Simultaneous determination of colistin sulfate and tigecycline in human plasma by liquid chromatography-tandem mass spectrometry method

Abstract Objective To establish a high-performance liquid chromatography–tandem mass spectrometry method (HPLC–MS/MS) to simultaneously determine colistin sulfate and tigecycline in human plasma. Methods Polymyxin B1 internal standard (20 µL) was added into 200 µL of plasma sample. The samples were...

Full description

Bibliographic Details
Main Authors: Ying-Chao Ma, Xi-Kun Wu, Xiu-Ling Yang, Zhi-Qing Zhang
Format: Article
Language:English
Published: BMC 2024-01-01
Series:BMC Chemistry
Subjects:
Online Access:https://doi.org/10.1186/s13065-023-01109-8
_version_ 1797356020009271296
author Ying-Chao Ma
Xi-Kun Wu
Xiu-Ling Yang
Zhi-Qing Zhang
author_facet Ying-Chao Ma
Xi-Kun Wu
Xiu-Ling Yang
Zhi-Qing Zhang
author_sort Ying-Chao Ma
collection DOAJ
description Abstract Objective To establish a high-performance liquid chromatography–tandem mass spectrometry method (HPLC–MS/MS) to simultaneously determine colistin sulfate and tigecycline in human plasma. Methods Polymyxin B1 internal standard (20 µL) was added into 200 µL of plasma sample. The samples were treated with methanol-5% trichloroacetic acid (50:50, V/V) solution, and the protein precipitation method was adopted for post-injection analysis. The chromatographic column was a Dikma C18 (4.6 mm × 150 mm, 5 μm). For the mobile phase, 0.1% formic acid in aqueous solution was used for phase A, 0.1% formic acid in acetonitrile solution for phase B, and gradient elution was also applied. The flow rate was 0.8 mL/min, the column temperature was 40 °C, and the injection volume was 10 µL; Electrospray ionization and multiple reaction ion monitoring were adopted and scanned by the HPLC–MS/MS positive ion mode. Results The endogenous impurities in the plasma had no interference in the determination of the analytes. There existed a good linear relationship of colistin sulfate within the range of 0.1–10 µg/mL (R2 = 0.9986), with the lower limit of quantification (LLOQ) of 0.1 µg/mL. There existed a good linear relationship of tigecycline within the range of 0.05–5 µg/ mL (R2 = 0.9987), with the LLOQ of 0.05 µg/mL. The intra- and inter-day relative standard deviations of colistin sulfate and tigecycline were both less than 15%, and the accuracy was between 88.21% and 108.24%. The extraction had good stability, the extraction recovery rate was 87.75–91.22%, and the matrix effect was 99.40–105.26%. Conclusion This study successfully established a method for simultaneously detecting colistin sulfate and tigecycline plasma concentrations. The method was simple, rapid, and highly sensitive and could be applied for therapeutic medication monitoring.
first_indexed 2024-03-08T14:19:35Z
format Article
id doaj.art-d115f9c0f38e4c0fba16a5a921b93b81
institution Directory Open Access Journal
issn 2661-801X
language English
last_indexed 2024-03-08T14:19:35Z
publishDate 2024-01-01
publisher BMC
record_format Article
series BMC Chemistry
spelling doaj.art-d115f9c0f38e4c0fba16a5a921b93b812024-01-14T12:07:40ZengBMCBMC Chemistry2661-801X2024-01-0118111310.1186/s13065-023-01109-8Simultaneous determination of colistin sulfate and tigecycline in human plasma by liquid chromatography-tandem mass spectrometry methodYing-Chao Ma0Xi-Kun Wu1Xiu-Ling Yang2Zhi-Qing Zhang3Department of Pharmacy, Second Hospital of Hebei Medical UniversityDepartment of Pharmacy, Second Hospital of Hebei Medical UniversityDepartment of Pharmacy, Second Hospital of Hebei Medical UniversityDepartment of Pharmacy, Second Hospital of Hebei Medical UniversityAbstract Objective To establish a high-performance liquid chromatography–tandem mass spectrometry method (HPLC–MS/MS) to simultaneously determine colistin sulfate and tigecycline in human plasma. Methods Polymyxin B1 internal standard (20 µL) was added into 200 µL of plasma sample. The samples were treated with methanol-5% trichloroacetic acid (50:50, V/V) solution, and the protein precipitation method was adopted for post-injection analysis. The chromatographic column was a Dikma C18 (4.6 mm × 150 mm, 5 μm). For the mobile phase, 0.1% formic acid in aqueous solution was used for phase A, 0.1% formic acid in acetonitrile solution for phase B, and gradient elution was also applied. The flow rate was 0.8 mL/min, the column temperature was 40 °C, and the injection volume was 10 µL; Electrospray ionization and multiple reaction ion monitoring were adopted and scanned by the HPLC–MS/MS positive ion mode. Results The endogenous impurities in the plasma had no interference in the determination of the analytes. There existed a good linear relationship of colistin sulfate within the range of 0.1–10 µg/mL (R2 = 0.9986), with the lower limit of quantification (LLOQ) of 0.1 µg/mL. There existed a good linear relationship of tigecycline within the range of 0.05–5 µg/ mL (R2 = 0.9987), with the LLOQ of 0.05 µg/mL. The intra- and inter-day relative standard deviations of colistin sulfate and tigecycline were both less than 15%, and the accuracy was between 88.21% and 108.24%. The extraction had good stability, the extraction recovery rate was 87.75–91.22%, and the matrix effect was 99.40–105.26%. Conclusion This study successfully established a method for simultaneously detecting colistin sulfate and tigecycline plasma concentrations. The method was simple, rapid, and highly sensitive and could be applied for therapeutic medication monitoring.https://doi.org/10.1186/s13065-023-01109-8Colistin sulfateTigecyclineLiquid chromatography–tandem mass spectrometryPlasma drug concentrationTherapeutic medication monitoring
spellingShingle Ying-Chao Ma
Xi-Kun Wu
Xiu-Ling Yang
Zhi-Qing Zhang
Simultaneous determination of colistin sulfate and tigecycline in human plasma by liquid chromatography-tandem mass spectrometry method
BMC Chemistry
Colistin sulfate
Tigecycline
Liquid chromatography–tandem mass spectrometry
Plasma drug concentration
Therapeutic medication monitoring
title Simultaneous determination of colistin sulfate and tigecycline in human plasma by liquid chromatography-tandem mass spectrometry method
title_full Simultaneous determination of colistin sulfate and tigecycline in human plasma by liquid chromatography-tandem mass spectrometry method
title_fullStr Simultaneous determination of colistin sulfate and tigecycline in human plasma by liquid chromatography-tandem mass spectrometry method
title_full_unstemmed Simultaneous determination of colistin sulfate and tigecycline in human plasma by liquid chromatography-tandem mass spectrometry method
title_short Simultaneous determination of colistin sulfate and tigecycline in human plasma by liquid chromatography-tandem mass spectrometry method
title_sort simultaneous determination of colistin sulfate and tigecycline in human plasma by liquid chromatography tandem mass spectrometry method
topic Colistin sulfate
Tigecycline
Liquid chromatography–tandem mass spectrometry
Plasma drug concentration
Therapeutic medication monitoring
url https://doi.org/10.1186/s13065-023-01109-8
work_keys_str_mv AT yingchaoma simultaneousdeterminationofcolistinsulfateandtigecyclineinhumanplasmabyliquidchromatographytandemmassspectrometrymethod
AT xikunwu simultaneousdeterminationofcolistinsulfateandtigecyclineinhumanplasmabyliquidchromatographytandemmassspectrometrymethod
AT xiulingyang simultaneousdeterminationofcolistinsulfateandtigecyclineinhumanplasmabyliquidchromatographytandemmassspectrometrymethod
AT zhiqingzhang simultaneousdeterminationofcolistinsulfateandtigecyclineinhumanplasmabyliquidchromatographytandemmassspectrometrymethod