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Carbon dots are emerging in the nanotechnology field as the newest class of fluorescent probes, owing to their high water-solubility, good chemical and photo-stability and tunable photoluminescence. The ability of metal cations to quench carbon dots fluorescence is already well known. Anyway, a dedicated study directed to the rational design of the optimal carbon dot probe is still missing. Herein we present a novel synthetic method for the production of carbon nanodots from an economic and environmental polluting starting material: olive solid wastes. The obtained carbon dots are efficiently quenched in presence of Fe3+, allowing the cation detection. Starting from a comprehensive study on their quenching mechanism, we have been able to develop effective strategies to modulate the sensing properties of these carbon dots. The sensitivity and linear range of the probe have been tuned by modulating the surface functionalization of the nanoparticles. The selectivity toward Fe3+ has been improved by growing around the dots a porous microsphere of ion imprinted polymer. The results highlighted in this work demonstrate that the carbon dots sensing properties can be modulated to meet the requirement of the users, allowing the design of tailored probes for a wide range of applications.

Supramolecular adducts formed by a commercial porphyrin derivative and silver nanoparticles have been obtained using exclusively light as an external trigger that is able to promote the formation of the plasmonic nanostructures. In particular, a water-soluble porphyrin, i.e. tetrakis(4-carboxyphenyl)porphyrin, has been used. It has been thoroughly characterized by means of UV-vis and fluorescence spectroscopy in order to explain its peculiar behavior when illumined with visible photons. Herein we demonstrate that, by means of light illumination, it is possible to tune the porphyrin aggregation state. Furthermore, when the monomeric form of the organic macrocycle is induced and a controlled amount of AgNO[Formula: see text] is simultaneously dissolved, it is possible to promote the formation of silver nanostructures using visible light. The proposed approach allowed porphyrin derivatives/Ag nanoparticles hybrid nanostructures to be obtained without using a chemical reducing agent: the porphyrin derivative simultaneously acts as reducing agent when irradiated by visible light and as a capping agent for the silver nanostructures. The organic/inorganic adduct was characterized by means of steady-state fluorescence that highlights a strong energetic or electronic communication between the two species. XRD and SEM investigations evidence that silver nanoparticles are formed without using any reducing agent.

Many strategies have been adopted to improve the photoinduced features of zinc oxide nanostructures for different application fields. In this work, zinc oxide has been synthesised and decorated by plasmonic metal nanoparticles to enhance its photocatalytic activity in the visible range. Furthermore, an insulating layer of SiO2 has been grown between the surface of zinc oxide nanoflakes and silver nanoparticles. A synthetic procedure that allows the accurate modulation of the insulating layer thickness in the range 5–40 nm has been developed. Evidences highlight the crucial role of the SiO2 layer in dramatically increasing photocatalytic water oxidation promoted by the nanostructure under both UV and visible illumination. An ideal thickness value of about 10 nm has been demonstrated to guarantee the plasmon-induced resonance energy-transfer process and to quench the Förster resonance energy-transfer mechanism; thus, optimising the local surface plasmon resonance effect and water oxidation properties.

Cellulose nanocrystals (CNCs) are renewable, sustainable and biocompatible nanomaterials, which have gained great attention in last years for their potentialities in several fields of application. With their polyelectrolyte behaviour, sulphated CNCs are suitable to produce multilayered architectures with cationic molecules. In this work, we have investigated the ability of anionic CNCs to assist the two-dimensional organization of two cationic fulleropyrrolidines at the air/water interface, leading to hybrid Langmuir-Schaeurofer films with improved (photo)electrical properties. We demonstrated that CNCs interact with the fulleropyrrolidines at the air/water interface, favouring the assembly of organized hybrid C-60/CNC films. The transfer efficiency of Langmuir layers and the morphological regularity of supported films proved to be influenced by the extent of positive charge on the fullerene counterpart. Interestingly, the electrochemical characterization of hybrid films revealed that sulphated nanocellulose strongly improves the electrical properties of organized fullerene layers, by increasing their conductivity and favouring the hydrogen evolution reaction. Moreover, the well-established C-60 photoactivity proved to be enhanced by CNCs, as demonstrated by the higher intensity of photocurrents. This outstanding nanocellulose impact on fullerene film electrical properties paves the way to the development of more performing C-60-based electrochemical devices, able to better exploit the unique properties of carbon nanostructures. (C) 2020 Elsevier Ltd. All rights reserved.

Peripheral nerve injuries may lead to a significant function loss, which deeply affect patient’s quality of life. In this context, tissue engineered collagen-based nerve guides are a promising alternative to autografts. To enhance the regeneration of the injured nerve tract, several bioactive molecules can be adopted as further components of the collagen-based conduits. Herein, sericin (Ser), a waste product of textile industry, was combined with type I collagen (Col), for the development of a bioactive substrate potentially able to support and enhance the regeneration of the peripheral nervous system. In particular, in order to identify an optimal substrate composition in terms of physicochemical and biological properties, thin Ser-Col films with different Ser:Col ratios were produced by air-drying and subsequently crosslinked through two different crosslinking methods. Then, Ser:Col films were characterized from a physicochemical point of view by examining secondary protein structure modifications via FTIR spectroscopy, swelling ratios, degradation rates and Ser release kinetics. Moreover, Ser:Col films ability to promote adhesion and proliferation of Schwann cells was evaluated in vitro. The results obtained in this study, although preliminary, suggest that Ser:Col blends could represent a promising strategy to enhance the repair of damaged peripheral nerves, by providing a sustained release of Ser from collagen-based nerve substrates.

Calcium carbonate has many applications in different fields; its use in environment remediation is particularly considered, due to its non-toxicity and potentially high efficiency. The structure, morphology and surface features of calcium carbonate can greatly affect its performance. Hierarchical porosity, in particular, can be beneficial for several functional properties. In this study, we report the synthesis of biomorphic calcium carbonate using a sustainable template agent – waste cork powder. Pyrolysed cork powder was infiltrated by an appropriate calcium-containing salt and successively thermally treated. Selected precursors, different impregnation-solution concentrations and thermal conditions were tested. The resulting materials were characterised by XRD, Raman spectroscopy and SEM. Surface area and porosity features were studied by BET analysis, with a detailed study on the effect of synthesis on the mesoporosity of the materials, average sizes varying between 4−15 nm. The most valuable results were achieved with calcium acetate followed by pyrolysis performed for relatively short time period. This maintained the porous 3D honeycomb cork structure made of ∼20 μm hexagonal cells, while consisting of highly mesoporous single-phase CaCO3. Such samples showed the highest surface area ever reported for CaCO3 prepared using a plant-based template; moreover, it also exhibited a dual-scale hierarchical porosity as, in addition to micrometer scale cellular macroporosity, it contained a significant mesoporosity in the cell walls, with a very narrow range of 3.6–3.9 nm. These promising characteristics enable the potential employment of cork-derived CaCO3 for environment remediation.

Perylene bisimide derivatives show peculiar physical chemical features, such as a highly conjugated system, high extinction coefficients and elevated fluorescence quantum yields, making them suitable for the development of optical sensors of compounds of interest. In particular, they are characterized by the tendency to aggregate into π-π stacked supramolecular structures. In this contribution, the behavior of the PBI derivative N, N'-bis(2-(trimethylammonium)ethylene)perylene bisimide dichloride was investigated both in aqueous solution and on solid support. The electronic communication between PBI aggregates and biogenic amines was exploited in order to discriminate aromatic amines down to subnanomolar concentrations by observing PBI fluorescence variations in the presence of various amines and at different concentrations. The experimental findings were corroborated by density functional theory calculations. In particular, phenylethylamine and tyramine were demonstrated to be selectively detected down to 10-10 M concentration. Then, in order to develop a surface plasmon resonance (SPR) device, PBI was deposited onto a SPR support by means of the layer-by-layer method. PBI was deposited in the aggregated form and was demonstrated to preserve the capability to discriminate, selectively and with an outstanding analytical sensitivity, tyramine in the vapor phase and even if mixed with other aromatic amines.

The possibility to employ carbon nanodots (CNDs) in solar devices was exploited by combining them with a fulleropyrrolidine derivative (FP2). The interaction between the two species was promoted by the presence of opposite electrostatic charges on CNDs (negatively charged) and FP2 (positively charged). The supramolecular dyad CNDs/FP2 generation was induced at the air/water interface of a Langmuir trough: water soluble CNDs were dissolved in the subphase and FP2 chloroform solution was spread on the subphase; the electrostatic interaction promoted the formation of the supramolecular adduct FP2/CNDs, which was then transferred onto solid substrates. Photo-induced charge transfer was promoted in the FP2/CNDs dyad and we demonstrated that the presence of CNDs increased the short-circuit current density, under light illumination, of a porphyrin-FP2/CNDs thin film by about 300% when compared with a more traditional porphyrin-FP2 solar device.

Heteroplasmy is the presence of more than one type of mitochondrial genome within an individual, a condition commonly reported as unfavorable and affecting mitonuclear interactions. So far, no study has investigated heteroplasmy at protein level, and whether it occurs within tissues, cells, or even organelles. The only known evolutionarily stable and natural heteroplasmic system in Metazoa is the Doubly Uniparental Inheritance (DUI)—reported so far in ∼100 bivalve species—in which two mitochondrial lineages are present: one transmitted through eggs (F-type) and the other through sperm (M-type). Because of such segregation, mitochondrial oxidative phosphorylation proteins reach a high amino acid sequence divergence (up to 52%) between the two lineages in the same species. Natural heteroplasmy coupled with high sequence divergence between F- and M-type proteins provides a unique opportunity to study their expression and assess the level and extent of heteroplasmy. Here, for the first time, we immunolocalized F- and M-type variants of three mitochondrially-encoded proteins in the DUI species Ruditapes philippinarum, in germline and somatic tissues at different developmental stages. We found heteroplasmy at organelle level in undifferentiated germ cells of both sexes, and in male soma, whereas gametes were homoplasmic: eggs for the F-type and sperm for the M-type. Thus, during gametogenesis, only the sex-specific mitochondrial variant is maintained, likely due to a process of meiotic drive. We examine the implications of our results for DUI proposing a revised model, and we discuss interactions of mitochondria with germ plasm and their role in germline development. Molecular and phylogenetic evidence suggests that DUI evolved from the common Strictly Maternal Inheritance, so the two systems likely share the same underlying molecular mechanism, making DUI a useful system for studying mitochondrial biology.

The burst of research papers focused on the tissue engineering and regeneration recorded in the last years is justified by the increased skills in the synthesis of nanostructures able to confer peculiar biological and mechanical features to the matrix where they are dispersed. Inorganic, organic and hybrid nanostructures are proposed in the literature depending on the characteristic that has to be tuned and on the effect that has to be induced. In the field of the inorganic nanoparticles used for decorating the bio-scaffolds, the most recent contributions about the paramagnetic and superparamagnetic nanoparticles use was evaluated in the present contribution. The intrinsic properties of the paramagnetic nanoparticles, the possibility to be triggered by the simple application of an external magnetic field, their biocompatibility and the easiness of the synthetic procedures for obtaining them proposed these nanostructures as ideal candidates for positively enhancing the tissue regeneration. Herein, we divided the discussion into two macro-topics: the use of magnetic nanoparticles in scaffolds used for hard tissue engineering for soft tissue regeneration.

It is well known that energetic demand and environmental pollution are strictly connected, the side products of vehicle and industrial exhausts are considered extremely dangerous for both human and environmental health. In the last years, the possibility to simultaneously photo-degrade water dissolved pollutants by means of ZnO nanostructures and to use their piezoelectric features to enhance the photo-degradation process has been investigated. In the present contribution, an easy and low-cost wet approach to synthetize hexagonal elongated ZnO microstructures in the wurtzite phase was developed. ZnO performances as photo-catalysts, under UV-light irradiation, were confirmed on water dissolved methylene blue dye. Piezoelectric responses of the synthetized ZnO microstructures were evaluated, as well, by depositing them into films onto flexible substrates, and a home-made layout was developed, in order to stimulate the ZnO microstructures deposited on solid supports by means of mechanical stress and UV photons, simultaneously. A relevant increment of the photo-degradation efficiency was observed when the piezopotential was applied, proposing the present approach as a completely eco-friendly tool, able to use renewable energy sources to degrade water solved pollutants.

Collagen represents one of the most widely used biomaterial for scaffolds fabrication in tissue engineering as it represents the mechanical support of natural tissues. It also provides physical scaffolding for cells and it influences their attachment, growth, and tissue regeneration. Among all fibrillary collagens, type I is considered one of the gold standard for scaffolds fabrication, thanks to its high biocompatibility, biodegradability, and hemostatic properties. It can be extracted by chemical and enzymatic protocols from several collagen-rich tissues, such as tendon and skin, of different animal species. Both the extraction processes and the manufacturing protocols for scaffolds fabrication provide structural and mechanical changes that can be tuned in order to deeply impact the properties of the final biomaterial. The aim of this review is to discuss the role of X-rays to study structural changes of type I collagen from fresh collagen-rich tissues (bovine, equine, fish) to the final scaffolds, with the aim to screen across available collagen sources and scaffolds fabrication protocols to be used in tissue regeneration.

Superparamagnetic magnetite nanoparticles were synthetized and capped by a SiO2 shell in order to avoid oxidation and aggregation of the iron oxide nanostructures. The inorganic capping was then further decorated by folic acid molecules, by using a very simple procedure exploiting supramolecular interactions among the organic moieties and the inorganic nanoparticles. The supramolecular nanoadduct thanks to folic acid molecules could act as a "Trojan horse" for the cancer cells and due to its superparamagnetic properties could induce local heat generation upon an appropriate magnetic field application. In fact, temperature was increased up to 42 °C when a 18 mT magnetic field was applied to the nanoparticles and the hybrid nanostructures were verified to be selectively internalized by HeLa cells, a human cervical cancer line known to overexpress the folic acid receptor.

For the first time, highly porous ZnO-based biomorphic materials were synthesised using cork as a natural sustainable template. In the first step, waste cork powder was pyrolysed and converted into inorganic carbon. This template was then infiltrated using a novel approach employing an aerosol of zinc-containing solutions. The infiltrated powders were calcined to convert the precursors into zinc oxide. Depending on temperature, these could form either a ZnO-graphite composite material, or pure ZnO. Their morphology, porosity, microstructure and composition were characterised; their optical band gap energies, ability to adsorb and photodegrade organic pollutants and UV absorption were also assessed. When heated to 350 degrees C they maintained the 3D porous cork structure, producing a graphite-containing composite material, with both physical adsorption and photocatalytic activity (E-g = 3.19 eV), suitable for environmental remediation. When heated to 700 degrees C, the powders were pure ZnO (no graphite), and they absorbed in the UV region, hence suitable for use as sunscreen. Doped ZnO ecoceramics were also produced, using silver and aluminium. An addition of 1 mol% Ag improved photocatalysis under solar light. Conversely, adding 2 mol% Al and calcining at 700 degrees C deactivated photocatalysis, but maintained strong UV absorption, producing a safer sunscreen material (no generation of free radicals). This is the first time that photocatalytic or UV absorption properties of any wood-derived biomorphic material or ecoceramic have been reported.

Ethane-bridged bis-porphyrin derivatives are reported for the selective detection of various analytes in sensing applications. The central metal ion is able to rule specific molecular arrangements upon analyte binding. Three bis-porphyrin compounds: a free base (metal free), Ni complex, and Cu complex, have been tested for histidine detection in aqueous media. Histidine is involved in various biological processes, including such deadly disease as lung cancer. The conformational changes of bis-porphyrins, induced by histidine binding, can be detected by monitoring the Soret band position. The spectroscopic characterization, at the air-water subphase interface, indicates that, in the presence of histidine, the Ni and Cu metallated derivatives undergo conformational changes. This behaviour was confirmed when these two derivatives were deposited onto the solid support by Langmuir-Schaefer (LS) technique. A prototypal Surface Plasmon Resonance (SPR) detection system for histidine based on these two porphyrin LS films was developed. The Cu substituted compound based SPR system allows the histidine sensing down to nanomolar concentration. Furthermore, a SPR response of the Ni bis-porphyrin shows a semilogarithmic dependence on the histidine concentration up to 10−6 M proposing the use of these two porphyrins in a sensor array for the monitoring of histidine levels in plasma.