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Tytuł:
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A sensitive capillary GC-MS method for analysis of topiramate from plasma obtained from single-dose studies.
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Autorzy:
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Conway JM; Experimental and Clinical Pharmacology, College of Pharmacy, University of Minnesota, Minneapolis, MN, USA.
Birnbaum AK
Marino SE
Cloyd JC
Remmel RP
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Źródło:
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Biomedical chromatography : BMC [Biomed Chromatogr] 2012 Sep; Vol. 26 (9), pp. 1071-6. Date of Electronic Publication: 2012 Jan 04.
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Typ publikacji:
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Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
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Język:
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English
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Imprint Name(s):
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Publication: 1990- : Chichester : Wiley
Original Publication: London : Heyden & Son, c1986-1990
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MeSH Terms:
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Fructose/*analogs & derivatives
Gas Chromatography-Mass Spectrometry/*methods
Dibenzocycloheptenes/blood ; Fructose/blood ; Fructose/isolation & purification ; Fructose/pharmacokinetics ; Humans ; Reproducibility of Results ; Sensitivity and Specificity ; Solid Phase Extraction ; Topiramate
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References:
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Grant Information:
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K01 NS050309 United States NS NINDS NIH HHS; P50 NS016308 United States NS NINDS NIH HHS; P50-NS16308 United States NS NINDS NIH HHS
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Substance Nomenclature:
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0 (Dibenzocycloheptenes)
0H73WJJ391 (Topiramate)
30237-26-4 (Fructose)
6R22P8K61P (cyheptamide)
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Entry Date(s):
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Date Created: 20120107 Date Completed: 20130220 Latest Revision: 20211021
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Update Code:
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20240104
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PubMed Central ID:
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PMC3776594
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DOI:
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10.1002/bmc.1749
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PMID:
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22223467
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Topiramate (Topamax®) is an antiepileptic medication used as adjunctive and monotherapy in patients with epilepsy and for migraine prophylaxis. A GC-MS assay was developed that was capable of detecting topiramate plasma concentrations following a single rectal or oral dose administration. Topiramate plasma samples were prepared by solid-phase extraction and were quantified by GC-MS analysis. The topiramate standard curves were split from 0.1 to 4 µg/mL and from 4 to 40 µg/mL in order to give a more accurate determination of the topiramate concentration. The accuracy of the standards ranged from 94.6 to 107.3% and the precision (%CV) ranged from 1.0 to 5.3% for both curves at all concentrations. The %CV for quality controls was <7.6%. The assay is both accurate and precise and will be used to complete future pharmacokinetic studies.
(Copyright © 2012 John Wiley & Sons, Ltd.)