Background: Tacrolimus has a low therapeutic index requiring strict control of whole blood concentrations. Although random access immunoassay platforms exist that rapidly provide quantitative values for tacrolimus, LC-MS/MS may provide more accurate quantitation. However, batch testing in many LC-MS/MS assays is not efficient, particularly when testing patients suspected of having tacrolimus toxicity. Extending calibration curve stability beyond the traditionally accepted single batch may facilitate improved turnaround time and reduce testing costs. A 24-h extended calibration of LC-MS/MS tacrolimus was designed and validated to reduce calibrator usage, improve turnaround time, and provide a more efficient workflow for urgent requests.
Methods: Patient samples included in the study were extracted and assayed with coextracted calibrators and quality control in real time. The same patient samples were extracted again 24 h later without coextracted calibrators. The data acquired from the second patient sample extraction was applied to the original calibration curve acquired 24 h prior and compared to the data for the same samples coextracted with calibrators, creating a value set utilizing extended curve stability.
Results: A linear regression compared the results using the extended curve to the results of the coextracted acquisitions. This yielded a strong correlation between the 2 data populations, with a slope of 1.0061 and a correlation coefficient of >0.95. The average bias between original patient values and patient values 24 h later was 3.4% across all patient samples.
Conclusions: Patient tacrolimus values were comparable when extracted within 24 h of calibration versus values coextracted with calibrators. Demonstrating comparability within 24 h of calibration allows the laboratory to provide rapid turnaround time for urgent samples without the need for an entirely new calibration curve.
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http://dx.doi.org/10.1093/jalm/jfab048 | DOI Listing |
Rapid Commun Mass Spectrom
November 2024
Faculty of Environment and Natural Resources, University of Freiburg, Freiburg im Breisgau, Germany.
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December 2024
Department of Pharmacy, Faculty of Medicine and Surgery, University of Malta, Msida, Malta.
Accurate and precise analysis of cannabinoids is important for elucidating their therapeutic potential and developing therapies, which are targeted toward different medical conditions. A wide range of cannabis products are present on the market and are available in different dosage forms, including dried flowers, extracts, and consumables. The aim of this article is to provide an updated narrative review of literature on challenges of analyzing cannabinoids in plant material, oils, and edibles.
View Article and Find Full Text PDFAnal Chem
June 2024
Department of Chemistry, University of Minnesota, 207 Pleasant Street, Minneapolis, Minnesota 55455, United States.
The response range of an ion-selective electrode (ISE) has been described by counterion interference at the lower and Donnan failure at the upper detection limit. This approach fails when the potentiometric response at the upper detection limit exhibits an apparently super-Nernstian response, as has been reported repeatedly for H-selective electrodes. While also observed when samples contain other anions, super-Nernstian responses at low pH are a problem in particular for samples that contain phthalate, a common component of commercial pH calibration solutions.
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February 2024
Department of Chemistry and Biochemistry, College of Natural Sciences and Mathematics, The University of Toledo, Toledo, Ohio 43606, United States.
This study addresses the challenges of matrix effects and interspecies plasma protein binding (PPB) on measurement variability during method validation across diverse plasma types (human, rat, rabbit, and bovine). Accurate measurements of small molecules in plasma samples often require matrix-matched calibration approaches with the use of specific plasma types, which may have limited availability or affordability. To mitigate the costs associated with human plasma measurements, we explore in this work the potential of cross-matrix-matched calibration using Bayesian hierarchical modeling (BHM) to correct for matrix effects associated with PPB.
View Article and Find Full Text PDFFood Chem
July 2024
Institute of National Analytical Research and Service (INARS), Bangladesh Council of Scientific and Industrial Research (BCSIR), Dr. Kudrat-i-Khuda Road, Dhanmondi, Dhaka 1205, Bangladesh. Electronic address:
The aim of the study was to develop a modified QuEChERS method coupled with liquid chromatography-tandem mass spectrometry (LC-MS/MS) for the simultaneous determination of five multi-class pesticides in country beans collected from Dhaka, Bangladesh. Pesticides were extracted using ACN, and to minimize the co-extraction matrix, optimized d-SPE cleanup was done using sorbents (GCB, PSA, and C18). In the calibration range, the method showed excellent linearity with a correlation coefficient of R ≥ 0.
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