Literature DB >> 12543490

Resolution of chiral drugs by liquid chromatography based upon diastereomer formation with chiral derivatization reagents.

Toshimasa Toyo'oka1.   

Abstract

Chiral derivatization reagents for resolution of biologically important compounds, such as chiral drugs by high-performance liquid chromatography (HPLC), based upon pre-column derivatization and diastereomer formation, are reviewed. The derivatization reagents for various functional groups, i.e., amine, carboxyl, carbonyl, hydroxyl and thiol, are evaluated in terms of reactivity, stability, wavelength, handling, versatility, sensitivity, and selectivity. The applicability of the reagents to the analyses of drugs and bioactive compounds are included in the text. Copyright 2002 Elsevier Science B.V.

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Year:  2002        PMID: 12543490     DOI: 10.1016/s0165-022x(02)00127-6

Source DB:  PubMed          Journal:  J Biochem Biophys Methods        ISSN: 0165-022X


  5 in total

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Authors:  Jiri Brichac; Ales Honzatko; Matthew J Picklo
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Review 2.  Significance and challenges of stereoselectivity assessing methods in drug metabolism.

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Journal:  J Pharm Anal       Date:  2015-12-21

3.  Simultaneous Quantitative Determination of Synthetic Cathinone Enantiomers in Urine and Plasma Using GC-NCI-MS.

Authors:  Rashed Alremeithi; Mohammed A Meetani; Anas A Alaidaros; Adnan Lanjawi; Khalid Alsumaiti
Journal:  J Anal Methods Chem       Date:  2018-04-01       Impact factor: 2.193

4.  Chiral drugs: an overview.

Authors:  Lien Ai Nguyen; Hua He; Chuong Pham-Huy
Journal:  Int J Biomed Sci       Date:  2006-06

5.  Validation of LC-MS/MS Coupled with a Chiral Column for the Determination of 3- or 15-Acetyl Deoxynivalenol Mycotoxins from Fusarium graminearum in Wheat.

Authors:  Lan Wang; Zheng Yan; Haiyan Zhou; Yingying Fan; Cheng Wang; Jingbo Zhang; Yucai Liao; Aibo Wu
Journal:  Toxins (Basel)       Date:  2021-09-16       Impact factor: 4.546

  5 in total

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