Establishment and Evaluation of the Novel Tetramethylammonium‐L‐Hydroxyproline Chiral Ionic Liquid Synergistic System Based on Clindamycin Phosphate for Enantioseparation by Capillary Electrophoresis. Issue 9 (11th June 2015)
- Record Type:
- Journal Article
- Title:
- Establishment and Evaluation of the Novel Tetramethylammonium‐L‐Hydroxyproline Chiral Ionic Liquid Synergistic System Based on Clindamycin Phosphate for Enantioseparation by Capillary Electrophoresis. Issue 9 (11th June 2015)
- Main Title:
- Establishment and Evaluation of the Novel Tetramethylammonium‐L‐Hydroxyproline Chiral Ionic Liquid Synergistic System Based on Clindamycin Phosphate for Enantioseparation by Capillary Electrophoresis
- Authors:
- Xu, Guangfu
Du, Yingxiang
Du, Fan
Chen, Jiaquan
Yu, Tao
Zhang, Qi
Zhang, Jinjing
Du, Shuaijing
Feng, Zijie - Abstract:
- <abstract abstract-type="main"> <title>Abstract</title> <p>Much attention has been paid to chiral <named-content content-type="chemicalTechnology" xlink:type="simple" xmlns:xlink="http://www.w3.org/1999/xlink">ionic liquids</named-content> (ILs) in <named-content content-type="chemicalTechnology" xlink:type="simple" xmlns:xlink="http://www.w3.org/1999/xlink">analytical chemistry</named-content>, especially its application in <named-content content-type="chemicalTechnology" xlink:type="simple" xmlns:xlink="http://www.w3.org/1999/xlink">capillary electrophoresis</named-content> (CE) enantioseparation. However, the investigation of chiral <named-content content-type="chemicalTechnology" xlink:type="simple" xmlns:xlink="http://www.w3.org/1999/xlink">ionic liquids</named-content> synergistic systems based on antibiotic chiral selectors has been reported in only one article. In this work, a novel chiral ionic liquid, tetramethylammonium‐L‐hydroxyproline (TMA‐L‐Hyp), was applied for the first time in CE chiral separation to evaluate its potential synergistic effect with clindamycin phosphate (CP) as the chiral selector. As observed, significantly improved separation was obtained in this TMA‐L‐Hyp/CP synergistic system compared to TMA‐L‐Hyp or a CP single system. Several primary factors that might influence the separation were investigated, including CP concentration, TMA‐L‐Hyp concentration, buffer pH, types and concentrations of organic modifier, applied voltage, and capillary<abstract abstract-type="main"> <title>Abstract</title> <p>Much attention has been paid to chiral <named-content content-type="chemicalTechnology" xlink:type="simple" xmlns:xlink="http://www.w3.org/1999/xlink">ionic liquids</named-content> (ILs) in <named-content content-type="chemicalTechnology" xlink:type="simple" xmlns:xlink="http://www.w3.org/1999/xlink">analytical chemistry</named-content>, especially its application in <named-content content-type="chemicalTechnology" xlink:type="simple" xmlns:xlink="http://www.w3.org/1999/xlink">capillary electrophoresis</named-content> (CE) enantioseparation. However, the investigation of chiral <named-content content-type="chemicalTechnology" xlink:type="simple" xmlns:xlink="http://www.w3.org/1999/xlink">ionic liquids</named-content> synergistic systems based on antibiotic chiral selectors has been reported in only one article. In this work, a novel chiral ionic liquid, tetramethylammonium‐L‐hydroxyproline (TMA‐L‐Hyp), was applied for the first time in CE chiral separation to evaluate its potential synergistic effect with clindamycin phosphate (CP) as the chiral selector. As observed, significantly improved separation was obtained in this TMA‐L‐Hyp/CP synergistic system compared to TMA‐L‐Hyp or a CP single system. Several primary factors that might influence the separation were investigated, including CP concentration, TMA‐L‐Hyp concentration, buffer pH, types and concentrations of organic modifier, applied voltage, and capillary temperature. The best results were obtained with a 40 mM borax buffer (pH 7.6) containing 30 mM TMA‐L‐Hyp, 80 mM CP, and 20% (v/v) methanol, while the applied voltage and temperature were set at 20 kV and 20°C, respectively. <italic>Chirality 27:598–604, 2015</italic>. © 2015 Wiley Periodicals, Inc.</p> </abstract> … (more)
- Is Part Of:
- Chirality. Volume 27:Issue 9(2015)
- Journal:
- Chirality
- Issue:
- Volume 27:Issue 9(2015)
- Issue Display:
- Volume 27, Issue 9 (2015)
- Year:
- 2015
- Volume:
- 27
- Issue:
- 9
- Issue Sort Value:
- 2015-0027-0009-0000
- Page Start:
- 598
- Page End:
- 604
- Publication Date:
- 2015-06-11
- Subjects:
- Chirality -- Periodicals
Pharmaceutical chemistry -- Periodicals
541.22 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1520-636X ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/chir.22463 ↗
- Languages:
- English
- ISSNs:
- 0899-0042
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3181.124450
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 3512.xml