Valproic acid binding to human serum and human placenta in vitro.

Abstract:

:The binding characteristics of the antiepileptic agent and teratogen valproic acid for human serum and human placenta were investigated utilizing equilibrium dialysis of the drugs in serum and in homogenates of whole placenta so that the transplacental transfer of the drug could be better defined. A low-capacity, high-affinity binder and a high-capacity, low-affinity binder for valproic acid were found in serum. However, there was only minimal, nonspecific binding of the drug to placenta. It appears that transplacental transfer of valproic acid is not mediated by binding to placenta. It is likely that such transfer occurs by passive diffusion, which may be facilitated by the lipophilicity of the drug and by development of a pH gradient across the placenta. These findings indicate that the placenta is not a depot for valproic acid.

journal_name

Ther Drug Monit

authors

Bailey DN,Briggs JR

doi

10.1097/01.ftd.0000158077.07836.9a

subject

Has Abstract

pub_date

2005-06-01 00:00:00

pages

375-7

issue

3

eissn

0163-4356

issn

1536-3694

pii

00007691-200506000-00019

journal_volume

27

pub_type

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