Ultrasensitive detection of cytokines enabled by nanoscale ZnO arrays

被引:61
作者
Adalsteinsson, Viktor [1 ]
Parajuli, Omkar [1 ]
Kepics, Stephen [1 ]
Gupta, Abhishek [1 ]
Reeves, W. Brian [2 ]
Hahm, Jong-in [1 ]
机构
[1] Penn State Univ, Dept Chem Engn, University Pk, PA 16802 USA
[2] Penn State Univ, Milton S Hershey Med Ctr, Coll Med, Hershey, PA 17033 USA
关键词
D O I
10.1021/ac800747q
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Early detection of disease markers can provide higher diagnostic power and improve disease prognosis. We demonstrate the use of zinc oxide nanorod (ZnO NR) arrays in a straightforward, reliable, and ultrasensitive detection of the cytokines interleukin-18 and tumor necrosis factor-alpha. Specifically, we exploit the fluorescence-enhancing properties of ZnO NR platforms in cytokine assays involving both a pure buffer and urine. The detection sensitivity achieved using this ZnO NR method is in the subfemtogram. per milliliter level, which is 3-4 orders of magnitude more sensitive than conventional assay detection limits. This unparalleled detection sensitivity is achieved without the need for indirect enzyme reactions or specialized instrumentation. We highlight various advantages of using ZnO NR arrays in the ultrasensitive profiling of cytokine levels. Key advantages include robustness of NR arrays, simple and direct assay schemes, high-throughput and multiplexing capabilities, and the ability to correlate directly measured signals to cytokine levels. In conjunction with the extremely high sensitivity demonstrated in this work, our ZnO NR array-based approach may be highly beneficial in early detection of many cytokine-implicated diseases.
引用
收藏
页码:6594 / 6601
页数:8
相关论文
共 52 条
[1]   Chemokine: Receptor structure, interactions, and antagonism [J].
Allen, Samantha J. ;
Crown, Susan E. ;
Handel, Tracy M. .
ANNUAL REVIEW OF IMMUNOLOGY, 2007, 25 :787-820
[2]   The biomarkers consortium: On the critical path of drug discovery [J].
Altar, C. A. .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 2008, 83 (02) :361-364
[3]   Mechanisms of disease: Cytokine pathways and joint inflammation in rheumatoid arthritis. [J].
Choy, EHS ;
Panayi, GS .
NEW ENGLAND JOURNAL OF MEDICINE, 2001, 344 (12) :907-916
[4]   Low-temperature growth and field emission of ZnO nanowire arrays -: art. no. 044315 [J].
Cui, JB ;
Daghlian, CP ;
Gibson, UJ ;
Püsche, R ;
Geithner, P ;
Ley, L .
JOURNAL OF APPLIED PHYSICS, 2005, 97 (04)
[5]   Early kidney TNF-α expression mediates neutrophil infiltration and injury after renal ischemia-reperfusion [J].
Donnahoo, KK ;
Meng, XZ ;
Ayala, A ;
Cain, MP ;
Harken, AH ;
Meldrum, DR .
AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY, 1999, 277 (03) :R922-R929
[6]   Nanoscale ZnO-enhanced fluorescence detection of protein interactions [J].
Dorfman, Adam ;
Kumar, Nitin ;
Hahm, Jong-in .
ADVANCED MATERIALS, 2006, 18 (20) :2685-+
[7]   Highly sensitive biomolecular fluorescence detection using nanoscale ZnO platforms [J].
Dorfman, Adam ;
Kumar, Nitin ;
Hahm, Jong-in .
LANGMUIR, 2006, 22 (11) :4890-4895
[8]   Protein arrays - Growing pains [J].
Eisenstein, Michael .
NATURE, 2006, 444 (7121) :959-964
[9]   Role of CXC chemokine receptor 3 pathway in renal ischemic injury [J].
Fiorina, Paolo ;
Ansari, Mohammed Javeed ;
Jurewicz, Mollie ;
Barry, Mark ;
Ricchiuti, Vincent ;
Smith, Rex Neal ;
Shea, Susan ;
Means, Terry K. ;
Auchincloss, Hugh, Jr. ;
Luster, Andrew D. ;
Sayegh, Mohamed H. ;
Abdi, Reza .
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2006, 17 (03) :716-723
[10]   Gene therapy expressing amino-terminal truncated monocyte chemoattractant protein-1 prevents renal ischemia-reperfusion injury [J].
Furuichi, K ;
Wada, T ;
Iwata, Y ;
Kitagawa, K ;
Kobayashi, K ;
Hashimoto, H ;
Ishiwata, Y ;
Tomosugi, N ;
Mukaida, N ;
Matsushima, K ;
Egashira, K ;
Yokoyama, H .
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2003, 14 (04) :1066-1071