Chemical Composition, Particle Size Range, and Biological Activity of some Low Molecular Weight Heparin Derivatives

1990 ◽  
Vol 79 (4) ◽  
pp. 339-343 ◽  
Author(s):  
George A. Neville ◽  
Fred Mori ◽  
Thomas J. Racey ◽  
Paul Rochon ◽  
Kevin R. Holme ◽  
...  
1995 ◽  
Vol 59 (11) ◽  
pp. 1517-1523 ◽  
Author(s):  
LEVENT M. AKYÜREK ◽  
KEIKO FUNA ◽  
ALKWIN WANDERS ◽  
ERIK LARSSON ◽  
BENGT C. FELLSTROM

1995 ◽  
Vol 59 (11) ◽  
pp. 1517-1523
Author(s):  
LEVENT M. AKYÜREK ◽  
KEIKO FUNA ◽  
ALKWIN WANDERS ◽  
ERIK LARSSON ◽  
BENGT C. FELLSTROM

2010 ◽  
Vol 148 (3) ◽  
pp. 317-326 ◽  
Author(s):  
Jin Woo Park ◽  
Ok Cheol Jeon ◽  
Sang Kyoon Kim ◽  
Taslim Ahmed Al-Hilal ◽  
Shun Ji Jin ◽  
...  

2019 ◽  
Vol 25 ◽  
pp. 107602961984070 ◽  
Author(s):  
Jianle Chen ◽  
Yanlei Yu ◽  
Jawed Fareed ◽  
Debra Hoppensteadt ◽  
Walter Jeske ◽  
...  

Heparin and its low-molecular-weight heparin derivatives are widely used clinical anticoagulants. These drugs are critical for the practice of medicine in applications, including kidney dialysis, cardiopulmonary bypass, and in the management of venous thromboembolism. Currently, these drugs are derived from livestock, primarily porcine intestine and less frequently bovine intestine and bovine lung. The worldwide dependence on the pig as a single dominant animal species has made the supply chain for this critical drug quite fragile, leading to the search for other sources of these drugs, including the expanded use of bovine tissues. A number of laboratories are now also examining the similarities between heparin and low-molecular-weight heparins prepared from porcine and ovine tissues. This study was designed to compare low-molecular-weight heparin prepared from ovine heparin through chemical β-elimination, a process currently used to prepare the low-molecular-weight heparin, enoxaparin. Using top-down, bottom-up, and compositional analyses as well as bioassays, low-molecular-weight heparin derived from ovine intestine was shown to closely resemble enoxaparin. Moreover, the compositions of daughter low-molecular-weight heparins prepared from three unfractionated ovine parent heparins were compared. Ovine enoxaparins had similar molecular weight and in vitro anticoagulant activities as Lovenox. Some disaccharide compositional, oligosaccharide composition at the reducing and nonreducing ends and intact chain compositional differences could be observed between porcine enoxaparin and ovine low-molecular-weight heparin. The similarity of these ovine and porcine heparin products suggests that their preclinical evaluation and ultimately clinical assessment is warranted.


1987 ◽  
Author(s):  
Y Morin ◽  
S Limon

The specific biological activity of low-molecular weight heparin prompted using CY 216 in ophtalmological surgery for thrombo-embolic prevention. We report preliminary results on 31 patients (9 males, 22 females, mean age 74,4) treated from 06/86 to 12/86 with a daily 0,3 ml sub-cutaneous injection of CY 216 started 2 hours prior to surgery until day 7, or day 10 for 7 patients. Coagulation tests included TCa and anti-Xa activity. All patients were checked daily for ocular haemorrnagies and thrombo-embolic manifestations. Anaesthesia was general in 16 cases and local in 15. Surgery was performed on 21 cataracts (67 %), 8 retinal detachments (26 %), 2 glaucomas (6 %).No patient developped any clinical thrombo-embolism condition. In that particular surgery where frequent local haemorrhagic complications occur and delay the onset of heparinotherapy, CY 216 treatment exhibited 3 minor eyelids ecchymosis, 1 choroid hematoma and 5 subconjonctival suffusions, all transient and not impacting specific surgical results ; and all already known as possible mechanical vascular aggression independant of heparinotherapy. 2 hyphemas (6 %) also occured, for which CY 216 was discontinued, still not impacting surgical results, and without excessive hypocoagulation according to tests. These biological tests showed no adverse effects ; TCa never raised more than 6" above controls, and anti-Xa activity raised to 4 times pre-treatment values ; in 3 patients, high values did not induce any haemorrhagic complications, a very strong argument in favor of excellent tolerance of CY 216 therapy.At this stage of preliminary results, the tolerance of CY 216 concerning local haemorrhagic risk in eye surgery can be evaluated as near to excellent.


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