Rapid method for the quantitation of mivacurium isomers in human and dog plasma by using liquid chromatography with fluorescence detection: Application to pharmacokinetic studies

A simple, selective and specific liquid chromatography method was used to simultaneously determine the cis-cis, cis-trans and trans-trans isomers of mivacurium in human and dog plasma. Solid phase extraction was used to separate interfering endogenous products from the compounds of interest. Fluorom...

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Published in:Journal of Pharmaceutical and Biomedical Analysis 1996-04, Vol.14 (6), p.675-683
Main Authors: Lugo, Sonia I., Eddington, Natalie D.
Format: Article
Language:English
Subjects:
Adult
Animals
Biological and medical sciences
Chromatography, High Pressure Liquid
Dogs
Female
Humans
Indicators and Reagents
Isoquinolines - blood
Isoquinolines - chemistry
Isoquinolines - pharmacokinetics
Medical sciences
Mivacurium
Muscle
Neuromuscular blockade
Neuromuscular Nondepolarizing Agents - blood
Neuromuscular Nondepolarizing Agents - chemistry
Neuromuscular Nondepolarizing Agents - pharmacokinetics
Pharmacokinetics
Pharmacology. Drug treatments
Reference Standards
Spectrometry, Fluorescence
Stereoisomerism
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cited_by cdi_FETCH-LOGICAL-c386t-9ebc232e31dc624d81af31a072464249320ee85aa9583066157545a2f54f003f3
cites cdi_FETCH-LOGICAL-c386t-9ebc232e31dc624d81af31a072464249320ee85aa9583066157545a2f54f003f3
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container_title Journal of Pharmaceutical and Biomedical Analysis
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creator Lugo, Sonia I.
Eddington, Natalie D.
description A simple, selective and specific liquid chromatography method was used to simultaneously determine the cis-cis, cis-trans and trans-trans isomers of mivacurium in human and dog plasma. Solid phase extraction was used to separate interfering endogenous products from the compounds of interest. Fluorometric detection was evaluated at excitation and emission maxima of 280 and 325 nm. The calibration curves were found to be linear in the range 50–500 ng ml −1. The method was applied to plasma samples collected from a human and dog study and was found to be satisfactory. Excellent recovery, linearity, accuracy and precision were achieved by the assay for each isomer.
doi_str_mv 10.1016/0731-7085(95)01684-8
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Solid phase extraction was used to separate interfering endogenous products from the compounds of interest. Fluorometric detection was evaluated at excitation and emission maxima of 280 and 325 nm. The calibration curves were found to be linear in the range 50–500 ng ml −1. The method was applied to plasma samples collected from a human and dog study and was found to be satisfactory. Excellent recovery, linearity, accuracy and precision were achieved by the assay for each isomer.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><pmid>8807542</pmid><doi>10.1016/0731-7085(95)01684-8</doi><tpages>9</tpages></addata></record>
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identifier ISSN: 0731-7085
ispartof Journal of Pharmaceutical and Biomedical Analysis, 1996-04, Vol.14 (6), p.675-683
issn 0731-7085
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source ScienceDirect Freedom Collection
subjects Adult
Animals
Biological and medical sciences
Chromatography, High Pressure Liquid
Dogs
Female
Humans
Indicators and Reagents
Isoquinolines - blood
Isoquinolines - chemistry
Isoquinolines - pharmacokinetics
Medical sciences
Mivacurium
Muscle
Neuromuscular blockade
Neuromuscular Nondepolarizing Agents - blood
Neuromuscular Nondepolarizing Agents - chemistry
Neuromuscular Nondepolarizing Agents - pharmacokinetics
Pharmacokinetics
Pharmacology. Drug treatments
Reference Standards
Spectrometry, Fluorescence
Stereoisomerism
title Rapid method for the quantitation of mivacurium isomers in human and dog plasma by using liquid chromatography with fluorescence detection: Application to pharmacokinetic studies
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