| Literature DB >> 17267147 |
Ji-Hui Zhao1, Ji-Hua Fu, Shu-Ming Wang, Chang-Hai Su, Ying Shan, Shu-Jia Kong, Yuan Wang, Wan-Liang Lu, Hua Zhang, Shuang Zhang, Lin Li, En-Hong Zhang, Li Wang, Qiu-Ling Pei, Jian-Cheng Wang, Xuan Zhang, Qiang Zhang.
Abstract
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.Entities:
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Year: 2006 PMID: 17267147 DOI: 10.1016/j.ijpharm.2006.12.030
Source DB: PubMed Journal: Int J Pharm ISSN: 0378-5173 Impact factor: 5.875