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Serum protein binding of drugs during and after pregnancy in humans
Author(s) -
Dean Margaret,
Stock Beresford,
Patterson Robert J,
Levy Gerhard
Publication year - 1980
Publication title -
clinical pharmacology and therapeutics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.941
H-Index - 188
eISSN - 1532-6535
pISSN - 0009-9236
DOI - 10.1038/clpt.1980.158
Subject(s) - free fraction , pregnancy , phenytoin , salicylic acid , medicine , gestation , drug , pharmacokinetics , pharmacology , post partum , sulfisoxazole , endocrinology , dexamethasone , diazepam , albumin , chemistry , biology , biochemistry , antibiotics , genetics , psychiatry , epilepsy , tetracycline
The serum protein binding of three weakly acidic drugs (salicylic acid, sulfisoxazole, and Phenytoin), one weak base (diazepam), and one steroid (dexamethasone) was determined in pregnant women at seven time periods during pregnancy and at two time periods post partum, as well as in a group of nonpregnant women of childbearing age. The serum free fraction values (ratio of concentrations, free to total drug) of all drugs rose during pregnancy, primarily after 15 wk of gestation, and remained elevated for at least 1 to 5 days post partum. Pregnancy had the greatest effect on protein binding of sulfisoxazole, diazepam, and salicylic acid. The magnitude of this effect is such that quantitatively significant changes in the pharmacokinetic and pharmacodynamic characteristics of certain drugs may be expected to occur during pregnancy (in addition to possible changes caused by other pregnancy‐related effects such as altered activity of drug‐metabolizing enzyme systems). All drugs but dexamethasone exhibited significant negative correlations between free fraction values and serum albumin concentrations during pregnancy. The serum protein binding of salicylic acid, but not the other drugs tested, was more extensive in nonpregnant women who were not taking oral contraceptives than in those who were. Clinical Pharmacology and Therapeutics (1980) 28, 253–261; doi: 10.1038/clpt.1980.158