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用于阴道给药塞克硝唑的热敏水凝胶,作为克服口服制剂全身副作用的一种方法。

Thermosensitive hydrogels for vaginal delivery of secnidazole as an approach to overcome the systemic side-effects of oral preparations.

作者信息

Argenta Débora Fretes, Bernardo Bianca da Costa, Chamorro Andrés Felipe, Matos Paulo Ricardo, Caon Thiago

机构信息

Department of Pharmaceutical Sciences, Federal University of Santa Catarina, Campus Reitor João David Ferreira Lima, s/n - Trindade, Florianópolis - SC, 88040-900, Brazil.

Department of Chemistry, Federal University of Santa Catarina, Campus Reitor João David Ferreira Lima, s/n - Trindade, Florianópolis - SC, 88040-900, Brazil.

出版信息

Eur J Pharm Sci. 2021 Apr 1;159:105722. doi: 10.1016/j.ejps.2021.105722. Epub 2021 Jan 19.

Abstract

Secnidazole (SEC) has been suggested as an alternative agent against Trichomonas vaginalis to overcome the adverse effects, antimicrobial resistance problems and poor adherence to the currently available therapy. Once no topical formulation may be found in the market until now, SEC was incorporated in thermosensitive bioadhesive systems to extend the contact time in the mucosa and to avoid a systemic drug disposition. Formulations containing 20% poloxamer 407, 1% poloxamer 188 and 1 or 2.5% chitosan showed suitable sol-gel transition temperature (> 30 °C), presenting a fast gelation time (100-115 s). Rheological, dynamic light scattering and infrared spectroscopy analysis suggested molecular interactions among polymers. Chitosan increased the mucoadhesion strength of the formulations. In addition, hydrogels showed a tendency to decrease the drug transport rate through mucosa when compared to the control. Mucin was also added onto mucosa for a more realistic simulation of permeability/retention. In the presence of this agent, hydrogels containing chitosan reduced the permeability/retention of the drug in approximately 2.0-fold when compared to the control. Therefore, the hydrogels presented suitable characteristics to remain in the vaginal environment, which would result in effective local treatment of trichomoniasis.

摘要

塞克硝唑(SEC)已被提议作为一种治疗阴道毛滴虫的替代药物,以克服现有疗法的不良反应、抗菌耐药性问题以及依从性差的问题。由于目前市场上尚未发现局部用制剂,因此将SEC纳入热敏性生物粘附系统中,以延长其在粘膜中的接触时间并避免全身药物分布。含有20%泊洛沙姆407、1%泊洛沙姆188和1%或2.5%壳聚糖的制剂显示出合适的溶胶-凝胶转变温度(>30°C),凝胶化时间较快(100-115秒)。流变学、动态光散射和红外光谱分析表明聚合物之间存在分子相互作用。壳聚糖提高了制剂的粘膜粘附强度。此外,与对照组相比,水凝胶显示出降低药物通过粘膜传输速率的趋势。还在粘膜上添加了粘蛋白,以更真实地模拟渗透性/滞留性。在这种药物存在的情况下,与对照组相比,含壳聚糖的水凝胶使药物的渗透性/滞留性降低了约2.0倍。因此,这些水凝胶具有适合留在阴道环境中的特性,这将导致滴虫病的有效局部治疗。

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