An isotope dilution-liquid chromatography-tandem mass spectrometry (ID-LC-MS/MS)-based candidate reference measurement procedure for the quantification of topiramate in human serum and plasma
Author:
Affiliation:
1. Dr. Risch Ostschweiz AG , Buchs , Switzerland
2. Roche Diagnostics GmbH , Penzberg , Germany
3. Chrestos Concept GmbH & Co. KG , Essen , Germany
Abstract
Funder
Roche Diagnostics GmbH
Publisher
Walter de Gruyter GmbH
Subject
Biochemistry (medical),Clinical Biochemistry,General Medicine
Link
https://www.degruyter.com/document/doi/10.1515/cclm-2022-1273/pdf
Reference35 articles.
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2. International Organization for Standardization. ISO 17511:2020. In vitro diagnostic medical devices-requirements for establishing metrological traceability of values assigned to calibrators, trueness control materials and human samples. Geneva, Switzerland: ISO; 2020.
3. Shank, RP, Maryanoff, BE. Molecular pharmacodynamics, clinical therapeutics, and pharmacokinetics of topiramate. CNS Neurosci Ther 2008;14:120–42. https://doi.org/10.1111/j.1527-3458.2008.00041.x.
4. Perucca, E. A pharmacological and clinical review on topiramate, a new antiepileptic drug. Pharmacol Res 1997;35:241–56. https://doi.org/10.1006/phrs.1997.0124.
5. Privitera, MD. Topiramate: a new antiepileptic drug. Ann Pharmacother 1997;31:1164–73. https://doi.org/10.1177/106002809703101010.
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