Porta M, Ricchetti I
Int J Clin Pharmacol Ther Toxicol. 1986 Dec;24(12):661-4.
Teicoplanin, a new glycopeptide antibiotic, was tested for its ability to induce agglutination and/or aggregation of fresh and fixed human platelets in vitro. Two chemically related substances, ristocetin and vancomycin, were used as controls in the same experimental conditions, as they are known to be active and, respectively, nonactive on platelets. The studies with fresh platelet rich plasma (PRP) taken from 10 healthy volunteers and the studies with fixed washed platelets (FWP) were carried out at the final concentrations of teicoplanin and vancomycin of 10, 100, 2000 and 5000 mg/l. Unlike ristocetin, teicoplanin did not exhibit any agglutinating or aggregating activity, even when tested for concentrations 50 times as high as those measured in vivo during the peak time. At high concentrations it induced protein precipitation, albeit to a lesser extent than vancomycin.
替考拉宁是一种新型糖肽类抗生素,对其在体外诱导新鲜及固定的人血小板凝集和/或聚集的能力进行了检测。在相同实验条件下,使用两种化学相关物质瑞斯托菌素和万古霉素作为对照,因为已知它们分别对血小板有活性和无活性。从10名健康志愿者采集的新鲜富血小板血浆(PRP)研究以及固定洗涤血小板(FWP)研究在替考拉宁和万古霉素的终浓度为10、100、2000和5000mg/l时进行。与瑞斯托菌素不同,替考拉宁即使在比体内峰值时间测量浓度高50倍的浓度下进行测试,也未表现出任何凝集或聚集活性。在高浓度下,它会诱导蛋白质沉淀,尽管程度比万古霉素小。