Method development and validation for simultaneous determination of ebastine and its active metabolite carebastine in human plasma by liquid chromatography–tandem mass spectrometry and its application to a clinical pharmacokinetic study in healthy Chinese volunteers. (7th August 2020)
- Record Type:
- Journal Article
- Title:
- Method development and validation for simultaneous determination of ebastine and its active metabolite carebastine in human plasma by liquid chromatography–tandem mass spectrometry and its application to a clinical pharmacokinetic study in healthy Chinese volunteers. (7th August 2020)
- Main Title:
- Method development and validation for simultaneous determination of ebastine and its active metabolite carebastine in human plasma by liquid chromatography–tandem mass spectrometry and its application to a clinical pharmacokinetic study in healthy Chinese volunteers
- Authors:
- Phiri, Margaret
Li, Duo
Li, Tengfei
Ji, Shunli
Ling, Tang
Li, Xianjing
Gao, Huaye
Ding, Li
Shu, Chang - Abstract:
- Abstract: A simple LC–tandem mass spectrometry (MS/MS) method to determine ebastine and carebastine (active metabolite) in human plasma was developed and validated. Analytes and internal standards were precipitated by protein precipitation and separated on Synergi Hydro‐RP 80A column (4 μm, 50 mm × 2.0 mm; Phenomenex) by gradient elution with mobile phase A comprising 0.1% formic acid in 5 mm ammonium acetate (NH4 Ac) and B comprising 100% methanol at a flow rate 0.4 mL/min. Ions were detected in positive multiple reaction monitoring mode, and they exhibited linearity over concentration range 0.01–8.0 and 1.00–300 ng/mL for ebastine and carebastine, respectively. A clinical pharmacokinetic study was conducted in healthy Chinese volunteers under fasting and fed conditions after a single oral administration of 10 mg ebastine. The maximum plasma concentration ( C max ), time to C max ( T max ) and elimination half‐life for ebastine were 0.679 ± 0.762 ng/mL, 1.67 ± 1.43 h and 7.86 ± 6.18 h, respectively, whereas these for carebastine were 143 ± 68.4 ng/mL, 5.00 ± 2.00 h and 17.4 ± 4.97 h, respectively under fasting conditions; the corresponding values under fed conditions were 4.13 ± 2.53 ng/mL, 3.18 ± 1.09 h and 21.6 ± 7.77 h for ebastine and 176 ± 68.4 ng/mL, 6.14 ± 2.0 h and 20.0 ± 4.97 h for carebastine.
- Is Part Of:
- Biomedical chromatography. Volume 34:Number 10(2020)
- Journal:
- Biomedical chromatography
- Issue:
- Volume 34:Number 10(2020)
- Issue Display:
- Volume 34, Issue 10 (2020)
- Year:
- 2020
- Volume:
- 34
- Issue:
- 10
- Issue Sort Value:
- 2020-0034-0010-0000
- Page Start:
- n/a
- Page End:
- n/a
- Publication Date:
- 2020-08-07
- Subjects:
- carebastine -- ebastine -- LC–MS/MS -- metabolite -- pharmacokinetics
Chromatographic analysis -- Periodicals
Biology -- Periodicals
Medicine -- Periodicals
Biology -- Periodicals
Chromatography -- methods -- Periodicals
Medicine -- Periodicals
543.089 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
- DOI:
- 10.1002/bmc.4904 ↗
- Languages:
- English
- ISSNs:
- 0269-3879
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
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- British Library DSC - 2087.758000
British Library DSC - BLDSS-3PM
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