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High-performance liquid chromatographic determination of tazobactam and piperacillin in human plasma and urine
Institution:1. Department of Obstetrics and Gynecology, University Hospital Innsbruck, Innsbruck;2. Department of Obstetrics and Gynecology, University Hospital Salzburg, Salzburg;3. Department of Obstetrics and Gynecology, Barmherzige Schwestern Linz, Linz;4. Department of Obstetrics and Gynecology, Hospital Bregenz, Bregenz;5. Department of Obstetrics and Gynecology, Wilhelminenspital, Vienna;6. Department of Obstetrics and Gynecology, University Hospital Vienna, Vienna;7. Department of Obstetrics and Gynecology, Eisenstadt General Hospital, Eisenstadt;8. Division of Biological Chemistry, Biocenter, Medical University, Innsbruck, Austria;1. Department of Pharmacy, Banner – University Medical Center Phoenix, Phoenix, AZ, United States;2. Department of Pharmacy, Rush University Medical Center, Chicago, IL, United States;1. Anesthesiology and Critical Care Department, CHU Bordeaux, 33000 Bordeaux, France;2. Pharmacy and Clinical Pharmacy Department, CHU Bordeaux, 33000 Bordeaux, France;3. Pharmacokinetics and PK/PD Group INSERM 1034, Univ. Bordeaux, 33000 Bordeaux, France;4. Univ. Bordeaux Segalen, 33000 Bordeaux, France;1. Faculty of Medicine and Health Sciences, Ghent University, Ghent, Belgium;2. Department of Intensive Care Medicine, Ghent University Hospital, Ghent, Belgium;3. Department of Clinical Chemistry, Microbiology and Immunology, Ghent University Hospital, Ghent, Belgium;1. Anesthesiology and Critical Care Department I, CHU Pellegrin, 33000 Bordeaux, France;2. Anesthesiology and Critical Care Department II, CHU Magellan, 33600 Pessac, France;3. Medical Intensive Care Unit, CHU Pellegrin, 33000 Bordeaux, France;4. Biostatistics Unit, Délégation Recherche Clinique & Innovation, CHU de Clermont-Ferrand, Clermont-Ferrand, France;5. Univ. Bordeaux Segalen, 33000 Bordeaux, France
Abstract:A high-performance liquid chromatographic (HPLC) method with ultraviolet (UV) absorbance was developed for the analysis of piperacillin-tazobactam (tazocillin), in plasma and urine. The detection was performed at 218 nm for tazobactam and 222 nm for piperacillin. The procedure for assay of these two compounds in plasma and of piperacillin in urine involves the addition of an internal standard (ceftazidime for tazobactam and benzylpenicillin for piperacillin) followed by a treatment of the samples with acetonitrile and chloroform. To quantify tazobactam in urine, diluted samples were analysed using a column-switching technique without internal standard. The HPLC column, LiChrosorb RP-select B, was equilibrated with an eluent mixture composed of acetonitrile-ammonium acetate (pH 5). The proposed technique is reproducible, selective, and reliable. The method has been validated, and stability tests under various conditions have been performed. Linear detector responses were observed for the calibration curve standards in the ranges 5–60 μg/ml for tazobactam, and 1–100 μg/ml for piperacillin and spans what is currently though to be the clinically relevant range for tazocillin concentrations in body fluids. The limit of quantification was 3 μg/ml for tazobactam and 0.5 μg/ml for piperacillin in plasma and urine. Extraction recoveries from plasma proved to be more than 85%. Precision, expressed as C.V., was in the range 0.4–18%.
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