Development of a sensitive ultra high performance liquid chromatography with tandem mass spectrometry method for the simultaneous quantification of nine active compounds in rat plasma and its application to a pharmacokinetic study after administration of Viscum coloratum extracts. Issue 3 (23rd December 2014)
- Record Type:
- Journal Article
- Title:
- Development of a sensitive ultra high performance liquid chromatography with tandem mass spectrometry method for the simultaneous quantification of nine active compounds in rat plasma and its application to a pharmacokinetic study after administration of Viscum coloratum extracts. Issue 3 (23rd December 2014)
- Main Title:
- Development of a sensitive ultra high performance liquid chromatography with tandem mass spectrometry method for the simultaneous quantification of nine active compounds in rat plasma and its application to a pharmacokinetic study after administration of Viscum coloratum extracts
- Authors:
- Fan, Rong‐Hua
Ding, Wei
Ma, Yu‐Ying
Lin, Hong‐Li
Men, Lei
Duan, Meng‐Meng
Zhao, Yun‐Li
Yu, Zhi‐Guo - Abstract:
- <abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <p>A simple, specific, and sensitive ultra high performance liquid chromatography with tandem mass spectrometry method was developed and validated for the simultaneous quantification of nine compounds including a new compound, rhamnazin‐3‐<italic>Ο</italic>‐β‐<sc>d</sc>‐(6″‐β‐hydroxy‐β‐methyglutaryl)<italic>‐</italic>β‐<sc>d</sc>‐glucoside‐4′<italic>‐Ο‐</italic>β‐<sc>d</sc>‐glucoside, in rat plasma using baicalin as an internal standard. The plasma samples were pretreated and extracted by protein precipitation with 0.2% formic acid in acetonitrile. The analytes were separated on a Thermo Syncronis C<sub>18</sub> column by gradient elution with a mobile phase consisting of acetonitrile and 0.1% aqueous formic acid at a flow rate of 0.25 mL/min. The detection of the analytes was performed on an electrospray ionization interface operating in positive‐ion and multiple reaction monitoring acquisition modes. The calibration curves of these analytes showed good linearity (<italic>r &gt;</italic> 0.99) within the test ranges. The lower limit of quantification ranged from 0.4 to 20.1 ng/mL for the analytes. The intra‐ and interday precision and accuracy were all within ±15%, and the recoveries were higher than 80.0%. The validated method was successfully applied to a pharmacokinetic study of the nine flavonoids after administration of the <italic>Viscum coloratum</italic> extracts by intravenous<abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <p>A simple, specific, and sensitive ultra high performance liquid chromatography with tandem mass spectrometry method was developed and validated for the simultaneous quantification of nine compounds including a new compound, rhamnazin‐3‐<italic>Ο</italic>‐β‐<sc>d</sc>‐(6″‐β‐hydroxy‐β‐methyglutaryl)<italic>‐</italic>β‐<sc>d</sc>‐glucoside‐4′<italic>‐Ο‐</italic>β‐<sc>d</sc>‐glucoside, in rat plasma using baicalin as an internal standard. The plasma samples were pretreated and extracted by protein precipitation with 0.2% formic acid in acetonitrile. The analytes were separated on a Thermo Syncronis C<sub>18</sub> column by gradient elution with a mobile phase consisting of acetonitrile and 0.1% aqueous formic acid at a flow rate of 0.25 mL/min. The detection of the analytes was performed on an electrospray ionization interface operating in positive‐ion and multiple reaction monitoring acquisition modes. The calibration curves of these analytes showed good linearity (<italic>r &gt;</italic> 0.99) within the test ranges. The lower limit of quantification ranged from 0.4 to 20.1 ng/mL for the analytes. The intra‐ and interday precision and accuracy were all within ±15%, and the recoveries were higher than 80.0%. The validated method was successfully applied to a pharmacokinetic study of the nine flavonoids after administration of the <italic>Viscum coloratum</italic> extracts by intravenous injection.</p> </abstract> … (more)
- Is Part Of:
- Journal of separation science. Volume 38:Issue 3(2015:Feb.)
- Journal:
- Journal of separation science
- Issue:
- Volume 38:Issue 3(2015:Feb.)
- Issue Display:
- Volume 38, Issue 3 (2015)
- Year:
- 2015
- Volume:
- 38
- Issue:
- 3
- Issue Sort Value:
- 2015-0038-0003-0000
- Page Start:
- 530
- Page End:
- 540
- Publication Date:
- 2014-12-23
- Subjects:
- Separation (Technology) -- Periodicals
Chromatographic analysis -- Periodicals
543.089 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1615-9314 ↗
http://www.interscience.wiley.com/jpages/1615-9306 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/jssc.201400804 ↗
- Languages:
- English
- ISSNs:
- 1615-9306
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5063.880000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 4370.xml