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Introduction Since most biologically active macromolecules are natural nanostructures, operating in the same scale of biomolecules gives the great advantage to enhance the interaction with cellular components. Noteworthy efforts in nanotechnology, particularly in biomedical and pharmaceutical fields, have propelled a high number of studies on the biological effects of nanomaterials. Moreover, the determination of specific physicochemical properties of nanomaterials is crucial for the evaluation and design of novel safe and efficient therapeutics and diagnostic tools. In this in vitro study, we report a physicochemical characterisation of fluorescent silica nanoparticles (NPs), interacting with biological models (U937 and PBMC cells), describing the specific triggered biologic response. Methods Flow Cytometric and Confocal analyses are the main method platforms. However TEM, NTA, DLS, and chemical procedures to synthesize NPs were employed. Results NT B 700 NPs, employed in this study, are fluorescent core-shell silica nanoparticles, synthesized through a micelle-assisted method, where the fluorescence energy transfer process, known as FRET, occurs at a high efficiency rate. Using flow cytometry and confocal microscopy, we observed that NT B 700 NP uptake seemed to be a rapid, concentration-, energy- and cell type-dependent process, which did not induce significant cytotoxic effects. We did not observe a preferred route of internalization, although their size and the possible aggregated state could influence their extrusion. At this level of analysis, our investigation focuses on lysosome and mitochondria pathways, highlighting that both are involved in NP co-localization. Despite the main mitochondria localization, NPs did not induce a significant increase of intracellular ROS, known inductors of apoptosis, during the time course of analyses. Finally, both lymphoid and myeloid cells are able to release NPs, essential to their biosafety. Discussion These data allow to consider NT B 700 NPs a promising platform for future development of a multifunctional system, by combining imaging and localized therapeutic applications in a unique tool.

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Chirality emergence in biological systems is common but the chiral expression from the molecular to macroscopic level in water‐based systems is poorly understood. Among water‐based systems, chromonic liquid crystals have recently received a lot of attention due to the spontaneous chirality they show when confined in curved geometries. Confinement of chiral‐induced chromonics is not trivial since they are three component systems whose time stability is a delicate thermodynamic balance. In this work, a well‐defined periodic Frank–Pryce texture, typical of chiral thermotropic liquid crystals, is observed in microspheres of a chiral induced chromonic embedded in a poly(dimethylsiloxane) matrix. This texture slowly degrades in time and a possible mechanism behind the degradation process is suggested via X‐ray diffraction and atomic force microscopy measurements on thin chromonic films. To stabilize this texture and to control the structure periodicity, cations are added to the three components system in an attempt to tune the non‐covalent interactions between molecules and supramolecular stacks. The study of the effects of this addition allows for better insight into the molecular interactions that occur in the chiral induced mesophase. This is a crucial point in view of possible biocompatible technological applications.

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