Search Results (111)

Potassium-ion batteries hold great promise for large-scale energy storage, but their commercialization is hindered by the large ionic radius of potassium, which causes sluggish kinetics and severe volume expansion in anode materials. To address this, we present a scalable spray-drying strategy coupled with NaCl salt-templating to synthesize hierarchical porous carbon/vanadium sulfide microspheres (p-V₃S₄/C MS). In this structure, V₃S₄ nanoparticles are uniformly encapsulated within a dextrin-derived amorphous carbon matrix, and pores are formed via selective NaCl etching. This unique architecture accommodates volume fluctuations while providing rapid ion diffusion pathways. As a result, the p-V₃S₄/C MS anode exhibits outstanding electrochemical performance, maintaining a reversible capacity of 107 mA h g⁻¹ after 2000 cycles at 2.0 A g⁻¹, and achieves a high pseudocapacitive contribution of 93% at 2.0 mV s⁻¹. Furthermore, a full cell paired with a Prussian blue (PB) cathode demonstrates practical viability and robust reversibility. Our findings demonstrate that this structural engineering effectively mitigates internal resistance and structural degradation, offering a cost-effective route for mass-producing high-performance anodes for next-generation energy storage. Full article

Background/Objectives: The precise elimination of Schistosoma japonicum eggs within host tissues poses a significant therapeutic obstacle due to the ineffectiveness of existing drugs in penetrating the eggs’ protective shields. This investigation sought to create a surface-modified magnetic nanoparticle (MNP) framework to surmount this hurdle and realize targeted theranostics for combating schistosomiasis. Methods: Fe₃O₄ MNPs, MNP-NH₂, and MNP-COOH were synthesized and characterized before systematically studying their interactions with parasites. The intrinsic autofluorescence of eggs and adult worms served as an optical background for the investigation. In vitro co-incubation assays, confocal microscopy, and Prussian blue staining were utilized to quantify both adsorption and internalization. The in vivo efficacy was assessed in a Schistosoma japonicum murine model following tail vein injection. Results: A pronounced surface chemistry-dependent interaction was noted. Fe₃O₄ MNP and MNP-NH₂ displayed remarkable adsorption and effective internalization into eggs in vitro, while MNP-COOH exhibited limited uptake. This varying effectiveness was similarly observed in vivo, with Fe₃O₄ MNP and MNP-NH₂ predominantly gathering in hepatic granulomas and effectively infiltrating deposited eggs. Within adult worms, Fe₃O₄ MNP and MNP-COOH exhibited distribution on the tegument and within adult worms. Conclusions: We developed a functional MNP platform in which surface charge governs parasiticidal targeting. Among the candidates investigated, MNP-NH₂ proved to be the most efficient for egg-targeted theranostics. This study introduces an innovative nanotechnology-based approach for accurate diagnosis and treatment of schistosomiasis by specifically tackling the challenge of impermeable eggs. Full article

Textile dyeing effluents are characterized by recalcitrant organics and high salinity, requiring robust pretreatments prior to biological polishing. The heterogeneous Fenton-type (HFT) oxidation over Prussian Blue nanoparticles supported on γ-alumina (PBNP/γ-Al₂O₃) was investigated in a liquid batch-recycle packed-bed reactor treating a synthetic textile wastewater (STW) reproducing an industrial dye bath with the Reactive Black 5 (RB5) dye, together with simplified RB5 and RB5 + NaCl matrices. Hydrogen peroxide decay followed pseudo-first-order kinetics. Using fixed initial doses (11, 20, 35 mmol L⁻¹), the catalyst exhibited an early adaptation phase and then reproducible operation: from the fourth reuse onward, both the H₂O₂ decomposition rate constant and DOC removal varied by <10% under identical conditions. Among matrices, STW exhibited the highest oxidant efficiency. With an initial H₂O₂ dose of 11 mmol L⁻¹, the treatment enabled complete discoloration and produced effluents with negligible toxicity. Increasing the initial dose to 20 or 35 mmol L⁻¹ did not improve treatment and led to a decrease in the hydrogen peroxide decomposition rate with reuses and loss of PB ν(C≡N) Raman bands, indicating surface transformation. Overall, PBNP/γ-Al₂O₃ demonstrated reproducible activity and structural resilience in saline, dyeing-relevant matrices at H₂O₂ doses that preserve catalytic integrity, confirming its feasibility as a stable and reusable pretreatment catalyst for saline dyeing effluents, and supporting its integration into hybrid AOP–biological treatment schemes for dyeing wastewater. Full article

The wound healing (WH) process is often severely hindered by bacterial infections and prolonged inflammatory responses. To address this problem, we developed a novel injectable nanocomposite DPB-ODQ hydrogel, which comprises polydopamine-modified Prussian blue nanoparticles (PB@PDA, also called DPB) and an oxidized dextran/quaternized chitosan (QCS)-based Schiff-base network. This hydrogel possesses a highly interconnected porous structure, an excellent swelling rate (730%), rapid gelling speed (45 s), a high mass retention rate over a three-day period (73.20%), and exceptional self-healing properties. Based on the presence of PDA and the Schiff base, it also exhibited good adhesive strength (13.5 kPa). In addition, under near-infrared irradiation at 1.0 W/cm², temperatures increased by more than 35 °C within 5 min, indicating excellent photothermal (PT) performance. The PT performance of DPB, synergized with the inherent antibacterial properties of QCS, endowed it with a bactericidal rate exceeding 96% against both Staphylococcus aureus and Escherichia coli. In vitro cell experiments have shown that it significantly promoted fibroblast proliferation and migration. In experiments involving mice infected with S. aureus, DPB-ODQ demonstrated an impressive WH rate of 92.82%, greatly promoting collagen deposition. Full article

Herein we first attempt to compare the catalytic and electrocatalytic properties of the most commonly used peroxidase-mimicking nanozymes based on transition metal ions, including magnetite, cerium oxide, and Prussian Blue. For the nanomaterials under consideration, the catalytic rate constant for reducing substrate increases upon decreasing its redox potential and reaches its maximum value for Prussian Blue in the presence of ferrocyanide (k_cat = 3.8 s⁻¹ per single redox-active site). In addition to the highest k_cat, Prussian Blue nanoparticles in electrochemical sensors exhibit sensitivity to H₂O₂ more than three orders of magnitude higher than other nanomaterials. The sensing properties of the electrodes modified with Prussian Blue nanoparticles appear to be dependent on their diameter; particles with a diameter of 140 nm provide optimal sensitivity and lifespan of the corresponding sensor. The achieved exceptional (electro)catalytic properties of Prussian Blue nanoparticles open prospects for their application as universal labels for personal analyzers with either optical or electrochemical readout. Full article

As the direct energy source in organisms, accurate and simple detection of adenosine triphosphate (ATP) is of great significance. Herein, a colorimetric aptasensor for ATP determination was designed by integrating the CRISPR/Cas12a system with an aptamer, and with Prussian blue nanocube and gold nanoparticle co-functionalized MoS₂ (MoS₂-PBNCs-AuNPs) nanozymes. As expected, the introduced CRISPR/Cas12a system and aptamer could efficiently amplify the detection signal and improve the specific recognition ability, respectively. Meanwhile, the catalytic activity of the MoS₂-PBNCs-AuNPs nanozymes can be regulated with the concentration of ATP. The high-affinity binding of ATP to the aptamer competitively inhibited aptamer-crRNA hybridization, causing fewer Cas12 proteins to be activated. As a result, the uncleaved single-stranded DNA (ssDNA) adsorbed onto the surface of nanozymes to effectively enhance their catalytic oxidation capability toward 3,3′,5,5′-tetramethylbenzidine (TMB). According to this phenomenon, this CRISPR-enhanced colorimetric aptasensor can detect down to 0.14 μM ATP with high selectivity, reproducibility, and stability. In addition, acceptable recoveries and low relative standard deviations of the aptasensor for ATP determination suggest that it is promising for application in early detection of clinical-related diseases. Full article

Precise remote temperature sensing at the micro- and nanoscale is a growing necessity in modern science and technology. We report a series of luminescent tris-acetylacetonate lanthanide complexes, Ln(acac)₃(H₂O)₂ (Ln = Eu (1Eu), Tb (1Tb), Yb (1Yb)); acac⁻ = acetylacetonate), operating as self-referenced thermometers in the 290–350 K range, both in the solid state and when embedded in hybrid nanoparticles. Among the investigated systems, the Eu³⁺ complex exhibits excellent lifetime-based thermometric performance, achieving a maximum relative sensitivity (S_rmax) of 2.9%·K⁻¹ at 340 K with a temperature uncertainty (δT) as low as 0.02 K and an average temperature uncertainty ($\overline{\delta T}$) of 0.5 K, placing it among the most effective ratiometric lanthanide-based luminescent thermometers reported to date. The Yb³⁺ analog enables intensity-based thermometry in the near-infrared domain with a good sensitivity S_rmax = 0.5%·K⁻¹ at 293 K, δT = 0.5 K at 303 K, and $\overline{\delta T}$ = 1.6 K. These molecular thermometers were further incorporated into the shell of Prussian Blue@SiO₂ core–shell nanoparticles. Among the resulting hybrids, PB@SiO₂-acac/(1Tb/1Eu) (with a Tb/Eu ratio of 2/8) stood out by enabling ratiometric temperature sensing based on the Eu³⁺⁵D₀ → ⁷F₂ lifetime, with satisfactory parameters (S_rmax = 0.9%·K⁻¹, δT = 0.21 K at 303 K, and $\overline{\delta T}$ = 1.1 K). These results highlight the potential of simple coordination complexes and their nanohybrids for advanced luminescent thermometry applications. Full article

MnFe₂O₄ magnetic nanoparticles have shown broad application prospects in the field of tumor diagnosis and treatment; however, precise particle size regulation within the 100–200 nm range, as well as the synergistic integration of physical and medical functionalities, remains challenging. As a commonly used method for synthesizing MnFe₂O₄ nanoparticles, the solvothermal method has been proven to enable the regulation of the particle size of products, particularly its ability to utilize the viscosity of solvents as a method for particle size regulation. Therefore, this work investigates the influence of the diethylene glycol (DEG) to ethylene glycol (EG) ratio on particle size regulation in solvothermal synthesis of MnFe₂O₄ nanoparticles, and constructs MnFe₂O₄@PB nanocomposite materials. The results demonstrate that with the DEG ratio increasing from 0 to 80% in a DEG:EG mixed solvent system, the average particle size of MnFe₂O₄ nanoparticles can be reduced from 266 nm to 105 nm. The MPB4.5 sample (MnFe₂O₄:PB molar ratio = 5:4.5 in the MnFe₂O₄@PB nanostructure) exhibits an optimal photothermal heating effect and good photothermal stability, demonstrating potential as a photothermal therapeutic agent. The resultant MnFe₂O₄@PB system provides a strategy for precise particle size regulation and functional integration for photothermal therapy of tumors with magnetic targeting potential. Full article

Background/Objectives: Gamma irradiation is a promising terminal sterilization method for nanoparticle-based biomedical systems. However, its potential effects on the physicochemical properties and biological performance of multifunctional nanomaterials must be carefully evaluated. This study aimed to assess the structural integrity, sterility, and cytocompatibility of magnetic nanoparticles (MNPs) and bioactive-glass-coated magnetic nanoparticles (MNPBGs), both based on magnetite (Fe₃O₄), after gamma irradiation. Methods: MNPs and MNPBGs were synthesized and subjected to gamma irradiation at 25 kGy, with additional doses explored in preliminary evaluations. Physicochemical characterizations were performed using XRD, TEM, SAED, and Raman spectroscopy. FTIR analyses were conducted on bioactive glass (BG) controls without magnetite. Sterility was evaluated via microbiological assays. Cytocompatibility and nitric oxide (NO) production were assessed using RAW 264.7 macrophages and Saos-2 osteosarcoma cells. Prussian blue staining was used to evaluate cellular uptake. Results: Gamma irradiation preserved the crystal structure, morphology, and size distribution of the nanoparticles. FTIR revealed only minor changes in the silicate network of BG, such as reduced intensity and slight shifting of Si-O-Si and Si-O-NBO bands, indicating limited radiation-induced structural rearrangement without affecting the material’s stability or cytocompatibility. Microbiological assays confirmed complete inhibition of microbial growth. All irradiated samples exhibited high cytocompatibility, with MNPBGs demonstrating enhanced biological responses. Notably, MNPBGs induced a more pronounced NO production in macrophages. Cellular uptake of nanoparticles by Saos-2 cells remained unaffected after irradiation. Conclusions: Gamma irradiation at 25 kGy is an effective sterilization strategy that maintains the structural and functional integrity of MNPs and MNPBGs. These findings support their safe use in sterile biomedical applications, particularly for bone-related therapies involving immunomodulation and drug delivery, with potential relevance for cancer treatment strategies such as osteosarcoma. Full article

Tracking T cells in vivo using MRI is a major challenge due to the difficulty of labeling these non-phagocytic cells with a sufficient contrast agent to generate a detectable signal change. In this study, we explored CD4-Superparamagnetic iron oxide nanoparticles (SPION), which is commonly used in magnetic cell sorting, as a potential receptor-mediated, specific CD4⁺ T cell MRI labeling agent. We optimized the labeling protocol for maximal CD4⁺ cell labeling and viability. Cell health was confirmed with trypan blue assay, and labeling efficacy was confirmed with Prussian blue staining, transmission electron microscopy, and MRI of labeled cell pellets. Key cell functionality was assessed by flow cytometry. Next, CD4-SPION-labeled T cells or unlabeled T cells were delivered via intravenous injection in naïve mice. Liver MRIs pre-, 24 h, and 72 h post-T cell injection were performed to determine in vivo tracking ability. Our results show that CD4-SPION induces significant attenuation of T2 signals in a concentration-dependent manner, confirming their potential as an effective MRI contrast agent. In vitro, analyses showed that CD4⁺ T cells were able to uptake CD4-SPION without affecting cellular activity and key functions, as evidenced by Prussian blue staining and flow cytometric analysis of IL-2 receptor and the IL-7 receptor α-chains, CD69 upregulation, and IFN-γ secretion. In vivo, systemically distributed CD4-SPION-labeled T cells could be tracked in the liver at 24 and 72 h after injection, contrary to controls. Histological staining of tissue sections validated the findings. Our results showed that SPION CD4⁺ T cell sorting coupled with longitudinal MR imaging is a valid method to track CD4⁺ T cells in vivo. This safe, specific, and sensitive approach will facilitate the use of SPION as an MRI contrast agent in clinical practice, allowing for non-invasive tracking of adoptive cell therapies in multiple disease conditions. Full article

Overuse of tert-butylhydroquinone (TBHQ) as a food antioxidant has the potential to pollute the environment and threaten human health. Therefore, it is imperative to develop precise and rapid methods to detect TBHQ in food products. In this study, Fe- and Mn-doped Prussian blue analogs (FeMn-PBAs) were prepared by co-precipitation, FeMn-PBAs/PAN was prepared by electrostatic spinning, and a novel FeMn@C/CNFs composite was prepared by carbonization in nitrogen. Bimetallic FeMn doping has been shown to reduce vacancy defects and enhance the structural stability of PBA. Furthermore, electrostatic spinning has been demonstrated to reduce the agglomeration of PBA nanoparticles, which are electrode-modifying materials with high stability and good electrical conductivity. The morphological and structural characteristics of the FeMn@C/CNF composites were examined using scanning electron microscopy (SEM), X-ray diffraction (XRD), transmission electron microscopy (TEM), and X-ray photoelectron spectroscopy (XPS). The electrochemical behavior of tert-butyl hydroquinone in FeMn@C/CNFs was studied by cyclic voltammetry (CV), differential pulse voltammetry (DPV), and chronocoulometry (CC). The results demonstrate that the sensor exhibits excellent repeatability, reproducibility, and anti-interference capabilities. The prepared electrochemical sensor can be effectively utilized for the detection of TBHQ in food samples such as soybean and peanut oil samples, proving its strong potential for practical applications. Full article

Polarized Small-Angle Neutron Scattering is a versatile low-energy neutron scattering technique that allows for the access of magnetic information on nanosize objects of size 2–100 nm, from individual properties like the magnetization distribution inside the object to the collective behaviors, e.g., spin-glass effects or long-range magnetic ordering. The multi-scale possibilities of this technique is particularly relevant to encompass simultaneously the individual and collective many-body phenomena. In this article, we report the direct measurement of the magnetic form factor of “Prussian Blue Analog” molecular-based Ferromagnetic nanoparticles ${\mathrm{Cs}}_{\mathrm{x}}^{\mathrm{I}}{\mathrm{Ni}}^{\mathrm{II}}\left[{\mathrm{Cr}}^{\mathrm{III}}{\left(\mathrm{CN}\right)}_6\right]$ embedded in a polymer matrix with use of Polarized Small-Angle Neutron Scattering. We show that PSANS is particularly adapted to evaluate the internal magnetization distribution in nanoparticles and determine their magnetic morphology. Full article

Prussian Blue (PB) is commonly incorporated into screen-printed enzymatic devices since it enables the determination of the enzymatically produced hydrogen peroxide at low potentials. Inkjet printing is gaining popularity in the development of electrochemical sensors as a substitute for screen printing. This work presents a fully inkjet-printed graphene–Prussian Blue platform, which can be paired with oxidase enzymes to prepare a biosensor of choice. The graphene electrode was inkjet-printed on a flexible polyimide substrate and then thermally and photonically treated with intense pulsed light, followed by inkjet printing of a PB nanoparticle suspension. The optimization of post-printing treatment and electrode deposition conditions was performed to yield a platform with minimal sheet resistance and peak potential differences. A thorough study of PB deposition was conducted: the fully inkjet-printed system was compared against sensors with PB deposited chemically or by drop casting the PB suspension on different kinds of carbon electrodes (glassy carbon, commercial screen-printed, and in-house inkjet-printed electrodes). For hydrogen peroxide detection, the fully inkjet-printed platform exhibits excellent sensitivity, a wider linear range, better linearity, and greater stability towards higher concentrations of peroxide than the other tested electrodes. Finally, lactate oxidase was immobilized in a chitosan matrix, and the prepared biosensor exhibited analytical performance comparable to other lactate sensors found in the literature in a wide, physiologically relevant linear range for measuring lactate concentration in sweat. The development of mediator-modified electrodes with a single fabrication technology, as demonstrated here, paves the way for the scalable production of low-cost, wearable, and flexible biosensors. Full article

Prussian blue nanoparticles (PBNPs) have been identified as a promising candidate for biomimetic peroxidase (POD)-like activity, specifically due to the metal centres (Fe³⁺/Fe²⁺) of Prussian blue (PB), which have the potential to function as catalytically active centres. The decoration of PBNPs with desired functional polymers (such as amino- or carboxylate-based) primarily facilitates the subsequent linkage of biomolecules to the nanoparticles for their use in biosensor applications. Thus, the elucidation of the catalytic POD mimicry of these systems is of significant scientific interest but has not been investigated in depth yet. In this report, we studied a series of poly(ethyleneimine) (PEI)-mediated PBNPs (PB/PEI NPs) prepared using various synthesis protocols. The resulting range of particles with varying size (~19–92 nm) and shape combinations were characterised in order to gain insights into their physicochemical properties. The POD-like nanozyme activity of these nanoparticles was then investigated by utilising a 3,3′,5,5′-tetramethylbenzidine (TMB)/H₂O₂ system, with the catalytic performance of the natural enzyme horseradish peroxidase (HRP) serving as a point of comparison. It was shown that most PB/PEI NPs displayed higher catalytic activity than the PBNPs, with higher activity observed in particles of smaller size, higher Fe content, and higher Fe²⁺/Fe³⁺ ratio. Furthermore, the nanoparticles demonstrated enhanced chemical stability in the presence of acid, sodium azide, or high concentrations of H₂O₂ when compared to HRP, confirming the viability of PB/PEI NPs as a promising nanozymatic material. This study disseminates fundamental knowledge on PB/PEI NPs and their POD-like activities, which will facilitate the selection of an appropriate particle type for future biosensor applications. Full article

Objectives: To design a multifunctional nanozyme hydrogel with antibacterial, photo-responsive nitric oxide-releasing, and antioxidative properties for promoting the healing of infected wounds. Methods: We first developed ultra-small silver nanoparticles (NPs)-decorated sodium nitroprusside-doped Prussian blue (SNPB) NPs, referred to as SNPB@Ag NPs, which served as a multifunctional nanozyme. Subsequently, this nanozyme, together with geniposide (GE), was incorporated into a thermo-sensitive hydrogel, formulated from Poloxamer 407 and carboxymethyl chitosan, creating a novel antibacterial wound dressing designated as GE/SNPB@Ag hydrogel. The physical properties of a GE/SNPB@Ag hydrogel were systematically investigated. Results: After embedding the nanozyme and GE, the resulting GE/SNPB@Ag hydrogel retains its thermosensitive properties and exhibits sustained release characteristics. In addition to its catalase-like activity, the nanozyme demonstrates high photothermal conversion efficiency, photo-induced nitric oxide release, and antibacterial activity. In addition, the hydrogel exhibits favorable antioxidant properties and high biocompatibility. The results of animal experiments demonstrate that the composite hydrogel combined with laser irradiation is an effective method for promoting infected wound healing. Conclusions: In vitro and in vivo studies indicate that the resulting GE/SNPB@Ag hydrogel holds significant potential for the treatment of infected wounds and for further clinical applications. Full article