Carbon Dots as Nontoxic and High-Performance Fluorescence Imaging Agents
文献类型:期刊论文
作者 | Yang, Sheng-Tao1,2,3; Wang, Xin2,3; Wang, Haifang1,4; Lu, Fushen2,3; Luo, Pengju G.2,3; Cao, Li2,3; Meziani, Mohammed J.2,3; Liu, Jia-Hui1; Liu, Yuanfang1,4; Chen, Min5 |
刊名 | JOURNAL OF PHYSICAL CHEMISTRY C
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出版日期 | 2009-10-22 |
卷号 | 113期号:42页码:18110-18114 |
ISSN号 | 1932-7447 |
DOI | 10.1021/jp9085969 |
英文摘要 | Fluorescent carbon dots (small carbon nanoparticles with the surface passivated by oligomeric PEG molecules) were evaluated for their cytotoxicity and in vivo toxicity and also for their optical imaging performance in reference to that of the commercially supplied CdSe/ZnS quantum dots. The results suggested that the carbon dots were biocompatible, and their performance as fluorescence imaging agents was competitive. The implication to the use of carbon dots for in vitro and in vivo applications is discussed. |
语种 | 英语 |
WOS记录号 | WOS:000270671100021 |
出版者 | AMER CHEMICAL SOC |
源URL | [http://ir.iccas.ac.cn/handle/121111/68587] ![]() |
专题 | 中国科学院化学研究所 |
通讯作者 | Wang, Haifang |
作者单位 | 1.Peking Univ, Coll Chem & Mol Engn, Beijing Natl Lab Mol Sci, Beijing 100871, Peoples R China 2.Clemson Univ, Dept Chem, Clemson, SC 29634 USA 3.Clemson Univ, Lab Emerging Mat & Technol, Clemson, SC 29634 USA 4.Shanghai Univ, Inst Nanochem & Nanobiol, Shanghai 200444, Peoples R China 5.Xiamen Univ, Lab Mass Spectrometry, Dept Oceanog, Xiamen 361005, Peoples R China |
推荐引用方式 GB/T 7714 | Yang, Sheng-Tao,Wang, Xin,Wang, Haifang,et al. Carbon Dots as Nontoxic and High-Performance Fluorescence Imaging Agents[J]. JOURNAL OF PHYSICAL CHEMISTRY C,2009,113(42):18110-18114. |
APA | Yang, Sheng-Tao.,Wang, Xin.,Wang, Haifang.,Lu, Fushen.,Luo, Pengju G..,...&Sun, Ya-Ping.(2009).Carbon Dots as Nontoxic and High-Performance Fluorescence Imaging Agents.JOURNAL OF PHYSICAL CHEMISTRY C,113(42),18110-18114. |
MLA | Yang, Sheng-Tao,et al."Carbon Dots as Nontoxic and High-Performance Fluorescence Imaging Agents".JOURNAL OF PHYSICAL CHEMISTRY C 113.42(2009):18110-18114. |
入库方式: OAI收割
来源:化学研究所
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