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β受体阻滞剂经猪口腔黏膜的体外药物渗透比较研究。

A comparative ex vivo drug permeation study of beta-blockers through porcine buccal mucosa.

作者信息

Amores Sonia, Lauroba Jacinto, Calpena Ana, Colom Helena, Gimeno Alvaro, Domenech José

机构信息

Pharmacy Pharmaceutical Technology Department, Biopharmaceutical Pharmacokinetics Unit, Faculty of Pharmacy, Av. Joan XXIII, s/n, Barcelona 08028, Spain.

Pharmacy Pharmaceutical Technology Department, Biopharmaceutical Pharmacokinetics Unit, Faculty of Pharmacy, Av. Joan XXIII, s/n, Barcelona 08028, Spain.

出版信息

Int J Pharm. 2014 Jul 1;468(1-2):50-4. doi: 10.1016/j.ijpharm.2014.03.050. Epub 2014 Apr 13.

Abstract

Apparent permeability coefficients (kp) of a series of beta-blockers: acebutolol, atenolol, labetalol, metoprolol, oxprenolol and propranolol, through porcine buccal mucosa were determined. The aim of the study was to determine the permeation parameters (apparent permeability coefficient, kp; flux, J; and lag time, TL) as a measure of the intrinsic permeability of porcine buccal mucosa to these drugs, in order to predict the efficacy of their possible administration through human buccal mucosa. A positive linear correlation was observed between the apparent permeability coefficient, kpand the partition coefficient, P. Oxprenolol and propranolol are the drugs that presented the highest values of kp: 0.3231×10(2) cm/h and 0.5666×10(2) cm/h, respectively. Multiple linear regression (MLR) using least square estimation was performed on the data set with logkpas dependent variable and the descriptors as predictor variables. The potential systemic capacity after a buccal administration was predicted by estimating the plasma concentrations at steady-stated (Css). Considering the entire process of permeation ex vivo, propranolol and oxprenolol would seem to be the best candidates for administration through the buccal mucosa.

摘要

测定了一系列β受体阻滞剂(醋丁洛尔、阿替洛尔、拉贝洛尔、美托洛尔、氧烯洛尔和普萘洛尔)通过猪口腔黏膜的表观渗透系数(kp)。本研究的目的是确定渗透参数(表观渗透系数kp、通量J和滞后时间TL),以衡量猪口腔黏膜对这些药物的内在渗透性,从而预测它们通过人口腔黏膜给药的疗效。观察到表观渗透系数kp与分配系数P之间存在正线性相关性。氧烯洛尔和普萘洛尔是kp值最高的药物,分别为0.3231×10² cm/h和0.5666×10² cm/h。以logkp为因变量、描述符为预测变量,对数据集进行了最小二乘估计的多元线性回归(MLR)。通过估计稳态血浆浓度(Css)预测口腔给药后的潜在全身作用能力。考虑到整个体外渗透过程,普萘洛尔和氧烯洛尔似乎是通过口腔黏膜给药的最佳候选药物。

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