Literature DB >> 32540081

Method screening strategies of stereoisomers of compounds with multiple chiral centers and a single chiral center.

Jessica Lin1, Charlotte Tsang1, Raymond Lieu1, Kelly Zhang2.   

Abstract

Analysis and control of stereoisomers is a major task in pharmaceutical analysis, and is a greater challenge when compounds with multiple chiral centers (MCC) are concerned. HPLC and SFC are commonly used for stereoisomer analysis in drug development, typically starting with chiral method screening. Although method screening for compounds with a single chiral center (SCC) has been well studied for 5-µm polysaccharide stationary phase particles, there are fewer reports on method screening for compounds with MCC and smaller particle sizes. In this study, we systematically evaluated the impact of key parameters in chiral method screening including column particle size (3-µm vs. sub-2 µm), nature of the chiral selector binding (coated vs. immobilized), mobile phase elution mode (isocratic vs. gradient), and separation approach (SFC vs. HPLC). A diverse set of pharmaceutical compounds with MCC and a SCC were studied. We found that the screening strategies differ between MCC and SCC compounds due to the difference in the recognition mechanism involved. Furthermore, we have developed an effective screening strategy with OD-3, AD-3 and IG-3 columns for SCC compounds which achieves larger than 90% success rate, and a combination of OD-3, AD-3, IG-3, IC-3 and AS-3 for MCC compounds which offers the best coverage.
Copyright © 2020 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Chiral separation; Method screening; Multiple chiral centers; Stereoisomers

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Year:  2020        PMID: 32540081     DOI: 10.1016/j.chroma.2020.461244

Source DB:  PubMed          Journal:  J Chromatogr A        ISSN: 0021-9673            Impact factor:   4.759


  1 in total

1.  Characteristic and complementary chiral recognition ability of four recently developed immobilized chiral stationary phases based on amylose and cellulose phenyl carbamates and benzoates.

Authors:  Takafumi Onishi; Takunori Ueda; Kenichi Yoshida; Kosuke Uosaki; Hiroyuki Ando; Ryota Hamasaki; Atsushi Ohnishi
Journal:  Chirality       Date:  2022-04-12       Impact factor: 2.183

  1 in total

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