Bilensoy Erem, Rouf M Abdur, Vural Imran, Sen Murat, Hincal A Atilla
Hacettepe University, Faculty of Pharmacy, Department of Pharmaceutical Technology, 06100 Ankara/Turkey.
AAPS PharmSciTech. 2006 Apr 14;7(2):E38. doi: 10.1208/pt070238.
The purpose of this study was to achieve a better therapeutic efficacy and patient compliance in the treatment for vaginitis. Clotrimazole (1%) has been formulated in a vaginal gel using the thermosensitive polymer Pluronic F127 (20%) together with mucoadhesive polymers such as Carbopol 934 and hydroxypropylmethylcellulose (0.2% for both). To increase its aqueous solubility, clotrimazole was incorporated as its inclusion complex with 1:1 molar ratio with beta-cyclodextrin. The inclusion complex was thoroughly characterized using various techniques, including 1H NMR spectroscopy, FT IR spectrophotometry, differential scanning calorimetry, scanning electron microscopy, phase solubility studies, and determination of stability constant (k(1:1)). The gelation temperature and rheological behavior of different formulations at varying temperatures were measured. In vitro release profiles of the gels were determined in pH 5.5 citrate buffer. It was observed that complexation with cyclodextrin slowed down the release of clotrimazole considerably. Carbopol 934, on the other hand, was found to interact with beta-cyclodextrin, inducing precipitation. As far as rheological properties are concerned, thermosensitive in situ gelling was obtained with formulations containing drug:cyclodextrin complex rather than with free drug. Thus, the optimum formulation for a controlled-release thermosensitive and mucoadhesive vaginal gel was determined to be clotrimazole:beta-cyclodextrin 1% with 0.2% hydroxypropylmethylcellulose in Pluronic F127 gel (20%) providing continuous and prolonged release of active material above MIC values.
本研究的目的是在阴道炎治疗中获得更好的治疗效果和患者依从性。克霉唑(1%)已与热敏聚合物泊洛沙姆F127(20%)以及诸如卡波姆934和羟丙基甲基纤维素(两者均为0.2%)等粘膜粘附聚合物一起制成阴道凝胶。为提高其水溶性,克霉唑以与β-环糊精1:1摩尔比的包合物形式加入。使用多种技术对该包合物进行了全面表征,包括1H核磁共振光谱、傅里叶变换红外光谱、差示扫描量热法、扫描电子显微镜、相溶解度研究以及稳定性常数(k(1:1))的测定。测量了不同配方在不同温度下的胶凝温度和流变行为。在pH 5.5的柠檬酸盐缓冲液中测定了凝胶的体外释放曲线。观察到与环糊精络合大大减缓了克霉唑的释放。另一方面,发现卡波姆934与β-环糊精相互作用,导致沉淀。就流变学性质而言,含有药物:环糊精络合物的配方获得了热敏原位胶凝,而不是游离药物。因此,控释热敏和粘膜粘附阴道凝胶的最佳配方被确定为在泊洛沙姆F127凝胶(20%)中含有1%克霉唑:β-环糊精和0.2%羟丙基甲基纤维素,可提供高于最低抑菌浓度值的活性物质的持续和延长释放。