软性明胶胶囊制剂中胰岛素的释放机制

M. Momoh, M. Adikwu, So Eragasa
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引用次数: 0

摘要

评价了试验制剂的药物释放动力学。使用了Kitazawa、Higuchi、Hixson-Crowell和Fickian模型。以新鲜屠宰的牛小肠为原料,经冷丙酮沉淀、风干、粉碎等工艺制备粘蛋白。分别以1:10、1:15、1:25的比例包封不同的胰岛素-粘蛋白制剂。体外释放研究表明,随着黏蛋白浓度的增加,其释放速率降低。1:10、1:15、1:25比例制剂的初始释放量分别为10min 41.4 mg、90min 54.5 mg、10min 24.2 mg、90min 50.9 mg、10min 34.0 mg、150min 45.1 mg。除了含有胰岛素和粘蛋白的制剂外,制剂中胰岛素的释放一般遵循Higuchi扩散模型机制。
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The release mechanism of insulin from soft gelatin capsule preparation
The kinetics of drug release from the test formulation was evaluated. Kitazawa, Higuchi, Hixson-Crowell and Fickian models were used. Mucin was processed from the small intestine of freshly slaughtered cow via precipitation with chilled acetone, air-drying and pulverization. Various preparations of insulin-mucin in the ratios 1:10, 1:15 and 1:25 were encapsulated. The in vitrorelease studies showed that the release rates decreased with increase in mucin concentration. The initial of releases were 41.4 mg in 10 min and 54.5 mg at 90 min , 24.2 mg in 10 min and 50.9 mg at 90 min and 34.0 mg in 10 min and 45.1 mg at 150 min for 1:10 1:15, 1:25 ratio preparations respectively. The release of insulin from the preparation generally followed the Higuchi diffusion model mechanisms with the exception of the formulation containing of insulin and mucin.
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