Detailed Information on Publication Record
2016
Highly Sensitive Laser Scanning of Photon-Upconverting Nanoparticles on a Macroscopic Scale
SEDLMEIER, Andreas, Antonín HLAVÁČEK, Lucia BIRNER, Matthias MICKERT, Verena MUHR et. al.Basic information
Original name
Highly Sensitive Laser Scanning of Photon-Upconverting Nanoparticles on a Macroscopic Scale
Authors
SEDLMEIER, Andreas (276 Germany), Antonín HLAVÁČEK (203 Czech Republic, guarantor, belonging to the institution), Lucia BIRNER (276 Germany), Matthias MICKERT (276 Germany), Verena MUHR (276 Germany), Thomas HIRSCH (276 Germany), Paul CORSTJENS (528 Netherlands), Hans TANKE (528 Netherlands), Tero SOUKKA (246 Finland) and Hans GORRIS (276 Germany)
Edition
Analytical Chemistry, WASHINGTON, AMER CHEMICAL SOC, 2016, 0003-2700
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
10406 Analytical chemistry
Country of publisher
United States of America
Confidentiality degree
není předmětem státního či obchodního tajemství
References:
Impact factor
Impact factor: 6.320
RIV identification code
RIV/00216224:14740/16:00089557
Organization unit
Central European Institute of Technology
UT WoS
000369471100050
Keywords in English
CONVERTING PHOSPHOR REPORTERS; LANTHANIDE-DOPED NANOCRYSTALS; UP-CONVERSION NANOPARTICLES; CIRCULATING ANODIC ANTIGEN; LATERAL FLOW ASSAY; IMAGING IN-VIVO; FLUORESCENT; CELLS; NANOPHOSPHORS; LUMINESCENCE
Tags
Změněno: 17/3/2017 13:40, Mgr. Eva Špillingová
Abstract
V originále
An upconversion laser scanner has been optimized to exploit the advantages of photon-upconverting nanoparticles (UCNPs) for background-free imaging on a macroscopic scale. A collimated 980 nm laser beam afforded high local excitation densities to account for the nonlinear luminescence response of UCNPs. As few as 2000 nano particles were detectable, and the linear dynamic range covered more than 5 orders of magnitude, which is essentially impossible by using conventional fluorescent dyes. UCNPs covered by a dye-doped silica shell were separated by agarose gel electrophoresis and scanned by a conventional fluorescence scanner as well as the upconversion scanner. Both optical labels could be detected independently. Finally, upconversion images of lateral flow test strips were recorded to facilitate the sensitive and quantitative detection of disease markers. A marker for the parasitic worm Schistosoma was used in this study.
Links
EE2.3.30.0009, research and development project |
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