Chiral separation of five antihistamine drug enantiomers and enantioselective pharmacokinetic study of carbinoxamine in rat plasma by HPLC-MS/MS. (30th March 2020)
- Record Type:
- Journal Article
- Title:
- Chiral separation of five antihistamine drug enantiomers and enantioselective pharmacokinetic study of carbinoxamine in rat plasma by HPLC-MS/MS. (30th March 2020)
- Main Title:
- Chiral separation of five antihistamine drug enantiomers and enantioselective pharmacokinetic study of carbinoxamine in rat plasma by HPLC-MS/MS
- Authors:
- Li, Meng
Zhang, Junyuan
Ma, Siman
Jiang, Zhen
Di, Xin
Guo, Xingjie - Abstract:
- Abstract : Chiral separation and pharmacokinetic study of antihistamine drugs. Abstract : The chiral separation of five antihistamine drugs including meclizine, cloperastine, azelastine, carbinoxamine and mequitazine was studied by HPLC combined with chiral stationary phases. The effect of chiral columns, the types and contents of organic modifiers, and the concentrations of basic additive on the chiral separation was evaluated and optimized in detail. The best enantioselectivity for these compounds was observed using Chiralpak IA and Chiralpak ID as chiral columns. In particular, baseline separation of carbinoxamine with the largest resolution of 3.82 was achieved using a Chiralpak ID column with the mobile phase of acetonitrile–water–ammonia solution (90 : 10 : 0.1, v/v/v). Based on this result, an enantioselective HPLC-MS/MS method was developed and validated for determination of carbinoxamine enantiomers in rat plasma. Also, this method was successfully applied in evaluating the pharmacokinetic profiles of carbinoxamine enantiomers. Good linearity ( r > 0.99) for both enantiomers over a concentration range of 0.1–100 ng mL −1 was obtained. The accuracy ranged from 87.4% to 113.8%, and the intra-day and inter-day precisions were below 9.4% for (+)- and (−)-carbinoxamine at three quality control levels. The pharmacokinetic parameters demonstrated that the absorption and elimination processes of carbinoxamine enantiomers were not stereoselective, and chiral inversion didAbstract : Chiral separation and pharmacokinetic study of antihistamine drugs. Abstract : The chiral separation of five antihistamine drugs including meclizine, cloperastine, azelastine, carbinoxamine and mequitazine was studied by HPLC combined with chiral stationary phases. The effect of chiral columns, the types and contents of organic modifiers, and the concentrations of basic additive on the chiral separation was evaluated and optimized in detail. The best enantioselectivity for these compounds was observed using Chiralpak IA and Chiralpak ID as chiral columns. In particular, baseline separation of carbinoxamine with the largest resolution of 3.82 was achieved using a Chiralpak ID column with the mobile phase of acetonitrile–water–ammonia solution (90 : 10 : 0.1, v/v/v). Based on this result, an enantioselective HPLC-MS/MS method was developed and validated for determination of carbinoxamine enantiomers in rat plasma. Also, this method was successfully applied in evaluating the pharmacokinetic profiles of carbinoxamine enantiomers. Good linearity ( r > 0.99) for both enantiomers over a concentration range of 0.1–100 ng mL −1 was obtained. The accuracy ranged from 87.4% to 113.8%, and the intra-day and inter-day precisions were below 9.4% for (+)- and (−)-carbinoxamine at three quality control levels. The pharmacokinetic parameters demonstrated that the absorption and elimination processes of carbinoxamine enantiomers were not stereoselective, and chiral inversion did not occur either in rats. … (more)
- Is Part Of:
- New journal of chemistry. Volume 44:Number 15(2020)
- Journal:
- New journal of chemistry
- Issue:
- Volume 44:Number 15(2020)
- Issue Display:
- Volume 44, Issue 15 (2020)
- Year:
- 2020
- Volume:
- 44
- Issue:
- 15
- Issue Sort Value:
- 2020-0044-0015-0000
- Page Start:
- 5819
- Page End:
- 5827
- Publication Date:
- 2020-03-30
- Subjects:
- Chemistry -- Periodicals
Chimie -- Périodiques
540 - Journal URLs:
- http://www.rsc.org/ ↗
http://www.rsc.org/is/journals/current/newjchem/njc.htm ↗ - DOI:
- 10.1039/d0nj00095g ↗
- Languages:
- English
- ISSNs:
- 1144-0546
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6084.319900
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 13848.xml