Laboratorio de Sistemas Farmacéuticos de Liberación Modificada (L-13, UIM), Facultad de Estudios Superiores Cuautitlán, Universidad Nacional Autónoma de México, 54714, Estado de México, Mexico.
Laboratorio de Investigación y Posgrado en Tecnología Farmacéutica (L-322, Campo 1), Facultad de Estudios Superiores Cuautitlán, Universidad Nacional Autónoma de México, 54740, Estado de México, Mexico.
AAPS PharmSciTech. 2024 Aug 22;25(7):197. doi: 10.1208/s12249-024-02914-7.
Vulvovaginal candidiasis (VVC) alters the innate cervicovaginal immunity, which provides an important barrier against viruses and other infections. The incidence of this disease has not decreased in the last 30 years, so effective treatments are still needed. Nanoparticles (NPs) of cellulose acetate phthalate (CAP) and clotrimazole (CLZ) were prepared by the emulsification-diffusion method. NPs were characterized using dynamic light scattering, atomic force microscopy and differential scanning calorimetry; their release profile was determined by the dialysis bag technique and mucoadhesion was evaluated with the mucin-particle method. The growth inhibition study of Candida albicans was carried out using the plate counting technique. Finally, accelerated physical stability tests of NPs were carried out, both in water and in SVF. The CAP-CLZ NPs had an average diameter of 273.4 nm, a PDI of 0.284, smooth surfaces and spherical shapes. In vitro release of CLZ from the CAP NPs was categorized with the Weibull model as a matrix system in which initial release was rapid and subsequently sustained. The inhibition of C. albicans growth by the CAP-CLZ NPs was greater than that of free CLZ, and the CAP-only NPs had a microbicidal effect on C. albicans. The NPs showed poor mucoadhesiveness, which could lead to studies of their mucopenetration capacities. An accelerated physical stability test revealed the erosion of CAP in aqueous media. A nanoparticulate system was developed and provided sustained release of CLZ, and it combined an antifungal agent with a microbial polymer that exhibited antifungal activity against C. albicans.
外阴阴道假丝酵母菌病(VVC)改变了先天的宫颈阴道免疫,为病毒和其他感染提供了重要的屏障。这种疾病在过去 30 年中并没有减少,因此仍然需要有效的治疗方法。采用乳化扩散法制备醋酸纤维素邻苯二甲酸酯(CAP)和克霉唑(CLZ)纳米粒子。采用动态光散射、原子力显微镜和差示扫描量热法对 NPs 进行了表征;采用透析袋技术测定其释放曲线,采用粘蛋白-颗粒法评价其粘膜粘附性。采用平板计数技术研究了念珠菌属的生长抑制作用。最后,对 NPs 在水和 SVF 中的加速物理稳定性进行了测试。CAP-CLZ NPs 的平均粒径为 273.4nm,PDI 为 0.284,表面光滑,呈球形。CLZ 从 CAP NPs 的体外释放符合 Weibull 模型,属于初始快速释放,随后持续释放的基质系统。CAP-CLZ NPs 对白色念珠菌的抑制作用大于游离 CLZ,而 CAP 单一组分对白色念珠菌具有杀菌作用。NPs 的粘膜粘附性较差,这可能导致对其粘膜穿透能力的研究。加速物理稳定性测试显示 CAP 在水介质中的侵蚀。开发了一种纳米颗粒系统,提供了 CLZ 的持续释放,并将抗真菌剂与具有抗白色念珠菌活性的微生物聚合物结合在一起。