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Photoluminescence is one of the most sensitive techniques for fingerprint detection, but it also suffers from background fluorescence and selectivity at the expense of generality. The method described herein integrates the advantages of near-infrared-light-mediated imaging and molecular recognition. In principle, upconversion nanoparticles (UCNPs) functionalized with a lysozyme-binding aptamer were used to detect fingerprints through recognizing lysozyme in the fingerprint ridges. UCNPs possess the ability to suppress background fluorescence and make it possible for fingerprint imaging on problematic surfaces. Lysozyme, a universal compound in fingerprints, was chosen as the target, thus simultaneously meeting the selectivity and generality criteria in photoluminescence approaches. Fingerprints on different surfaces and from different people were detected successfully. This strategy was used to detect fingerprints with cocaine powder by using UCNPs functionalized with a cocaine-binding aptamer. [ABSTRACT FROM AUTHOR]

Target practice: A novel photodynamic therapy system has been constructed by taking advantage of the specific molecular recognition of an aptamer, loading capability of a G‐quadruplex, and upconversion of nanoparticles using near‐infrared (NIR) light. This system selectively delivers a photosensitizer to targeted cells and upon irradiation with NIR light demonstrates phototoxicity effects. [ABSTRACT FROM AUTHOR]

Near‐infrared‐light‐mediated imaging and molecular recognition have been combined for the detection of latent fingerprints. Q. Yuan et al. describe in their Communication on page 1616 ff. how this general technique does not suffer from background fluorescence interference and simultaneously meets the selectivity and generality criteria for the detection of fingerprints, thus providing high evidential quality for individual identification. [ABSTRACT FROM AUTHOR]