Development and Validation of UPLC Tandem Mass Spectrometry Assay for Ceftibuten and Sulbactam in Human Plasma.
Karla Paulina Valero-RiveraMartin Magaña-AquinoMaría Del Carmen Romero-MéndezMiriam Nayeli Morales-BarragánJulia Sagahón-AzúaSusanna Edith Medellín-GaribayRosa Del Carmen Milán-SegoviaFidel Martínez-GutiérrezSilvia Romano MorenoPublished in: Journal of chromatographic science (2024)
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.
Keyphrases
- liquid chromatography
- tandem mass spectrometry
- simultaneous determination
- ultra high performance liquid chromatography
- high performance liquid chromatography
- mass spectrometry
- high resolution mass spectrometry
- liquid chromatography tandem mass spectrometry
- gas chromatography
- solid phase extraction
- high resolution
- clinical practice
- ms ms
- magnetic resonance
- molecularly imprinted
- acinetobacter baumannii
- magnetic resonance imaging
- cystic fibrosis
- drug resistant
- human health