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鱼精蛋白肝素中和能力的测定。

Measurement of the heparin neutralizing capacity of protamine.

作者信息

Graham D T, Pomeroy A R, Smythe D B

出版信息

Thromb Haemost. 1979 May 25;41(3):583-9.

PMID:462424
Abstract

Several methods of estimating the heparin neutralizing capacity of protamine were investigated for their reliability and practicability. The results from two chemical methods were compared with those from two in vitro biological assays, one of which was the method of the British Pharmacopoeia (1973). An in vivo method using mice was used to assess the accuracy of the in vitro test methods. Three standard heparin preparations were tested against the W.H.O. 1st International Reference Preparation for Protamine. Two of the heparin preparations were of mucosal origin, one of which was the 3rd International Standard, and the third heparin preparation was of lung origin (the 2nd International Standard for Heparin). The mean neutralization values (all methods) of heparin by protamine for a House Reference Preparation and the 3rd and 2nd International Standards for Heparin were 95.8, 109.8 and 89.9 units per mg of Protamine, respectively. All methods read the House Reference Preparation to have a lower value than the 3rd International Standard, which had a higher value than the 2nd International Standard for Heparin. There was a constant relationship between the results of any one method and those of another. The chemical and in vitro biological methods gave results of comparable precision although the latter required a greater degree of technical skill and time to perform.

摘要

研究了几种评估鱼精蛋白肝素中和能力的方法的可靠性和实用性。将两种化学方法的结果与两种体外生物学测定方法的结果进行了比较,其中一种是《英国药典》(1973年版)的方法。采用小鼠体内方法评估体外试验方法的准确性。针对世界卫生组织第一国际鱼精蛋白参考制剂对三种标准肝素制剂进行了测试。其中两种肝素制剂来源于黏膜,一种是第三国际标准品,第三种肝素制剂来源于肺(第二国际肝素标准品)。鱼精蛋白对一种内部参考制剂以及第三和第二国际肝素标准品的肝素平均中和值(所有方法)分别为每毫克鱼精蛋白95.8、109.8和89.9单位。所有方法均显示内部参考制剂的值低于第三国际标准品,而第三国际标准品的值高于第二国际肝素标准品。任何一种方法的结果与另一种方法的结果之间存在恒定关系。化学方法和体外生物学方法给出的结果精度相当,尽管后者需要更高的技术水平和更多的时间来操作。

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