Detail work on formulation development and evaluation of micro sponges gel of clotrimazole for treatment of vaginal fungal infection

Saloni Jaswal
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Abstract

Vaginal infection is so widespread that women have to seek medical counseling. In fact, almost 70% of women experience vaginal infections in their life. Vulvovaginal candidiasis is responsible for vaginal infections and Candida albicans is the major agent. Vaginal infections are caused by hormonal changes, negative sexual effects, irrelevant quality of life, high mortality rate, depressive mood and various kind of anxiety. Detail Work on Formulation Development and Evaluation of Micro sponges gel of Clotrimazole for Treatment of Vaginal fungal Infection. The microsponge-based novel delivery system has been developed for vaginal delivery of Clotrimazole. The method adopted was quasi-emulsion solvent diffusion. Formed microsponges were a spherical in shape Different drug–polymer ratio reflected good particle size, drug content and entrapment efficiency. Microsponge-based gel showed in vitro drug release reflected highest regression value for Koshmeyer-Peppas and in vitro antifungal activity of CLZ microsponges gel was higher than the market formulation. Drug, chemical and solvent to be used are listed as Clotrimazole, Eudragit RL-100, Polyvinyl alcohol, Carbopol 934, Sodium Citrate dihydrate, Citric Acid, Dichloromethane, Triethanolamine, Agar 1. Preparation of citrate buffer pH 4.5 solution 2. Preparation of standard curve of citrate buffer pH 4.5 solution: methanol 3. FTIR spectroscopy 4. Selection of method for the preparation of microsponges 5. Quasi emulsion solvent diffusion (two step method) is selected for the preparation of microsponges 6. Selection of amount of drug (clotrimazole): 7. Selection of optimum volume of solvent (dichloromethane): 8. Selection of amount of emulsifier (polyvinyl alcohol): 9. Preparation of microsponges. The f23 formulation, which had a manufacturing yield of 66.58%, an entrapment efficiency of 91.26%, and an actual drug content of 67.28 percent, was determined to be more trustworthy than the other formulations. The CDR was 66.18%, and the Flux value was 76.17(g/cm2/h).With (r2)0.9738 and a n value of 0.3981, Koshmeyer Peppas was judged to be the model that suited the data the best.A measurement of the viscosity revealed non-Newtonian flow. The ZOI, which exceeded the advertised preparation, was discovered to be 2.2 cm. For vaginal delivery of Clotrimazole, a new delivery mechanism based on microsponges has been created. The technique used was solvent diffusion from a quasi-emulsion. Microsponges that had been formed had a spherical shape. Different drug-polymer ratios were indicative of good drug content, entrapment effectiveness, and particle size. Microsponge-based gel demonstrated in vitro drug release that had the greatest regression value for Koshmeyer-Peppas, and CLZ microsponges gel had stronger in vitro antifungal activity than the commercial formulation.
克霉唑微海绵凝胶治疗阴道真菌感染的配方研制及疗效评价
阴道感染非常普遍,妇女不得不寻求医疗咨询。事实上,近70%的女性在一生中都经历过阴道感染。外阴阴道念珠菌病是阴道感染的主要原因,白色念珠菌是主要的病原体。阴道感染是由荷尔蒙变化、负面的性影响、生活质量不相关、高死亡率、抑郁情绪和各种焦虑引起的。克霉唑微海绵凝胶治疗阴道真菌感染的配方研制及评价。本研究开发了一种基于微海绵的新型阴道给药系统。采用准乳液溶剂扩散法。形成的微海绵呈球形,不同的药-聚合物比反映出良好的粒径、药物含量和包封效率。微海绵凝胶对Koshmeyer-Peppas的体外药物释放回归值最高,CLZ微海绵凝胶的体外抗真菌活性高于市场配方。所使用的药物、化学品和溶剂为:克曲霉唑、乌龙茶RL-100、聚乙烯醇、卡波波尔934、柠檬酸二水合物钠、柠檬酸、二氯甲烷、三乙醇胺、琼脂1。柠檬酸缓冲pH 4.5溶液的制备柠檬酸缓冲液ph4.5溶液:甲醇3标准曲线的制备。FTIR光谱微海绵制备方法的选择选择准乳液溶剂扩散法(两步法)制备微海绵6。药物用量选择(克霉唑):7。溶剂(二氯甲烷)最佳体积的选择:乳化剂(聚乙烯醇)用量选择:9。微型海绵的制备。f23制剂的制造得率为66.58%,包封效率为91.26%,实际药物含量为67.28%,比其他制剂更可信。CDR为66.18%,通量值为76.17(g/cm2/h)。(r2)0.9738, n值为0.3981,判断Koshmeyer Peppas是最适合数据的模型。粘度的测量揭示了非牛顿流动。结果发现,超过宣传材料的ZOI为2.2厘米。建立了一种基于微海绵的阴道给药机制。所使用的技术是溶剂从准乳液扩散。已经形成的微型海绵呈球形。不同的药物-聚合物比例表明良好的药物含量、包封效果和粒径。微海绵凝胶对Koshmeyer-Peppas的体外药物释放回归值最大,CLZ微海绵凝胶的体外抗真菌活性比市售配方更强。
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