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Determination of lopinavir cerebral spinal fluid and plasma ultrafiltrate concentrations by liquid chromatography coupled to tandem mass spectrometry.

Determination of lopinavir cerebral spinal fluid and plasma ultrafiltrate concentrations by liquid chromatography coupled to tandem mass spectrometry. Research Abstract Details 

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  • Determination of lopinavir cerebral spinal fluid and plasma ultrafiltrate concentrations by liquid chromatography coupled to tandem mass spectrometry. Abstract Text:

    robin difrancescoRobin DiFrancesco,robert dicenzoRobert DiCenzo,glorimar vicenteGlorimar Vicente,julie donnellyJulie Donnelly,troy m martinTroy M Martin,luis a colonLuis A Colon,giovanni schifitoGiovanni Schifito,gene d morseGene D Morse,

    A method for the determination of lopinavir (LPV) concentrations in cerebral spinal fluid (CSF) and plasma ultrafiltrate (UF) was developed and validated to analyze clinical specimens from patients receiving antiretroviral treatment with lopinavir/ritonavir. The CSF (400 microL sample volume) final calibration range for LPV was 0.313-25.0 ng/mL. The final calibration range for UF (50 microL sample volume) was 1.25-100 ng/mL. The samples were prepared using liquid-liquid extraction, concentrated, and analyzed using a reversed phase isocratic separation. Detection was achieved in positive mixed reaction monitoring mode on a triple quadrupole mass spectrometer. Isolation of LPV through chromatographic separation and proper selection of calibration matrix were important factors in achieving accurate results. Plasma UF was found to be an equivalent calibration matrix to CSF whereas plasma matrix produced a positive bias in samples with unknown concentrations. Artificial CSF media prepared chemically were biased and less superior than UF. Sources of plasma for the UF did not affect accuracy. Several CSF sources were tested for specificity of the method and LPV concentrations were accurately produced with atmospheric pressure chemical ionization source producing more accurate results than the electrospray source. The method successfully measured LPV concentrations in CSF that were previously undetectable by HPLC as well as UF from protein binding studies.

    Determination of lopinavir cerebral spinal fluid and plasma ultrafiltrate concentrations by liquid chromatography coupled to tandem mass spectrometry. Publishing Authors By Initials

    r difrancescoR DiFrancesco,r dicenzoR DiCenzo,g vicenteG Vicente,j donnellyJ Donnelly,tm martinTM Martin,la colonLA Colon,g schifitoG Schifito,gd morseGD Morse,

    For similar natural sciences: time: time factors research abstracts see: natural sciences: time: time factors research

    PUBMED ID PMID:

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    Determination of lopinavir cerebral spinal fluid and plasma ultrafiltrate concentrations by liquid chromatography coupled to tandem mass spectrometry. Journal Published:

    PUBLICATION TYPE: Research Support, Non-U.S. Gov

    Journal: Journal of pharmaceutical and biomedical analysis

    VOLUME: 44

    Page Numbers: 1139-46

    Journal Abbreviation:

    ISSN: 0731-7085

    DAY: 25

    MONTH: 05

    YEAR: 2007

    Determination of lopinavir cerebral spinal fluid and plasma ultrafiltrate concentrations by liquid chromatography coupled to tandem mass spectrometry. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 8309336

    Determination of lopinavir cerebral spinal fluid and plasma ultrafiltrate concentrations by liquid chromatography coupled to tandem mass spectrometry. Keywords Mesh Terms:

    KEYWORDS: Time Factors

    MESH TERMS: methods

    Chemical & Substance for Abstract: Determination of lopinavir cerebral spinal fluid and plasma ultrafiltrate concentrations by liquid chromatography coupled to tandem mass spectrometry. Information

    Substance Name: lopinavir

    Registry Number: 192725-17-0

    Grant and Affiliation Information for Determination of lopinavir cerebral spinal fluid and plasma ultrafiltrate concentrations by liquid chromatography coupled to tandem mass spectrometry.

    AFFILIATION: Department of Pharmacy Practice, University at Buffalo, NY 14260, United States. rda@buffalo.edu

    Country: England

    England Research PublicationEngland Research Publication

    AGENCY: United States PHS

    GRANT: SIORRR14572

    ACRONYM: DA

    MEDLINETA: J Pharm Biomed Anal

    REFSOURCE:

    DATABASENAME:

    ACCESSION NUMBER:

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