首页> 外文期刊>International Journal of Pharmaceutics >Transdermal iontophoretic delivery of tacrine hydrochloride: Correlation between in vitro permeation and in vivo performance in rats
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Transdermal iontophoretic delivery of tacrine hydrochloride: Correlation between in vitro permeation and in vivo performance in rats

机译:盐酸三碱的透皮离子渗透递送:大鼠体外渗透与体内性能之间的相关性

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摘要

The aim of present investigation is to evaluate the feasibility of transdermal iontophoretic delivery of tacrine hydrochloride in Sprague Dawley (SD) rats using anodal iontophoretic patches and to correlate plasma tacrine concentration profiles to in vitro tacrine permeation flux. In vitro skin permeation studies were carried out across artificial membrane CELGRAD (R) 2400, freshly excised SD rat abdominal skin, freshly excised hairless rat abdominal skin, and frozen pig skin to examine the role of permeation membranes. Furthermore, plasma profiles with an application of 0.1-0.3 mA current strength and tacrine concentration loading of 5-20 mg/ml were obtained in SD rats. The tacrine plasma profiles were fitted to one-compartmental model using WinNonlin and in vivo transdermal absorption rates were then correlated to in vitro permeation profiles using various approaches. Tacrine permeation across membranes revealed current dependent interspecies differences at lower current strength application which diminished at higher current strength application, whereas, no significant difference in tacrine permeation was observed across fresh and frozen SD rat skin under 0.2 mA current application. In vivo studies confirmed current and concentration dependent tacrine plasma profiles with possible tacrine depot formation under the skin in-line with earlier in vitro results. Correlation of in vivo transdermal absorption rates to in vitro permeation profiles revealed higher in vitro permeation fluxes compare to in vivo transdermal absorption rates at varied combination of current strength and concentrations. Present in vivo studies support the earlier published in vitro findings and tacrine plasma profiles show a potential to reach therapeutic effective concentration of tacrine hydrochloride to provide a platform for preprogrammed tacrine delivery. (C) 2016 Elsevier B. V. All rights reserved.
机译:本研究的目的是评估对SD(SD)大鼠经皮离子电渗递送的盐酸他克林的使用可行性阳极电离子透入贴片及关联血浆他克林浓度分布在体外他克林渗透通量。在体外皮肤渗透研究,跨人工膜CELGRAD(R)2400,新鲜切除的SD大鼠腹部皮肤,切除新鲜无毛老鼠腹部皮肤,和冻猪皮肤进行检查渗透膜的作用。此外,具有5-20 0.1-0.3 mA的电流的强度和他克林浓度装载的应用血浆分布毫克/ ml的在SD大鼠获得。所述他克林血浆曲线进行了利用WinNonlin符合一隔室模型和体内经皮吸收率,然后使用各种方法关联于在体外渗透曲线。他克林渗透跨膜显示在较低的电流强度的应用程序,减弱在较高的电流强度的应用,而横跨新鲜和冷冻SD大鼠皮肤中观察到低于0.2毫安的电流应用在他克林渗透无显著差值电流取决于种间差异。体内研究证实了行与先前的体外结果在皮肤下的电流和浓度依赖性的,可能的他克林贮库形成他克林血浆分布。的体内透皮吸收率的相关性,以在体外渗透谱分析结果发现在体外渗透通量更高比较在体内经皮吸收率在电流强度和浓度变化的组合。体内研究支持早期发表在体外发现和他克林血浆分布本显示达到盐酸他克林治疗有效浓度,以提供预编程的他克林递送的平台的潜力。 (c)2016年Elsevier B. V.保留所有权利。

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