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一种用于全自动临床分析仪的新型血清钙卫蛋白比浊免疫测定法。

A new turbidimetric immunoassay for serum calprotectin for fully automatized clinical analysers.

作者信息

Nilsen Tom, Sunde Kathrin, Larsson Anders

机构信息

Gentian Technology AS, Moss, Norway ; Department of Medical Sciences, Uppsala University Hospital, Uppsala, Sweden.

Gentian Technology AS, Moss, Norway.

出版信息

J Inflamm (Lond). 2015 Jul 25;12:45. doi: 10.1186/s12950-015-0090-3. eCollection 2015.

Abstract

Serum and plasma calprotectin concentration is shown to be elevated when neutrophils are activated, and may therefore be used as a marker for inflammatory diseases. A serum calprotectin immunoassay was developed based on calprotectin values observed in samples from the intensive care unit. The polyclonal avian antibodies were raised and affinity purified with calprotectin antigens. The performance was tested and it was observed that the assay was linear in the range 0.3-24.7 mg/L, the limit of quantitation was observed to be lower than 0.3 mg/L, no antigen excess was observed up to 54 mg/L, all CVs were lower than 1.8 % in the precision study, the calibration curve stability was longer than 6 weeks, and there was no significant interference detected for haemoglobin, intralipid or bilirubin. The serum calprotectin immunoassay presented in this paper performs well within the criteria carefully set from the limited clinical experience obtained in both serum and plasma. In addition it is commutable with Bühlmann MRP8/14 ELISA.

摘要

当中性粒细胞被激活时,血清和血浆中的钙卫蛋白浓度会升高,因此可用作炎症性疾病的标志物。基于在重症监护病房样本中观察到的钙卫蛋白值,开发了一种血清钙卫蛋白免疫测定法。制备了多克隆禽抗体并用钙卫蛋白抗原进行亲和纯化。对该测定法的性能进行了测试,观察到该测定法在0.3 - 24.7 mg/L范围内呈线性,定量限低于0.3 mg/L,在高达54 mg/L时未观察到抗原过量,在精密度研究中所有变异系数均低于1.8%,校准曲线稳定性超过6周,并且未检测到血红蛋白、脂肪乳剂或胆红素的显著干扰。本文介绍的血清钙卫蛋白免疫测定法在从血清和血浆中获得的有限临床经验所精心设定的标准范围内表现良好。此外,它与Bühlmann MRP8/14 ELISA具有互换性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9fa/4514941/d757d1687070/12950_2015_90_Fig1_HTML.jpg

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