RT Journal Article
SR Electronic
T1 Phencyclidine blood protein binding: influence of protein, pH and species.
JF Journal of Pharmacology and Experimental Therapeutics
JO J Pharmacol Exp Ther
FD American Society for Pharmacology and Experimental Therapeutics
SP 656
OP 660
VO 226
IS 3
A1 S M Owens
A1 M Mayersohn
A1 J R Woodworth
YR 1983
UL http://jpet.aspetjournals.org/content/226/3/656.abstract
AB We studied the influence of protein, pH and species on phencyclidine (PCP) protein binding. PCP binding to dog serum was unaffected by high concentrations of PCP and metabolites. The percentage of unbound PCP in pooled human serum and plasma specimens and pooled dog serum specimens was (mean +/- S.D.): 48.3 +/- 2.5; 42.5 +/- 1.8; and 43.3 +/- 1.9%, respectively. The percentage of unbound PCP in human serum albumin (HSA), 81.2 +/- 2.0%, was constant over the physiological HSA concentration range (3.5-5.5 g/dl). The binding of PCP to alpha 1-acid glycoprotein (alpha 1-AGP) increased with increasing alpha 1-AGP concentration (50-200 mg/dl). The binding to HSA or alpha 1-AGP separately did not account for the binding found in whole serum or plasma specimens. However, when a constant concentration of HSA (4.5 g/dl) was added to varying concentrations of alpha 1-AGP, the PCP binding increased dramatically and was similar to the binding found in human serum specimens. The association constant in the presence of both proteins (7.72 X 10(4) M-1) was 4.4 times greater than the association constant for alpha 1-AGP alone (1.74 X 10(4) M-1). This suggested an interaction between the proteins which resulted in enhanced PCP binding. The percentage of unbound PCP increased with decreasing pH in both dog serum and human serum specimens. This change could have possible effects on PCP distribution and elimination. The PCP blood to plasma ratio was 0.94 in pooled human heparinized blood and 1.25 in pooled dog heparinized blood. Neither species showed PCP concentration-dependent partitioning.