Surface Of Nanoparticles Research Articles

Dual-responsive nanoparticles for enhanced drug delivery in breast Cancer chemotherapy.

Drug delivery efficiency often affects chemotherapy outcome due to dense collagen barrier in tumor environment. Here, we report a nanoparticle capable of pH and glutathione dual-responsive drug delivery to enhance the efficacy of breast cancer chemotherapy. Maleiminated polyethylene glycol and polylactide block copolymer were synthesized as a core material, doxorubicin was encapsulated into the nanoparticle by self-assembly. Thiocollagenase and maleimide were connected on the nanoparticle surface by click chemistry, and further coated with chondroitin sulfate as a protective layer to form dual-responsive doxorubicin nanoparticle. The results showed that the nanoparticle had the ability to penetrate deep tumor tissue, to target on CD44 of cancer cell, and to release doxorubicin in cancer cell in response to pH and glutathione signals, demonstrating superior anticancer efficacy in breast cancer-bearing mice. In conclusion, the dual-responsive nanoparticle could be used as a drug carrier to enhance drug delivery in breast cancer chemotherapy.

Antimicrobial GL13K Peptide-Decorated ZnO Nanoparticles To Treat Bacterial Infections.

As a broad-spectrum antimicrobial material, ZnO nanoparticles (NPs) offer a novel approach to infected wounds in the clinic; however, it is very necessary to improve the antimicrobial performance of ZnO to satisfy the clinic requirements. In this work, a new antimicrobial hybrid ZnO@PDA/GL13K was prepared by attaching the antimicrobial GL13K peptide on the surface of ZnO NPs via polydopamine (PDA) as a covalent bonding agent, which can enhance the reactive oxygen species (ROS) production and damage the cell wall, showing superior antimicrobial efficacy. Besides, the ZnO@PDA/GL13K hybrid can promote the healing of bacterial infected wounds, with the wound area only remaining 1.8% on day 9, about 2 times smaller than that of the ZnO group. Moreover, ZnO@PDA/GL13K also showed good biocompatibility, and no side effect on normal tissue and organs was found, implying that the antimicrobial hybrid may possess prospective application in biomedical fields.

Characterization of Nano Calcium Carbonate Extracted from Eggshells

Organic waste, especially eggshells, represents a valuable resource for the synthesis of calcium carbonate nanoparticles, which have significant industrial and medical applications. This study describes the methodology for converting eggshells into calcium carbonate nanoparticles through heat treatment and nano milling processes. Advanced characterization techniques, including TEM, SEM, and AFM, were used to analyze the morphology and structure of the synthesized nanoparticles. The particles were found to be of nanometer dimensions, with a size of around 150 nm and a distinctive spherical shape, as shown in the TEM images. SEM images showed that the surface of calcium carbonate nanoparticles synthesized from eggshells is smooth, crystalline, and spherical or nearly spherical. FTIR analysis revealed the presence of distinct functional groups for calcium carbonate, with peaks at 713–868 cm⁻¹, consistent with previous studies. The results show that nanoparticles manufactured from calcium carbonate possess unique properties that enhance their applicability in various fields, and promote sustainability and environmental preservation.

Catalytic Syntheses of Thiol-End-Functionalized ROMP Polymers.

Thiol-functionalized polymers have become a crucial class of materials due to their distinct chemical properties and versatile reactivity, leading to a broad spectrum of applications. Herein, we report the straightforward syntheses of a wide range of thiol-end-functionalized ring-opening metathesis polymerization (ROMP) polymers exploiting our previously reported catalytic ROMP mechanisms using suitable chain transfer agents. All the synthesized polymers were characterized via SEC, 1H NMR spectroscopy and MALDI-ToF mass spectrometry techniques. Furthermore, the existence of thiol groups on the polymer chains was verified through the well-established thiol coating reaction on gold nanoparticle surfaces. We believe this method of synthesizing thiol-end-functionalized ROMP polymers (using a reduced amount of ruthenium metal compared to conventional living ROMP) will be of great importance to materials science and biochemical research.

Navigating the nano-bio immune interface: advancements and challenges in CNS nanotherapeutics

In recent years, significant advancements have been made in utilizing nanoparticles (NPs) to modulate immune responses within the central nervous system (CNS), offering new opportunities for nanotherapeutic interventions in neurological disorders. NPs can serve as carriers for immunomodulatory agents or platforms for delivering nucleic acid-based therapeutics to regulate gene expression and modulate immune responses. Several studies have demonstrated the efficacy of NP-mediated immune modulation in preclinical models of neurological diseases, including multiple sclerosis, stroke, Alzheimer’s disease, and Parkinson’s disease. While challenges remain, advancements in NPs engineering and design have led to the development of NPs using diverse strategies to overcome these challenges. The nano-bio interface with the immune system is key in the conceptualization of NPs to efficiently act as nanotherapeutics in the CNS. The biomolecular corona plays a pivotal role in dictating NPs behavior and immune recognition within the CNS, giving researchers the opportunity to optimize NPs design and surface modifications to minimize immunogenicity and enhance biocompatibility. Here, we review how NPs interact with the CNS immune system, focusing on immunosurveillance of NPs, NP-induced immune reprogramming and the impact of the biomolecular corona on NPs behavior in CNS immune responses. The integration of NPs into CNS nanotherapeutics offers promising opportunities for addressing the complex challenges of acute and chronic neurological conditions and pathologies, also in the context of preventive and rehabilitative medicine. By harnessing the nano-bio immune interface and understanding the significance of the biomolecular corona, researchers can develop targeted, safe, and effective nanotherapeutic interventions for a wide range of CNS disorders to improve treatment and rehabilitation. These advancements have the potential to revolutionize the treatment landscape of neurological diseases, offering promising solutions for improved patient care and quality of life in the future.

Effect of temperature and nanoparticle size on the interfacial layer thickness of TiO2–water nanofluids using molecular dynamics

Abstract In the design and optimization of nanofluids, it is crucial to investigate and characterize the thermal conductivity enhancement mechanisms and their influencing factors. Although the effect of the “liquid film” on the thermal conductivity of the solid–liquid interface in nanofluids has been extensively studied, most of the research in this area has examined metal–water nanofluids or Ar-based nanofluids. In this work, non-equilibrium molecular dynamics is utilized to explore the mechanism of thermal conductivity enhancement in TiO2–water nanofluids. It is noted that a distinct interfacial layer is formed within 5 Å from the nanoparticle surface. As the nanoparticle size increases, the number density also increases, resulting in a corresponding increase in the thermal conductivity. Moreover, adding 1% TiO2 nanoparticles to water leads to an increase in thermal conductivity of 1.5–3%. Notably, the interfacial layer thickness remains relatively constant with the change in temperature. The Materials Studio analysis results indicated that the water molecule will have stable chemisorption on the titanium dioxide surface with an adsorption energy of approximately −0.96 eV. The findings of this study offer new insights and useful information to support the selection of nanomaterials for the preparation of convective systems.

Trojan Horse Strategy for Wireless Electrical Stimulation-Induced Zn2+ Release to Regulate Neural Stem Cell Differentiation for Spinal Cord Injury Repair.

Due to the uncertain differentiation of neural stem cells (NSCs), replenishing lost neurons by endogenous neural differentiation to repair spinal cord injury (SCI) remains challenging. The electrical stimulation-induced drug release is a promising approach for the localized and controlled release of drugs to regulate the differentiation of NSCs into neurons. Here, we developed Zn-PDA@BT nanoparticles acted as Trojan Horse to enter cells through endocytosis for Zn2+-controlled release therapy by the potentials generated by the piezoelectric effect. Due to the presence of polydopamine (PDA), under ultrasound stimulation, the electrical signal derived from the piezoelectric effect of barium titanate nanoparticles can be attracted to the surface of Trojan Horse nanoparticles to facilitate the controlled release of Zn2+. And Zn2+ bonded with PDA can increase the intracellular Zn2+ concentration within mouse-derived NSCs (mNSCs) to regulate the differentiation of mNSCs, which could enhance excitatory neuronal differentiation and inhibit astrocyte differentiation of mNSCs by activating the TGF-β and p53 pathways. More importantly, this Trojan Horse therapy allowed mNSCs to differentiate into mature neurons in 5 days, while the natural differentiation process took 10 days. Moreover, the transplantation of mNSC-ingested Zn-PDA@BT nanoparticles effectively replenished lost neurons at the damaged site and promoted function recovery after SCI in vivo, demonstrating the great potential of electrical stimulation-induced Zn2+ release for SCI repair.

Preparation of Diisooctyl Phosphate‐Modified Ultra‐Small Zinc Oxide Nanoparticle and Investigation of Its Tribological Properties as Additive in Alkylnaphthalene

ABSTRACTZnO nanoparticle surface‐modified by diisooctyl phosphate (P204) was prepared by liquid‐phase in situ surface modification technique with zinc acetate as the raw material, P204 as the modifier and anhydrous ethanol as the solvent. The morphology and microstructure of the P204‐ZnO nanoparticle were characterised by transmission electron microscopy, X‐ray diffraction and Fourier transform infrared spectrometry. Its thermal stability was evaluated by thermogravimetric analysis; and its tribological properties as the additive in alkylnaphthalene were evaluated with an SRV‐5 friction and wear tester in reciprocal sliding mode. The results show that the as‐prepared P204‐ZnO nanoparticle has an average particle size of about 4 nm and a P204 content of about 42% (mass fraction); and the surface modifier is grafted onto the surface of ZnO nanoparticle by physical adsorption. With a mass fraction of 0.5% in alkylnaphthalene base oil, P204‐ZnO nano‐additive can mildly reduce the friction coefficient and drastically reduce the wear rate of the steel–steel sliding pair. This is due to the formation of the composite tribofilm via the adsorption and deposition of the nano‐additive on rubbed steel surfaces as well as the tribochemical reactions of the modifier P204 yielding phosphate and of steel substrate yielding iron oxides. The as‐formed composite tribofilm with a thickness of about 20 nm, consisting of phosphate and iron oxides as the binder as well as deposited ZnO nanoparticle as the filling phase, is responsible for the excellent friction‐reducing and antiwear abilities of P204‐ZnO nano‐additive for the steel sliding contact.

Application of a magnetic graphene nanocomposite modified with 5-aminoisophthalic acid amine group for chromium (VI) adsorption from aqueous solutions: kinetic and thermodynamic studies

ABSTRACT Polymer nanocomposites are composite materials that incorporate nanomaterials, such as magnetic graphene oxide (mGO), into a polymer matrix. To enhance its adsorption capacity, the surface of mGO nanoparticles was polymerised by a 5-aminoisophthalic acid amine group (mGO-AIPA) through a simplified co-precipitation method. The structural and morphological characteristics of the synthesised nanoparticles were evaluated through techniques such as X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), Field emission scanning electron microscopy (FESEM), Thermogravimetric analysis (TGA), and Vibrating sample magnetometer (VSM). Response surface method (RSM) was used to evaluate the effectiveness of mGO-AIPA nanocomposite in removing chromium (VI) ions by examining variables such as solution of pH, contact time, adsorbent dose and initial concentration. Also, the study of kinetic models, adsorption isotherms and thermodynamic modelling of the process were evaluated. The results found that the mGO-AIPA nanocomposite has the maximum removal of chromium (VI) ions from the aqueous solution by 83.11% in optimal conditions including pH 3.5, contact time of 35 min, an adsorbent dosage of 25 mg g−1 and an initial concentration of 55 mg L−1. The pseudo-second-order kinetic and Langmuir isotherm models had a better fit with the experimental data of adsorption and the maximum adsorption capacity of chromium (VI) the base of the Langmuir model was 90.91 mg g−1. Moreover, the thermodynamic analysis indicated that the process was exothermic and nonspontaneous process, implying that it was energetically unfavourable. These findings suggest that the mGO-AIPA nanocomposite has a high performance as an effectual adsorbent to eliminate chromium heavy metal from an aqueous medium.

Cerium Oxide‐Armored Composite Latex Particles by Visible Light Emulsion Photopolymerization: From Synthesis to Film Properties

AbstractCerium dioxide (CeO2) has huge potential in many applications ranging from biochemical engineering to the coating industry. Here, the first example of visible light photo‐mediated Pickering emulsion polymerization of (meth)acrylate monomers is reported using CeO2 nanoparticles (NPs) as solid stabilizer. A ω,ω′−dicarboxylic acid diphenyl disulfide photoinitiator is anchored on the surface of the CeO2 NPs and used to initiate the emulsion polymerization of methyl methacrylate (MMA) and of MMA/n‐butyl acrylate (MMA/BA) under visible light leading to CeO2‐armored latexes. Radicals generated upon light irradiation trigger the formation of polymer chains chemically attached to the CeO2 NPs, promoting their subsequent adsorption on the latex surface. The composite films obtained from the CeO2‐armored P(MMA‐co‐BA) latexes exhibit a unique honeycomb nanostructure with the nanoceria located in the walls giving the materials excellent mechanical, anti‐UV, and photocatalytic properties.

Gold Nanoparticles Stabilized by δ‐Cyclodextrin in Aqueous Media: Characterization and Evaluation of their Catalytic Properties in the Reduction of 4‐Nitrophenol

AbstractThe synthesis of gold nanoparticles stabilized by cyclomaltononaose (δ‐CD) in aqueous phase was performed. Protection of the gold nanoparticles by standard native cyclodextrins such as α‐CD, β‐CD and γ‐CD has also been considered for comparison. All of these colloidal suspensions were fully characterized by FT‐IR, DLS, UV‐Vis spectroscopy, TEM, XPS and also NMR experiments. Finally, their catalytic activity was evaluated in the reduction of 4‐nitrophenol to 4‐aminophenol in the presence of an excess of sodium borohydride. Gold nanoparticles stabilized by δ‐CD presented good activity and exhibited better long‐term stability. This study highlighted the fact that the obtention of the best catalytic activity corresponds to not only a compromise between the size of the nanoparticles and the interaction of the substrate with the metal nanoparticles surface, but also the supramolecular interactions between the substrate and the cyclodextrin.

Amino Acid Adsorption Onto Magnetic Nanoparticles Reveals Correlations With Physicochemical Parameters

AbstractWe analyze the adsorption of the proteinogenic amino acids (AAs) glutamine, glutamic acid, lysine, tyrosine, proline, and valine onto bare iron oxide nanoparticles (approx. 10 nm). Aiming to identify the governing principles of low molecular weight coronae, which remain underinvestigated, our study covers broad concentration ranges up to the solubility limit of the AAs. Isothermal experiments reveal that the highly soluble AAs valine, proline, and lysine form extensive multilayers on the nanoparticle surface, and infrared measurements indicate intermolecular interactions, particularly with valine and lysine, for higher AA contents. Conversely, the low solubility of tyrosine and glutamic acid restricts their adsorption capacity, despite their higher partitioning on the solid surface. Parameters derived from fitting a classic saturation model seem to align with well‐documented physicochemical properties such as the hydrophobicity and the complexity indices – a promising first step towards formulating design principles. Scaling these parameters by the AA solubility reveals a clear correlation with the adsorption behavior. In adsorption experiments with AA model mixtures, sequential incubation increases the adsorption capacity for valine and proline, whereas simultaneous incubation with these AAs reduces tyrosine's capacity. Future studies should seek to elucidate adsorption patterns to advance our understanding of corona growth and evolution mechanisms.

Recent Advances in Simulation Studies on the Protein Corona

When flowing through the blood stream, drug carriers such as nanoparticles encounter hundreds of plasma proteins, forming a protein layer on the nanoparticle surface, known as the “protein corona”. Since the protein corona influences the size, shape, and surface properties of nanoparticles, it can modulate their circulating lifetime, cytotoxicity, and targeting efficiency. Therefore, understanding the mechanism of protein corona formation at the atomic scale is crucial, which has become possible due to advances in computer power and simulation methodologies. This review covers the following topics: (1) the structure, dynamics, and composition of protein corona on nanoparticles; (2) the effects of protein concentration and ionic strength on protein corona formation; (3) the effects of particle size, morphology, and surface properties on corona formation; (4) the interactions among lipids, membranes, and nanoparticles with the protein corona. For each topic, mesoscale, coarse-grained, and all-atom molecular dynamics simulations since 2020 are discussed. These simulations not only successfully reproduce experimental observations but also provide physical insights into the protein corona formation. In particular, these simulation findings can be applied to manipulate the formation of a protein corona that can target specific cells, aiding in the rational design of nanomedicines for drug delivery applications.

Tetrahedral DNA Framework‐Based Spherical Nucleic Acids for Efficient siRNA Delivery

Spherical nucleic acids (SNAs) hold substantial therapeutic potential for the delivery of small interfering RNAs (siRNAs). Nevertheless, their potential remains largely untapped due to the challenges of cytosolic delivery. Inspired by the dynamic, spiky architecture of coronavirus, an interface engineering approach based on a tetrahedral DNA framework (tDF) is demonstrated for the development of coronavirus‐mimicking SNAs. By exploiting their robustness and precise construction, tDFs are evenly arranged on the surface of core nanoparticles (NPs) with flexible conformations, generating a dynamic, spiky architecture. This spiky architecture in tetrahedral DNA framework‐based SNAs (tDF‐SNAs) substantially improve siRNAs duplex efficiency from 20% to 95%. Meanwhile, tDF‐SNAs changed the endocytosis pathway to clathrin‐independent cellular engulfment pathway and enhanced the cellular uptake efficiency. Due to these advances, the delivery efficiency of siRNA molecules by tDF‐SNAs is 1‐2 orders of magnitude higher than that of SNAs, resulting in a 2‐fold increase in gene silencing efficacy. These results show promise in the development of bioinspired siRNAs delivery systems for intracellular applications.

Tetrahedral DNA Framework-Based Spherical Nucleic Acids for Efficient siRNA Delivery.

Spherical nucleic acids (SNAs) hold substantial therapeutic potential for the delivery of small interfering RNAs (siRNAs). Nevertheless, their potential remains largely untapped due to the challenges of cytosolic delivery. Inspired by the dynamic, spiky architecture of coronavirus, an interface engineering approach based on a tetrahedral DNA framework (tDF) is demonstrated for the development of coronavirus-mimicking SNAs. By exploiting their robustness and precise construction, tDFs are evenly arranged on the surface of core nanoparticles (NPs) with flexible conformations, generating a dynamic, spiky architecture. This spiky architecture in tetrahedral DNA framework-based SNAs (tDF-SNAs) substantially improve siRNAs duplex efficiency from 20% to 95%. Meanwhile, tDF-SNAs changed the endocytosis pathway to clathrin-independent cellular engulfment pathway and enhanced the cellular uptake efficiency. Due to these advances, the delivery efficiency of siRNA molecules by tDF-SNAs is 1-2 orders of magnitude higher than that of SNAs, resulting in a 2-fold increase in gene silencing efficacy. These results show promise in the development of bioinspired siRNAs delivery systems for intracellular applications.

Developments in Localized Surface Plasmon Resonance

AbstractLocalized surface plasmon resonance (LSPR) is a nanoscale phenomenon associated with noble metal nanostructures that has long been studied and has gained considerable interest in recent years. These resonances produce sharp spectral absorption and scattering peaks, along with strong electromagnetic near-field enhancements. Over the past decade, advancements in the fabrication of noble metal nanostructures have propelled significant developments in various scientific and technological aspects of LSPR. One notable application is the detection of molecular interactions near the nanoparticle surface, observable through shifts in the LSPR spectral peak. This document provides an overview of this sensing strategy. Given the broad and expanding scope of this topic, it is impossible to cover every aspect comprehensively in this review. However, we aim to outline major research efforts within the field and review a diverse array of relevant literature. We will provide a detailed summary of the physical principles underlying LSPR sensing and address some existing inconsistencies in the nomenclature used. Our discussion will primarily focus on LSPR sensors that employ metal nanoparticles, rather than on those utilizing extended, fabricated structures. We will concentrate on sensors where LSPR acts as the primary mode of signal transduction, excluding hybrid strategies like those combining LSPR with fluorescence. Additionally, our examination of biological LSPR sensors will largely pertain to label-free detection methods, rather than those that use metal nanoparticles as labels or as means to enhance the efficacy of a label. In the subsequent section of this review, we delve into the analytical theory underpinning LSPR, exploring its physical origins and its dependency on the material properties of noble metals and the surrounding refractive index. We will discuss the behavior of both spherical and spheroidal particles and elaborate on how the LSPR response varies with particle aspect ratio. Further, we detail the fundamentals of nanoparticle-based LSPR sensing. This includes an exploration of single-particle and ensemble measurements and a comparative analysis of scattering, absorption, and extinction phenomena. The discussion will extend to how these principles are applied in practical sensing scenarios, highlighting the key experimental approaches and measurement techniques.

Enhanced efficiency of carbon based all perovskite tandem solar cells via cubic plasmonic metallic nanoparticles with dielectric nano shells

This study investigates a carbon-based all-perovskite tandem solar cell (AP-TSC) with the structure ITO, SnO₂, Cs₀.₂FA₀.₈Pb(I₀.₇Br₀.₃)₃, WS₂, MoO₃, ITO, C₆₀, MAPb₀.₅Sn₀.₅I₃, PEDOT: PSS, Carbon. The bandgap configuration of the cell is 1.75 eV/1.17 eV, which is theoretically limited to 36% efficiency. The effectiveness of embedding cubic plasmonic metallic nanoparticles (NPs) made of Gold (Au) and Silver (Ag) within the absorber layers to eliminate the requirement for thicker absorber layers, decrease manufacturing costs and Pb toxicity is demonstrated in our analysis. This analysis was conducted using 3D Finite Element Method (FEM) simulations for both optical and electrical calculations. Prior to delving into the primary investigation of the tandem structure, a validation simulation was conducted to demonstrate the accuracy and reliability of the simulations. Notably, the efficiency mismatch observed during the validation simulation, specifically in relation to the incorporation of metallic nanoparticles (NPs), amounted to a mere 0.01%. To mitigate the potential issues of direct contact between metallic NPs and perovskite materials, such as increased thermal and chemical instability and recombination at the NP surface, a 5 nm dielectric shell was applied to the NPs. The incorporation of cubic core-shell Ag NPs resulted in a 15.32% enhancement in short-circuit current density, from 16.39 mA/cm² to 18.90 mA/cm², and a 15.68% increase in overall efficiency, from 26.9 to 31.12%. This research paves the way for the integration of core-shell metallic NPs in AP-TSCs, highlighting a significant potential for efficiency and stability improvements. In a dedicated section the band alignment of the sub-cell was addressed. Additionally, a thermal investigation of the proposed tandem structure was conducted, demonstrating the robustness of the proposed AP-TSC. Finally, the sensitivity analyses related to input parameters and the challenges associated with large-scale fabrication of the proposed AP-TSC were extensively discussed.

Probing Active Sites on Pd/Pt Alloy Nanoparticles by CO Adsorption.

We studied the adsorption of CO on Pd/Pt nanoparticles (NPs) with varying compositions using polarization-dependent Fourier transform infrared reflection absorption spectroscopy (FT-IRRAS) and theoretical calculations (DFT). We prepared PtPd alloy NPs via physical vapor codeposition on α-Al2O3(0001) supports. Our morphological and structural characterization by scanning electron microscopy and grazing incidence X-ray diffraction revealed well-defined, epitaxial NPs. We used CO as a probe molecule to identify the particles' surface active sites. Polarization-dependent FT-IRRAS enabled us to distinguish CO adsorption on top and side facets of the NPs. The role of the Pd/Pt alloy ratio on CO adsorption was investigated by comparing the experimental CO stretching band frequency for different alloy arrangements to the results for pure Pd and Pt NPs. Moreover, we studied the influence of hydrogen adsorption on the NP surface composition. We determined the dependence of the IR bands on the local atomic arrangement via DFT calculations, revealing that both bulk alloy composition and neighboring atoms influence the wavenumber of the bands.

The “gut” corona at the surface of nanoparticle is dependent on exposure to bile salts and phospholipids

The “gut” corona at the surface of nanoparticle is dependent on exposure to bile salts and phospholipids

Formation of Superhydrophobic Coatings Based on Dispersion Compositions of Hexyl Methacrylate Copolymers with Glycidyl Methacrylate and Silica Nanoparticles.

In the last decade, the task of developing environmentally friendly and cost-effective methods for obtaining stable superhydrophobic coatings has become topical. In this study, we examined the effect of the concentrations of filler and polymer binder on the hydrophobic properties and surface roughness of composite coatings made from organic-aqueous compositions based on hexyl methacrylate (HMA) and glycidyl methacrylate (GMA) copolymers. Silicon dioxide nanoparticles were used as a filler. A single-stage "all-in-one" aerosol application method was used to form the coatings without additional intermediate steps for attaching the adhesive layer or texturing the substrate surface, as well as pre-modification of the surface of filler nanoparticles. As the ratio of the mass fraction of polymer binder (Wn) to filler (Wp) increases, the coatings show the lowest roll-off angles among the whole range of samples studied. Coatings with an optimal mass fraction ratio (Wn/Wp = 1.2 ÷ 1.6) of the filler to polymer binder maintained superhydrophobic properties for 24 h in contact with a drop of water in a chamber saturated with water vapor and exhibited roll-off angles of 6.1° ± 1°.