Skip to main content
AAPS PharmSciTech logoLink to AAPS PharmSciTech
. 2006 Sep 1;7(3):E107–E113. doi: 10.1208/pt070370

5-methyl-pyrrolidinone chitosan films as carriers for buccal administration of proteins

Claudia Colonna 1, Ida Genta 1, Paola Perugini 1, Franca Pavanetto 1, Tiziana Modena 1, Maurizia Valli 2, Corrado Muzzarelli 3, Bice Conti 1,
PMCID: PMC2750512  PMID: 17025236

Abstract

The purpose of this research was to investigate 5-methyl-pyrrolidinone chitosan (MPC) films as carriers for buccal delivery of protein drugs. Placebo and protein-loaded MPC films were prepared by casting and were then cross-linked with tripolyphosphate at different pH conditions. Myoglobin (MHb) was chosen as the model protein because its molecular weight is under the permeability limit of the buccal mucosa. The observed characteristics like bioadhesiveness, swelling behavior, and in vitro release of MHb from loaded films furnish information on the functional behavior of these films. The results obtained show that the modulation of Mhb release was achieved only through chitosan cross-linking; the best results in release rate control were obtained by cross-linking performed at pH 6.5. Good bioadhesion properties were maintained even with high cross-linking degrees; the swelling index of MHb-loaded films at different cross-linking degrees evaluated at pH 7.4 and pH 6.4 were comparable to those of placebo films. By setting suitable tripolyphosphate cross-linking conditions for MPC films, one can control protein release without affecting bioadhesion.

Keywords: 5-methyl-pyrrolidinone chitosan, tripolyphosphate cross-linked films, protein delivery, buccal cavity

Full Text

The Full Text of this article is available as a PDF (232.4 KB).

References

  • 1.Paul W, Sharma CP. Chitosan, a drug carrier for the 21 st century: a review. STP Pharma Sci. 2000;10:5–22. [Google Scholar]
  • 2.Muzzarelli RAA, Ilari P, Tomasetti M. Preparation and characteristic properties of 5-methylpyrrolidinone chitosan. Carbohydr Polym. 1993;20:99–105. doi: 10.1016/0144-8617(93)90084-H. [DOI] [Google Scholar]
  • 3.Sandri G, Rossi S, Ferrari F, Bonferoni MC, Muzzarelli C, Caramella C. Assessment of chitosan derivatives as buccal and vaginal penetration enhancers. Eur J Pharm Sci. 2004;21:351–359. doi: 10.1016/j.ejps.2003.10.028. [DOI] [PubMed] [Google Scholar]
  • 4.Berscht PC, Nies B, Liebendöfer A, Kreuter J. In vitro evaluation of biocompatibility of different wound dressing materials. J Mater Sci Mater Med. 1995;6:201–205. doi: 10.1007/BF00146856. [DOI] [Google Scholar]
  • 5.Smith J, Wood E, Dornish M. Effect of chitosan on epithelial cell tight junctions. Pharm Res. 2004;21:43–49. doi: 10.1023/B:PHAM.0000012150.60180.e3. [DOI] [PubMed] [Google Scholar]
  • 6.Senel S, Ikinci G, Kas S, Yousefi-Rad A, Hincal AA. Chitosan films and hydrogels of chlorhexidine gluconate for oral mucosal delivery. Int J Pharm. 2000;193:197–203. doi: 10.1016/S0378-5173(99)00334-8. [DOI] [PubMed] [Google Scholar]
  • 7.Needleman I, Martin GP, Smales FC. Characterization of bioadhesives for periodontal and oral mucosal drug delivery. J Clin Periodontol. 1998;25:74–82. doi: 10.1111/j.1600-051X.1998.tb02366.x. [DOI] [PubMed] [Google Scholar]
  • 8.Senel S, Kremer MJ, Kas S, Wertz PW, Hincal AA, Squier CA. Enhancing effect of chitosan on peptide drug delivery across buccal mucosa. Biomaterials. 2000;21:2067–2071. doi: 10.1016/S0142-9612(00)00134-4. [DOI] [PubMed] [Google Scholar]
  • 9.Berger J, Reist M, Mayer JM, Felt O, Peppas NA, Gurny R. Structure and interactions in covalently and ionically crosslinked chitosan hydrogels for biomedical applications. Eur J Pharm Biopharm. 2004;57:19–34. doi: 10.1016/S0939-6411(03)00161-9. [DOI] [PubMed] [Google Scholar]
  • 10.Genta I, Colonna C, Perugini P, et al. Evaluation of bioadhesive performance of chitosan derivatives as films for buccal application. J Drug Deliv Sci Technol. 2005;15:459–463. [Google Scholar]
  • 11.Shu XZ, Zhu KJ. The influence of multivalent phosphate structure on the properties of ionically cross-linked chitosan films for controlled drug release. Eur J Pharm Biopharm. 2002;54:235–243. doi: 10.1016/S0939-6411(02)00052-8. [DOI] [PubMed] [Google Scholar]
  • 12.Remunan-Lopez C, Bodmeir R. Mechanical water uptake and permeability properties of cross-linked chitosan glutamate and alginate films. J Control Release. 1997;44:215–225. doi: 10.1016/S0168-3659(96)01525-8. [DOI] [Google Scholar]
  • 13.Mi F, Shyu SS, Lee ST, Wong TB. Kinetic study of chitosan-tripolyphosphate complex reaction and acid-resistive properties of the chitosan-tripolyphosphate gel beads prepared by in-liquid curing method. J Polym Sci Part B: Polym Phys. 1999;37:1551–1564. doi: 10.1002/(SICI)1099-0488(19990715)37:14<1551::AID-POLB1>3.0.CO;2-H. [DOI] [Google Scholar]
  • 14.Mi FL, Shyu SS, Lee ST, Wong TB. Chitosan-polyelectrolyte complexation for the preparation of gel beads and controlled release of anticancer drug, II: effect of pH-dependent ionic cross-linking or interpolymer complex using tripolyphosphate or polyphosphate as reagent. J Appl Polym Sci. 1999;74:1093–1107. doi: 10.1002/(SICI)1097-4628(19991031)74:5<1093::AID-APP6>3.0.CO;2-C. [DOI] [Google Scholar]
  • 15.Patel D, Smith AW, Grist N, Barnett P, Smart JD. An in vitro mucosal model of bioadhesive agents in the oral cavity. J Control Release. 1999;61:175–183. doi: 10.1016/S0168-3659(99)00117-0. [DOI] [PubMed] [Google Scholar]

Articles from AAPS PharmSciTech are provided here courtesy of American Association of Pharmaceutical Scientists

RESOURCES