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一种使用标记抗体测定半抗原的酶免疫分析设计。应用于甲氨蝶呤测定。

An enzyme immunoassay design using labelled antibodies for the determination of haptens. Application to methotrexate assay.

作者信息

Ferrua B, Milano G, Ly B, Guennec J Y, Masseyeff R

出版信息

J Immunol Methods. 1983 May 27;60(1-2):257-68. doi: 10.1016/0022-1759(83)90353-8.

Abstract

A competitive enzyme immunoassay with labelled antibodies has been developed for methotrexate (MTX). Methotrexate in the sample and a constant quantity of this hapten physically absorbed to polystyrene spheres through a methylated bovine albumin carrier were allowed to compete for a limiting amount of peroxidase labelled antibody. After washing, the residual enzyme activity bound to the solid phase was measured. This test was able to detect 10 fm of MTX per sample. A comparative study of this test with a commercial radioimmunoassay kit using the same antiserum and a high pressure liquid chromatography method showed that the sensitivity, specificity and precision of this test were as good as of the radioimmunoassay. The high pressure liquid chromatography method was 500 times less sensitive. Good agreement was found among the 3 methods on 83 serum samples from patients receiving methotrexate therapy.

摘要

已开发出一种用于甲氨蝶呤(MTX)的标记抗体竞争性酶免疫测定法。样品中的甲氨蝶呤以及通过甲基化牛血清白蛋白载体物理吸附到聚苯乙烯球上的恒定数量的该半抗原,被允许竞争有限量的过氧化物酶标记抗体。洗涤后,测量与固相结合的残留酶活性。该测试能够检测每个样品中10飞摩尔的MTX。使用相同抗血清的该测试与商业放射免疫测定试剂盒以及高压液相色谱法的比较研究表明,该测试的灵敏度、特异性和精密度与放射免疫测定法相当。高压液相色谱法的灵敏度低500倍。在接受甲氨蝶呤治疗的患者的83份血清样本中,这三种方法之间发现了良好的一致性。

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