氟康唑固体分散剂阴道片剂配方中的质量设计方法

Pranita S. Kanojiya, Rita Wadetwar, Amit Godbole, Nilesh P. Gawande, Samiksha S. Dadmal, Adesh L. Fasate, Chandu B. Karad
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摘要

摘要 阴道念珠菌病是妇科常见病。氟康唑是一种抗真菌药物,其溶解性较差,阻碍了溶解和抗真菌活性。本研究旨在通过实验设计法配制氟康唑固体分散体阴道缓释片,以保证质量不打折扣。第一步,采用 Plackett Burman 设计对影响片剂性能的重要因素进行初步筛选。对重要因素进一步采用 32 因子设计,并对反应进行研究。药物释放、生物黏附强度和膨胀指数被视为阴道片剂的关键质量属性。通过等值线图和响应面图确定了设计空间。在设计空间内制备的片剂药物释放率(99.97±0.1%)、生物黏附强度(1671.62±43.23 达因/平方厘米)和溶胀指数(342.47±5%)均符合之前确定的产品质量目标值。与普通药物片剂(36±2 毫米)相比,固体分散体片剂对白茨球菌的抗真菌活性抑制区(51±3 毫米)更大。图表摘要
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Quality by design approach in the formulation of vaginal tablet of fluconazole solid dispersion
Abstract Vaginal Candidiasis had caused quite frequent gynecological medical consultations. Fluconazole is an antifungal drug that has poor solubility that hinders dissolution and antifungal activity. The study aimed to formulate the sustained release vaginal tablet of Fluconazole solid dispersion through the Design of Experiment approach to guarantee no compromise with the quality. In the first step, Plackett Burman Design was employed for the preliminary screening of the essential factors that would affect the tablet’s property. The significant factors were used further in applying the 32 factorial design and the responses were studied. The drug release, bioadhesive strength and swelling index were taken as the responses and considered as the vital critical quality attributes of the vaginal tablet. The design space was determined through the contour and response surface plots. The tablet was prepared within the design space with the drug release (99.97±0.1%), bioadhesive strength (1671.62±43.23 dynes/cm2), and swelling index (342.47±5 %) that suggested the values lie within the quality target product profile determined previously. The antifungal activity against C. albicans resulted in a larger inhibition zone for the solid dispersion-based tablet (51±3 mm) than the plain drug-based tablet (36±2 mm). GRAPHICAL ABSTRACT
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