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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 >Absorption characteristics of compounds with different molecular weights after application to the unilateral kidney surface in rats.
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Absorption characteristics of compounds with different molecular weights after application to the unilateral kidney surface in rats.

机译:应用于大鼠单侧肾脏表面后,不同分子量化合物的吸收特性。

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The aim of the present study is to clarify the absorption mechanism of a drug from the kidney surface membrane in rats. We studied the absorption characteristics of phenolsulfonphthalein (PSP) and other compounds with different molecular weights after their application to the rat kidney surface in vivo, employing a cylindrical diffusion cell (i.d. 6 mm, area 0.28 cm(2)). The time course of free PSP amounts remaining in the diffusion cell obeyed first-order kinetics at a dose of 1 mg, and its rate constant [Formula: see text] was calculated to be 0.0137 min(-1). Absorption ratios of PSP in 4 h were calculated (from the amount recovered from the diffusion cell) to be 91.4, 96.4 and 97.7% at doses of 0.5, 1 and 1.5 mg, respectively. The area under the curve for the plasma concentration profile of free PSP was proportional to the application dose. It is thus suggested that the absorption process of PSP from the rat kidney surface does not approach saturation at a dose of 1.5 mg. Also, no significant difference was seen in the [Formula: see text] values within the dose range of 0.5-1.5 mg, which were estimated by curve-fitting the plasma concentration profiles of free PSP in a two-compartment model with first-order absorption. Furthermore, we examined the importance of molecular weight on the absorption from the kidney surface using fluorescein isothiocyanate-dextrans (FDs) with molecular weights of 4400 (FD-4), 11,000 (FD-10), 40,500 (FD-40) or 69,000 (FD-70), including the organic anions bromphenol blue and bromosulfonphthalein. The absorption ratios of FDs from the rat kidney surface in 6 h decreased with an increase in the molecular weight (76.1% for FD-4, 54.4% for FD-10, 11.5% for FD-40 and 3.9% for FD-70). A linear relationship was observed between [Formula: see text] and the reciprocal value of z the square root of the molecular weight of these compounds. The limit of absorption from the rat kidney surface was extrapolated to be at a molecular weight of approximately 130,000.
机译:本研究的目的是阐明大鼠肾脏表面膜对药物的吸收机制。我们研究了使用圆柱形扩散池(直径6 mm,面积0.28 cm(2))将苯酚磺酞(PSP)和其他具有不同分子量的化合物体内应用到大鼠肾脏表面后的吸收特性。剂量为1 mg时,扩散池中残留的游离PSP量随时间的变化遵循一级动力学,其速率常数[公式:参见文字]计算为0.0137 min(-1)。在0.5h,0.5mg和1mg的剂量下(从扩散池回收的量)计算出PSP在4小时内的吸收率分别为91.4%,96.4%和97.7%。游离PSP血浆浓度曲线的曲线下面积与施用剂量成正比。因此建议在1.5mg剂量下从大鼠肾脏表面吸收PSP的过程不会达到饱和。同样,在0.5-1.5 mg剂量范围内的[配方:参见文本]值中也没有观察到显着差异,这是通过对一室两室模型中游离PSP的血浆浓度曲线进行曲线拟合来估算的吸收。此外,我们使用分子量为4400(FD-4),11,000(FD-10),40,500(FD-40)或69,000的异硫氰酸荧光素(FDs)检查了分子量对从肾脏表面吸收的重要性(FD-70),包括有机阴离子溴酚蓝和溴磺酞。随着分子量的增加,FDs在大鼠肾脏表面的吸收率在6小时内降低(FD-4为76.1%,FD-10为54.4%,FD-40为11.5%,FD-70为3.9%)。 。在[分子式:见正文]和这些化合物的分子量的平方根z的倒数值之间观察到线性关系。从大鼠肾脏表面的吸收极限被推断为分子量约为130,000。

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