Self-assembly Technique Research Articles

Silver nanostar films for surface-enhanced Raman spectroscopy (SERS) of the pesticide imidacloprid

Strategies for synthetic control of anisotropic metal nanostructures have grown in recent years in part due to their great potential for application as surface-enhanced Raman scattering (SERS) sensing substrates. It has been shown that SERS using silver substrates is a powerful tool for identification and qualification of trace chemical analysis on the basis of their unique molecular vibrations. In this work, we synthesized star-shaped silver nanostructures and fabricated SERS substrates to use the SERS enhancement of the Raman signal to detect neonicotinoid pesticides. These silver nanostar substrates were prepared by assembling the nanostar particles on a glass substrate surface using a self-assembly technique with various layers of silver nanostars film. The silver nanostar distribution on the solid substrate surface was found to have good reproducibility, reusability and were a stable SERS substrate giving SERS enhancements for pesticide detection at concentrations as low as 10−6 mg/ml. The distribution of these silver nanostars on the surface allowed excellent reproducibility of the detection with a low relative standard derivation (RSD) of SERS intensity of 8%. This work potentially builds a platform for an ultrasensitive detector where samples can be probed with little to no pre-processing and a range of pollutants can be detected at very low levels.

A Review on Self-Assembly of Colloidal Nanoparticles into Clusters, Patterns, and Films: Emerging Synthesis Techniques and Applications.

The colloidal synthesis of functional nanoparticles has gained tremendous scientific attention in the last decades. In parallel to these advancements, another rapidly growing area is the self-assembly or self-organization of these colloidal nanoparticles. First, the organization of nanoparticles into ordered structures is important for obtaining functional interfaces that extend or even amplify the intrinsic properties of the constituting nanoparticles at a larger scale. The synthesis of large-scale interfaces using complex or intricately designed nanostructures as building blocks, requires highly controllable self-assembly techniques down to the nanoscale. In certain cases, for example, when dealing with plasmonic nanoparticles, the assembly of the nanoparticles further enhances their properties by coupling phenomena. In other cases, the process of self-assembly itself is useful in the final application such as in sensing and drug delivery, amongst others. In view of the growing importance of this field, this review provides a comprehensive overview of the recent developments in the field of nanoparticle self-assembly and their applications. For clarity, the self-assembled nanostructures are classified into two broad categories: finite clusters/patterns, and infinite films. Different state-of-the-art techniques to obtain these nanostructures are discussed in detail, before discussing the applications where the self-assembly significantly enhances the performance of the process.

Bio-Template Synthesis of V2O3@Carbonized Dictyophora Composites for Advanced Aqueous Zinc-Ion Batteries

In terms of new-generation energy-storing devices, aqueous zinc-ion batteries (AZIBs) are becoming the prime candidates because of their inexpensive nature, inherent safety, environmental benignity and abundant resources. Nevertheless, due to a restrained selection of cathodes, AZIBs often perform unsatisfactorily under long-life cycling and high-rate conditions. Consequently, we propose a facile evaporation-induced self-assembly technique for preparing V2O3@carbonized dictyophora (V2O3@CD) composites, utilizing economical and easily available biomass dictyophora as carbon sources and NH4VO3 as metal sources. When assembled in AZIBs, the V2O3@CD exhibits a high initial discharge capacity of 281.9 mAh g-1 at 50 mA g-1. The discharge capacity is still up to 151.9 mAh g-1 after 1000 cycles at 1 A g-1, showing excellent long-cycle durability. The extraordinary high electrochemical effectiveness of V2O3@CD could be mainly attributed to the formation of porous carbonized dictyophora frame. The formed porous carbon skeleton can ensure efficient electron transport and prevent V2O3 from losing electrical contact due to volume changes caused by Zn2+ intercalation/deintercalation. The strategy of metal-oxide-filled carbonized biomass material may provide insights into developing high-performance AZIBs and other potential energy storage devices, with a wide application range.

Development of Crosslinker-Free Polysaccharide-Lysozyme Microspheres for Treatment Enteric Infection

Antibiotic abuse in the conventional treatment of microbial infections, such as inflammatory bowel disease, induces cumulative toxicity and antimicrobial resistance which requires the development of new antibiotics or novel strategies for infection control. Crosslinker-free polysaccharide-lysozyme microspheres were constructed via an electrostatic layer-by-layer self-assembly technique by adjusting the assembly behaviors of carboxymethyl starch (CMS) on lysozyme and subsequently outer cationic chitosan (CS) deposition. The relative enzymatic activity and in vitro release profile of lysozyme under simulated gastric and intestinal fluids were investigated. The highest loading efficiency of the optimized CS/CMS-lysozyme micro-gels reached 84.9% by tailoring CMS/CS content. The mild particle preparation procedure retained relative activity of 107.4% compared with free lysozyme, and successfully enhanced the antibacterial activity against E. coli due to the superposition effect of CS and lysozyme. Additionally, the particle system showed no toxicity to human cells. In vitro digestibility testified that almost 70% was recorded in the simulated intestinal fluid within 6 h. Results demonstrated that the cross-linker-free CS/CMS-lysozyme microspheres could be a promising antibacterial additive for enteric infection treatment due to its highest effective dose (573.08 μg/mL) and fast release at the intestinal tract.

Dual-functional lanthanide-MOF probe nanocomposite based on hydroxyapatite nanowires as fluorescent sensor for ascorbic acid.

Adual-functional lanthanide-MOF nanocomposite probewas designed and constructed for the detection of ascorbic acid (AA). The magnetically functionalized hydroxyapatite nanowires are selected as the carriers and simultaneously loaded with ciprofloxacin (CIP) and terbium metal organic framework to form the internal reference fluorescence probe nanocomposite (Fe3O4-HAPNWs-Tb/MOF-CIP). This dual-functional lanthanide-MOF probe not only combines the respectively unique fluorescence properties of lanthanide MOFs and CIP, but also takes full advantage of the rapid separation properties of the magnetic component. Structural and spectroscopic characterization results have demonstrated the successful synthesis of probe material and the fluorescence mechanism. At a suitable excitation wavelength (295nm), the probe can simultaneously emit characteristic fluorescence of CIP (445nm) and Tb3+ (543nm). In the presence of AA, the ratio of I543/I445 decreases rapidly with increasing of AA concentration. The linear range of determinationis 0.3-40μM with a detection limit of 20.4nM. Thecontents of AA in vitamin C tablets and four fruit juice samples were detected by the composite probe. The spiked recoveries ranged from 82.6 to 104.2% with relative standard deviations (RSD) less than 2.1%, revealing the practical application value of the developed sensor in healthcare and food fields. A novel internal reference fluorescence sensor (Fe O -HAPNWs-Tb/MOF-CIP) was constructed for detecting ascorbic acid by solvothermal and self-assembly techniques, showing excellent selectivity and sensitivity based on the different responses of Tb/MOF and CIP to the target.

High performance laser-driven flyers based on a refractory metamaterial perfect absorber.

Laser-driven flyers (LDFs), which can drive metal particles to ultra-high speeds by feeding high-power laser, have been widely used in many fields, such as ignition, space debris simulation, and dynamic high-pressure physics. However, the low energy-utilization efficiency of the ablating layer hinders the development of LDF devices towards low power consumption and miniaturization. Herein, we design and experimentally demonstrate a high-performance LDF based on the refractory metamaterial perfect absorber (RMPA). The RMPA consists by a layer of TiN nano-triangular array, a dielectric layer and a layer of TiN thin film, and is realized by combing the vacuum electron beam deposition and colloid-sphere self-assembled techniques. RMPA can greatly improve the absorptivity of the ablating layer to about 95%, which is comparable to the metal absorbers, but obviously larger than that of the normal Al foil (∼10%). This high-performance RMPA brings a maximum electron temperature of ∼7500 K at ∼0.5 µs and a maximum electron density of ∼1.04 × 1016 cm-3 at ∼1 µs, which are higher than that the LDFs based on normal Al foil and metal absorbers due to the robust structure of RMPA under high-temperature. The final speed of the RMPA-improved LDFs reaches to about 1920 m/s measured by the photonic Doppler velocimetry system, which is about 1.32 times larger than the Ag and Au absorber-improved LDFs, and about 1.74times larger than the normal Al foil LDFs under the same condition. This highest speed unambiguously brings a deepest hole on the Teflon slab surface during the impact experiments. The electromagnetic properties of RMPA, transient speed and accelerated speed, transient electron temperature and density have been systematically investigated in this work.

Magnetic-driving giant multilayer polyelectrolyte microcapsules for intelligent enhanced oil recovery

With the worldwide energy crisis breaking out, the global demand for petroleum is increasing tremendously. However, it is still a major challenge to improve oil recovery from oil reservoirs in the petroleum industry. Here, the multilayer giant polyelectrolyte microcapsules (PEM), sodium dodecyl benzene sulfonate-Fe3O4 @ (polyacrylamine hydrochloride/polystyrene sulfonate)3-poly(N-isopropylacrylamide-co-diallyl dimethyl ammonium chloride) (SFe@(PAH/PSS)3-PND), were prepared through electrostatic self-assembly technique. PND was polymerized from N-isopropylacrylamide (NIPAM) and dimethyl diallyl ammonium chloride (DMDAAC). The oil recovery efficiency of the polyelectrolyte microcapsules was all higher than 50 %, and which was significantly increased to over 70 % after heating above the lower critical solution temperature (LCST). Attributed to the temperature-adjusted intelligent mechanisms of the NIPAM molecular in PND, the contraction of NIPAM molecular chains affected with high temperature, coupled with the reduction of microcapsule volume, led to expansion of the pores in the capsule walls, which significantly increased the permeability of SDBS. Meanwhile, oil droplets combined with SDBS were encapsuled with the hydrophobic PND layer based on hydrophobic interaction, part of which entered into amphiphilic phospholipid core layer. Inspired by cellular cytokinesis, the SFe@ (PAH/PSS)3-PND was capable of intelligently capturing and carrying oil droplets driven with magnetism. The oil recovery efficiency of SFe@ (PAH/PSS)3-PND significantly improved and were all more than 78 % after heating above the LCST With magnetron drive, which is much higher than the traditional method. Hence, this work revealed the novel approaches in potential applications for intelligent enhanced oil recovery (EOR) in the petroleum industry.

Biocompatibility and osteoinductive ability of casein phosphopeptide modified polyetheretherketone.

Polyetheretherketone (PEEK) is a potential implant material for dental application due to its excellent mechanical properties. However, its biological inertness and poor osteoinductive ability limited its clinical application. Based on a lay-by-layer self-assembly technique, here we incorporated casein phosphopeptide (CPP) onto PEEK surface by a simple two-step strategy to address the poor osteoinductive ability of PEEK implants. In this study, the PEEK specimens were positively charged by 3-ammoniumpropyltriethoxysilane (APTES) modification, then the CPP was adsorbed onto the positively charged PEEK surface electrostatically to obtain CPP-modified PEEK (PEEK-CPP) specimens. The surface characterization, layer degradation, biocompatibility and osteoinductive ability of the PEEK-CPP specimens were studied in vitro. After CPP modification, the PEEK-CPP specimens had a porous and hydrophilic surface and presented enhanced cell adhesion, proliferation, and osteogenic differentiation of MC3T3-E1 cells. These findings indicated that CPP modification could significantly improve the biocompatibility and osteoinductive ability of PEEK-CPP implants in vitro. In a word, CPP modification is a promising strategy for the PEEK implants to achieve osseointegration.

Construction of functionalized graphene nanoplatelets/SiC nanowires hybrid skeleton for epoxy composites with enhanced thermal conductivity and thermomechanical properties

Functionalized graphene nanoplatelets/SiC nanowires (f-GnP/SiCnw) and unmodified (u-GnP/SiCnw) hybrid skeletons with different amounts of SiCnw were successfully constructed through a vacuum-assisted self-assembly technique. Subsequently, the hybrid skeletons were incorporated into an epoxy resin to fabricate nanocomposites with excellent thermal and thermomechanical properties. The study revealed that the f-GnP/SiCnw hybrid skeletons exhibit a more pronounced reinforcing effect than the f-GnP-only skeleton without SiCnw and the unmodified (u-GnP/SiCnw) counterparts at the same filler loading. Incorporating the f-GnP/SiCnw hybrid skeleton with 5 wt% SiCnw resulted in through-plane and in-plane thermal conductivity of the epoxy composites as high as 1.58 W/m·K and 6.20 W/m·K, which is 690 and 3000% higher than that of the neat epoxy, respectively. Meanwhile, the storage modulus and glass transition temperature of the epoxy composites were also evidently enhanced after the introduction of the hybrid skeletons. This work provides an insight into the fabrication of high-performance thermally conductive composites.

Preparation of Hexagonal Boron Nitride-Containing Foam with Improved Thermal Conductivity of Epoxy Resins

With the continuous development of electrical and electronic devices, the thermal conductivity of dielectric polymer composites within devices is becoming increasingly important. However, improving the thermal conductivity usually requires the incorporation of a large amount of filler in polymer material, which undoubtedly increases the production cost while destroying the processability and the dielectric properties of the material. In this work, an efficient heat transfer network was constructed inside the resin matrix to overcome this drawback. Using the opposite surface potentials of hexagonal boron nitride (h-BN) and polyethyleneimine (PEI) in solvent, h-BN was anchored on the surface of melamine foam (MF) by an electrostatic self-assembly technique to construct a thermal conductive skeleton with a three-dimensional open pore structure, and the corresponding epoxy (EP) composite was prepared by vacuum-assisted impregnation. This EP–MF@BN composite showed a significant increase in the heat arrival rate at an extremely low filler loading. At a h-BN loading of 2.1 wt %, the thermal conductivity of the composite reached 0.433 W/(m·K), which was 147% higher than that of the pure resin matrix. This is mainly attributed to the unique three-dimensional open-hole structure of the MF foam, which formed a three-dimensional frame structure with extremely low thermal resistance after anchoring by h-BN, thus providing a great degree of weakening of the scattering behavior during phonon transport. In addition, the transport behavior of carriers inside the composite under strong electric field conditions was analyzed in the current study. This strategy of constructing an efficient heat transfer network inside the polymer matrix provides an idea and method for the preparation of composites in the field of electrical insulation.

Capsule structured Al/FeF3/AP energetic microspheres with enhanced combustion performance and energy release efficiency by a microexplosion reaction

The agglomeration and sintering of aluminum (Al) metal fuels lead to inadequate combustion and low energy release efficiency in the solid propellant systems. Herein, we assemble Al particles with gas generator of ferric trifluoride (FeF3) into capsule structured microspheres to detonate a microexplosion reaction by the evaporation-induced self-assembly technique, with encapsulating by ammonium perchlorate (AP) oxidant. The generated ternary Al/FeF3/AP microspheres achieved superior heat of combustion (12719.75 J g−1) and combustion temperature (1639.6 °C) owing to the full contact between components, reduced reaction transport distance, and the fierce shattering microexplosion combustion. Combustion mechanism analysis indicated that Al2O3 layer that hindered the oxidation reaction of Al was etched by the hydrogen fluoride (HF) from FeF3 decomposition, which caused the rapid splashing of nano Al clusters to detonate shattering microexplosion combustion. Furthermore, the ternary Al/FeF3/AP microspheres dramatically improve the combustion performance of hydroxy-terminated polybutadiene (HTPB)-based propellants and achieve a burning rate of 2.975 mm s−1, higher than most of the published HTPB/AP/Al propellants to date. The construction of Al/FeF3/AP microspheres exhibits a huge potential for the improvement of the propulsion power of rockets and weapons.

Nucleopeptide-Coupled Injectable Bioconjugated Guanosine-Quadruplex Hydrogel with Inherent Antibacterial Activity.

The multicomponent reaction-directed self-assembled hydrogels offer the opportunities to fabricate materials with ubiquitous properties which sometimes are not possible to generate from single components. Therefore, multicomponent-derived hydrogels have enormous applications in biomedical fields, and the number of such systems is increasing day by day. Herein, the multicomponent self-assembly techniques have been employed to develop a biomimetic low-molecular-weight G-quadruplex hydrogel under physiological conditions. The bioconjugation of guanosine, 4-formylphenylboronic acid, and cytosine-functionalized nucleopeptide (NP) is important to generate the multicomponent self-assembled dynamic imino-boronate ester-mediated bioconjugated G-quadruplex hydrogels. Using thioflavin T fluorescence assay, powder X-ray diffraction, and circular dichroism spectroscopic techniques, we confirm the existence of a G-quartet-like structure as the key parameter for the formation of nanofibrillar hydrogels. The multicomponent self-assembled G-quadruplex hydrogel possesses excellent inherent antibacterial activity against a broad range of bacterial species. The in vitro cytocompatibility of the synthesized hydrogel was evaluated on MCF-7 and HEK 293T cell lines to study the biocompatibility of the hydrogel. The proposed injectable, biocompatible, and NP-coupled G-quadruplex hydrogel with inherent antibacterial efficiency holds promising importance to prevent localized bacterial infections.

Regulation of Released Alkali from Gel Polymer Electrolyte in Quasi-Solid State Zn-Air Battery.

Gel polymer electrolyte (GPE) in quasi-solid state Zn-air battery (QSZAB) will release alkali during cycling, resulting in gradual dehydration of GPE, corrosion of Zn electrode, Zn dendrites growth, and therefore inferior performance. Here, hollow Sn microspheres are prepared on Zn substrate by the technique of colloidal self-assembly. The inner surfaces of hollow Sn microspheres are modified by 2-hydroxypropyl-β-cyclodextrin (hollow Sn-inner HPβCD) to regulate the released alkali at GPE|anode interface. The hollow Sn-inner HPβCD can lessen the leakage of released alkali, make stored alkali diffuse back to GPE during the charging process, and mitigate the loss of soluble Zn(OH)4 2- to suppress Zn dendrites growth. Resultantly, GPE in QSZAB with hollow Sn-inner HPβCD exhibits a high retention capacity for alkaline solution. The cell also exhibits a long cyclic lifespan of 127h due to the effective regulation of released alkali, which outperforms QSZAB without hollow Sn-inner HPβCD by 7.94 times. This work rivets the regulation of released alkali at GPE|anode interface, providing new insight to improve QSZABs' performance.

Engineered Living Oriented Electrospun Fibers Regulate Stem Cell Para-Secretion and Differentiation to Promote Spinal Cord Repair.

Living biomaterials directly couple with live cells to synthesize functional molecules and respond to dynamic environments, allowing the design, construction and application of next generation composite materials. Improving the coordination and communication between artificial materials and living cells is essential. In this study, collagen self-assembly and micro-sol electrospinning techniques are used to prepare oriented living fiber bundles that can increase the transplantation rate of stem cells in the early stages of inflammation, indirectly enhancing the dynamic regulation of stem cells during inflammation. Additionally, brain-derived neurotrophic factor (BDNF) contained in the fiber can improve the differentiation of bone marrow mesenchymal stem cells (BMSCs) into neurons once the inflammatory storm subsides. The living oriented fiber bundles fully simulate the 3D structure of the central nervous system, activate integrin β1, promote the growth and adhesion of stem cells in the acute stage of inflammation, upregulate anti-inflammatory genes by more than twofold via BMSCs in response to inflammation, and stably release BDNF for up to 4 weeks post-inflammation storm subsidence. Finally, the BDNF induces the differentiation of BMSCs to neurons by enhancing the expression of neural-related genes, which enables the recovery of neurological functions in the later stages of spinal cord injury.

Improvement of flame-retardant and antistatic property of wood using a spray-assisted layer-by-layer self-assembly technique

ABSTRACT Wood has the characteristics of shrinkage and swelling, flammability, and insulation, which can lead to poor user experience and accidents during its application in wood structure buildings and wood products. In this study, multifunctional chitosan/sodium phytate/TiO2-CuO nanoparticle composite coatings were sprayed on a wood surface through spray-assisted layer-by-layer (SP-LBL) self-assembly. By designing different spraying distances and other process parameters combined with a surface resistance test, thermogravimetric analysis, and combustion test, the antistatic and flame-retardant properties of modified wood were investigated. Antistatic property test results confirmed a positive effect between TiO2 and CuO nanoparticles on discharging electrostatic charge. Moreover, the surface resistance value of the wood remained unchanged after 15 days of spraying treatment. Additionally, the antistatic stability of the composite coatings was more effective in the short-term application. However, long-term stability needs to be observed. The results of thermogravimetric analysis and combustion test confirmed that chitosan, sodium phytate, and TiO2-CuO nanoparticles synergically improved the flame retardant of wood.

Thermochromic Photonic Crystal Microspheres with Uniform Color Display and Wide Coloration Range.

Thermochromic microspheres based on poly(N-isopropylacrylamide) attract much attention in detection and sensor due to the noticeable color response and fast response rate. However, some issues such as uneven color display and narrow coloration range still limit their practical applications. Herein, novel thermochromic microspheres with homogeneous color displays and wide thermochromic range are designed by combining the microfluidic technology with the magnetically-induced self-assembly technique and copolymerizing acrylamide (AM) with N-isopropylacrylamide. The photonic crystal structure with especially even colors is fast and conveniently constructed by magnetic assembly. The addition of AM makes the microspheres more hydrophilic and thus leading to a broader coloration range. The relationship between the structural color display and both the microstructures of photonic crystals and the thermo-responsive properties of gel matrix are elucidated. The detectable temperature of microspheres rises to as high as 60°C, and displays bright iridescent color variations from orange to blue-violet in the heating process. Importantly, their shrinking or swelling equilibrium can be reached in 80 and 105 s. Such microspheres are successfully used to visually indicate the appropriate temperature of enzymatic reaction, and have great potential in practical applications such as visual temperature detection and efficiency monitoring of chemical reactions.

Does freezing induce self-assembly of polymers? A molecular dynamics study.

This work investigates the freezing-induced self-assembly (FISA) of polyvinyl alcohol (PVA) and PVA-like polymers using molecular dynamics simulations. In particular, the effect of the degree of supercooling, degree of polymerization, polymer type, and initial local concentration on the FISA was studied. It was found that the preeminent factor responsible for FISA is not the diffusion of the polymers away from the nucleating ice front, but the increase in the polymer's local concentration upon freezing of the solvent (water). At a higher degree of supercooling, the polymers are engulfed by the growing ice front, impeding their diffusion into the supercooled solution and finally inhibiting their self-assembly. Conversely, at a relatively lower degree of supercooling, the rate of diffusion of the polymers into the supercooled solution is higher, which increases their local concentration and results in FISA. FISA was also observed to depend on the polymer-solvent interactions. Strongly favorable solute-solvent interactions hinder the self-assembly, whereas unfavorable solute-solvent interactions promote the self-assembly. The polymer and aggregate morphology were investigated using the radius of gyration, end-to-end distance, and asphericity analysis. This study brings molecular insights into the quintessential factors governing self-assembly via freezing of the solvent, which is a novel self-assembly technique especially suitable for biomedical applications.

Casting liquid PDMS on self-assembled bilayer polystyrene nanospheres to prepare a SERS substrate with two layers of nanopits for detection of p-nitrophenol.

p-Nitrophenol (PNP) is widely used in pesticides, pharmaceuticals, and dyestuffs. It is vital to detect trace PNP in the environment, because it poses significant environmental hazards due to its high toxicity. In this paper, a new method was reported for preparing a SERS substrate with excellent SERS activity by combining self-assembly techniques and flexible materials. First, the three-dimensional (3D) polystyrene (PS) photonic crystal (PC) structural master was fabricated by stacking two layers of self-assembled PS nanospheres with different diameters. Polydimethylsiloxane (PDMS) with a complementary structure to the master was obtained by casting, curing and peeling off. Finally, the PDMS-Ag substrate was fabricated by sputtering a thin Ag layer on the PDMS structure. The enhancement factor (EF) of the PDMS-Ag substrate was calculated to be 2.90 × 109 by using 4-amino thiophenol (ATP) as the probe molecule, and the limit of detection (LOD) for ATP can reach 10-11 M. And the RSD of the SERS intensity for the peak at 1078 cm-1 on the PDMS-Ag substrates from batch to batch was within 2%, indicating the high reproducibility of the as-prepared substrate. The quantitative analysis of PNP was achieved with a LOD of 10-8 M. Therefore, the PDMS-Ag substrate exhibits high sensitivity and reproducibility, and it can detect PNP in trace amounts, with great potential for detecting other contaminants.

Comparison of Endoscopic Hemostasis for Endoscopic Sphincterotomy Bleeding between a Novel Self-Assembling Peptide and Conventional Technique

Introduction: Recently, a novel self-assembling peptide hemostatic gel has become available in Japan. However, the safety and efficacy of this novel self-assembling peptide hemostatic gel remain unclear for bleeding after EST. The aim of this study was to evaluate the safety and efficacy of a novel self-assembling peptide hemostatic gel for bleeding after EST, and to perform a comparison to a conventional endoscopic hemostasis technique. Method: This retrospective study was carried out between January 2019 and October 2022. Patients who developed bleeding associated with EST were enrolled. The patients were divided into two groups based on the hemostasis technique used: a conventional hemostasis technique (Group A) or a novel self-assembling peptide hemostatic gel hemostasis technique (Group B). Result: A total of 62 patients (Group A, n = 36; Group B, n = 26) were included. Endoscopic hemostasis was initially obtained in 72.2% (26/32) of patients in Group A and in 88.4% (23/26) of patients in Group B, which was not significantly different (p = 0.1320). However, the procedure time was significantly shorter in Group B (mean, 9.38 min) compared with Group A (mean, 15.4 min) (p = 0.0103). There were no significant differences in the severity of bleeding between the two groups (p = 0.4530). Post-EST bleeding was observed in six patients (Group A, n = 4; Group B, n = 2). Adverse events were more frequently observed in Group A (n = 12) than in Group B (n = 1) (p = 0.0457). Conclusions: PuraStat application for EST bleeding might be safe and effective, and is comparable to the conventional endoscopic hemostasis technique, although further prospective randomized trials are needed.

Eco-friendly Approach for Creation of Resonant Silicon Nanoparticle Colloids

The commercial application of Mie-resonant nanophotonic technologies currently used in various laboratory studies, from biosensing to quantum optics, appears to be challenging. Development of colloidal-based fabrication approaches is a solution to face the issue. In our research, we studied the fabrication of resonant Si nanoparticle (NP) arrays on a surface with controlled wettability. First, we use nanosecond (ns) laser ablation in water and subsequent density gradient separation to obtain colloids of resonant spherical crystalline silicon NPs with a low polydispersity index. Then, the same industrial ns laser is applied to create a wetting gradient on the steel substrate to initiate a self-assembly of the NPs deposited by drop casting. Thus, we use a single commercial ns laser for producing both the NPs and the hydrophilic wetting gradient. We apply an easily operating size separation technique and only non-toxic media. This research contributes to the large-scale fabrication of various optical devices based on resonant high-refractive index nanostructures by ecologically friendly self-assembly techniques.