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Article: Determination of trimetazidine in human plasma by high performance liquid chromatography-mass spectrometry

TitleDetermination of trimetazidine in human plasma by high performance liquid chromatography-mass spectrometry
Authors
KeywordsHigh performance liquid chromatography/mass spectrometry
Pharmacokinetics
Plasma
Trimetazidine
Issue Date2007
Citation
Fenxi Huaxue/ Chinese Journal of Analytical Chemistry, 2007, v. 35, n. 4, p. 541-544 How to Cite?
AbstractA sensitive and specific high performance liquid chromatography/ electrospray ionization-mass spectrometry (HPLC/ESI-MS) method has been developed and validated for the identification and quantification of trimetazidine (TMZ) in human plasma. The TMZ and internal standard, lidocaine, were isolated from plasma by protein precipitation with methanol. The acidified supernatant was dried in a rotational-vacuum-concentrator, and the residue was dissolved with mobile phase prior to analysis. Chromatographic separation was performed on a Xterra MS C18column (150 mm ×4.6 mm, with 5 μm particle size) with the mobile phase consisting of methanol and water (pH-2.0 adjusted with trifluoroacetic acid) (40:60, V/V), and the flow rate was 0.6 mL/min. Detection was performed on a single quadrupole mass spectrometer with selected ion monitoring (SIM) mode via electrospray ionization (ESI) source. The method was linear over the concentration range of 2.5-100 |Xg/L for TMZ. The intra- and inter-day precisions were less than 7%, relative recovery ranged from 96.45% to 103. 03% and the exaction recovery was between 72.45% and 80.47%. The presented work offers a relatively simple and sensitive methodology within short turn-around time, which has also been successfully applied to a clinical pharmacoki-netic study.
Persistent Identifierhttp://hdl.handle.net/10722/342230
ISSN
2021 Impact Factor: 1.193
2019 SCImago Journal Rankings: 0.569

 

DC FieldValueLanguage
dc.contributor.authorJiao, Yang-
dc.contributor.authorSu, Ming Ming-
dc.contributor.authorChen, Min Jun-
dc.contributor.authorJia, Wei-
dc.contributor.authorTao, Ping-
dc.contributor.authorQiu, Yi Qun-
dc.contributor.authorHuang, Zhong Yi-
dc.date.accessioned2024-04-17T07:02:12Z-
dc.date.available2024-04-17T07:02:12Z-
dc.date.issued2007-
dc.identifier.citationFenxi Huaxue/ Chinese Journal of Analytical Chemistry, 2007, v. 35, n. 4, p. 541-544-
dc.identifier.issn0253-3820-
dc.identifier.urihttp://hdl.handle.net/10722/342230-
dc.description.abstractA sensitive and specific high performance liquid chromatography/ electrospray ionization-mass spectrometry (HPLC/ESI-MS) method has been developed and validated for the identification and quantification of trimetazidine (TMZ) in human plasma. The TMZ and internal standard, lidocaine, were isolated from plasma by protein precipitation with methanol. The acidified supernatant was dried in a rotational-vacuum-concentrator, and the residue was dissolved with mobile phase prior to analysis. Chromatographic separation was performed on a Xterra MS C18column (150 mm ×4.6 mm, with 5 μm particle size) with the mobile phase consisting of methanol and water (pH-2.0 adjusted with trifluoroacetic acid) (40:60, V/V), and the flow rate was 0.6 mL/min. Detection was performed on a single quadrupole mass spectrometer with selected ion monitoring (SIM) mode via electrospray ionization (ESI) source. The method was linear over the concentration range of 2.5-100 |Xg/L for TMZ. The intra- and inter-day precisions were less than 7%, relative recovery ranged from 96.45% to 103. 03% and the exaction recovery was between 72.45% and 80.47%. The presented work offers a relatively simple and sensitive methodology within short turn-around time, which has also been successfully applied to a clinical pharmacoki-netic study.-
dc.languageeng-
dc.relation.ispartofFenxi Huaxue/ Chinese Journal of Analytical Chemistry-
dc.subjectHigh performance liquid chromatography/mass spectrometry-
dc.subjectPharmacokinetics-
dc.subjectPlasma-
dc.subjectTrimetazidine-
dc.titleDetermination of trimetazidine in human plasma by high performance liquid chromatography-mass spectrometry-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.scopuseid_2-s2.0-46749113113-
dc.identifier.volume35-
dc.identifier.issue4-
dc.identifier.spage541-
dc.identifier.epage544-
dc.identifier.eissn1872-2040-

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