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Optimized Chitosan/Anion Polyelectrolyte Complex Based Inserts for Vaginal Delivery of Fluconazole: In Vitro/In Vivo Evaluation

机译:优化的壳聚糖/阴离子聚电解质复合物用于氟康唑阴道输送的插入物:体外/体内评估

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摘要

(1) Background: Fluconazole, used orally for vaginal candidiasis, has reported gastrointestinal side effects. Therefore, researchers directed towards the drug vaginal delivery. However, vaginal delivery is limited by poor retention and leakage. Thus, this work aimed at exploring chitosan/anion polyelectrolyte complex (PEC) for the formulation of fluconazole vaginal inserts with controlled release and appreciable mucoadhesion. (2) Methods: PECs were prepared and assessed for interactions. Fluconazole PEC based vaginal inserts were prepared by lyophilization using mannitol. 3151 factorial design was applied to investigate the effect of the anion type and Chitosan/anion ratio on the inserts mucoadhesion and release properties. The optimized insert [based on 5:5 chitosan: anionic polymer (sodium alginate)] release was modulated by the release retardant; Compritol® 888. The selected formulation was subjected to microbiological and histological evaluation. (3) Results: Fluconazole inserts showed satisfactory drug content, acceptable friability percentages and highest swelling indices at six hours. Statistical analysis showed significant effect of the studied factors on detachment force and release properties. Microbiological assays revealed significantly higher antifungal activity of inserts compared to fluconazole solution. Reduced inflammatory cells were confirmed by histological evaluation. (4) Conclusion: CH/Alg based vaginal insert could be a promising platform for vaginal delivery of antifungal drugs used for vaginal candidiasis treatment.
机译:(1)背景:氟康唑口服用于阴道念珠​​菌病,有胃肠道副作用。因此,研究人员针对药物的阴道输送。但是,阴道输送受限于不良的保留和渗漏。因此,这项工作旨在探索壳聚糖/阴离子聚电解质复合物(PEC)用于氟康唑阴道插入物的控制释放和明显的粘膜粘附。 (2)方法:准备PEC并评估其相互作用。通过使用甘露醇冻干制备基于氟康唑PEC的阴道插入物。采用3 1 5 1 析因设计,研究了阴离子类型和壳聚糖/阴离子比对插入物黏膜黏附和释放性能的影响。优化的插入物[基于5:5壳聚糖:阴离子聚合物(藻酸钠)]的释放受释放抑制剂的调节; Compritol ®888。对选定的制剂进行微生物学和组织学评估。 (3)结果:氟康唑插件在6小时内显示出令人满意的药物含量,可接受的脆性百分比和最高溶胀指数。统计分析表明,所研究的因素对剥离力和释放性能有显着影响。微生物测定显示,与氟康唑溶液相比,插入物的抗真菌活性明显更高。通过组织学评估证实炎性细胞减少。 (4)结论:基于CH / Alg的阴道插入物可能是用于阴道念珠​​菌病治疗的抗真菌药物向阴道输送的有前途的平台。

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