Vishnu Y Vamshi, Chandrasekhar K, Ramesh G, Rao Y Madhusudan
Centre for Biopharmaceutics and Pharmacokinetics, University College of Pharmaceutical Sciences, Kakatiya University, Warangal - 506 009 (A.P.) India.
Curr Drug Deliv. 2007 Jan;4(1):27-39. doi: 10.2174/156720107779314785.
A buccal patch for systemic administration of carvedilol in the oral cavity has been developed using two different mucoadhesive polymers. The formulations were tested for in vitro drug permeation studies, buccal absorption test, in vitro release studies, moisture absorption studies and in vitro bioadhesion studies. The physicochemical interactions between carvedilol and polymers were investigated by Fourier transform infrared (FTIR) Spectroscopy. According to FTIR the drug did not show any evidence of an interaction with the polymers used and was present in an unchanged state. XRD studies reveal that the drug is in crystalline state in the polymer matrix. The results indicate that suitable bioadhesive buccal patches with desired permeability could be prepared. Bioavailability studies in healthy pigs reveal that carvedilol has got good buccal absorption. The bioavailability of carvedilol from buccal patches has increased 2.29 folds when compared to that of oral solution. The formulation AC5 (HPMC E 15) shows 84.85 + 0.089% release and 38.69 + 6.61% permeated through porcine buccal membrane in 4 hr. The basic pharmacokinetic parameters like the C(max), T(max) and AUC(total) were calculated and showed statistically significant difference (P<0.05) when given by buccal route compared to that of oral solution.
已使用两种不同的粘膜粘附聚合物开发出一种用于在口腔内全身给药的卡维地洛口腔贴片。对这些制剂进行了体外药物渗透研究、口腔吸收试验、体外释放研究、吸湿研究和体外生物粘附研究。通过傅里叶变换红外(FTIR)光谱研究了卡维地洛与聚合物之间的物理化学相互作用。根据FTIR,药物未显示出与所用聚合物相互作用的任何证据,且处于未改变的状态。X射线衍射(XRD)研究表明,药物在聚合物基质中呈结晶状态。结果表明,可以制备出具有所需渗透性的合适的生物粘附口腔贴片。在健康猪身上进行的生物利用度研究表明,卡维地洛具有良好的口腔吸收。与口服溶液相比,卡维地洛口腔贴片的生物利用度提高了2.29倍。制剂AC5(羟丙甲纤维素E 15)在4小时内显示84.85±0.089%的释放率和38.69±6.61%透过猪口腔黏膜的渗透率。计算了C(max)、T(max)和AUC(total)等基本药代动力学参数,与口服溶液相比,经口腔途径给药时显示出统计学上的显著差异(P<0.05)。