Author: David E. Moody
Abstract:
This is a progress report on a project that is testing the
hypothesis that inhibition of in vitro drug metabolism can predict potential
drug interactions with the opioids buprenorphine, methadone, and oxycodone.
The overall assessment is that substantial progress has been
made in meeting project objectives. Researchers have optimized incubation
conditions for buprenorphine, methadone, and oxycodone in human liver
microsomes (HLM) and with the relevant DNA-expressed cytochrome P450s (rCYPs)
(i.e., CYP3A4 for all three substrates, 2C8 for buprenorphine, 2B6 for
methadone, and 2D6 and 2C18 for oxycodone).
Researchers also established the following positive controls
for the system: troleandomycin (TAO) with CYP3A4 metabolism of buprenorphine,
oxycodone and methadone, and gemfibrozil glucuronide for CYP2C8 metabolism of
buprenorphine.
Progress was made in another area in screening the
inhibitory potential of three drug classes in HLM using the project's ±
15-minute pre-incubation of inhibitor with HLM and source of NADPH protocol
that indicates both in vitro inhibition and TDI. This has been done for four
H2-receptor antagonists, and five proton pump inhibitors (PPIs) with methadone
and oxycodone at 2.0 ìM substrate concentration, and for twelve antifungal
azole compounds at 20 ìM substrate for all three opioids.
In addition, for the relevant compounds (most), researchers
have determined IC50 values for the inhibition of relevant CYP450s, and have
performed in vivo extrapolations to estimate in vivo inhibitory potential.
Further, for the relevant compounds (most), the project determined IC50 values
for the inhibition of relevant CYP450s, and have performed in vivo
extrapolations to estimate in vivo inhibitory potential.
Following further mechanistic studies, the project will
submit manuscripts on TDI by cimetidine and PPIs. Although much remains to be
done in the project's studies on in vitro inhibition of opioid metabolism,
significant in-roads have been achieved.
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