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首页> 外文期刊>International Journal of Pharmaceutical Sciences and Research >DESIGN, FORMULATION AND IN VITRO EVALUATION OF MICROSPONGES BASED GEL FOR TOPICAL DELIVERY OF KETOCONAZOLE
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DESIGN, FORMULATION AND IN VITRO EVALUATION OF MICROSPONGES BASED GEL FOR TOPICAL DELIVERY OF KETOCONAZOLE

机译:基于微海绵的酮康唑局部给药凝胶的设计,配方和体外评价

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The aim of the present study was to formulate topical microsponge-based delivery system containing ketoconazole for controlled release of the drug for proficient treatment of fungal infections. Ketoconazole loaded microsponges were prepared by quasi emulsion solvent diffusion method using ethyl cellulose N22 polymer with varied drug polymer ratios. The prepared microsponges were characterized by SEM, FTIR, and evaluated for surface morphology, % drug loading, particle size, % entrapment efficiency and in vitro drug release. The effect of formulation variables such as drug to polymer ratio, stirring speed on the physical characteristics of microsponges was examined. Compatibility studies using UV and FTIR indicated that there is no chemical interaction between drug and polymers. SEM studies revealed that the prepared micro sponges were spherical and porous with a mean particle size of 82.25μm. The formulations were subjected to in vitro release studies for 8 hr which showed sustained release. Microsponges were further incorporated in to carbopol gel formulation for topical delivery. Prepared gel formulations were evaluated for physical parameters like pH, spreadability and in vitro drug diffusion. Hydrogel loaded with ketoconazole microsponges showed desirable physical properties and in vitro drug release, i.e. 54.66% in 6 h, which is more controlled than the gel prepared with the pure drug i.e. 82.64% in 6 h.
机译:本研究的目的是制定包含酮康唑的局部基于微海绵的递送系统,以控制药物的释放,从而有效地治疗真菌感染。负载酮康唑的微海绵是通过准乳液溶剂扩散法使用乙基纤维素N22聚合物制成的,该聚合物具有不同的药物聚合物比率。通过SEM,FTIR表征制备的微海绵,并评估其表面形态,药物载量%,粒径,包封率和体外药物释放。检查了诸如药物与聚合物的比例,搅拌速度等配方变量对微海绵物理特性的影响。使用UV和FTIR进行的兼容性研究表明,药物与聚合物之间没有化学相互作用。扫描电镜研究表明,制备的微海绵为球形,多孔,平均粒径为82.25μm。对制剂进行体外释放研究8小时,其显示出持续释放。将微海绵进一步掺入卡波普凝胶制剂中以进行局部递送。评价制备的凝胶制剂的物理参数,如pH,可扩展性和体外药物扩散。载有酮康唑微海绵的水凝胶显示出理想的物理性能和体外药物释放,即6小时内释放率为54.66%,比纯药物制备的凝胶(6小时内释放率为82.64%)更受控制。

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