Upconversion nanoparticles (UCNPs) have attracted enormous interest over the past few years because of their unique optical properties and potential for use in various applications such as bioimaging probes, biosensors, and light-harvesting materials for photovoltaics. The improvement of imaging resolution is one of the most important goals for UCNPs used in biological applications. Super-resolution imaging techniques that overcome the fundamental diffraction limit of light rely on the photochemistry of organic dyes or fluorescent proteins. Here we report our progress toward super-resolution microscopy with UCNPs. We found that the red emission (655 nm) of core/shell UCNPs with the structure NaYF:Yb,Er/NaYF could be modulated by emission depletion (ED) of the intermediate state that interacts resonantly with an infrared beam (1540 nm). In contrast, the green emission bands (525 and 545 nm) of the UCNPs were less affected by irradiation with the infrared beam. The origin of such distinct behaviors between the green and red emissions was attributed to their different photophysical pathways.
Because of their well-known optical properties, upconversion nanoparticles (UCNPs) are regarded as some of the most promising nanomaterials for bioimaging, biosensors, and solar cells. The nonblinking nature of their upconversion emissions has been a particularly beneficial advantage for live-cell imaging. However, the origin of this unique property has never been seriously investigated. We report, for the first time, the observation of stochastic photon emission (SPEM) in core/shell UCNPs (NaYF 4 :Yb 3+ ,Er 3+ /NaYF 4 ) on the microsecond and nanosecond time scales, even under continuous irradiation at 980 nm. This SPEM was attributed to slow "upconversion cycles". We consider that the conventionally reported, nonblinking nature of UCNP emissions can be attributed to the averaging of SPEMs from multiple Er 3+ ions and the low temporal resolution of previous observation. The off-time distribution, which possesses kinetics information for the upconversion pathways, was well fitted to a single exponential indicating involvement of a single rate-determining step. The distinct behaviors of the green and red emissions confirm their different photophysical pathways.
The detection of mycotoxins is crucial because of their toxicity in plants, animals, and humans. It is very important to determine whether food products are contaminated with mycotoxins such as ochratoxin A (OTA), as mycotoxins can survive heat treatments and hydrolysis. In this study, we designed a fluorescence resonance energy transfer (FRET)-based system that exploits antibody-antigen binding to detect mycotoxins more rapidly and easily than other currently available methods. In addition, we were able to effectively counteract the matrix effect in the sample by using a nitrocellulose membrane that enabled fluorescence measurement in coffee samples. The developed FRET on lateral flow immunoassay (FRET-LFI) system was used to detect OTA at a limit of detection (LOD) of 0.64 ng∙mL−1, and the test can be completed in only 30 min. Moreover, OTA in coffee samples was successfully detected at a LOD of 0.88 ng∙mL−1, overcoming the matrix effect, owing to the chromatographic properties of the capillary force of the membrane. We believe that the developed system can be used as a powerful tool for the sensitive diagnosis of harmful substances such as mycotoxins and pesticides for environmental and food quality control monitoring.
Py-12-O-2-DMA was used for a quantitative magnetic field imaging in mild conditions with 375 nm LED excitation. It was ca. 24.7 times brighter than a previously reported phenanthrene-based complex when excited by 355 nm excitation.
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