以卡波波尔675和PVP为黏附基元的黏附持续递送双氯芬酸钠

A. Attama, P. Akpa, Cw Nwokeabia
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引用次数: 0

摘要

研究了卡波波尔675与聚乙烯吡咯烷酮(PVP)及其物理混合物制备的黏附片对双氯芬酸钠的黏附性、溶胀特性和释放特性,以评价其在持续给药中的适用性。采用leomte du Nuoy张力仪和猪空肠张力法测定片剂的离体黏附强度。在三种不同pH培养基(1.2、7.0和7.5)中进行释放研究。黏附试验结果表明,以卡波波尔675与PVP 1:1物理混合配制的片剂黏附强度最高,表明其与猪空肠黏附紧密。它们的低溶胀和低释放特性也表明该片剂是缓释型制剂的很好候选,因为该片剂能维持双氯芬酸钠的释放。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mucoadhesive sustained delivery of diclofenac sodium using carbopol 675 and PVP admixtures as mucoadhesive motif
The mucoadhesiveness, swelling characteristics and release profile of diclofenac sodium from mucoadhesive tablets prepared with Carbopol 675 and polyvinyl pyrrolidone (PVP) and their physical mixtures were studied to evaluate their applicability in sustained drug delivery. The ex-vivo mucoadhesive strengths of the tablet compacts were determined by tensiometry using Lecomte du Nuoy tensiometer and everted pig jejunum. Release studies were carried out in three different pH media (1.2, 7.0 and 7.5). The results of mucoadhesive test revealed that tablets formulated from 1:1 physical mixture of Carbopol 675 and PVP had the highest mucoadhesive strength, which showed they bound tightly to the mucus pig jejunum. Their low swelling and release behaviours also indicated that the tablet compacts are very good candidates for sustained release formulation since release of diclofenac sodium was sustained by the compacts.
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