乙酰氯芬酸缓释微球的制备:表征及体内研究

Rakesh Sharma, Anil Midda
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引用次数: 1

摘要

http://dx.doi.org/10.21276/IJRDPL.22780238.2017.6(7).2862-2866摘要:目的:探讨醋氯芬酸微球缓释模型,建立水凝胶形成黏附聚合物对药物释放的影响。方法:以羧甲基纤维素(CMC)和卡波波尔934P (CP)为水凝胶形成聚合物,采用乳液溶剂蒸发法制备微球。结果与讨论:以羧甲基纤维素钠和卡波姆934P水凝胶形成聚合物为原料制备了醋酸氯芬酸黏附缓释微球。羧甲基纤维素钠和卡波姆934P分别以1/3和1/6w/w的比例进行制备。扫描电镜显示微球的外表面不均匀。在模拟胃液pH 1.2和模拟肠液pH 6.8条件下进行体外溶出试验。发现乙酰氯芬酸从微球中持续释放,依赖于卡波波尔934P交联的侵蚀。对新鲜鸡胃黏膜和鸡蛋壳膜进行了体外黏附研究。在雄性Sprague-Dawley大鼠体内进行微球胃肠道输送。结论:体外释药持续时间为14 h。体外黏附评价可在鸡胃粘膜或鸡蛋壳膜上进行。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Preparation of Sustained Release Microspheres of Aceclofenac: Characterization & in-vivo studies
http://dx.doi.org/10.21276/IJRDPL.22780238.2017.6(7).2862-2866 ABSTRACT:Objective: To explore the sustained drug release model of Aceclofenac from microspheres to establish the result of hydrogel forming mucoadhesive polymers on drug release. Methods: Microspheres were produced by Emulsion solvent evaporation method using Carboxy Methyl cellulose (CMC) and Carbopol 934P (CP) as hydrogel forming polymers. Results and Discussion: Mucoadhesive sustained release microspheres of Aceclofenac were prepared using carboxymethyl cellulose sodium and carbomer 934P hydrogel forming polymers. Carboxymethyl cellulose sodium and Carbomer 934P were used in 1/3 and 1/6w/w proportion in the preparation. Scanning electron microscopy revealed the uneven outer surface of the microspheres. Invitro dissolution test was carried out in simulated gastric fluid pH 1.2 and simulated intestinal fluid pH 6.8. Release of Aceclofenac from microspheres was found sustained, dependent on the erosion of crosslinking of carbopol 934P. Invitro mucoadhesive study was done on fresh stomach mucosa of chicken and chicken egg shell membrane. Invivo gastroenteric conveyance of microspheres was done in Male Sprague-Dawley rats. Conclusion: Invitro drug release is sustained for the period of 14 hrs. In-vitro Mucoadhesion evaluation can be done either on chicken stomach mucous membrane or chicken eggshell membrane.
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