Lack of metabolic racemisation of ropivacaine, determined by liquid chromatography using a Chiral AGP column

被引:14
作者
Arvidsson, T [1 ]
Bruce, HF [1 ]
Halldin, MM [1 ]
机构
[1] ASTRA PAIN CONTROL AB,DEPT DRUG METAB,S-15185 SODERTALJE,SWEDEN
关键词
local anaesthetics; enantiomers; stereoselective; liquid chromatography; Chiral AGP column; bioanalysis; urine samples;
D O I
10.1002/chir.530070414
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Ropivacaine hydrochloride monohydrate (ropivacaine) is a new local anaesthetic agent which is administered exclusively as the (-)-(S)-form. The aim of the study was to determine whether metabolic racemisation of (-)-(S)-ropivacaine occurs. This was tested in man, rat, dog, and sheep after different routes of administration. The enantiomers of ropivacaine and two of the major metabolites, 3-hydroxy-ropivacaine and 2',6'-pipecoloxylidide (PPX), were determined in urine samples by liquid chromatography on a Chiral AGP column after liquid-liquid extraction. It was possible to detect <1% of the (+)-(R)-enantiomer of both ropivacaine and the two major metabolites. In the samples examined, no trace of metabolic racemisation was observed, In pharmacokinetic, pharmacodynamic, toxicological, and metabolic studies, therefore, nonchiral assays are considered to be adequate. (C) 1995 Wiley-Liss, Inc.
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页码:272 / 277
页数:6
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