Auto-phase-locked time-gated luminescence detection for background-free upconversion spectra measurement and true-color biological imaging

被引:22
作者
Zhu, Zece [1 ,2 ]
Tian, Di [3 ]
Shu, Xuewen [1 ,2 ]
机构
[1] Wuhan Natl Lab Optoelect, Wuhan, Hubei, Peoples R China
[2] Sch Opt & Elect Informat, Wuhan, Hubei, Peoples R China
[3] Huazhong Univ Sci & Technol, Sch Chem & Chem Engn, Minist Educ, Key Lab Mat Chem Energy Convers & Storage HUST, Wuhan 430074, Hubei, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
Time-gated; Lanthanide luminescence; Microscopic imaging; Upconversion; Chopper; NANOPARTICLES; FLUORESCENCE; NANOCRYSTALS; NANOPROBES; MICROSCOPY;
D O I
10.1016/j.snb.2018.01.012
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Time-resolved technique is widely used in biological detection and imaging, since this technique can eliminate the background signals from scattering and short-lived autofluorescence and greatly increase the signal-to-noise ratio. However, the relative apparatus always require pulse source, gated detector and electronic phase matching circuitry, which are expensive to implement and maintain. Herein, a simple method for time-gated upconversion luminescence spectra measurement and biological imaging was developed. By adjusting the exciting and detecting optical paths to pass through the same chopper wheel, only one mechanical chopper was needed, which simultaneously acted as pulse generator and detecting shutter. The phases of each excitation and time gate were synchronized and locked automatically as the optical paths fixed. Therefore, no complex electronic phase matching circuitry or control system was needed. By equipping with a 980 nm CW laser as exciting source, the time-gated spectra of upconversion lanthanide luminescence free from the scattering light was measured. Moreover, smart phones or the human eyes could easily detect the delayed luminescence of these materials, promising the true-color biological imaging with common cameras. This approach could be used in many other time-gated luminescence detection for long-lived luminescence materials and probes excited by other light sources. (c) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:289 / 294
页数:6
相关论文
共 36 条
[1]   Direct observation of intersystem crossing in a thermally activated delayed fluorescence copper complex in the solid state [J].
Bergmann, Larissa ;
Hedley, Gordon J. ;
Baumann, Thomas ;
Braese, Stefan ;
Samuel, Ifor D. W. .
SCIENCE ADVANCES, 2016, 2 (01)
[2]   Nanoscopic ultrafast space-time-resolved spectroscopy [J].
Brixner, T ;
de Abajo, FJG ;
Schneider, J ;
Pfeiffer, W .
PHYSICAL REVIEW LETTERS, 2005, 95 (09)
[3]   Taking advantage of luminescent lanthanide ions [J].
Bünzli, JCG ;
Piguet, C .
CHEMICAL SOCIETY REVIEWS, 2005, 34 (12) :1048-1077
[4]   A Device for Gated Autosynchronous Luminescence Detection [J].
Connally, Russell .
ANALYTICAL CHEMISTRY, 2011, 83 (12) :4782-4787
[5]   Time-gated luminescence microscopy [J].
Connally, Russell E. ;
Piper, James A. .
FLUORESCENCE METHODS AND APPLICATIONS: SPECTROSCOPY, IMAGING, AND PROBES, 2008, 1130 :106-116
[6]   Overcoming Autofluorescence: Long-Lifetime Infrared Nanoparticles for Time-Gated In Vivo Imaging [J].
del Rosal, Blanca ;
Ortgies, Dirk H. ;
Fernandez, Nuria ;
Sanz-Rodriguez, Francisco ;
Jaque, Daniel ;
Martin Rodriguez, Emma .
ADVANCED MATERIALS, 2016, 28 (46) :10188-10193
[7]   Versatile Spectral and Lifetime Multiplexing Nanoplatform with Excitation Orthogonalized Upconversion Luminescence [J].
Dong, Hao ;
Sun, Ling-Dong ;
Feng, Wei ;
Gu, Yuyang ;
Li, Fuyou ;
Yan, Chun-Hua .
ACS NANO, 2017, 11 (03) :3289-3297
[8]   Responsive lanthanide luminescent cyclen complexes: from switching/sensing to supramolecular architectures [J].
Gunnlaugsson, T ;
Leonard, JP .
CHEMICAL COMMUNICATIONS, 2005, (25) :3114-3131
[9]  
Jin D., 2014, Curr. Protoc. Cytom, V67, p2.22.1
[10]   Time-Gated Luminescence Microscopy Allowing Direct Visual Inspection of Lanthanide-Stained Microorganisms in Background-Free Condition [J].
Jin, Dayong ;
Piper, James A. .
ANALYTICAL CHEMISTRY, 2011, 83 (06) :2294-2300