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Thrombosis |
From the Department of Biochemistry (J.F.W.K., T.L.) and the Cardiovascular Research Institute (S.J.H.W., T.L.), Maastricht University, 6200 MD Maastricht, The Netherlands; and the Medtronic Bakken Research Center B.V. (A.D., M.V., M.H.), 6229 GW Maastricht, The Netherlands.
Correspondence to Dr. T. Lindhout, Department of Biochemistry, Maastricht University, PO Box 616, 6200 MD Maastricht, The Netherlands. E-mail t.lindhout{at}bioch.unimaas.nl
Objective Blood compatibility of artificial surfaces depends on their immunogenic and thrombogenic properties. Collagens weak antigenicity makes it an attractive candidate for stent coatings or fabrication of vascular grafts. However, the thrombogenic nature of collagen limits its application. We examined whether heparinization can make collagen more thromboresistant.
Methods and Results Collagen was heparinized by crosslinking collagen with extensively periodate oxidized heparin and/or by covalently bonding of mildly periodate oxidized heparin. Both ways of heparinization have no effect on platelet adhesion and could not abolish induction of platelet procoagulant activity. However, thrombin generation was completely prevented under static and flow conditions. The functionality of immobilized heparin was confirmed by specific uptake of antithrombin, 13.5±4.7 pmol/cm2 and 1.95±0.21 pmol/cm2 for mildly and heavily periodated heparin, respectively.
Conclusions These results indicate that immobilization of heparin on collagen, even as a crosslinker, is a very effective way to prevent surface thrombus formation. These data encourage the application of heparinized collagen as stent-graft material in animal and eventually human studies.
Key Words: collagen heparin thrombogenicity thrombosis blood flow
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