Four strategies for water transfer of oil-soluble near-infrared-emitting PbS quantum dots

被引:8
|
作者
Xue, Bing [1 ]
Cao, Jie [1 ]
Deng, Dawei [1 ,2 ]
Xia, Junfei [1 ]
Jin, Jing [1 ]
Qian, Zhiyu [3 ]
Gu, Yueqing [1 ]
机构
[1] China Pharmaceut Univ, Dept Biomed Engn, Sch Life Sci & Technol, Nanjing 210009, Peoples R China
[2] Southeast Univ, Sch Biol Sci & Med Engn, State Key Lab Bioelect, Nanjing 210096, Peoples R China
[3] Nanjing Univ Aeronaut & Astronaut, Dept Biomed Engn, Sch Automat, Nanjing 210016, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
CDTE NANOCRYSTALS; FLUORESCENT; PHOTOLUMINESCENCE; LUMINESCENCE; SYSTEM;
D O I
10.1007/s10856-012-4548-z
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
The successful transfer of oil-soluble quantum dots (QDs) into water is critical for many of their bioapplications. In this paper, the impacts of four various strategies (i.e., via micelles, nanohydrogels, amphiphilic polymers and water-soluble thiol small molecules) on the phase transfer of oil-soluble oleic acid-capped NIR-emitting PbS QDs into water were evaluated systematically. It was found that the process of water transfer and the optical property of the resulting water-soluble QDs highly hinge on the type of the phase transfer agents used due to their different interactions with QD surface. Among all these phase transfer agents, SOC micelles and glutathione (thiol) molecules are more favorable for retaining the optical property of the initial oil-soluble PbS QDs. As a result, the obtained water-soluble QDs show strong NIR fluorescence (PL QY > 30% in water). However, in the case of nanohydrogel and amphiphilic polymers, the corresponding water-soluble ones display relatively weak fluorescence emission. These results suggest fully that "correct" phase transfer agents should be selected in order to obtain high-quality water-soluble PbS QDs. The possible reasons for this obvious difference were further analyzed and revealed. Besides, the preliminary results obtained also indicate that the NIR-emitting PbS QDs will be a potential probe in the in vivo biomedical imaging of small animals.
引用
收藏
页码:723 / 732
页数:10
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