N. Srinivas et S. Kaul, PHARMACOKINETICS OF A NOOTROPIC AGENT, BMY-21502, AND ITS METABOLITESIN BEAGLE DOGS, European journal of drug metabolism and pharmacokinetics, 23(1), 1998, pp. 61-65
A preliminary investigation into the pharmacokinetics of BMY-21502, a
nootropic agent, and two of its metabolites, BMY-42191 and BMY-40440,
was performed in 4 beagle dogs. Following oral dosing of a solution of
BMY-21502 (0.61 mmoles), plasma samples were obtained for 24 h and an
alyzed for the three analytes by a validated HPLC assay. BMY-21502 was
rapidly absorbed (T-max = 0.5 +/- 0.3 h), followed by a rapid decline
of the plasma levels (T-1/2 = 0.95 +/- 0.1 h). The hydroxy metabolite
, BMY-42191, was rapidly formed and the peak concentrations in plasma
were obtained by 2.88 +/- 0.2 h. On the contrary, there was a consider
able delay in the peaking of the ketone metabolite, BMY-40440 (T-max =
6 h). The T-1/2 values for BMY-40440 (5.58 +/- 0.5 h) were longer tha
n those for BMY-42191 (4.28 +/- 1.2 h). Comparison of AUC values for B
MY-42191 (326.43 +/- 63.3 h.mu M) with those of BMY-40440 (67.52 +/- 8
.4 h.mu M) or BMY-21502 (69.35 +/- 7.3 h.mu M) indicated that BMY-4219
1 was the major circulating species in dog plasma. In conclusion, the
preliminary data indicate that the metabolism of BMY-21502 is complex
and may encompass hydroxy-ketone metabolic interconversions, as report
ed for other xenobiotics.