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在日立912分析仪上开发针对14种人血清蛋白的免疫比浊测定法。

Development of immunoturbidimetric assays for fourteen human serum proteins on the Hitachi 912.

作者信息

Ledue Thomas B, Collins Marilyn F, Ritchie Robert F

机构信息

Foundation for Blood Research, Scarborough, ME 04070-0190, USA.

出版信息

Clin Chem Lab Med. 2002 May;40(5):520-8. doi: 10.1515/CCLM.2002.090.

DOI:10.1515/CCLM.2002.090
PMID:12113299
Abstract

Many laboratories rely on dedicated nephelometers or turbidimeters and commercial reagent kits for the evaluation of serum proteins. However, with growing emphasis on cost containment, laboratories are forced to seek additional operational efficiencies by capitalizing on the use of existing analyzers whenever possible. In the present paper we describe the development of immunoturbidimetric assays for routine analysis of 14 human serum proteins (alpha1-antitrypsin, alpha2-macroglobulin, albumin, apolipoproteins Al and B, complement components 3 and 4, haptoglobin, immunoglobulins A, G, and M, orosomucoid, prealbumin, and transferrin) on the Hitachi 912, a general chemistry analyzer. With this system, we obtained excellent precision at levels corresponding to low, normal, and high physiologic concentrations of each protein (within-run imprecision CVs < or = 3.4%, total imprecision CVs < or = 4.1%). Linearity for each method was within 5% of the expected value throughout the calibration range, and method comparisons with either the Roche turbidimetric or Dade Behring nephelometric assays were in good agreement (r >0.97). We observed no significant interference from bilirubin (up to 718 micromol/l), hemoglobin (up to 8 g/l), triglyceride (up to 14.7 mmol/l) or rheumatoid factor (up to 4,140 IU/ml). Calibration for the 14 protein assays was stable for at least 7 days and onboard refrigerated reagents were stable for at least 3 months. The instrument's automated sample re-run feature minimized sample handling and helped to conserve specimens. In conclusion, the newly developed assays on the Hitachi 912 offer high throughput (>250 tests per hour) without the associated cost of a dedicated instrument for protein assays.

摘要

许多实验室依靠专用的比浊计或浊度仪以及商业试剂盒来评估血清蛋白。然而,随着对成本控制的日益重视,实验室被迫尽可能利用现有分析仪来提高运营效率。在本文中,我们描述了在日立912型通用化学分析仪上开发的免疫比浊法,用于常规分析14种人血清蛋白(α1-抗胰蛋白酶、α2-巨球蛋白、白蛋白、载脂蛋白A1和B、补体成分3和4、触珠蛋白、免疫球蛋白A、G和M、类粘蛋白、前白蛋白和转铁蛋白)。使用该系统,我们在每种蛋白质的低、正常和高生理浓度水平上都获得了出色的精密度(批内不精密度CVs≤3.4%,总不精密度CVs≤4.1%)。在整个校准范围内,每种方法的线性度在预期值的5%以内,并且与罗氏比浊法或达德拜林比浊法的方法比较结果吻合良好(r>0.97)。我们未观察到胆红素(高达718微摩尔/升)、血红蛋白(高达8克/升)、甘油三酯(高达14.7毫摩尔/升)或类风湿因子(高达4140国际单位/毫升)的显著干扰。14种蛋白质测定的校准至少稳定7天,机载冷藏试剂至少稳定3个月。该仪器的自动样品重新运行功能最大限度地减少了样品处理,并有助于保存标本。总之,在日立912上新开发的测定方法提供了高通量(每小时>250次检测),而无需专用蛋白质测定仪器的相关成本。

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