首页> 外文OA文献 >Comparative Study on the Effects of Some Polyoxyethylene Alkyl Ether and Sorbitan Fatty Acid Ester Surfactants on the Performance of Transdermal Carvedilol Proniosomal Gel Using Experimental Design
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Comparative Study on the Effects of Some Polyoxyethylene Alkyl Ether and Sorbitan Fatty Acid Ester Surfactants on the Performance of Transdermal Carvedilol Proniosomal Gel Using Experimental Design

机译:实验设计比较一些聚氧乙烯烷基醚和山梨聚糖脂肪酸酯表面活性剂对透皮卡维地洛前体凝胶性能的影响

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摘要

The aim of this work was to investigate the effects of formulation variables on development of carvedilol (CAR) proniosomal gel formulations as potential transdermal delivery systems. Different non-ionic surfactants; polyoxyethylene alkyl ethers, namely Brij 78, Brij 92, and Brij 72; and sorbitan fatty acid esters (Span 60) were evaluated for their applicability in preparation of CAR proniosomal gels. A 23 full factorial design was employed to evaluate individual and combined effects of formulation variables, namely cholesterol content, weight of proniosomes, and amount of CAR added on performance of proniosomes. Prepared proniosomes were evaluated regarding entrapment efficiency (EE%), vesicle size, and microscopic examination. Also, CAR release through cellulose membrane and permeation through hairless mice skin were investigated. Proniosomes prepared with Brij 72 and Span 60 showed better niosome forming ability and higher EE% than those prepared with Brij 78 and Brij 92. Higher EE% was obtained by increasing both weight of proniosomes and amount of CAR added, and decreasing cholesterol content. Release rate through cellulose membrane was inversely affected by weight of proniosomes. In Span 60 proniosomes, on increasing percent of cholesterol, a decrease in release rate was observed. While in Brij 72 proniosomes, an enhancement in release rate was observed on increasing amount of CAR added. Permeation experiments showed that skin permeation was mainly affected by weight of proniosomes and that Span 60 proniosomal gels showed higher permeation enhancing effect than Brij 72. Proniosomal gel could constitute a promising approach for transdermal delivery of CAR.
机译:这项工作的目的是调查配方变量对卡维地洛(CAR)早代凝胶制剂作为潜在的透皮给药系统的发展的影响。不同的非离子表面活性剂;聚氧乙烯烷基醚,即Brij 78,Brij 92和Brij 72;评估了山梨糖醇酐和脱水山梨糖醇脂肪酸酯(Span 60)在制备CAR原核生物凝胶中的适用性。采用23个全因子设计来评估配方变量(即胆固醇含量,proniosome的重量以及所添加的CAR的量)对proniosome的性能的个体和综合影响。评估准备的前体的包封率(EE%),囊泡大小和显微镜检查。此外,还研究了CAR通过纤维素膜的释放和通过无毛小鼠皮肤的渗透。与使用Brij 78和Brij 92制备的脂质体相比,使用Brij 72和Span 60制备的脂质体显示出更好的脂质体形成能力和更高的EE%。通过增加proniosomes的重量和所添加的CAR量以及降低胆固醇含量,可以获得更高的EE%。通过纤维素膜的释放速率受脂质体重量的反作用。在Span 60原核小体中,随着胆固醇百分比的增加,观察到释放速率降低。而在Brij 72 proniosomes中,随着CAR添加量的增加,释放速率得到了提高。渗透实验表明,皮肤渗透主要受proniosomes重量的影响,Span 60 proiosiosomal凝胶显示出比Brij 72更高的渗透增强作用。proniosomal凝胶可构成有希望的CAR透皮递送方法。

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