Sekhar K Chandra, Naidu K V S, Vishnu Y Vamshi, Gannu Ramesh, Kishan V, Rao Y Madhusudan
College of Pharmacy and Health Sciences, Mercer University, Atlanta, Georgia, USA.
Drug Deliv. 2008 Mar-Apr;15(3):185-91. doi: 10.1080/10717540801952639.
This article describes buccal permeation of chlorpheniramine maleate (CPM) and its transbuccal delivery using mucoadhesive buccal patches. Permeation of CPM was calculated in vitro using porcine buccal membrane and in vivo in healthy humans. Buccal formulations were developed with hydroxyethylcellulose (HEC) and evaluated for in vitro release, moisture absorption, mechanical properties, and bioadhesion, and optimized formulation was subjected for bioavailability studies in healthy human volunteers. In vitro flux of CPM was calculated to be 0.14 +/- 0.03 mg.h(-1).cm(-2) and buccal absorption also was demonstrated in vivo in human volunteers. In vitro drug release and moisture absorbed were governed by HEC content and formulations exhibited good tensile and mucoadhesive properties. Bioavailability from optimized buccal patch was 1.46 times higher than the oral dosage form and the results showed statistically significant difference.
本文描述了马来酸氯苯那敏(CPM)的颊部渗透及其使用粘膜粘附性颊贴剂的经颊给药。CPM的渗透在体外使用猪颊膜进行计算,并在健康人体中进行体内研究。用羟乙基纤维素(HEC)开发了颊部制剂,并对其体外释放、吸湿、机械性能和生物粘附性进行了评估,优化后的制剂在健康人类志愿者中进行了生物利用度研究。计算得出CPM的体外通量为0.14±0.03 mg·h⁻¹·cm⁻²,并且在人类志愿者体内也证明了颊部吸收。体外药物释放和吸湿受HEC含量的控制,制剂表现出良好的拉伸和粘膜粘附性能。优化后的颊贴剂的生物利用度比口服剂型高1.46倍,结果显示有统计学上的显著差异。