Evaluation of the stereoselective metabolism of the chiral analgesic drug etodolac by high-performance liquid chromatography-Reference-Cited by-同舟云学术

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Evaluation of the stereoselective metabolism of the chiral analgesic drug etodolac by high-performance liquid chromatography

Published:1993-11 Issue:2 Volume:621 Page:199-207
ISSN:0378-4347
Container-title:Journal of Chromatography B: Biomedical Sciences and Applications
language:en
Short-container-title:Journal of Chromatography B: Biomedical Sciences and Applications

Author:

Becker-Scharfenkamp U.,Blaschke G.

Publisher

Elsevier BV

Subject

General Chemistry

Reference13 articles.

2. Disposition and biotransformation of14C-etodolac in man

3. Resolution of etodolac and antiinflammatory and prostaglandin synthetase inhibiting properties of the enantiomers

4. American Home Products Corporation (N. A. Abraham, C. A. Demerson, Inv.), U.S. Pat., 4520 203 (28.5.1985).

5. American Home Products Corporation (N. A. Abraham, C. A. Demerson, Inv.), U.S. Pat., 4501 899 (26.2.1985).

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1. Liquid chromatographic methods for separation, determination, and bioassay of enantiomers of etodolac: A review;Journal of Separation Science;2019-08-23

2. Ultrasound-assisted chiral derivatization of etodolac with (1R)-(−)-menthyl chloroformate for the determination of etodolac enantiomers;Arabian Journal of Chemistry;2016-11

3. Thin-layer chromatographic enantioseparation of (RS)-etodolac using indirect approach;JPC - Journal of Planar Chromatography - Modern TLC;2016-10

4. Enantioselective analysis of etodolac in human plasma by LC–MS/MS: Application to clinical pharmacokinetics;Journal of Pharmaceutical and Biomedical Analysis;2016-02

5. A novel approach for enantioseparation as applied to (RS)-etodolac from pharmaceutical formulations: LC MS and density functional theory support for confirmation of diastereomers so separated;Biomedical Chromatography;2015-02-01

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