Nanomedicine is considered a new trend in the world. It is concerned with the biomedical application of nanotechnology in the early diagnosis and treatment of diseases. In recent years, many types of research tried to use the unique properties of nanoparticles; especially zinc oxide nanoparticles in the treatment of some diseases [4]. Zinc oxide nanoparticles have bioavailability, biocompatibility, and high solubility. Therefore, they can mimic the biomolecules' activity, and can localize in many body systems wherein biomolecules can regulate the cellular cycle, and maintain cellular homoeostasis [5]. In the last decades, chemotherapy, radiation therapy, and surgery were the primary choices for cancer treatment, but they had many adverse effects due to their non-selective effects on the cells; as they might affect normal cells as well. Therefore, searching for another substitute therapy that has the ability to both destroy cancer cells and overcome the various adverse effects of the traditional cancer therapy has become mandatory [6].

Zinc oxide nanoparticles were approved by Food and Drug Administration (FDA) as a new and potent anticancer therapy [7]. Zinc oxide nanoparticles can produce selective cytotoxicity towards cancer cells via the induction of disequilibrium of zinc-dependent protein activity, in addition to the production of reactive oxygen species [8]. Rasmussen et al. [9] emphasized the ability of zinc oxide nanoparticles to kill cancer cells through the induction of oxidative stress in the cancerous cells. Furthermore, zinc is involved in all cellular protecting processes against cancer through the activation of DNA repair, and hence preventing both apoptosis and cancer cell growth [10].

Zinc channels create a balance between cell survival and cell death via controlling the free and intracellular zinc movements [11]. Zinc also plays an important role to maintain the tumor suppressor gene p53 activity that regulates apoptosis activity [12]. Moreover, zinc can also help in the activation of the caspase-6 enzyme which is responsible for apoptosis. Therefore, zinc deficiency causes DNA damage and p53 disruption, resulting in the loss of DNA integrity and the potential for increased cancer risk. Hence, zinc oxide nanoparticles are considered potent therapy for many cancers [13].

Many published articles have mentioned that zinc oxide nanoparticles had more than 30 times selective cytotoxicity towards cancer cells compared to healthy cells, and that they could kill cancer cells selectively in vitro and vivo via inferring the selective localization [14-16]. Zinc oxide nanoparticles were characterized by their enhanced permeation, and by their retention inside the tumor cells. The small size and the surface properties of zinc oxide nanoparticles enabled them to diffuse easily through the blood vessels towards the tumor cells, and to be localized inside these cells specifically, and hence act on them [17]. Moreover, as zinc oxide nanoparticles show positive charges in the physiological conditions; such as in tissue fluid or in blood, while the cancerous cells have negatively charged phospholipids on their outer membranes, an electrostatic attraction occurs between zinc oxide nanoparticles and the cancerous cells [18, 19]. Bisht and Rayamajhi [20] reported that zinc oxide nanoparticles have shown anti-proliferative effects, and that zinc nanoparticles succeeded to treat a human gastric adenocarcinoma cell line, resulting in a significant inhibition of cellular proliferation. Therefore, Bisht and Rayamajhi supported the use of zinc oxide nanoparticles as a promising anticancer agent with fewer side effects in comparison to the traditional anticancer therapy.

Badkoobeh et al. [21] suggested that zinc oxide nanoparticles could be used as a potent antioxidant, and as an effective adjuvant treatment to chemotherapeutic drugs that cause reproductive dysfunction in males. This was based upon the ability of zinc oxide nanoparticles to increase the therapeutic efficacy of doxorubicin, and to reduce doxorubicin gonado-toxic properties. Furthermore, several studies revealed the ability of zinc to ameliorate the oxidative stress and glutathione depletion. Other studies emphasized the ability of zinc to enhance the reproductive function, and reported that zinc was found in high levels in the male reproductive system and in the seminal fluid. Therefore, zinc is thought to play an important role in spermatogenesis process [22]. In the same context, Dawei et al. [23] indicated that zinc oxide nanoparticles had the ability to increase antioxidant enzymes levels, and to decrease malondialdehyde (MDA) level. Therefore, zinc oxide nanoparticles could protect the cell membrane integrity against oxidative stress damage. On the contrary, Sharma et al. [24] reported that sub-acute oral exposure of zinc oxide nanoparticles could induce oxidative stress, DNA damage, and apoptosis in the liver.

Atef et al. [25] showed that low doses of zinc oxide nanoparticles had cytoprotective effects. These particles could improve antioxidant activity, and decrease the levels of free radicals resulting from Aflatoxin B1. Aflatoxin B1 induced detrimental effects on humans as well as on animals eating Aflatoxins contaminated feedstuff. Aflatoxins-induced toxic effects included teratogenic, carcinogenic, mutagenic and immunosuppressive effects. Studies have shown a direct correlation between dietary aflatoxins intake in humans and liver cancer [26]. Therefore, according to Atef et al. [25], zinc oxide nanoparticles could protect the hepatic cells from the damaging effect of Aflatoxin B1 through scavenging free radicals [25].

Zinc oxide nanoparticles affected the growth of both gram positive and gram negative bacteria; so, they could be considered as potent antibacterial agents. The antibacterial effect of zinc oxide nanoparticles is due to the high sensitivity of the lipid bilayer of bacteria to the reactive oxygen species produced by these nanoparticles [27-29]. Moreover, zinc oxide nanoparticles could also be considered as antifungal agents; because they could completely stop the growth of some types of fungi when administered at high concentrations. However, recent studies show that the impact of zinc oxide nanoparticles on some organisms is not yet sufficiently understood despite their widespread use in biomedicine [29].

In the field of cosmetics, zinc oxide nanoparticles powder is widely used in sunscreens and ointments [30]. Zinc oxide nanoparticles are considered as ultraviolet blockers and semiconductor agents because they could absorb and scatter the visible ultraviolet rays. The photocatalytic activity of zinc oxide nanoparticles increases with decreasing their sizes [31]. Numerous studies on healthy human skin suggested that zinc oxide nanoparticles don't penetrate beyond the stratum corneum when they are used in sunscreens [32].

Zinc oxide nanoparticles are widely used in dietary supplements. They were found to produce an immunomodulatory effect. Roy et al. reported that zinc oxide nanoparticles increased antigen-specific immune reactions in mice. They enhanced antigen-specific antibodies production in serum, especially immunoglobulin E (IgE) and immunoglobulin G (IgG), and they also could enhance the functionality of T cells. It was also detected that zinc oxide nanoparticles had an adjuvant effect toward Th2 response; increasing the production and activation of cytokines [33].

In recent years, a number of studies have shown the possibility of using zinc oxide nanoparticles as therapeutic agents and as gene carriers. At the same time, many published research studies showed the toxic effects of zinc oxide nanoparticles on some specific organs and cell lines. These toxic effects were attributed to the high solubility of the particles, resulting in cytotoxicity, oxidative stress, and mitochondrial dysfunction. Therefore, an urgent necessity exists to evaluate both the toxicological hazards and the therapeutic benefits for the use of zinc oxide nanoparticles in medicine. Furthermore, it is important to determine if their toxicity is reversible, and if this toxicity depends on the concentration and the time of exposure to the particles [34].

Inhalation of zinc oxide nanoparticles induced inflammation and fibrosis in the alveolar and tracheobronchial tissues depending on the size and solubility of the particles. Acidic lung fluid resulted in the dissolution of zinc oxide nanoparticles, and consequently increased their concentration leading to pulmonary toxicity [35]. Furthermore, zinc oxide nanoparticles induced cytotoxicity in human lung epithelial cells via inducing oxidative stress in a concentration-dependent manner, resulting in DNA damage and apoptosis [36].

Intra-peritoneal injection of zinc oxide nanoparticles was found to cause neurotoxic effects in the form of attenuation of the learning ability and memory according to the study of Han et al. [37]. Elshama et al. [38] found that the prolonged use of zinc oxide nanoparticles via intra-peritoneal route induced histopathological and ultrastructural changes in the brains and spinal cords of rats, depending on the dose, and based on reactive oxygen species generation.

Moreover, Li et al. [39] reported that both intraperitoneal and oral administration of zinc oxide nanoparticles led to systemic distribution and toxic accumulation of the particles in the liver, spleen, kidney, and lung; which were the target organs where the toxic manifestations of zinc oxide nanoparticle have appeared. In male rats, zinc oxide nanoparticles elevated liver enzymes, and led to harmful effects on the body metabolism [40]. In the same context, Soheili et al. [41] reported that the administration of zinc oxide nanoparticles increased significantly all liver enzymes (e.g. aspartate transaminase “AST”, alanine transaminase “ALT”, alkaline phosphatase “ALP” and lactate dehydrogenase “LDH”) in a dose-dependent manner. Furthermore, the authors reported an increase in the blood glucose level, suggesting the defective effects of zinc oxide nanoparticles on the pancreatic cells. Administration of zinc oxide nanoparticles was also found to induce severe anemia and significant histopathological changes on the livers and hearts of rats. The histopathological changes were in the form of hyaline degeneration of the cardiac muscle and focal hemorrhages associated with hepatic apoptosis. Esmaeilloua et al. [42] demonstrated that zinc oxide nanoparticles had severe oxidative toxic effects on kidney, lung, and liver. The effects were dependent on the physicochemical properties of nanoparticles such as the specific surface area and the nanoparticle size.

In addition, Ko et al. [43] reported that zinc oxide nanoparticles adversely altered the hematological indices such as hemoglobin, hematocrit, mean corpuscular volume, mean corpuscular hemoglobin, mean corpuscular hemoglobin concentration, platelets, and white blood cells (total and differential). They also reported histopathological changes in the spleen, stomach, and pancreas associated with zinc oxide nanoparticles administration. In the same context, Seoka et al. [44] showed that oral intake of high dose zinc oxide nanoparticles led to pancreatitis and anemia.

Kim et al. [45] showed that the oral administration of different doses of 100 nm zinc oxide nanoparticles with different surface charges and for a prolonged period induced significant histopathological changes, such as squamous and glandular cell hyperplasia in the stomach, acinar cell apoptosis in the pancreas, retinal atrophy, and suppurative inflammation in the prostate. They also detected disturbances in most hematological indices, and in other biochemical parameters such as blood urea nitrogen, blood glucose and calcium, albumin, and alkaline phosphatase. The previously reported toxic effects were observed at doses greater than 125 mg/kg, while the No Observed Adverse Effect Level (NOAEL) was 31.25 mg/kg.

Sub-chronic use of zinc oxide nanoparticles was found to induce toxic manifestations in the lymphatic system and in the blood cell count depending on the administered dose. The nanoparticles induced a decrease in the total blood cell count (white blood cells, red blood cells, and platelets), a disturbance in the differential white blood cell count, and produced histopathological and ultrastructural changes in thymus, spleen and lymph nodes in rats [46].

Reza et al. [47] conducted a study to investigate the deleterious effects of treating rats with different doses of zinc oxide nanoparticles on Thyroid Stimulating Hormone (TSH), Follicular Stimulating Hormone (FSH) and Luteinizing Hormone (LH) levels, and on cholesterol level in the blood. The authors detected a decrease in FSH level and an increase in TSH level; however, they found an increase in the cholesterol level. The induced effects on rats were associated with the administration of high doses only.

Although available data about the effects of zinc oxide nanoparticles on reproduction and on fetal development are not enough so far, Hong et al. [48] reported that the administration of repeated oral doses of zinc oxide nanoparticles in rats during pregnancy and for short periods of time -not exceeding 15 days- led to maternal and developmental toxicity.