Locke Matthew, Rigsby Peter, Longstaff Colin
Haemostasis Section, Biotherapeutics Division, National Institute for Biological Standards and Control, South Mimms, Herts, UK.
Biostatistics Section, National Institute for Biological Standards and Control, South Mimms, Herts, UK.
J Thromb Haemost. 2020 Jun;18(6):1501-1505. doi: 10.1111/jth.14787.
Streptokinase is used worldwide as a cost-effective treatment for acute myocardial infarction. Manufacturers use the World Health Organization (WHO) International Standard (IS) for Streptokinase to potency label their products, ensuring consistent, safe, and effective dosing. Stocks of the third IS for streptokinase (coded 00/464) are running low, and an international collaborative study was organized to calibrate a replacement. A total of 15 laboratories from nine countries took part, using chromogenic and/or fibrin clot lysis methods to determine the potency of two candidate preparations, coded 16/356 (sample B) and 16/358 (sample C), relative to the third IS (00/464). A third sample (88/824, sample A), which was used in the collaborative studies to establish the second and third IS, was also included. There was good agreement in potency estimates from different assay methods and low variability both within and between laboratories. Long-term stability modeling indicated the candidates are very stable. Comparison of potency estimates for 88/824 (sample A) with potencies calculated in previous studies revealed a variability of only 1.9% over the course of three collaborative studies spanning 30 years and more than 50 years of streptokinase standardization. This indicates excellent continuity of the International Unit (IU) and assay methods. Following agreement by study participants and Scientific and Standardization Committee experts of the International Society on Thrombosis and Haemostasis, the WHO Expert Committee on Biological Standardization established 16/358 (sample C) as the fourth IS for Streptokinase with a potency of 1013 IU per ampoule in October 2019.
链激酶在全球范围内被用作治疗急性心肌梗死的一种经济有效的药物。制造商使用世界卫生组织(WHO)链激酶国际标准品(IS)对其产品进行效价标注,以确保给药剂量的一致性、安全性和有效性。链激酶的第三个国际标准品(编号00/464)库存正在减少,因此组织了一项国际合作研究来校准替代品。来自9个国家的15个实验室参与其中,使用显色法和/或纤维蛋白凝块溶解法来确定两种候选制剂(编号16/356,样品B;编号16/358,样品C)相对于第三个国际标准品(00/464)的效价。还纳入了第三个样品(88/824,样品A),该样品曾用于合作研究以建立第二个和第三个国际标准品。不同检测方法的效价估计结果具有良好的一致性,并且实验室内部和实验室之间的变异性都很低。长期稳定性模型表明候选品非常稳定。将88/824(样品A)的效价估计值与先前研究中计算的效价进行比较,发现在跨越30年以及链激酶标准化超过50年的三项合作研究过程中,变异性仅为1.9%。这表明国际单位(IU)和检测方法具有出色的连续性。在研究参与者以及国际血栓与止血学会科学与标准化委员会专家达成一致后,世界卫生组织生物标准化专家委员会于2019年10月将16/358(样品C)确立为链激酶的第四个国际标准品,每安瓿效价为1013 IU。