Abstract
Two cytochrome P450 (CYP)-based immobilized enzyme reactors (IMERs) were developed to perform automated on-line phase I drug metabolism studies. For this purpose, biotinylated recombinant CYP2D6 or CYP3A4 reconstituted systems were anchored to the surface of two monolithic mini-columns (2 mm x 6 mm I.D.), which had been covalently grafted with NeutrAvidin. After optimization of immobilization conditions, the obtained IMERs were integrated on-line into a LC hyphenated to an electrospray ionization MS/MS system. Studies with probe substrates and a known competitive inhibitor were performed, showing the potential of CYP-based IMERs in drug metabolism. In the optimized conditions, ca. 15 experiments were carried out with each bioreactor.
MeSH terms
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Avidin
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Bioreactors*
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Biotinylation
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Chromatography, Liquid / instrumentation
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Chromatography, Liquid / methods*
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Cytochrome P-450 CYP2D6 / metabolism*
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Cytochrome P-450 CYP2D6 Inhibitors
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Cytochrome P-450 CYP3A / metabolism*
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Cytochrome P-450 CYP3A Inhibitors
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Drug Evaluation, Preclinical / methods*
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Enzyme Inhibitors / pharmacology
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Enzyme Stability
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Enzymes, Immobilized / metabolism*
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Humans
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Kinetics
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Microsomes, Liver / chemistry
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Recombinant Proteins / metabolism
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Spectrometry, Mass, Electrospray Ionization / instrumentation
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Spectrometry, Mass, Electrospray Ionization / methods*
Substances
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Cytochrome P-450 CYP2D6 Inhibitors
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Cytochrome P-450 CYP3A Inhibitors
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Enzyme Inhibitors
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Enzymes, Immobilized
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Recombinant Proteins
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neutravidin
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Avidin
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Cytochrome P-450 CYP2D6
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Cytochrome P-450 CYP3A
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CYP3A4 protein, human