Volume 11 Issue 6
Dec.  2021
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Huiya Yuan, Shihui Yu, Guihong Chai, Junting Liu, Qi (Tony) Zhou. An LC-MS/MS method for simultaneous analysis of the cystic fibrosis therapeutic drugs colistin, ivacaftor and ciprofloxacin[J]. Journal of Pharmaceutical Analysis, 2021, 11(6): 732-738. doi: 10.1016/j.jpha.2021.02.004
Citation: Huiya Yuan, Shihui Yu, Guihong Chai, Junting Liu, Qi (Tony) Zhou. An LC-MS/MS method for simultaneous analysis of the cystic fibrosis therapeutic drugs colistin, ivacaftor and ciprofloxacin[J]. Journal of Pharmaceutical Analysis, 2021, 11(6): 732-738. doi: 10.1016/j.jpha.2021.02.004

An LC-MS/MS method for simultaneous analysis of the cystic fibrosis therapeutic drugs colistin, ivacaftor and ciprofloxacin

doi: 10.1016/j.jpha.2021.02.004
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Research reported in this publication was supported by the National Institute of Health's National Institute of Allergy and Infectious Diseases under Award Nos. R01AI146160 and R01AI132681. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institute of Health.

  • Received Date: Jun. 01, 2020
  • Accepted Date: Feb. 22, 2021
  • Rev Recd Date: Jan. 25, 2021
  • Available Online: Jan. 12, 2022
  • Publish Date: Dec. 15, 2021
  • Inhaled antibiotics such as colistin and ciprofloxacin are increasingly used to treat bacterial lung infections in cystic fibrosis patients. In this study, we established and validated a new HPLC-MS/MS method that could simultaneously detect drug concentrations of ciprofloxacin, colistin and ivacaftor in rat plasma, human epithelial cell lysate, cell culture medium, and drug transport media. An aliquot of 200 μL drug-containing rat plasma or cell culture medium was treated with 600 μL of extraction solution (acetonitrile containing 0.1% formic acid and 0.2% trifluoroacetic acid (TFA)). The addition of 0.2% TFA helped to break the drug-protein bonds. Moreover, the addition of 0.1% formic acid to the transport medium and cell lysate samples could significantly improve the response and reproducibility. After vortexing and centrifuging, the sample components were analyzed by HPLC-MS/MS. The multiple reaction monitoring mode was used to detect the following transitions: 585.5–101.1 (colistin A), 578.5–101.1 (colistin B), 393.2–337.2 (ivacaftor), 332.2–314.2 (ciprofloxacin), 602.3–101.1 (polymyxin B1 as internal standard (IS)) and 595.4–101.1 (polymyxin B2 as IS). The running time of a single sample was only 6 min, making this a time-efficient method. Linear correlations were found for colistin A at 0.029–5.82 μg/mL, colistin B at 0.016–3.14 μg/mL, ivacaftor at 0.05–10.0 μg/mL, and ciprofloxacin at 0.043–8.58 μg/mL. Accuracy, precision, and stability of the method were within the acceptable range. This method would be highly useful for research on cytotoxicity, animal pharmacokinetics, and in vitro drug delivery.
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