In vivo molecular and cellular imaging with quantum dots

被引:981
作者
Gao, XH
Yang, LL
Petros, JA
Marshal, FF
Simons, JW
Nie, SM
机构
[1] Emory Clin, Dept Biomed Engn, Atlanta, GA 30322 USA
[2] Georgia Inst Technol, Atlanta, GA 30322 USA
[3] Emory Clin, Dept Chem, Atlanta, GA 30322 USA
[4] Emory Clin, Dept Hematol & Oncol, Atlanta, GA 30322 USA
[5] Emory Clin, Winship Canc Inst, Atlanta, GA 30322 USA
[6] Emory Clin, Dept Surg, Atlanta, GA 30322 USA
[7] Emory Clin, Dept Urol, Atlanta, GA 30322 USA
[8] Hunan Univ, Biotechnol & Bioengn Ctr, Changsha, Peoples R China
基金
美国国家卫生研究院;
关键词
D O I
10.1016/j.copbio.2004.11.003
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Quantum dots (QDs), tiny light-emitting particles on the nanometer scale, are emerging as a new class of fluorescent probe for in vivo biomolecular and cellular imaging. In comparison with organic dyes and fluorescent proteins, QDs have unique optical and electronic properties: size-tunable light emission, improved signal brightness, resistance against photobleaching, and simultaneous excitation of multiple fluorescence colors. Recent advances have led to the development of multifunctional nanoparticle probes that are very bright and stable under complex in vivo conditions. A new structural design involves encapsulating luminescent QDs with amphiphilic block copolymers and linking the polymer coating to tumor-targeting ligands and drug delivery functionalities. Polymer-encapsulated QDs are essentially nontoxic to cells and animals, but their long-term in vivo toxicity and degradation need more careful study. Bioconjugated QDs have raised new possibilities for ultrasensitive and multiplexed imaging of molecular targets in living cells, animal models and possibly in humans.
引用
收藏
页码:63 / 72
页数:10
相关论文
共 61 条
[1]   Nanocrystal targeting in vivo [J].
Åkerman, ME ;
Chan, WCW ;
Laakkonen, P ;
Bhatia, SN ;
Ruoslahti, E .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (20) :12617-12621
[2]   Semiconductor clusters, nanocrystals, and quantum dots [J].
Alivisatos, AP .
SCIENCE, 1996, 271 (5251) :933-937
[3]   The use of nanocrystals in biological detection [J].
Alivisatos, P .
NATURE BIOTECHNOLOGY, 2004, 22 (01) :47-52
[4]   Photopolymerizable degradable polyanhydrides with osteocompatibility [J].
Anseth, KS ;
Shastri, VR ;
Langer, R .
NATURE BIOTECHNOLOGY, 1999, 17 (02) :156-159
[5]   Alloyed semiconductor quantum dots: Tuning the optical properties without changing the particle size [J].
Bailey, RE ;
Nie, SM .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2003, 125 (23) :7100-7106
[6]   Noninvasive imaging of quantum dots in mice [J].
Ballou, B ;
Lagerholm, BC ;
Ernst, LA ;
Bruchez, MP ;
Waggoner, AS .
BIOCONJUGATE CHEMISTRY, 2004, 15 (01) :79-86
[7]   Targeting metastatic prostate cancer with radiolabeled monoclonal antibody J591 to the extracellular domain of prostate specific membrane antigen [J].
Bander, NH ;
Trabulsi, EJ ;
Kostakoglu, L ;
Yao, D ;
Vallabhajosula, S ;
Smith-Jones, P ;
Joyce, MA ;
Milowsky, M ;
Nanus, DM ;
Goldsmith, SJ .
JOURNAL OF UROLOGY, 2003, 170 (05) :1717-1721
[8]   Semiconductor nanocrystals as fluorescent biological labels [J].
Bruchez, M ;
Moronne, M ;
Gin, P ;
Weiss, S ;
Alivisatos, AP .
SCIENCE, 1998, 281 (5385) :2013-2016
[9]   Luminescent quantum dots for multiplexed biological detection and imaging [J].
Chan, WCW ;
Maxwell, DJ ;
Gao, XH ;
Bailey, RE ;
Han, MY ;
Nie, SM .
CURRENT OPINION IN BIOTECHNOLOGY, 2002, 13 (01) :40-46
[10]   Quantum dot bioconjugates for ultrasensitive nonisotopic detection [J].
Chan, WCW ;
Nie, SM .
SCIENCE, 1998, 281 (5385) :2016-2018