首页> 外文期刊>Journal of Controlled Release: Official Journal of the Controlled Release Society >Oral colon-specific drug delivery for bee venom peptide: development of a coated calcium alginate gel beads-entrapped liposome
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Oral colon-specific drug delivery for bee venom peptide: development of a coated calcium alginate gel beads-entrapped liposome

机译:蜂毒肽的口服结肠特异性药物递送:包被有藻酸盐钙微珠的脂质体的开发

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摘要

Colon-specific drug delivery systems (CDDSs) can be used to improve the bioavailability of protein and peptide drugs through the oral route. A novel formulation for oral administration using coated calcium alginate gel beads-entrapped liposome and bee venom peptide as a model drug has been investigated for colon-specific drug delivery in vitro. Drug release studies under conditions mimicking stomach to colon transit have shown that the drug was protected from being released completely in the physiological environment of the stomach and small intestine. The release rate of bee venom from the coated calcium alginate gel beads-entrapped liposome was dependent on the concentration of calcium and sodium alginate, he amount of bee venom in the liposome, as well as the coating. Furthermore, a human gamma-scintigraphy technique was used in vivo to determine drug delivery more precisely. The colonic arrival time of the tablets was found to be 4-5 h. The results clearly demonstrated that the coated calcium alginate gel beads-entrapped liposome is a potential system for colon-specific drug delivery. (C) 2003 Elsevier B.V. All rights reserved. [References: 19]
机译:结肠特异性药物递送系统(CDDS)可用于通过口服途径改善蛋白质和肽类药物的生物利用度。已经研究了使用包衣有藻酸钙凝胶珠的脂质体和蜂毒肽作为模型药物进行口服给药的新型制剂,用于体外结肠特异性药物递送。在模拟胃到结肠转运的条件下进行的药物释放研究表明,可以防止药物在胃和小肠的生理环境中完全释放。蜂毒从包被的藻酸钙凝胶珠包裹的脂质体中的释放速率取决于钙和海藻酸钠的浓度,脂质体中蜂毒的量以及包衣。此外,在体内使用了人类伽玛闪烁显像技术来更精确地确定药物的传递。发现片剂的结肠到达时间为4-5小时。结果清楚地表明,包被的藻酸钙凝胶珠包裹的脂质体是结肠特异性药物递送的潜在系统。 (C)2003 Elsevier B.V.保留所有权利。 [参考:19]

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