Wang Lei, Tang Xing
Department of Pharmaceutics, Shenyang Pharmaceutical University, 110016 Shenyang, People's Republic of China.
Int J Pharm. 2008 Feb 28;350(1-2):181-7. doi: 10.1016/j.ijpharm.2007.08.042. Epub 2007 Aug 31.
Bioadhesive tablet formulations of ketoconazole for vaginal delivery were studied. Carbomer (Carbopol 974P, Carbopol 934P), hydroxypropylmethyl cellulose (HPMC) and hydroxypropyl cellulose (HPC) were used as candidate bioadhesive polymers. Effervescent was incorporated into the formulations as a disintegration agent. The swelling behavior and bioadhesive strength of the drug-free tablets were investigated. Carbopol 934P was selected as biopolymer in combination with HPMC or HPC at different ratios to develop five drug-loaded formulations. The swellings, tackiness and in vitro release were studied on the tablets. A good sustained effect and a moderate bioadhesion were obtained with the tablets. The formulation containing 100mg of effervescent, with the Carbopol 934P:HPC ratio of 1:9, seemed to be the optimum one for the tablet. In vivo drug residence tests were carried out by administering the preferred formulation to female rats. The results showed that the drug remaining followed a one-order model. Even after 24h of administration in vagina of rats, 17% of the original employed drug was retained on the vaginal tissue. Our study may provide a potential vaginal tablet formulation of ketoconazole against Candida albicans.
对用于阴道给药的酮康唑生物黏附片制剂进行了研究。使用卡波姆(卡波普974P、卡波普934P)、羟丙基甲基纤维素(HPMC)和羟丙基纤维素(HPC)作为候选生物黏附聚合物。将泡腾剂作为崩解剂加入到制剂中。研究了不含药物的片剂的溶胀行为和生物黏附强度。选择卡波普934P与不同比例的HPMC或HPC组合作为生物聚合物,以开发五种载药制剂。对这些片剂的溶胀性、黏性和体外释放进行了研究。这些片剂获得了良好的缓释效果和适度的生物黏附性。含有100mg泡腾剂、卡波普934P与HPC比例为1:9的制剂似乎是该片剂的最佳配方。通过将优选的制剂给予雌性大鼠进行体内药物滞留试验。结果表明,药物残留遵循一级模型。即使在大鼠阴道给药24小时后,仍有17%的原用药物保留在阴道组织上。我们的研究可能为抗白色念珠菌的酮康唑阴道片制剂提供一种潜在的配方。