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A UHPLC–MS/MS method for the simultaneous determination of piperacillin and tazobactam in plasma (total and unbound), urine and renal replacement therapy effluent

机译:UHPLC-MS / MS方法同时测定血浆(全部和未结合),尿液和肾脏替代治疗废水中的哌拉西林和他唑巴坦

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摘要

Piperacillin-tazobactam is a beta-lactam/beta-lactamase combination antibiotic used in patients with moderate to severe infection. Dosing of piperacillin-tazobactam requires an understanding of this patient group to maximise the effectiveness of this antibiotic and limit a further emergence of resistant pathogens. This is the first method that measures piperacillin and tazobactam simultaneously, across this range of clinically-relevant biological matrices. The calibration line was linear across the concentration range of 0.5–500 μg/mL for piperacillin and 0.625–62.5 μg/mL for tazobactam. All validation testing for matrix effects, precision and accuracy, specificity and stability were within 15%. A calibration equivalence study was performed to investigate the suitability of applying calibration curves prepared in an alternative matrix, with a mean bias of −10.8% identified for the application of a calibration line prepared for tazobactam in plasma only. Bias for all other calibration lines prepared in alternate matrices was within the 5% acceptance criteria. The method was successfully applied to a pharmacokinetic study of a critically ill patient receiving renal replacement therapy, with the results included.
机译:哌拉西林-他唑巴坦是一种β-内酰胺/β-内酰胺酶联合抗生素,用于中度至重度感染患者。哌拉西林-他唑巴坦的剂量需要对该患者组有一个了解,以使这种抗生素的效力最大化并限制耐药病原体的进一步出现。这是在该临床相关的生物基质范围内同时测量哌拉西林和他唑巴坦的第一种方法。哌拉西林的浓度范围为0.5–500μg/ mL,他唑巴坦的浓度范围为0.625–62.5μg/ mL,校准线呈线性。所有关于基质效应,精度和准确性,特异性和稳定性的验证测试均在15%以内。进行了一项校准当量研究,以研究使用在另一种基质中制备的校准曲线的适用性,对于仅将他唑巴坦制备的校准线应用于血浆中,其平均偏差为-10.8%。在备用矩阵中准备的所有其他校准线的偏差均在5%接受标准之内。该方法已成功应用于接受肾脏替代疗法的重症患者的药代动力学研究,其结果包括在内。

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