Nappinnai M, Chandanbala R, Balaijirajan R
Department of Pharmaceutics, C. L. Baid Mehta College of Pharmacy, Jyothi Nagar, Thoraipakkam, Old Mahabalipuram Road, Chennai-600 096, India.
Indian J Pharm Sci. 2008 Sep;70(5):631-5. doi: 10.4103/0250-474X.45402.
A mucoadhesive drug delivery system for systemic delivery of nitrendipine, a calcium channel blocker through buccal route was formulated. Mucoadhesive polymers like hydroxypropylmethylcellulose K-100, hydroxypropylcellulose, sodium carboxymethylcellulose, sodium alginate, polyvinyl alcohol, polyvinyl pyrrolidone K-30 and carbopol-934P were used for film fabrication. The films were evaluated for their weight, thickness, percentage moisture absorbed and lost, surface pH, folding endurance, drug content uniformity, In vitro residence time, In vitro release and ex vivo permeation. Based on the evaluation of these results, it was concluded that buccal films made of hydroxylpropylcellulose and sodium carboxymethylcellulose (5±2% w/v; F-4), which showed moderate drug release (50% w/w at the end of 2 h) and satisfactory film characteristics could be selected as the best among the formulations studied.
制备了一种用于通过颊部途径全身递送钙通道阻滞剂尼群地平的粘膜粘附给药系统。使用了诸如羟丙基甲基纤维素K - 100、羟丙基纤维素、羧甲基纤维素钠、海藻酸钠、聚乙烯醇、聚乙烯吡咯烷酮K - 30和卡波姆 - 934P等粘膜粘附聚合物来制备薄膜。对薄膜的重量、厚度、吸湿和失重百分比、表面pH值、耐折性、药物含量均匀性、体外停留时间、体外释放和离体渗透进行了评估。基于这些结果的评估,得出结论:由羟丙基纤维素和羧甲基纤维素钠(5±2% w/v;F - 4)制成的颊部薄膜显示出适度的药物释放(2小时结束时为50% w/w)且具有令人满意的薄膜特性,可被选为所研究制剂中的最佳制剂。