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In recent years, lanthanide-containing upconversion nanoparticles (UCNPs) have aroused the extensive interest in bioimaging due to their unique upconversion fluorescent properties, such as the high tissue penetration depth, good biocompatibility, low auto-fluorescence, and high imaging sensitivity. In this work, we synthesize a series of NaYF4:Yb, Tm@NaYF4 core-shell structured nanoparticles with various shell thicknesses. A “hot injection” strategy is introduced to fabricate the core-shell UCNPs through using high boiling-point mixtures (sodium/rare-earth trifluoroacetates dissolved in oleic acid and octadecene at 150 °C) as shell precursor solutions. The as-synthesized UCNPs are characterized by transmission electron microscope, particle size analysis and fluorescence spectra. The experimental results show that the shell thickness of UCNPs can be well controlled within a range from 4.2 nm to 32.6 nm by simply tuning the added quantity of the shell precursors. Meanwhile, the upconversion luminescence intensity of NaYF4:Yb, Tm@NaYF4 shows tens times higher than that of NaYF4:Yb, Tm owing to the effective suppression of surface quenching. The optimized thickness of the shell is determined to be 22.7 nm. An ultrathick inert shell (>22.7 nm) is not beneficial to upconversion luminescence mainly due to a strong scattering effect. In addition, the in vitro upconversion luminescent bioimaging application is demonstrated by using the as-synthesized core-shell structured UCNPs. Typically, the prepared OA capped UCNPs are dispersed in HCl solution to obtain hydrophilic ones, followed by polyethylene glycol (PEG) modification to improve their biological compatibility. The hydrophilic NaYF4:Yb, Tm@NaYF4@PEG nanostructures (denoted as UCNP@PEG) show a good biocompatibility with HeLa cells, as the viability of HeLa cells do not decrease obviously when the concentration of UCNP@PEG increases to 0.2 mg/mL. Then, we evaluate the upconversion luminescent signals of UCNP@PEG in HeLa cells under the excitation of 980 nm laser. An obviously increasing upconversion luminescent signal can be observed in HeLa cells with the incubation time increasing from 0.5 h to 6.0 h, indicating that the UCNP@PEG can be used as an excellent luminescence probe for cell imaging and monitoring the cell endocytosis process. All in all, we offer an efficient “hot injection” strategy of fabricating the core-shell structured UCNPs with various shell thickness for improving the upconversion efficiency of UCNPs, which will pave the way for new bioimaging and medical applications.
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Keywords:
- upconversion luminescence /
- hot injection /
- core-shell /
- bioimaging
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图 1 热注射法可控制备核壳型稀土上转换发光纳米材料的设计原理图
Figure 1. Schematic design of core-shell structured upconversion nanoparticles synthesized with the hot injection method.
图 2 (a), (b) β相的NaYF4:Yb, Tm的TEM图; (c) NaYF4:Yb, Tm的粒径分布统计图
Figure 2. (a), (b) TEM images and (c) the corresponding size distribution of the of NaYF4: Yb, Tm.
图 3 (a)−(d) NaYF4:Yb, Tm@NaYF4纳米粒子(粒径约43.8 nm)的结构示意图, TEM图和粒径分布图; (e)−(h) NaYF4:Yb, Tm@NaYF4纳米粒子(粒径约63.2 nm)的结构示意图, TEM图和粒径分布图; (i)−(l) NaYF4:Yb, Tm@NaYF4纳米粒子(粒径约80.8 nm)的结构示意图, TEM图和粒径分布图; (m)−(p) NaYF4:Yb, Tm@NaYF4纳米粒子(粒径约100.7 nm)的结构示意图, TEM图和粒径分布图
Figure 3. (a)−(d) The schematic core-shell structure, TEM images and size distribution of NaYF4:Yb, Tm@NaYF4 (about 43.8 nm); (e)−(h) the schematic core-shell structure, TEM images and size distribution of NaYF4:Yb, Tm@NaYF4 (about 63.2 nm); (i)−(l) the schematic core-shell structure, TEM images and size distribution of NaYF4:Yb, Tm@NaYF4 (about 80.8 nm); (m)−(p) the schematic core-shell structure, TEM images and size distribution of NaYF4:Yb, Tm@NaYF4 (about 100.7 nm).
图 4 (a) 980 nm激发下NaYF4:Yb, Tm@NaYF4纳米粒子的上转换机制; (b)不同壳层厚度的UCNPs的上转换发光光谱; (c)不同壳层厚度的UCNPs的上转换发光强度的柱状统计图
Figure 4. (a) The energy transfer mechanisms of NaYF4:Yb, Tm@NaYF4 UCNPs; (b) the upconversion luminescent spectra and (c) the relative luminescent intensity of core-shell structured UCNPs with different shell thicknesses.
图 5 (a) UCNP@PEG的结构示意图; (b) UCNP@PEG的TEM图; (c)与不同浓度UCNP@PEG培养后, HeLa的细胞活性
Figure 5. (a) Schematic structure of UCNP@PEG; (b) TEM image of UCNP@PEG; (c) cell viabilities of HeLa cells after incubation with various concentrations of UCNP@PEG
图 6 与UCNP@PEG共同培养0.5, 3.0 和6.0 h后的HeLa的上转换荧光成像照片
Figure 6. Upconversion luminescent images of HeLa cells after culturing with UCNP@PEG for 0.5, 3.0 and 6.0 h.
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[1] Wen S, Zhou J, Zheng K, Bednarkiewicz A, Liu X, Jin D 2018 Nat. Commun. 9 2415
Google Scholar
[2] Chen Q, Xie X, Huang B, Liang L, Han S, Yi Z, Liu X 2017 Angew. Chem. 129 7713
Google Scholar
[3] Li X, Zhang F, Zhao D 2013 Nano Today 8 643
Google Scholar
[4] Li X, Zhang F, Zhao D 2015 Chem. Soc. Rev. 44 1346
Google Scholar
[5] Zhu X, Su Q, Feng W, Li F 2017 Chem. Soc. Rev. 46 1025
Google Scholar
[6] Auzel F 2004 Chem. Rev. 104 139
Google Scholar
[7] Dong H, Sun L D, Yan C H 2015 Chem. Soc. Rev. 44 1608
Google Scholar
[8] Wang F, Deng R, Wang J, Wang Q, Han Y, Zhu H, Chen X H, Liu X G 2011 Nat. Mater. 10 968
Google Scholar
[9] Hu F, Liu B, Chu H, Liu C, Li Z, Chen D, Li L 2019 Nanoscale 11 9201
Google Scholar
[10] 丁庆磊, 肖思国, 张向华, 夏艳琴, 刘政威 2006 55 5140
Google Scholar
Ding Q L, Xiao S G, Zhang X H, Xia Y Q, Liu Z W 2006 Acta Phys. Sin. 55 5140
Google Scholar
[11] Haase M, SchäfTm H 2011 Angew. Chem. Int. Ed. 50 5808
Google Scholar
[12] Rao L, Bu L L, Cai B, Xu J H, Li A, Zhang W F, Zhao X Z 2016 Adv. Mater. 28 3460
Google Scholar
[13] Liu K, Liu X, Zeng Q, Zhang Y, Tu L, Liu T, AaldTms M C 2012 ACS Nano 6 4054
Google Scholar
[14] Wang M, Mi C C, Wang W X, Liu C H, Wu Y F, Xu Z R, Xu S K 2009 ACS Nano 3 1580
Google Scholar
[15] Nyk M, Kumar R, Ohulchanskyy T Y, BTmgey E J, Prasad P N 2008 Nano Lett. 8 3834
Google Scholar
[16] Peng J, Samanta A, Zeng X, Han S, Wang L, Su D, Jiang W 2017 Angew. Chem. Int. Ed. 56 4165
Google Scholar
[17] Liang L, Xie X, All A. H, Huang L, Liu X 2016 Chem. Eur. J. 22 10801
Google Scholar
[18] Wang S, Fan Y, Li D, Sun C, Lei Z, Lu L, Zhang F 2019 Nat. Commun. 10 1058
Google Scholar
[19] Lei X, Li R, Tu D, Shang X, Liu Y, You W, Chen X 2018 Chem. Sci. 9 4682
Google Scholar
[20] Liu L, Wang S, Zhao B, Pei P, Fan Y, Li X, Zhang F 2018 Angew. Chem. Int. Ed. 57 7518
Google Scholar
[21] H. Kobayashi, M. Ogawa, R. Alford, P. L. Choyke, Y. Urano 2010 Chem. Rev. 110 2620
Google Scholar
[22] Liu X, Qiu J 2015 Chem. Soc. Rev. 44 8714
Google Scholar
[23] Liu X, Yan C H, Capobianco J A 2015 Chem. Soc. Rev. 44 1299
Google Scholar
[24] Park W, Lu D, Ahn S 2015 Chem. Soc. Rev. 44 2940
Google Scholar
[25] Nadort A, Zhao J, Goldys E M 2016 Nanoscale 8 13099
Google Scholar
[26] Liu B, Chen Y, Li C, He F, Hou Z, Huang S, Zhu H, Chen X, Lin J 2015 Adv. Funct. Mater. 25 4717
Google Scholar
[27] Liu B, Li C, Cheng Z, Hou Z, Huang S, Lin J 2016 Biomater. Sci. 4 890
Google Scholar
[28] Zhai X, Lei P, Zhang P, Wang Z, Song S, Xu X, Liu X, Feng J, Zhang H 2015 Biomaterials 65 115
Google Scholar
[29] Ye S, Chen G, Shao W, Qu J, Prasad P N 2015 Nanoscale 7 3976
Google Scholar
[30] Li W, Chen Z, Zhou L, Li Z, Ren J, Qu X 2015 J. Am. Chem. Soc. 137 8199
Google Scholar
[31] Hao S, Yang L, Qiu H, Fan R, Yang C, Chen G 2015 Nanoscale 7 10775
Google Scholar
[32] Chen D, Liu L, Huang P, Ding M, Zhong J, Ji Z 2015 J. Phys. Chem. Lett. 6 2833
Google Scholar
[33] Gu Z, Yan L, Tian G, Li S, Cha Z, Zhao Y 2013 Adv. Mater. 25 3758
Google Scholar
[34] Dou Q, Idris N M, Zhang Y 2013 Biomaterials 34 1722
Google Scholar
[35] Liu X, Kong X, Zhang Y, Tu L, Wang Y, Zeng Q, Li C, Shi Z, Zhang H 2011 Chem. Commun. 47 11957
Google Scholar
[36] Yi G S, Chow G M 2006 Chem. Mater. 19 341
[37] Wang F, Liu X 2008 J. Am. Chem. Soc. 130 5642
Google Scholar
[38] Zhang S L, Li J, Lykotrafitis G, Bao G, Suresh S 2009 Adv. Mater. 21 419
Google Scholar
[39] Cabral H, Matsumoto Y, Mizuno K, Chen Q, Murakami M, Kimura M, Terada Y, Kano M R, Miyazono K, Uesaka M, Hishiyama N, Kataoka K 2011 Nat. Nanotechnol. 6 815
Google Scholar
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