Quantitative determination of isoniazid in biological samples by cation-selective exhaustive injection-sweeping-micellar electrokinetic chromatography
Journal
Analytical and Bioanalytical Chemistry
Journal Volume
401
Journal Issue
7
Pages
2205-2214
Date Issued
2011
Author(s)
Abstract
Tuberculosis (TB), an infectious disease caused by Mycobacterium tuberculosis, infects approximately one third of the current world population. Isoniazid is one of the most frequently used first-line anti-TB drugs. In this study, we developed a sensitive cation-selective exhaustive injection-sweeping- micellar electrokinetic chromatography method (CSEI-Sweep-MEKC) for analyzing isoniazid in human plasma. Parameters including acetonitrile (ACN) percentage in the separation buffer; the injection time, and concentration of the high-conductivity buffer; sodium dodecyl sulfate (SDS) concentration; phosphate concentration in the sample matrix; and the sample injection time were all optimized to obtain the best analytical performance. The optimal background electrolyte comprised 50 mM phosphate buffer, 100 mM SDS, and 15% ACN. Non-micelle background electrolyte, containing 75 mM phosphate buffer and 15% ACN, was first injected into the capillary, followed by a short plug of 200 mM phosphate (high-conductivity buffer). Run-to-run repeatability (n?=?3) and intermediate precision (n?=?3) of peak area ratios were found to be lower than 8.7% and 11.4% RSD, respectively. The accuracy of the method was within 98.1-106.9%. The limit of detection of isoniazod in human plasma was 9 ng mL -1. Compared with conventional MEKC, the enhancement factor of the CSEI-Sweep-MEKC method was 85 in plasma samples. The developed method was successfully used to determine isoniazid concentration in patient plasma. The results demonstrated that CSEI-Sweep-MEKC has the potential to analyze isoniazid in human plasma for therapeutic drug monitoring and clinical research. ? 2011 Springer-Verlag.
SDGs
Other Subjects
Analytical performance; Back ground electrolyte; Biological samples; Cation-selective exhaustive injection; Clinical research; Electrokinetic chromatography; Enhancement factor; Human plasmas; Infectious disease; Injection time; Isoniazid; Limit of detection; Micellar electrokinetic chromatography; Mycobacterium tuberculosis; Peak area ratios; Phosphate buffers; Phosphate concentration; Plasma samples; Quantitative determinations; Run to run; Sample injection; Sample matrix; Separation buffers; Sodium dodecyl sulfate; Sweeping; Therapeutic drug monitoring; World population; Acetonitrile; Concentration (process); Electrodynamics; Electrolytes; Liquid chromatography; Optimization; Patient monitoring; Plasma (human); Plasmas; Positive ions; Sodium sulfate; Hydrazine; acetonitrile; acetonitrile derivative; buffer; cation; dodecyl sulfate sodium; isoniazid; tuberculostatic agent; article; chemistry; human; metabolism; micellar electrokinetic chromatography; micelle; Acetonitriles; Antitubercular Agents; Buffers; Cations; Chromatography, Micellar Electrokinetic Capillary; Humans; Isoniazid; Micelles; Sodium Dodecyl Sulfate; Mycobacterium tuberculosis
Type
journal article