氯霉唑透皮贴剂的研制与评价

Yelamanda Jagadeesh, Hari Kiran, Reddy Naveena B, Chandra Prakash D, Bhagya Lakshmi G, Vaishnavi P, Varshini S, Vadamala Prudhvi Raj
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引用次数: 0

摘要

本研究的目的是研制氯霉唑透皮贴剂,以提高药物的有效性和避免药物的副作用。以不同比例的EC和HPMC制备氯霉唑透皮贴剂,以改善药物的扩散。采用溶剂蒸发法制备了氯霉唑透皮贴剂。用傅里叶变换红外光谱对药物和聚合物进行了表征。FTIR光谱表明,制剂与辅料无相互作用。对氯曲霉唑透皮贴剂的评价主要包括质量变化、厚度、耐折试验等物理参数,以及药物含量和体外药物扩散研究。补丁由溶剂蒸发技术通过准备补丁被发现非刺激物,重量差异被发现在39±5.81 48±2.90毫克,厚度在0.08±0.09,0.04±0.08毫米,耐折度的补丁被发现在98年到128±0.57±0.59,补丁的抗拉强度从1.95±1.2,3.98±1.9,伸长率范围从10.6到18.6,药物含量均匀度在78.25 - 89.76%之间。在pH 7.4条件下,制剂的体外药物扩散曲线因其组成而异。通过扩散试验观察各制剂的A Tran皮肤斑块。同时观察到F6的药物释放最高。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Formulation and Evaluation of Transdermal Patches of Clotrimazole
The aim of the present research work was to formulate Transdermal patches of Clotrimazole and to enhance effectiveness and to avoid side effects of the drug. Transdermal patch of clotrimazole was prepared with EC and HPMC in different ratios in order to improve the drug diffusion. Clotrimazole has formulated Transdermal patches were prepared by solvent evaporation technique. Drug and polymers has been characterized by FT-IR. The FTIR spectra of formulation shows that no interaction between drug and excipient. The evaluation of Transdermal patches of Clotrimazole were performed mainly for their Physical parameters such as Weight variation, Thickness, Folding endurance test And also for their Drug content and In-vitro Drug diffusion studies. The patch prepared by solvent evaporation technique passes the prepared patch were found to be non irritant, weight variation was found in the range of 39±5.81 to 48±2.90mg, thickness in the range of 0.08±0.09 to 0.04±0.08 mm, Folding endurance of patches was found to be in the range of 98 ±0.57 to 128±0.59, The tensile strength of the patches was ranging from 1.95±1.2to 3.98±1.9, The percentage elongation ranges from 10.6 to 18.6, drug content uniformity was in between 78.25 to 89.76 %. The in-vitro drug diffusion profiles of the formulations in pH 7.4 show differences depending on their composition. A Tran’s dermal patches of all the preparations were observed by the diffusion test. It was also observed that F6 showed highest drug release.
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