4.8 Article

Quantum-Dot-Functionalized Poly(styrene-co-acrylic acid) Microbeads: Step-Wise Self-Assembly, Characterization, and Applications for Sub-femtomolar Electrochemical Detection of DNA Hybridization

期刊

ADVANCED FUNCTIONAL MATERIALS
卷 20, 期 7, 页码 1173-1179

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adfm.200901721

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资金

  1. National Natural Science Foundation of China [20845005, 20710087, 20535010, 90713015, 20875044, 20821063]
  2. National Basic Research Program [201003732400]
  3. Important National S&T Specific Project [2009ZX10004-313]
  4. Department of Health of Jiangsu [RC2007069]
  5. Natural Science Foundation of Jiangsu [BK2008014]

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A novel nanoparticle label capable of amplifying the electrochemical signal of DNA hybridization is fabricated by functionalizing poly(styrene-co-acrylic acid) microbeads with CdTe quantum dots. CdTe-tagged polybeads are prepared by a layer-by-layer self-assembly of the CdTe quantum dots (diameter = 3.07 nm) and polyelectrolyte on the polybeads (diameter = 323 nm). The self-assembly procedure is characterized using scanning and transmission electron microscopy, and X-ray photoelectron, infrared and photoluminescence spectroscopy. The mean quantum-dot coverage is (9.54 +/- 1.2) x 10(3) per polybead. The enormous coverage and the unique properties of the quantum dots make the polybeads an effective candidate as a functionalized amplification platform for labelling of DNA or protein. Herein, as an example, the CdTe-tagged polybeads are attached to DNA probes specific to breast cancer by streptavidin biotin binding to construct a DNA biosensor. The detection of the DNA hybridization process is achieved by the square-wave voltammetry of Cd2+ after the dissolution of the CdTe tags with HNO3. The efficient carrier-bead amplification platform, coupled with the highly sensitive stripping voltammetric measurement, gives rise to a detection limit of 0.52 fmol L-1 and a dynamic range spanning 5 orders of magnitude. This proposed nanoparticle label is promising, exhibits an efficient amplification performance, and opens new opportunities for ultrasensitive detection of other biorecognition events.

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