Gümüşderelioglu M, Deniz G
Hacettepe University, Chemical Engineering Department, Ankara, Turkey.
J Biomater Sci Polym Ed. 2000;11(10):1039-50. doi: 10.1163/156856200743562.
Mitomycin-C (MMC)-loaded poly(DL-lactide) (PLA)/poly(DL-lactide-co-glycolide) (PLGA) films which have different drug loading capacities and thicknesses were prepared by a solvent-evaporation technique. Degradation and release studies were conducted at 37 degrees C in pH 7.4 phosphate buffered saline. The results showed that both the rate and the percentage of released MMC increased as the glycolide content in the copolymer increased from 10 to 30% (w/w) and the drug load increased from 0.5 to 2 mg MMC per 300 mg of polymer. In contrast, they decreased depending upon increasing film thickness from 80 to 300 microm and polymer molecular weight. It was found that the drug release mechanism is diffusion-controlled according to a non-Fickian diffusion mechanism.
通过溶剂蒸发技术制备了具有不同载药量和厚度的载丝裂霉素-C(MMC)的聚(DL-丙交酯)(PLA)/聚(DL-丙交酯-共-乙交酯)(PLGA)薄膜。在37℃、pH 7.4的磷酸盐缓冲盐水中进行降解和释放研究。结果表明,随着共聚物中乙交酯含量从10%(w/w)增加到30%(w/w)以及载药量从每300mg聚合物0.5mg MMC增加到2mg MMC,MMC的释放速率和释放百分比均增加。相反,随着薄膜厚度从80μm增加到300μm以及聚合物分子量增加,它们会降低。发现药物释放机制根据非菲克扩散机制是扩散控制的。