Development and validation of a UHPLC-MS/MS method to measure cefotaxime and metabolite desacetylcefotaxime in blood plasma: a pilot study suitable for capillary microsampling in critically ill children

• Published in: Analytical and bioanalytical chemistry Vol. 413; no. 17; pp. 4483 - 4491
• Main Authors: Guerra Valero, Yarmarly C., Dorofaeff, Tavey, Roberts, Jason A., Lipman, Jeffrey, Coulthard, Mark G., Sparkes, Louise, Wallis, Steven C., Parker, Suzanne L.
• Format: Journal Article
• Language: English
• Published: Berlin/Heidelberg Springer Berlin Heidelberg 01.07.2021; Springer; Springer Nature B.V
• Subjects: Acetic acid; Acetonitrile; Ammonium; Ammonium acetate; Analysis; Analytical Chemistry; Antibiotics; Biochemistry; Blood plasma; Cefotaxime; Characterization and Evaluation of Materials; Chemistry; Chemistry and Materials Science; Children; Composition; Deuteration; Dosage; Food Science; High performance liquid chromatography; Identification and classification; Ionization; Ions; Laboratory Medicine; Liquid chromatography; Mass spectrometry; Mass spectroscopy; Measurement; Metabolites; Methods; Monitoring/Environmental Analysis; Pharmacokinetics; Pharmacology; Research Paper; Australia; UHPLC-MS/MS; Cefotaxime; Desacetylcefotaxime; Capillary microsampling; Bioanalysis
• ISSN: 1618-2642; 1618-2650
• DOI: 10.1007/s00216-021-03411-7

Critical illness has been shown to affect the pharmacokinetics of antibiotics, which can lead to ineffective antibiotic exposure and the potential emergence of resistant bacteria. The lack of studies describing antibiotic pharmacokinetics in critically ill children has led to significant off-label dosing. This is, in part, due to the ethical and physiological challenges of removing frequent, large-volume samples from children. Capillary microsampling facilitates the collection of small volumes of blood samples to conduct clinical pharmacokinetic studies. A sensitive, rapid, and accurate ultra-high-performance liquid chromatography tandem mass spectrometry (UHPLC-MS/MS) bioanalytical method to measure cefotaxime and desacetylcefotaxime in 2.8 μL of plasma was developed and validated. Plasma samples were treated with acetonitrile and analytes were separated using a Kinetex C8 (100 × 2.1 mm) column. The chromatographic separation was established using a gradient method, with the mobile phases consisting of acetonitrile and ammonium acetate. An electrospray ionization source interface operated in a positive mode for the multiple reaction monitoring MS/MS analysis of cefotaxime, desacetylcefotaxime, and deuterated cefotaxime (internal standard). The bioanalytical method using microsample volumes met requirements for method validation for both analytes. Cefotaxime had precision within ± 7.3% and accuracy within ± 5% (concentration range of 0.5 to 500 mg/L). Desacetylcefotaxime had precision within ± 9.5% and accuracy within ± 3.5% (concentration range of 0.2 to 10 mg/L). The bioanalytical method was applied for the quantification of cefotaxime and its metabolite to 20 capillary microsamples collected at five time points in one dosing interval from five critically ill children. Graphical abstract