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Validation of a HPLC method for quantification of midazolam in rat plasma: Application during a Maytenus ilicifolia –drug interaction study
Author(s) -
Nascimento Sara Batista,
Lima Nascimento Mariana,
DuarteAlmeida Joaquim Maurício,
Oliveira Flávio Martins,
Carmo Vieira Maria,
Siqueira João Máximo,
Andrade Frank Pereira,
Costa César Isabela,
Castro Whocely Victor
Publication year - 2021
Publication title -
biomedical chromatography
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.4
H-Index - 65
eISSN - 1099-0801
pISSN - 0269-3879
DOI - 10.1002/bmc.4999
Subject(s) - chemistry , chromatography , high performance liquid chromatography , methanol , solvent , analyte , pharmacokinetics , midazolam , elution , acetonitrile , pharmacology , biochemistry , organic chemistry , medicine , sedation
Abstract Midazolam (MDZ) is routinely employed as a marker compound of cytochrome P450 3A (CYP3A) activity. Despite the many HPLC–UV methods described to quantify MDZ in plasma, all of them use acetonitrile (ACN) or a mixture of methanol–isopropanol as organic solvent of the mobile phase. Since the ACN shortage in 2008, efforts have been made to replace this solvent during HPLC analysis. A simple, sensitive, accurate and repeatable HPLC–UV method (220 nm) was developed and validated to quantify MDZ in rat plasma using methanol instead. The method was applied during a herb–drug interaction study involving Maytenus ilicifolia , a Brazilian folk medicine used to treat gastric disorders. Plasma samples were alkalinized and MDZ plus alprazolam (internal standard) were extracted with diethyl ether. After solvent removal, the residue was reconstituted with methanol–water (1:1). The analyte was eluted throughout a C 18 column using sodium acetate buffer (10 m m , pH 7.4)–methanol (40:60, v/v). The precision at the lower limit of quantification never exceeded 19.40%, and 13.86% at the higher levels of quality control standards, whereas the accuracy ranged from −19.81 to 14.33%. The analytical curve was linear from 50 to 2,000 ng/ml. The activity of the hepatic CYP3A enzymes was not affected by the extract.