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Detecting and quantifying multiple proteins in clinical samples in high-throughput using antibody microarrays.使用抗体微阵列以高通量方式检测和定量临床样本中的多种蛋白质。
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Protein microarray platforms for clinical proteomics.蛋白质微阵列平台在临床蛋白质组学中的应用。
Proteomics Clin Appl. 2007 Sep;1(9):934-52. doi: 10.1002/prca.200700154. Epub 2007 Aug 10.
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A panel of kallikrein markers can reduce unnecessary biopsy for prostate cancer: data from the European Randomized Study of Prostate Cancer Screening in Göteborg, Sweden.一组激肽释放酶标志物可减少前列腺癌不必要的活检:来自瑞典哥德堡前列腺癌筛查欧洲随机研究的数据。
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ENSAM: Europium Nanoparticles for Signal enhancement of Antibody Microarrays on nanoporous silicon.ENSAM:用于增强纳米多孔硅上抗体微阵列信号的铕纳米颗粒
J Proteome Res. 2008 Mar;7(3):1308-14. doi: 10.1021/pr700591j. Epub 2008 Feb 8.
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Diagnostic value of free prostate-specific antigen among men with a prostate-specific antigen level of <3.0 microg per liter.前列腺特异性抗原水平<3.0微克/升男性中游离前列腺特异性抗原的诊断价值
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Reverse-phase versus sandwich antibody microarray, technical comparison from a clinical perspective.反相抗体芯片与夹心抗体芯片:从临床角度进行的技术比较
Anal Chem. 2007 Aug 1;79(15):5817-25. doi: 10.1021/ac0709955. Epub 2007 Jul 3.
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An integrated approach to prognosis using protein microarrays and nonparametric methods.一种使用蛋白质微阵列和非参数方法进行预后评估的综合方法。
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High-speed biomarker identification utilizing porous silicon nanovial arrays and MALDI-TOF mass spectrometry.利用多孔硅纳米管阵列和基质辅助激光解吸电离飞行时间质谱进行高速生物标志物鉴定。
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多孔硅抗体微阵列用于定量分析:临床血浆样本中游离和总 PSA 的测量。

Porous silicon antibody microarrays for quantitative analysis: measurement of free and total PSA in clinical plasma samples.

机构信息

Dept. of Laboratory Medicine, Div. of Clinical Chemistry, Lund University, Skåne University Hospital, 205 02, Malmö, Sweden.

Dept. of Measurement Technology and Industrial Electrical Engineering, Div. Nanobiotechnology, Lund University, 223 63, Lund, Sweden.

出版信息

Clin Chim Acta. 2012 Dec 24;414:76-84. doi: 10.1016/j.cca.2012.08.009. Epub 2012 Aug 18.

DOI:10.1016/j.cca.2012.08.009
PMID:22921878
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4201342/
Abstract

The antibody microarrays have become widespread, but their use for quantitative analyses in clinical samples has not yet been established. We investigated an immunoassay based on nanoporous silicon antibody microarrays for quantification of total prostate-specific-antigen (PSA) in 80 clinical plasma samples, and provide quantitative data from a duplex microarray assay that simultaneously quantifies free and total PSA in plasma. To further develop the assay the porous silicon chips was placed into a standard 96-well microtiter plate for higher throughput analysis. The samples analyzed by this quantitative microarray were 80 plasma samples obtained from men undergoing clinical PSA testing (dynamic range: 0.14-44 ng/ml, LOD: 0.14 ng/ml). The second dataset, measuring free PSA (dynamic range: 0.40-74.9 ng/ml, LOD: 0.47 ng/ml) and total PSA (dynamic range: 0.87-295 ng/ml, LOD: 0.76 ng/ml), was also obtained from the clinical routine. The reference for the quantification was a commercially available assay, the ProStatus PSA Free/Total DELFIA. In an analysis of 80 plasma samples the microarray platform performs well across the range of total PSA levels. This assay might have the potential to substitute for the large-scale microtiter plate format in diagnostic applications. The duplex assay paves the way for a future quantitative multiplex assay, which analyzes several prostate cancer biomarkers simultaneously.

摘要

抗体微阵列已经得到了广泛的应用,但它们在临床样本中的定量分析尚未得到确立。我们研究了一种基于纳米孔硅抗体微阵列的免疫分析方法,用于定量分析 80 份临床血浆样本中的总前列腺特异性抗原 (PSA),并提供了来自双微阵列分析的定量数据,该分析同时定量检测血浆中的游离和总 PSA。为了进一步开发该分析方法,我们将多孔硅芯片放入标准的 96 孔微量滴定板中,以实现更高的通量分析。通过这种定量微阵列分析的样本是 80 份来自接受临床 PSA 测试的男性的血浆样本(动态范围:0.14-44 ng/ml,LOD:0.14 ng/ml)。第二个数据集,测量游离 PSA(动态范围:0.40-74.9 ng/ml,LOD:0.47 ng/ml)和总 PSA(动态范围:0.87-295 ng/ml,LOD:0.76 ng/ml),也来自临床常规。定量的参考是一种商业上可用的检测方法,即 ProStatus PSA Free/Total DELFIA。在对 80 份血浆样本的分析中,微阵列平台在总 PSA 水平范围内表现良好。该分析方法有可能替代诊断应用中的大规模微量滴定板格式。双分析为未来同时分析多个前列腺癌生物标志物的定量多重分析铺平了道路。