J. Shen et al., A CLINICAL-TRIAL OF A SLOW-RELEASE FORMULATION OF ACETYLSALICYLIC-ACID IN PATIENTS AT RISK FOR PREECLAMPSIA, British journal of clinical pharmacology, 35(6), 1993, pp. 664-667
The formation of thromboxane A2 (TXA2) in maternal and foetal cord ser
um was measured at birth in eight control patients and in 13 patients
taking 100 mg of a slow-release formulation of acetylsalicylic acid. T
he serum concentrations of TXB2 (a stable end product of TXA2 hydrolys
is) in both maternal and cord serum from patients who ingested the ace
tylsalicylic acid formulation were significantly lower (P < 0.01) than
those in control subjects. Acetylsalicylic acid was not detected (< 3
0 ng ml-1) in maternal plasma from six mothers and in cord plasma from
seven foetuses in the acetylsalicylic acid-treated group. The mean co
rd to maternal plasma concentration ratios for detectable acetylsalicy
lic acid and salicylate were 0.62 +/- 0.19 (s.d.) (n = 6) and 0.84 +/-
0.16 (n = 13), respectively. We conclude that low doses of acetylsali
cylic acid given in a slow-release form to mothers during pregnancy ca
use depression of TXA2 formation in the foetal blood.