## Abstract Heparin immobilization chemistry using alkyl spacer arms was adapted to optimize yield on polyurethane (PU) surfaces. The resultant biological activity of immobilized heparin (HI) was examined __in vitro__ and __in vivo__, and compared with a heparin releasing (HR) system. Immobilized h
In vitro andin vivo studies of heparinized-collageno-elastic tubes
โ Scribed by Senatore, Fred ;Shankar, Hariharan ;Chen, Jyh-Herng ;Avantsa, Srinivas ;Feola, Mario ;Posteraro, Robert ;Blackwell, Eric
- Publisher
- John Wiley and Sons
- Year
- 1990
- Tongue
- English
- Weight
- 902 KB
- Volume
- 24
- Category
- Article
- ISSN
- 0021-9304
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โฆ Synopsis
Heparin was covalently coupled to collageno-elastic grafts (CET) derived from lamb carotid arteries, by u s i n g t h e crosslinking agent 1-ethyl-3 (3-dimethylaminopropyl) carbodiimide (EDC). The collagenous grafts were pretreated with various aminating agents in order to enhance the number of available binding sites on the collagen surface. By varying the EDC/heparin weight ratio, the pH of the immobilization media, and the pretreatment agent, a global search pattern maximized heparin loading at 3.90 * 0.36 USP heparin/cm* collagenous graft surface when the EDC/heparin ratio was 2:l at a pH of 1.5 with 1 M hydroxylamine sulfate as the pretreatment agent. Heparinized CETs were superior to nonheparinized CETs by exhibiting b o t h e n h a n c e d antiplatelet activity in using an in vitro differential recirculation reactor with chromium-51 tagged platelets and enhanced patency when interposed in canine carotid arteries. Both antiplatelet activity and patency duration for heparinized CETs were independent of heparin loading.
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