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Letters |
University of Alabama at Birmingham, Department of Clinical Pharmacology, Birmingham, AL 35294-0019
a Address correspondence to this author at: University of Alabama at Birmingham, Department of Clinical Pharmacology, 1530 3rd Ave. South, VH 116, Birmingham, AL 35294-0019. Fax 205-975-4871; e-mail
Edward.Acosta@ccc.uab.edu.
To the Editor:
Nelfinavir mesylate (NFV) is an HIV protease inhibitor approved for the treatment of HIV infection. Since its introduction, NFV has become a common component of standard highly active antiretroviral regimens. Although the drug has been available since 1997, the pharmacokinetic and pharmacodynamic properties of NFV and its active hydroxy-t-butylamide (M8) metabolite have not been well characterized. We recently completed investigations into the stability of NFV and M8 in plasma stored at -20 and -70 °C for up to 19 months. We observed significant degradation of both compounds in heparinized plasma samples stored at -20 °C. These results may have implications for those involved with the collection and analysis of NFV and M8 pharmacokinetic data.
To facilitate our investigations, we prepared NFV and M8 calibrators in
drug-free heparinized
References
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