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一种用于标准化肝素制剂的体内测定法。

A in vivo assay for standardizing heparin preparations.

作者信息

Pomeroy A R

出版信息

Thromb Haemost. 1979 May 25;41(3):576-82.

PMID:462423
Abstract

The limitations of currently used in vitro assays of heparin have demonstrated the need for an in vivo method suitable for routine use. The in vivo method which is described in this paper uses, for each heparin preparation, four groups of five mice which are injected intravenously with heparin according to a "2 and 2 dose assay" procedure. The method is relatively rapid, requiring 3 to 4 hours to test five heparin preparations against a standard preparation of heparin. Levels of accuracy and precision acceptable for the requirements of the British Pharmacopoeia are obtained by combining the results of 3 to 4 assays of a heparin preparation. The similarity of results obtained in vivo method and in vitro method of the British Pharmacopoeia for heparin preparations of lung and mucosal origin validates this in vivo method and, conversely, demonstrates that the in vitro method of the British Pharmacopoeia gives a reliable estimation of the in vivo activity of heparin.

摘要

目前肝素体外检测方法的局限性表明需要一种适用于常规使用的体内方法。本文所述的体内方法针对每种肝素制剂,使用四组每组五只小鼠,按照“2和2剂量检测”程序静脉注射肝素。该方法相对快速,测试五种肝素制剂与一种肝素标准制剂相对比需要3至4小时。通过合并肝素制剂3至4次检测的结果,可获得符合英国药典要求的准确度和精密度水平。体内方法与英国药典肝素肺源和粘膜源制剂体外方法所得结果的相似性验证了该体内方法,反之,也证明英国药典的体外方法能够可靠地估计肝素的体内活性。

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