Skip to main content
Log in

Compression Behavior of Orthorhombic Paracetamol

  • Published:
Pharmaceutical Research Aims and scope Submit manuscript

Abstract

Purpose. Orthorhombic crystals of paracetamol exhibit good technological properties during compression. The purpose of this study was to investigate the compression behavior of this substance and to compare it to that of monoclinic paracetamol. From the crystal structure, it could be hypothesized that sliding planes are present in the orthorhombic form, and could be responsible for an increase in crystal plasticity.

Methods. Compression of pure orthorhombic or monoclinic paracetamol tablets was carried out on a fully instrumented single punch machine. Data was used to establish Heckel's profiles. Images of compressed crystals were obtained by scanning electron microscopy.

Results. Tabletability of the orthorhombic crystals was far better than that of the monoclinic ones, and capping was not observed even at high compression pressure. Compared to the monoclinic form, orthorhombic paracetamol exhibited greater fragmentation at low pressure, increased plastic deformation at higher pressure, and lower elastic recovery during decompression. Plastic behavior was confirmed by SEM - micrographs showing that crystals folded under pressure. A compactibility study showed that the nature of interparticle bonds was similar for both polymorphs, the number of bonds being greater for orthorhombic paracetamol.

Conclusions. Unlike the monoclinic form, orthorhombic paracetamol is suitable for the direct compression process. The crystalline structure accounts for its better compression behavior, because of the presence of sliding planes.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

REFERENCES

  1. M. Duberg and C. Nyström. Studies on Direct Compression of Tablets. XVII. Porosity-pressure curves for the characterization of volume reduction mechanisms in powder compression. Powder Technol. 46:67–75 (1994).

    Google Scholar 

  2. D. Train. An investigation into the compaction of powder. J. Pharm. Pharmacol. 8:745–761 (1956).

    Google Scholar 

  3. J. S. M. Garr and M. H. Rubinstein. An investigation into the capping of paracetamol at increasing speeds of compression. Int. J. Pharm. 72:117–122 (1991).

    Google Scholar 

  4. R. Hüttenrauch. New concepts in pharmaceutics. Labo-Pharma-Probl. Tech. 31:644–655 (1983).

    Google Scholar 

  5. P. York. Crystal engineering and particle design for the powder compaction process. Drug Dev. Ind. Pharm. 18:677–721 (1992).

    Google Scholar 

  6. J. M. Fachaux, A. M. Guyot-Hermann, J. C. Guyot, P. Conflant, M. Drache, S. Veesler, and R. Boistelle. Pure paracetamol for direct compression. Part I. Development of sintered—like crystals of paracetamol. Powder Technol. 82:123–128 (1995).

    Google Scholar 

  7. A. Ettabia, E. Joiris, A. M. Guyot-Hermann, and J. C. Guyot. Preparation of a pure paracetamol for direct compression by spherical agglomeration. Pharm. Ind. 59:625–631 (1997).

    Google Scholar 

  8. P. Di Martino, A. M. Guyot-Hermann, P. Conflant, and J. C. Guyot. A new pure paracetamol for direct compression: the orthorhombic form Int. J. Pharm. 128:1–8 (1996).

    Google Scholar 

  9. M. Haïsa, S. Kashino, and H. Maeda. The orthorhombic form of p-hydroxyacetanilide. Acta Cryst. B30:2510–2513 (1974).

    Google Scholar 

  10. M. Haïsa, S. Kashino, R. Kawai, and H. Maeda. The monoclinic form of p-hydroxyacetanilide. Acta Cryst. B32:1283–1285 (1976).

    Google Scholar 

  11. H. Hess. Tablets under the microscope. Pharm. Technol. 9:37–58 (1978)

    Google Scholar 

  12. P. Di Martino, P. Conflant, M. Drache, J. P. Huvenne, and A. M. Guyot-Hermann. Preparation and physical characterization of Forms II and III of paracetamol. J. Thermal Anal. 48:447–458 (1997).

    Google Scholar 

  13. C. Lefebvre, F. Guillaume, R. Bouché, R. Bouaziz, and J. C. Guyot. Etude de différentes formes polymorphes du méprobamate. 5th International Conference On Pharmaceutical Technology. Paris. I: 211–221 (1989).

    Google Scholar 

  14. M. J. Juslin and T. P. Paronen. On the accuracy of displacement measurements by instrumented single-punch machines. J. Pharm. Pharmacol. 32:796–798 (1980).

    Google Scholar 

  15. J. T. Fell and J. M. Newton. Determination of tablet strength by the diametral-compression test. J. Pharm. Sci. 5:688–691 (1970).

    Google Scholar 

  16. N. A. Armstrong and R. F. Haines-Nutt. Elastic recovery and surface area changes in compacted powder systems. Powder Technol. 9:287–290 (1974).

    Google Scholar 

  17. R. W. Heckel. Density—pressure relationships in powder compaction. Trans. Metall. Soc. AIME, 221:661–675 (1961).

    Google Scholar 

  18. E. Doelker. Assessment of powder compaction. In D. Chulia, M. Deleuil and Y. Pourcelot (eds), Powder technology and pharmaceutical processes, Elsevier, Amsterdam, 1994, pp. 403–471.

    Google Scholar 

  19. M. Eriksson and G. Alderborn. The effect of original particle size and tablet porosity on the increase in tensile strength during storage of sodium chloride tablets in a dry atmosphere. Int. J. Pharm. 113:199–207 (1995).

    Google Scholar 

  20. P. Paronen and J. Ilkka. Porosity-pressure functions. In G. Alderborn and C. Nyström (eds), Pharmaceutical powder compaction technology, Marcel Dekker, New York, 1996, pp. 55–75.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Joiris, E., Martino, P.D., Berneron, C. et al. Compression Behavior of Orthorhombic Paracetamol. Pharm Res 15, 1122–1130 (1998). https://doi.org/10.1023/A:1011954800246

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1023/A:1011954800246

Navigation