Hydrophilic Modification Research Articles

Selective Adsorption to Pathogenic Bacteria Augments Antibacterial Activity via Adjusting the Physicochemical Property of Nanoparticles

AbstractOral antibiotics are the primary method used to treat bacterial infections in clinical practice. However, the non‐selectivity of antibiotics reduces the efficacy of treatment while also tending to damage normal flora and cause dysbiosis. Obviously, it is crucial to enhance the selectivity of antibiotics against bacteria. It is possible to modulate the physicochemical properties of orally administered nanosystems to achieve selective adsorption to bacteria, thereby achieving improving bactericidal effects. A series of nanoparticles are examined bacterial adhesion characteristics focusing on five aspects: particle size, shape, charge, surface hydrophilicity, and surface modification. Selective adsorption of nanoparticles is investigated pathogenic bacteria (S. aureus as an example), normal bacteria (E. coli as an example), and probiotic bacteria (E. faecium as an example). The results show that ≈50 nm chitosan‐modified spherical Poly(lactide‐co‐glycolide) (PLGA) nanoparticles exhibit a stronger adsorption capacity for pathogenic bacteria (Staphylococcus aureus). After loading with amoxicillin, the antibacterial nanoparticles are able to destroy pathogenic bacteria without disrupting the normal intestinal bacterial flora and reducing the typical side effects of ecological disruption caused by broad‐spectrum antibiotics. Thus, this work presents a convenient and versatile strategy for targeting bacteria to enhance the antibacterial efficacy of current antibiotics.

Development of Off-On Near-Infrared Fluorescent Probes for Sensitive In Vivo Imaging of Amyloid-β Species with Enhanced Pharmacokinetics.

The fluorescent imaging of pathologically accumulated β-amyloid (Aβ) proteins is of significant importance to the diagnosis of Alzheimer's disease (AD). In the paper, we prepare two new NIR probes, NIR-1 and NIR-2, through hydrophilic modification of introducing water-soluble bioactive groups such as polyethylene glycol (PEG) and morpholine to tune in vivo pharmacokinetics for specific detection of soluble and insoluble Aβ species. The in vitro assessments confirm that both NIR-1 and NIR-2 display strong near-infrared (NIR) fluorescence (FL) enhancement upon interaction with Aβ42 monomers, oligomers or aggregates (λem>670 nm) and show highly sensitive, rapid and selective response towards Aβ42 species. After i. v. injection, each probe showed fast blood-brain barrier (BBB) penetration and immediately produced intense FL signals in the brain of APP/PS1 AD model mice at 10 min. Moreover, compared with NIR-2, NIR-1 bearing a hydrophilic PEG chain displayed not only more rapid clearance but also lower background signal to efficiently distinguish APP/PS1 mice and wild-type mice with higher signal-to-background ratio, which was further validated by ex vivo histological staining of brain tissues. Therefore, due to its excellent pharmacokinetics, NIR-1 shows great promise as an effective NIR probe for specific detection of Aβ species.

Tuning surface hydrophilicity of a BiVO4 photoanode through interface engineering for efficient PEC water splitting.

This study presents a novel approach to enhance photoelectrochemical (PEC) water oxidation by integrating cobalt phthalocyanine (CoPc) with bismuth vanadate (BVO) via a direct solvothermal method. The as-prepared BVO@CoPc photoanode demonstrated a photocurrent density of 4.0 mA cm-2 at 1.23 V vs. RHE, which is approximately 3.1 times greater than that of the unmodified BVO, and has superior stability. The incident photon-to-current conversion efficiency (IPCE) of the BVO@CoPc photoanode reaches an impressive value of 81%, accompanied by significant enhancements in charge injection efficiency. This excellent performance can be ascribed to the enhanced hydrophilicity with the BVO/CoPc interface engineering, which facilitates interfacial interaction between the electrode and electrolyte, accelerates photogenerated charge carrier transfer and separation. Furthermore, compared to the immersion and drop-casting methods, the BVO@CoPc-S composite photoanode prepared via the solvothermal method exhibits a significant improvement in interfacial contact and surface hydrophilicity. These findings highlight the potential of the strategy based on interfacial hydrophilicity modification to overcome key limitations in PEC water splitting, providing a pathway to more efficient and durable photoanode design.

High‐Density Polyethylene Janus Fibrous Membrane with Enhanced Breathability and Moisture Permeability via PDA Assisted Hydrophilic Modification

AbstractFunctional fibrous membranes with high mechanical properties are intensively developed for different application fields. In this study, to enhance moisture and air permeability without compromising mechanical strength, a facile float‐surface modification strategy is employed to fabricate Janus fibrous membranes with distinct hydrophobicity/hydrophilicity using the high‐density polyethylene (HDPE) fibrous membranes. By coating one side of the HDPE fibrous membranes with polydopamine (PDA) and a superhydrophilic polyelectrolyte, the obtained Janus HDPE fibrous membranes demonstrate an excellent water transmission rate (577.61 ± 72.66 g m−2 h−1), water vapor transmission rate (WVTR, 131.62 ± 24.34 g m−2 h−1) and gas permeability (17,496 ± 235 m3 m−2 h−1 bar−1), which are much better than those commercial membranes (Tyvek with water transmission rate 518.93 ± 23.20 g m−2 h−1, WVTR 53.09 ± 6.19 g m−2 h−1, and gas permeability 2,871 ± 145 m3 m−2 h−1 bar−1). Further, the Janus HDPE fibrous membranes keep outstanding mechanical strength (17.00 ± 4.26 MPa of tensile strength, 45.49 ± 8.75% of strain at break), and exhibit an asymmetric wettability on each side which is demonstrated by the separation experiments with various oil‐water mixtures. This simple modification approach not only improves the serviceability of HDPE fibrous membranes but also offers scalable potential for apparel applications and other industrial applications.

Li-Based Nanoprobes with Boosted Photoluminescence for Temperature Visualization in NIR Imaging-Guided Drug Release.

Lanthanide-doped fluoride nanocrystals have emerged as promising tools in biomedicine, yet their applications are still limited by their low luminescence efficiency. Herein, we developed highly efficient lithium-based core-shell-shell (CSS) nanoprobes (NPs) featuring a rhombic active domain and a spherical inert protective shell. By introducing Yb3+ as an energy transfer bridge and optimizing the CSS design, a remarkable 1643-fold enhancement in visible emission and a 33-fold increase in NIR emission are achieved compared to original nanoparticles. The upconversion quantum yield and brightness are 5-fold and 10-fold higher than those of typical sodium-based NPs, respectively, supported by the finite-difference time-domain simulations revealing stronger light absorption in rhombic LiYF4. Furthermore, the hydrophilic modification enabled the CSS NPs to conjugate with Rose Bengal hexanoic acid, thereby achieving upconversion-activated drug release. Meanwhile, the robust NIR emission of Yb3+ allows for precise lifetime-based thermal mapping and high-resolution imaging, advancing the development of noninvasive clinical diagnostics and targeted cancer therapies.

An innovative and rapid method for permanent hydrophilic modification of polydimethylsiloxane (PDMS) chip surfaces

An innovative and rapid method for permanent hydrophilic modification of polydimethylsiloxane (PDMS) chip surfaces

Enhanced surface hydrophilicity improves osseointegration of titanium implants via integrin-mediated osteoimmunomodulation.

Titanium (Ti) implants have become widespread especially in dentistry and orthopedics, where macrophage-driven osteoimmunomodulation is crucial to their success. Hydrophilic modification of Ti represents a promising strategy to enhance its immune and osteogenic responses. Herein, the osteoimmunomodulatory performance and integrin-mediated mechanism of novel non-thermal atmospheric plasma (NTAP) treatment to induce a hydrophilic Ti were investigated for the first time. Compared to a hydrophobic surface, NTAP-modified Ti possessed a 3-fold increase of pro-healing M2 macrophage makers, and the doubled osteogenic differentiation of mesenchymal stem cells was demonstrated in this immune microenvironment, thus improving early osseointegration. Mechanistically, the ameliorative osteoimmunomodulatory properties of NTAP were attributed to its positive and negative modulation in macrophages' integrin β1 or β2, and the subsequent FAK-PI3K/Akt or NF-κB signaling pathway. Collectively, this study highlighted the role of integrins and related signaling pathways in hydrophilic implant-caused macrophage polarization, therefore inventively unveiling the underlying mechanism of NTAP-enhanced osteoimmunomodulation. Furthermore, it established a robust theoretical foundation for the clinical application of this cost-effective, versatile, and transformation-valuable surface engineering strategy for the development of next-generation Ti implants.

Surface Hydrophilic Modification of Polypropylene by Nanosecond Pulsed Ar/O2 Dielectric Barrier Discharge.

Polypropylene (PP) membranes have found diverse applications, such as in wastewater treatment, lithium-ion batteries, and pharmaceuticals, due to their low cost, excellent mechanical properties, thermal stability, and chemical resistance. However, the intrinsic hydrophobicity of PP materials leads to membrane fouling and filtration flux reduction, which greatly hinders the applications of PP membranes. Dielectric barrier discharge (DBD) is an effective technique for surface modification of materials because it generates a large area of low-temperature plasma at atmospheric pressure. In this study, O2 was added to nanosecond pulsed Ar DBD to increase its reactivity. Electrical and optical diagnostic techniques were used to study the discharge characteristics of the DBD at varying O2 contents. The uniformity of the discharge was quantitatively analyzed using the observed discharge images. Water contact angle measurements were used to assess the surface hydrophilicity of polypropylene. The surface morphology and chemical composition of the PP materials before and after treatment were analyzed using field emission scanning electron microscopy (FE-SEM), atomic force microscopy (AFM), Fourier-transform infrared spectroscopy (FTIR), and X-ray photoelectron spectroscopy (XPS). The results show that the moderate addition of O2 enhances surface hydrophilicity and the uniformity of the modification. By increasing the O2 addition from 0% to 0.1%, the average power increased from 4.19 W to 5.79 W, and the energy efficiency increased from 17.78% to 21.51%. The water contact angle of the DBD-treated PP showed a tendency to decrease and then increase with increasing O2 content, with the optimum O2 addition determined to be 0.1%. Under this condition, the water contact angle of the PP surface decreased by 31.88°, which is 52.31% lower than the untreated surface. O2 increases the number of oxygen-containing polar groups (-OH, C=O, and O-C=O) on the surface of the material, and deepens and densifies the grooves on the surface of the PP material, resulting in an increase in the hydrophilicity of the PP surface.

Diamine Crosslinked Addition-Type Diblock Poly(Norbornene)s-Based Anion Exchange Membranes with High Conductivity and Stability for Fuel Cell Applications.

Anion exchange membranes (AEMs) as a kind of important functional material are widely used in fuel cells. However, synthetic AEMs generally suffer from low conductivity, poor alkaline stability, and poor dimensional stability. Constructing efficient ion transport channels is widely regarded as one of the most effective strategies for developing AEMs with high conductivity and low swelling ratio. Herein we demonstrate a versatile strategy to prepare the AEMs with both high conductivity and excellent alkali stability via all-carbon hydrogen block copolymer backbone hydrophilic crosslinking and introducing flexible alkoxy spacer chains. Additionally, we investigated the impact of the crosslinking degree on the AEMs' performances. It was found that the dosage of the hydrophilic crosslinker has a significant impact on the construction of efficient ion transport channels in the AEMs. Amazingly, the CL30-aPNB-TMHDA-TMA exhibited the highest hydroxide conductivity (138.84 mS cm-1), reasonable water uptake (54.96%), and a low swelling ratio (14.07%) at 80 °C. Meanwhile, the membrane showed an excellent alkaline stability in a 1 M NaOH solution at 80 °C for 1008 h (ion exchange capacity (IEC) and OH- conductivity remained at 91.9% and 89.12%, respectively). The single cells assembled with CL30-aPNB-TMHDA-TMA exhibited a peak power density of 266.2 mW cm-2 under a current density of 608 mA cm-2 at 80 °C. The novel developed composite strategy of flexible alkoxy side chains with hydrophilic crosslinking modification is potentially promised to be an effective approach to develop the high-performance AEMs.

Atmospheric Pressure Nitrogen Corona Discharge and Its Application in Hydrophilicity Modification of Polypropylene Fibber Surfaces

Atmospheric Pressure Nitrogen Corona Discharge and Its Application in Hydrophilicity Modification of Polypropylene Fibber Surfaces

Urushiol-Based Coating with High Surface Hydrophilicity for Easy-Cleaning of Oil Pollutants.

Urushiol is recognized as a sustainable coating material with superior properties; however, it faces significant challenges in applications such as petrochemicals and marine engineering due to surface oil contamination. This study aimed to enhance the cleanability of urushiol-based coatings through hydrophilic modification. Polyethylene glycol monooleate (PEGMO) was identified as an appropriate hydrophilic macromonomer and utilized as a modifier to develop a novel urushiol-based coating, termed P(U-PEGMO), via thermal curing. The results indicated that copolymerization occurred between urushiol and PEGMO during the curing process, forming a stable urushiol copolymer with favorable compatibility. The incorporation of PEGMO greatly improved the surface hydrophilicity of the coatings, as evidenced by a reduction in the water contact angle to below 30° when the modifier content reached 30% or higher, demonstrating a high degree of surface hydrophilicity. This enhanced property imparted the modified coating with underwater superoleophobicity and reduced oil adhesion, thereby facilitating the removal of oil. The cleaning performance was evaluated using a simple water rinsing method, after which, less than 2.5 wt% of oil residues remained on the surface of the modified coating. The high hydrophilicity is considered responsible for the coating's easy-cleaning capability. In addition, the modified coatings exhibited improved flexibility and impact resistance, albeit with a slight decrease in hardness.

Hydrophilic Modification of Macroscopically Hydrophobic Mineral Talc and Its Specific Application in Flotation.

Sodium diethyldithiocarbamate (DDTC), a common collector used to enhance the hydrophobicity of minerals in froth flotation, nevertheless weakens the hydrophobicity of the talc surface. To rationalize this anomaly, the interactions of a hydrophobic alkyl group and hydrophilic mineralophilic group (-NCS2-) of heteropolar surfactant DDTC, and a water molecule with the talc (001) surface, were investigated. Herein, DFT simulations found that the talc (001) surface features natural hydrophobicity determined by the competition between adhesion (surface water) and cohesion (water-water interactions). The interaction of the hydrophobic alkyl group of DDTC with the talc surface is more favorable compared to that of the -NCS2- group and H2O, favoring the hydrophilic modification of the talc surface. Additionally, adsorption isotherms, time-of-flight secondary ion mass spectrometry (ToF-SIMS), microflotation tests, and contact angle measurements also indicate that the differences in adsorption orientation of the heteropolar surfactant DDTC on the talc surface enhance the hydrophilicity of the talc surface, leading to a decreased recovery of the talc. This study provides crucial surface chemistry evidence for the selective adsorption of heteropolar surfactants and contributes to the understanding of the mechanism for the efficient flotation separation of molybdenite from talc.

Adsorption Behavior of Fluorocarbon Surfactants on Polytetrafluoroethylene Surface

By using the sessile drop method, the wetting properties of nonionic fluorocarbon surfactants (FNS-1 and FNS-2) and anionic fluorocarbon surfactant (FAS) solutions on the surface of polytetrafluoroethylene (PTFE) were investigated. Meanwhile, the effects of surfactant concentration on the contact angle, adhesion tension, PTFE–liquid interfacial tension, and work of adhesion of the fluorocarbon surfactant with different structures were detected. The results demonstrate that the adsorption amount of the three fluorocarbon surfactants at the air–liquid interface is 1.5~2 times higher than their adsorption amount at the PTFE–solution interface. Before critical micelle concentration (CMC), the fluorocarbon surfactant molecules rely on their hydrophobic groups to adsorb on the PTFE surface. The smallest molecular size of FNS-2 results in the largest adsorption amount, while electrostatic repulsion and large steric hindrance result in the smallest adsorption amount for FAS. Above CMC, the fluorocarbon surfactants form semi-micelles to adsorb on the PTFE surface. The hydrophilic modification ability of the three fluorocarbon surfactants for the PTFE surface is stronger than that of reported surfactants, and the contact angle can be reduced to about 20° at high concentrations. The order of the hydrophilic modification ability is FNS-2 > FNS-1 > FAS. Hydrophilic EO groups can effectively enhance the hydrophilicity of FNS-1 and FNS-2. Due to the hydrophobic -CH3 group and the smaller adsorption amount, FNS-1 possesses a weaker hydrophilic modification ability than FNS-2. Investigating the adsorption behavior of fluorocarbon surfactants on the PTFE surface can help us to better utilize fluorocarbon surfactants. This could have broad implications for colloid and interface science.

Performance study of integrated aftercool-humidifier based on surface foaming hydrophilic modification

Performance study of integrated aftercool-humidifier based on surface foaming hydrophilic modification

Typical Heterotrophic and Autotrophic Nitrogen Removal Process Coupled with Membrane Bioreactor: Comparison of Fouling Behavior and Characterization.

There is limited research on the relationship between membrane fouling and microbial metabolites in the nitrogen removal process coupled with membrane bioreactors (MBRs). In this study, we compared anoxic-oxic (AO) and partial nitritation-anammox (PNA), which were selected as representative heterotrophic and autotrophic biological nitrogen removal-coupled MBR processes for their fouling behavior. At the same nitrogen loading rate of 100 mg/L and mixed liquor suspended solids (MLSS) concentration of 4000 mg/L, PNA-MBR exhibited more severe membrane fouling compared to AO-MBR, as evidenced by monitoring changes in transmembrane pressure (TMP). In the autotrophic nitrogen removal process, without added organic carbon, the supernatant of PNA-MBR had higher concentrations of protein, polysaccharides, and low-molecular-weight humic substances, leading to a rapid flux decline. Extracellular polymeric substances (EPS) extracted from suspended sludge and cake sludge in PNA-MBR also contributed to more severe membrane fouling than in AO-MBR. The EPS subfractions of PNA-MBR exhibited looser secondary structures in protein and stronger surface hydrophobicity, particularly in the cake sludge, which contained higher contents of humic substances with lower molecular weights. The higher abundances of Candidatus Brocadia and Chloroflexi in PNA-MBR could lead to the production of more hydrophobic organics and humic substances. Hydrophobic metabolism products as well as anammox bacteria were deposited on the hydrophobic membrane surface and formed serious fouling. Therefore, hydrophilic membrane modification is more urgently needed to mitigate membrane fouling when running PNA-MBR than AO-MBR.

Hydrophilicity modification of polyphenylene sulfide: A comparative study on the introduction of Zr by physical blending and copolymerization

Hydrophilicity modification of polyphenylene sulfide: A comparative study on the introduction of Zr by physical blending and copolymerization

A simple and efficient approach for pore structure optimization and hydrophilic modification of PTFE nanofiber membrane

A simple and efficient approach for pore structure optimization and hydrophilic modification of PTFE nanofiber membrane

A Polymer-Based Polar Stationary Phase Grafted With Modified Lysine for Hydrophilic Interaction Chromatography.

The high hydrophobicity and chemical inertness of poly(styrene-divinylbenzene) (PS-DVB) microspheres make their surface hydrophilic modification difficult. Here we describe a facile way to convert PS-DVB microspheres to hydrophilic, then can be used as polar stationary phase for hydrophilic interaction chromatography. This approach utilizes the grafting of an acrylamide-terminated lysine zwitterionic monomer onto PS-DVB microspheres via free radical polymerization. The obtained stationary phase shows good hydrophilicity and a typical retention mechanism of hydrophilic interaction chromatography toward several model polar analytes. It also exhibits obvious zwitterionic properties and is capable of separating cationic and anionic analytes simultaneously. The column shows negligible bleeding level, much superior to silica-based ones.

Surfactant hydrophilic modification of expanded graphite to fabricate water-based composite phase change material with high latent heat for cold energy storage

Surfactant hydrophilic modification of expanded graphite to fabricate water-based composite phase change material with high latent heat for cold energy storage

Enhanced Antifouling Capability of In Situ-Grown Hydrophilic-Hydrophobic Nanodomains on Membrane Surface in the Ultralow Pressurized Ultrafiltration Process.

Although hydrophilic modification of the membrane surface is widely adopted, polymeric membranes still suffer from irreversible fouling caused by hydrophilic components in surface water. Here, an ultrathin hydrogel layer (40 nm) with hydrophilic-hydrophobic textures was in situ grown onto the polysulfone ultrafiltration membrane surface using an organic-radical-initiated interfacial polymerization technique. The interfacial polymerization of hydrophilic and hydrophobic monomers ensured the molecular-scale distribution of hydrophilic and hydrophobic nanodomains on the membrane surface. These nanodomains, with their molecular lengths, facilitated dynamic repulsion interactions between the uniformly textured surface and foulant components with different degrees of hydrophilicity. Chemical force characterization confirmed that the adhesion force between the hydrophilic-hydrophobic textured membrane surface and foulants (dodecane, bovine serum albumin, and humic acid) was greatly reduced. Dynamic filtration experiments showed that a hydrophilic-hydrophobic textured membrane always possessed the largest water flux and the best antifouling performance. Furthermore, the foulant coverage ratio on the membrane surface was first evaluated by measuring changes in surface streaming potentials, which demonstrated a 69% reduction in the amount of foulant adhering to the hydrophilic-hydrophobic textured membrane surface. Therefore, the construction of hydrophilic-hydrophobic nanodomains on the membrane surface provides a promising strategy for alleviating membrane fouling caused by both hydrophobic and hydrophilic components during ultralow pressurized ultrafiltration processes.