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The ability to replicate the microenvironment of biological tissues creates unique biomedical possibilities for stem cell applications. Current fabrication methods are limited by either the control on feature size and shape, or by the throughput and size of the replicas. Here, a novel platform is reported that combines thermal scanning probe lithography (tSPL) with innovative methodologies for the low‐cost and high‐throughput nanofabrication of large area quasi‐3D bone tissue replicas with high fidelity, sub‐15 nm lateral precision, and sub‐2 nm vertical resolution. This bio‐tSPL platform features a biocompatible polymer resist that withstands multiple cell culture cycles, allowing the reuse of the replicas, further decreasing costs and fabrication times. The as‐fabricated replicas support the culture and proliferation of human induced mesenchymal stem cells, which display broad therapeutic and biomedical potential. Furthermore, it is demonstrated that bio‐tSPL can be used to nanopattern the bone tissue replicas with amine groups, for subsequent tissue‐mimetic biofunctionalization. The achieved level of time and cost‐effectiveness, as well as the cell compatibility of the replicas, make bio‐tSPL a promising platform for the production of tissue‐mimetic replicas to study stem cell‐tissue microenvironment interactions, test drugs, and ultimately harness the regenerative capacity of stem cells and tissues for biomedical applications. [ABSTRACT FROM AUTHOR]

The combination of highly sensitive techniques such as electrochemiluminescence (ECL) with nanotechnology sparked new analytical applications, in particular for immunoassay‐based detection systems. In this context, nanomaterials, particularly dye‐doped silica nanoparticles (DDSNPs) are of high interest, since they can offer several advantages in terms of sensitivity and performance. In this work we synthesized two sets of monodispersed and biotinylated [Ru(bpy)3]2+‐doped silica nanoparticles, named bio‐Triton@RuNP and bio‐Igepal@RuNP, obtained following the reverse microemulsion method using two different types of nonionic surfactants. Controlling the synthetic procedures, we were able to obtain nanoparticles (NPs) offering highly intense signal, using tri‐n‐propylamine (TPrA) as coreactant, with bio‐Triton@RuNps being more efficient than bio‐Igepal@RuNP. [ABSTRACT FROM AUTHOR]

The combination of highly sensitive techniques such as electrochemiluminescence (ECL) with nanotechnology sparked new analytical applications, in particular for immunoassay‐based detection systems. In this context, nanomaterials, particularly dye‐doped silica nanoparticles (DDSNPs) are of high interest, since they can offer several advantages in terms of sensitivity and performance. In this work we synthesized two sets of monodispersed and biotinylated [Ru(bpy)3]2+‐doped silica nanoparticles, named bio‐Triton@RuNP and bio‐Igepal@RuNP, obtained following the reverse microemulsion method using two different types of nonionic surfactants. Controlling the synthetic procedures, we were able to obtain nanoparticles (NPs) offering highly intense signal, using tri‐n‐propylamine (TPrA) as coreactant, with bio‐Triton@RuNps being more efficient than bio‐Igepal@RuNP. [ABSTRACT FROM AUTHOR]

The use of electrochemiluminescence (ECL), i.e., chemiluminescence triggered by electrochemical stimulus, as emitting light source for microscopy is an emerging approach with different applications ranging from the visualization of nanomaterials to cell mapping. In this trend article, we give an overview of the state of the art in this new field with the purpose to illustrate all the possible applications so far explored as well as describing the mechanism underlying this transduction technique. The results discussed here would highlight the great potential of the combination between ECL and microscopy and how this marriage can turn into an innovative approach with specific application in analytical sciences. [ABSTRACT FROM AUTHOR]

Bone microenvironment, human induced pluripotent stem cells, nanofabrication, thermal scanning probe lithography, tissue engineering Tissue Engineering: Cost and Time Effective Lithography of Reusable Millimeter Size Bone Tissue Replicas With Sub-15 nm Feature Size on A Biocompatible Polymer (Adv. Funct. Keywords: bone microenvironment; human induced pluripotent stem cells; nanofabrication; thermal scanning probe lithography; tissue engineering EN bone microenvironment human induced pluripotent stem cells nanofabrication thermal scanning probe lithography tissue engineering 1 1 1 05/12/21 20210510 NES 210510 In article number 2008662, Elisa Riedo, Giuseppe Maria de Peppo, and co-workers describe a novel thermochemi cal scanning probe lithography (tSPL)-based platform for the low-cost and high throughput fabrication of bone tissue replicas in a biocompatible material with nanoscale resolution. [Extracted from the article]

Frontispiz: Dye-Doped Silica Nanoparticles for Enhanced ECL-Based Immunoassay Analytical Performance Keywords: ECL imaging; electrochemiluminescence; electrochemistry; nanomaterials; silica nanoparticles EN ECL imaging electrochemiluminescence electrochemistry nanomaterials silica nanoparticles 1 1 1 11/26/20 20201201 NES 201201 B Kontrastmittel b In der Zuschrift auf S. 22042 berichten L. Prodi et al. über die Synthese einer neuen Familie von farbstoffdotierten Silika-Nanopartikeln und deren Anwendung in der effizienten Elektrochemilumineszenz-Bildgebung. ECL imaging, electrochemiluminescence, electrochemistry, nanomaterials, silica nanoparticles. [Extracted from the article]

Electrogenerated chemiluminescence (ECL) stands out as a remarkable phenomenon of light emission at electrodes initiated by electrogenerated species in solution. Characterized by its exceptional sensitivity and minimal background optical signals, ECL finds applications across diverse domains, including biosensing, imaging, and various analytical applications. This review aims to serve as a comprehensive guide to the utilization of ECL in analytical applications. Beginning with a brief exposition on the theory at the basis of ECL generation, we elucidate the diverse systems employed to initiate ECL. Furthermore, we delineate the principal systems utilized for ECL generation in analytical contexts, elucidating both advantages and challenges inherent to their use. Additionally, we provide an overview of different electrode materials and novel ECL-based protocols tailored for analytical purposes, with a specific emphasis on biosensing applications. [ABSTRACT FROM AUTHOR]

Silicon carbide (SiC) is one of the hardest known materials. Its exceptional mechanical properties combined with its high thermal conductivity make it a very attractive material for a variety of technological applications. Recently, it is discovered that two‐layer epitaxial graphene films on SiC can undergo a pressure activated phase transition into a sp3 diamene structure at room temperature. Here, it is shown that epitaxial graphene films grown on SiC can increase the hardness of SiC up to 100% at low loads (up to 900 µN), and up to 30% at high loads (10 mN). By using a Berkovich diamond indenter and nanoindentation experiments, it is demonstrated that the 30% increase in hardness is present even for indentations depths of 175 nm, almost three hundred times larger than the graphene film thickness. The experiments also show that the yield point of SiC increases up to 77% when the SiC surface is coated with epitaxial graphene. These improved mechanical properties are explained with the formation of diamene under the indenter's pressure. [ABSTRACT FROM AUTHOR]

Nanoelectrode arrays (NEAs) are increasingly applied for a variety of electroanalytical applications; however, very few studies dealt with the use of NEAs as an electrochemical generator of electrogenerated chemiluminescence (ECL). In the present study, arrays of nanodisc and nanoband electrodes with different dimensions and inter-electrode distances were fabricated by e-beam lithography on a polycarbonate layer deposited on boron-doped diamond (BDD) substrates. In particular, NEAs with 16 different geometries were fabricated on the same BDD sample substrate obtaining a multiple nanoelectrode and ultramicroelectrode array platform (MNEAP). After electrochemical and morphological characterization, the MNEAP was used to capture simultaneously with a single image the characteristic behaviour of ECL emission from all the 16 arrays. Experiments were performed using Ru(bpy) as the ECL luminophore and tri- n-propylamine (TPrA) as the co-reactant. With a relatively limited number of experiments, such an imaging procedure allowed to study the role that geometrical and mechanistic parameters play on ECL generation at NEAs. In particular, at high concentrations of TPrA, well-separated individual ECL spots or bands revealed an ECL signal which forms a pattern matching the nanofabricated structure. The analysis of the imaging data indicated that the thickness of the ECL-emitting zone at each nanoelectrode scales inversely with the co-reactant concentration, while significantly stronger ECL signals were detected for NEAs operating under overlap conditions. [ABSTRACT FROM AUTHOR]

Detection of nucleic acids is crucial in many medical applications, and in particular for monitoring infectious diseases, as it has become perfectly clear after the pandemic infection of COVID-19. In this context, the development of innovative detection methods based on signal-amplification rather than analyte-amplification represents a significant breakthrough compared to existing PCR-based methodologies, allowing the development of new nucleic acid detection technologies suitable to be integrated in portable and low-cost sensor devices while keeping high sensitivities, thus enabling massive diagnostic screening. In this work, we present a novel molecular sensor for the ultrasensitive PCR-free detection of Hepatitis B Virus (HBV) based on electrochemiluminescence (ECL). Thanks to the combination of surface cooperative hybridization scheme with ECL detection strategy, our novel DNA sensor is able to detect HBV genome – both synthetic and extracted – with the unprecedented limit of detection (LoD) of 0.05 cps μL−1 for extracted sample, that is even lower than the typical LoD of PCR methodologies. The detection concept presented here for HBV detection is very versatile and can be extended to other pathogens, paving the way for future development of rapid molecular test for infectious diseases, both viral and bacterial, in Point-of-Care (PoC) format. • We have developed a versatile platform based on electrochemiluminescence for ultrasensitive amplification-free detection of virus genome. •Surface cooperative hybridization combined with ECL detection strategy allow the ultrasensitive detection of HBV genome. •Molecular sensor based on ECL is used to quantify extracted viral DNA in ultralow concentrations (0.06cps/μL). [ABSTRACT FROM AUTHOR]

Electrochemiluminescence (ECL), an intriguing luminescent phenomenon induced by electrochemical stimulation, has evolved from studying electron transfer reactions to a powerful analytical method and imaging technique. ECL can be generated through annihilation or co-reactant methods, with recent advancements integrating it into imaging devices for diverse applications. This review traces the evolution of ECL from its early applications to recent developments in imaging technology. Notably, the utilization of charge-coupled devices (CCD) and electron multiplying charge-coupled devices (EMCCD) in ECL microscopy has revolutionized imaging capabilities, making it a cost-effective option for point-of-care testing. The review explores the heterogeneous ECL mechanism, emphasizing its limitations and challenges in visualizing objects away from the electrode surface. The synergy between ECL and microscopy is highlighted, showcasing its diverse applications and contributions to understanding ECL mechanisms and improving its use in biological contexts. Finally, the review encapsulates innovative approaches in material design, surface modification, and electrode architecture, providing a comprehensive overview of strategies to control the active layer of the ECL and advance ECL microscopy. [ABSTRACT FROM AUTHOR]

Carbon dots (CDs), defined by their size of less than 10 nm, are a class of photoluminescent (PL) and electrochemiluminescent (ECL) nanomaterials that include a variety of carbon‐based nanoparticles. However, the control of their properties, especially ECL, remains elusive and afflicted by a series of problems. Here, the authors report CDs that display ECL in water via coreactant ECL, which is the dominant mechanism in biosensing applications. They take advantage of a multicomponent bottom‐up approach for preparing and studying the luminescence properties of CDs doped with a dye acting as PL and ECL probe. The dependence of luminescence properties on the surface chemistry is further reported, by investigating the PL and ECL response of CDs with surfaces rich in primary, methylated, or propylated amino groups. While precursors that contribute to the core characterize the PL emission, the surface states influence the efficiency of the excitation‐dependent PL emission. The ECL emission is influenced by surface states from the organic shell, but states of the core strongly interact with the surface, influencing the ECL efficiency. These findings offer a framework of pre‐ and post‐synthetic design strategies to improve ECL emission properties, opening new opportunities for exploring biosensing applications of CDs. [ABSTRACT FROM AUTHOR]

Carbon dots (CDs), defined by their size of less than 10 nm, are a class of photoluminescent (PL) and electrochemiluminescent (ECL) nanomaterials that include a variety of carbon‐based nanoparticles. However, the control of their properties, especially ECL, remains elusive and afflicted by a series of problems. Here, the authors report CDs that display ECL in water via coreactant ECL, which is the dominant mechanism in biosensing applications. They take advantage of a multicomponent bottom‐up approach for preparing and studying the luminescence properties of CDs doped with a dye acting as PL and ECL probe. The dependence of luminescence properties on the surface chemistry is further reported, by investigating the PL and ECL response of CDs with surfaces rich in primary, methylated, or propylated amino groups. While precursors that contribute to the core characterize the PL emission, the surface states influence the efficiency of the excitation‐dependent PL emission. The ECL emission is influenced by surface states from the organic shell, but states of the core strongly interact with the surface, influencing the ECL efficiency. These findings offer a framework of pre‐ and post‐synthetic design strategies to improve ECL emission properties, opening new opportunities for exploring biosensing applications of CDs. [ABSTRACT FROM AUTHOR]

The coupling of nanomaterials, and nanoparticles in particular, with one of the most powerful transduction techniques, electrochemiluminescence (ECL), i.e., chemiluminescence triggered by electrochemical reactions at electrodes, has recently provided sensing tools with unprecedented sensitivity limits. This review aims to give an overview of the state of the art in the field over the last 5 years, i.e., a time span covering over 80% of the scientific production in this context. The results herein discussed would demonstrate that the use of nanoparticles in the ECL technique represents one of the most interesting research lines for the development of ultrasensitive analytical tools, offering an insight to recognize and select the best nanomaterials for ECL signal amplification, with particular emphasis in biosensing. [ABSTRACT FROM AUTHOR]

We report the nanopatterning of the methylammonium lead iodide (MAPbI 3 ) perovskite, a polycrystalline hybrid organic-inorganic semiconductor with very promising perspectives for photovoltaic and optoelectronic applications. Nanopatterning of MAI is obtained via Pulsed-NIL technology, an ultrafast version of the thermal nanoimprint lithography (NIL) based on stamps with integrated heaters. By Pulsed-NIL we were able to replicate onto the hybrid perovskite structures with details at the sub-100 nm scale, in spite of its crystalline nature. This work shows a new possibility for the exploitation of organo-metal halide perovskites in optoelectronic devices with more complex architectures than just planar films. [ABSTRACT FROM AUTHOR]

[Display omitted] • Polycrystalline cerium oxide thin films (CeO 2 /GC) were studied as an electrode for ECL detection of sarcosine (SA). • CeO 2 /GC was applied for detection of SA in the concentration range used in clinical assays for prostate cancer diagnostics. • Modification of the GC electrode by CeO 2 increases the electrode's electroactive area and enhances its catalytic properties. • CeO 2 /GC electrode revealed higher ECL signal stability due to its higher surface area. Prostate cancer (PCa) is widely spread in male population, especially over 65 years. Currently used medical methods of PCa diagnosis often lead to false-positive results thus new non-invasive methods for PCa detection, such as urine tests for cancer metabolites, are actively studied. Herein, nanostructured polycrystalline cerium oxide thin films (CeO 2 /GC) prepared by magnetron sputtering on a glassy carbon substrate are tested for electrochemiluminescent (ECL) detection of sarcosine exploiting the oxidative-reduction mechanism using Ru(bpy) 3 2+ as luminophore. Non-functionalized CeO 2 /GC electrodes revealed a higher ECL signal stability compared to bare glassy carbon electrodes. Moreover, CeO 2 /GC electrodes were successfully applied for rapid and sensitive detection of different sarcosine concentrations ranging from 50 to 5000 µM. These results open new possibilities for developing sensing platforms for sarcosine detection based on the CeO 2 /GC working electrode via surface modification and functionalization, aiming to further investigate and improve their sensitivity and selectivity. [ABSTRACT FROM AUTHOR]

Glucocorticoids are universally used in the treatment of acute lymphoblastic leukemia (ALL), and resistance to glucocorticoids in leukemia cells confers poor prognosis. To elucidate mechanisms of glucocorticoid resistance, we determined the prednisolone sensitivity of primary leukemia cells from 444 patients newly diagnosed with ALL and found significantly higher expression of CASP1 (encoding caspase 1) and its activator NLRP3 in glucocorticoid-resistant leukemia cells, resulting from significantly lower somatic methylation of the CASP1 and NLRP3 promoters. Overexpression of CASP1 resulted in cleavage of the glucocorticoid receptor, diminished the glucocorticoid-induced transcriptional response and increased glucocorticoid resistance. Knockdown or inhibition of CASP1 significantly increased glucocorticoid receptor levels and mitigated glucocorticoid resistance in CASP1-overexpressing ALL. Our findings establish a new mechanism by which the NLRP3-CASP1 inflammasome modulates cellular levels of the glucocorticoid receptor and diminishes cell sensitivity to glucocorticoids. The broad impact on the glucocorticoid transcriptional response suggests that this mechanism could also modify glucocorticoid effects in other diseases. [ABSTRACT FROM AUTHOR]