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表面活性剂对药物肠道吸收影响的实验研究。以头孢羟氨苄为模型药物,月桂醇硫酸酯钠为模型表面活性剂:大鼠结肠研究。

Experimental studies on the influence of surfactants on intestinal absorption of drugs. Cefadroxil as model drug and sodium lauryl sulfate as model surfactant: studies in rat colon.

作者信息

Sancho-Chust V, Fabra-Campos S, Gómez-Meseguer V, Bengochea M, Martín-Villodre A

机构信息

Department of Pharmaceutics, University of Valencia, Spain.

出版信息

Arzneimittelforschung. 1995 May;45(5):595-601.

PMID:7612059
Abstract

The effect of the anionic surfactant, sodium lauryl sulfate (CAS 151-21-3), on the absorption of cefadroxil (CAS 50370-12-2) as model antibiotic in colon has been studied by means of an in situ rat gut technique, as a previous step to investigate the influence of the surfactant on the intestinal, carrier-mediated absorption of the antibiotic. Microbial degradation tests were initially performed, which demonstrated that cefadroxil disappearance from luminal content was only due to absorption. Micelle solubilization of cefadroxil was also previously assessed through dialysis tests in order to adequately correct absorption rate constant values found in the presence of the surfactant at supramicellar concentration. Micelle solubilization was minimal, although statistically significant. Apparent passive absorption rate constants, ka(h-1), were determined in the presence of variable concentrations of lauryl sulfate in perfusion fluids. Results showed that ka values greatly increased as surfactant luminal concentration increased until an asymptotic value (about 7-fold higher than cefadroxil alone) was obtained; this was assumed to be due to a direct effect of the surfactant on membrane polarity. Moreover, the results were satisfactorily adjusted using a functional hyperbolic-type equation, as occurs with many other saturable processes. This was supposed to be indicative that the surfactant effect is due to an adsorption process of the surfactant ions or molecules to the intestinal absorbent membrane.

摘要

作为研究表面活性剂对该抗生素肠道载体介导吸收影响的前期步骤,已通过原位大鼠肠道技术研究了阴离子表面活性剂月桂醇硫酸酯钠(CAS 151-21-3)对头孢羟氨苄(CAS 50370-12-2)作为结肠中模型抗生素吸收的影响。最初进行了微生物降解试验,结果表明头孢羟氨苄从肠腔内容物中的消失仅归因于吸收。此前还通过透析试验评估了头孢羟氨苄的胶束增溶作用,以便对在超胶束浓度的表面活性剂存在下测得的吸收速率常数进行适当校正。胶束增溶作用极小,尽管具有统计学意义。在灌注液中存在不同浓度月桂醇硫酸酯的情况下测定了表观被动吸收速率常数ka(h-1)。结果表明,随着表面活性剂肠腔浓度的增加,ka值大幅升高,直至获得一个渐近值(比单独使用头孢羟氨苄时高约7倍);这被认为是表面活性剂对膜极性的直接作用所致。此外,使用函数双曲线型方程对结果进行了令人满意的拟合,许多其他可饱和过程也是如此。这被认为表明表面活性剂的作用是由于表面活性剂离子或分子吸附到肠道吸收膜上。

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