Next Article in Journal
Validation of the 2H-SNIF NMR and IRMS Methods for Vinegar and Vinegar Analysis: An International Collaborative Study
Next Article in Special Issue
Rana chensinensis Ovum Oil Based on CO2 Supercritical Fluid Extraction: Response Surface Methodology Optimization and Unsaturated Fatty Acid Ingredient Analysis
Previous Article in Journal
Purification of Aqueous Media by Biochars: Feedstock Type Effect on Silver Nanoparticles Removal
Previous Article in Special Issue
Mangiferin Rich Products from Aphloia theiformis (Vahl) Benn Leaves: Extraction, Fractionation, Phytochemical Characterization, and Antioxidant Properties
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Review

Green and Sustainable Valorization of Bioactive Phenolic Compounds from Pinus By-Products

by
Pedro Ferreira-Santos
,
Elisa Zanuso
,
Zlatina Genisheva
,
Cristina M. R. Rocha
and
José A. Teixeira
*
CEB—Centre of Biological Engineering, University of Minho, Campus de Gualtar, 4710-057 Braga, Portugal
*
Author to whom correspondence should be addressed.
Molecules 2020, 25(12), 2931; https://doi.org/10.3390/molecules25122931
Submission received: 2 June 2020 / Revised: 22 June 2020 / Accepted: 23 June 2020 / Published: 25 June 2020

Abstract

:
In Europe, pine forests are one of the most extended forests formations, making pine residues and by-products an important source of compounds with high industrial interest as well as for bioenergy production. Moreover, the valorization of lumber industry residues is desirable from a circular economy perspective. Different extraction methods and solvents have been used, resulting in extracts with different constituents and consequently with different bioactivities. Recently, emerging and green technologies as ultrasounds, microwaves, supercritical fluids, pressurized liquids, and electric fields have appeared as promising tools for bioactive compounds extraction in alignment with the Green Chemistry principles. Pine extracts have attracted the researchers’ attention because of the positive bioproperties, such as anti-inflammatory, antimicrobial, anti-neurodegenerative, antitumoral, cardioprotective, etc., and potential industrial applications as functional foods, food additives as preservatives, nutraceuticals, pharmaceuticals, and cosmetics. Phenolic compounds are responsible for many of these bioactivities. However, there is not much information in the literature about the individual phenolic compounds of extracts from the pine species. The present review is about the reutilization of residues and by-products from the pine species, using ecofriendly technologies to obtain added-value bioactive compounds for industrial applications.

1. Introduction

Agroforestry industries are an important part of the manufacturing industry, and their growth can help to achieve the objectives of European Union (EU) industrial policy, acting in different strategic areas, such as increasing energy efficiency, deploying renewable sources, circular economy, bioeconomy, and natural carbon sinks [1,2]. Moreover, the development of these industries should also be in line with the 17 sustainable development goals by 2030 dictated by the United Nations; in particular, the agroindustry can directly impact on at least 4 of these goals related to the use of clean energy, industry innovation, responsible consumption, and climate action [3].
Nowadays, 5 billion tons of biomass residues from agroforestry and food industries are estimated worldwide and represent an emission for 3.3 billion tonnes of carbon dioxide each year [4,5]. In the EU, the total annual biowaste is estimated at around 100 million tonnes, generating a negative ecological impact [6].
One of the strategies for the reduction of generated environmental impact is the reuse of industrial biowastes to obtain new natural ingredients. Concomitantly, the growing interest in the development of effective/intensified processes and application of green technologies to obtain sustainable, ecological, safe and high-quality products has become a reality [7,8]. This idea is in close association with the principles governing the concept of green chemistry, which are mainly aimed at reducing wastes and promoting a more efficient use of energy and resources [9].
The decrease in the use of “non-recyclable” fossil derivatives and the increase in the use of biowastes and by-products is in the sights of the EU and the world, contributing to the reduction of the negative impact of processes in the environment and the fight against climate changes [2]. In this sense, the use of different plant by-products as sources of materials, biofuels, energy, and bioactive compounds has come to be explored following the concept of biorefinery, contributing to a circular economy [6].
The present review focuses on the appreciation of different green extraction strategies related to the recovery of high added-value compounds (such as polyphenols) from pine by-products, their potential bioactivities, and possible industrial applications.

2. Biorefinery and Lignocellulosic By-Products

Resources depletion, waste accumulation, and climate change are a combination of forces driving the need for the sustainable practices we are facing nowadays. Additionally, urbanization and population growth are causing the global energy demand to be in continuous rise. With the energy demand increasing, the necessity of detachment from fossil fuels and the transition to renewable resources is mandatory to reduce the environmental problems. Energy resources such as biomass, wind, and solar energy can meet the energy requirements if large-scale technologies are well developed [10]. In this sense, biorefinery is analogous to fossil fuel refinery. The biorefinery term dates back to 1980. Since then, several definitions have been considered. These definitions are based on the type of feedstock used, type of processes, and type of products obtained [11]. In general, the biorefinery concept is the synergy of technologies that convert biomass into their building blocks to produce a variety of biofuels, chemicals, and high added-value compounds. Hereof, the development of a sustainable process involves not only the use of biomass but also implies reducing the use of harmful chemicals, transition to greener processes, efficient use of energy, and elimination of wastes (Figure 1) [9].
Ethanol is a well-known biofuel product of the second generation biorefinery. Second generation or lignocellulosic biorefinery usually begins with the pretreatment of the biomass in order to increase the digestibility of cellulose, to solubilize the hemicellulose, and to relocate the lignin [12]. Pretreatments can be mechanical, chemical, physicochemical, or biological [13]. Afterward, to liberate the fermentable sugars (i.e., monosaccharide units) from the pretreated biomass, acid or enzymatic hydrolysis processes are applied [14]. Then, the fermentation of the obtained sugars to obtain ethanol can be carried out using microorganisms as yeast or bacteria [15,16], where, in an integrated biorefinery, ethanol can also be considered as a precursor for chemicals, hydrocarbon fuels, and aromatic compounds [17]. Hence, the research and development of sustainable processes are growing not only for biofuels but also for the high added-value compounds than can allow an economically viable process (Figure 1).
Currently, lignocellulosic biomass has been largely studied as a potential substrate in fermentation processes, and mainly for biofuel production. Nevertheless, innovative and new emerging technologies are being studied to increase the obtainment of high-value compounds of interest, particularly bioactive ones. The recovery of these of high-value compounds is linked to the biorefinery concept and the green chemistry principles. Lignocellulosic biomass (in which pine by-products may be included) is mostly considered as a residue from crops as straw, sugarcane bagasse, corn stover, and wood waste. Cellulose is the major component of the lignocellulosic materials, followed by hemicellulose and lignin. Cellulose is the world’s most abundant biopolymer made up of glucose units. Applications of cellulose extracted from lignocellulosics include the manufacture of cellulosic fiber and nanocrystalline cellulose in a wide range of industries such as automotive, textile, and medicine due to the strength on its structure, availability, modifiable surface, renewability, and low cost [18,19]. Hemicellulose is the second most abundant polysaccharide in lignocellulosic biomass mainly composed by monomeric units as xylose, mannose, arabinose, glucose, galactose, and acids such as uranic acid [20]. Hemicellulose and specific target products from hemicellulose are used in a variety of areas as food, medicine, and chemicals due to the biocompatibility and bioactivity properties they show [20]. Pine sawdust has been used to produce levulinic, formic, and acetic acid and furfural form hemicellulose extracted by steam explosion [21]. In addition, pinewood (Pinus eldarica) pretreated with dilute sodium hydroxide was used to produce ethanol from the pretreated solid where the solubilized hemicellulose fraction was used to produce biogas [22]. The third main component of lignocellulosic materials is lignin, which is an amorphous phenolic polymer that provides mechanical strength and rigidity to plants [23]. In the biorefinery process, lignin cannot be used as a substrate for fermentation as it contains no sugars. Therefore, a wide area of research is on lignin valorization. Lignin is mainly used to generate heat and electricity due to the high heating value although other applications are possible, including the use as a precursor for carbon fiber synthesis, resins, and low molecular weight aromatic and phenolic compounds [24,25]. Nowadays, the modern polymer industry from natural sources of aromatic compounds is limited due to the high prices of the final product. Here, lignin plays an important role, since phenolic compounds can be obtained from lignin deconstruction [26].
Historically, wood has been a major energy source for human beings. Forest biomass is the most abundant feedstock on earth, representing 89.3% of the total biomass [27]. In Europe, forest area is one of the most important renewable resources, representing near 5% of the world’s forest and covering 43% of its land, comprising close to 182 million hectares of forest. Forest is also considered as a resource for improving life quality and job generation [28]. Wood biomass can be densified into solid fuels, as pellets, or converted into heat, electricity, biofuels, and other bioproducts through a variety of chemical, thermochemical, and biochemical processes [29]. On the other hand, the lumber industry generates a considerable amount of waste that includes leaves, barks, sawdust, chips, cones, resins, and branches. These residues are not usually well valued and are thrown out, burned, or used for animal bedding, although they can be a profitable source of high added-value compounds [30]. Therein, wood biomass residues increase their overall value due to the metabolites that are present in lower abundance compared with cellulose, hemicellulose, and lignin. These extractive compounds combine alkaloids, waxes, phenolics, pectins, resins, and essential oils [31], and they are of great importance considering the wide industry applications, more precisely, in food and pharmaceutical industries due to the antioxidant, antimicrobial, anti-inflammatory, and antitumoral effects they show [32].

3. Pine as Feedstocks

This work is mainly focused on the valorization of the Pinus species (and its by-products), which are evergreen trees of resinous conifers group from the Pinaceae family. In the EU, there are more than 14 different species, representing one of the largest forest occupations. Table 1 describes the main Pinus species distributed in the European countries according to the “European forest genetic resources program (EUFORGEN)” [33]. In Portugal, pine forests are the third forest formation after eucalyptus and cork oaks, with an area of approximately 1 million hectares, representing an important part of the total forest, about 23% [34].
The chemical composition of pine and its constituents (wood, bark, leaves, cones, seeds, and resin) varies depending on the Pinus tree and also on many other factors, such as genotypic, ecological, and seasonal, among others [35]. The methodology used for the determination of chemical composition of plant resources is also a factor to consider, since different methods lead to different results [36].
The general chemical/nutritional composition of pine by-products has been described by several authors (wood [37,38,39,40,41,42], bark [43,44,45,46,47], needles [48,49], cones [41,50], seeds (nuts) [51,52,53], and resin or oleoresin [54,55]) and is summarized in Figure 2.

Pine Applications

At present, agroforestry residues and by-products are mainly used as combustion feedstock for biofuels production [56]. The most important biomasses are obtained from lumber industry (bark and sawdust) or forest activities, the residues from farms and agro-business, the organic fraction of municipal solid wastes, and the plants deliberately grown for energetic purposes. In this sense, it is important to reduce and give a “second life” to these residues, moving to “zero waste”.
The Pinus plant is very important economically, as it is considered good feedstock for the bioeconomy (Figure 1) [57]. In its natural environment, it has an important protective function, such as improving water infiltration, preventing soil erosion on dry slopes, and serving as a windbreak [33]. Trees are also used as ornamental plants in urban and industrial contexts. Other uses include Christmas trees and fuelwood.
Interestingly, in a study by Ehn and co-workers [58], it has been found that pine forest aroma (for its content in volatile compounds, terpenes) can limit climate change, preventing the global warming.
The main industrial activities are related to the usage of pine wood and wooden products, including sawmills, wood panels, cellulose pulp and paper production, wood fuels, carpentry, packing, and wood furniture [33]. These feedstock, their components, and their by-products are considered a good source for wood biorefineries, transforming the lignocellulosic fractions into biofuels, chemical products, and composite materials, as previously mentioned [57].
Pine bark, the by-product obtained in larger quantities that is produced when wood is transformed, is almost exclusively used as fuel, being also subjected to composting to filling substrate in nurseries, utilized for cover in public gardens, or simply thrown away on landscapes [44,59]. Nowadays, this by-product has been used as low-cost and green alternatives waste-based biosorbents for the removal of a wide range of water pollutants [60].
The pine leaves (needles) are normally used in agriculture to enrich the soil, and the seeds are used for human consumption because they are highly nutritious and much appreciated by consumers in cooked/prepared dishes (food industry) or simply as edible pine nuts. The resins, a product resulting from the exploitation of these species, are more regularly used as a sealant, glue, varnish, and also as a solvent and paint thinner (turpentine oil) [55,57,61].
In addition to the “traditional” uses of these by-products, it is important to take advantage of these bio-resources to create high value-added products.
Currently, the agroforestry by-products have been increasingly exploited to isolate biocompounds with high industrial interest. Studies using natural matrices as a potential source of bioactive compounds have been published in recent decades [7,62,63,64,65,66,67]. For instance, in a new review paper [68], the authors report that in addition to fruits and vegetables, tree barks are rich in phenolic compounds with excellent biological properties (such as antioxidant, immunostimulatory, anticancer, antibacterial, anti-inflammatory, antimutagenic, etc.) and may used to obtain functional ingredients.
Pine bark is one of the most sought after sources of antioxidant biocompounds of natural origin. The extracts obtained from this by-product are mostly composed of phenolic compounds with high biological activity [46,59,62,69,70,71,72]. Nowadays, there are numerous studies reporting the applicability of pine bioactive extracts in various areas, such as health care, food, agrochemical, and others [73,74,75]. One of the most promising applications for these extracts is in the preservation and enrichment of foods, thus replacing synthetic antioxidants, as well as a nutraceutical, cosmeceutical, or pharmaceutical.
The pine wood/sawdust extractives, rich in phenolic antioxidant compounds, have a potential for food and pharmaceutical applications, such as preservatives or nutraceuticals [40,76].
Pine tars, a by-product of pine wood and bark, are known to contain tricyclic diterpenoid resin acids, tricyclic diterpene hydrocarbons, alkylphenanthrenes, and fatty acids. This water-resistant by-product has a wide range of applications, for example, as a multipurpose adhesive, sealant, and in medicine [77,78].
Knowing the chemical composition and physicochemical properties, pine seeds or nuts appear to have a positive effect on human health [52,53]. The seed lipids, rich in linoleic acid, have a beneficial effect on blood pressure and cholesterol. The fatty acid composition and the relatively high polyphenol content present high protection against oxidative stress. In this sense, pine seeds can potentially be used in the food industry and other non-food industries, such as pharmaceutical and cosmetics [79,80,81].
Oleoresins are widely used in the synthesis of perfumed compounds for cosmetics, essences as additives for food and beverages, food protection (antimicrobial), bioinsecticides (high repellent activity), tapping green chemicals, biofuels, and carbon sequestration from multipurpose trees [54,55,57,61].
Interestingly, this search for functional extracts, new natural molecules, and the creation of new high value-added products has increased the use/study of agroforestry by-products and residues, including pine bark, sawdust, leaves, seeds, and resin. This makes it possible to potentially bring these “wastes” back to the market.

4. Extraction Processes for Phenolic Compounds Recovery

The recovery of bioactive and functional purified biomolecules or extracts from plant materials is an important step to enable the reuse of natural resources for subsequent application in pharmaceutical and cosmetic products, food enrichment and preservatives, dietary supplements, and nutraceuticals.
The extraction process of natural extracts depends on several factors, including the applied extraction technique, the parameters associated with the technique (such as temperature, time, and the extraction solvent), and the raw materials composition [63]. It is known that the phenolic compounds are metabolites present in the cell vacuoles [82]. Therefore, it is also important to promote the opening of pores or even the rupture of the cell wall to facilitate the release of the compounds into the extraction medium.
In this sense, it is important to study all variables of the process in order to maximize the potential of the extraction method, developing a highly efficient process [8]. On the other hand, all variables in the process have to make it possible to obtain a safe and high quality final product (eco-extract), in addition to maximizing the extraction of the compounds of interest. Figure 3 illustrates the main principles of an efficient extraction process, following the concept of green extraction.

4.1. Extraction Solvents

The reduction use of hazardous solvents is also considered one of the priorities of the EU policy for the 2010 to 2050 period [7]. Nowadays, extraction using conventional organic solvents is the most commonly used procedure to prepare extracts from plant materials due to their ease of use, efficiency, and wide applicability. The efficiency of the extraction methods depends on the choice of the solvent, since solvents with different polarities are needed for the isolation of compounds with different chemical constitution. In addition, it is difficult to define a single method for the efficient extraction of all compounds, since the polarities of the molecules to be extracted vary [63].
A suitable solvent has to be able to obtain safe and high-quality extracts and to preserve the biological effects of the extracted compounds without exhibiting toxicity when consumed. Furthermore, it should be recyclable and reusable, preventing negative environmental effects. Other parameters, such as flammability, explosiveness, volatility, mass transfer, and (in)ability to dissociate the complex extract should be considered [65]. The extraction yield depends not only on the solvent used but also on several other factors such as sample/solvent ratio, temperature, extraction time, stirring, and raw material composition [83].
Conventional solvents from “non-natural”/petroleum resources, such as methanol, ethanol, acetone, ethyl acetate, dichloromethane, hexane, etc. and their aqueous solutions have been used for the extraction of bioactive compounds from plant materials. Several studies have been done demonstrating the importance of these solvents in the recovery of natural molecules and active extracts from different plants and by-products [65,84,85,86], including the lignocellulosic by-products [87]. Researchers also studied the influence of these different solvents in obtaining antioxidant phenolic compounds from pine by-products, and depending on the solvent used, the extracted fraction (extract composition) is different [59,85,88]. For example, in a work by Venkatesan and collaborators [85], the impact of different extraction solvents (such as ethanol, methanol, isopropanol, acetonitrile, and acetone) was analyzed to obtain phenolic extracts with antioxidant activity from Pinus densiflora bark. Their results showed that low concentrations of ethanol and acetonitrile are favorable for the extraction of phenolics with high antioxidant activity. In another study, using Pinus niruri, methanol was more efficient than other solvents such as ethanol, hexane, and ethyl acetate, showing an enhanced extraction rate of phenolic and flavonoid compounds with higher biological activities [88].
It is known that water is an efficient solvent for the extraction of various compounds, due to its properties and thanks to the fact that water is easily available, safe, non-toxic, non-flammable, and environmentally friendly [8]. In this sense, it is considered the cleanest/greenest solvent (apart from the use of no solvent, which is the greenest), according to the principles of green chemistry [64,89]. However, it is not suitable for the extraction of less polar substances.
Other possible environmental friendly solvents’ option is to replace petroleum-based solvents by “bio-solvents”. For instance, “bioethanol” can be produced from bioresources, by fermentation. This second-generation solvent could be made cost-competitive by the development of biorefinery-based processes for the integral use of lignocellulosic biomass, substituting ethanol obtained from petroleum derivatives [90].
As alternatives to conventional solvents, the use of green solvents such as ionic liquids (ILs) and natural deep eutectic solvents (NADES) is emerging, in order to make the extraction process eco-friendly and more effective [91]. In general, ILs and NADES are derived from cheap, abundant, low toxic, and biodegradable natural components [6,7]. NADES can be defined as “mixtures of pure naturally occurring compounds that present an eutectic point temperature below an ideal liquid mixture” [6,92]. ILs are liquid molten salts at temperatures below 100 °C composed by cations and organic or inorganic anions with exclusive and adjusted physicochemical properties [93].
However, a lack of information on the biological activity and toxicity of the obtained extracts limits the use and industrial applications of ILs and NADES [7], leading to these solvents not being regulated by the Federal Drug Administration (FDA) [94]. Furthermore, although they can be tuned for enhanced affinity toward the compound of interest, their separation from the final mixture may be hindered by the high boiling point characteristic of these solvents.
Murador and collaborators [95] summarize the main chemical constituents of these ILs and NADES and mention some works where they are applied in the extraction of antioxidant compounds, such as phenolic compounds and carotenoids, among others. Specifically, ILs and NADES have been applied to the phenolic compounds and other antioxidant compounds extraction from lignocellulosic biomass and agri-food wastes [4,6,93,96,97,98].
In the case of pine plants as feedstock, the process of extracting bioactive compounds with added value (such as phenolics) using these green solvents is not widely explored. In a recent study, ILs were combined with enzymes and microwave technology to promote cell wall disruption for the extraction of essential oil and procyanidins from pine cones of Pinus koraiensis [99]. However, there are no reports using ILs and NADES as alternative solvents for extraction of bioactive molecules of other parts of pine plant, despite the advantage they showed for obtaining functional compounds in other lignocellulosic residues.

4.2. Extraction Technologies

Conventional methods of extraction, such as the solid–liquid method, hydrodistillation, maceration, and Soxhlet require the use of large amounts of water or organic solvents, agitation, long extraction time, high temperatures, and energy consumption, as well as the generation of a considerable quantity of wastes [8,100,101].
The need for obtaining greener, sustainable, and viable processes has led scientists and industries to develop new processes in full correspondence with the green extraction concept [102,103]. In this context, the search for alternative extraction technologies with environmental and economic advantages, taking into account the characteristics of the final products has emerged [104]. As a result, techniques such as ultrasound-assisted extraction (UAE), microwave-assisted extraction (MAE), supercritical fluid extraction (SFE), pressurized liquid extraction (PLE), and ohmic heating (OH) electrotechnology have been developed, optimized, and applied to improve the extraction process of antioxidant phenolic compounds from plant resources, such as pine by-products (Table 2).
In the following sub-sections, a brief introduction to these extraction technologies and some examples of their application in obtaining phenolic compounds from pine by-products will be presented.

4.2.1. Ultrasound-Assisted Extraction

Ultrasound produces high-intensity sound waves (typically higher than 20 kHz) [104]. The operation mechanism of UAE is based in pressure variations that form microbubbles resulting in microturbulence and a high collision of particles. The collapse of microparticles caused by ultrasound waves can promote higher penetration of the solvent into the cellular material causing the cell walls disruption and increasing the release of intracellular compounds into the extraction medium [105,106]. UAE is an alternative technology with advantages compared to conventional techniques, since less processing time, low solvent usage, and lower extraction temperatures are required, preserving heat-sensitive compounds. In addition, it leads to an increase in extraction yield, requiring less energy in the process [106]. Due to its advantages, ultrasound technology is mentioned as an eco-friendly and cheap process and can be easily implemented to extract phenolic compounds from plants and plant by-products [76,107,108,109,110].
In the last decade, UAE has been used to obtain extracts rich in phenolic compounds from pine by-products. In a study of Liazid and co-workers [111], UAE was used to obtain phenolic extracts from seeds of two pine species (Pinus maritima and Pinus d’Alpes). The results of this work showed that the application of ultrasound waves, using water as a solvent at 75 °C during 20 min, doubled the recovery of phenolic compounds compared to a conventional maceration technique, increasing the antioxidant activity of these extracts. Using the bark of the Pinus radiata as a raw material, Aspé and collaborators [112] verified that the synergetic effect of ultrasounds (35 kHz/85 W) with acetone 70% (v/v) allows the formation of pores in the matrix cells, promoting the rapid rupture of the cell wall, facilitating the extraction of phenolic compounds, and drastically reducing the extraction time (from 180 min for conventional extraction in a water bath or Soxhlet, for 6 min when using UAE).
In another study, authors used ultrasound technology in combination with methanol 70% (v/v) as a solvent to extract phenolic compounds, such as flavonoids from leaves (needles) of four different pine species (Pinus peuce, P. nigra, P. mugo and P. sylvestris) [113]. UAE proved to be a potential tool for the sustainable recovery of phenolic compounds from pine leaves, without using temperature in the process.
Recently, Meullemiestre and co-workers [76] reported that the UAE, in addition to increasing the extraction of phenolic compounds from maritime pine wood (sawdust waste) by 40% compared to conventional extraction techniques (solid–liquid), also allowed reducing the time of the process. On the other hand, they also reported that UAE is a scalable technique and can be applied industrially to obtain bio-functional extracts.

4.2.2. Microwave Assisted Extraction

MAE is a heating process using electromagnetic waves of frequency between 300 MHz and 300 GHz that interact with samples to extract analytes from a matrix to a solvent. The microwave irradiation increases the internal pressure of the plant cells by heating the cells from the inside, leading to cell disruption and releasing the compounds of interest. Some of the advantages of MAE are a lower time of extraction compared with other extraction processes, the possibility of multiple extractions, low solvent volume, an attainment of high temperatures, and more effective, uniform and selective heating [107,114]. To have better extraction yields, it is important to consider the capability of the solvent to absorb microwaves, as it can be a drawback when the solvent lacks the capacity of energy absorption. Furthermore, the thickness of the sample to be heated may also be a drawback, particularly in the scalability of the extraction process, as the ability of microwaves to penetrate a sample is limited. Liazid et al. [111] studied the extraction of phenolic compounds from Pinus pinaster seeds using water as solvent and demonstrated that MAE produces extracts with great polyphenols content, since it can achieve high temperatures, which is a decisive factor in phenolic compounds extraction, as most of these processes are temperature dependent. In this work, the polyphenolic extracts obtained at 75 °C demonstrated high antioxidant activity. In another work, the extraction time to obtain phenolic compounds from Pinus radiata bark was reduced by 98.3% using MAE compared with the Soxhlet technique process, which required 3 h [112]. In addition, the extraction time was significantly reduced in a study performed by Chupin et al. [115] using MAE to extract tannins, flavonoids, and sugars compared with hot water-based extraction. The time was reduced to 3 min instead of 2 h. Moreover, they compared different bark particle sizes and conclude that small particle size (400 μm) improved the amount of extracts obtained. Therefore, MAE can be considered as a simple and rapid method to extract phenolic compounds from Pinus bark. The extraction of other valuable pine faction, such as oil or sugars, may also be improved [72].

4.2.3. Supercritical Fluid Extraction

The SFE process enhances solvents’ behavior by working at pressures and temperatures near or above the critical point. Supercritical fluids exhibit different physicochemical properties which are advantageous in solvent extractions: they possess gas-like properties, such as diffusion, viscosity and surface tension, and liquid-like density and solvation power. This mixed behavior, as both liquid and gas, of the solvent in the supercritical region facilitates and enhances mass transfer [116]. Some solvents used for SFE are ethane, argon, methanol, water, and carbon dioxide, being this last one the most commonly used due to its non-toxicity, safety, easy removal from the extract, and low critical temperature (near room temperature, which is particularly important for termolabile compounds). However, for polar polyphenols extraction and owing to its non-polar character, CO2 is usually used in combination with co-solvents such as solvents as ethanol. In this way, the solvating power of CO2 is increased [117]. Typically, for polyphenols extraction, fractionated SFE is performed, where a first extraction is carried out usually with supercritical CO2 followed by a second extraction adding a polar solvent to increase the solubility of the phenolic compounds. For example, Braga et al. [118] performed a fractionated SFE of maritime pine bark; in the first extraction step, low-polarity CO2 soluble compounds were removed, and in the second step, they added 10% EtOH into the system to extract polar compounds and obtained a higher recovery yield of catechin and epicatechin than with Soxhlet extraction. Since the addition of EtOH enhances the extraction of polyphenols, Seabra and co-workers [119] studied the influence of the CO2:EtOH ratio and concluded that a 30:70 ratio was the most appropriate mixture to obtain the highest extract from maritime pine bark in the shortest time. An optimization study of SFE carried out by Ghoreishi et al. [120] achieved a 34% taxifolin recovery from Pinus nigra bark using ethanol as solvent at a flow rate of 1/20 of CO2. They also proposed a prediction model that can be used to scale up the SFE process for taxifolin extraction, thus reinforcing that SFE is a suitable process for polyphenols extraction. Therefore, SFE proved to have advantages over conventional extraction processes by reducing the amount of solvent used, being manageable in a way that specific compounds can be extracted and operating at low temperatures, which preserves the quality of the extracts. However, the final prices of products obtained with high-pressure technologies tend to be higher compared with conventional processes.

4.2.4. Pressurized Liquid Extraction

The PLE method is also referred to as accelerated solvent extraction, pressurized solvent extraction, and enhanced solvent extraction [36,106]. This technology is based on the use of liquid solvents at temperature and pressure values above the atmospheric boiling point and below the critical point values, decreasing the viscosity of the solvent, promoting accelerated dissolution kinetics, and increasing the solutes’ solubility. It also increases mass transfer rates and decreases surface tension, facilitating the penetration of solvents into the matrix, changing its structure, and disintegrating it [106,121]. For example, in the case of water as an extraction solvent in PLE (subcritical water extraction), the water is heated over 100 °C increasing pressure above atmospheric conditions. In the particular case of water, the dielectric constant decreases and water can reach behaviors similar to organic solvents [4,106,122]. Moreover, the possibility of using organic solvents decreases the polarity of the extraction fluid, making the extraction more selective and directed to the compounds of interest, such as phenolic compounds [122]. This method is considered a viable eco-friendly alternative to replace other extraction techniques, such as SFE or Soxhlet, which have the disadvantages of being expensive and, in the last case, of being slow and using large amounts of organic solvents.
In recent years, PLE has been widely applied in the extraction of antioxidant compounds from different plants, by-products, and agro-industrial waste [87]. Moreover, PLE has been used for recovering antioxidant phenolic compounds with industrial potential from different parts of pine plants [81,111,123]. Lixia et al. [81] investigated the influence of different extraction technologies in the antioxidant compounds of oils from Pinus koraiensis nuts. The results of this study concluded that subcritical extraction preserves the quality of pine nuts oil, containing considerable amounts of fatty acids, tocopherols, and tocotrienols. In addition, Liazid and co-workers [111] applied subcritical water technology at 100 °C and 4 Mpa conditions to obtain phenolic extracts from seeds of Pinus maritima and Pinus d’Alpes. In another work using pine leaves (P. taiwanensis and P. morrisonicola needles) as raw material [123], the combination of enzymes and ethanol using the PLE technique showed interesting results in obtaining bio-functional extracts with high amounts of phenolic compounds.

4.2.5. Ohmic Heating Extraction

OH is a non-pulsed electrotechnology based on the conversion of electric energy into thermal energy with technological purposes [124]. This technique is based in the Joule effect (heat is generated inside a conductive matrix, in the presence of an electric current) and provides a fast and homogeneous heating rate in a semi-conductive material (0.1–10 S/cm). One advantage is the reduction of energy consumption in comparison to other heating extraction techniques [100,125]. The voltage applied in the OH process normally varies between 400 and 4000 V (electric field from 0.001 to 1 kV/cm), and the heating rates achieved depend on the power supply output, the equipment (reactor design), and the properties of the matrix (such as conductivity and viscosity) [124].
Furthermore, this “green” technology allows to reduce the ecological impacts caused by the extraction processes, decreasing the water use and waste generation [126]. OH can further induce not only thermal but also promote the formation of pores (electro-permeabilization) in cell membranes, showing a promising potential to obtain extracts that are more sterile [100,127]. This phenomenon is considered to be relevant in the extraction of bioactive compounds from different agri-food wastes and forestry by-products [125,128,129,130].
This novel and emergent electrotechnology has been proposed for the extractions of phenolic compounds from Pinus pinaster bark [59]. Interestingly, OH (5–15 V/cm) in combination with a hydroethanolic solvent (EtOH 50%) showed a marked increase in the extraction yield of antioxidant phenolic compounds compared to conventional solid–liquid extraction with the same solvent in a thermal bath (approximately 90 to 40 mg gallic acid equivalent /g bark, respectively). Specifically, the individual phenolic compounds such as taxifolin, quercetin, narigenin, apigenin, resveratrol, and some phenolic acids are most benefited by ohmic extraction. In this work, the effect of electric fields on the pine bark tissues disruption was visible, and a reduction of more than 50% in energy consumption compared to conventional heating was achieved.
Besides OH, pulsed electric fields (PEF) could also be an interesting option to explore, as it acts by destroying the cell wall and plant tissue structure and facilitating extraction. Though to our knowledge it has never been applied to pine matrices, it was successfully applied in the extraction of different compounds from many agri-food wastes (e.g., Norway spruce bark, tomato, and potato peels, among others) [131,132,133].

5. Polyphenols as Extracted Biocompounds

Polyphenols are chemical compounds distributed in herb plants, vegetables, and fruits with a wide range of applicability. Currently, more than 8000 phenolic compounds are known, and among them, 4000 flavonoids have been identified. The polyphenols are secondary metabolites essential for the growth and development of the plants [68]. They also protect the plants against insects and other animals. Polyphenols in plants are involved in functions related with sensory properties such as color, bitterness, and astringency.
The common characteristics between all polyphenols are the presence of benzene ring(s) and hydroxyl groups. However, they are highly diverse and can be divided in several sub-groups. There are different ways of categorizing these compounds, based on their source of origin, biological function, or chemical structure. According to their chemical structure, polyphenols can be divided in two main groups: flavonoid and non-flavonoid. The non-flavonoid group incorporates the phenolic acids (hydroxybenzoic acids and hydroxycinnamic acids), stilbenes, and lignans. The flavonoids include compounds from the groups of anthocyanins, flavanols, flavonols, flavones, flavanones, isoflavones, and tannins (Figure 4). Phenolic acids are present in the free and bound form and can be divided in two main groups: hydroxybenzoic acids and hydroxycinnamic acids. Hydroxybenzoic acids are based on a C6–C1 structure and include protocatechuic, vanillic, gallic, and syringic acids. Hydroxycinnamic acids are compounds with a three-carbon side chain (C6–C3) and include coumaric, caffeic, and ferulic acids [135]. The demand of phenolic acids is very high in the industries as they work for precursors of other significant bioactive molecules, which are needed on regular basis for therapeutic, cosmetics, and food industries [136]. Phenolic acids are also available commercially as dietary supplements.
Stilbens are small number of compounds, composed of a 1,2-diphenylethylene nucleus with some hydroxyls. The main representative of this group is the resveratrol with strong antioxidant and anti-inflammatory properties. Lignans are produced by the oxidative dimerization of two phenylpropane units and are found in many plants, in particular in flax seeds [135].
The group of flavonoids is the most studied of both groups. Anthocyanins are polyphenols that determine the color of plant raw materials, imparting them a red, blue, purple, or pink color [137]. Tannins are highly polymerized substances and one of the most widespread organic compounds in nature. They have a relatively high molecular weight. Tannins can be further divided into two sub-groups, including hydrolysable tannins and condensed tannins [135]. The hydrolysable tannins are subdivided to gallotannins and ellagitannins, while condensed tannins are oligomers or polymers of flavan-3-ol monomers, which are linked by an interflavan carbon bond.
The distribution of the polyphenols in plants is not uniform. The phenolic content depends on factors such as the stage of ripening, time of harvest, and environmental factors [137]. In plants, the majority of polyphenols are linked with different sugar units at different positions of the polyphenol skeleton.
Before extraction of the polyphenol, the raw material must be collected, properly transported, and stored. The handling of the sample before extraction is extremely important, as polyphenols are unstable molecules that can be easily oxidized. They can be easily deteriorated by light and high temperatures. Before storage, normally, samples are dried, frozen, or lyophilized. The extraction of phenolic compounds from plant materials depends on the nature of the sample matrix and also on the chemical properties of desired phenolic compounds, such as the number of aromatic rings and hydroxyl groups in its structure, polarity, and concentration [136].
The main solvents used for the extraction of these compounds are water, methanol, ethanol, acetonitrile, and acetone, or their mixtures with different proportions of water. Depending on the solvent used for the exaction, a mixture of phenolics soluble in the solvent will be extracted from plant materials. The choice of solvent used influences the phenolic final composition and bioactivity of the extract [59].
There is no universal extraction procedure suitable for the extraction of all plant phenolics [122]. For the estimation of total phenolics, flavonoids, and anthocyanins content, spectrophotometric methods are used [100,129]. Although these methods are rapid and simple, they do not give any information about individual compounds. To be identified and quantified, the phenolic compounds must be separated first. The most used method for polyphenol separation is the high-performance liquid chromatography (HPLC) coupled with a diode array detector (DAD). For the unequivocal identification, a mass spectrometric detector is usually used after the chromatograph (LC/MS).
The search of functional products enriched with polyphenol extracts has been exploding. The aim is to increase the products’ antioxidant activity, giving rise to one or more types of biological activity [111]. Polyphenols are known to have diverse bioactivities. They are strong antioxidants, together with the vitamins and carotenoids, acting against the oxidative stress caused by reactive oxidative species. This is due to the hydroxyl group present in the molecule of the polyphenols. The hydrogen ion is dissociated and neutralizes the free radicals and other reactive oxygen species, scavenging the free radicals [138]. In that sense, the antioxidant power of a phenolic compound depends mostly on its chemical structure: for the phenolic acids, the number of hydroxyl groups in the molecule is the main driver [139]; in other polyphenols, the double bonds of the benzene ring and the double bond of the oxo functional group are also important [140].
There is controversy in the studies trying to connect the antioxidant capacity with the total phenolics content of a sample. In some studies, the total phenolic compounds were highly correlated with the antioxidant power of the samples [59]. In others, no significant correlations between total phenolic compounds and antioxidant power were found, such as in the case of wine samples [139]. Moreover, some groups of polyphenols were found to be more correlated to the antioxidant capacity of the extracts than others. It was concluded that the antioxidant activity has very strong correlation with anthocyanins and total procyanidins content. However, no correlation was found between the antioxidant capacity and the content of flavonols, flavanols (sum of (+)-catechins and (−)-epicatechins), and total gallotannins [137]. In addition, it was concluded that procyanidins and anthocyanins are included in the polyphenols responsible for the total antioxidant capacity of the investigated rhubarb varieties. Another study concluded that flavonoids and phenolic acids, as the main components of R. maderensis, are responsible for its antioxidant properties [141].
Moreover, extracts from medicinal plants in which the polyphenols are the main constituents are also known to have anti-diabetic properties [142]. For instance, R. maderensis extracts exhibited important inhibitory capacity toward key enzymes linked to type-2 diabetes and obesity [141].
Polyphenols have become target study compounds in the fight against cancer, as they are natural compounds that are safe and of low toxicity. Polyphenols are able to prevent cancer by reducing or blocking the harmful effects of free radicals on cells through their antioxidant properties [143]. Phenolic extracts of vine pruning residues demonstrated a decrease in the cell proliferation of four different cancer cell lines [144]. Polyphenols from oolong and black tea demonstrated various health benefits including anticancer, antioxidant, anti-cardiovascular, antimicrobial, anti-hyperglycemic, and anti-obesity activities [145]. Polyphenol extracts rich in β-carotene and rutin showed to have not only antioxidant but also anti-inflammatory effect [146]. Polyphenol extracts also demonstrated antimicrobial activity [144,147].
Lately, a lot of studies refer to the wood bark as an important source of polyphenols with a potential biological effect [68]. Extracts from pine contain a considerable amount of flavonoids and condensed tannins [115]. The amount of these active constituents varies depending on the pine specie and geographical location of growth [71]. Moreover, the solvent polarity and different methods of extraction used contribute to the different content in natural antioxidant and antioxidant activity of the extracts [88]. It is very important to ensure the chemical stability of polyphenols during the extraction processes, using mild extraction methods. The emergent technologies mentioned before in this review are important options to be considered [111].
As previously mentioned, different parts of the pine can be used for the extraction of polyphenols compounds (needles, seeds, bark, and cone), but the most studied is the pine bark. In Europe, there are 14 different known pine species. Although all extracts from pine have high amounts of total polyphenols regardless of the solvent, the method, the plant part or pine species used, there are differences in the concentrations and type of the individual compounds as well as in the strength of the bioactivities. This is due to the natural variability such as genotype, differences in growing and harvesting conditions, climate, soil type, etc. In a comparative study of three different species of pine bark extracts (P. pinea, P. pinaster, and P. halepensis), it was found that all extracts had induced cell-cycle arrest and apoptosis in Caco-2 cells (human colorectal adenocarcinoma). However, the extracts were different in terms of individual polyphenol compounds and the strength of the bioactivities. The extract of P. pinaster was the one with the highest biological activity and the one with the highest amount of procyanidin B2. The most abundant compounds in the pine samples were taxifolin and catechin. Procyanidin A2 was only present in samples of P. halepensis. Procyanidin B1 was found in P. pinea in concentrations two times higher compared to the other two species of pine in the study. Extracts of P. pinaster had the highest antioxidant capacity, while P. halepensis had the lowest antioxidant capacity [148].
Barks of various pine species from different regions of Turkey (P. pinea, P. sylvestris, P. nigra) and Germany (P. parfliora, P. ponderosa, P. sylvestris, P. nigra) were compared in terms of their flavonoids content and antioxidant activity [71]. The highest antioxidant activity was achieved by P. pinea (81.0%), while P. parfliora showed the lowest activity (31.9%). Moreover, a very good correlation was found between the antioxidant activity of the extracts and its total phenolic compounds, i.e., species P. pinea had the highest total phenol content, while P. parfliora had the lowest total phenol content. The main polyphenol compounds found in all extracts were catechin, catechin gallate, epicatechin, and taxifolin. The P. pinea had the highest amount of individual phenolic compounds.
Four different methods (maceration with magnetic stirring, ultrasound-assisted extraction, microwave-assisted extraction, and extraction with pressurized liquids) were used to obtain the extracts of seeds from P. pinaster. A direct relationship was found between the antioxidant activity and total polyphenol content of pine seeds extracts. Moreover, it was concluded that high extraction temperatures in any of the methods used brought lower bioactivities [111].
Needle and twig extracts of five different pine species (P. brutia, P. halepensis, P. nigra, P. pinea, and P. sylvestris) together with Pycnogenol®, a pine bark commercial extract, besides the strong antioxidant activity presented cholinesterase inhibitory potential [149]. Extract from Pinus brutia bark had 3.3-fold more total catechins and 9.8-fold more taxifolin than Pycnogenol®, showing strong anti-inflammatory activity [150]. A total of 17 phenolic compounds (mainly flavonoids) were identified in the needles of four pine species, P. peuce, P. nigra, P. mugo, and P. sylvestris from the Macedonian flora [113]. The authors concluded that there are no differences between the studied species of pine in terms of polyphenols. Taxifolin and quercetin were not found in any of the Macedonian pine species.
Moreover, the impact of the particle size of pine bark (between 0.05 and 1 mm) in the extracts was evaluated [115]. Mass transfer kinetics and the access of the solvent to the soluble components depends on the particle size [76]. The particle size has a direct effect on the amount of the polyphenol extracted. The smaller the particle size is, the more extracts are obtained (best results were registered for size 0.4 mm). However, there is no impact on the nature of the extract and on the types of the compounds extracted [115]. There is a lower limit of the particle size beyond which the quantity of extracted polyphenols decreased. It was registered that very fine particles stayed in suspension at the surface of the solvent and therefore were not subjected to proper extraction [76].
The extraction of polyphenols would also depend on the solid/liquid ratio. Meullemiestre et al. [76] found the optimum ratio to be about 6 g of dry material/100 mL; when concentrations were higher than 7.5 g of dry material/100 mL, the maritime pine wood absorbed all available liquid.
Eighteen phenolic compounds were identified in the extracts of P. pinaster by Ferreira-Santos and co-workers [45,59]. In one of the studies, the authors tried to understand the action of the type of solvent (water and ethanol) and method of extraction (conventional or ohmic heating) over the chemical profile of the extracts. Extracts made with the different solvents were found to be statistically different in terms of content of phenolic compounds [59]. The antioxidant activity of the extracts were always higher in the hydroethanolic extracts comparing with the aqueous extracts. Moreover, significant correlations were found between total phenolic content and antioxidant activities of the obtained extracts [59]. In a second study, from the same author, pine bark extracts made with different concentrations of ethanol (from 0% to 90%) were evaluated for their bioactivities (antioxidant, antimicrobial, and antidiabetic) and in vitro cell viability (in normal and cancer cell lines). The study demonstrated that the pine bark extracts have high potential antioxidant, antidiabetic, and antimicrobial activities, especially when made with 50% and 70% of ethanol [45]. Moreover, the authors concluded that pine bark extracts act selectively on cancer cells, as these are negatively selected and the non-tumor cells are not.
In general, both studies [45,59] showed that the compounds with the highest concentrations in all samples were ellagic acid and taxifolin. The concentrations of ellagic acid accounted for between 9.0% and 50% of the total phenolic compounds, while taxifolin accounted for between 15% and 42% of the total phenolic compounds. Individual concentrations of phenolic compounds such as catechin, taxifolin, quercetin, caffeic acid, o-coumaric acid, ferulic acid, and ellagic acid in the extracts made with 50% ethanol were almost twice as high as in the correspondent extracts obtained with water.
There are not many studies showing the identification and even less studies showing the quantification of polyphenols in extracts from Pine species. The extracts are obtained mostly from the pine bark, and fewer are obtained from needles (Table 3). The chemical composition of the extracts depends on the type of pine used (species, location), on the part of the plant, on the method of extraction, and on the solvent. For example, the main group of polyphenols compounds found in the P. sylvestris is the group of stilbenes [151], while in P. pinaster, the main group of compounds are the flavonoids [59].
As one can see from Table 3, the main polyphenol compounds found in extracts from pine needles are p-coumaric acid and epicatechin, in pine seeds eriodictyol and taxifolin, and in pine bark catechin, gallic acid, and taxifolin. In the following text, we summarize the bioactivities of the individual compound found in the extracts of pine species. However, we want to draw the attention of the reader to the idea that, in terms of expressing biological activities, the polyphenols act as group of compounds rather than individual compounds, and synergistic and/or antagonist or simply different effects may be found.
The p-coumaric acid together with ferulic and caffeic acids are the most common hydroxycinnamic acids in pine-based extracts. The hydroxylation of p-coumaric acid results in the formation of ferulic acid, while the oxymethylation of p-coumaric acid produces caffeic acid, respectively. These phenolic acids are used as precursors in the synthesis of lignins and other phenolics [136]. Taofiq et al. [156] conducted a study on individual compounds as possible ingredients in cosmeceutical formulations. The authors concluded that p-coumaric, protocatechuic, and cinnamic acids displayed anti-tyrosinase, antimicrobial, and anti-inflammatory activities, showing their potential for the cosmeceutical industry. Caffeic acid and, at a higher degree, ferulic acid proved to protect the skin against UVB-induced erythema. Besides as antioxidants, these two hydroxycinnamic acids can be used as photoprotectors in skin cosmetics [163].
The protocatechuic, vanillic, and syringic acids are the three commonly found hydroxybenzoic acids [136]. This tree hydroxybenzoic acids were also found in pine extracts (Table 3). Vanillic acid demonstrated anti-inflammatory activity with neuroprotective activity and was found to be a promising candidate for preventing and/or delaying the onset and progression of ischemic injury and vascular dementia [158]. In other cases, the use of a mixture of phenolic compounds rather than the individual compounds exhibits stronger activities. For example, the combined use of syringic acid, resveratrol, and gallic acid, in rats, revealed antioxidant and cardioprotective activities [159]. Resveratrol also showed an anticancer effect when examined in lung, prostate, breast, skin, and gastrointestinal cancers [172]. Resveratrol is the most known constituent of wines and grapes, but it was also found in pine bark extracts (Table 3). It was also proven that resveratrol has anti-inflammatory capacity, especially in the skeletal muscle, but it is less active in liver [171]. Moreover, gallic and p-coumaric acids were considered as promising adjuvant agents against the progression of neurodegeneration in the brain by diabetes [155]. Rosmarinic acid is known to have a number of potentially beneficial biological effects and is an acid ester of caffeic acid and 3(3,4-dihydroxyphenyl)lactic acid. The use of rosmarinic acid in gelatin edible film showed long-term antibacterial activity. Rosmarinic acid edible films may have promising application in the fields of food and pharmaceutical packaging, as they showed a good antibacterial activity even after 3 months of storage [173]. Rosmarinic acid was found in extracts of pine bark in concentrations between 0.4 and 0.8 mg/g [59]. This acid was found to be the predominant compound of Salvia species. Strong correlations between the rosmarinic acid contents and bioactivites of Salvia samples were established [165]. Moreover, this acid demonstrated potent antiviral properties [164]. 3,4 dihydroxybenzoic acid is universal in the Angiosperm plants, as it is constituent of lignin. It is a strong antioxidant, as well as a neuroprotective against Aβ-induced neuronal damage [168]. This acid can be used in formulations for phytonematode control, as it showed nematicidal activity against juveniles of M. incognita [174].
As we can see from the Table 3, in different pine extracts, many catechin compounds with diphenylpropane (C6–C3–C6–) skeletons were found. Epigallocatechin, epigallocatechin gallate, and epicatechin are the main constituents of the leaves of Camellia sinensis (the tea plant), while catechin gallate is a minor polyphenolic constituent in green tea: 1.28% (by weight) of the total catechin content in green tea [166]. These catechins are responsible for the astringent and bitter taste of the green tea [153]. Catechin is the main phenolic compound present in P. pinaster bark extract followed by epicatechin and epicatechin gallate [161]. Gallocatechin was found also in Norway spruce and confirmed to be a strong inhibitor of melanin biosynthesis; however, there is little information on the biological activities of this compound [162]. All these catechins have strong antioxidants and anticancer activities against different types of cancer [166]. Catechins have received considerable attention as promising candidates for development of therapeutic agents.
Taxifolin, as an individual compound, is extensively studied. It was found in the pine extracts of seeds and bark; in bark, it is present in much higher concentrations than in seeds [45,59,157]. For instance, this compound was recovered from P. nigra bark [120] with a maximum extraction recovery of 34%. Taxifolin was detected as the major compound in other needle leaved trees such as the Japanese larch, Larix kaempferi [175]. Its main bioactivities are antioxidant, anticancer, and anti-inflammatory [148,167]. Quercetin is a taxifolin-related flavonoid found in onions, and it showed anti-inflammatory, antimicrobial, and anticancer properties (in vitro and in vivo) [176]. Quercetin-rich extracts from onion skin can be used in functional bread production [176].
According to Lantto and co-workers [157], eriodictyol was one of the main compounds found in extracts of Siberian pine bark. Eriodictyol, as taxifolin, can be find in citrus fruits. It has showed antioxidant and anti-inflammatory activities. Recent findings indicated that eriodictyol might be a new preventative agent for psteoarthritis [177]. Another promising therapeutic agent for the treatment of osteoarthritis is ellagic acid [169]. It is found in high concentrations in the ethanolic extracts of P. pinaster [59], which is also a constituent in the fruit peel of berries and nuts [169].
Apigenin is found abundantly in herbs, fruits, and vegetables (peppermint, grape fruit, parsley). It has potent antioxidant, anti-inflammatory, and anticancer properties [170]. Gascon et al. [148] found three procyanidin compounds in pine bark extracts: A2, B1, and B2. The activities of procyanidins depend on their structure, especially on their degree of polymerization. Procyanidin B2 is one of the most active molecules within the procyanidins, as well as the most studied. It is also found in cocoa and grape seeds. The three compounds have antioxidant activity; B-type procyanidins have also neuroprotective activity. The richest set of bioactivities agglomerates for the procyanidins B2, but as we mentioned, this is also the most studied one.
There are several pine bark commercial extracts: Oligopin®, Pycnogenol®, and Flavangenol®. Pycnogenol® is the most known and most studied one. Its extraction involves standardized consecutive steps using water and ethanol as solvents. It is a polyphenol-rich extract prepared from P. pinaster (French maritime pine). The main constituents are procyanidins (85%), flavonoids (catechin, taxifolin), as well as some phenolic acids in minor amounts (gallic, caffeic, and ferulic acid) [149]. This extract proved to have excellent antioxidant properties that can promote various health properties such as cardioprotective, anticancer, antihypertensive, and anti-inflammatory [118,150]. In another study, the clinical efficiency of Pycnogenol® in the management, treatment, and control of chronic venous insufficiency and venous microangiopathy was proven [178]. This extract showed also anti-diabetic property, as the supplementation of Pycnogenol® to conventional diabetes treatment lowered glucose levels and improved endothelial function [179]. Oligopin® is another extract obtained from the pine tree P. pinaster from a specific location in France (Landes of Gascony). Its production includes two extraction steps and one purification step. This methodology ensure that the obtained extract has a specific and constant composition. The main compounds found in Oligopin® are flavonoids (catechin and taxifolin) and acids (ferulic, gallic, caffeic, p-coumaric, and protocatechic) [180].
As a final remark, the individual polyphenol compounds found in the extracts of pine bark have diverse bioactivities that align with the mentioned previously bioactivities of the hole extracts such as antioxidant, anticancer, cardioprotective, antidiabetic, anti-inflammatory, etc. Pine extracts have active ingredients that are useful for the food industry as supplements or natural pigments, for food preservation and as active food packaging. In the cosmetic formulations, they can be used for protecting the skin against oxygen reactive species, formed by pollution, stress, or ultraviolet reaction.

6. Conclusions and Future Perspectives

Pine residues and by-products are an important source of biocompounds with high industrial interest. They can be recovered using the biorefinery concept, thus contributing to the circular economy.
More environmentally friendly techniques have been explored to avoid the large amounts of (organic) solvents, energy consumption, and waste generation typical of conventional solvent extraction processes. Although replacing conventional technologies by non-conventional ones has emerged, improvements are necessary in terms of deep knowledge of the extraction processes and scaling up. UAE, MAE, SFE, PLE, and OH are some of these emerging promising technologies for bioactive compounds extraction in alignment with the Green Chemistry principles. Regarding the extraction step, the selection of the most appropriate techniques differs according to the type of compounds targeted for recovery and final aimed functionality/application. However, there is not a universal extraction method suitable for the extraction of all pine phenolics. The different pine species have different individual phenolic composition. For example, the main phenolic compound found in extracts of Portuguese pine is the taxifolin, whereas it was not found in Macedonian pine species. Depending on the final purpose for the extraction, an individual study must be carried on to tune the best extraction procedure.
Interestingly, all extracts from pine, regardless the solvent, the method, pine species, and the plant part used, have high amounts of polyphenols.
However, there are differences in the concentrations and type of the individual compounds as well as in the strength of the bioactivities. There are not many studies showing identification and even less studies showing quantification of the individual polyphenols in extracts from pine species.
Pine extracts have a number of described bioactivities that may be beneficial for the human health. As a consequence, pine extracts have high potential as constituents in formulation for the food, cosmeceutical, and pharmaceutical industries.
The possible reutilization of the pine residues is yet limited, compared to its potential. In this context, more studies are needed to find and develop new products and uses resulting from pine residues and by-products.

Funding

This work was funded by the Portuguese Foundation for Science and Technology (FCT) under the scope of the strategic funding of UIDB/04469/2020 unit and BioTecNorte operation (NORTE-01-0145-FEDER-000004) funded by the European Regional Development Fund under the scope of Norte2020 - Programa Operacional Regional do Norte and by program INTERREG V-B Sudoe (REDVALUE, SOE1/P1/E0123). Zlatina Genisheva is supported by the project OH2O (POCI-01-0145-FEDER-029145) funded by FCT and Fundo Europeu de Desenvolvimento Regional (FEDER) under the scope of Programa Operacional de Competividade e Internacionalizaçao (POCI)-COMPETE 2020 and Portugal 2020. Elisa Zanuso is recipient of a PhD fellowship supported by the Mexican Science and Technology Council (CONACYT ID 639021/495314). Pedro Santos is recipient of a PhD fellowship supported by a doctoral advanced training (call NORTE-69-2015-15), funded by the European Social Fund under the scope of Norte2020 - Programa Operacional Regional do Norte (NORTE-08-5369-FSE-000036).

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. European Commission. Going Climate-Neutral by 2050: A Strategic Long-Term Vision for a Prosperous, Modern, Competitive and Climate-Neutral EU Economy. Available online: https://ec.europa.eu/clima/sites/clima/files/long_term_strategy_brochure_en.pdf (accessed on 21 January 2020).
  2. 2050 Long-Term Strategy | Energy. Available online: https://ec.europa.eu/energy/en/topics/energy-strategy-and-energy-union/2050-long-term-strategy (accessed on 21 January 2020).
  3. United Nations. Transforming our world: The 2030 Agenda for Sustainable Development. Available online: https://sustainabledevelopment.un.org/post2015/transformingourworld (accessed on 21 May 2020).
  4. Torres-Valenzuela, L.S.; Ballesteros-Gómez, A.; Rubio, S. Green solvents for the extraction of high added-value compounds from agri-food waste. Food Eng. Rev. 2019, 12, 83–100. [Google Scholar] [CrossRef]
  5. Naidu, D.S.; Hlangothi, S.P.; John, M.J. Bio-based products from xylan: A review. Carbohydr. Polym. 2018, 179, 28–41. [Google Scholar] [CrossRef] [PubMed]
  6. Jablonský, M.; Škulcová, A.; Malvis, A.; Šima, J. Extraction of value-added components from food industry based and agro-forest biowastes by deep eutectic solvents. J. Biotechnol. 2018, 282, 46–66. [Google Scholar] [CrossRef] [PubMed]
  7. Cvjetko Bubalo, M.; Vidović, S.; Radojčić Redovniković, I.; Jokić, S. New perspective in extraction of plant biologically active compounds by green solvents. Food Bioprod. Process. 2018, 109, 52–73. [Google Scholar] [CrossRef]
  8. Chemat, F.; Abert-Vian, M.; Fabiano-Tixier, A.S.; Strube, J.; Uhlenbrock, L.; Gunjevic, V.; Cravotto, G. Green extraction of natural products. Origins, current status, and future challenges. Trac Trends Anal. Chem. 2019, 118, 248–263. [Google Scholar] [CrossRef]
  9. Herrero, M.; Ibañez, E. Green extraction processes, biorefineries and sustainability: Recovery of high added-value products from natural sources. J. Supercrit. Fluids 2018, 134, 252–259. [Google Scholar] [CrossRef] [Green Version]
  10. Gielen, D.; Boshell, F.; Saygin, D. Climate and energy challenges for materials science. Nat. Publ. Gr. 2016, 15, 117–120. [Google Scholar] [CrossRef]
  11. Wenger, J.; Stern, T. Reflection on the research on and implementation of biorefinery systems—A systematic literature review with a focus on feedstock. Biofuels Bioprod. Bior. 2019, 13, 1347–1364. [Google Scholar] [CrossRef] [Green Version]
  12. Ruiz, H.A.; Conrad, M.; Sun, S.-N.; Sanchez, A.; Rocha, G.J.M.; Romaní, A.; Castro, E.; Torres, A.; Rodríguez-Jasso, R.M.; Andrade, L.P.; et al. Engineering aspects of hydrothermal pretreatment: From batch to continuous operation, scale-up and pilot reactor under biorefinery concept. Bioresour. Technol. 2020, 299, 122685. [Google Scholar] [CrossRef] [Green Version]
  13. Pachapur, V.L.; Kaur Brar, S.; Le Bihan, Y. Integrated wood biorefinery: Improvements and tailor-made two-step strategies on hydrolysis techniques. Bioresour. Technol. 2020, 299, 122632. [Google Scholar] [CrossRef]
  14. Pino, M.S.; Rodríguez-Jasso, R.M.; Michelin, M.; Flores-Gallegos, A.C.; Morales-Rodriguez, R.; Teixeira, J.A.; Ruiz, H.A. Bioreactor design for enzymatic hydrolysis of biomass under the biorefinery concept. Chem. Eng. J. 2018, 347, 119–136. [Google Scholar] [CrossRef] [Green Version]
  15. Avelino Gonçaves, F.; Ruiz, H.A.; Silvino dos Santos, E.; Teixeira, J.A.; Ribeiro de Macedo, G. Bioethanol production by Saccharomyces cerevisiae, Pichia stipitis and Zymomonas mobilis from delignified coconut fibre mature and lignin extraction according to biorefinery concept. Renew. Energy 2016, 94, 353–365. [Google Scholar] [CrossRef] [Green Version]
  16. Akhtar, N.; Gupta, K.; Goyal, D.; Goyal, A. Recent advances in pretreatment technologies for efficient hydrolysis of lignocellulosic biomass. Env.. Prog. Sustain. Energy 2016, 35, 498–511. [Google Scholar] [CrossRef]
  17. Sorokina, K.N.; Taran, O.P.; Medvedeva, T.B.; Samoylova, Y.V.; Piligaev, A.V.; Parmon, V.N. Cellulose biorefinery based on a combined catalytic and biotechnological approach for rroduction of 5-HMF and ethanol. ChemSusChem 2017, 10, 562–574. [Google Scholar] [CrossRef] [PubMed]
  18. Brinchi, L.; Cotana, F.; Fortunati, E.; Kenny, J.M. Production of nanocrystalline cellulose from lignocellulosic biomass: Technology and applications. Carbohydr. Polym. 2013, 94, 154–169. [Google Scholar] [CrossRef] [PubMed]
  19. Nuruddin, M.; Hosur, M.; Uddin, M.J.; Baah, D.; Jeelani, S. A novel approach for extracting cellulose nanofibers from lignocellulosic biomass by ball milling combined with chemical treatment. J. Appl. Polym. Sci. 2016, 133. [Google Scholar] [CrossRef]
  20. Luo, Y.; Li, Z.; Li, X.; Liu, X.; Fan, J.; Clark, J.H. The production of furfural directly from hemicellulose in lignocellulosic biomass: A review. Catal. Today 2019, 319, 14–24. [Google Scholar] [CrossRef]
  21. Clauser, N.M.; Gutiérrez, S.; Area, M.C.; Felissia, F.E.; Vallejos, M.E. Techno-economic assessment pellet production in a pine sawdust. BiofuelsBioprod. Biorefining 2018, 12, 997–1012. [Google Scholar] [CrossRef]
  22. Safari, A.; Karimi, K.; Shafiei, M. Dilute alkali pretreatment of softwood pine: A biorefinery approach. Bioresour. Technol. 2017, 234, 67–76. [Google Scholar] [CrossRef]
  23. Charisteidis, I.; Lazaridis, P.; Fotopoulos, A.; Pachatouridou, E.; Matsakas, L.; Rova, U.; Christakopoulos, P.; Triantafyllidis, K. Catalytic fast pyrolysis of lignin isolated by hybrid organosolv — Steam explosion pretreatment of hardwood and softwood biomass for the production of phenolics and aromatics. Catalyst 2019, 9, 935. [Google Scholar] [CrossRef] [Green Version]
  24. Ragauskas, A.J.; Ragauskas, A.J.; Beckham, G.T.; Biddy, M.J.; Chandra, R.; Chen, F.; Davis, M.F.; Davison, B.H.; Dixon, R.A.; Gilna, P.; et al. Lignin valorization: Improving lignin processing in the biorefinery. Science. 2014, 344, 1246843. [Google Scholar] [CrossRef] [PubMed]
  25. Yuan, T.-Q.; Xu, F.; Sun, R.-C. Role of lignin in a biorefinery: Separation characterization and valorization. J. Chem. Technol. Biotechnol. 2013, 88, 346–352. [Google Scholar] [CrossRef]
  26. Paone, E.; Tabanelli, T.; Mauriello, F. The rise of lignin biorefinery. Curr. Opin. Green Sustain. Chem. 2019, 24, 1–6. [Google Scholar] [CrossRef]
  27. Chen, J.; Yuan, Z.; Zanuso, E.; Trajano, H.L. Response of biomass species to hydrothermal pretreatment. In Hydrothermal Processing in Biorefineries: Production of Bioethanol and High Added-Value Compounds of Second and Third Generation Biomass; Springer International Publishing: Cham, Switzerland, 2017. [Google Scholar]
  28. Forests, Forestry and Logging - Statistics Explained. Available online: https://ec.europa.eu/eurostat/statistics-explained/index.php/Forests,_forestry_and_logging (accessed on 21 January 2020).
  29. Cambero, C.; Sowlati, T.; Pavel, M. Economic and life cycle environmental optimization of forest-based biorefinery supply chains for bioenergy and biofuel production. Chem. Eng. Res. Des. 2016, 107, 218–235. [Google Scholar] [CrossRef]
  30. Vega, L.Y.; López, L.; Valdés, C.F.; Chejne, F. Assessment of energy potential of wood industry wastes through thermochemical conversions. Waste Manag. 2019, 87, 108–118. [Google Scholar] [CrossRef]
  31. Belt, T.; Keplinger, T.; Hänninen, T.; Rautkari, L. Cellular level distributions of Scots pine heartwood and knot heartwood extractives revealed by Raman spectroscopy imaging. Ind. Crop. Prod. 2017, 108, 327–335. [Google Scholar] [CrossRef]
  32. Tungmunnithum, D.; Thongboonyou, A.; Pholboon, A.; Yangsabai, A. Flavonoids and other phenolic compounds from medicinal plants for pharmaceutical and medical aspects: An overview. Medicines 2018, 5, 93. [Google Scholar] [CrossRef]
  33. Species - EUFORGEN European Forest Genetic Resources Programme. Available online: http://www.euforgen.org/species/ (accessed on 27 March 2020).
  34. IFN6 — ICNF. Available online: http://www2.icnf.pt/portal/florestas/ifn/ifn6 (accessed on 27 March 2020).
  35. Tümen, İ.; Akkol, E.K.; Taştan, H.; Süntar, I.; Kurtca, M. Research on the antioxidant, wound healing, and anti-inflammatory activities and the phytochemical composition of maritime pine (Pinus pinaster Ait). J. Ethnopharmacol. 2018, 211, 235–246. [Google Scholar] [CrossRef]
  36. del Río, P.G.; Gomes-Dias, J.S.; Rocha, C.M.R.; Romaní, A.; Garrote, G.; Domingues, L. Recent trends on seaweed fractionation for liquid biofuels production. Bioresour. Technol. 2019, 299, 122613. [Google Scholar] [CrossRef] [Green Version]
  37. Räisänen, T.; Athanassiadis, D. Basic chemical composition of the biomass components of pine, spruce and birch. Sci. Res. 2013. [Google Scholar]
  38. Shemfe, M.B.; Gu, S.; Ranganathan, P. Techno-economic performance analysis of biofuel production and miniature electric power generation from biomass fast pyrolysis and bio-oil upgrading. Fuel 2015, 143, 361–372. [Google Scholar] [CrossRef] [Green Version]
  39. Akgül, M.; Çöpür, Y.; Temiz, S. A comparison of kraft and kraft-sodium borohydrate brutia pine pulps. Build. Env. 2007, 42, 2586–2590. [Google Scholar] [CrossRef]
  40. Chaula, Z.; Said, M.; John, G.; Manyele, S.; Mhilu, C. Modelling the Suitability of Pine Sawdust for Energy Production via Biomass Steam Explosion. Smart Grid Renew. Energy 2014, 5, 1–7. [Google Scholar] [CrossRef] [Green Version]
  41. Gulsoy, S.K.; Ozturk, F. Kraft pulping properties of european black pine cone. Maderas Cienc. Y Tecnol. 2016, 17, 875–882. [Google Scholar] [CrossRef] [Green Version]
  42. Cotana, F.; Cavalaglio, G.; Gelosia, M.; Nicolini, A.; Coccia, V.; Petrozzi, A. Production of bioethanol in a second generation prototype from pine wood chips. Energy Procedia. 2014, 45, 42–51. [Google Scholar] [CrossRef] [Green Version]
  43. Miranda, I.; Mirra, I.; Gominho, J.; Pereira, H. Fractioning of bark of Pinus pinea by milling and chemical characterization of the different fractions. Maderas. Cienc. Y Tecnol. 2017, 19, 185–194. [Google Scholar] [CrossRef] [Green Version]
  44. Fradinho, D.M.; Neto, C.P.; Evtuguin, D.; Jorge, F.C.; Irle, M.A.; Gil, M.H.; Pedrosa de Jesus, J. Chemical characterisation of bark and of alkaline bark extracts from maritime pine grown in Portugal. Ind. Crop. Prod. 2002, 16, 23–32. [Google Scholar] [CrossRef]
  45. Ferreira-Santos, P.; Genisheva, Z.; Botelho, C.; Santos, J.; Ramos, C.; Teixeira, J.A.; Rocha, C.M.R. Unravelling the biological potential of pinus pinaster bark extracts. Antioxidants 2020, 9, 334. [Google Scholar] [CrossRef] [Green Version]
  46. Miranda, I.; Gominho, J.; Mirra, I.; Pereira, H. Chemical characterization of barks from Picea abies and Pinus sylvestris after fractioning into different particle sizes. Ind. Crop. Prod. 2012, 36, 395–400. [Google Scholar] [CrossRef]
  47. Vieito, C.; Pires, P.; Fernandes, É.; Velho, M. Chemical characterization of pine bark (Pinus pinaster Aiton subsp. atlantica), antioxidant properties and phenolic profile of its extracts. Millenium J. Educ. Technol. Heal. 2019, 8, 79–87. [Google Scholar] [CrossRef] [Green Version]
  48. Khan, I.U.; Shah, A.A.; Sahibzada, F.A.; Hayyat, A.; Nazar, M.; Mobashar, M.; Tariq, A.; Sultana, N. Carcass characteristics and serum biochemical profile of Japanese quail by the supplementation of pine needles and vitamin E powder. Biologia (Bratisl). 2019, 74, 993–1000. [Google Scholar] [CrossRef]
  49. Ramay, M.S.; Yalçın, S. Effects of supplemental pine needles powder (Pinus brutia) on growth performance, breast meat composition, and antioxidant status in broilers fed linseed oil-based diets. Poult. Sci. 2019, 2019.99, 479–486. [Google Scholar] [CrossRef] [PubMed]
  50. Dönmez, I.E.; Hafizoǧlu, H.; Kilic, A.; Tümen, I.; Sivrikaya, H. Chemical composition of fourteen different coniferous species cones growing naturally in Turkey. Wood Res. 2012, 57, 339–344. [Google Scholar]
  51. López-Mata, L. Proteins, amino acids and fatty acids composition of nuts from the mexican endemic rarity, Pinus maximartinezii, and its conservation implications. Interciencia 2001, 26, 606–610. [Google Scholar]
  52. Cheikh-Rouhou, S.; Hentati, B.; Besbes, S.; Blecker, C.; Deroanne, C.; Attia, H. Chemical composition and lipid fraction characteristics of Aleppo pine (pinus halepensis Mill.) seeds cultivated in Tunisia. Food Sci. Technol. Int. 2006, 12, 407–416. [Google Scholar] [CrossRef]
  53. Tukan, S.K.; Al-Ismail, K.; Ajo, R.Y.; Al-Dabbas, M.M. Seeds and seed oil compositions of Aleppo pine (Pinus halepensis Mill.) grown in Jordan. Riv. Ital. Delle Sostanze Grasse 2013, 90, 87–93. [Google Scholar]
  54. Rodrigues-Corrêa, K.C.d.S.; de Lima, J.C.; Fett-Neto, A.G. Pine oleoresin: Tapping green chemicals, biofuels, food protection, and carbon sequestration from multipurpose trees. Food Energy Secur. 2012, 1, 81–93. [Google Scholar]
  55. Wiyono, B.; Tachibana, S.; Tinambunan, D. Chemical compositions of pine resin, rosin and turpentine oil from west java. Indones. J. Res. 2006, 3, 7–17. [Google Scholar] [CrossRef]
  56. Wang, Z.; Lei, T.; Yan, X.; Chen, G.; Xin, X.; Yang, M.; Guan, Q.; He, X.; Gupta, A.K. Common characteristics of feedstock stage in life cycle assessments of agricultural residue-based biofuels. Fuel 2019, 253, 1256–1263. [Google Scholar] [CrossRef]
  57. Mitchell, G.R.; Biscaia, S.; Mahendra, V.S.; Mateus, A. High value materials from the forests. Adv. Mater. Phys. Chem. 2016, 6, 54–60. [Google Scholar] [CrossRef] [Green Version]
  58. Ehn, M.; Thornton, J.A.; Kleist, E.; Sipilä, M.; Junninen, H.; Pullinen, I.; Springer, M.; Rubach, F.; Tillmann, R.; Lee, B.; et al. A large source of low-volatility secondary organic aerosol. Nature 2014, 506, 476–479. [Google Scholar] [CrossRef] [PubMed]
  59. Ferreira-Santos, P.; Genisheva, Z.; Pereira, R.N.; Teixeira, J.A.; Rocha, C.M.R. Moderate electric fields as a potential tool for sustainable recovery of phenolic compounds from pinus pinaster bark. Acs Sustain. Chem. Eng. 2019, 7, 8816–8826. [Google Scholar] [CrossRef] [Green Version]
  60. Silva, B.; Martins, M.; Rosca, M.; Rocha, V.; Lago, A.; Neves, I.C.; Tavares, T. Waste-based biosorbents as cost-effective alternatives to commercial adsorbents for the retention of fluoxetine from water. Sep. Purif. Technol. 2020, 235. [Google Scholar] [CrossRef] [Green Version]
  61. Kim, K.H.; Daugaard, T.J.; Smith, R.; Mba-Wright, M.; Brown, R.C. Recovery of resin acids from fast pyrolysis of pine. J. Anal. Appl. Pyrolysis 2019, 138, 132–136. [Google Scholar] [CrossRef]
  62. Shi, J.; Nawaz, H.; Pohorly, J.; Mittal, G.; Kakuda, Y.; Jiang, Y. Extraction of polyphenolics from plant material for functional foods - Engineering and technology. Food Rev. Int. 2005, 21, 139–166. [Google Scholar] [CrossRef]
  63. Wen, L.; Zhang, Z.; Sun, D.W.; Sivagnanam, S.P.; Tiwari, B.K. Combination of emerging technologies for the extraction of bioactive compounds. Crit. Rev. Food. Sci. Nutr. 2020, 60, 1826–1841. [Google Scholar] [CrossRef]
  64. Chemat, F.; Fabiano-tixier, A.S.; Abert, M.; Allaf, T.; Vorobiev, E. Trends in analytical chemistry solvent-free extraction of food and natural products. Trends Anal. Chem. 2015, 71, 157–168. [Google Scholar] [CrossRef] [Green Version]
  65. Lourenço, S.C.; Moldão-Martins, M.; Alves, V.D. Antioxidants of natural plant origins: From sources to food industry applications. Molecules 2019, 24, 4132. [Google Scholar] [CrossRef] [Green Version]
  66. Maqsood, S.; Adiamo, O.; Ahmad, M.; Mudgil, P. Bioactive compounds from date fruit and seed as potential nutraceutical and functional food ingredients. Food Chem. 2019, 308, 125522. [Google Scholar] [CrossRef]
  67. Fidelis, M.; De Moura, C.; Kabbas, T.; Pap, N.; Mattila, P.; Mäkinen, S.; Putnik, P.; Kovačević, D.B.; Tian, Y.; Yang, B.; et al. Fruit seeds as sources of bioactive compounds: Sustainable production of high value-added ingredients from by-products within circular economy. Molecules 2019, 24, 3854. [Google Scholar] [CrossRef] [Green Version]
  68. Tanase, C.; Cosarcă, S.; Muntean, D.L. A critical review of phenolic compounds extracted from the bark of woody vascular plants and their potential biological activity. Molecules 2019, 24, 1182. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  69. Sharma, A.; Goyal, R.; Sharma, L. Potential biological efficacy of Pinus plant species against oxidative, inflammatory and microbial disorders. Bmc Complement. Altern. Med. 2016, 16, 1–11. [Google Scholar] [CrossRef] [Green Version]
  70. Ku, C.S.; Jang, J.P.; Mun, S.P. Exploitation of polyphenol-rich pine barks for potent antioxidant activity. J. Wood Sci. 2007, 53, 524–528. [Google Scholar] [CrossRef]
  71. Yesil-Celiktas, O.; Otto, F.; Parlar, H. A comparative study of flavonoid contents and antioxidant activities of supercritical CO2 extracted pine barks grown in different regions of Turkey and Germany. Eur. Food Res. Technol. 2009, 229, 671–677. [Google Scholar] [CrossRef]
  72. Mellouk, H.; Meullemiestre, A.; Maache-Rezzoug, Z.; Bejjani, B.; Dani, A.; Rezzoug, S.A. Valorization of industrial wastes from French maritime pine bark by solvent free microwave extraction of volatiles. J. Clean. Prod. 2016, 112, 4398–4405. [Google Scholar] [CrossRef]
  73. Iravani, S.; Zolfaghari, B. Pharmaceutical and nutraceutical effects of Pinus pinaster bark extract. Res. Pharm. Sci. 2011, 6, 1–11. [Google Scholar] [PubMed]
  74. Mármol, I.; Quero, J.; Jiménez-Moreno, N.; Rodríguez-Yoldi, M.J.; Ancín-Azpilicueta, C. A systematic review of the potential uses of pine bark in food industry and health care. Trends Food Sci. Technol. 2019, 88, 558–566. [Google Scholar] [CrossRef]
  75. Maimoona, A.; Naeem, I.; Saddiqe, Z.; Jameel, K. A review on biological, nutraceutical and clinical aspects of French maritime pine bark extract. J. Ethnopharmacol. 2011, 133, 261–277. [Google Scholar] [CrossRef]
  76. Meullemiestre, A.; Petitcolas, E.; Maache-Rezzoug, Z.; Chemat, F.; Rezzoug, S.A. Impact of ultrasound on solid-liquid extraction of phenolic compounds from maritime pine sawdust waste. Kinetics, optimization and large scale experiments. Ultrason. Sonochem. 2016, 28, 230–239. [Google Scholar] [CrossRef]
  77. Egenberg, I.M.; Aasen, J.A.B.; Holtekjølen, A.K.; Lundanes, E. Characterisation of traditionally kiln produced pine tar by gas chromatography-mass spectrometry. J. Anal. Appl. Pyrolysis 2002, 62, 143–155. [Google Scholar] [CrossRef]
  78. Stacey, R.J.; Dunne, J.; Brunning, S.; Devièse, T.; Mortimer, R.; Ladd, S.; Parfitt, K.; Evershed, R.; Bull, I. Birch bark tar in early Medieval England – Continuity of tradition or technological revival? J. Archaeol. Sci. Rep. 2020, 29, 102118. [Google Scholar] [CrossRef] [PubMed]
  79. Hoon, Y.L.; Choo, C.; Watawana, M.I.; Jayawardena, N.; Waisundara, V.Y. Short communications Evaluation of the total antioxidant capacity and antioxidant compounds of different solvent extracts of Chilgoza pine nuts ( Pinus gerardiana ). J. Funct. Foods 2015, 18, 1014–1021. [Google Scholar] [CrossRef]
  80. Lin, S.; Liang, R.; Xue, P.; Zhang, S.; Liu, Z.; Dong, X. Antioxidant activity improvement of identified pine nut peptides by pulsed electric field (PEF) and the mechanism exploration. LWT Food Sci. Technol. 2017, 75, 366–372. [Google Scholar] [CrossRef]
  81. Hou, L.; Li, C.; Qiu, J. Comparison of the physicochemical characteristics of Pinus koraiensis L. nut oils from different extraction technologies. Grain Oil Sci. Technol. 2018, 1, 113–118. [Google Scholar]
  82. Silva, S.; Costa, E.M.; Calhau, C.; Morais, R.M.; Pintado, M.E. Anthocyanin extraction from plant tissues: A review. Crit. Rev. Food Sci. Nutr. 2017, 57, 3072–3083. [Google Scholar] [CrossRef]
  83. da Silva, R.P.F.F.; Rocha-Santos, T.A.P.; Duarte, A.C. Supercritical fluid extraction of bioactive compounds. Trac - Trends Anal. Chem. 2016, 76, 40–51. [Google Scholar] [CrossRef] [Green Version]
  84. Marcheafave, G.G.; Tormena, C.D.; Pauli, E.D.; Rakocevic, M.; Bruns, R.E.; Scarminio, I.S. Experimental mixture design solvent effects on pigment extraction and antioxidant activity from Coffea arabica L. leaves. Microchem. J. 2019, 146, 713–721. [Google Scholar] [CrossRef]
  85. Venkatesan, T.; Choi, Y.W.; Kim, Y.K. Impact of different extraction solvents on phenolic content and antioxidant potential of pinus densiflora bark extract. Biomed Res. Int. 2019, 2019, 1–14. [Google Scholar] [CrossRef] [Green Version]
  86. Mokrani, A.; Madani, K. Effect of solvent, time and temperature on the extraction of phenolic compounds and antioxidant capacity of peach (Prunus persica L.) fruit. Sep. Purif. Technol. 2016, 162, 68–76. [Google Scholar] [CrossRef]
  87. Fierascu, R.C.; Fierascu, I.; Avramescu, S.M.; Sieniawska, E. Recovery of Natural Antioxidants from Agro-Industrial Side Streams through Advanced Extraction Techniques. Molecules 2019, 24, 4212. [Google Scholar] [CrossRef] [Green Version]
  88. Hadzri, H.M.; Yunus, M.A.C.; Zhari, S.; Rithwan, F. The effects of solvents and extraction methods on the antioxidant activity of P. niruri. J. Teknol. Sci. Eng. 2014, 68, 47–52. [Google Scholar] [CrossRef] [Green Version]
  89. Prat, D.; Wells, A.; Hayler, J.; Sneddon, H.; McElroy, C.R.; Abou-Shehada, S.; Dunn, P.J. CHEM21 selection guide of classical- and less classical-solvents. Green Chem. 2015, 18, 288–296. [Google Scholar] [CrossRef] [Green Version]
  90. Domínguez, E.; Romaní, A.; Domingues, L.; Garrote, G. Evaluation of strategies for second generation bioethanol production from fast growing biomass Paulownia within a biorefinery scheme. Appl. Energy 2017, 187, 777–789. [Google Scholar] [CrossRef] [Green Version]
  91. Liu, Y.; Friesen, J.B.; McAlpine, J.B.; Lankin, D.C.; Chen, S.N.; Pauli, G.F. Natural deep eutectic solvents: Properties, applications, and perspectives. J. Nat. Prod. 2018, 81, 679–690. [Google Scholar] [CrossRef] [PubMed]
  92. Martins, M.A.R.; Pinho, S.P.; Coutinho, J.A.P. Insights into the nature of eutectic and deep eutectic mixtures. J. Solut. Chem. 2019, 48, 962–982. [Google Scholar] [CrossRef] [Green Version]
  93. Ventura, S.P.M.E.; Silva, F.A.; Quental, M.V.; Mondal, D.; Freire, M.G.; Coutinho, J.A.P. Ionic-liquid-mediated extraction and separation processes for bioactive compounds: Past, present, and future trends. Chem. Rev. 2017, 117, 6984–7052. [Google Scholar] [CrossRef]
  94. Martins, P.L.G.; Braga, A.R.; de Rosso, V.V. Can ionic liquid solvents be applied in the food industry? Trends Food Sci. Technol. 2017, 66, 117–124. [Google Scholar] [CrossRef]
  95. Murador, D.C.; de Souza Mesquita, L.M.; Vannuchi, N.; Braga, A.R.C.; de Rosso, V.V. Bioavailability and biological effects of bioactive compounds extracted with natural deep eutectic solvents and ionic liquids: Advantages over conventional organic solvents. Curr. Opin. Food Sci. 2019, 26, 25–34. [Google Scholar] [CrossRef]
  96. Passos, H.; Freire, M.G.; Coutinho, J.A.P. Ionic liquid solutions as extractive solvents for value-added compounds from biomass. Green Chem. 2014, 16, 4786–4815. [Google Scholar] [CrossRef] [Green Version]
  97. da Costa Lopes, A.M.; Brenner, M.; Falé, P.; Roseiro, L.B.; Bogel-Łukasik, R. Extraction and purification of phenolic compounds from lignocellulosic biomass assisted by ionic liquid, polymeric resins, and supercritical CO2. Acs Sustain. Chem. Eng. 2016, 4, 3357–3367. [Google Scholar] [CrossRef]
  98. Ivanović, M.; Alañón, M.E.; Arráez-Román, D.; Segura-Carretero, A. Enhanced and green extraction of bioactive compounds from Lippia citriodora by tailor-made natural deep eutectic solvents. Food Res. Int. 2018, 111, 67–76. [Google Scholar] [CrossRef] [PubMed]
  99. Hou, K.; Bao, M.; Wang, L.; Zhang, H.; Yang, L.; Zhao, H.; Wang, Z. Aqueous enzymatic pretreatment ionic liquid–lithium salt based microwave–assisted extraction of essential oil and procyanidins from pinecones of Pinus koraiensis. J. Clean. Prod. 2019, 236, 117581. [Google Scholar] [CrossRef]
  100. Rocha, C.M.R.; Genisheva, Z.; Ferreira-Santos, P.; Rodrigues, R.; Vicente, A.A.; Teixeira, J.A.; Pereira, R.N. Electric field-based technologies for valorization of bioresources. Bioresour. Technol. 2018, 254, 325–339. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  101. Heleno, S.A.; Diz, P.; Prieto, M.A.; Barros, L.; Rodrigues, A.; Barreiro, M.F.; Ferreira, I.C.F.R. Optimization of ultrasound-assisted extraction to obtain mycosterols from Agaricus bisporus L. by response surface methodology and comparison with conventional Soxhlet extraction. Food Chem. 2016, 197, 1054–1063. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  102. Alara, O.R.; Abdurahman, N.H.; Ukaegbu, C.I.; Azhari, N.H. Vernonia cinerea leaves as the source of phenolic compounds, antioxidants, and anti-diabetic activity using microwave-assisted extraction technique. Ind. Crop. Prod. 2018, 122, 533–544. [Google Scholar] [CrossRef]
  103. Goula, A.M.; Ververi, M.; Adamopoulou, A.; Kaderides, K. Green ultrasound-assisted extraction of carotenoids from pomegranate wastes using vegetable oils. Ultrason. Sonochem. 2017, 34, 821–830. [Google Scholar] [CrossRef]
  104. Okolie, C.L.; Akanbi, T.O.; Mason, B.; Udenigwe, C.C.; Aryee, A.N.A. Influence of conventional and recent extraction technologies on physicochemical properties of bioactive macromolecules from natural sources: A review. Food Res. Int. 2019, 116, 827–839. [Google Scholar] [CrossRef]
  105. Bouras, M.; Chadni, M.; Barba, F.J.; Grimi, N.; Bals, O.; Vorobiev, E. Optimization of microwave-assisted extraction of polyphenols from Quercus bark. Ind. Crop. Prod. 2015, 77, 590–601. [Google Scholar] [CrossRef]
  106. Barba, F.J.; Zhu, Z.; Koubaa, M.; Sant’Ana, A.S.; Orlien, V. Green alternative methods for the extraction of antioxidant bioactive compounds from winery wastes and by-products: A review. Trends Food Sci. Technol. 2016, 49, 96–109. [Google Scholar] [CrossRef]
  107. Vinatoru, M.; Mason, T.J.; Calinescu, I. Ultrasonically assisted extraction (UAE) and microwave assisted extraction (MAE) of functional compounds from plant materials. Trac Trends Anal. Chem. 2017, 97, 159–178. [Google Scholar] [CrossRef]
  108. Deng, Y.; Zhao, Y.; Padilla-Zakour, O.; Yang, G. Polyphenols, antioxidant and antimicrobial activities of leaf and bark extracts of Solidago canadensis L. Ind. Crop. Prod. 2015, 74, 803–809. [Google Scholar] [CrossRef]
  109. Ghitescu, R.-E.; Volf, I.; Carausu, C.; Bühlmann, A.-M.; Gilca, A.; Popa, V.I. Optimization of ultrasound-assisted extraction of polyphenols from spruce wood bark. Ultrason. Sonochem. 2015, 22, 535–541. [Google Scholar] [CrossRef] [PubMed]
  110. Contreras, M.d.M.; Lama-Muñoz, A.; Espínola, F.; Moya, M.; Romero, I.; Castro, E. Valorization of olive mill leaves through ultrasound-assisted extraction. Food Chem. 2020, 314, 126218. [Google Scholar] [CrossRef]
  111. Liazid, A.; Schwarz, M.; Varela, R.M.; Palma, M.; Guillén, D.A.; Brigui, J.; Macías, F.A.; Barroso, C.G. Evaluation of various extraction techniques for obtaining bioactive extracts from pine seeds. Food Bioprod. Process. 2010, 88, 247–252. [Google Scholar] [CrossRef]
  112. Aspé, E.; Fernández, K. The effect of different extraction techniques on extraction yield, total phenolic, and anti-radical capacity of extracts from Pinus radiata Bark. Ind. Crop. Prod. 2011, 34, 838–844. [Google Scholar] [CrossRef]
  113. Karapandzova, M.; Stefkov, G.; Cvetkovikj, I.; Stanoeva, J.P.; Stefova, M.; Kulevanova, S. Flavonoids and other phenolic compounds in needles of pinus peuce and other pine species from the macedonian flora. Nat. Prod. Commun. 2015, 10, 987–990. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  114. Wang, H.; Ding, J.; Ren, N. Recent advances in microwave-assisted extraction of trace organic pollutants from food and environmental samples. Trac Trends Anal. Chem. 2016, 75, 197–208. [Google Scholar] [CrossRef]
  115. Chupin, L.; Maunu, S.L.; Reynaud, S.; Pizzi, A.; Charrier, B.; Charrier-EL Bouhtoury, F. Microwave assisted extraction of maritime pine (Pinus pinaster) bark: Impact of particle size and characterization. Ind. Crop. Prod. 2015, 65, 142–149. [Google Scholar] [CrossRef]
  116. Wrona, O.; Rafińska, K.; Mozenski, C.; Byszewski, B. Supercritical fluid extraction of bioactive compounds from plant materials. J. Aoac Int. 2017, 100, 1624–1635. [Google Scholar] [CrossRef]
  117. Ferrentino, G.; Morozova, K.; Mosibo, O.K.; Ramezani, M.; Scampicchio, M. Biorecovery of antioxidants from apple pomace by supercritical fluid extraction. J. Clean. Prod. 2018, 186, 253–261. [Google Scholar] [CrossRef]
  118. Braga, M.E.M.; Santos, R.M.S.; Seabra, I.J.; Facanali, R.; Marques, M.O.M.; de Sousa, H.C. Fractioned SFE of antioxidants from maritime pine bark. J. Supercrit. Fluids 2008, 47, 37–48. [Google Scholar] [CrossRef]
  119. Seabra, I.J.; Dias, A.M.A.; Braga, M.E.M.; de Sousa, H.C. High pressure solvent extraction of maritime pine bark: Study of fractionation, solvent flow rate and solvent composition. J. Supercrit. Fluids 2012, 62, 135–148. [Google Scholar] [CrossRef]
  120. Ghoreishi, S.M.; Hedayati, A.; Mohammadi, S. Optimization of periodic static-dynamic supercritical CO2 extraction of taxifolin from pinus nigra bark with ethanol as entrainer. J. Supercrit. Fluids 2016, 113, 53–60. [Google Scholar] [CrossRef]
  121. Soquetta, M.B.; Terra, L.d.M.; Bastos, C.P. Green technologies for the extraction of bioactive compounds in fruits and vegetables. Cyta - J. Food 2018, 16, 400–412. [Google Scholar] [CrossRef]
  122. Dai, J.; Mumper, R.J. Plant phenolics: Extraction, analysis and their antioxidant and anticancer properties. Molecules 2010, 15, 7313–7352. [Google Scholar] [CrossRef] [PubMed]
  123. Lin, S.C.; Chang, C.M.J.; Deng, T.S. Enzymatic hot pressurized fluids extraction of polyphenolics from Pinus taiwanensis and Pinus morrisonicola. J. Taiwan Inst. Chem. Eng. 2009, 40, 136–142. [Google Scholar] [CrossRef]
  124. Jaeger, H.; Roth, A.; Toepfl, S.; Holzhauser, T.; Engel, K.H.; Knorr, D.; Vogel, R.F.; Bandick, N.; Kulling, S.; Heinz, V.; et al. Opinion on the use of ohmic heating for the treatment of foods. Trends Food Sci. Technol. 2016, 55, 84–97. [Google Scholar] [CrossRef]
  125. Pereira, R.N.; Vicente, A.A. Environmental impact of novel thermal and non-thermal technologies in food processing. Food Res. Int. 2010, 43, 1936–1943. [Google Scholar] [CrossRef] [Green Version]
  126. Chemat, F.; Rombaut, N.; Meullemiestre, A.; Turk, M.; Périno, S.; Fabiano-Tixier, A.-S.; Abert-Vian, M. Review of green food processing techniques. Preservation, transformation, and extraction. Innov. Food Sci. Emerg. Technol. 2017, 41, 357–377. [Google Scholar] [CrossRef]
  127. Sastry, S. Ohmic heating and moderate electric field processing. Food Sci. Technol. Int. 2008, 14, 419–422. [Google Scholar] [CrossRef]
  128. Lebovka, N.I.; Praporscic, I.; Ghnimi, S.; Vorobiev, E. Does electroporation occur during the ohmic heating of food? J. Food Sci. 2005, 70, E308–E311. [Google Scholar] [CrossRef]
  129. Pereira, R.N.; Rodrigues, R.M.; Genisheva, Z.; Oliveira, H.; de Freitas, V.; Teixeira, J.A.; Vicente, A.A. Effects of ohmic heating on extraction of food-grade phytochemicals from colored potato. LWT Food Sci. Technol. 2016, 74, 493–503. [Google Scholar] [CrossRef] [Green Version]
  130. Puértolas, E.; Barba, F.J. Electrotechnologies applied to valorization of by-products from food industry: Main findings, energy and economic cost of their industrialization. Food Bioprod. Process. 2016, 100, 172–184. [Google Scholar] [CrossRef]
  131. Bouras, M.; Grimi, N.; Bals, O.; Vorobiev, E. Impact of pulsed electric fields on polyphenols extraction from Norway spruce bark. Ind. Crop. Prod. 2016, 80, 50–58. [Google Scholar] [CrossRef]
  132. Andreou, V.; Dimopoulos, G.; Dermesonlouoglou, E.; Taoukis, P. Application of pulsed electric fields to improve product yield and waste valorization in industrial tomato processing. J. Food Eng. 2020, 270, 109778. [Google Scholar] [CrossRef]
  133. Frontuto, D.; Carullo, D.; Harrison, S.M.; Brunton, N.P.; Ferrari, G.; Lyng, J.G.; Pataro, G. Optimization of pulsed electric fields-assisted extraction of polyphenols from potato peels using response surface methodology. Food Bioprocess Technol. 2019, 12, 1708–1720. [Google Scholar] [CrossRef]
  134. Conde, E.; Hemming, J.; Smeds, A.; Reinoso, B.D.; Moure, A.; Willför, S.; Domínguez, H.; Parajó, J.C. Extraction of low-molar-mass phenolics and lipophilic compounds from Pinus pinaster wood with compressed CO2. J. Supercrit. Fluids 2013, 81, 193–199. [Google Scholar] [CrossRef]
  135. Xu, C.C.; Wang, B.; Pu, Y.Q.; Tao, J.S.; Zhang, T. Advances in extraction and analysis of phenolic compounds from plant materials. Chin. J. Nat. Med. 2017, 15, 721–731. [Google Scholar] [CrossRef]
  136. Kumar, N.; Goel, N. Phenolic acids: Natural versatile molecules with promising therapeutic applications. Biotechnol. Rep. 2019, 24, e00370. [Google Scholar] [CrossRef]
  137. Kalisz, S.; Oszmiański, J.; Kolniak-Ostek, J.; Grobelna, A.; Kieliszek, M.; Cendrowski, A. Effect of a variety of polyphenols compounds and antioxidant properties of rhubarb (Rheum rhabarbarum). Lwt 2020, 118, 108775. [Google Scholar] [CrossRef]
  138. Yan, Z.; Zhong, Y.; Duan, Y.; Chen, Q.; Li, F. Antioxidant mechanism of tea polyphenols and its impact on health benefits. Anim. Nutr. 2020, 6, 115–123. [Google Scholar] [CrossRef] [PubMed]
  139. Reis Giada, M.d.L. Food phenolic compounds: main classes, sources and their antioxidant power. In Oxidative Stress and Chronic Degenerative Diseases - A Role for Antioxidants; InTechOpen: London, UK, 2013. [Google Scholar]
  140. Minatel, I.O.; Borges, C.V.; Ferreira, M.I.; Gomez, H.A.G.; Chen, C.-Y.O.; Lima, G.P.P. Phenolic compounds: Functional properties, impact of processing and bioavailability. In Phenolic Compounds - Biological Activity; InTechOpen: London, UK, 2017. [Google Scholar]
  141. Spínola, V.; Llorent-Martínez, E.J.; Castilho, P.C. Inhibition of α-amylase, α-glucosidase and pancreatic lipase by phenolic compounds of Rumex maderensis (Madeira sorrel). Influence of simulated gastrointestinal digestion on hyperglycaemia-related damage linked with aldose reductase activity and protein glacation. LWT 2020, 118, 108727. [Google Scholar]
  142. Castro, M.C.; Villagarcía, H.; Nazar, A.; Arbeláez, L.G.; Massa, M.L.; Del Zotto, H.; Ríos, J.L.; Schinella, G.R.; Francini, F. Cacao extract enriched in polyphenols prevents endocrine-metabolic disturbances in a rat model of prediabetes triggered by a sucrose rich diet. J. Ethnopharmacol. 2020, 247, 112263. [Google Scholar] [CrossRef] [PubMed]
  143. Dzah, C.S.; Duan, Y.; Zhang, H.; Wen, C.; Zhang, J.; Chen, G.; Ma, H. The effects of ultrasound assisted extraction on yield, antioxidant, anticancer and antimicrobial activity of polyphenol extracts: A review. Food Biosci. 2020, 35, 100547. [Google Scholar] [CrossRef]
  144. Jesus, M.S.; Ballesteros, L.F.; Pereira, R.N.; Genisheva, Z.; Carvalho, A.C.; Pereira-Wilson, C.; Teixeira, J.A.; Domingues, L. Ohmic heating polyphenolic extracts from vine pruning residue with enhanced biological activity. Food Chem. 2020, 316, 126298. [Google Scholar] [CrossRef] [Green Version]
  145. Zhang, H.; Qi, R.; Mine, Y. The impact of oolong and black tea polyphenols on human health. Food Biosci. 2019, 29, 55–61. [Google Scholar] [CrossRef]
  146. Cabral, F.L.; Bernardes, V.M.; Passos, D.F.; de Oliveira, J.S.; Doleski, P.H.; Silveira, K.L.; Horvarth, M.C.; Bremm, J.M.; Barbisan, F.; Azzolin, V.F.; et al. Astrocaryum aculeatum fruit improves inflammation and redox balance in phytohemagglutinin-stimulated macrophages. J. Ethnopharmacol. 2020, 247, 112274. [Google Scholar] [CrossRef]
  147. Fei, P.; Ali, M.A.; Gong, S.; Sun, Q.; Bi, X.; Liu, S.; Guo, L. Antimicrobial activity and mechanism of action of olive oil polyphenols extract against Cronobacter sakazakii. Food Control 2018, 94, 289–294. [Google Scholar] [CrossRef]
  148. Gascón, S.; Jiménez-Moreno, N.; Jiménez, S.; Quero, J.; Rodríguez-Yoldi, M.J.; Ancín-Azpilicueta, C. Nutraceutical composition of three pine bark extracts and their antiproliferative effect on Caco-2 cells. J. Funct. Foods 2018, 48, 420–429. [Google Scholar] [CrossRef]
  149. Ustun, O.; Senol, F.S.; Kurkcuoglu, M.; Orhan, I.E.; Kartal, M.; Baser, K.H.C. Investigation on chemical composition, anticholinesterase and antioxidant activities of extracts and essential oils of Turkish Pinus species and pycnogenol. Ind. Crop. Prod. 2012, 38, 115–123. [Google Scholar] [CrossRef]
  150. Ince, I.; Yesil-Celiktas, O.; Karabay-Yavasoglu, N.U.; Elgin, G. Effects of Pinus brutia bark extract and Pycnogenol® in a rat model of carrageenan induced inflammation. Phytomedicine 2009, 16, 1101–1104. [Google Scholar] [CrossRef] [PubMed]
  151. Venugopal, P.; Julkunen-Tiitto, R.; Junninen, K.; Kouki, J. Phenolic compounds in scots pine heartwood: Are kelo trees a unique woody substrate? Can. J. Res. 2015, 46, 225–233. [Google Scholar] [CrossRef] [Green Version]
  152. Yen, G.C.; Der Duh, P.; Huang, D.W.; Hsu, C.L.; Fu, T.Y.C. Protective effect of pine (Pinus morrisonicola Hay.) needle on LDL oxidation and its anti-inflammatory action by modulation of iNOS and COX-2 expression in LPS-stimulated RAW 264.7 macrophages. Food Chem. Toxicol. 2008, 46, 175–185. [Google Scholar] [CrossRef] [PubMed]
  153. Pauli, E.D.; Malta, G.B.; Sanchez, P.M.; Moreira, I.C.; Scarminio, I.S. Mixture design analysis of solvent extractor effects on epicatechin, epigallocatechin gallate, epigallocatechin and antioxidant activities of the Camellia sinensis L. leaves. Anal. Chem. Res. 2014, 2, 23–29. [Google Scholar] [CrossRef] [Green Version]
  154. Latha, R.C.R.; Daisy, P. Insulin-secretagogue, antihyperlipidemic and other protective effects of gallic acid isolated from Terminalia bellerica Roxb. in streptozotocin-induced diabetic rats. Chem. Biol. Interact. 2011, 189, 112–118. [Google Scholar] [CrossRef]
  155. Abdel-Moneim, A.; Yousef, A.I.; Abd El-Twab, S.M.; Abdel Reheim, E.S.; Ashour, M.B. Gallic acid and p-coumaric acid attenuate type 2 diabetes-induced neurodegeneration in rats. Metab. Brain Dis. 2017, 32, 1279–1286. [Google Scholar] [CrossRef]
  156. Taofiq, O.; Heleno, S.A.; Calhelha, R.C.; Fernandes, I.P.; Alves, M.J.; Barros, L.; González-Paramás, A.M.; Ferreira, I.C.F.R.; Barreiro, M.F. Phenolic acids, cinnamic acid, and ergosterol as cosmeceutical ingredients: Stabilization by microencapsulation to ensure sustained bioactivity. Microchem. J. 2019, 147, 469–477. [Google Scholar] [CrossRef] [Green Version]
  157. Lantto, T.A.; Dorman, H.J.D.; Shikov, A.N.; Pozharitskaya, O.N.; Makarov, V.G.; Tikhonov, V.P.; Hiltunen, R.; Raasmaja, A. Chemical composition, antioxidative activity and cell viability effects of a Siberian pine (Pinus sibirica Du Tour) extract. Food Chem. 2009, 112, 936–943. [Google Scholar] [CrossRef]
  158. Khoshnam, S.E.; Sarkaki, A.; Rashno, M.; Farbood, Y. Memory deficits and hippocampal inflammation in cerebral hypoperfusion and reperfusion in male rats: Neuroprotective role of vanillic acid. Life Sci. 2018, 211, 126–132. [Google Scholar] [CrossRef]
  159. Sammeturi, M.; Shaik, A.H.; Bongu, S.B.R.; Cheemanapalli, S.; Mohammad, A.; Kodidhela, L.D. Protective effects of syringic acid, resveratrol and their combination against isoprenaline administered cardiotoxicity in wistar rats. SaudiJ. Biol. Sci. 2019, 26, 1429–1435. [Google Scholar] [CrossRef]
  160. Wang, Y.; Chen, Y.; Chen, Y.; Zhou, B.; Shan, X.; Yang, G. Eriodictyol inhibits IL-1β-induced inflammatory response in human osteoarthritis chondrocytes. Biomed. Pharm. 2018, 107, 1128–1134. [Google Scholar] [CrossRef] [PubMed]
  161. Chupin, L.; Motillon, C.; Charrier-El Bouhtoury, F.; Pizzi, A.; Charrier, B. Characterisation of maritime pine (Pinus pinaster) bark tannins extracted under different conditions by spectroscopic methods, FTIR and HPLC. Ind. Crop. Prod. 2013, 49, 897–903. [Google Scholar] [CrossRef]
  162. Hammerbacher, A.; Raguschke, B.; Wright, L.P.; Gershenzon, J. Gallocatechin biosynthesis via a flavonoid 3′,5′-hydroxylase is a defense response in Norway spruce against infection by the bark beetle-associated sap-staining fungus Endoconidiophora polonica. Phytochemistry 2018, 148, 78–86. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  163. Saija, A.; Tomaino, A.; Trombetta, D.; De Pasquale, A.; Uccella, N.; Barbuzzi, T.; Paolino, D.; Bonina, F. In vitro and in vivo evaluation of caffeic and ferulic acids as topical photoprotective agents. Int. J. Pharm. 2000, 199, 39–47. [Google Scholar] [CrossRef]
  164. Chung, Y.C.; Hsieh, F.C.; Lin, Y.J.; Wu, T.Y.; Lin, C.W.; Lin, C.T.; Tang, N.Y.; Jinn, T.R. Magnesium lithospermate B and rosmarinic acid, two compounds present in Salvia miltiorrhiza, have potent antiviral activity against enterovirus 71 infections. Eur. J. Pharm. 2015, 755, 127–133. [Google Scholar] [CrossRef]
  165. Adımcılar, V.; Kalaycıoğlu, Z.; Aydoğdu, N.; Dirmenci, T.; Kahraman, A.; Erim, F.B. Rosmarinic and carnosic acid contents and correlated antioxidant and antidiabetic activities of 14 Salvia species from Anatolia. J. Pharm. Biomed. Anal. 2019, 175, 112763. [Google Scholar] [CrossRef]
  166. Babich, H.; Zuckerbraun, H.L.; Weinerman, S.M. In vitro cytotoxicity of (-)-catechin gallate, a minor polyphenol in green tea. Toxicol. Lett. 2007, 171, 171–180. [Google Scholar] [CrossRef]
  167. Talmaciu, A.I.; Ravber, M.; Volf, I.; Knez, Ž.; Popa, V.I. Isolation of bioactive compounds from spruce bark waste using sub- and supercritical fluids. J. Supercrit. Fluids 2016, 117, 243–251. [Google Scholar] [CrossRef]
  168. Ban, J.Y.; Cho, S.O.; Jeon, S.Y.; Bae, K.H.; Song, K.S.; Seong, Y.H. 3,4-Dihydroxybenzoic acid from Smilacis chinae rhizome protects amyloid β protein (25-35)-induced neurotoxicity in cultured rat cortical neurons. Neurosci. Lett. 2007, 420, 184–188. [Google Scholar] [CrossRef]
  169. Lin, Z.; Lin, C.; Fu, C.; Lu, H.; Jin, H.; Chen, Q.; Pan, J. The protective effect of Ellagic acid (EA) in osteoarthritis: An in vitro and in vivo study. Biomed. Pharm. 2020, 125, 109845. [Google Scholar] [CrossRef]
  170. Silvan, S.; Manoharan, S. Apigenin prevents deregulation in the expression pattern of cell-proliferative, apoptotic, inflammatory and angiogenic markers during 7,12-dimethylbenz[a]anthracene-induced hamster buccal pouch carcinogenesis. Arch. Oral Biol. 2013, 58, 94–101. [Google Scholar] [CrossRef] [PubMed]
  171. Szkudelska, K.; Okulicz, M.; Hertig, I.; Szkudelski, T. Resveratrol ameliorates inflammatory and oxidative stress in type 2 diabetic Goto-Kakizaki rats. Biomed. Pharm. 2020, 125, 110026. [Google Scholar] [CrossRef] [PubMed]
  172. Sajadimajd, S.; Bahramsoltani, R.; Iranpanah, A.; Kumar Patra, J.; Das, G.; Gouda, S.; Rahimi, R.; Rezaeiamiri, E.; Cao, H.; Giampieri, F.; et al. Advances on natural polyphenols as anticancer agents for skin cancer. Pharm. Res. 2020, 151, 104584. [Google Scholar] [CrossRef] [PubMed]
  173. Ge, L.; Zhu, M.; Li, X.; Xu, Y.; Ma, X.; Shi, R.; Li, D.; Mu, C. Development of active rosmarinic acid-gelatin biodegradable films with antioxidant and long-term antibacterial activities. Food Hydrocoll. 2018, 83, 308–316. [Google Scholar] [CrossRef]
  174. Nguyen, D.M.C.; Seo, D.J.; Kim, K.Y.; Park, R.D.; Kim, D.H.; Han, Y.S.; Kim, T.H.; Jung, W.J. Nematicidal activity of 3,4-dihydroxybenzoic acid purified from Terminalia nigrovenulosa bark against Meloidogyne incognita. Microb. Pathog. 2013, 59–60, 52–59. [Google Scholar] [CrossRef]
  175. Muramatsu, D.; Uchiyama, H.; Kida, H.; Iwai, A. Cell cytotoxity and anti-glycation activity of taxifolin-rich extract from Japanese larch, Larix kaempferi. Heliyon 2019, 5, e02047. [Google Scholar] [CrossRef] [Green Version]
  176. Świeca, M.; Gawlik-Dziki, U.; Dziki, D.; Baraniak, B.; Czyz, J. The influence of protein-flavonoid interactions on protein digestibility in vitro and the antioxidant quality of breads enriched with onion skin. Food Chem. 2013, 141, 451–458. [Google Scholar] [CrossRef]
  177. Wang, L.; Li, X.; Wang, H. Physicochemical properties, bioaccessibility and antioxidant activity of the polyphenols from pine cones of Pinus koraiensis. Int. J. Biol. Macromol. 2019, 126, 385–391. [Google Scholar] [CrossRef]
  178. Cesarone, M.R.; Belcaro, G.; Rohdewald, P.; Pellegrini, L.; Ledda, A.; Vinciguerra, G.; Ricci, A.; Ippolito, E.; Fano, F.; Dugall, M.; et al. Improvement of signs and symptoms of chronic venous insufficiency and microangiopathy with Pycnogenol®: A prospective, controlled study. Phytomedicine 2010, 17, 835–839. [Google Scholar] [CrossRef]
  179. Liu, X.; Wei, J.; Tan, F.; Zhou, S.; Würthwein, G.; Rohdewald, P. Antidiabetic effect of Pycnogenol® French maritime pine bark extract in patients with diabetes type II. Life Sci. 2004, 75, 2505–2513. [Google Scholar] [CrossRef]
  180. Segal, L.; Penman, M.G.; Piriou, Y. Evaluation of the systemic toxicity and mutagenicity of OLIGOPIN®, procyanidolic oligomers (OPC) extracted from French Maritime Pine Bark extract. Toxicol. Rep. 2018, 5, 531–541. [Google Scholar] [CrossRef] [PubMed]
Figure 1. Pine valorization under biorefinery concept.
Figure 1. Pine valorization under biorefinery concept.
Molecules 25 02931 g001
Figure 2. General chemical/nutritional composition of pine by-products.
Figure 2. General chemical/nutritional composition of pine by-products.
Molecules 25 02931 g002
Figure 3. Principles of efficient process for obtaining natural extracts. Adapted from Chemat et al. [8].
Figure 3. Principles of efficient process for obtaining natural extracts. Adapted from Chemat et al. [8].
Molecules 25 02931 g003
Figure 4. Polyphenol groups according to their chemical structure.
Figure 4. Polyphenol groups according to their chemical structure.
Molecules 25 02931 g004
Table 1. Pinus trees species implemented in European countries, as well as its geographical distribution.
Table 1. Pinus trees species implemented in European countries, as well as its geographical distribution.
Latin NameCommon NameGeographical Distribution
Pinus sylvestrisScots pineAll countries of Europa and Asia
Pinus nigraEuropean black pineMountain areas of Europe, United States, and Asia Minor
Pinus brutiaBrutia pineEastern Coast of the Mediterranean (Turkey, Greece, Italy)
Pinus pinasterMaritime pineWestern Mediterranean Sea, Central and Southern Europe, and North Africa
Pinus halepensisAleppo pineCoastal areas of the Western Mediterranean region, Southern France and Italy, and North Africa
Pinus cembraSwiss stone pineContinental Alps and regions of the Carpathian Mountains
Pinus uncinataMountain pineMountains of Western Europe, Northern Europe, and Mediterranean
Pinus pineaStone pineMediterranean Basin, extending from Portugal to Syria
Pinus strobusWhite pineEastern North America and Carpathian Mountains in Czech Republic and Southern Poland
Pinus mugoMountain pineMountains of Central and Eastern Europe
Pinus heldreichiiBosnian pineSouthern and Western part of the Balkans, near the Mediterranean basin
PinuscontortaLodgepole pineWestern North America, Europe, and New Zealand
Pinus peuceMacedonian pineMountain areas of the Balkan Peninsula
Pinus radiataMonterey pine Central Coast of California, Australia, New Zealand, Mexico, Argentina, Chile, Uruguay, Kenya, Spain, and South Africa
Table 2. Green technologies for phenolic compounds recovery from pine by-products and possible applications.
Table 2. Green technologies for phenolic compounds recovery from pine by-products and possible applications.
Extraction MethodPine SpeciesPart of TreeOptimum Extraction ConditionsForeseen ApplicationsReference
Ultrasound-Assisted Extraction
(UAE)
P. pinaster
P. d’Alpes
seedsWater; 75 °C; 20 minBioactive extracts for food supplements[111]
P. radiatabarkAcetone (70%, v/v); 25 °C; 6 min; 35 kHz/85 WNutraceutical action[112]
P. mugo
P. nigra
P. peuce
P. sylvestris
needlesMethanol (70%, v/v); RT; 30 minMedicinal and pharmaceutical [113]
P. pinasterwoodAcidified water; 40 °C; 43 min; 0.67 W/cm2Diet supplement[76]
Microwave-Assisted Extraction (MAE)P. pinaster
P. d’Alpes
seedsWater; 75 ºC; 20 minBioactive extracts for food supplements[111]
P. radiatabarkAcetone (70%, v/v); 25 °C; 1–2 min; 2450 MHz/900 WBioactive extracts as promising pharmaceutical and food applications[112]
P. pinasterbarkEthanol (80%, v/v); 3 min; 100WDiet supplement[115]
P. pinasterbark92.4 min; 803.5 WAntioxidant essential oils[72]
P. koraiensisconesEnzymatic pretreatment; ionic liquid–lithium salt; 15.95 min; 581.49 WCosmetic or health-related applications[99]
Pressurised Liquid Extraction
(PLE)
P. taiwanensis
P. morrisonicola
needlesEnzymatic hydrolysis (ethanol 70% v/v); 70 °C; 180 min; 4.12 MPaFood, cosmetic, or health applications[123]
P. pinaster
P. d’Alpes
seedsWater; 100 °C; 20–23 min; 4 MPaBioactive extracts for food supplements[111]
P. koraiensisseedsn-butane; 21 °C; 0.5 MPaOils for cosmetology and pharmaceutical application[81]
Supercritical Fluid Extraction
(SFE)
P. pinasterbarkCO2 + ethanol (10%, v/v); 50 °C; 35 min; 25 MPaAroma/flavor, food, and pharmaceutical industries[118]
P. pinasterbarkCO2:ethanol (30:70, v/v); 30 °C; 360 min; 25 MPaAntioxidant extracts[119]
P. pinea
P. sylvestris
P. nigra
P. parviflora
P. ponderosa
barkCO2 + ethanol (3% v/v); 40 and 60 °C; 200 barFood, cosmetic, or health-related applications[71]
P. niruri--CO2; 90 min; 60 °C; 30 MPaAntioxidant extracts[88]
P. nigrabarkCO2 + ethanol; 42.8 °C; 137.9 min; 19.3 MPaPharmaceutical industry[120]
P. pinasterwoodCO2 + ethanol (10%, v/v); 50 °C; 35 min; 25 MPaAntioxidant extracts for food and pharmaceutical applications[134]
Ohmic Heating Extraction
(OH)
P. pinasterbarkEthanol (50%, v/v); 83 °C; 30 min; 5-15 V/cmAntioxidant extracts for food and pharmaceutical applications[59]
Table 3. Individual phenolic compounds found in pine by-products and their reported bioactivities.
Table 3. Individual phenolic compounds found in pine by-products and their reported bioactivities.
NameChemical
Formula
Concentration
Range (mg/g)
BioactivitiesReference
NEEDLES
EpicatechinC15H14O61.5antioxidant[152,153]
p-Coumaric AcidC9H8O32.3antioxidant, anti-inflammatory, hepatoprotective and renoprotective, anti-neurodegenerative, anti-cholesterolemic, improve insulin resistance, anti-tyrosinase, antimicrobial [152,154,155,156]
SEEDS
Protocatechuic AcidC7H6O40.5anti-tyrosinase, antimicrobial, and anti-inflammatory activities[156,157]
CatechinC15H14O60.5hepatoprotective activity[145,157]
Epigallocatechin GallateC22H18O110.5antimicrobial, antioxidant, photoprotective[145,157]
Vanillic AcidC8H8O40.9anti-inflammatory, neuroprotective[157,158]
Syringic AcidC9H10O51.0cardioprotective, antioxidant, antimicrobial, anti-inflammatory, neuro and hepatoprotective activities[157,159]
EpicatechinC15H14O61.3antioxidant[157]
TaxifolinC15H14O71.7antioxidant, anticancer, anti-inflammatory[157]
Cinnamic AcidC9H8O20.1anti-tyrosinase, antimicrobial, and anti-inflammatory[156,157]
EriodictyolC15H12O63.8anti-inflammatory[157,160]
m-Coumaric AcidC9H8O3tracesnot found[157]
BARK
Gallic AcidC7H6O5traces–5.5anti-inflammatory, antihyperlipidemic, antioxidant, antitumor, antihyperglycemic, and anti-neurodegenerative, cardioprotective[59,154,155,159,161]
GallocatechinC15H14O70.07–0.95inhibitor of melanin biosynthesis[45,59,162]
EpicatechinC15H14O60.06–1.9antioxidant[71,161]
Epicatechin GallateC22H18O100.3–0.9antioxidant[161]
CatechinC15H14O60.095–7.7antioxidant, anticancer, cardioprotective, antifungal[45,59,71,161,162]
Vanillic AcidC8H8O40.02–0.07neuroprotective, anti-inflammatory[45,59,158]
Caffeic AcidC9H8O40.03–0.2antioxidant, photoprotective[45,59,163]
Rosmaniric AcidC18H16O80.4–0.8antioxidant, antidiabetic, antibacterial, antiviral[59,164,165]
Catechin GallateC22H18O100.002–1.5antioxidant, anticancer[71,166]
TaxifolinC15H12O70.01–4.7antioxidant, anticancer, anti-inflammatory[45,59,148,167]
3,4 Dihydroxy-Benzoic AcidC9H10O40.08–0.8neuroprotective, antioxidant, nematicidal activity[45,59,168]
Ellagic acidC14H6O80.4–4.0anti-inflammatory, antioxidant[45,59,169]
NaringinC27H32O170.8–2.0not found[45,59]
ApigeninC15H10O50.3–0.5anticancer, antioxidant, anti-inflammatory[45,59,170]
ResveratrolC14H12O30.03–0.4antioxidant, anti-cancer, cardioprotective, anti-inflammatory[45,59,159,171]
Ferulic acidC10H10O40.06–0.5antioxidant, photoprotective[45,59,163]
p-coumaric acidC9H8O3n.q.antioxidant, anti-inflammatory, hepatoprotective and renoprotective, anti-neurodegenerative, anti-cholesterolemic, improve insulin resistance, anti-tyrosinase, antimicrobial[59,154,155,156]
QuercetinC15H10O70.06–1.1inflammatory, antimicrobial, anticancer[45,59]
Procyanidin A2C30H24O12n.q.antioxidant[148]
Procyanidin B1C30H26O12n.q.antioxidant, neuroprotective, anti-proliferative activity[148]
Procyanidin B2C30H26O12n.q.antioxidant, anti-inflammatory, cardioprotective, neuroprotective, anti-proliferative activity[148]
n.q.–not quantified.

Share and Cite

MDPI and ACS Style

Ferreira-Santos, P.; Zanuso, E.; Genisheva, Z.; Rocha, C.M.R.; Teixeira, J.A. Green and Sustainable Valorization of Bioactive Phenolic Compounds from Pinus By-Products. Molecules 2020, 25, 2931. https://doi.org/10.3390/molecules25122931

AMA Style

Ferreira-Santos P, Zanuso E, Genisheva Z, Rocha CMR, Teixeira JA. Green and Sustainable Valorization of Bioactive Phenolic Compounds from Pinus By-Products. Molecules. 2020; 25(12):2931. https://doi.org/10.3390/molecules25122931

Chicago/Turabian Style

Ferreira-Santos, Pedro, Elisa Zanuso, Zlatina Genisheva, Cristina M. R. Rocha, and José A. Teixeira. 2020. "Green and Sustainable Valorization of Bioactive Phenolic Compounds from Pinus By-Products" Molecules 25, no. 12: 2931. https://doi.org/10.3390/molecules25122931

Article Metrics

Back to TopTop