抗凝血酶
肝素
衍生化
亲和层析
还原胺化
琼脂糖
色谱法
胺化
化学
显色的
低聚糖
高分子化学
材料科学
生物化学
高效液相色谱法
酶
催化作用
作者
Shengmei Yuan,Gyongyi Szakalas‐Gratzl,Nicholas P. Ziats,Donald W. Jacobsen,Kandice Kottke‐Marchant,Roger Marchant
出处
期刊:Journal of Biomedical Materials Research
[Wiley]
日期:1993-06-01
卷期号:27 (6): 811-819
被引量:27
标识
DOI:10.1002/jbm.820270614
摘要
Oligosaccharides of heparin with high affinity for antithrombin III (ATIII) have been immobilized onto surface-modified NHLBI Primary Reference low density polyethylene (PE). PE was modified by radiofrequency plasma polymerized (< 150 nm thick) films derived from N-vinyl-2-pyrrolidone (PPNVP) or allyl alcohol (PPAA), and coupled by chemical derivatization to either 3-aminopropyltriethoxysilane or amino-terminated poly(ethylene oxide). High affinity heparin oligosaccharides (HA-heparin, anti-factor Xa activity of 592 +/- 120 IU/mg) prepared by partial deaminative cleavage of commercial crude heparin and fractionated by agarose-ATIII affinity chromatography, were immobilized to surface-modified PE by reductive amination. The anticoagulant activity, as determined by a chromogenic assay for the inhibition of factor Xa, was estimated to be 30-70 mIU/cm2, with binding estimated to be 56-119 ng/cm2. The highest activity was obtained for the HA-heparin immobilized to PE modified by PPNVP with a PEO spacer. Visual confirmation of ATIII binding to immobilized HA-heparin was demonstrated by a gold-labeled double antibody method with imaging by SEM.
科研通智能强力驱动
Strongly Powered by AbleSci AI