4.6 Article

Development of ELISA formats for polymyxin B monitoring in serum of critically ill patients

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ELSEVIER
DOI: 10.1016/j.jpba.2021.114275

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Polymyxin B; Colistin; Enzyme-linked immunosorbent assay; Drug monitoring

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Treating infections in critically ill patients often requires the use of last-line antibacterial drugs such as polymyxins. In critically ill patients, drug pharmacokinetics change significantly, affecting antibiotic concentrations and necessitating individual dosage adjustment to avoid therapeutic failures or toxic manifestations.
Treating infections in critically ill patients often requires the use of last-line antibacterial drugs such as polymyxins with a narrow therapeutic window and high toxicity. In critically ill patients, the drug pharmacokinetics changes significantly, and as a result, the antibiotic concentrations in blood and infection foci become suboptimal, which leads to therapeutic failures or toxic manifestations. For timely dosage adjustments, a competitive ELISA-based method using antibodies to polymyxin B (PMB) was developed. Among the several considered assays, a direct antibody-coated format was selected for its short duration (1.5 h) and the best agreement with the LC-MS/MS data (R-2 = 98 %). The assay dynamic measurement range (IC20-IC80) could be substantially shifted by changing the ratio of immunoreagents. To conveniently measure the therapeutic range of PMB concentrations, it was adjusted to 5.0-192 ng/mL, allowing the samples to be analyzed after a simple 100-fold dilution with the assay buffer. The ELISA sensitivity expressed in half-inhibition concentration (IC50) and the limit of detection were 30.6 and 1.8 ng/mL, respectively. The assay cross-reactivity towards the related analogue colistin (COL) was 95 %, and this compound could also be adequately quantified by the same assay. The PMB and COL recovery from the spiked serum samples was similar and constituted 98-109 %. The trial drug monitoring was carried out in 3 patients with Gram-negative sepsis, and the established pharmacokinetic profiles of PMB revealed the necessity for individual dosage adjustment. (C) 2021 Elsevier B.V. All rights reserved.

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