Yang V C, Bernstein H, Cooney C L, Kadam J C, Langer R
Thromb Res. 1986 Dec 1;44(5):599-610. doi: 10.1016/0049-3848(86)90162-3.
Recently, the development of low molecular weight heparin fractions and fragments (LMHF) as potential antithrombotic agents has gained increased attention. However, the lack of antagonists to neutralize the anticoagulant effects of these drugs may seriously exclude them from possible uses in extracorporeal therapy. This is mainly because of the concern that the high dosage of the drugs employed in extracorporeal therapy could lead to serious bleeding risks. Our earlier work has demonstrated that immobilized heparinase can remove polydisperse heparin both in vitro and in vivo. To examine whether such a system may be used as a novel approach to neutralize the anticoagulant effects of LMHF, different LMHF were tested using heparinase. In vitro data showed that both the APTT and anti-FXa activities of the LMHF including Kabi 2165, PK 10169, Cy 216 and CY 222 were nearly completely eliminated by heparinase in less than 20 min. This study suggests that an immobilized heparinase system may be an useful element for the acceptance of the LMHF for their use in extracorporeal therapy.
最近,低分子量肝素级分和片段(LMHF)作为潜在抗血栓形成药物的开发受到了越来越多的关注。然而,缺乏能够中和这些药物抗凝作用的拮抗剂可能会严重阻碍它们在体外治疗中的应用。这主要是因为担心体外治疗中使用的高剂量药物会导致严重的出血风险。我们早期的研究表明,固定化肝素酶在体外和体内都能去除多分散肝素。为了研究这样的系统是否可以作为一种中和LMHF抗凝作用的新方法,我们使用肝素酶对不同的LMHF进行了测试。体外数据显示,包括卡比2165、PK 10169、Cy 216和CY 222在内的LMHF的活化部分凝血活酶时间(APTT)和抗Xa因子活性在不到20分钟内几乎被肝素酶完全消除。这项研究表明,固定化肝素酶系统可能是使LMHF被接受用于体外治疗的一个有用因素。