Microdialysis for pharmacokinetic analysis of drug transport to the brain

被引:60
作者
de Lange, ECM [1 ]
de Boer, BAG [1 ]
Breimer, DD [1 ]
机构
[1] Leiden Amsterdam Ctr Drug Res, Div Pharmacol, Sylvius Labs, NL-2300 RA Leiden, Netherlands
关键词
microdialysis; brain extracellular fluid; blood-brain barrier;
D O I
10.1016/S0169-409X(98)00089-1
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The intracerebral microdialysis technique represents an important tool for monitoring free drug concentrations in brain extracellular fluid (brain(EcF)) as a function of time. With knowledge of associated free plasma concentrations, it provides information on blood-brain barrier (BBB) drug transport. However, as the implantation of the microdialysis probe evokes tissue reactions, it should be established if the BBB characteristics are maintained under particular microdialysis experimental conditions. Several studies have been performed to evaluate the use of intracerebral microdialysis as a technique to measure drug transport across the BBB and to measure regional pharmacokinetics of drugs in the brain. Under carefully controlled conditions, the intracerebral microdialysis data did reflect passive BBB transport under normal conditions, as well as changes induced by hyperosmolar opening or by the presence of a tumor in the brain. Studies on active BBB transport by the mdr1a-encoded P-glycoprotein (Pgp) were performed, comparing mdr1a(-/-) with wild-type mice. Microdialysis surgery and experimental procedures did not affect Pgp functionality, but the latter did influence in vivo concentration recovery, which was in line with theoretical predictions. It is concluded that intracerebral microdialysis provides meaningful data on drug transport to the brain, only if appropriate methods are applied to determine in vivo concentration recovery. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:211 / 227
页数:17
相关论文
共 72 条
[1]  
AGON P, 1989, POSITRON EMISSION TO, P1087
[2]   A STUDY OF INTRATHECAL, CEREBROSPINAL FLUID-TO-BRAIN EXCHANGE [J].
AIRD, RB .
EXPERIMENTAL NEUROLOGY, 1984, 86 (02) :342-358
[3]   4-TRIMETHYLAMMONIUM ANTIPYRINE - A QUATERNARY AMMONIUM NONRADIONUCLIDE MARKER FOR BLOOD-BRAIN-BARRIER INTEGRITY DURING INVIVO MICRODIALYSIS [J].
ALLEN, DD ;
CROOKS, PA ;
YOKEL, RA .
JOURNAL OF PHARMACOLOGICAL AND TOXICOLOGICAL METHODS, 1992, 28 (03) :129-135
[4]   F-19 NUCLEAR-MAGNETIC-RESONANCE SPECTROSCOPY OF NEUROLEPTICS - THE 1ST INVIVO PHARMACOKINETICS OF TRIFLUOPERAZINE IN THE RAT-BRAIN AND THE 1ST INVIVO SPECTRUM OF FLUPHENAZINE IN THE HUMAN BRAIN [J].
BARTELS, M ;
GUNTHER, U ;
ALBERT, K ;
MANN, K ;
SCHUFF, N ;
STUCKSTEDTE, H .
BIOLOGICAL PSYCHIATRY, 1991, 30 (07) :656-662
[5]   REGIONAL CEREBRAL GLUCOSE PHOSPHORYLATION AND BLOOD-FLOW AFTER INSERTION OF A MICRODIALYSIS FIBER THROUGH THE DORSAL HIPPOCAMPUS IN THE RAT [J].
BENVENISTE, H ;
DREJER, J ;
SCHOUSBOE, A ;
DIEMER, NH .
JOURNAL OF NEUROCHEMISTRY, 1987, 49 (03) :729-734
[6]   MICRODIALYSIS - THEORY AND APPLICATION [J].
BENVENISTE, H ;
HUTTEMEIER, PC .
PROGRESS IN NEUROBIOLOGY, 1990, 35 (03) :195-215
[7]   STEADY-STATE THEORY FOR QUANTITATIVE MICRODIALYSIS OF SOLUTES AND WATER INVIVO AND INVITRO [J].
BUNGAY, PM ;
MORRISON, PF ;
DEDRICK, RL .
LIFE SCIENCES, 1990, 46 (02) :105-119
[8]  
COLOMBO T, 1982, CANCER CHEMOTH PHARM, V7, P127
[9]   MULTIDRUG-RESISTANCE GENE (P-GLYCOPROTEIN) IS EXPRESSED BY ENDOTHELIAL-CELLS AT BLOOD-BRAIN BARRIER SITES [J].
CORDONCARDO, C ;
OBRIEN, JP ;
CASALS, D ;
RITTMANGRAUER, L ;
BIEDLER, JL ;
MELAMED, MR ;
BERTINO, JR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (02) :695-698
[10]   KINETIC-MODEL FOR DISPOSITION OF 6-MERCAPTOPURINE IN MONKEY PLASMA AND CEREBROSPINAL-FLUID [J].
COVELL, DG ;
NARANG, PK ;
POLACK, DG .
AMERICAN JOURNAL OF PHYSIOLOGY, 1985, 248 (02) :R147-R156