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微透析探针校准:无净通量和反向透析方法中梯度及组织依赖性变化

Microdialysis probes calibration: gradient and tissue dependent changes in no net flux and reverse dialysis methods.

作者信息

Le Quellec A, Dupin S, Genissel P, Saivin S, Marchand B, Houin G

机构信息

Laboratoire de Pharmacologie Pharmacocinétique, Faculté des Sciences Pharmaceutiques, Toulouse, France.

出版信息

J Pharmacol Toxicol Methods. 1995 Feb;33(1):11-6. doi: 10.1016/1056-8719(94)00049-a.

DOI:10.1016/1056-8719(94)00049-a
PMID:7727803
Abstract

Probe calibrations are required for accurate estimations of extracellular concentrations in microdialysis experiments. Several methods have been developed and validated for in vivo determination of dialysis membrane recovery such as the perfusion rate method and the No Net Flux method. In this study, the No Net Flux and the reverse dialysis methods were investigated. Both measure the net transport of drug across the dialysis membrane. The recovery was defined as R = (Cin - Cout)/Cin, where Cin and Cout were the concentrations of a compound in the perfusate and in the dialysate, respectively. First, the accuracy of the No Net Flux method to estimate in vivo recovery was compared in two situations: diffusion from the probe into the dialysis medium and diffusion from the outer medium into the probe. The point of no net transport was used to estimate the concentration surrounding the probe. Neither difference between extracellular concentrations (intercept values) nor difference between recoveries were observed. Then the reverse dialysis method was tested to estimate the relative loss of drug from the perfusate when the probe was placed in a drug-free medium. Finally comparisons of the behavior of the drug diffusion across the membrane under increasing gradient conditions have shown an asymptotic profile, specific of the tissue; blood, muscle, and adipose tissue. The faster a drug was removed by microvascular transport (blood > muscle > adipocytes), the higher was the recovery, until the perfusate concentration reached a threshold value where the transport process became gradient limited and no more tissue limited.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在微透析实验中,为了准确估计细胞外浓度,需要进行探针校准。已经开发并验证了几种用于体内测定透析膜回收率的方法,如灌注速率法和无净通量法。在本研究中,对无净通量法和反向透析法进行了研究。两者都测量药物跨透析膜的净转运。回收率定义为R = (Cin - Cout)/Cin,其中Cin和Cout分别是灌注液和透析液中化合物的浓度。首先,在两种情况下比较了无净通量法估计体内回收率的准确性:从探针扩散到透析介质中以及从外部介质扩散到探针中。无净转运点用于估计探针周围的浓度。未观察到细胞外浓度(截距值)之间的差异或回收率之间的差异。然后测试了反向透析法,以估计当探针置于无药物介质中时灌注液中药物的相对损失。最后,在梯度增加的条件下对药物跨膜扩散行为的比较显示出一种渐近曲线,这是组织特有的;血液、肌肉和脂肪组织。药物通过微血管转运去除得越快(血液>肌肉>脂肪细胞),回收率就越高,直到灌注液浓度达到一个阈值,此时转运过程变得受梯度限制,不再受组织限制。(摘要截断于250字)

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