Thromb Haemost 2002; 87(05): 831-835
DOI: 10.1055/s-0037-1613092
Review Article
Schattauer GmbH

Absence of Placental Transfer of Pentasaccharide (Fondaparinux, Arixtra®) in the Dually Perfused Human Cotyledon in vitro

F. Lagrange
1   Departments of Pharmacology, Pharmacokinetics & Clinical Pharmacy and Therapeutics, Bordeaux 2 University, France
3   Department of Obstetrics and Gynecology, University Hospitals Bordeaux, France
,
C. Vergnes
2   Thrombosis and Haemostasis Unit, Laboratory of Haematology, University Hospitals Bordeaux, France
,
J.L. Brun
3   Department of Obstetrics and Gynecology, University Hospitals Bordeaux, France
,
F. Paolucci
4   Sanofi-Synthelabo Research, Montpellier, France, and Riells, Spain
,
T. Nadal
4   Sanofi-Synthelabo Research, Montpellier, France, and Riells, Spain
,
J.J. Leng
3   Department of Obstetrics and Gynecology, University Hospitals Bordeaux, France
,
M.C. Saux
1   Departments of Pharmacology, Pharmacokinetics & Clinical Pharmacy and Therapeutics, Bordeaux 2 University, France
,
B. Banwarth
1   Departments of Pharmacology, Pharmacokinetics & Clinical Pharmacy and Therapeutics, Bordeaux 2 University, France
› Author Affiliations
Further Information

Publication History

Received 08 October 2001

Accepted after revision 17 January 2002

Publication Date:
11 December 2017 (online)

Summary

The synthetic pentasaccharide, fondaparinux, is the first of a new antithrombotic class: selective factor Xa inhibitors. Comparative clinical trials of fondaparinux versus heparins in prevention and treatment of venous thromboembolism are ongoing. Little is known about fondaparinux during pregnancy, as women of child-bearing potential were excluded from clinical trials. No particular safety issue, for either mother or fetus, has been reported for heparins. The objective of this study was to compare in vitro the steady state placental transfer of fondaparinux and enoxaparin at the plasma concentrations reached during acute treatment of venous thromboembolism (1.75 µg/mL and 1 anti- Xa IU/mL respectively), using antipyrine (20 mg/L) as reference. No biological activity was detectable in the fetal venous effluent during perfusion of enoxaparin-antipyrine, fondaparinux-antipyrine or control media. Furthermore, fetal venous samples did not differ significantly from fetal arterial samples. This apparent absence of placental transfer supports further evaluation of fondaparinux in pregnant women.

 
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