Zhao Ji-Hui, Fu Ji-Hua, Wang Shu-Ming, Su Chang-Hai, Shan Ying, Kong Shu-Jia, Wang Yuan, Lu Wan-Liang, Zhang Hua, Zhang Shuang, Li Lin, Zhang En-Hong, Wang Li, Pei Qiu-Ling, Wang Jian-Cheng, Zhang Xuan, Zhang Qiang
State Key Laboratory of Natural and Biomimetic Drugs and School of Pharmaceutical Sciences, Peking University, Beijing 100083, China.
Int J Pharm. 2007 Jun 7;337(1-2):88-101. doi: 10.1016/j.ijpharm.2006.12.030. Epub 2006 Dec 28.
The combination therapy of nitrate and selective beta-adrenoceptor antagonist has shown benefits for treatment of hypertension and heart disease than either drug alone. The objectives of the present study were to define effects on the anti-hypertension activity and pharmacokinetics of a novel transdermal patch incorporating isosorbide dinitrate (ISDN) with bisoprolol (BP). The 3:2 ratio of ISDN to BP (mg/mg) in the transdermal patches exhibited better anti-hypertension effect synergistically with a similar inhibiting heart rates effect to that of BP alone in renovascular hypertensive rats, and was therefore selected as a final formulation. The in vitro transdermal penetration of both ISDN and BP from the patches displayed a zero-order process, and the penetration rate constants were 7.4 microg/(cm(2)h) for ISDN, and 5.9 microg/(cm(2)h) for BP, respectively. After transdermal administration at single dose or multiple doses, the synergistic anti-hypertension effect was confirmed in spontaneously hypertensive rats also. The effect of each patch lasts for 3 days, and increased with the total dose of two drugs (2mg/cm(2), ISDN:BP=3:2, mg/mg), showing a dose dependant manner. After transdermal administration to rabbits, the absolute bioavailabilities were 33.6% for ISDN, and 31.3% for BP, respectively. The maximal concentrations (C(max)) of both drugs were significantly reduced while the areas under the plasma concentration-time curve (AUC), and mean residence times (MRT) were evidently increased and extended, respectively. As a patient-friendly, convenient, and multi-day dosing therapeutic system, the transdermal patches incorporating ISDN and BP could be promising for prevention and treatment of hypertension.
与单独使用任何一种药物相比,硝酸盐与选择性β-肾上腺素能受体拮抗剂的联合治疗已显示出对高血压和心脏病治疗的益处。本研究的目的是确定一种新型透皮贴剂(含二硝酸异山梨酯(ISDN)和比索洛尔(BP))对降压活性和药代动力学的影响。透皮贴剂中ISDN与BP的比例为3:2(mg/mg),在肾血管性高血压大鼠中,与单独使用BP相比,具有更好的协同降压效果,且对心率的抑制作用相似,因此被选为最终制剂。ISDN和BP从贴剂中的体外透皮渗透均显示为零级过程,渗透速率常数分别为ISDN 7.4μg/(cm²h),BP 5.9μg/(cm²h)。在自发性高血压大鼠中,单剂量或多剂量经皮给药后,协同降压效果也得到证实。每个贴剂的效果持续3天,并随两种药物的总剂量(2mg/cm²,ISDN:BP = 3:2,mg/mg)增加而增强,呈剂量依赖性。经皮给药于兔后,ISDN的绝对生物利用度为33.6%,BP为31.3%。两种药物的最大浓度(Cmax)均显著降低,而血浆浓度-时间曲线下面积(AUC)和平均驻留时间(MRT)分别明显增加和延长。作为一种对患者友好、方便且多日给药的治疗系统,含ISDN和BP的透皮贴剂在高血压的预防和治疗方面可能具有前景。