Development and validation of a high-performance liquid chromatography method for determination of lisinopril in human plasma by magnetic solid-phase extraction and pre-column derivatization-Reference-Cited by-同舟云学术

Development and validation of a high-performance liquid chromatography method for determination of lisinopril in human plasma by magnetic solid-phase extraction and pre-column derivatization

Published:2017-11-16 Issue:3 Volume:32 Page:e4120
ISSN:0269-3879
Container-title:Biomedical Chromatography
language:en
Short-container-title:Biomedical Chromatography

Author:

Rastkari Noushin¹^ORCID,Ahmadkhaniha Reza²^ORCID

Affiliation:

1. Center for Air Pollution Research, Institute for Environmental Research; Tehran University of Medical Sciences; Tehran Iran

2. Department of Human Ecology, School of Public Health; Tehran University of Medical Sciences; Tehran Iran

Funder

Tehran University of Medical Sciences and Health Services

Publisher

Wiley

Subject

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

Reference44 articles.

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2. Development and validation of RP-HPLC method for the estimation of lisinopril in tablet dosage form;Chander;Analytical Chemistry Letters,2012

3. Adsorption of organic compounds onto multiwall and nitrogen-doped carbon nanotubes: Insights into the adsorption mechanisms;Díaz-Flores;Water, Air, & Soil Pollution,2017

4. Determination of Lisinopril in dosage forms and spiked human plasma through derivatization with 7-chloro-4-nitrobenzo-2-oxa-1,3-diazole (NBD-cl) followed by spectrophotometry or HPLC with fluorimetric detection;El-Emam;Journal of Pharmaceutical and Biomedical Analysis,2004

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4. Determination of Lisinopril in Pure and Tablet form by Using 2-Hydroxynaphthaldehyde as Derivatizing Reagent;Pakistan Journal of Analytical & Environmental Chemistry;2021-06-23

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