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  • Simple and accurate quantitative analysis of 20 anti-tuberculosis drugs in human plasma using liquid chromatography-electrospray ionization-tandem mass spectrometry.

Simple and accurate quantitative analysis of 20 anti-tuberculosis drugs in human plasma using liquid chromatography-electrospray ionization-tandem mass spectrometry.

Journal of pharmaceutical and biomedical analysis (2014-09-15)
Hyo-Ji Kim, Kyung-Ah Seo, Hyun-Mi Kim, Eun-Sook Jeong, Jong Lyul Ghim, Seung Heon Lee, Young Min Lee, Dong Hyun Kim, Jae-Gook Shin
ABSTRACT

A simple and accurate liquid chromatography (LC)-tandem mass spectrometry (MS/MS) method for the quantitation of 20 anti-tuberculosis (anti-TB) drugs in human plasma, was developed as a tool for therapeutic drug monitoring. Two protein precipitation methods were adopted; one using methanol containing 0.13N HCl, for precipitation of amikacin, kanamycin, streptomycin and pyrazinamide, and the other using acetonitrile, for precipitation of preamoxicillin, ciprofloxacin, clarithromycin, clofazimine, cycloserine, ethambutol, ethionamide, isoniazid, levofloxacin, linezolid, moxifloxacin, p-aminosalicylic acid (PAS), prothionamide, rifabutin, rifampin and roxithromycin. Separation was performed either on an HILIC silica column or a reversed-phase dC18 column, with a gradient elution. Detection was carried out in multiple reaction-monitoring (MRM) mode. The calibration curves were linear over a 50-fold concentration range, with correlation coefficients (r) greater than 0.9969 for all anti-TB drugs. The intra- and inter-day precision was less than 14.3%, and the accuracy ranged between 84.8 and 113.0%. The developed method was successfully applied to the identification and quantitation of anti-TB drugs in patients with multi-drug resistant TB.

MATERIALS
Product Number
Brand
Product Description

Rifampicin, European Pharmacopoeia (EP) Reference Standard
Isoniazid, European Pharmacopoeia (EP) Reference Standard
Supelco
Levofloxacin, analytical standard
Amikacin for system suitability, European Pharmacopoeia (EP) Reference Standard
Ethambutol for system suitability, European Pharmacopoeia (EP) Reference Standard
USP
Amikacin sulfate, United States Pharmacopeia (USP) Reference Standard
USP
Methyl alcohol, United States Pharmacopeia (USP) Reference Standard
Ciprofloxacin, European Pharmacopoeia (EP) Reference Standard
Amikacin sulfate, European Pharmacopoeia (EP) Reference Standard
Ethionamide for system suitability, European Pharmacopoeia (EP) Reference Standard
Supelco
Methanol solution, contains 0.10 % (v/v) formic acid, UHPLC, suitable for mass spectrometry (MS), ≥99.5%
Sigma-Aldrich
4-Aminosalicylic acid, 99%
Sigma-Aldrich
Formic acid, ≥95%, FCC, FG
Supelco
Acetonitrile, HPLC grade, ≥99.93%
Sigma-Aldrich
Methanol-12C, 99.95 atom % 12C
Sigma-Aldrich
Acetonitrile
Sigma-Aldrich
Acetonitrile, SAJ first grade, ≥99.0%
Sigma-Aldrich
Ciprofloxacin, ≥98% (HPLC)
Sigma-Aldrich
Formic acid, JIS special grade, ≥98.0%
Sigma-Aldrich
Acetonitrile, JIS special grade, ≥99.5%
Sigma-Aldrich
Acetonitrile, ≥99.8%, suitable for HPLC
Sigma-Aldrich
Levofloxacin, 98.0-102.0% anhydrous basis (HPLC)
Sigma-Aldrich
Acetonitrile, ≥99.5%, ACS reagent
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Amikacin disulfate salt, potency: 674-786 μg per mg (as amikacin base)
Supelco
Isoniazid, analytical standard, ≥99% (TLC)
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D-Cycloserine
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Amoxicillin, 95.0-102.0% anhydrous basis
Sigma-Aldrich
D-Cycloserine, synthetic
Sigma-Aldrich
Formic acid solution, BioUltra, 1.0 M in H2O
Supelco
Streptomycin solution, ~1 mg/mL in 1 mM EDTA, analytical standard