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Antimicrobial Agents and Chemotherapy, September 1999, p. 2245-2250, Vol. 43, No. 9
Department of Clinical Pharmacology, The
Liver Center, Center for AIDS Research, University of Alabama at
Birmingham, Birmingham, Alabama 35294,1 and
Triangle Pharmaceuticals, Inc., Durham, North Carolina
277072
Received 25 March 1999/Returned for modification 24 May
1999/Accepted 1 July 1999
An analytical methodology combining solid-phase extraction (SPE)
and high-performance liquid chromatography (HPLC) was developed to
quantitate the intracellular active 5'-triphosphate (TP) of
0066-4804/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Quantitation of Intracellular Triphosphate of
Emtricitabine in Peripheral Blood Mononuclear Cells from Human
Immunodeficiency Virus-Infected Patients
-L-2',3'-dideoxy-5-fluoro-3'-thiacytidine
(emtricitabine) (FTC) in human peripheral blood mononuclear cells
(PBMCs). The FTC nucleotides, including 5'-mono-, di-, and
triphosphates, were successively resolved on an anion-exchange SPE
cartridge by applying a gradient of potassium chloride. The FTC-TP was
subsequently digested to release the parent nucleoside that was finally
analyzed by HPLC with UV detection (HPLC-UV). Validation of the
methodology was performed by using PBMCs from healthy donors exposed to
an isotopic solution of [3H]FTC with known specific
activity, leading to the formation of intracellular FTC-TP that was
quantitated by an anion-exchange HPLC method with radioactive
detection. These levels of FTC-TP served as reference values and were
used to validate the data obtained by HPLC-UV. The assay had a limit of
quantitation of 4.0 pmol of FTC-TP (amount on column from approximately
107 cells). Intra-assay precision (coefficient of variation
percentage of repeated measurement) and accuracy (percentage deviation
of the nominal reference value), estimated by using quality control samples at 16.2, 60.7, and 121.5 pmol, ranged from 1.3 to 3.3% and
1.0 to 4.8%, respectively. Interassay precision and accuracy varied
from 3.0 to 10.2% and from 2.5 to 6.7%, respectively. This methodology was successfully applied to the determination of FTC-TP in
PBMCs of patients infected with human immunodeficiency virus after oral
administration of various dosing regimens of FTC monotherapy.
*
Corresponding author. Mailing address: Department of
Clinical Pharmacology, University of Alabama at Birmingham, Box 600, Volker Hall G019, University Station, Birmingham, AL 35294-0019. Phone:
(205) 934-8226. Fax: (205) 975-4871. E-mail:
Jean-Pierre.Sommadossi{at}CCC.UAB.EDU.
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