Non-bleaching fluorescence emission difference microscopy using single 808-nm laser excited red upconversion emission

被引:36
|
作者
Wu, Qiusheng [1 ]
Huang, Bingru [1 ]
Peng, Xingyun [1 ]
He, Sailing [2 ]
Zhan, Qiuqiang [1 ,3 ,4 ]
机构
[1] SCNU, COER, Guangdong Prov Key Lab Opt Informat Mat & Technol, South China Acad Adv Optoelect, Guangzhou 510006, Guangdong, Peoples R China
[2] Royal Inst Technol, Dept Electromagnet Engn, JORCEP, S-10044 Stockholm, Sweden
[3] South China Normal Univ, Natl Ctr Int Res Green Optoelect, Guangzhou 510006, Guangdong, Peoples R China
[4] Shenzhen Univ, Minist Educ & Guangdong Prov, Key Lab Optoelect Devices & Syst, Shenzhen, Peoples R China
来源
OPTICS EXPRESS | 2017年 / 25卷 / 25期
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
UPCONVERTING NANOPARTICLES; STIMULATED-EMISSION; RESOLUTION LIMIT; LUMINESCENCE; ENHANCEMENT; NANOCRYSTALS; DEEP; NM;
D O I
10.1364/OE.25.030885
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
Optical super-resolution microscopy has become a powerful technique to help scientists to monitor the sample of interest at nanoscale. Fluorescence emission difference (FED) microscopy, a very facile super-resolution method, does not require high depleting laser intensity and is independent on the species of agents, which makes FED microscopy possess great potential. However, to date, the biomarkers applied in FED microscopy usually suffer from a photo-bleaching problem. In this work, by introducing Er3+ activated upconverting nanoparticles with red-color emission and non-photobleaching properties, we demonstrate nonbleaching super-resolution imaging with FED microscopy. The dopant neodymium ions (Nd3+) can work as highly efficient sensitizing ions and enable near infrared 808-nm CW laser excitation of relatively low power, which would potentially reduce high intensity/short-wavelength light induced tissue damage. Both simulations and experiments on monodispersed NaYF4:Nd3+/Yb3+/Er3+@NaYF4:Nd3+ UCNPs also indicate that the easy saturation of the multiphoton properties of these UCNPs is beneficial to resolution enhancement in FED microscopy. (C) 2017 Optical Society of America under the terms of the OSA Open Access Publishing Agreement
引用
收藏
页码:30885 / 30894
页数:10
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