Preparation and In Vitro Evaluation Of Transdermal Patch Of Aceclofenac

K. Sravanthi, D. R. Reddy, A. Sirisha, A. Pavani, B. Mahalakshmi, B. Sowjanya
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引用次数: 4

Abstract

The purpose of this research was to develop a matrix-type transdermal therapeutic system containing drug Aceclofenac with different ratios of hydrophilic (hydroxyl propyl methyl cellulose) and hydrophobic (methyl cellulose) polymeric systems by the solvent casting technique. Formulated transdermal patches were physically evaluated with regard to thickness, weight variation, drug content, flatness, tensile strength, folding endurance, percentage of moisture content and water vapour transmission rate. All prepared formulations indicated good physical stability. In-vitro drug studies of formulations were performed by using Franz diffusion cells. The results followed the release profile of Aceclofenac followed mixed zero-order. However, the release profile of the optimized formulation F9 (99.50±0.09) indicated that the permeation of the drug from the patches was governed by a diffusion mechanism. Formulation F9 showed highest flux among all the formulations and 217±7.42 fold enhancements in drug permeation.
乙酰氯芬酸透皮贴剂的制备及体外评价
本研究的目的是通过溶剂铸造技术,以不同比例的亲水性(羟丙基甲基纤维素)和疏水性(甲基纤维素)聚合物体系为原料,制备含药物乙酰氯芬酸的基质型透皮治疗体系。对配方透皮贴片的厚度、重量变化、药物含量、平整度、拉伸强度、折叠耐久性、含水量百分比和水蒸气透射率进行物理评价。所制备的制剂均具有良好的物理稳定性。采用Franz扩散细胞对制剂进行体外药物研究。结果符合阿氯芬酸的释放曲线为混合零阶。F9的释药曲线(99.50±0.09)表明药物以扩散机制渗透。F9的药通率最高,药透率提高了217±7.42倍。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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