Chitosan-g-poly(vinyl alcohol) (PVA) copolymers with different grafting percent were prepared by grafting water-soluble PVA onto chitosan. The drug-release behavior was studied using the chitosan-g-PVA copolymer matrix containing prednisolone in a drug-delivery system under various conditions. The r
Properties of chitosan/poly(vinyl alcohol) films for drug-controlled release
β Scribed by Qun Wang; Yu-min Du; Li-hong Fan
- Publisher
- John Wiley and Sons
- Year
- 2005
- Tongue
- English
- Weight
- 173 KB
- Volume
- 96
- Category
- Article
- ISSN
- 0021-8995
No coin nor oath required. For personal study only.
β¦ Synopsis
Abstract
With bovine serum albumin (BSA) as a model drug, drugβloaded films of chitosan (CS) and poly(vinyl alcohol) (PVA) were obtained by a casting/solvent evaporation method and crosslinked by tripolyphosphate (TPP). The films were characterized by FTIR, XRD, and SEM. The influential factors of drugβloaded films on drugβcontrolled release were studied. These factors included, primarily, the component ratio of CS and PVA, the loaded amount of BSA, the pH and ionic strength of the release solution, and the crosslinking time with TPP. The results showed that within 25 h, when the weight ratios of CS to PVA in the drugβloaded films were 90 : 10, 70 : 30, 50 : 50, and 30 : 50, the cumulative release rates of BSA were 63.3, 72.9, 81.8, and 91.8%, respectively; when the amounts of model drug were 0.1, 0.2, and 0.3 g, the release rates were 100, 81.8, and 59.6%, respectively; when the pH values of the drug release medium were 1.0, 3.8, 5.4, and 7.4, the release rates reached 100, 100, 37.9, and 7.8%, respectively; the cumulative release rates of BSA were 78.4, 82.3, 84.3, and 91.7% when the ionic strengths of the release solution were, respectively, 0.1, 0.2, 0.3, and 0.4__M__; when the crosslinking times of these drug films in the TPP solution were 0, 5, 15, 30, and 60 min, the release rates attained 100, 100, 81.8, 65, and 43.3%, respectively. All the results indicated that the CS/PVA film was useful in drug delivery systems. Β© 2005 Wiley Periodicals, Inc. J Appl Polym Sci 96: 808β813, 2005
π SIMILAR VOLUMES
## Abstract Physically crosslinked chitosanβ__g__βpoly(vinyl alcohol) hydrogels with controllable graft percent were prepared in three steps. Poly(vinyl acetate) (PVAc) was first grafted onto chitosan via radical copolymerization. Then the copolymer was converted into chitosanβ__g__βpoly(vinyl alco