Surface Of Nanoparticles Research Articles

Selectivity Modulation of Multistep Reduction Reactions by Gold Nanoclusters

The selective synthesis of valuable azo‐ and azoxyaromatic chemicals via transfer coupling of nitroaromatic compounds has been achieved by fine‐tuning the catalyst structure. Here, a direct method to modulate nitrobenzene reduction and selectively alter the product from azobenzene to azoxybenzene by employing the size effect of Au is reported. Au nanoclusters (NCs) with smaller sizes embedded in ZIF‐8 controllably converted nitrobenzene into azoxybenzene, while supported Au nanoparticles (NPs) catalyzed nitrobenzene reduction to azobenzene. X‐ray photoelectron spectroscopy (XPS) and Diffuse reflectance infrared Fourier transform spectroscopy on CO adsorption (CO‐DRIFTS) of Au NC/ZIF‐8 revealed a higher valence state and a lower electron density of Au than that of Au NP/ZIF‐8, combined with the desorption of azoxybenzene from the Au NC and Au NP surface, suggesting that the Au NCs with lower electron density exhibit stronger adsorption. Density functional theory (DFT) calculations and charge density difference maps indicated that azoxybenzene bonded to Au NC/ZIF‐8 with greater adsorption energy, resulting in more electron transfer between azoxybenzene and the generated Au sites, which inhibited further reduction of azoxybenzene and resulted in high azoxybenzene selectivity. The application of the size effect of Au particles to regulate nitrobenzene transfer coupling provided new insights into the structure‐selectivity relationships.

Selectivity Modulation of Multistep Reduction Reactions by Gold Nanoclusters.

The selective synthesis of valuable azo- and azoxyaromatic chemicals via transfer coupling of nitroaromatic compounds has been achieved by fine-tuning the catalyst structure. Here, a direct method to modulate nitrobenzene reduction and selectively alter the product from azobenzene to azoxybenzene by employing the size effect of Au is reported. Au nanoclusters (NCs) with smaller sizes embedded in ZIF-8 controllably converted nitrobenzene into azoxybenzene, while supported Au nanoparticles (NPs)catalyzed nitrobenzene reduction to azobenzene. X-ray photoelectron spectroscopy (XPS) and Diffuse reflectance infrared Fourier transform spectroscopy on CO adsorption (CO-DRIFTS) of Au NC/ZIF-8 revealed a higher valence state and a lower electron density of Au than that of Au NP/ZIF-8, combined with the desorption of azoxybenzene from the Au NC and Au NP surface, suggesting that the Au NCs with lower electron density exhibit stronger adsorption. Density functional theory (DFT) calculations and charge density difference maps indicated that azoxybenzene bonded to Au NC/ZIF-8 with greater adsorption energy, resulting in more electron transfer between azoxybenzene and the generated Au sites, which inhibited further reduction of azoxybenzene and resulted in high azoxybenzene selectivity. The application of the size effect of Au particles to regulate nitrobenzene transfer coupling provided new insights into the structure-selectivity relationships.

L-Type amino acid transporter 1-targeting nanoparticles for antisense oligonucleotide delivery to the CNS

L-type amino acid transporter 1 (LAT1)-specific ligands and polyion complexes are used as brain-specific targets to deliver RNA-based drugs across the blood-brain barrier. We characterized a LAT1-targeting antisense oligonucleotide (ASO) encapsulated nanoparticle, “Phe-NPs/ASO.” A 25% density of phenylalanine effectively binds to the surface of LAT1 targeting nanoparticles in the GL261-Luc cells and Phe-NPs/ASO showed higher binding affinity compared to that without phenylalanine by cellular binding assay. To further characterize the blood-brain barrier-targeting effect and tissue distribution following a single-dose intravenous injection in mice, we performed in vivo biodistribution studies using fluorescence imaging. The Phe-NPs/ASO were detected in the brain tissue 1 h post-intravenous at an approximately 64-fold higher ratio than that of the same ASOs administered in the absence of any nanoparticle carrier. The brain tissue delivery of antisense oligonucleotide-loaded Phe-NPs was also confirmed in a fluorescence imaging study performed in non-human primates. These results demonstrate that Phe-NPs may successfully deliver an ASO to the brain tissue across brain regions. Phe-nanoparticles loaded with RNA-based drugs have the potential to treat diseases of the central nervous system, including all forms of neurodegenerative diseases.

Silica Nanoparticles Decorated with Ceria Quantum Dots Modulate Intra- and Extracellular Reactive Oxygen Species Formation and Selectively Reduce Human A375 Melanoma Cell Proliferation.

Nanomaterials show great promise for cancer treatment. Nonetheless, most nanomaterials lack selectivity for cancer cells, damaging healthy ones. Cerium dioxide (ceria, CeO2) nanoparticles have been shown to exert selective toxicity toward cancer cells due to the redox modulating properties they display as their size decreases. However, these particles suffer from poor suspension stability. The efficacy of CeO2 nanoparticles for cancer treatment is hampered by their innate high surface energy, which leads to particle agglomeration and, consequently, reactivity loss. This effect increases as particle size decreases; as such, quantum dots (QDs) suffer most from this phenomenon. In this study, it is proposed that silicon dioxide (silica, SiO2) nanoparticles can provide an inert platform for surface encrusted CeO2 QDs and that the resulting nanocomposite (hereafter QDCeO2/SiO2) not only will exhibit negligible agglomeration compared with CeO2 alone but also will improve the modulation of reactive oxygen species (ROS) leading to selective reduction of human A375 melanoma cell proliferation. The SiO2 nanoparticles had a bimodal size distribution with median particle size of 66 and 168 nm, while the CeO2 quantum dots encrusted on their surface had a size of 3.2 nm. An elevated Ce3+/Ce4+ ratio led to the QDCeO2/SiO2 nanocomposite displaying synergistic superoxide dismutase- and catalase-like activity, favoring the accumulation of ROS at pH 6.5 which translated into QDCeO2/SiO2 exerting selective oxidative stress in, and toward, the melanoma cells. Treatment with 50 μg mL-1 QDCeO2/SiO2 significantly reduced cell proliferation by 27% compared to untreated control cells in the colony formation assay. Treatment with either SiO2 or CeO2 alone did not affect the cell proliferation. These results highlight the benefit of dispersing CeO2 QDs on the surface of core nanoparticles and the resulting enhancement of selective redox reactivity and proliferation arrest when compared to CeO2 nanoparticles alone. Furthermore, the method employed here to encrust CeO2 QDs could lead to the facile synthesis of new nanocomposites with enhanced control of ROS activity, not only for in vitro studies using other cancer cell lines of interest but also in animal models and perhaps leading to clinical trials in melanoma patients.

Key Control Characteristics of Carbon Black Materials for Fuel Cells and Batteries for a Standardized Characterization of Surface Properties

AbstractCarbon Blacks (CBs) are primarily used in electrocatalysis as support materials for nanoparticulate electrocatalysts. In fuel cells, CBs, catalysts, and proton conductive polymers (ionomers) undergo a dispersion/homogenization process for electrode coating. The interactions between components in dispersion and the surface of CB particles are complex. The surface characteristics of CB particles impact slurry formulation, electrode coating, and the resulting electrode layer, affecting fuel cell and battery performance and durability. This study investigates commercially available CBs such as Vulcan XC72R, Ketjen Black EC‐300J, Ketjen Black EC‐600JD, and Super C65, focusing on application‐relevant key control characteristics (KCCs). The KCCs include physicochemical features like electrical conductivity (electron transport through the catalyst layer, CL), oxygen‐containing surface groups (hydrophilicity/phobicity of the CL, catalyst functionalization), surface basicity/acidity, ionomer adsorption, and particle dispersibility (catalyst ink stability). KCCs are determined by particle bulk electrical conductivity, Boehm titration (BT), isoelectric point (IEP), and Hansen solubility parameters (HSP). HSP, understood as similarity parameters for particles, indicate how nanoparticle surfaces interact with liquids during dispersion. The proposed KCCs serve as a starting point for characterizing CBs and guiding product design to obtain meaningful structure‐property relationships, essential for a successful energy transition.

Mass Spectrometry-Based Top-Down Proteomics in Nanomedicine: Proteoform-Specific Measurement of Protein Corona.

Conventional mass spectrometry (MS)-based bottom-up proteomics (BUP) analysis of the protein corona [i.e., an evolving layer of biomolecules, mostly proteins, formed on the surface of nanoparticles (NPs) during their interactions with biomolecular fluids] enabled the nanomedicine community to partly identify the biological identity of NPs. Such an approach, however, fails to pinpoint the specific proteoforms─distinct molecular variants of proteins in the protein corona. The proteoform-level information could potentially advance the prediction of the biological fate and pharmacokinetics of nanomedicines. Recognizing this limitation, this study pioneers a robust and reproducible MS-based top-down proteomics (TDP) technique for characterizing proteoforms in the protein corona. Our TDP approach has successfully identified about 900 proteoforms in the protein corona of polystyrene NPs, ranging from 2 to 70 kDa, revealing proteoforms of 48 protein biomarkers with combinations of post-translational modifications, signal peptide cleavages, and/or truncations─details that BUP could not fully discern. This advancement in MS-based TDP offers a more advanced approach to characterize NP protein coronas, deepening our understanding of NPs' biological identities. We, therefore, propose using both TDP and BUP strategies to obtain more comprehensive information about the protein corona, which, in turn, can further enhance the diagnostic and therapeutic efficacy of nanomedicine technologies.

Metal alkoxides as models for metal oxides—the concept revisited

Sol-Gel synthesis of metal oxides constitutes a tremendously exciting domain of inorganic chemistry, where molecular and supramolecular science meet the physical chemistry and materials science. Structure and reactivity, especially surface complexation of biologically important molecules on the surface of metal oxide nanoparticles can efficiently be traced through structural studies of metal oxo-paperbags—the product of partial hydrolysis of alkoxide precursors. Paperbag is a recently proposed term to denote oligonuclear complexes not featuring intrinsic metal-metal bonding and thus not qualified to be called “clusters”. Another important insight, provided recently by the studies of heterometallic species, is dealing with visualization of bonding modes of single atom catalysts on metal oxide substrates and reveals possible coordination environments of heteroatoms on doping. The studies of large paperbag aggregates can contribute to understanding of factors influencing the bandgap and photocatalytic activity of related oxides. The use of these species directly as photo or electro catalysts is rather debatable, however, in the view of high reactivity of these alkoxide intermediates, easily transforming them into metal oxide nanoparticles on hydrolysis or thermolysis.Graphical

Insights of oxygen vacancies engineered structural, morphological, and electrochemical attributes of Cr-doped Co3O4 nanoparticles as redox active battery-type electrodes for hybrid supercapacitors

The global warming issue is spurring the development of renewable energy solutions, where supercapacitors are emerging as promising options for energy storage. Despite advancements in battery-type materials, doping is a practical approach to enhancing electrochemical performance. In this study, using the solution combustion method, we synthesized spinel Co3O4 nanoparticles doped with chromium (Cr) at 2.5 % and 5 % concentrations. The addition of Cr significantly modifies the structural, morphological, surface, and electrochemical properties of Co3O4 nanoparticles. Raman and X-ray photoelectron spectroscopy confirm that this doping method effectively regulates the oxygen vacancy defect level. Moreover, Cr dopants and oxygen vacancies modify electronic states, facilitating more accessible contact to active sites, improving electrical conductivity and more intricate redox chemistry. Notably, the 2.5 % Cr-doped Co3O4 configuration demonstrates substantially enhanced specific capacity (334.64 C g−1/92.95 mAh g−1 at 1 A g−1) and rate performance (59 %), surpassing those of 5 % Cr-doped Co3O4 and undoped Co3O4. Furthermore, the as-fabricated 2.5 % Cr-doped Co3O4//activated carbon (AC) hybrid supercapacitor (HSC) device exhibits a noteworthy energy density of 42.5 Wh kg−1 at 1295.73 W kg−1, withstanding 33.54 Wh kg−1 even at a power density of 5720.46 W kg−1. The HSC device showcases outstanding cyclic performance with 100 % capacity retention after 5000 cycles. Therefore, our work offers a viable way to improve the efficiency of hybrid supercapacitors by providing essential insights into the design of defect-engineered battery-type electrode materials.

Radial dependence of ionization clustering around a gold nanoparticle irradiated by X-rays under charged particle equilibrium

Objective.This work explores the enhancement of ionization clustering and its radial dependence around a gold nanoparticle (NP), indicative of the induction of DNA lesions, a potential trigger for cell-death.Approach.Monte Carlo track structure simulations were performed to determine (a) the spectral fluence of incident photons and electrons in water around a gold NP under charged particle equilibrium conditions and (b) the density of ionization clusters produced on average as well as conditional on the occurrence of at least one interaction in the NP using Associated Volume Clustering. Absorbed dose was determined for comparison with a recent benchmark intercomparison. Reported quantities are normalized to primary fluence, allowing to establish a connection to macroscopic dosimetric quantities.Main results.The modification of the electron spectral fluence by the gold NP is minor and mainly occurs at low energies. The net fluence of electrons emitted from the NP is dominated by electrons resulting from photon interactions. Similar to the known dose enhancement, increased ionization clustering is limited to a distance from the NP surface of up to200nm. The number of clusters per energy imparted is increased at distances of up to150nm, and accordingly the enhancement in clustering notably surpasses that of dose enhancement. Smaller NPs cause noticeable peaks in the conditional frequency of clusters between50nm-100nmfrom the NP surface.Significance.This work shows that low energy electrons emitted by NPs lead to an increase of ionization clustering in their vicinity exceeding that of energy imparted. While the electron component of the radiation field plays an important role in determining the background contribution to ionization clustering and energy imparted, the dosimetric effects of NPs are governed by the interplay of secondary electron production by photon interaction and their ability to leave the NP.

Proline-Functionalized Magnetic Nanoparticles as Highly Performing Asymmetric Catalysts.

Amino acids have a crucial role in the field of asymmetric organocatalysis for the production of chiral compounds with high added value and specific biological activity. In particular, proline offers high activity and stereoselectivity for catalyzing aldol reactions in organic solvents. However, proline-based catalysts often lack water-solubility, accessibility, catalytic performance, or recovery in aqueous media. This work reports the design of proline-functionalized poly(methyl methacrylate) (PMMA) nanoparticles with a magnetic core that offer high availability of chiral units in water and high recyclability. A proline-based copolymerizable surfactant is designed and integrated onto the surface of PMMA nanoparticles through a miniemulsion polymerization process without using additional surfactants. The miniemulsion technique allows the incorporation of magnetite to the system to create a magnetically separable catalyst. The chiral nanocatalyst presents a high diastereoselective catalytic activity for the intermolecular aldol reaction between p-nitrobenzaldehyde and cyclohexanone in water.

Unmasking Fluorinated Moieties on the Surface of Hydride-Terminated Silicon Nanoparticles.

Despite the widespread use of hydrofluoric acid (HF) in the preparation of silicon surfaces, the true nature of fluorinated surface species remains unclear. Here, we employ an array of characterization techniques led by solid-state nuclear magnetic resonance spectroscopy to uncover the nature of fluorinated moieties on the surface of hydride-terminated silicon nanoparticles (H-SiNPs). A structural model that explains the observed trends in 19F and 29Si magnetic shielding is proposed and further supported by quantum chemical computations. Fluorine is incorporated into local oxidation domains on the surface and clustered at the interface of the oxide and surrounding hydride-terminated surface. Silicon sites capped by a single fluorine are also identified by their distinct 19F and 29Si chemical shifts, providing insight into how fluorine termination influences the electronic structure. The extent of fluorine passivation and the effects of fluorine on the optical properties of SiNPs are also discussed. Finally, challenges associated with Teflon contamination are highlighted that future explorations of nanomaterials may have to contend with.

Constructing stress-release layer on Si nanoparticles for high-performance lithium storage

Tailing structures of silicon anode to alleviate the mechanical stress has an important significance in the development of lithium-ion batteries (LIBs). Herein, the stress-released layer of N-doped cubic carbon on the surface of Si nanoparticles (Si@NCC) is explored to stabilize the electrode. Endowed with the unique superiority, the Si@NCC electrode delivers an impressive lithium storage performance with high specific capacity of 630 mAh/g at 0.1 A/g, excellent cycling stability (72.0 % capacity retention after 100 cycles at 0.1 A/g) and good rate capability (375 mAh/g at 2 A/g). It has been demonstrated that the N-doped cubic carbon shell with high conductivity can effectively limit the expansion and agglomeration of Si nanoparticles. Besides, the COMSOL simulations of the stress distributions in materials confirm that the N-doped cubic carbon layer could remarkably decrease the stress originated from the volume expansion of Si nanoparticles during the lithiation. Therefore, this work provides ideas for the mechanical effect of Si-based anodes for lithium storage and sheds lights on the designing advanced materials toward high-performance energy storage devices.

Deep Plasma Proteome Profiling by Modulating Single Nanoparticle Protein Corona with Small Molecules.

The protein corona, a dynamic biomolecular layer that forms on nanoparticle (NP) surfaces upon exposure to biological fluids is emerging as a valuable diagnostic tool for improving plasma proteome coverage analyzed by liquid chromatography-mass spectrometry (LC-MS/MS). Here, we show that spiking small molecules, including metabolites, lipids, vitamins, and nutrients (namely, glucose, triglyceride, diglycerol, phosphatidylcholine, phosphatidylethanolamine, L-α-phosphatidylinositol, inosine 5'-monophosphate, and B complex), into plasma can induce diverse protein corona patterns on otherwise identical NPs, significantly enhancing the depth of plasma proteome profiling. The protein coronas on polystyrene NPs when exposed to plasma treated with an array of small molecules (n=10) allowed for detection of 1793 proteins marking an 8.25-fold increase in the number of quantified proteins compared to plasma alone (218 proteins) and a 2.63-fold increase relative to the untreated protein corona (681 proteins). Furthermore, we discovered that adding 1000 µg/ml phosphatidylcholine could singularly enable the detection of 897 proteins. At this specific concentration, phosphatidylcholine selectively depleted the four most abundant plasma proteins, including albumin, thus reducing the dynamic range of plasma proteome and enabling the detection of proteins with lower abundance. By employing an optimized data-independent acquisition (DIA) approach, the inclusion of phosphatidylcholine led to the detection of 1436 proteins in a single plasma sample. Our molecular dynamic results revealed that phosphatidylcholine interacts with albumin via hydrophobic interactions, h-bonds, and water-bridges. Addition of phosphatidylcholine also enabled the detection of 337 additional proteoforms compared to untreated protein corona using a top-down proteomics approach. These significant achievements are made utilizing only a single NP type and one small molecule to analyze a single plasma sample, setting a new standard in plasma proteome profiling. Given the critical role of plasma proteomics in biomarker discovery and disease monitoring, we anticipate widespread adoption of this methodology for identification and clinical translation of proteomic biomarkers into FDA approved diagnostics.

Growth Mediated Disassembly of Cucurbit[8]uril Cross‐linked Static Cubic Self‐assembly of Silver Nanoparticles

AbstractStatic self‐assembly resides in thermodynamically stable global minima of the energy landscape, whereas dynamic self‐assembly occupies local minima of the energy profile and remains in the ordered state for a limited time via dissipation of energy to surroundings. This makes the spatiotemporal control over the assembly and disassembly mechanism easily controllable in the case of dynamic self‐assembly. However, due to the higher thermal stability of static self‐assembly, it is very challenging to perform reverse engineering on these types of systems. Herein we report growth reaction‐based reversal of static silver cubes obtained via cucurbit[8]uril (CB[8]) crosslinked self‐assembly of silver nanoparticles (AgNP). The AgNP building units with variable CB[8] surface coverage have been used as seeds onto which deposition of gold via growth reaction has been performed. The disassembly of supracube structure has been controlled by the formation of [AuCl4]−–CB[8] complex and successive reduction of [AuCl4]− to Au0 on the surface of the seed. The resulting monodispersed isotropic nanoparticles, formed from the CB[8] based cubic self‐assembly after growth, exhibit Au−Ag bimetallic nature. Quenching of the fluorogenic response from the hydrophobic dye coumarin‐7, added after growth, suggests direct interaction with the metallic nanoparticle surface after disassembly and thereby confirms successful growth reaction mediated reversal of self‐assembly.

Alloying and Segregation in PdRe/Al2O3 Bimetallic Catalysts for Selective Hydrogenation of Furfural

X-ray absorption fine structure (XAFS) spectroscopy, temperature-programmed reduction (TPR), and temperature-programmed hydride decomposition (TPHD) were employed to elucidate the structures of a series of PdRe/Al2O3 bimetallic catalysts for the selective hydrogenation of furfural. TPR evidenced low-temperature Re reduction in the bimetallic catalysts consistent of the migration of [ReO4]− (perrhenate) species to hydrogen-covered Pd nanoparticles on highly hydroxylated γ-Al2O3. TPHD revealed a strong suppression of β-PdHx formation in the reduced catalysts prepared by (i) co-impregnation and (ii) [HReO4] impregnation of the reduced Pd/Al2O3, indicating the formation of Pd-rich alloy nanoparticles; however, reduced catalysts prepared by (iii) [Pd(NH3)4]2+ impregnation of calcined Re/Al2O3 and subsequent re-calcination did not. Re LIII X-ray absorption edge shifts were used to determine the average Re oxidation states after reduction at 400 °C. XAFS spectroscopy and high-angle annular dark field (HAADF)-scanning transmission electron microscopy (STEM) revealed that a reduced 5 wt.% Re/Al2O3 catalyst contained small Re clusters and nanoparticles comprising Re atoms in low positive oxidation states (~1.5+) and incompletely reduced Re species (primarily Re4+). XAFS spectroscopy of the bimetallic catalysts evidenced Pd-Re bonding consistent with Pd-rich alloy formation. The Pd and Re total first-shell coordination numbers suggest that either Re is segregated to the surface (and Pd to the core) of alloy nanoparticles and/or segregated Pd nanoparticles are larger than Re nanoparticles (or clusters). The Cowley short-range order parameters are strongly positive indicating a high degree of heterogeneity (clustering or segregation of metal atoms) in these bimetallic catalysts. Catalysts prepared using the Pd(NH3)4[ReO4]2 double complex salt (DCS) exhibit greater Pd-Re intermixing but remain heterogeneous on the atomic scale.

Catechol-modified stabilizer facilitates impulsive ligand functionalization of particulates and membrane modification of cells

Ligand-functionalized particulates have received considerable attention for targeted drug delivery. Previous studies have reported several methods for functionalizing various molecules on the surfaces of nano- and micro-particulates which involve multiple steps, reaction buffers and chemicals, and long reaction times. Here, we report a single-step method that uses catechol chemistry to rapidly functionalize ligands on the surfaces of polymeric nanoparticles (NPs). We synthesized dopamine-conjugated poly (ethylene-alt-maleic acid) (D-PEMA) by performing a nucleophilic addition reaction between dopamine and poly (ethylene-alt-maleic anhydride) (PEMAnh). We then used D-PEMA as a stabilizer while preparing NPs which led to the construction of NPs that were non-adhesive per se but provided active sites for conjugating multiple different ligands in an alkaline buffer via Michael's addition and Schiff's base substitution reactions. The ligand-functionalized NPs were nontoxic and effectively internalized by both primary and cancer cells. In addition, NPs prepared using the modified stabilizer conjugated rapidly on the surfaces of pancreatic islets in alkaline conditions. Our study provides evidence that the modified stabilizer is versatile and has the potential for drug delivery applications and cell surface modifications.

Conversion of Ultrasmall Glutathione-Coated Silver Nanoparticles during Dispersion in Water into Ultrasmall Silver Sulfide Nanoparticles.

Ultrasmall silver nanoparticles (2 nm) were prepared by reduction with sodium borohydride (NaBH4) and stabilized by the ligand glutathione (a tripeptide: glycine-cysteine-glutamic acid). NMR spectroscopy and optical spectroscopy (UV and fluorescence) revealed that these particles initially consist of silver nanoparticles and fluorescing silver nanoclusters, both stabilized by glutathione. Over time, the silver nanoclusters disappear and only the silver nanoparticles remain. Furthermore, the capping ligand glutathione eliminates hydrogen sulfide (H2S) from the central cysteine and is released from the nanoparticle surface as tripeptide glycine-dehydroalanine-glutamic acid. Hydrogen sulfide reacts with the silver core to form silver sulfide. After four weeks in dispersion at 4 °C, this process is completed. These processes cannot be detected by transmission electron microscopy (TEM), small-angle X-ray scattering (SAXS), or differential centrifugal sedimentation (DCS) as these methods cannot resolve the mixture of nanoparticles and nanoclusters or the nature of the nanoparticle core. X-ray photoelectron spectroscopy showed the mostly oxidized state of the silver nanoparticle core, Ag(+I), both in freshly prepared and in aged silver nanoparticles. These results demonstrate that ultrasmall nanoparticles can undergo unnoticed changes that considerably affect their chemical, physical, and biological properties. In particular, freshly prepared ultrasmall silver nanoparticles are much more toxic against cells and bacteria than aged particles because of the presence of the silver clusters.

Preparation and characterization of pickering emulsions stabilized by zein/quercetin/quaternary ammonium chitosan composite nanoparticles with antibacterial effect

The role of nanoparticles in the stabilizing interface is very important in the preparation of stable Pickering emulsions. In this study, ternary composite nanoparticles (ZQ-HC) were synthesized by complexing zein-quercetin covalent complex (ZQ) with quaternary ammonium chitosan (HTCC) and subsequently stabilized Pickering emulsions (ZQ-HC) with antibacterial activity. Results revealed that HTCC covers the surface of ZQ nanoparticles successfully, which designates an effective improvement in the surface wettability of ZQ effectively. Among them, ZQ-HC2:1 possesses the closest three-phase contact angle of 90° and the highest emulsification activity and emulsion stability. The results of ultra-high resolution microscopy showed that ZQ-HC nanoparticles were adsorbed at the oil-water interface to prevent droplet aggregation and improved the pH, ionic strength, and storage stability of the prepared Pickering emulsions. ZQ-HC nanoparticles construct an antioxidant barrier at the oil-water interface, improving the lipid oxidation stability of the emulsion. The ZQ-HC2:1 stabilized Pickering emulsion exhibits the most superior stability and strongest antibacterial activity against other emulsions. The ZQ-HC stabilized Pickering emulsions prepared in this study exhibit potential for use as carriers of bioactive ingredients in food applications.

Highly efficient nucleic acid encapsulation method for targeted gene therapy using antibody conjugation system

Gene therapy has surfaced as a promising avenue for treating cancers, offering the advantage of deliberate adjustment of targeted genes. Nonetheless, the swift degradation of nucleic acids in the bloodstream necessitates an effective and secure delivery system. The widespread utilization of poly lactic-co-glycolic acid (PLGA) nanoparticles as drug delivery systems has highlighted challenges in controlling particle size and release properties. Moreover, the encapsulation of nucleic acids exacerbates these difficulties due to the negatively charged surface of PLGA nanoparticles. In this study, we aimed to improve the encapsulation efficiency of nucleic acids by employing negatively charged microbeads and optimizing the timing of the specific formulation steps. Furthermore, by conjugating PSMA-617, a ligand for the prostate-specific membrane antigen (PSMA), with PLGA nanoparticles, we assessed the antitumor effects and the efficacy of a nucleic acid delivery system on prostate cancer model. The employed technique within the nucleic acid encapsulation system represents a novel approach that could be adapted to encapsulate various kinds of nucleic acids. Moreover, it enables the attachment of targeting moieties to different cell membrane proteins, thereby unveiling new prospects for precise therapeutics in cancer therapy.

Self-Assembled Nanoparticles of Silicon (IV)-NO Donor Phthalocyanine Conjugate for Tumor Photodynamic Therapy in Red Light.

The combination of photodynamic therapy (PDT) and pneumatotherapy is emerging as one of the most effective strategies for increasing cancer treatment efficacy while minimizing side effects. Photodynamic forces affect nitric oxide (NO) levels as activated photosensitizers produce NO, and NO levels in the tumor and microenvironment directly impact tumor cell responsiveness to PDT. In this paper, 3-benzenesulfonyl-4-(1-hydroxy ether)-1,2,5-oxadiazole-2-oxide NO donor-silicon phthalocyanine coupling (SiPc-NO) was designed and prepared into self-assembled nanoparticles (SiPc-NO@NPs) by precipitation method. By further introducing arginyl-glycyl-aspartic acid (RGD) on the surface of nanoparticles, NO-photosensitizer delivery systems (SiPc-NO@RGD NPs) with photo-responsive and tumor-targeting properties were finally prepared and preliminarily evaluated in terms of their formulation properties, NO release, and photosensitizing effects. Furthermore, high reactive oxygen species (ROS) generation efficiency and high PDT efficiency in two breast cancer cell lines (human MCF-7 and mouse 4T1) under irradiation were also demonstrated. The novel SiPc-NO@RGD NPs show great potential for application in NO delivery and two-photon bioimaging-guided photodynamic tumor therapy.