Design of highly emissive polymer dot bioconjugates for in vivo tumor targeting.
Design of highly emissive polymer dot bioconjugates for in vivo tumor targeting.
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DOI:
10.1002/anie.201007461
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发表时间:
2011-04-04
影响因子:
16.6
通讯作者:
Chiu, Daniel T.
中科院分区:
文献类型:
--
作者:
Wu, Changfeng;Hansen, Stacey J.;Hou, Qiong;Yu, Jiangbo;Zeigler, Maxwell;Jin, Yuhui;Burnham, Daniel R.;McNeill, Jason D.;Olson, James M.;Chiu, Daniel T.
Nanoparticle-based diagnostic and therapeutic agents have attracted considerable interest because of their potential for clinical oncology and other biomedical research.[1] Versatile nanostructures have been demonstrated for in vivo applications, such as lipid and polymeric nanocapsules for drug delivery,[2] iron oxide nanoparticles for magnetic resonance imaging,[3] gold nanoparticles for X-ray computed tomography,[4] and quantum dots (Qdots) for fluorescence imaging.[5] Qdots represent one of the exciting nanotechnologies translated to biology in the past decade. The size-tunable luminescence makes them appealing as multicolor fluorophores for biological labelling, imaging, and sensing.[6, 7] For in vivo applications, however, the intrinsic toxicity of Qdots is of critical concern,[8] which may impede their final clinical translation. Therefore, the design of bright probes with biologically benign materials is highly desirable for many in vivo clinical applications.
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