We report intracellular fluorescence lifetime imaging (FLIM) and fluorescence anisotropy measurements of two meso-substituted fluorophores based on the boron-dipyrrin (BODIPY) structure.Both dyes incorporate hydrophobic groups, which render them membrane-soluble. We have obtained quantum yields, radiative and non-radiative rate constants, fluorescence lifetimes and time-resolved fluorescence anisotropy of the dyes in homogeneous methanol/glycerol solutions of varying viscosity from 0.6 cP to 950 cP. We find that the fluorescence lifetimes and rotational correlation times for both dyes increase with increasing viscosity, as predicted by theory. These molecules can thus serve as fluorescent molecular rotors to report on local microviscosity, including that in live cells. The dyes are readily taken up by cells as imaged using confocal fluorescence microscopy. Using FLIM we have detected two distinct fluorescence lifetime populations for both dyes in live SK-OV-3 human ovarian carcinoma cells, corresponding to apparent viscosity values of 160 ± 20 cP and 260 ± 40 cP, each found in distinct intracellular domains. In both cellular domains, independent of the fluorophore used, the viscosity values significantly exceed that expected for the aqueous phase of cellular cytoplasm, suggesting slower diffusion and reaction rates in this hydrophobic microenvironment. FLIM measurements were complemented with time-resolved fluorescence anisotropy measurements, which confirm the high viscosity values in the immediate environment of both rotors. The present study highlights the power of FLIM to map heterogeneous microenvironments of complex biological systems and also the use of fluorescent molecular rotors as microviscosity sensors.3

A novel method is proposed using nanometer-sized diamond particles as detection probes for biolabeling. The advantages of nanodiamond's unique properties were demonstrated in its biocompatibility, nontoxicity, easily detected Raman signal, and intrinsic fluorescence from its natural defects without complicated pretreatments. Carboxylated nanodiamond's (cND's) penetration ability, noncytotoxicity, and visualization of cND-cell interactions are demonstrated on A549 human lung epithelial cells. Protein-targeted cell interaction visualization was demonstrated with cND-lysozyme complex interaction with bacteria Escherichia coli. It is shown that the developed biomolecule-cND complex preserves the original functions of the test protein. The easily detected natural fluorescent and Raman intrinsic signals, penetration ability, and low cytotoxicity of cNDs render them promising agents in multiple medical applications.

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Bactericidal activity of traditional titanium dioxide (TiO 2 ) photocatalyst is effective only upon irradiation by ultraviolet light, which restricts the potential applications of TiO 2 for use in our living environments. Recently carbon-containing TiO 2 was found to be photoactive at visible-light illumination that affords the potential to overcome this problem; although, the bactericidal activity of these photocatalysts is relatively lower than conventional disinfectants. Evidenced from scanning electron microscopy and confocal Raman spectral mapping analysis, we found the interaction with bacteria was significantly enhanced in these anatase/rutile mixed-phase carbon-containing TiO 2 . Bacteria-killing experiments indicate that a significantly higher proportion of all tested pathogens including Staphylococcus aureus, Shigella flexneri and Acinetobacter baumannii, were eliminated by the new nanoparticle with higher bacterial interaction property. These findings suggest the created materials with high bacterial interaction ability might be a useful strategy to improve the antimicrobial activity of visible-light-activated TiO 2 .

We present polarization-resolved fluorescence measurements of fluorescent molecular rotors 9-(2-carboxy-2-cyanovinyl)julolidine (CCVJ), 9-(2,2-dicyanovinyl)julolidine (DCVJ), and a meso-substituted boron dipyrromethene (BODIPY-C(12)). The photophysical properties of these molecules are highly dependent on the viscosity of the surrounding solvent. The relationship between their quantum yields and the viscosity of the surrounding medium is given by an equation first described and presented by Förster and Hoffmann and can be used to determine the microviscosity of the environment around a fluorophore. Herein we evaluate the applicability of molecular rotors as probes of apparent viscosity on a microscopic scale based on their viscosity dependent fluorescence depolarization. We develop a theoretical framework, combining the Förster-Hoffmann equation with the Perrin equation and compare the dynamic ranges and usable working regimes for these dyes in terms of utilising fluorescence anisotropy as a measure of viscosity. We present polarization-resolved fluorescence spectra and steady-state fluorescence anisotropy imaging data for measurements of intracellular viscosity. We find that the dynamic range for fluorescence anisotropy for CCVJ and DCVJ is significantly lower than that of BODIPY-C(12) in the viscosity range 0.6<η<600 cP. Moreover, using steady-state anisotropy measurements to probe microviscosity in the low (<3 cP) viscosity regime, the molecular rotors can offer a better dynamic range in anisotropy compared with a rigid dye as a probe of microviscosity, and a higher total working dynamic range in terms of viscosity.

In this work, the spectroscopic properties of surface functionalized nanodiamond particles are investigated via Fourier transform infrared spectroscopy. The functionalization of the nanodiamond surface was achieved chemically using strong acid treatment method. The size dependent C=O stretching frequency (between 1680 and 1820 cm(-1)) are studied for particle diameter sizes from the 5 to 500 nm range. The surface C=O stretching frequencies at approximately 1820 cm(-1), for large particle size (500 nm), down shifted to 1725 cm(-1) (5 nm) with decreasing particle sizes. We attributed the shift as a result of hydrogen bond formation between the COOH groups in the carboxylated nanodiamond surfaces. Particle size was characterized with dynamic light scattering method and surface morphology of the particles was investigated with scanning electron microscopy. The influence of pH value on C=O stretching frequency is also analyzed. This finding affords useful information for the studying of surface functionalized nanodiamonds with implications for their interaction with biomolecules.

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