一种新的化学发光免疫法测定三碘甲状腺原氨酸和甲状腺素:用实验室间调查的质控血清进行评价。

G C Zucchelli, A Pilo, S Masini, M R Chiesa, C Prontera
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引用次数: 3

摘要

最近由Byk-Sangtec diagnostics (Dietzenbach, Germany)建立的用于三碘甲状腺原氨酸和甲状腺素的化学发光免疫测定系统(LIA-mat)已被评估并与放射免疫测定法和化学发光增强酶免疫测定法(Amerlite)进行比较,使用在国家实验室间质量控制中循环的对照材料以及患者血清。LIA-mat检测是使用包被单克隆抗体和三碘甲状腺原氨酸-或甲状腺素- abei(氨基丁基异亮醇)偶联物作为示踪剂的竞争性方法。LIA-mat T3的工作范围(根据测定内精度曲线计算)从1.4 nmol/l扩展到12.3 nmol/l;测定间精密度为8.1 ~ 19.3 CV%。LIA-mat T3结果(y)与全国实验室间调查参与者的共识均值(x)的回归分析得出:y = -0.14 + 1.05 x, r = 0.95。LIA-mat T4的工作范围从33 ~ 515 nmol/l;测定间精密度为5.4 ~ 9.2 CV%。LIA-mat T4结果(y)与参与全国实验室间调查的实验室的共识均值(x)非常一致(y = 3.79 + 1.02 x, r = 0.98)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A new chemiluminescence immunoassay for triiodothyronine and thyroxine: evaluation using quality control sera assayed in an interlaboratory survey.

A recently developed chemiluminescence immunoassay system (LIA-mat) for triiodothyronine and thyroxine, set up by Byk-Sangtec Diagnostica (Dietzenbach, Germany), has been evaluated and compared with radioimmunoassays and with a chemiluminescence enhanced enzyme immunoassay (Amerlite), using control materials circulated in a national interlaboratory quality control, as well as patient sera. The LIA-mat assays are competitive methods which use coated monoclonal antibodies and triiodothyronine- or thyroxine-ABEI (aminobutylethylisoluminol) conjugate as tracers. The working range of LIA-mat T3 (computed from the within-assay precision profile) extended from 1.4 to 12.3 nmol/l; the between-assay precision was 8.1 - 19.3 CV%. Regression analysis of the LIA-mat T3 results (y) against the consensus means (x) of the participants in the national interlaboratory survey yielded: y = -0.14 + 1.05 x, r = 0.95. The working range of LIA-mat T4 extended from 33 to 515 nmol/l; the between-assay precision was 5.4 - 9.2 CV%. An excellent agreement was found between LIA-mat T4 results (y) and the consensus means (x) of the laboratories participating in the national interlaboratory survey (y = 3.79 + 1.02 x, r = 0.98).

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