元素标记免疫分析法联合电感耦合血浆质谱法在HCG检测中的应用

Q4 Health Professions
Danna Pu, W. Jiang, Xinyu Wen, Guang-hong Guo, Ping Li, Chengbin Wang
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引用次数: 0

摘要

目的建立一种基于电感耦合等离子体质谱(ICP-MS)的免疫分析法定量检测人绒毛膜促性腺激素(HCG)的方法,并评价该方法的临床适用性。方法选择Sm作为元素标签,采用双抗体夹心法建立HCG定量检测体系。优化了生物素化抗体的用量和反应时间。根据美国临床与实验室标准协会(CLSI)的EP文件及相关标准,在建立方法后对分析性能进行评价,包括空白限(LOB)、线性度、精密度、回收率、交叉反应性和干扰试验。并与电化学免疫分析法(ECLIA)进行了比较,对88例临床样品进行了检测。结果优化后总流程在30min内完成,最佳生物素化抗体用量为0.5 μl。LOB为0.29 mIU/ml。在1.16 ~ 8 365.62 mIU/ml范围内线性良好,线性相关系数大于0.995 (R2=0.998 0),加样回收率为97.53% ~ 102.01%。高值样品和低值样品的测定内变异系数和测定间变异系数均小于10%。与黄体生成素(LH)、促卵泡激素(FSH)、促甲状腺激素(TSH)无明显交叉反应。不同浓度干扰物质引起的干扰偏置小于10%。与ECLIA法进行临床样品检测相比,本方法具有显著的相关性(R2=0.960 0)。结论ICP-MS碱基免疫分析法检测HCG具有较好的准确性、较高的灵敏度和特异性,分析性能验证结果符合临床要求,为本方法的临床应用提供了实验依据。关键词:绒毛膜促性腺激素;免疫测定;分光光度法、原子;质谱分析
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Application of element-tagged immunoassay combined with inductively coupled plasma mass spectrometry in HCG detection
Objective To establish an inductively coupled plasma mass spectrometry (ICP-MS) based immunoassay method for the quantitative detection of human chorionic gonadotropin (HCG), and evaluate the clinical applicability of this method. Methods Sm was selected as element tags, and the HCG quantitative detection system was established by double antibody sandwich method. The dosage of biotinylated antibody and reaction time were optimized. According to EP documents of Clinical and Laboratory Standards Institute (CLSI) and related standards, the analytical performance was evaluated after the establishment of the assay, including the limit of blank (LOB), linearity, precision, recovery, cross reactivity and interference test. And 88 clinical samples were measured using the new method compared to the electrochemical immunoassay (ECLIA) method. Results Total process completed within 30 min after optimization, and the optimal biotinylated antibody dosage was 0.5 μl. The LOB was 0.29 mIU/ml. The linearity was good within the range of 1.16-8 365.62 mIU/ml with the linear correlation coefficient greater than 0.995 (R2=0.998 0), the recovery was 97.53%-102.01%. Both intra-and inter-assay coefficients of variation of the high-value sample and the low-value sample were less than 10%. And there was no significant cross-reaction with Luteinizing hormone (LH), follicular stimulating hormone (FSH), and thyroid-stimulating hormone (TSH). The interference bias caused by different concentrations of interference substances was less than 10%. When compared with the ECLIA method for clinical sample detection, the proposed method showed a significant correlation(R2=0.960 0). Conclusion The proposed ICP-MS base immunoassay for HCG detection has good accuracy, high sensitivity and specificity, and the results of analytical performance verification meet the clinical requirements, which provides experimental basis for the clinical application of this method. Key words: Chorionic gonadotropin; Immunoassay; Spectrophotometry, atomic; Mass spectrometry
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来源期刊
中华检验医学杂志
中华检验医学杂志 Health Professions-Medical Laboratory Technology
CiteScore
0.40
自引率
0.00%
发文量
8037
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