Bradbrook I D, Magnani H N, Moelker H C, Morrison P J, Robinson J, Rogers H J, Spector R G, Van Dinther T, Wijnand H
Br J Clin Pharmacol. 1987 Jun;23(6):667-75. doi: 10.1111/j.1365-2125.1987.tb03100.x.
ORG 10172 is a heparinoid with mean molecular weight 6500 daltons. Intravenous bolus injections of ORG 10172 were compared with placebo and heparin injections in 91 separate studies in 83 healthy male subjects. 6400 units ORG 10172 produced a mean maximum change of 14.7 s in kaolin cephalin time (c.f. greater than 120 s for 5000 units heparin). Changes in prothrombin time were minimal (1.6 s for 6400 units ORG 10172 and 4.5 s after 5000 units heparin). A dose-related increase in bleeding time occurred after ORG 10172 and at high doses (greater than 3200 units) some secondary bleeding, which was never serious, occurred at between 1 and 4 h after incision. A dose-dependent reduction in ex vivo platelet adhesiveness was found at 10 min after ORG 10172 injection. ORG 10172 promoted a much smaller release of lipoprotein lipase as compared with heparin. The effect of ORG 10172 on plasma factor Xa activity (one measure of its action) was described by a biexponential decay with a mean distribution half-life of 2.34 (s.e. mean 0.16) h and mean disposition half-life of 17.6 (s.e. mean 1.1) h. It thus has a much longer duration of effect than heparin. There was a linear relationship of plasma anti-Xa response to increasing dose although there was some variability only partly explained by differences in body weight or surface area. ORG 10172 administration by bolus intravenous injection was well tolerated and there was no evidence of adverse effects on clinical chemistry or haematology tests.
ORG 10172是一种平均分子量为6500道尔顿的类肝素。在83名健康男性受试者中进行的91项独立研究中,将ORG 10172静脉推注与安慰剂和肝素注射进行了比较。6400单位的ORG 10172使高岭土部分凝血活酶时间的平均最大变化为14.7秒(相比之下,5000单位肝素的变化大于120秒)。凝血酶原时间的变化最小(6400单位ORG 10172为1.6秒,5000单位肝素后为4.5秒)。ORG 10172注射后出血时间呈剂量相关增加,高剂量(大于3200单位)时,在切口后1至4小时出现一些继发性出血,但从未严重。ORG 10172注射后10分钟发现离体血小板黏附性呈剂量依赖性降低。与肝素相比,ORG 10172促进脂蛋白脂肪酶释放的作用要小得多。ORG 10172对血浆因子Xa活性(其作用的一种衡量指标)的影响表现为双指数衰减,平均分布半衰期为2.34(标准误均值0.16)小时,平均处置半衰期为17.6(标准误均值1.1)小时。因此,其作用持续时间比肝素长得多。血浆抗Xa反应与剂量增加呈线性关系,尽管存在一些变异性,部分原因仅由体重或体表面积差异解释。静脉推注ORG 10172耐受性良好,没有证据表明对临床化学或血液学检查有不良影响。