Danielsson B, Gadd K, Mattiasson B, Mosbach K
Clin Chim Acta. 1977 Dec 1;81(2):163-75. doi: 10.1016/0009-8981(77)90008-0.
An enzyme thermistor assay for serum glucose is described. The glucose present in the sample is reacted in a small column containing glucose oxidase immobilized to controlled pore glass (single thermistor device). The heat produced in the primary reaction is measured directly in the column without any need for coupling reactions. The useful linear range is 0.01-0.45 mM glucose, permitting 50-fold dilution of serum samples. Advantages are low enzyme cost, due to the immobilization, insensitivity for the color or any turbidity of the sample, and no requirement for coenzyme or any ancillary reaction. Improved sensitivity and extended linear range (0.01--0.9 mM) can be attained through a secondary reaction using catalase. The application to glucose analysis of a split-flow enzyme thermistor equipped with a reference column to eliminate unspecific heat effects is also described. The enzyme thermistor determinations were also compared with a spectrophotometric continuous flow technique using a small column with immobilized glucose oxidase and 4-aminoantipyrine and phenol as color reagents.
本文描述了一种用于血清葡萄糖检测的酶热敏电阻测定法。样品中的葡萄糖在一个装有固定在可控孔径玻璃上的葡萄糖氧化酶的小柱中进行反应(单热敏电阻装置)。初级反应中产生的热量可直接在柱中测量,无需偶联反应。有用的线性范围是0.01 - 0.45 mM葡萄糖,允许血清样品进行50倍稀释。优点包括由于固定化导致酶成本低、对样品的颜色或任何浊度不敏感,以及不需要辅酶或任何辅助反应。通过使用过氧化氢酶的二级反应可以提高灵敏度并扩展线性范围(0.01 - 0.9 mM)。还描述了一种配备参考柱以消除非特异性热效应的分流酶热敏电阻在葡萄糖分析中的应用。酶热敏电阻测定法还与使用装有固定化葡萄糖氧化酶以及4 - 氨基安替比林和苯酚作为显色试剂的小柱的分光光度连续流动技术进行了比较。