National Brain Research Program(2017-1.2.1-NKP-201700002)
GINOP(2.3.2-15-2016-00050) Támogató: GINOP
(EFOP-3.6.1.-16-2016-00004) Támogató: EFOP
(GINOP-2.2.1-15-2016-00020)
(K123836)
Szakterületek:
Általános orvostudomány
Farmakológia és gyógyszerészet
Orvos- és egészségtudomány
SZV 1287 is our novel multi-target analgesic, which seems to be a promising drug candidate
for the treatment of neuropathic pain. Therefore, the drug development process has
been started in 2016. Since the pharmacokinetic characterization of a drug candidate
is essential and albumin binding of drugs can strongly affect their pharmacokinetic
properties, herein we provided the detailed investigation and characterization of
the interaction of SZV 1287 and its known metabolites with serum albumin. In a preliminary
animal study, we demonstrated the appearance of SZV 1287, oxaprozin, L 2799, L 2805,
and L 2811 in the circulation after the per os administration of the parent compound
to rats. Then albumin-ligand interactions were examined employing fluorescence spectroscopy,
affinity chromatography, ultrafiltration, ultracentrifugation, and molecular modeling.
Finally, we tested the potential species dependent differences in the albumin binding
of SZV 1287, employing human, bovine, porcine, and rat serum albumins. Our results
demonstrated that SZV 1287 and its metabolites form highly stable complexes with albumin
(Ka = 105 to 106 L/mol). Furthermore, SZV 1287 occupies Sudlow’s Site II on human
serum albumin. Therefore, it is reasonable to hypothesize that SZV 1287-albumin interaction
is an important issue regarding the pharmacokinetics of this drug candidate.