Literature DB >> 12706639

Comparative study of the pharmacokinetic profiles of two LMWHs--bemiparin (3500 IU, anti-Xa) and tinzaparin (4500 IU, anti-Xa)--administered subcutaneously to healthy male volunteers.

F Depasse1, M J González de Suso, I Lagoutte, J Fontcuberta, M Borrell, M M Samama.   

Abstract

Pharmacokinetic profiles of bemiparin (3500 IU, anti-Xa) and tinzaparin (4500 IU, anti-Xa) administered subcutaneously to 12 healthy male volunteers were compared in a monocentric study. Each of the 12 subjects underwent successively the two low-molecular-weight heparin (LMWH) preparations in a randomised order and was considered as its own control. Anti-Xa activity, free and total tissue factor pathway inhibitor (TFPI), and thromboplastin-thrombomodulin-mediated time were determined as main variables. Activated partial thromboplastin time (APTT), thrombin clotting time, and anti-IIa activity were also determined. Bemiparin (3500 IU, anti-Xa) exerts a significantly more rapid, more potent, and more prolonged anti-Xa activity than tinzaparin (4500 IU, anti-Xa). The plasma level increase for free and total TFPI is significantly lower with bemiparin than with tinzaparin. Free and total TFPI peak levels occur earlier than anti-Xa activity peak levels for both LMWH preparations, but no statistical difference appeared between the two preparations for TFPI T(max). No significant effect was observed for both preparations for thromboplastin-thrombomodulin-mediated time. Subcutaneous injection of bemiparin exerts only minimal anti-IIa activity and does not prolong thrombin time, whereas tinzaparin elicits significant anti-IIa activity and prolongs thrombin clotting time. Bemiparin exerts a significantly lower prolongation of APTT than tinzaparin. No difference was observed for APTT prolongation T(max) between the two preparations. Globally, the overall tolerability of both formulations revealed no relevant adverse effects. In conclusion, bemiparin and tinzaparin are not bioequivalent. Bemiparin exerts an important and more prolonged anti-Xa activity in comparison with tinzaparin. An original finding of this study is the difference observed between the two formulations for free TFPI release.

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Year:  2003        PMID: 12706639     DOI: 10.1016/s0049-3848(03)00141-5

Source DB:  PubMed          Journal:  Thromb Res        ISSN: 0049-3848            Impact factor:   3.944


  7 in total

Review 1.  Bemiparin: pharmacological profile.

Authors:  Carlos F Sánchez-Ferrer
Journal:  Drugs       Date:  2010-12-14       Impact factor: 9.546

Review 2.  Tinzaparin sodium: a review of its use in the prevention and treatment of deep vein thrombosis and pulmonary embolism, and in the prevention of clotting in the extracorporeal circuit during haemodialysis.

Authors:  Sheridan M Hoy; Lesley J Scott; Greg L Plosker
Journal:  Drugs       Date:  2010-07-09       Impact factor: 9.546

Review 3.  Tinzaparin sodium: a review of its pharmacology and clinical use in the prophylaxis and treatment of thromboembolic disease.

Authors:  Susan M Cheer; Christopher J Dunn; Rachel Foster
Journal:  Drugs       Date:  2004       Impact factor: 9.546

Review 4.  Bemiparin: a review of its use in the prevention of venous thromboembolism and treatment of deep vein thrombosis.

Authors:  Therese M Chapman; Karen L Goa
Journal:  Drugs       Date:  2003       Impact factor: 9.546

5.  Effects of antithrombotic drugs fondaparinux and tinzaparin on in vitro proliferation and osteogenic and chondrogenic differentiation of bone-derived mesenchymal stem cells.

Authors:  Argiris Papathanasopoulos; Dimitrios Kouroupis; Karen Henshaw; Dennis McGonagle; Elena A Jones; Peter V Giannoudis
Journal:  J Orthop Res       Date:  2011-03-22       Impact factor: 3.494

Review 6.  Tinzaparin-a review of its molecular profile, pharmacology, special properties, and clinical uses.

Authors:  Marina Amerali; Marianna Politou
Journal:  Eur J Clin Pharmacol       Date:  2022-07-23       Impact factor: 3.064

Review 7.  Tinzaparin and other low-molecular-weight heparins: what is the evidence for differential dependence on renal clearance?

Authors:  Kristian B Johansen; Torben Balchen
Journal:  Exp Hematol Oncol       Date:  2013-08-08
  7 in total

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