蔓荆子乙素负载外用草药凝胶的配方及其对关节炎治疗的评估

Q4 Pharmacology, Toxicology and Pharmaceutics
Pratiksha S. Dhembare, Priyanka G. Kusarkar, Archana S. Murgunde
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引用次数: 0

摘要

目前的研究旨在开发和测试一种用于荆芥局部给药的囊状药物载体系统,以提供持续给药。研究人员采用薄膜水合法制备了藤黄乙素体,并对其体外药物释放曲线、大小、药物含量及其他特性进行了研究。为了获得理想的药物释放和夹持效果,改变了卵磷脂和乙醇的成分以形成乙硫体。经测量,优化配方批次的乙质体囊泡大小为 13.47 nm 单位,zeta 电位为 -3.97 mV。乙硫体凝胶的药物释放率为 83.24%,包埋效率为 89.40%。光学和扫描电子显微镜观察证实了球形囊泡的形成。据观察,随着乙醇浓度的增加,制剂的体外药物释放量增加,而脂质浓度降低。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
FORMULATION OF VITEX NEGUNDO ETHOSOMAL LOADED TOPICAL HERBAL GEL AND ITS EVALUATION FOR ARTHRITIS TREATMENT
The current research aims to develop and test a system of vesicular drug carriers for topical drug administration of Vitex negundo Linn. to provide sustained drug delivery. The ethosomes of V. negundo Linn. were produced using thin-film hydration, and their in vitro drug release profiles, size, drug content, and other characteristics were examined. To attain the desired results, for drug release and entrapment effectiveness, the composition of lecithin and ethanol was changed to form ethosomes. The ethosomal size of the vesicle of the optimized formulation batch was measured to be the units 13.47 nm with -3.97 mV as zeta potential. The percent drug release of ethosomal gel was 83.24 %, and the percent entrapment efficiency was 89.40 %. The formation of spherically shaped vesicles was confirmed by optical and scanning electron microscopy observations. It was observed that as the ethanol concentration increased, the formulation’s in vitro profile for drug release increase, and lipid concentration decreases.
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来源期刊
INDIAN DRUGS
INDIAN DRUGS Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
0.30
自引率
0.00%
发文量
98
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