The new, so-called molecular weight heparins (mean MW : about 5,000 daltons) are less heterogeneous than the old, fractionated heparins (mean MW: about 15,000 daltons). Both types of preparations contain molecules with affinity for antithrombin III (AT III) and anticoagulant activity, as well as other molecules without affinity for AT III but which are thought to contribute to the antithrombotic activity of heparin. The anticoagulant effect of low molecular weight heparins (defined as their ability to prolong the activated cephalin time) in 3 to 4 times lower than that of standard heparin, but their activity against the activated factor X (Xa) is approximately the same. The half-life of the anti-Xa activity of low molecular weight heparins is twice that of standard heparin. The bioavailability of low molecular weight heparins administered subcutaneously is greater than 90%, as against less than 30% with standard heparin. Clinical trails have shown that one single subcutaneous injection of low molecular weight heparin 2 hours before an operation, then every 24 hours reduces the incidence of isotopic venous thrombosis in general surgery at least as much as 2 daily injections of calcium heparinate 5000 I.U. Low molecular weight heparins are virtually devoid of the pro-platelet aggregation activity exhibited by standard heparin.
新型的所谓分子量肝素(平均分子量:约5000道尔顿)比旧型的、经分级分离的肝素(平均分子量:约15000道尔顿)的异质性更低。这两种制剂都含有对抗凝血酶III(AT III)有亲和力且具有抗凝活性的分子,以及对AT III无亲和力但被认为有助于肝素抗血栓活性的其他分子。低分子量肝素的抗凝作用(定义为其延长活化部分凝血活酶时间的能力)比标准肝素低3至4倍,但其对活化因子X(Xa)的活性大致相同。低分子量肝素抗Xa活性的半衰期是标准肝素的两倍。皮下注射低分子量肝素的生物利用度大于90%,而标准肝素则低于30%。临床试验表明,术前2小时单次皮下注射低分子量肝素一次,然后每24小时注射一次,其降低普通外科手术中同位素静脉血栓形成的发生率至少与每日两次注射5000国际单位肝素钙的效果相同。低分子量肝素几乎没有标准肝素所表现出的促血小板聚集活性。