Nanosize Dimensions Research Articles

Polychaeta-mediated synthesis of gold nanoparticles: A potential antibacterial agent against Acute Hepatopancreatic Necrosis Disease (AHPND)–causing bacteria, Vibrio parahaemolyticus.

Gold nanoparticles (AuNPs) have emerged as a promising application in aquaculture. Their nano-sized dimensions, comparable to pathogens offer potential solutions for combating antibiotic resistance. In this study, AuNPs were synthesized by using polychaetes, Marphysa moribidii as the bio-reducing agent. Modifications were made to reduce agglomeration in green-synthesized AuNPs through ultrasonication. The antibacterial activities of AuNPs against V. parahaemolyticus were evaluated. The physicochemical characteristics of the green synthesized AuNPs were comprehensively investigated. The successful formation of AuNPs was confirmed by the appearance of a red ruby colour and the presence of surface Plasmon resonance (SPR) absorption peaks at 530 nm as observed from UV–vis spectroscopy. Scanning electron microscopy (SEM) revealed spherical-shaped AuNPs with some agglomerations. Transmission electron microscopy (TEM) showed particle size of AuNPs ranging from 10 nm to 60 nm, meanwhile dynamic light scattering (DLS) analysis indicated an average particle size of 24.36 nm. X-ray diffraction (XRD) analysis confirmed the high crystallinity of AuNPs, and no AuNPs were detected in the polychaetes extracts prior to synthesis. A brief ultrasonication significantly reduced the tendencies for AuNPs to coalesce. The green-synthesized AuNPs demonstrated a remarkable antibacterial efficacy against V. parahaemolyticus. The minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC) tests revealed that a concentration of 0.3 g/ml of AuNPs effectively inhibited V. parahaemolyticus. These findings highlighted the potential of green-synthesized AuNPs as antibacterial agents for the prevention and management of AHPND in aquaculture.

Thermal Lattice Field during Ultra-Short Laser Pulse Irradiation of Metal Targets: A Fokker–Planck Analytical Model

The ultrafast fs laser pulse heating of thin metal films is studied for the first time using the two-temperature model on the basis of the Fokker–Planck formalism. The incident laser radiation is multi-modal, while the electron temperature is described during the first 2 fs. The predictions are intended for use by experimentalists in optoelectronics, photonics, laser processing, electronics, and bio- and nanomedicine. The crucial role of the nano-sized spatial dimensions of the metal sample is highlighted. A significant result of this study is the interdependence between the target’s size, the phonon/lattice characteristics, and the coefficient β (the quotient of non-diffusive phenomena), which varies between zero (pure diffusive case) and one (pure non-diffusive case).

Annealing effect on the magneto-electric properties of SOT-MTJs from micro to nano-sized dimensions

Spin–orbit torque magnetic random-access memory exhibits great potential for next-generation memory. Annealing is an essential process for SOT magnetic tunnel junctions (SOT-MTJs) thin films. To optimize the SOT-MTJ thin films, studying the different dimensions from micro-size to nano-size is very necessary. Here, we investigate the annealing effect on magneto-electric properties of micro-scaled and nano-scaled SOT-MTJs. The tunnel magnetoresistance (TMR) and critical current density (J c) increase after annealing, attributing to the improved crystallization of CoFeB layers and perpendicular magnetic anisotropy (PMA), respectively. However, the TMR increment of micro-scaled SOT-MTJ is larger than that in nano-scale, due to the reduced defects of micro-scaled SOT-MTJs by annealing. Additionally, the J c of nano-scaled SOT-MTJ is decoupled from that of micro-scaled SOT-MTJ because of the improved PMA and diminished thermal effect. This work assesses the different annealing effects in micro- and nano-sized dimensions and supplies experiment foundations to optimize the performance of SOT-MTJs.

Drug-delivery research and much more: interview with Dan Peer.

Drug-delivery research and much more: interview with Dan Peer.

A novel electrochemical sensor for the detection of zearalenone in food matrices using PEGylated Fe3O4 nanoparticles supported by in-silico and multidetector AF4

It is widely known that zearalenone (ZEN) is a carcinogenic mycotoxin that is found in a wide variety of grains, cereals, and dairy products, causing cancer in both humans and animals. Thus, there is a growing demand for sensitive, selective, and inexpensive sensors that can detect toxic mycotoxins in real food samples. In this paper, the impact of PEGylated Fe3O4 nanoparticles (NPs) intercalated with carboxylic acid functionalized multiwalled carbon nanotubes (PEG-Fe3O4 NPs/cMWCNTs) was investigated for the design of an electrochemical sensor for ZEN analysis. Results showed that the nanocomposite-enhanced electrode exhibited a strong cathodic redox response of ZEN using cyclic voltammetry (CV). The developed sensor provided significantly low limits of detection and quantification of 0.34 and 1.12 fg mL−1 respectively over a calibration range of 1.00 to 10.00 fg mL−1 by differential pulse voltammetry (DPV). Excellent spike recoveries ranging from 92 to 106% were obtained for real samples of rice and corn flour. The multidetector Asymmetrical Flow Field-Flow Fractionation (AF4) measurements on the synthesized PEG-Fe3O4 NPs verified their nano-sized dimensions (rg≈ 31 nm) contributing to the exceptionally high electron transfer in DPV sensing. On the other hand, the simulated Monte Carlo (MC) adsorption studies demonstrated that the ZEN/PEG-Fe3O4 NP/cMWCNTs electrode interaction was the strongest on the GCE surface. The charge transfer was further enhanced by the combination of the strong cMWCNTs/GCE platform, due to their inherent conductive properties. The study suggests that the incorporation of the nanocomposite-enhanced electrode can be extended to prevent ZEN mycotoxin exposure.

Degradable Bottlebrush Polypeptides and the Impact of their Architecture on Cell Uptake, Pharmacokinetics, and Biodistribution In Vivo.

Bottlebrush polymers are highly promising as unimolecular nanomedicines due to their unique control over the critical parameters of size, shape and chemical function. However, since they are prepared from biopersistent carbon backbones, most known bottlebrush polymers are non-degradable and thus unsuitable for systemic therapeutic administration. Herein, wereport the design and synthesis of novel poly(organo)phosphazene-g-poly(α-glutamate) (PPz-g-PGA) bottlebrush polymers with exceptional control over their structure and molecular dimensions (Dh ≈ 15-50 nm). These single macromolecules show outstanding aqueous solubility, ultra-high multivalency and biodegradability, making them ideal as nanomedicines. While well-established in polymer therapeutics, it has hitherto not been possible to prepare defined single macromolecules of PGA in these nanosized dimensions. A direct correlation wasobserved between the macromolecular dimensions of the bottlebrush polymers and their intracellular uptake in CT26 colon cancer cells. Furthermore, the bottlebrush macromolecular structure visibly enhanced the pharmacokinetics by reducing renal clearance and extending plasma half-lives. Real-time analysis of the biodistribution dynamics showed architecture-driven organ distribution and enhanced tumor accumulation. This work, therefore, introduces a robust, controlled synthesis route to bottlebrush polypeptides, overcoming limitations of current polymer-based nanomedicines and, in doing so, offers valuable insights into the influence of architecture on the in vivo performance of nanomedicines.

Amphotericin B Nano-Assemblies Circumvent Intrinsic Toxicity and Ensure Superior Protection in Experimental Visceral Leishmaniasis with Feeble Toxic Manifestation.

In spite of its high effectiveness in the treatment of both leishmaniasis as well as a range of fungal infections, the free form of the polyene antibiotic amphotericin B (AmB) does not entertain the status of the most preferred drug of choice in clinical settings. The high intrinsic toxicity of the principal drug could be considered the main impedance in the frequent medicinal use of this otherwise very effective antimicrobial agent. Taking into consideration this fact, the pharma industry has introduced many novel dosage forms of AmB to alleviate its toxicity issues. However, the limited production, high cost, requirement for a strict cold chain, and need for parenteral administration are some of the limitations that explicitly compel professionals to look for the development of an alternate dosage form of this important drug. Considering the fact that the nano-size dimensions of drug formulation play an important role in increasing the efficacy of the core drug, we employed a green method for the development of nano-assemblies of AmB (AmB-NA). The as-synthesized AmB-NA manifests desirable pharmacokinetics in the treated animals. The possible mechanistic insight suggested that as-synthesized AmB-NA induces necrosis-mediated cell death and severe mitochondrial dysfunction in L. donovani promastigotes by triggering depolarization of mitochondrial membrane potential. In vivo studies demonstrate a noticeable decline in parasite burden in the spleen, liver, and bone marrow of the experimental BALB/c mice host. In addition to successfully suppressing the Leishmania donovani, the as-formed AmB-NA formulation also modulates the host immune system with predominant Th1 polarization, a key immune defender that facilitates the killing of the intracellular parasite.

Thermoresponsive in-situ gel containing hyaluronic acid and indomethacin for the treatment of corneal chemical burn

Ocular chemical burns are prevalent injuries that must have immediate and effective treatment to avoid complications. Aiming to improve bioavailability and efficacy, a poloxamer-based thermoresponsive in-situ gelling system containing hyaluronic acid and indomethacin was developed. Formulations with different polymeric proportions were screened through rheological measurements resulting in an optimized system (F2) with gelling temperature of 34.2 ± 0.11 °C. Its maximum viscosity varied from 77.33 mPa (25 °C) to 82.95 mPa (34 °C) following a non-Newtonian profile and a pH of 6.86 ± 0.01. No incompatibilities were found after infrared analysis. Polarized light microscopy and cryo-transmission electron microscopy have demonstrated micelles of nano-sized dimensions (21.86 nm) with indomethacin entrapped in the core, forming a polymeric network under heating. In vitro tests revealed a cumulative release of 59.75 ± 3.17 % up to 24 h under a sustained release profile. Results from HET-CAM assay indicated that F2 was well tolerated. Corneal wound healing was significantly faster in animals treated with F2 compared to a commercial formulation and an untreated group. These findings suggests that F2 could be an efficient system to delivery drugs into the ocular surface improving wound healing.

Unique Role of GeO2 as a Noninvasive Promoter of Nano-Sized Zeolite Crystals.

The synthesis of zeolites with nano-sized dimensions is often limited to a narrow design space that conventionally relies upon the design of organics to direct hierarchical materials. Here, it is demonstrated that the addition of an inorganic modifier, germanium oxide (GeO2 ), to a zeolite growth mixture directs the formation of crystals with ultrasmall dimensions. This effect is observed for zeolites ZSM-11and ZSM-5 over a range of synthesis conditions wherein the role of GeO2 in zeolite crystallization deviates from its typical function as a heteroatom. Notably, the final products contain trace amounts of Ge, which indicates the inorganic modifier does not compete for sites in the zeolite framework based on its formation of a discrete phase that enables GeO2 recovery. Catalytic tests using the methanol-to-hydrocarbons reaction reveal significant enhancement in the performance of zeolite catalysts prepared with GeO2 compared to reported examples of nano-sized zeolites. These findings highlight a potentially generalizable and commercially viable synthesis method to reduce mass-transport limitations in zeolites for diverse applications.

Synthesis and Characterization of Curcumin-Loaded Nanoparticles of Poly(Glycerol Sebacate): A Novel Highly Stable Anticancer System.

The research for alternative administration methods for anticancer drugs, towards enhanced effectiveness and selectivity, represents a major challenge for the scientific community. In the last decade, polymeric nanostructured delivery systems represented a promising alternative to conventional drug administration since they ensure secure transport to the selected target, providing active compounds protection against elimination, while minimizing drug toxicity to non-target cells. In the present research, poly(glycerol sebacate), a biocompatible polymer, was synthesized and then nanostructured to allow curcumin encapsulation, a naturally occurring polyphenolic phytochemical isolated from the powdered rhizome of Curcuma longa L. Curcumin was selected as an anticancer agent in virtue of its strong chemotherapeutic activity against different cancer types combined with good cytocompatibility within healthy cells. Despite its strong and fascinating biological activity, its possible exploitation as a novel chemotherapeutic has been hampered by its low water solubility, which results in poor absorption and low bioavailability upon oral administration. Hence, its encapsulation within nanoparticles may overcome such issues. Nanoparticles obtained through nanoprecipitation, an easy and scalable technique, were characterized in terms of size and stability over time using dynamic light scattering and transmission electron microscopy, confirming their nanosized dimensions and spherical shape. Finally, biological investigation demonstrated an enhanced cytotoxic effect of curcumin-loaded PGS-NPs on human cervical cancer cells compared to free curcumin.

Structural and surface studies of luminescent Ca/Eu phosphate nanomaterials: From the bulk to surface features

Three luminescent Eu-containing phosphate materials (Ca-doped europium phosphate monohydrate, Eu-doped carbonated-apatite, and europium phosphate monohydrate) were prepared and analyzed on the level of bulk structure and surface properties and compared to the biomimetic non-luminescent counterpart hydroxyapatite. Europium-containing phosphate materials exhibited nanosized dimensions but different luminescence emissions and luminescence lifetimes depending on their crystalline structures (i.e., lanthanide phosphate or apatites) and chemical composition. The introduction of Eu in the crystal lattice leads to a notable decrease in the overall Lewis acidity of the surface cationic sites detected by CO probing. Further, the mixed Eu/Ca-containing materials surfaces were found to be very similar to the reference hydroxyapatite in terms of water adsorption energy, while the pure europium phosphate resulted to have the notably higher energy values of direct interaction of water molecules with the surface cations with no detected propagation of this effect towards water overlayers.

The effect of drying process of cellulose nanofiber from oil palm empty fruit bunches on morphology

One major manufacturing challenge in nanocellulose production is getting the dry form of nanocellulose while maintaining its nano-size dimensions. Different drying techniques will produce nanocellulose with different sizes and morphologies. Each has its own specific application. This study performed three methods to dry nanocellulose suspension, specifically cellulose nanofiber, including freeze-drying, spray-drying, and oven drying. The morphology and particle size of the dried CNF were analyzed using Field Emission Scanning Electron Microscope (FE SEM). Sponge-like material, also known as aerogel with low density (0.01 – 0.02 g/cm3) and high porosity (98%), was obtained via freeze-drying. Meanwhile, finely grounded solidly in a spherical and irregular form has resulted from the spray drying process of CNF, with an average diameter of less than 2 μm. Oven-dried CNF formed rigid thin film with a rough surface. However, the FE-SEM micrograph indicated that the nanoscale dimension of the oven-dried CNF has no longer existed. Therefore, oven-drying is not suggested as a drying method for nanocellulose.

A comparative study of the nonlinear rheological properties of three different cellulose nanofibril suspensions

This study focused on the nonlinear rheological characterization of three types of cellulose nanofibril (CNF) suspensions under large amplitude oscillatory shear (LAOS) flow. Three different CNFs were produced, two by mechanical fibrillation alone under different conditions [here named microfibrillated cellulose (MFC) and U-CNF] and the other by mechanical fibrillation after carboxymethylation (CM-CNF). MFC and U-CNF had broad width distributions, whereas CM-CNF had narrower fibril width and width distribution due to the presence of charged carboxymethyl groups. Nonlinear stress responses of the prepared suspensions were analyzed using the sequence of physical processes method. All CNF suspensions exhibited intracycle rheological transitions composed of three physical processes: (1) structure recovery, (2) elastic deformation to early stage yielding, and (3) late-stage yielding. MFC and U-CNF suspensions exhibited similar rheological transitions overall. However, CM-CNF suspension had a higher network recovery rate within a shorter time and showed an additional yielding step due to the complex interplay between recovery and yielding dynamics. This result originated from complete nanofibrillation and charged functional groups on fibril surfaces. Rapid reformation of effective fibril–fibril contacts in CM-CNF suspension was attributed to electrostatic repulsions and complete nanosized lateral dimensions. In addition, excitation frequency was found to influence intracycle rheological transitions. A range of intracycle rheological transitions became narrower on increasing frequency because the time period for each transition was not enough under faster flow conditions. In particular, the characteristic yielding step of CM-CNF suspension disappeared on increasing frequency, which suggested that high-frequency excitation might be unfavorable for the nonlinear viscoelastic characterization of soft materials under LAOS flow.

Interfaces and Interphases in Batteries: How to Identify and Monitor Them Properly Using Surface Sensitive Characterization Techniques

AbstractInterfaces, interphases, surfaces, and bulk are the main elements in a battery that require to be monitored and understood to control battery life during cycling and electrochemical ageing. To date, bulk‐related processes are generally easier to address in terms of characterization techniques because in‐depth investigations of most of these processes can be performed in operando mode (that is, during battery cycling). However, investigations of surfaces, interfaces, and interphases possess some challenges due to the involved nanosize dimensions, which render it difficult to select adequate techniques and interpret data appropriately. In addition, the evolving chemistry can suffer beam damage during investigation, and the use of postmortem/ex situ samples are not fully reliable. Moreover, the definitions of the terms “interface,” “interphase,” “interfacial,” and “interfacial region” are not clearly consistent, the details of which will be discussed in this study. Finally, techniques that can address interfacial processes in batteries are reviewed by highlighting their primary advantages and disadvantages.

"Nano-ghosts": Risk assessment of submicron-sized particles in food biased towards fictional "nano".

Much confusion has been generated in the safety assessment of food-grade TiO2 (E171) by the comingling of studies conducted on submicron-sized particles with those examining the toxicity of more minuscule counterparts. As E171 displays a nano-sized tail in its particle distribution (up to 36 % of particles with a diameter < 100 nm), it was thought that potential hazards of this food additive can be extrapolated from studies on thoroughly nanoscale formulations. This simplistic procedure may, however, overestimate the effects of the nano-sized tail of E171 because TiO2 particles readily aggregate or agglomerate in aqueous suspensions and biological matrices. The resulting larger clusters display a reduced oral bioavailability in comparison to the same material in nano-sized dimensions. Also, even if taken up in trace amounts, the smaller particles likely remain appended to larger particles or clusters and these aggregates or conglomerates may nullify to a great extent their “nano” characteristics. The purpose of this review is, therefore, to reevaluate the literature on the toxicity of TiO2 particles focusing on studies that are directly relevant for the assessment of E171. The purpose is not to avert a ban on the use of E171 in food, which might well be justified in light of the uncertainties associated with this additive employed solely for its colorant properties. Instead, it will be important to avoid in the future this same bias towards a fictional “nano” hazard, especially when evaluating more innovative engineered particles that confer true benefits for example by enhancing nutritional properties, quality, freshness, traceability or sustainability of food.

Diamond membrane production: The critical role of radicals in the non-contact electrochemical etching of sp2 carbon

Sub-micrometre single crystal diamond membranes are of huge importance for next generation optical, quantum and electronic device applications. Electrochemical etching has proven a critical step in the production of such membranes. Etching is used to selectively remove a very thin layer of sub-surface sp2 carbon, prepared by ion implantation in bulk diamond, releasing the diamond membrane. Due to the nanosized dimensions, etching is typically carried out using non-contact electrochemistry in low conductivity solutions (bipolar arrangement) which whilst effective, results in extremely slow etch rates. In this work, a new method of non-contact electrochemical etching is presented which uses high conductivity, high concentration, fully dissociated aqueous electrolytes. Careful choice of the electrolyte anion results in significant improvements in the sp2 carbon etch rate. In particular, we show both chloride and sulfate electrolytes increase etch rates significantly (up to × 40 for sulfate) compared to our measurements using the current state-of-the-art solutions and methodologies. Electron paramagnetic resonance experiments, recorded after the electrode potential has been switched off, reveal sizeable hydroxyl radical concentrations at timescales > 107 longer than their lifetime (≤μs). These measurements highlight the importance of electrochemically initiated, solution chemistry radical generation and regeneration pathways in high concentration sulfate and chloride solutions for nano-etching applications.

Characterizing the Heterogeneity of Small Extracellular Vesicle Populations in Multiple Cancer Types via an Ultrasensitive Chip.

Identifying small extracellular vesicle (sEV) subpopulations based on their different molecular signatures could potentially reveal the functional roles in physiology and pathology. However, it is a challenge to achieve this aim due to the nano-sized dimensions of sEVs, low quantities of biological cargo each sEV carries, and our incomplete knowledge of identifying features capable of separating heterogeneous sEV subpopulations. Here, a sensitive, multiplexed, and nano-mixing-enhanced sEV subpopulation characterization platform (ESCP) is proposed to precisely determine the sEV phenotypic heterogeneity and understand the role of sEV heterogeneity in cancer progression and metastasis. The ESCP utilizes spatially patterned anti-tetraspanin-functionalized micro-arrays for sEV subpopulation sorting and nanobarcode-based surface-enhanced Raman spectroscopy for multiplexed read-outs. An ESCP has been used for investigating sEV phenotypic heterogeneity in terms of canonical sEV tetraspanin molecules and cancer-associated protein biomarkers in both cancer cell line models and cancer patient samples. Our data explicitly demonstrate the selective enrichment of tetraspanins and cancer-associated protein biomarkers, in particular sEV subpopulations. Therefore, it is believed that the ESCP could enable the evaluation and broader application of sEV subpopulations as potential diagnostic disease biomarkers.

Biosensors and biomarkers for determining gestational diabetes mellitus and jaundice in children.

Gestational diabetes and jaundice are the correlated diseases predominantly found in mother and newborn child. Jaundice is a neonatal complication with an increased risk when mother has gestational diabetes. Mothers with diabetes at an early stage of gestational age are at higher risk for hyperbilirubinemia (jaundice) and hypoglycemia. So, it is mandatory to monitor the condition of diabetes and jaundice during the pregnancy period for a healthy child and safest delivery. On the other hand, nanotechnology has displayed a rapid advancement that can be implemented to overcome these issues. The development of high-performance diagnosis using appropriate biomarkers provides their efficacy in the detection gestational diabetes and jaundice. This review covers the aspects from a fast-developing field to generate nanosensors in the nanosized dimensions for the applications to overcome these complications by coupling diagnostics with biomarkers. Further, the serum-based biomarkers have been discussed for these inborn complications and also the diagnosis with the current trend.

"Two Ships in a Bottle" Design for Zn-Ag-O Catalyst Enabling Selective and Long-Lasting CO2 Electroreduction.

Electrochemical CO2 reduction (CO2RR) using renewable energy sources represents a sustainable means of producing carbon-neutral fuels. Unfortunately, low energy efficiency, poor product selectivity, and rapid deactivation are among the most intractable challenges of CO2RR electrocatalysts. Here, we strategically propose a "two ships in a bottle" design for ternary Zn-Ag-O catalysts, where ZnO and Ag phases are twinned to constitute an individual ultrafine nanoparticle impregnated inside nanopores of an ultrahigh-surface-area carbon matrix. Bimetallic electron configurations are modulated by constructing a Zn-Ag-O interface, where the electron density reconfiguration arising from electron delocalization enhances the stabilization of the *COOH intermediate favorable for CO production, while promoting CO selectivity and suppressing HCOOH generation by altering the rate-limiting step toward a high thermodynamic barrier for forming HCOO*. Moreover, the pore-constriction mechanism restricts the bimetallic particles to nanosized dimensions with abundant Zn-Ag-O heterointerfaces and exposed active sites, meanwhile prohibiting detachment and agglomeration of nanoparticles during CO2RR for enhanced stability. The designed catalysts realize 60.9% energy efficiency and 94.1 ± 4.0% Faradaic efficiency toward CO, together with a remarkable stability over 6 days. Beyond providing a high-performance CO2RR electrocatalyst, this work presents a promising catalyst-design strategy for efficient energy conversion.

An Overview of Exosomes in Cancer Therapy: A Small Solution to a Big Problem

Exosomes are defined as a type of extracellular vesicle released when multivesicular bodies of the endocytic pathway fuse with the plasma membrane. They are characterized by their role in extracellular communication, partly due to their composition, and present the ability to recognize and interact with cells from the immune system, enabling an immune response. Their targeting capability and nanosized dimensions make them great candidates for cancer therapy. As chemotherapy is associated with cytotoxicity and multiple drug resistance, the use of exosomes targeting capabilities, able to deliver anticancer drugs specifically to cancer cells, is a great approach to overcome these disadvantages. The objective is to assess treatment efficiency in reducing tumor cells, as well as overall safety and response by cancer carriers. So far, results show exosomes as a promising therapeutic strategy in the fight against cancer. This review summarizes the characteristics and composition of exosomes, as well as explaining in detail the involved parties in the origin of exosomes. Furthermore, some considerations about exosome application in immunotherapy are addressed. The main isolation and loading methods are described to give an insight into how exosomes can be obtained and manipulated. Finally, some therapeutic applications of exosomes in cancer therapy are described.