Nanodiagnostics: A new frontier for clinical laboratory medicine

被引:126
作者
Azzazy, Hassan M. E.
Mansour, Mai M. H.
Kazmierczak, Steven C.
机构
[1] Amer Univ Cairo, Dept Chem, Cairo, Egypt
[2] Amer Univ Cairo, Sci & Technol Res Ctr, Cairo, Egypt
[3] Oregon Hlth & Sci Univ, Dept Pathol, Portland, OR 97201 USA
关键词
D O I
10.1373/clinchem.2006.066654
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Background: The use of nanotechnologies for diagnostic applications shows great promise to meet the rigorous demands of the clinical laboratory for sensitivity and cost-effectiveness. New nanodiagnostic tools include quantum dots (QDs), gold nanoparticles, and cantilevers. QDs, which are the most promising nanostructures for diagnostic applications, are semiconductor nanocrystals characterized by high photostability, single-wavelength excitation, and size-tunable emission. QDs and magnetic nanoparticles can be used for barcoding of specific analytes. Gold and magnetic nanoparticles are key components of the bio-barcode assay, which has been proposed as a future alternative to the PCR. Methods: We examined articles published over the past 10 years investigating the use of QDs, gold nanoparticles, cantilevers, and other nanotechnologies in promising diagnostic applications. Results: Several nanodiagnostic assays have been developed, including a QD-based assay capable of detecting biotinylated prostate-specific antigen (PSA) at 0.38 ng/L, a bio-barcode assay capable of detecting 30 amol/L PSA in a 10-mu L sample, and another able to detect 50 molecules of the Alzheimer marker amyloid beta-derived diffusible ligand in 10 mu L of cerebrospinal fluid. Conclusions: Nanodiagnostics promise increased sensitivity, multiplexing capabilities, and reduced cost for many diagnostic applications as well as intracellular imaging. Further work is needed to fully optimize these diagnostic nanotechnologies for clinical laboratory setting and to address the potential health and environmental risks related to QDs. (c) 2006 American Association for Clinical Chemistry.
引用
收藏
页码:1238 / 1246
页数:9
相关论文
共 50 条
[41]   Three-layer composite magnetic nanoparticle probes for DNA [J].
Stoeva, SI ;
Huo, FW ;
Lee, JS ;
Mirkin, CA .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2005, 127 (44) :15362-15363
[42]   Homogeneous detection of unamplified genomic DNA sequences based on colorimetric scatter of gold nanoparticle probes [J].
Storhoff, JJ ;
Lucas, AD ;
Garimella, V ;
Bao, YP ;
Müller, UR .
NATURE BIOTECHNOLOGY, 2004, 22 (07) :883-887
[43]   Scanometric DNA array detection with nanoparticle probes [J].
Taton, TA ;
Mirkin, CA ;
Letsinger, RL .
SCIENCE, 2000, 289 (5485) :1757-1760
[44]   A general strategy for nanocrystal synthesis [J].
Wang, X ;
Zhuang, J ;
Peng, Q ;
Li, YD .
NATURE, 2005, 437 (7055) :121-124
[45]   Fluorescence spectroscopy of single biomolecules [J].
Weiss, S .
SCIENCE, 1999, 283 (5408) :1676-1683
[46]   Engineered nanomaterials for biophotonics applications: Improving sensing, imaging, and therapeutics [J].
West, JL ;
Halas, NJ .
ANNUAL REVIEW OF BIOMEDICAL ENGINEERING, 2003, 5 :285-292
[47]   Bioassay of prostate-specific antigen (PSA) using microcantilevers [J].
Wu, GH ;
Datar, RH ;
Hansen, KM ;
Thundat, T ;
Cote, RJ ;
Majumdar, A .
NATURE BIOTECHNOLOGY, 2001, 19 (09) :856-860
[48]   Immunofluorescent labeling of cancer marker Her2 and other cellular targets with semiconductor quantum dots [J].
Wu, XY ;
Liu, HJ ;
Liu, JQ ;
Haley, KN ;
Treadway, JA ;
Larson, JP ;
Ge, NF ;
Peale, F ;
Bruchez, MP .
NATURE BIOTECHNOLOGY, 2003, 21 (01) :41-46
[49]   Homogeneous point mutation detection by quantum dot-mediated two-color fluorescence coincidence analysis [J].
Yeh, HC ;
Ho, YP ;
Shih, IM ;
Wang, TH .
NUCLEIC ACIDS RESEARCH, 2006, 34 (05)
[50]   Multiplexed electrical detection of cancer markers with nanowire sensor arrays [J].
Zheng, GF ;
Patolsky, F ;
Cui, Y ;
Wang, WU ;
Lieber, CM .
NATURE BIOTECHNOLOGY, 2005, 23 (10) :1294-1301