Chi D S, Chen J P
Thromb Haemost. 1976 Apr 30;35(2):423-36.
A new modification of hemagglutination inhibition immunoassay for measuring fibrinogen/fibrin degradation products (FDP) using glutaraldehyde as a coupling reagent was introduced. This method was compared with the tanned-red-cell hemagglutination inhibition immunoassay (TRCHII). Sheep erythrocytes (SRBC) were sensitized with fragment D or E, respectively. The procedure of sensitizing SRBC is simple and can be achieved within 2 hrs. The sensitized SRBC stored at 4 degrees C for 6 months did not lose their activities. The sensitivities for assaying D and E relative FDP were 0.32 mug/ml, respectively, which were slightly better than those of TRCHII. This represents the first adaptation of glutaraldehyde erythrocyte hemagglutination inhibition immunoassay (GEHII) for the estimation of FDP employing either microtiter plate or test tube. The microtechnique and test tube method were found to be essentially equivalent. The FDP level in the sera of normal individuals and patients suspected of elevation of FDP were assayed by both TRCHII and GEHII. By linear least squares analysis, the results show a significant correlation between these two methods. These results indicate GEHII is a simple, rapid and sensitive immunoassay for FDP in human serum.
介绍了一种以戊二醛作为偶联剂,用于检测纤维蛋白原/纤维蛋白降解产物(FDP)的血凝抑制免疫测定法的新改良方法。该方法与鞣酸红细胞血凝抑制免疫测定法(TRCHII)进行了比较。分别用D片段或E片段致敏绵羊红细胞(SRBC)。致敏SRBC的操作简单,可在2小时内完成。在4℃下储存6个月的致敏SRBC未丧失其活性。检测D和E相关FDP的灵敏度分别为0.32μg/ml,略优于TRCHII。这是首次将戊二醛红细胞血凝抑制免疫测定法(GEHII)应用于采用微量滴定板或试管检测FDP。发现微量技术和试管法基本等效。采用TRCHII和GEHII对正常个体血清及疑似FDP升高患者的血清中的FDP水平进行检测。通过线性最小二乘法分析,结果表明这两种方法之间存在显著相关性。这些结果表明,GEHII是一种用于检测人血清中FDP的简单、快速且灵敏的免疫测定法。