Literature DB >> 3334165

Enantiomeric resolution of drug compounds by liquid chromatography.

H T Karnes1, M A Sarkar.   

Abstract

Novel techniques have recently emerged to separate chiral drug compounds into pure enantiomers. The mechanism, experimental difficulties, and applicability of these methods can very greatly, and the choices involved are not straightforward. The most significant new advances in the field of chiral separations have come from work done with liquid chromatographic systems and chiral stationary-phase columns. This review describes several commonly used approaches to chiral separation, dia-stereomeric derivatization, chiral mobile-phase additives, and three major types of chiral stationary phases. Although no single method can be judged superior for every drug application, it appears that chiral stationary phases have received the most attention recently and they are emphasized here.

Mesh:

Substances:

Year:  1987        PMID: 3334165     DOI: 10.1023/a:1016437018323

Source DB:  PubMed          Journal:  Pharm Res        ISSN: 0724-8741            Impact factor:   4.200


  19 in total

1.  Stereochemical factors in biological activity.

Authors:  A H BECKETT
Journal:  Fortschr Arzneimittelforsch       Date:  1959

2.  Optical isomer separation by liquid chromatography.

Authors:  D W Armstrong
Journal:  Anal Chem       Date:  1987-01-15       Impact factor: 6.986

3.  Separation of drug stereoisomers by the formation of beta-cyclodextrin inclusion complexes.

Authors:  D W Armstrong; T J Ward; R D Armstrong; T E Beesley
Journal:  Science       Date:  1986-05-30       Impact factor: 47.728

Review 4.  The chromatographic analysis of enantiomers in drug metabolism studies.

Authors:  B Testa
Journal:  Xenobiotica       Date:  1986-03       Impact factor: 1.908

5.  Separation of acebutolol and diacetolol diastereomers by reversed-phase high-performance liquid chromatography.

Authors:  A A Gulaid; G W Houghton; A R Boobis
Journal:  J Chromatogr       Date:  1985-01-18

6.  The direct enantiomeric determination of (-)- and (+)-propranolol in human serum by high-performance liquid chromatography on a chiral stationary phase.

Authors:  I W Wainer; T D Doyle; K H Donn; J R Powell
Journal:  J Chromatogr       Date:  1984-03-09

7.  Enantiomeric purity of naproxen by liquid chromatographic analysis of its diastereomeric octyl esters.

Authors:  D M Johnson; A Reuter; J M Collins; G F Thompson
Journal:  J Pharm Sci       Date:  1979-01       Impact factor: 3.534

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

Authors:  C A Demerson; L G Humber; N A Abraham; G Schilling; R R Martel; C Pace-Asciak
Journal:  J Med Chem       Date:  1983-12       Impact factor: 7.446

9.  Separation of enantiomeric amines by ion-pair chromatography.

Authors:  C Pettersson; G Schill
Journal:  J Chromatogr       Date:  1981-01-16

10.  Resolution of enantiomeric amides on a cellulose-based chiral stationary phase. Steric and electronic effects.

Authors:  I W Wainer; M C Alembik
Journal:  J Chromatogr       Date:  1986-05-16
View more
  1 in total

Review 1.  Chirality. Clinical pharmacokinetic and pharmacodynamic considerations.

Authors:  E J Lee; K M Williams
Journal:  Clin Pharmacokinet       Date:  1990-05       Impact factor: 6.447

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.