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Simple and robust LC-MS/MS method for quantification of colistin methanesulfonate and colistin in human plasma for therapeutic drug monitoring.
Kim, Kwang-Youl; Kim, Bo-Hyung; Kwack, Won Gun; Kwon, Hyun-Jung; Cho, Sang-Heon; Kim, Cheol-Woo.
Afiliación
  • Kim KY; Department of Clinical Pharmacology, Inha University Hospital, Inha University School of Medicine, Incheon, the Republic of Korea.
  • Kim BH; Department of Clinical Pharmacology and Therapeutics, Kyung Hee University Hospital, Seoul, the Republic of Korea; East-West Medical Research Institute, Kyung Hee University, Seoul, the Republic of Korea.
  • Kwack WG; Department of Internal Medicine, Kyung Hee University Hospital, Seoul, the Republic of Korea.
  • Kwon HJ; Department of Clinical Pharmacology, Inha University Hospital, Inha University School of Medicine, Incheon, the Republic of Korea.
  • Cho SH; Department of Clinical Pharmacology, Inha University Hospital, Inha University School of Medicine, Incheon, the Republic of Korea.
  • Kim CW; Department of Clinical Pharmacology, Inha University Hospital, Inha University School of Medicine, Incheon, the Republic of Korea; Department of Internal Medicine, Inha University Hospital, Inha University School of Medicine, Incheon, the Republic of Korea. Electronic address: cwkim1805@inha.ac.kr.
J Pharm Biomed Anal ; 236: 115734, 2023 Nov 30.
Article en En | MEDLINE | ID: mdl-37776629
A rapid, simple, and robust LC-MS/MS method was developed and validated for the quantitation of colistin and colistin methanesulfonate (CMS) in human plasma. The method also prevented overestimation of colistin concentration by establishing the stability of CMS under sample preparation conditions, including blood and plasma storage conditions. Polymyxin B1 was used as an internal standard, and positive-ion electrospray ionization in multiple reaction monitoring mode was used for quantification. Chromatographic separation was achieved using a Zorbax eclipse C18 column (3.5 µm, 2.1 mm i.d. × 100 mm), with a flow rate of 0.5 mL/min, 5 µL injection volume, and gradient elution with a mixture of acetonitrile-water (containing 0.1 % trifluoroacetic acid). The method had a quantifiable range of 0.043-8.61 and 0.057-11.39 µg/mL for colistin A and B in human plasma, respectively, under a total runtime of 6.0 min. Further, it demonstrated appropriate extraction efficiency, no significant interference from co-eluting endogenous compounds, and satisfactory intraday and interday precision and accuracy. The proposed procedure for sample preparation successfully addressed the issue of CMS instability, consequently diminishing the probability of overestimating the concentration of colistin. Therefore, this simple and robust LC-MS/MS method for CMS and colistin quantification in human plasma is a valuable tool for clinicians to accurately monitor colistin treatment in patients with infections caused by multidrug-resistant (MDR) Gram-negative bacteria.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: J Pharm Biomed Anal Año: 2023 Tipo del documento: Article Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: J Pharm Biomed Anal Año: 2023 Tipo del documento: Article Pais de publicación: Reino Unido