On-line protein capture on magnetic beads for ultrasensitive microfluidic immunoassays of cancer biomarkers

被引:99
作者
Otieno, Brunah A. [1 ]
Krause, Colleen E. [1 ]
Latus, Alina [1 ,2 ]
Chikkaveeraiah, Bhaskara V. [1 ]
Faria, Ronaldo C. [1 ,3 ]
Rusling, James F. [1 ,4 ,5 ,6 ]
机构
[1] Univ Connecticut, Dept Chem, 55 North Eagleville Rd, Storrs, CT 06269 USA
[2] Romanian Acad, Inst Phys Chem I Murgulescu, Bucharest 060021, Romania
[3] Univ Fed Sao Carlos, Dept Quim, BR-13565905 Sao Paulo, SP, Brazil
[4] Univ Connecticut, Ctr Hlth, Dept Cell Biol, Farmington, CT 06232 USA
[5] Univ Connecticut, Inst Mat Sci, Storrs, CT 06269 USA
[6] Natl Univ Ireland Galway, Sch Chem, Galway, Ireland
关键词
Protein detection; Cancer biomarkers; Magentic beads; Immunoarray; Microfluidics; PROSTATE-SPECIFIC ANTIGEN; SQUAMOUS-CELL CARCINOMA; GROWTH-FACTOR RECEPTOR; BICINCHONINIC ACID; HEAD; NECK; POINT; SERUM; AMPLIFICATION; INTERLEUKIN-8;
D O I
10.1016/j.bios.2013.09.054
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Accurate, sensitive, multiplexed detection of biomarker proteins holds significant promise for personalized cancer diagnostics. Here we describe the incorporation of a novel on-line chamber to capture cancer biomarker proteins on magnetic beads derivatized with 300,000 enzyme labels and 40,000 antibodies into a modular microfluidic immunoarray. Capture and detection chambers are produced from PDMS on machined molds and do not require lithography. Protein analytes are captured from serum or other biological samples in the stirred capture chamber on the beads held in place magnetically. The beads are subsequently washed free of sample components, and wash solutions sent to waste. Removal of the magnet and valve switching sends the magnetic bead-protein bioconjugates into a detection chamber where they are captured on 8 antibody-decorated gold nanoparticle-film sensors and detected amperometrically. Most steps in the immunoassay including protein capture, washing and measurement are incorporated into the device. In simultaneous assays, the microfluidic system gave ultralow detection limits of 5 fg mL(-1) for interleukin-6 (IL-6) and 7 fg mL(-1) for IL-8 in serum. Accuracy was demonstrated by measuring IL-6 and IL-8 in conditioned media from oral cancer cell lines and showing good correlations with standard ELISAs. The on-line capture chamber facilitates rapid, sensitive, repetitive protein separation and measurement in 30 min in a semi-automated system adaptable to multiplexed protein detection. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:268 / 274
页数:7
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