The effect of cross-linking of chitosan microspheres with genipin on protein release

被引:247
作者
Yuan, Y. [1 ]
Chesnutt, B. M. [1 ]
Utturkar, G. [1 ]
Haggard, W. O. [1 ]
Yang, Y. [1 ]
Ong, J. L. [1 ]
Bumgardner, J. D. [1 ]
机构
[1] Univ Memphis, Univ Memphis Univ Tennessee Joint Biomed Engn Pro, Hlth Sci Ctr, Dept Biomed Engn, Memphis, TN 38152 USA
关键词
chitosan microsphere; drug/protein delivery; degree of cross-linking; swelling ratio; genipin;
D O I
10.1016/j.carbpol.2006.10.023
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Genipin, a natural and non-toxic cross-linking reagent, was evaluated for its effects on the drug/protein release and swelling of chitosan microspheres. Chitosan microspheres, using albumin as a model protein, were prepared and cross-linked with 0.5 mM genipin for 4 to 16 h or for 4 h using 0.5 to 2.0 mM genipin. The degree of cross-linking, swelling and the release of albumin from the microspheres was determined by the ninhydrin assay, measuring change in mass between dry and wet spheres, and in 3 1 -day elution tests, respectively. The degree of cross-linking increased up to maximum of 33% to 34% with up to 8 hour cross-linking time or with up to 1.0 mM genipin concentration. Additional cross-linking time or concentration did not significantly increase degree of cross-linking. Swelling ratios decreased significantly from 119.2% in the uncross-linked condition to 108.8% at 16 h cross-linking time. However, increasing the genipin concentration resulted in much smaller decreases in swelling. The release of albumin was reduced with as little as 4 h cross-linking time to 30.9% of uncross-linked microspheres for up to 24 days and by as much as 52.3-60.0% for up to 31 days with 8-16 h cross-linking time. Using genipin concentrations of 1.0 to 2.0 mM for 4 h, greatly reduced albumin release to only 12.4% to 27.1 % on day 24. These data demonstrate that protein and drug delivery rates from chitosan microspheres may be controlled and extended by controlling the degree of cross-linking with genipin. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:561 / 567
页数:7
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