Photocatalytic hydrogen (H₂) production is a promising route for alternative energetics. Understanding structure–activity relationships is a crucial step towards the rational design of photocatalysts, which requires the application of operando spectroscopy under relevant working conditions. We performed an operando investigation on a catalytic system during the photodeposition of Pt on TiO₂ and photostimulated H₂ production, using simultaneous laboratory X-ray absorption spectroscopy (XAS), UV–Vis spectroscopy, and mass spectrometry. XAS showed a progressive increase in Pt fluorescence for Pt deposited on TiO₂ for over an hour, which is correlated with the signal of the produced H₂. The final Pt/TiO₂ catalyst contained Pt(0) particles. The electronic features corresponding to the Pt⁴⁺ species in the UV–Vis spectrum of the solution disappear as soon as UV radiation is applied in the presence of formic acid, which acts as a hole scavenger, resulting in the presence of Pt(0) particles in solution.

The development of advanced methods for the synthesis of nano- and microparticles in the field of biomedicine is of high interest due to a range of reasons. The current synthesis methods may have limitations in terms of efficiency, scalability, and uniformity of the particles. Here, we investigate the synthesis of submicron calcium carbonate using a microfluidic chip with a T-shaped oil supply for droplet-based synthesis to facilitate control over the formation of submicron calcium carbonate particles. The design of the chip allowed for the precise manipulation of reaction parameters, resulting in improved porosity while maintaining an efficient synthesis rate. The pore size distribution within calcium carbonate particles was estimated via small-angle X-ray scattering. This study showed that the high porosity and reduced size of the particles facilitated the higher loading of a model peptide: 16 vs. 9 mass.% for the particles synthesized in a microfluidic device and in bulk, correspondingly. The biosafety of the developed particles in the concentration range of 0.08–0.8 mg per plate was established by the results of the cytotoxicity study using mouse fibroblasts. This innovative approach of microfluidically assisted synthesis provides a promising avenue for future research in the field of particle synthesis and drug delivery systems.

Microfluidic devices have opened new opportunities for functional material chemical synthesis in a few applications. The screening of microfluidic synthesis processes is an urgent task of the experimental process in terms of automation and intellectualization. This study proposes a methodology and software for extracting the morphological and dynamic characteristics of generated monodisperse droplets from video data streams obtained from a digital microscope. For this purpose, the paper considers an approach to generating an extended feature space characterizing the process of droplet generation using a microfluidic device based on the creation of synthetic image datasets. YOLOv7 was used as an algorithm for detecting objects in the images. When training this algorithm, the values in the test dataset mAP@0.5 0.996 were obtained. The algorithms proposed for image processing and analysis implement the basic functionality to extract the morphological and dynamic characteristics of monodisperse droplets in the synthesis process. Laboratory validation and verification of the software demonstrated high results of the identification of key characteristics of the monodisperse droplets generated by the microfluidic device with the average deviation from the real values not exceeding 8%.

Rare-earth-doped nanoscaled BaGdF₅ is known as an efficient contrasting agent for X-ray micro-CT and NMR as well as a promising candidate for X-ray photodynamic therapy, thereby opening an opportunity for theragnostic applications. Conventional synthesis of Ln-doped BaGdF₅ consider a long-lasting batch procedure, while a conjugation with photosensitizer usually implies a separate stage requiring active mixing. To the best of our knowledge, in this work, we for the first time obtain BaGdF₅:Tb³⁺ nanophosphors in a microfluidic route at temperatures as low as 100 °C while decreasing the time of thermal treatment down to 6 min. The proposed synthesis route allows for the obtaining of single-phase and monodisperse BaGd_1−xF5:Tb_x³⁺ nanoparticles with an averaged particle size of ca. 7–9 nm and hydrodynamic radius around 22 nm, as estimated from TEM and DLS, respectively. In addition, X-ray-excited optical luminescence has been recorded in situ for the series of nanophosphors synthesis with varied flow rates of Tb³⁺ and Gd³⁺ stock solutions, thereby anticipating a possible application of microfluidics for screening a wide range of possible co-dopants and reaction conditions and its effect on the optical properties of the synthesized materials. Moreover, we demonstrated that BaGd_1−xF₅:Tb_x³⁺@RoseBengal conjugates might be obtained in a single-stage route by implementing an additional mixer at the synthesis outcome, namely, by mixing the resulting reaction mixture containing nanoparticles with an equivalent flow of photosensitizer aqueous solution. In vitro cytotoxicity test declares moderate toxicity effect on different cell lines, while the results of flow cytometry indirectly confirm cellular uptake. Finally, we report long-term biodistribution monitoring of the synthesized nanocomposites assessed by X-ray micro-CT in the in vivo experiments on balb/c mice, which depicts an unusual character of agents’ accumulation.

A multichannel microfluidic cell (MFC) obtained using 3D printing for studying the structure of complex solutions by small-angle X-ray scattering (SAXS) is described. MFC was tested at the BioMUR beamline of the Kurchatov synchrotron. A comparative analysis of SAXS signal from the standard capillary and from the developed MFC was carried out, with MFC showing significant advantages. The dynamics of SAXS scattering curves for lysozyme solutions with NaCl precipitant were studied when the protein and precipitant concentrations changed. The obtained time series of data are well consistent with the known data for the lysozyme solution.