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[Display omitted] • LD-VP emits fluorescence at 520 nm in dioxane and 600 nm in viscous media without any interference from biological entities. • The LD-VP probe is pH-independent. • The quantum yield of probe LD-VP has changed from 0.5 % to 30% as the viscosity rises from 0.9 cP to 953 cP. • Probe LD-VP has provided green images in nonpolar intracellular milieu detection and red images for high viscosity. • Probe LD-VP concurrently labeled mitochondria, lysosomes, and lipid droplets in red and green channels based on intracellular viscosity and polarity. The viscosity and polarity of cells are inherent physical parameters, and changes to these attributes are frequently linked to malfunctioning conditions or different diseases. Cancer cells often harbor elevated nonpolar lipid droplets (LDs), acting as energy reserves. The rise in lipid droplets (LDs) and viscosity, distinctive traits of cancer cells, has motivated us to develop a fluorescent probe based on naphthalimide. The fluorescent marker LD-VP exhibits fluorescence signals at 520 nm in nonpolar dioxane and 600 nm in highly viscous glycerol. This implies that probe LD-VP can furnish details regarding cellular microviscosity and lipid droplets within live cells by providing dual-channel images. The probe LD-VP is chemically inert and harmless, enabling its safe utilization in live cell imaging. We conducted fluorescence imaging based on viscosity using probe LD-VP in the red channel, which is found to be co-localized in both mitochondria and lysosomes. Moreover, the probe effectively marks lipid droplets in the green channel. The probe LD-VP represents a distinctive fluorescent tool capable of monitoring both viscosity and lipid droplet expression in live cells. This tool holds the potential for visualizing physiological abnormalities or pathological conditions. [ABSTRACT FROM AUTHOR]

A novel NIR probe based on oxazolonaphthoimidazo[1,2- a ]pyridine-malononitrile (ONIM) conjugate linked by vinyl linkage was designed and synthesized for the detection of cyanide ion. [Display omitted] • An orange emitting sensor ONIM (712 nm) with D-π-A framework is synthesized. • The ONIM emission is retained in the solid state. • ONIM could sense cyanide ion without interference of other anions. • Sensing mechanism of cyanide sensing was confirmed by 1H NMR and DFT calculations. • Live cell imaging in human breast cancer cell MDA-MB 231 and as solid state sensor was achieved. Cyanide is undoubtedly dangerous and fast acting chemical employed in various industrial applications with toxic side effects, which raises urgent need for its monitoring. In this context, oxazolonaphthoimidazo[1,2- a ]pyridine-malononitrile (ONIM) conjugate linked by vinyl linkage was designed, synthesized and characterised by FT-IR, NMR and mass spectrometry. The developed probe has been evaluated for the colorimetric and fluorometric detection of cyanide ion. An obvious color change with unique rapid " turn-off " fluorometric response was observed within 5 s upon addition of CN– thus reflecting its better acuteness and sensitivity over other competing anions. The developed probe exhibits a detection limit of 9.54 nM which is very low in comparison to maximum permitable amount of cyanide in drinking water (1.9 µM). The probe is stable within the p H range of 2–9 and suitable for the recognition of CN– in the p H range of 7 to 10, specially at neutral p H conditions. The chemodosimetric approach based detection mechanism was authenticated by 1H NMR titration and DFT calculations. The solid state applications were established by utilising ONIM impregnated TLC plates and filter paper in cyanide recognition. The solid state emissive behaviour of ONIM offers on-spot detection of the cyanide anion. Additionally, the practicability of ONIM has been extended in live cell imaging of CN– in human breast cancer cell (MDA-MB-231), which revealed a " turn-off " fluorescence response for the probe in the presence of CN– ion. [ABSTRACT FROM AUTHOR]

Conjugated polymer nanoparticles have been regarded as promising fluorescent materials for biological application, due to their high emission efficiency, good photostability and low cytotoxicity. In this contribution, we synthesized a conjugated polymer which integrates blue-, green- and red-emitting components into the backbone in an appropriate molar ratio. After being transferred from solution to nanoparticles, its fluorescence color turns from blue to pink with enhanced fluorescence quantum yield. After incorporation of an amphiphilic polymer as matrix, white-emissive polymer nanoparticles are obtained as a result of optimized energy transfer degree among the three components. Finally, their good performance on cell imaging are demonstrated by incubation with HeLa cells, after being proved to be safe for biological application. [ABSTRACT FROM AUTHOR]