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Formulation Characterization and Clinical Evaluation of Microemulsion Containing Clotrimazole for Topical Delivery

机译:含克霉唑局部给药的微乳的配制表征和临床评价

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摘要

The objective of the present study was to formulate and evaluate microemulsion systems for topical delivery of clotrimazole (CTM). The solubility of CTM in various oils was determined to select the oil phase of the microemulsion systems. Pseudoternary phase diagrams were constructed to identify the area of microemulsion existence. Five CTM microemulsion formulations (M1–M5) were prepared and evaluated for their thermodynamic stability, pH, refractive index, droplet size, viscosity, and in vitro release across cellulose membrane. Among the prepared microemulsion formulations, M3 (lemon oil/Tween 80-butanol/water) and M4 (isopropyl myristate/Tween 80-butanol/water) microemulsion systems were found to be promising according to their physical properties and CTM cumulative percentage release. Gel form of M3 and M4 were prepared using 1% Carbopol 940 as the hydrogel matrix. Both formulations were evaluated in the liquid and gel forms for drug retention in the skin in comparison to the marketed CTM topical cream and their stability examined after storage at 40°C for 6 months. Microemulsion formulations achieved significantly higher skin retention for CTM over the CTM cream. Stability studies showed that M4 preparations were more stable than M3. The in vitro anti-fungal activity of M4 against Candida albicans was higher than that of the conventional cream. Moreover, clinical evaluation proved the efficacy and tolerability of this preparation in the treatment of various topical fungal infections.
机译:本研究的目的是制定和评估克霉唑(CTM)局部给药的微乳体系。确定CTM在各种油中的溶解度以选择微乳液系统的油相。构造伪三元相图以识别微乳液存在的区域。制备了五种CTM微乳液配方(M1-M5),并对其热力学稳定性,pH,折射率,液滴尺寸,粘度和在整个纤维素膜上的体外释放进行了评估。在制备的微乳液配方中,M3(柠檬油/吐温80 /正丁醇/水)和M4(肉豆蔻酸异丙酯/吐温80 /正丁醇/水)微乳液系统根据其物理性质和CTM累积性被认为是很有前途的百分比释放。使用1%Carbopol 940作为水凝胶基质制备M3和M4的凝胶形式。与市售的CTM局部乳霜相比,两种制剂均以液体和凝胶形式评估了药物在皮肤中的滞留性,并在40°C储存6个月后检查了它们的稳定性。与CTM面霜相比,微乳液配方对CTM的皮肤保留率更高。稳定性研究表明,M4制剂比M3更稳定。 M4对白色念珠菌的体外抗真菌活性高于常规乳膏。此外,临床评估证明了该制剂在治疗各种局部真菌感染中的功效和耐受性。

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