Development and validation of an ultra-performance liquid chromatography method for simultaneous analysis of 20 antihistaminics in dietary supplements-Reference-Cited by-同舟云学术

Development and validation of an ultra-performance liquid chromatography method for simultaneous analysis of 20 antihistaminics in dietary supplements

Published:2014-07-31 Issue:3 Volume:29 Page:465-474
ISSN:0269-3879
Container-title:Biomedical Chromatography
language:en
Short-container-title:Biomed. Chromatogr.

Author:

Kim Jung Yeon¹,Do Jung-Ah¹^ORCID,Choi Ji Yeon¹,Cho Sooyeul¹,Kim Woo-Seong¹,Yoon Chang-Yong¹

Affiliation:

1. Advanced Analysis Team, National Institute of Food and Drug Safety Evaluation, Ministry of Food and Drug Safety, Osong Health Technology Administration Complex; 187 Osongsaengmyeong2-ro, Osongeup Cheongwon-gun Chungcheongbuk-do 363-700 Republic of Korea

Funder

Ministry of Food and Drug Safety

Publisher

Wiley

Subject

Clinical Biochemistry,Drug Discovery,Pharmacology,Molecular Biology,General Medicine,Biochemistry,Analytical Chemistry

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4. Simultaneous screeming and quantitiation of 18 antihistamine drugs in blood by liquid chromatography ionspray tandem mass spectrometry;Gergov;Forensic Science International,2001

5. Simultaneous determination of ten antihistamine drugs in human plasma using pipette tip solid-phase extraction and gas chromatography/mass spectrometry;Hasegawa;Rapid Communications in Mass Spectrometry,2006

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