首页> 外文期刊>Asian Journal of Pharmaceutical and Clinical Research >FORMULATION AND EVALUATION OF MICONAZOLE NITRATE NANOEMULSION AND CREAM
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FORMULATION AND EVALUATION OF MICONAZOLE NITRATE NANOEMULSION AND CREAM

机译:硝酸咪康唑纳米乳和乳膏的配方与评价

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Objective: The present study is to determine the evaluation profile of the preparations nanoemulsion and cream of miconazole nitrate. Methods: Preparation of nanoemulsi with concentrations 1%, 1.5%, and 2% using the principle of low-energy emulsification and miconazole nitrate cream was then performed physical evaluation of the preparation which included organoleptic test, pH measurement, viscosity test, emulsion type, cycling test, centrifugation test, particle size measurement with particle size analyzer, and homogeneity test of cream preparations. Result: Based on organoleptic test, it can be seen that the miconazole nitrate nanoemulsion preparations produced are clear, colored weak yellow, and the cream is white. The average pH of the nanoemulsion preparations ranged from 6.01 to 6.25, while the cream preparations were 5.95–6.52. The average viscosity values of nanoemulsion preparations were 1707 cps, 1920 cps, and 1987 cps, respectively. In the cycling test, the nanoemulsion preparation remained weak yellow and odorless, and the cream preparation remained white and did not experience phase separation. In the centrifugation test, the nanoemulsion preparation and the cream were centrifuged at a rate of 3800 for 5 h, after centrifugation tests, both the nanoemulsing and cream preparations did not show any phase separation, in the nanoemulsion preparation possibly due to the high viscosity of the preparation. On the type nanoemulsi test, by dripping methylene blue on the formula. After observed, the blue methylene is evenly dispersed into the formula, indicating that all four formulas have an oil-in-water emulsion type (o/w). The particle size of the nanoemulsion preparation ranged from 102.36 nm to 309.11 nm. Conclusion: The results of evaluation of miconazole nitrate nanoemulsion preparations were better than cream preparations.
机译:目的:本研究旨在确定硝酸咪康唑纳米乳剂和乳膏制剂的评价概况。方法:采用低能乳化原理制备浓度分别为1%,1.5%和2%的纳米乳剂,并对硝酸咪康唑乳膏进行物理评价,包括感官测试,pH测量,粘度测试,乳液类型,循环测试,离心测试,使用粒度分析仪进行粒度测量以及乳膏制剂的均匀性测试。结果:根据感官测试,可以看出所生产的硝酸咪康唑纳米乳液制剂是透明的,有色的淡黄色,乳白色。纳米乳剂的平均pH值在6.01至6.25之间,而乳膏剂的平均pH在5.95–6.52之间。纳米乳液制剂的平均粘度值分别为1707cps,1920cps和1987cps。在循环测试中,纳米乳液制剂保持弱黄色和无味,并且乳膏制剂保持白色并且没有经历相分离。在离心试验中,将纳米乳液制剂和乳膏以3800的速率离心5小时,在离心试验后,纳米乳液制剂和乳膏制剂均未显示出任何相分离,这可能是由于纳米乳制剂的高粘度所致。准备。在类型纳米乳化试验中,通过在配方上滴加亚甲基蓝。观察后,蓝色亚甲基均匀分散在配方中,表明所有四个配方均具有水包油乳液类型(o / w)。纳米乳液制剂的粒度为102.36nm至309.11nm。结论:硝酸咪康唑纳米乳剂的评价结果​​优于乳膏剂。

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