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预防右旋糖酐对血清蛋白双缩脲法检测的干扰。

Prevention of interference by dextran with biuret-type assay of serum proteins.

作者信息

Flack C P, Woollen J W

出版信息

Clin Chem. 1984 Apr;30(4):559-61.

PMID:6200256
Abstract

In assay of serum proteins by use of the biuret reaction, dextran can cause turbidity by formation of an insoluble complex of dextran with copper and tartrate (or EDTA) in strongly alkaline solution. Whether or not the turbidity occurs depends on the tartrate concentration: turbidity is maximal at about 10 g/L, absent at 20 g/L or more, and only slight and delayed at 4 g/L. Two biuret reagents, containing respectively 5.6 and 22.5 g of tartrate per liter, obviate the interference, but the former is suitable only when a short (5 min) incubation is used. Both reagents show linear calibration curves and yield virtually identical results.

摘要

在利用双缩脲反应测定血清蛋白时,葡聚糖在强碱性溶液中可通过与铜和酒石酸盐(或乙二胺四乙酸)形成不溶性复合物而导致浑浊。浑浊是否出现取决于酒石酸盐浓度:在约10 g/L时浑浊度最大,在20 g/L或更高时无浑浊,在4 g/L时只有轻微且延迟的浑浊。两种双缩脲试剂,分别每升含有5.6 g和22.5 g酒石酸盐,可消除干扰,但前者仅在采用短时间(5分钟)孵育时适用。两种试剂均显示线性校准曲线,且产生的结果几乎相同。

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