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논문 기본 정보

자료유형
학술저널
저자정보
Yusung Choi (Kangwon National University) Thuy-Vy Pham (Kangwon National University) Xuan-Lan Mai (Kangwon National University) Quoc-Ky Truong (Pham Ngoc Thach University of Medicine) Thi-Anh-Tuyet Le (Kangwon National University) Thi-Ngoc-Van Nguyen (Can Tho University of Medicine and Pharmacy) Gunhee Lee (Kangwon National University) Jong-Seong Kang (Chungnam National University) Woongchon Mar (Seoul National University) Kyeong Ho Kim (Kangwon National University)
저널정보
한국분석과학회 분석과학 분석과학 제32권 제5호
발행연도
2019.10
수록면
185 - 195 (11page)

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초록· 키워드

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Over the past decades, chiral switch of the proton pump inhibitors (PPIs) has been received widespread attention in therapeutic advantages as well as pharmaceutical analysis. In present study, the influence of cyclodextrins (CDs) on the chiral separation of four common PPIs (lansoprazole, omeprazole, pantoprazole, and rabeprazole) was investigated. The results demonstrated that capillary electrophoresis (CE) with dual CDs as a chiral selector system is a possible and promising method for the enantioseparation of these PPIs. Rabeprazole, which is the most challenging and acid-labile candidate among four PPIs, was selected for further development of the technique. To optimize CE condition, the effects of capillary parameters and background electrolytes on the enantioseparation were investigated. Finally, the best chiral separation was acheived by using sulfobutyl ether-β-CD, and γ-CD as dual chiral selectors. The developed CE method not only provided the effective chiral separation but also showed the good stability of rabeprazole. The proposed method was successfully validated according to the International Conference on Harmonization guideline and effectively applied to determine rabeprazole enantiomers in commercial rabeprazole tablets, with recoveries ranging from 97.17 % to 103.29 % of the label content.

목차

Abstract
1. Introduction
2. Experimental
3. Results and Discussion
4. Conclusions
References

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