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The Effect of Niosomal System (Span 60-Cholesterol) on Diclofenac Sodium Preparation Characteristics and Diclofenac Sodium Preparation of Hydroxypropyl Cellulose Gel Base (HPC)

机译:憩室系统(跨度60-胆固醇)对双丙基纤维素凝胶碱(HPC)的双氯芬酸钠制备特性和双氯芬酸钠制剂的影响

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摘要

Diclofenac sodium is a lipophilic drug. That characteristic makes it difficult to disperse well in hydrophilic gel base. The niosome with its vesicle system could overcome that low dispersibility. It affects penetration by reducing water loss in trans-epidermal layer and change lipid bilayer conformation. The present study was designed to investigate the effect of niosomal system (Span 60–Cholesterol) on preparation characteristics and diclofenac sodium penetration of hydroxypropyl cellulose (HPC) gel base. We examined three different formulas in HPC gel base. Formula III was made in niosomal system.  Preparation  characteristics were  evaluated with organoleptic and acidity tests. Drug penetration was checked using apparatus 5-paddle over disk and 0.45 μm Milipore membrane impregnated with isopropyl myristate. The solution is phosphate buffer saline pH 7.4±0.05 in temperature 37±0.5°C. All of the data were evaluated based on one way ANOVA and continued with HSD test. It was concluded that niosomal system (span 60-cholesterol) has an influence in increasing pH value and penetration (based on flux value and permeability) of diclofenac sodium in HPC gel base.
机译:双氯芬酸钠是一种亲脂性药物。该特征使得难以在亲水凝胶碱中分散良好。具有囊泡系统的定期可以克服这种低分散性。它通过降低反式表皮层中的水分损失来影响渗透,并改变脂质双层构象。本研究旨在探讨憩室系统(跨度60-胆固醇)对羟丙基纤维素(HPC)凝胶碱的制备特性和双氯芬酸钠渗透性的影响。我们在HPC凝胶基础上检查了三种不同的公式。式III是在憩室系统中进行的。用有机酸和酸度试验评估制备特征。使用液体5型焊盘检查药物渗透,并浸渍有异丙基肌酯的0.45μmmilipore膜。溶液是磷酸盐缓冲盐水pH 7.4±0.05温度37±0.5℃。所有数据都是基于单向ANOVA进行评估,并继续使用HSD测试。得出结论认为,憩室系统(跨度60-胆固醇)对HPC凝胶碱中双氯芬酸钠钠的pH值和渗透率(基于助熔剂)的渗透率和渗透率)有影响。

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