Automated Multiplexed ECL Immunoarrays for Cancer Biomarker Proteins

化学 微流控 多路复用 前列腺癌 生物标志物 试剂 谷氨酸羧肽酶Ⅱ 前列腺特异性抗原 微处理器 蛋白质微阵列 抗原 纳米技术 癌症 计算机硬件 计算机科学 微阵列 免疫学 生物化学 材料科学 生物 医学 内科学 电信 基因表达 物理化学 基因
作者
Karteek Kadimisetty,Spundana Malla,Naimish P. Sardesai,Amit A. Joshi,Ronaldo C. Faria,Norman H. Lee,James F. Rusling
出处
期刊:Analytical Chemistry [American Chemical Society]
卷期号:87 (8): 4472-4478 被引量:116
标识
DOI:10.1021/acs.analchem.5b00421
摘要

Point-of-care diagnostics based on multiplexed protein measurements face challenges of simple, automated, low-cost, and high-throughput operation with high sensitivity. Herein, we describe an automated, microprocessor-controlled microfluidic immunoarray for simultaneous multiplexed detection of small protein panels in complex samples. A microfluidic sample/reagent delivery cassette was coupled to a 30-microwell detection array to achieve sensitive detection of four prostate cancer biomarker proteins in serum. The proteins are prostate specific antigen (PSA), prostate specific membrane antigen (PSMA), platelet factor-4 (PF-4), and interlukin-6 (IL-6). The six channel system is driven by integrated micropumps controlled by an inexpensive programmable microprocessor. The reagent delivery cassette and detection array feature channels made by precision-cut 0.8 mm silicone gaskets. Single-wall carbon nanotube forests were grown in printed microwells on a pyrolytic graphite detection chip and decorated with capture antibodies. The detection chip is housed in a machined microfluidic chamber with a steel metal shim counter electrode and Ag/AgCl reference electrode for electrochemiluminescent (ECL) measurements. The preloaded sample/reagent cassette automatically delivers samples, wash buffers, and ECL RuBPY-silica-antibody detection nanoparticles sequentially. An onboard microcontroller controls micropumps and reagent flow to the detection chamber according to a preset program. Detection employs tripropylamine, a sacrificial reductant, while applying 0.95 V vs Ag/AgCl. Resulting ECL light was measured by a CCD camera. Ultralow detection limits of 10-100 fg mL(-1) were achieved in simultaneous detection of the four protein in 36 min assays. Results for the four proteins in prostate cancer patient serum gave excellent correlation with those from single-protein ELISA.
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