Literature DB >> 8396956

A cross-over comparison of the anti-clotting effects of three low molecular weight heparins and glycosaminoglycuronan.

J C Stiekema1, J M Van Griensven, T G Van Dinther, A F Cohen.   

Abstract

1. The anti-clotting effects after intravenous administration of three low molecular weight (LMW) heparins, Fragmin (KABI 2165), Fraxiparine (CY 216), Clexane (PK 10169) and the LMW mixture of glycosaminoglycuronans Orgaran (Org 10172) were compared in a randomized cross-over study in 12 healthy male volunteers. 2. The time courses of the anti-Xa activity of Fragmin, Fraxiparine and Clexane (five subjects) were best fitted by a monoexponential function and had comparable half-lives of 1.9 h, 2.3 h and 2.8 h, respectively. The time courses of the anti-Xa activity of Orgaran and Clexane (four subjects) were described by a biexponential function with terminal half-lives of 56.8h and 27.7 h, respectively. They were longer than those of Fraxiparine and Fragmin. Orgaran injection was associated with a significantly smaller 'clearance' (0.8 +/- 0.2 l h-1) of the plasma anti-Xa activity compared with Fragmin (2.0 +/- 0.5), Fraxiparine (1.7 +/- 0.5) and Clexane (1.6 +/- 0.5). 3. In comparison with the three LMW heparins, the terminal half-life of plasma anti-IIa activity after Orgaran was longer and the 'clearance' of Orgaran was lower than that after Clexane. The area under the curve of the plasma anti-IIa activity after administration of Orgaran was negligible compared with that obtained after injection of the LMW heparins. 4. Orgaran caused the smallest and Fragmin the greatest prolongation of the activated partial thromboplastin time (Orgaran 5.8 +/- 1.2 s vs Fragmin 18.5 +/- 5.2 s) and the thrombin clotting time (Orgaran 2.9 +/- 1.7 s vs Fragmin 47.8 +/- 0.9 s).(ABSTRACT TRUNCATED AT 250 WORDS)

Entities:  

Mesh:

Substances:

Year:  1993        PMID: 8396956      PMCID: PMC1364554          DOI: 10.1111/j.1365-2125.1993.tb05891.x

Source DB:  PubMed          Journal:  Br J Clin Pharmacol        ISSN: 0306-5251            Impact factor:   4.335


  14 in total

1.  Bioavailability and antagonization of the low molecular weight heparin CY 216 in man.

Authors:  J Harenberg; B Würzner; R Zimmermann; G Schettler
Journal:  Thromb Res       Date:  1986-11-15       Impact factor: 3.944

2.  ORG 10172: a low molecular weight heparinoid anticoagulant with a long half-life in man.

Authors:  I D Bradbrook; H N Magnani; H C Moelker; P J Morrison; J Robinson; H J Rogers; R G Spector; T Van Dinther; H Wijnand
Journal:  Br J Clin Pharmacol       Date:  1987-06       Impact factor: 4.335

3.  Relationship between biological activity and concentration of a low-molecular-weight heparin (PK 10169) and unfractionated heparin after intravenous and subcutaneous administration.

Authors:  J Dawes; L Bara; E Billaud; M Samama
Journal:  Haemostasis       Date:  1986

4.  Low molecular weight heparin (KABI 2165, Fragmin): pharmacokinetics after intravenous and subcutaneous administration in human volunteers.

Authors:  G Bratt; E Törnebohm; L Widlund; D Lockner
Journal:  Thromb Res       Date:  1986-06-01       Impact factor: 3.944

5.  Assay of plasma heparin using thrombin and the chromogenic substrate H-D-Phe-Pip-Arg-pNA (S-2238).

Authors:  M L Larsen; U Abildgaard; A N Teien; K Gjesdal
Journal:  Thromb Res       Date:  1978-08       Impact factor: 3.944

6.  Catalysis of thrombin inhibition provides an index for estimating the antithrombotic potential of glycosaminoglycans in rabbits.

Authors:  F A Fernandez; M R Buchanan; J Hirsh; J W Fenton; F A Ofosu
Journal:  Thromb Haemost       Date:  1987-06-03       Impact factor: 5.249

7.  Comparative pharmacokinetics of a low molecular weight heparin (PK 10 169) and unfractionated heparin after intravenous and subcutaneous administration.

Authors:  L Bara; E Billaud; G Gramond; A Kher; M Samama
Journal:  Thromb Res       Date:  1985-09-01       Impact factor: 3.944

8.  Heparan sulfate and dermatan sulfate inhibit the generation of thrombin activity in plasma by complementary pathways.

Authors:  F A Ofosu; G J Modi; L M Smith; A L Cerskus; J Hirsh; M A Blajchman
Journal:  Blood       Date:  1984-09       Impact factor: 22.113

9.  A novel anti-thrombotic heparinoid (Org 10172) devoid of bleeding inducing capacity: a survey of its pharmacological properties in experimental animal models.

Authors:  D G Meuleman; P M Hobbelen; G van Dedem; H C Moelker
Journal:  Thromb Res       Date:  1982-08-01       Impact factor: 3.944

10.  The antithrombotic activity and pharmacokinetics of enoxaparine, a low molecular weight heparin, in humans given single subcutaneous doses of 20 to 80 mg.

Authors:  A M Frydman; L Bara; Y Le Roux; M Woler; F Chauliac; M M Samama
Journal:  J Clin Pharmacol       Date:  1988-07       Impact factor: 3.126

View more
  7 in total

Review 1.  What do we learn from repeated population analyses?

Authors:  Stephen B Duffull; Daniel F B Wright
Journal:  Br J Clin Pharmacol       Date:  2015-01       Impact factor: 4.335

2.  Comparison of biological activities of two low molecular weight heparins in 10 healthy volunteers.

Authors:  M Azizi; C Veyssier-Belot; M Alhenc-Gelas; G Chatellier; E Billaud-Mesguish; J N Fiessinger; M Aiach
Journal:  Br J Clin Pharmacol       Date:  1995-12       Impact factor: 4.335

Review 3.  Pharmacokinetic optimisation of the treatment of deep vein thrombosis.

Authors:  A Iorio; G Agnelli
Journal:  Clin Pharmacokinet       Date:  1997-02       Impact factor: 6.447

Review 4.  Dalteparin: an update of its pharmacological properties and clinical efficacy in the prophylaxis and treatment of thromboembolic disease.

Authors:  C J Dunn; B Jarvis
Journal:  Drugs       Date:  2000-07       Impact factor: 9.546

Review 5.  Danaparoid. A review of its pharmacology and clinical use in the management of heparin-induced thrombocytopenia.

Authors:  M I Wilde; A Markham
Journal:  Drugs       Date:  1997-12       Impact factor: 9.546

Review 6.  Dalteparin sodium. A review of its pharmacology and clinical use in the prevention and treatment of thromboembolic disorders.

Authors:  C J Dunn; E M Sorkin
Journal:  Drugs       Date:  1996-08       Impact factor: 9.546

Review 7.  Enoxaparin. A reappraisal of its pharmacology and clinical applications in the prevention and treatment of thromboembolic disease.

Authors:  S Noble; D H Peters; K L Goa
Journal:  Drugs       Date:  1995-03       Impact factor: 9.546

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.