Development and Validation of UPLC Tandem Mass Spectrometry Assay for Ceftibuten and Sulbactam in Human Plasma

Author:

Valero-Rivera Karla Paulina12,Magaña-Aquino Martin3,del Carmen Romero-Méndez María12,Morales-Barragán Miriam Nayeli12,Sagahón-Azúa Julia12,Medellín-Garibay Susanna Edith12,del Carmen Milán-Segovia Rosa12,Martínez-Gutiérrez Fidel12,Romano-Moreno Silvia12ORCID

Affiliation:

1. Department of Pharmacy , Faculty of Chemical Sciences, , #6 Ave. Manuel Nava, C.P. 78210, San Luis Potosi , Mexico

2. Autonomous University of San Luis Potosi , Faculty of Chemical Sciences, , #6 Ave. Manuel Nava, C.P. 78210, San Luis Potosi , Mexico

3. Central Hospital “Dr. Ignacio Morones Prieto” , #2395 Ave. Venustiano Carranza, C.P. 78290, San Luis Potosi , Mexico

Abstract

Abstract A sensitive and rapid ultra-performance liquid chromatography coupled with -tandem mass spectrometry (UPLC-MS/MS) method was developed and validated to determine ceftibuten (CTB) and sulbactam (SUL) in human plasma. An ACQUITY UPLC HSS T3 C18 (2.1 × 100 mm), 1.8 μm column with gradient elution of water (0.1% formic acid) and acetonitrile was used for separation at a flow rate of 0.2 mL/min. This method involves a simple sample preparation with acetonitrile. The calibration curves of CTB and SUL in plasma showed good linearity over the concentration range of 0.50–25 μg/mL and with a correlation coefficient (r2) >0.99. This method was validated in terms of selectivity, linearity, precision, accuracy and stability. High precision was obtained with coefficients of variation <15%. Excellent recovery in the range of 90–104% was achieved for CTB and SUL was 86–110%. The method has the potential utility to support pharmacometric modeling in clinical practice and biopharmaceutic studies.

Funder

Consejo Nacional de Humanidades, Ciencias y Tecnologías

Publisher

Oxford University Press (OUP)

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