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首页> 外文期刊>European journal of pharmaceutics and biopharmaceutics: official journal of Arbeitsgemeinschaft fuer Pharmazeutische Verfahrenstechnik e.V >Dual-directional regulation of drug permeating amount by combining the technique of ion-pair complexation with chemical enhancers for the synchronous permeation of indapamide and bisoprolol in their compound patch through rabbit skin
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Dual-directional regulation of drug permeating amount by combining the technique of ion-pair complexation with chemical enhancers for the synchronous permeation of indapamide and bisoprolol in their compound patch through rabbit skin

机译:通过将离子对络合技术与化学增强剂相结合的双向调节药物渗透量,通过兔皮

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To achieve the synchronous skin permeation of indapamide (IND) and bisoprolol (BSP) in their compound patch, the techniques of ion-pair complexation and chemical enhancers were combined to dual-directionally regulate drug permeating amounts. Ion-pair complexes of BSP and various organic acids were formed by the technique of ion-pair complexation. Among the complexes formed, bisoprolol tartrate (BSP.T) down-regulated the permeating amount of BSP to the same extent as that of IND. Then, to simultaneously up-regulate the amounts of the two drugs, an enhancer combination of 15.8% Span80 (SP), 6.0% Azone (AZ) and 2.2% N-methyl pyrrolidone (NMP) was obtained by central composite design and exhibited an outstanding and simultaneous enhancement on IND and BSP with enhancing ratio (ER) of 4.52 and 3.49, respectively. The effect of the dual-directional regulation was evaluated by in vitro permeation experiments and in vivo pharmacokinetic studies. For IND and BSP, their observed permeation profiles were comparable and their MAT (mean absorption time) showed no significant difference, which both demonstrated these two drugs achieved the synchronous skin permeation in their compound patch by the dual-directional regulation strategy of combining the technique of ion-pair complexation with chemical enhancers. (C) 2015 Elsevier B.V. All rights reserved.
机译:为了在其复合贴剂中实现吲达咪唑(IND)和双子丙醇(BSP)的同步皮肤渗透,将离子对络合和化学增强剂的技术合并到双向调节药物渗透量。通过离子对络合技术形成BSP和各种有机酸的离子对复合物。在形成的复合物中,双戊醛(BSP.T)下调BSP的渗透量与IND的程度相同。然后,通过中央复合设计获得15.8%SPAN80(SP),6.0%Azone(AZ)和2.2%N-甲基吡咯烷酮(NMP)的增强子组合,并通过中央复合设计获得了15.8%SCAN80(SP),6.0%氮杂(SZ)和2.2%N-甲基吡咯烷酮(NMP)。 ID和BSP的出色和同时增强分别增强4.52和3.49的增强率(ER)。通过体外渗透实验和体内药代动力学研究评价双向调节的效果。对于IND和BSP,它们所观察到的渗透型材是可比性的,并且它们的垫(平均吸收时间)显示出没有显着差异,这两者都证明了这两种药物通过组合技术的双向调节策略实现了它们的复合贴片中的同步皮肤渗透与化学增强剂的离子对络合。 (c)2015 Elsevier B.v.保留所有权利。

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