Design of poly(ethylene glycol)/streptavidin coimmobilized upconversion nanophosphors and their application to fluorescence biolabeling

被引:98
作者
Kamimura, Masao [1 ]
Miyamoto, Daisuke [1 ,2 ]
Saito, Yu [3 ,5 ]
Soga, Kohei [3 ,5 ,6 ]
Nagasaki, Yukio [1 ,2 ,3 ,4 ,6 ,7 ]
机构
[1] Univ Tsukuba, Grad Sch Pure & Appl Sci, Tsukuba, Ibaraki 3068575, Japan
[2] Univ Tsukuba, Tsukuba Res Ctr Interdisciplinary Mat Sci TIMS, Tsukuba, Ibaraki 3068575, Japan
[3] Univ Tsukuba, Ctr Tsukuba Adv Res Alliance TARA, Tsukuba, Ibaraki 3068575, Japan
[4] Univ Tsukuba, Masters Sch Med Sci, Grad Sch Comprehens Human Sci, Tsukuba, Ibaraki 3068575, Japan
[5] Tokyo Univ Sci, Dept Mat Sci & Technol, Chiba 2788510, Japan
[6] Tokyo Univ Sci, PTRC, Chiba 2788510, Japan
[7] Natl Inst Mat Sci, Satellite Lab, Int Ctr Mat Nanoarchitecton MANA, Tsukuba, Ibaraki 3050047, Japan
关键词
D O I
10.1021/la801056c
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Infrared-to-visible upconversion phosphors (i.e., rare earth ion-doped Y2O3 nanoparticles (UNPs)) were synthesized by the homogeneous precipitation method. Because the charge on the erbium (Er) ion-doped Y2O3 (Y2O3:Er) NP (UNP1) surface is positive under neutral conditions, the UNP1 surface was electrostatically PEGylated using negatively charged poly(ethylene glycol)-b-poly (acrylic acid) (PEG-b-PAAc). The adsorption of PEG-b-PAAc was confirmed by Fourier transform infrared (FT-IR) measurements and thermal gravimetric analysis (TGA). The surface charge of the PEGylated UNP1s (PEG-UNP1s) was effectively shielded by the PEGylation. The dispersion stability of the UNP1s was also significantly improved by the PEGylation. The PEG-UNP1s were dispersed over 1 week under physiological conditions as a result of the steric repulsion between the PEG chains on the UNP1 surface. The upconversion emission spectrum of PEG-UNP1s was observed under physiological conditions and was confirmed by near-infrared excited fluorescence microscope observation. Streptavidin (SA)-installed ytterbium (Yb) and Er ion-codoped Y2O3 (Y2O3: Yb,Er) NPs (UNP2s) were prepared by the coimmobilization of PEG-b-PAAc and streptavidin. The PEG/SA coimmobilized UNP2s (PEG/SA-UNP2s) specifically recognized biotinylated antibodies and emitted strong upconversion luminescence upon near-infrared excitation. The obtained PEG/streptavidin coimmobilized UNPs are promising as high-performance near-infrared biolabeling materials.
引用
收藏
页码:8864 / 8870
页数:7
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