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肿瘤相关抗原免疫放射分析中造影剂的体外效应

In vitro effect of contrast agents during immunoradiometric assay for tumour-associated antigens.

作者信息

Watanabe N, Oriuchi N, Higuchi T, Yukihiro M, Fukushima Y, Tomiyoshi K, Hirano T, Inoue T, Endo K

机构信息

Department of Nuclear Medicine, Gunma University School of Medicine, Japan.

出版信息

Nucl Med Commun. 1998 Jan;19(1):63-70. doi: 10.1097/00006231-199801000-00009.

Abstract

The aim of this study was to investigate if contrast agents interfere with the performance of an immunoradiometric assay (IRMA) in vitro for serum tumour-associated antigen. Each of five carcinoembryonic antigen (CEA)-positive sera, CA-130-positive sera and tissue polypeptide antigen (TPA)-positive sera was mixed with six contrast agents: Ioversol 350, Iopamidol 370, Iomeprol 300, Iomeprol 400, Iohexol 300 and Gadopenteic acid in 50:50, 50:20, 50:5.0, 50:1.0, 50:0.5 and 50:0.1 microl proportions. Following IRMA, the interference of binding rates in each mixture was calculated, and the serum concentrations of CEA, CA-130 and TPA were estimated and compared with the originals. All contrast agents used were able to inhibit the binding rate with IRMA and the inhibition rates were in proportion to the amount of contrast agent. The detection of serum concentrations of CEA, CA-130 and TPA was significantly inhibited in the mixtures with more than 5.0 microl of contrast agent in all cases. Apart from Iomeprol 400, there was no significant inhibition of detection at the lowest concentrations of contrast agents. Iomeprol 400 was the strongest inhibitor and Gadopenteic acid the weakest inhibitor for each IRMA of the contrast agents employed. In conclusion, our results demonstrate that contrast agents may reduce the immunoreaction of antibody and antigen and lead to in vitro inhibition during immunoassays. It would be unwise to perform any plasma/serum immunoassay on a sample collected within 24 h of the administration of contrast agent considering the pharmacokinetics.

摘要

本研究旨在调查造影剂是否会在体外干扰血清肿瘤相关抗原的免疫放射分析(IRMA)。将5份癌胚抗原(CEA)阳性血清、CA - 130阳性血清和组织多肽抗原(TPA)阳性血清分别与6种造影剂以50:50、50:20、50:5.0、50:1.0、50:0.5和50:0.1微升的比例混合,这6种造影剂分别为碘海醇350、碘帕醇370、碘美普尔300、碘美普尔400、碘克沙醇300和钆喷酸。进行IRMA后,计算每种混合物中结合率的干扰情况,并估计CEA、CA - 130和TPA的血清浓度并与原液进行比较。所有使用的造影剂均能抑制与IRMA的结合率,且抑制率与造影剂的量成正比。在所有情况下,造影剂用量超过5.0微升的混合物中,CEA、CA - 130和TPA血清浓度的检测均受到显著抑制。除碘美普尔400外,在最低造影剂浓度下检测未受到显著抑制。在所使用的造影剂中,碘美普尔400对每种IRMA的抑制作用最强,钆喷酸最弱。总之,我们的结果表明,造影剂可能会降低抗体与抗原的免疫反应,并在免疫测定过程中导致体外抑制。考虑到药代动力学,在注射造影剂后24小时内采集的样本上进行任何血浆/血清免疫测定都是不明智的。

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