Trace Analysis With Nanomaterials 2010
DOI: 10.1002/9783527632015.ch1
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Photoswitchable Nanoprobes for Biological Imaging Applications

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Cited by 4 publications
(7 citation statements)
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“…7,27,29,[75][76][77][78][79] The bottleneck is that multiple emitting fluorophores located within the diffraction-limited area cannot be resolved simultaneously. However, the diffraction limit originating from the wave properties of light restricts the optical microscope resolution to ∼300 nm, a level two of orders of magnitude coarser than nanoscale molecules; thus many intracellular organelles and their associated molecular structures remained unresolvable.…”
Section: Photoswitchable Fluorescent Nps Enable High-resolution Imagingmentioning
confidence: 99%
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“…7,27,29,[75][76][77][78][79] The bottleneck is that multiple emitting fluorophores located within the diffraction-limited area cannot be resolved simultaneously. However, the diffraction limit originating from the wave properties of light restricts the optical microscope resolution to ∼300 nm, a level two of orders of magnitude coarser than nanoscale molecules; thus many intracellular organelles and their associated molecular structures remained unresolvable.…”
Section: Photoswitchable Fluorescent Nps Enable High-resolution Imagingmentioning
confidence: 99%
“…6,[23][24][25] In this review, we outline the major classes of SP/DAE-based photoswitchable fluorescent NPs developed in recent years while photoswitchable single-molecule fluorophores and fluorescent proteins, as well as NPs constructed from other types of photoswitches are beyond the scope of this review. Additionally, considering that SP/DAE-based dynamic materials have been reviewed extensively, 6,7,[26][27][28][29] we emphasize on the emerging applications of photoswitchable fluorescent NPs in biological fluorescence assays and detection with a few representative paradigms.…”
Section: Jie Wangmentioning
confidence: 99%
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“…Since the resolution can be measured based on the switching of the fluorescent probes between two distinctively different fluorescent states, either fluorescent “ON” and “OFF” states or two fluorescent states with distinct color. Furthermore, the fluorescent probes must be actively varied (usually via photoswitching or photoactivation) in time to ensure that only an optically resolvable subset of fluorophores is activated at any time in a diffraction—limited region, thereby allowing their localization with high accuracy [ 29 ]. For example, Santra’s group described a method for synthesis of dopamine dithiocarbamate (DDTC) capped with CdS:Mn/ZnS core/shell QDs using a water-in-oil (W/O) microemulson mechanism [ 30 ].…”
Section: Semiconductor Qds-based Fluorescence Approaches For Biomomentioning
confidence: 99%