Skip to main content
Log in

The Effect of Microcrystalline Cellulose Crystallinity on the Hydrophilic Property of Tablets and the Hydrolysis of Acetylsalicylic Acid as Active Pharmaceutical Ingredient Inside Tablets

  • Research Article
  • Published:
AAPS PharmSciTech Aims and scope Submit manuscript

Abstract

The crystal structures of active pharmaceutical ingredients and excipients should be strictly controlled because they influence pharmaceutical properties of products which cause the change in the quality or the bioavailability of the products. In this study, we investigated the effects of microcrystalline cellulose (MCC) crystallinity on the hydrophilic properties of tablets and the hydrolysis of active pharmaceutical ingredient, acetylsalicylic acid (ASA), inside tablets by using tablets containing 20% MCC as an excipient. Different levels of grinding were applied to MCC prior to tablet formulation, to intentionally cause structural variation in the MCC. The water penetration and moisture absorbability of the tablets increased with decreasing the crystallinity of MCC through higher level of grinding. More importantly, the hydrolysis of ASA inside tablets was also accelerated. These results indicate that the crystallinity of MCC has crucial effects on the pharmaceutical properties of tablets even when the tablets contain a relatively small amount of MCC. Therefore, controlling the crystal structure of excipients is important for controlling product qualities.

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.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5
Fig. 6

Similar content being viewed by others

References

  1. FDA paper: guideline for submitting supporting documentation in drug applications for the manufacture of drug substances. 1987.

  2. Otsuka M, Matsuda Y. Polymorphism: pharmaceutical aspects. In: Swarbrick J, Boylan JC, editors. Encyclopedia of pharmaceutical technology vol. 12. New York: Marcel Dekker, Inc; 1995. p. 305–26.

    Google Scholar 

  3. Maggio RM, Castellano PM, Kaufman TS. PCA-CR analysis of dissolution profiles. A chemometric approach to probe the polymorphic form of the active pharmaceutical ingredient in a drug product. Int J Pharm. 2009;378:187–93.

    Article  CAS  PubMed  Google Scholar 

  4. Engel GL, Farid NA, Faul MM, Richardson LA, Winneroski LL. Salt form selection and characterization of LY333531 mesylate monohydrate. Int J Pharm. 2000;198:239–47.

    Article  CAS  PubMed  Google Scholar 

  5. McNamara DP, Childs SL, Giordano J, Iarriccio A, Cassidy J, Shet MS, et al. Use of a glutaric acid cocrystal to improve oral bioavailability of a low solubility API. Pharm Res. 2006;23:1888–97.

    Article  CAS  PubMed  Google Scholar 

  6. Ando M, Ito R, Ozeki Y, Nakayama Y, Nabeshima T. Evaluation of a novel sugar coating method for moisture protective tablets. Int J Pharm. 2007;336:319–28.

    Article  CAS  PubMed  Google Scholar 

  7. Sebhatu T, Elamin AA, Ahlnek C. Effect of moisture sorption on tabletting characteristics of spray dried (15% amorphous) lactose. Pharm Res. 1994;11:1233–8.

    Article  CAS  PubMed  Google Scholar 

  8. Shinzawa H, Awa K, Ozaki Y. Compression effect on sustained-release and water absorption properties of cellulose tablets studied by heterospectral two-dimensional (2D) correlation analysis. Anal Methods. 2012;4:1530–7.

    Article  CAS  Google Scholar 

  9. Awa K, Shinzawa H, Ozaki Y. An effect of cellulose crystallinity on moisture-absorbability of a pharmaceutical tablet studied by near-infrared spectroscopy and scanning electron microscopy. Appl Spectrosc. 2014;68:625–32.

    Article  CAS  PubMed  Google Scholar 

  10. Suzuki T, Nakagami H. Effect of crystallinity of microcrystalline cellulose on the compactability and dissolution of tablets. Eur J Pharm Biopharm. 1999;47:225–30.

    Article  CAS  PubMed  Google Scholar 

  11. Yano S, Hatakeyama H. Dynamic viscoelasticity and structural changes of regenerated cellulose during water sorption. Polymer. 1988;29:566–70.

    Article  CAS  Google Scholar 

  12. Klemm D, Phillip B, Heinze T, Heinze U, Wagenknecht W. Comprehensive cellulose chemistry: vol. 1 fundamentals and analytical methods. Weinheim: Wiley-VCH Verlag GmbH; 1998.

    Book  Google Scholar 

  13. Shinzawa H, Awa K, Ozaki Y. Compression-induced morphological and molecular structural changes of cellulose tablets probed with near infrared imaging. J Near Infrared Spectrosc. 2011;19:15–22.

    Article  CAS  Google Scholar 

  14. Shinzawa H, Awa K, Ozaki Y, Sato H. Near-infrared imaging analysis of cellulose tablets by a band position shift. Appl Spectrosc. 2009;63:974–7.

    Article  CAS  PubMed  Google Scholar 

  15. Merck Index. Twelfth Edition. Merck Research Laboratories; 1996. P. 886.

  16. Ciolacu D, Ciolacu F, Pola VI. Amorphous cellulose-structure and characterization. Cellul Chem Technol. 2011;45:13–21.

    CAS  Google Scholar 

  17. Sinka IC, Burch SF, Tweed JH, Cunningham JC. Measurement of density variations in tablets using X-ray computed tomography. Int J Pharm. 2004;271:215–24.

    Article  CAS  PubMed  Google Scholar 

  18. Shinzawa H, Morita S, Awa K, Okada M, Noda I, Ozaki Y, et al. Multiple perturbation two-dimensional correlation analysis of cellulose by attenuated total reflection infrared spectroscopy. Appl Spectrosc. 2009;63:501–6.

    Article  CAS  PubMed  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Kimie Awa.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Awa, K., Shinzawa, H. & Ozaki, Y. The Effect of Microcrystalline Cellulose Crystallinity on the Hydrophilic Property of Tablets and the Hydrolysis of Acetylsalicylic Acid as Active Pharmaceutical Ingredient Inside Tablets. AAPS PharmSciTech 16, 865–870 (2015). https://doi.org/10.1208/s12249-014-0276-7

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1208/s12249-014-0276-7

Keywords

Navigation