Point-of-Care Assay Platform for Quantifying Active Enzymes to Femtomolar Levels Using Measurements of Time as the Readout

被引:82
作者
Lewis, Gregory G. [1 ]
Robbins, Jessica S. [1 ]
Phillips, Scott T. [1 ]
机构
[1] Penn State Univ, Dept Chem, University Pk, PA 16802 USA
基金
美国国家科学基金会;
关键词
PAPER-BASED MICROFLUIDICS; SELF-IMMOLATIVE POLYMERS; LATERAL-FLOW ASSAY; HYDROGEN-PEROXIDE; IMMUNOCHROMATOGRAPHIC ASSAY; ALKALINE-PHOSPHATASE; WHOLE-BLOOD; ELECTROCHEMICAL DETECTION; SIGNAL AMPLIFICATION; ANALYTICAL DEVICES;
D O I
10.1021/ac402415v
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
This Article describes a strategy for quantifying active enzyme analytes in a paper-based device by measuring the time for a reference region in the paper to turn green relative to an assay region. The assay requires a single step by the user, yet accounts for variations in sample volume, assay temperature, humidity, and contaminants in a sample that would otherwise prevent a quantitative measurement. The assay is capable of measuring enzymes in the low to mid femtomolar range with measurement times that range from similar to 30 s to similar to 15 min (lower measurement times correspond to lower quantities of the analyte). Different targets can be selected in the assay by changing a small molecule reagent within the paper-based device, and the sensitivity and dynamic range of the assays can be tuned easily by changing the composition and quantity of a signal amplification reagent or by modifying the configuration of the paper-based microfluidic device. By tuning these parameters, limits-of-detection for assays can be adjusted over an analyte concentration range of low femtomolar to low nanomolar, with dynamic ranges for the assays of at least 1 order of magnitude. Furthermore, the assay strategy is compatible with complex fluids such as serum.
引用
收藏
页码:10432 / 10439
页数:8
相关论文
共 74 条
[1]   Hybrid Nanoparticle-Liposome Detection of Phospholipase Activity [J].
Aili, Daniel ;
Mager, Morgan ;
Roche, David ;
Stevens, Molly M. .
NANO LETTERS, 2011, 11 (04) :1401-1405
[2]  
ALLEN MP, 1990, CLIN CHEM, V36, P1591
[3]   A Two-Component Small Molecule System for Activity-Based Detection and Signal Amplification: Application to the Visual Detection of Threshold Levels of Pd(II) [J].
Baker, Matthew S. ;
Phillips, Scott T. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2011, 133 (14) :5170-5173
[4]   Characterization of a monomeric Escherichia coli alkaline phosphatase formed upon a single amino acid substitution [J].
Boulanger, RR ;
Kantrowitz, ER .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (26) :23497-23501
[5]  
BOWERS GN, 1966, CLIN CHEM, V12, P70
[6]   Understanding Wax Printing: A Simple Micropatterning Process for Paper-Based Microfluidics [J].
Carrilho, Emanuel ;
Martinez, Andres W. ;
Whitesides, George M. .
ANALYTICAL CHEMISTRY, 2009, 81 (16) :7091-7095
[7]   Simple, distance-based measurement for paper analytical devices [J].
Cate, David M. ;
Dungchai, Wijitar ;
Cunningham, Josephine C. ;
Volckens, John ;
Henry, Charles S. .
LAB ON A CHIP, 2013, 13 (12) :2397-2404
[8]   Contribution of hydrogen peroxide to the cytotoxicity of green tea and red wines [J].
Chai, PC ;
Long, LH ;
Halliwell, B .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2003, 304 (04) :650-654
[9]   "Flow Valve" Microfluidic Devices for Simple, Detectorless, and Label-Free Analyte Quantitation [J].
Chatterjee, Debolina ;
Mansfield, Danielle S. ;
Anderson, Neil G. ;
Subedi, Sudeep ;
Woolley, Adam T. .
ANALYTICAL CHEMISTRY, 2012, 84 (16) :7057-7063
[10]  
CHEN R, 1987, CLIN CHEM, V33, P1521