Delivery and reveal of localization of upconversion luminescent microparticles and quantum dots in the skin in vivo by fractional laser microablation, multimodal imaging, and optical clearing.

Delivery and spatial localization of upconversion luminescent microparticles [Y2O3:Yb, Er] (mean size ∼1.6 µm) and quantum dots (QDs) (CuInS2/ZnS nanoparticles coated with polyethylene glycol-based amphiphilic polymer, mean size ∼20 nm) inside rat skin was studied in vivo using a multimodal optical imaging approach. The particles were embedded into the skin dermis to the depth from 300 to 500 µm through microchannels performed by fractional laser microablation. Low-frequency ultrasound was applied to enhance penetration of the particles into the skin. Visualization of the particles was revealed using a combination of luminescent spectroscopy, optical coherence tomography, confocal microscopy, and histochemical analysis. Optical clearing was used to enhance the image contrast of the luminescent signal from the particles. It was demonstrated that the penetration depth of particles depends on their size, resulting in a different detection time interval (days) of the luminescent signal from microparticles and QDs inside the rat skin in vivo. We show that luminescent signal from the upconversion microparticles and QDs was detected after the particle delivery into the rat skin in vivo during eighth and fourth days, respectively. We hypothesize that the upconversion microparticles have created a long-time depot localized in the laser-created channels, as the QDs spread over the surrounding tissues.

Fluorescent ZnCdS nanoparticles for glucose sensing.

The effect of glucose on fluorescence of synthesized ZnCdS nanoparticles in the presence of glucose oxidase or in a mixture of glucose oxidase and peroxidase has been investigated. Behavior of fluorescence characteristics of ZnCdS nanoparticles with nonstabilized surface and coated with polymer shell is compared. It has been shown that, for uncoated ZnCdS nanoparticles, hydrogen peroxide formed by glucose oxidation with glucose oxidase causes static quenching of the nanoparticle fluorescence. A quenching mechanism is proposed in which surface centers of fluorescence, which include cationic vacancies, trap oxygen ions supplied by hydrogen peroxide. It has been shown that the linear Stern-Volmer plot has no threshold within the investigated concentrations of glucose. The sensitivity of ZnCdS nanoparticles to glucose, determined from the slope of linear Stern-Volmer plot, is maximum for polymer-coated nanoparticles and is 12.2 ml/mg. With peroxidase, there is a threshold concentration of glucose (160 µM) below which the nanoparticles become insensitive to glucose.