Hydrolysis Resistance Research Articles

Conjugate Position of Glucuronide and Sulfate in Piceatannol Derivatives Affects the Stability and Hydrolytic Resistance of the Conjugate in Biological Matrices.

Piceatannol, a stilbene compound, undergoes a comprehensive phase II metabolism mediated by UDP-glucuronosyltransferases (UGTs) and sulfotransferases (SULTs) in humans. Despite their well-documented beneficial effects on health, their detailed pharmacokinetic fate, including the metabolite structure and properties, is poorly understood. Thus, we determined the structure of seven glucuronides and six sulfates transformed from piceatannol and its methylated derivatives in recombinant yeast cells expressing UGTs or SULTs. We evaluated their properties in human and rat plasma samples. The conjugate that was substituted at the 3'- or 4'-catecholic hydroxy moiety exhibited increased stability. The sulfatase-mediated hydrolysis assay results in incomplete digestion or compound degradation of certain sulfates, suggesting a potential risk of underestimation by using indirect quantification methods. These findings emphasize the importance of an authentic standard for accurate pharmacokinetic studies of phase II metabolites that will be useful for understanding the mechanisms underlying the functional contribution of piceatannol in the body.

Insights of the trypsin inhibitory activity and ultrasound effect of ovomucoid based on molecular docking and spectroscopic

Ovomucoid (OVM) is the most abundant trypsin inhibitor in egg white, considered as one of the anti-nutritional factors in egg processing. In this study, the molecular mechanism of the interaction between OVM and trypsin was explored. Besides, the effect of food processing methods on the activity of OVM and structural change of OVM was analyzed. The results showed that OVM mainly inhibited trypsin activity through hydrogen bonding in its first domain and it was a non-competitive inhibitor. Surprisingly, ultrasound treatment could reduce trypsin inhibitory activity of OVM to 30%. The hydrolytic resistance to digestive enzymes and the thermal stability of the OVM was also significantly reduced. The spectroscopic results indicated ultrasound treatment affected the trypsin inhibitory activity of OVM by reducing β-sheet content and increasing hydrophobicity. In conclusion, this study reveals the molecular mechanism by which OVM inhibits trypsin activity, and provides an ultrasound treatment method to effectively reduce this activity of OVM.

Synthesis, Antibacterial Activity and Hydrolytic Resistance of (Meth)acrylamide-based Monomers for Dental Resin Adhesive

Synthesis, Antibacterial Activity and Hydrolytic Resistance of (Meth)acrylamide-based Monomers for Dental Resin Adhesive

Millimeter-scale Na2SiF6:Mn4+ red-emitting crystals with intense zero phonon line at 617 nm and enhanced hydrolysis resistance

Millimeter-scale Na2SiF6:Mn4+ red-emitting crystals with intense zero phonon line at 617 nm and enhanced hydrolysis resistance

Evaluation of extreme depyrogenation conditions on the surface hydrolytic resistance of glass containers for pharmaceutical use.

This paper is the result of a round robin activity run by the Technical Committee TC12, Pharma Packaging, of the International Commission on Glass (ICG). The study was motivated by a concern about the risk that the depyrogenation treatment of glass vials, when performed in an abnormal way that deviates from the usual procedure, may have a negative impact on the hydrolytic resistance of the container inner surface. The study was executed by using 10 ml clear type I Borosilicate glass vials representing four different compositions. For the applied depyrogenation process extreme parameters were chosen to with maximum temperature up to 400°C, exposure times up to 72 hours and different amounts of residual water inside as starting conditions. Those treated samples were tested in seven different laboratories as a round robin test.. A large amount of data was obtained, which clearly indicate that the hydrolytic resistance performance of the Type I Borosilicate glass vials is not affected even by such extreme depyrogenation conditions (e.g. 400°C, 72hours and not perfect dried inside). This is an important and useful result, both for glass and pharma companies, based on the 12.000 analytical data collected during the interlaboratory activity.

Advancements in Gelatin-Based Wound Dressings: Cross-Linking Techniques, Biocompatibility, and Biodegradability for Enhanced Angiogenesis and Healing

Uncontrolled hemorrhage from wounds is a significant cause of morbidity, highlighting the need for rapid and effective hemostatic interventions. Wound dressings play a crucial role in managing blood loss and fluid exudation while supporting the dynamic wound-healing process. This process involves hemostasis, inflammation, proliferation, angiogenesis, and remodeling to restore the skin's barrier function. Among available options, dry absorbable local hemostats offer practical advantages by absorbing wound exudates and promoting healing. Gelatin sponges, known for their hemostatic properties, biocompatibility, and biodegradability, are excellent candidates for wound dressings. They effectively stop bleeding and support tissue repair. However, gelatin’s inherent sensitivity to environmental conditions limits its direct application. To address these challenges, cross-linking techniques are employed to improve mechanical strength, hydrolysis resistance, and stability while refining the pore morphology of gelatin sponges for enhanced biomedical applications. Various cross-linkers, such as aldehydes, carbodiimides, reducing sugars, genipin, and acyl azides, have been investigated for gelatin modification. While glutaraldehyde achieves effective cross-linking, its high cytotoxicity restricts its use in biocompatible products. Alternatives like 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide (EDC) and genipin offer reduced cytotoxicity, though genipin's cost poses a limitation. Reducing sugars, such as glucose and fructose, provide a promising, non-toxic, and cost-effective solution for commercial-scale production. Optimizing cross-linking methods is essential for developing safe, effective, and affordable gelatin-based wound dressings. Addressing cross-linker toxicity remains critical to advancing their clinical applicability.

Identification, characterization, and distribution of novel amidase gene aphA in sphingomonads conferring resistance to amphenicol antibiotics.

Amphenicol antibiotics, such as chloramphenicol (CHL), thiamphenicol (TAP), and florfenicol (Ff), are high-risk emerging pollutants. Their extensive usage in aquaculture, livestock, and poultry farming has led to an increase in bacterial antibiotic resistance and facilitated the spread of resistance genes. Yet, limited research has been conducted on the co-resistance of CHL, TAP, and Ff. Herein, a novel amidase AphA was identified from a pure cultured strain that can concurrently mediate the hydrolytic inactivation of CHL, TAP, and Ff, yielding products p-nitrophenylserinol, thiamphenicol amine (TAP-amine), and florfenicol amine (Ff-amine), respectively. The antibacterial activity of these antibiotic hydrolysates exhibited a significant reduction or complete loss in comparison to the parent compounds. Notably, AphA shared less than 26% amino acid sequence identity with previously reported enzymes and exhibited high conservation within the sphingomonad species. Through enzymatic kinetic analysis, the AphA exhibited markedly superior affinity and catalytic activity toward Ff in comparison to CHL and TAP. Site-directed mutagenesis analysis revealed the indispensability of catalytic triad residues, particularly serine 153 and histidine 277, in forming crucial hydrogen bonds essential for AphA's hydrolytic activity. Comparative genomic analysis showed that aphA genes in some species are closely adjacent to various transposable elements, indicating that there is a high potential risk of horizontal gene transfer (HGT). This study established a hydrolysis resistance mechanism of amphenicol antibiotics in sphingomonads, which offers theoretical guidance and a novel marker gene for assessing the prevalent risk of amphenicol antibiotics in the environment.IMPORTANCEAmphenicol antibiotics are pervasive emerging contaminants that present a substantial threat to ecological systems. Few studies have elucidated resistance genes or mechanisms that can act on CHL, TAP, and Ff simultaneously. The results of this study fill this knowledge gap and identify a novel amidase AphA from the bacterium Sphingobium yanoikuyae B1, which mediates three typical amphenicol antibiotic inactivation, and the molecular mechanism is elucidated. The diverse types of transposable elements were identified in the flanking regions of the aphA gene, indicating the risk of horizontal transfer of this antibiotic resistance genes (ARG). These findings offer new insights into the bacterial resistance to amphenicol antibiotics. The gene reported herein can be utilized as a novel genetic diagnostic marker for monitoring the environmental fate of amphenicol antibiotics, thereby enriching risk assessment efforts within the context of antibiotic resistance.

Hydrolytic‐Resistance Long‐Persistent Luminescence SrAl2O4:Eu2+,Dy3+ Ceramics for Optical Information Storage

AbstractSrAl2O4:Eu2+, Dy3+ (SAED) is one of the most popular materials for information storage and night display applications because it has a wide excitation range and long afterglow duration. However improving the hydrolytic resistance of SAED remains a challenge. In this study, the SAED is presented to be the ceramic type by a solid‐state reaction in a vacuum ambiance. The achieved SAED ceramic has 8200 mcd m−2 initial luminescence intensity. It can also obtain long‐persistent luminescence after UV light irradiation even soaking in water for more than 30 days. This ceramic demonstrates sustained imaging capability irradiated under 365 nm UV light and X‐ray, as well as erasability and reproducibility of storage by lighting and heating. These results indicate the promising applications of SAED ceramics in optical information storage and night display in complex environments. The phase evolution in the SAED ceramic is identified directly in the micromorphology for the first time based on scanning electron microscopy coupled with a cathodoluminescence system.

Improved properties of glass vials for primary packaging with atomic layer deposition

Novel pharmaceuticals and drug delivery devices may require better performance from the packaging material e.g., in terms of extractables and leachables, and unwanted interactions. To address this, we applied atomic layer deposition (ALD) to build nanometer-range SiO2, ZrO2 and Al2O3-TiO2 films on primary packaging glass. Controlled modification of the surface also enabled creation of functionality without affecting visual appearance of the material. ALD-coated Type I borosilicate vials were compared to uncoated ones, and tailored functionality was presented by appropriate measurements. The tested ALD coatings formed a barrier on glass against extractables and leachables, from the vial and the coating alike. A good ALD coating prevents any leakage into the stored drug product. Hydrolytic resistance results improved by 85–92 %, and these results correlated well with straightforward water conductivity measurements. Opposite to uncoated borosilicate glass vials, no extracted elements could be detected from the extracts of the coated vials with stable ALD films. Improved surface integrity was observed with electron microscopy as well. ALD films increased hydrophilicity of the surface and tuning the ALD film thickness and composition allowed precise blocking of UV light wavelengths, without affecting transparency. As a conclusion, ALD is a versatile method to create barrier and functional films on primary packaging materials.

Development of oriented microbial consortium-based compound enzyme strengthens food waste hydrolysis and antibiotic resistance genes removal: Deciphering of performance, metabolic pathways and microbial communities

Enzymatic hydrolysis has been considered as an eco-friendly pretreatment method for enhancing bioconversion process of food waste (FW). However, existing commercial enzymes and microbial monomer-based compound enzymes (MME) have the issues of uneven distribution of enzymatic activity and low matching degree with the components of FW, leading to low efficiency with enzymatic hydrolysis and removal of antibiotic resistance genes (ARGs). This study used FW as the substrate, under the co-culture system, produced a microbial consortium-based compound enzymes (MCE) with oriented and well-matching degree for FW hydrolysis and ARGs removal, of which the performance, metabolic pathways and microbial communities were also investigated in depth. Results showed that the best performance for ARGs was achieved by the MCE prepared by mixing 1:5 of Aspergillus oryzae and Aspergillus niger after 12 days fermentation. The highest soluble chemical oxygen demand (SCOD) concentration and ARGs removal could respectively reach 83.90 ± 1.67 g/L and 45.95% after MCE pretreatment. The analysis of metabolic pathways revealed that 1:5 MCE pretreatment strengthened the catalytic activity of carbohydrate-active enzymes, increased the abundances of genes involved in cellulose and starch degradation, polysaccharide synthesis, ATP binding cassette (ABC) transporters and global regulation, while decreased the abundances of genes involved in mating pair formation system, two-component regulatory systems and quorum sensing, thereby enhanced FW hydrolysis and restrained ARGs dissemination. Microbial community analysis further indicated that the 1:5 MCE pretreatment promoted growth, metabolism and richness of functional microbes, while inhibited the host microbes of ARGs. It is expected that this study can provide useful insights into understanding the fate of ARGs in food waste during MCE pretreatment process.

Hydrothermal aging behavior of poly(butylene adipate-co-terephthalate) mulch: influence of the hydrolysis resistance based on the different filling materials

Hydrothermal aging behavior of poly(butylene adipate-co-terephthalate) mulch: influence of the hydrolysis resistance based on the different filling materials

Characterization of the Alkali and Hydrolysis Resistance of Polymer-Impregnated, Alkali-Resistant Glass Filaments.

The aim of this series of tests was to characterize the alkali and water resistance of alkali-resistant (durability) glass filaments, which were optimized with two non-vulcanized formulations based on co-polymerizing styrene-butadiene rubbers (CemFil-SBR1 and CemFil-SBR2). Furthermore, it was assessed which of the two polymer-impregnated multifilament yarns is the better alternative for use in cementitious binders. For this purpose, the impregnated multifilament yarns were chemically conditioned for up to twelve months at temperatures of 23 and 50 °C in 2.5 percent sodium hydroxide solution and 2.5 percent potassium hydroxide solution as well as in 3 percent salt and distilled water. The samples were then subjected to material science tests. The liquid absorption capacities and the changes in the mass of the composite materials were determined at different times during conditioning. The load-bearing capacity of the samples was also tested using uniaxial fiber strand tensile tests. The durability of the polymer-impregnated multifilament yarns was described in detail in conjunction with scanning electron microscopy images and nominal cross-section determinations. The test liquids caused a reduction in strength during the storage period, which was accelerated by increased temperatures. The reduction in strength is mainly due to glass corrosion of the filaments. Glass corrosion is delayed due to the good impregnation quality, which fundamentally improves the durability of the yarns. The results of the durability tests show that the polymer-impregnated multifilament yarns CemFil-SBR2 are probably more suitable for use in cementitious binders, as they have better alkali and hydrolysis resistance.

Structure, chemical durability, and melting properties of aluminosilicate glass

AbstractBorosilicate glasses possess excellent melting properties and high stability against chemical attack by aqueous solutions, enabling this glass family to be used in various fields. In this article, we design a novel glass network in order to achieve a chemically robust glass with a low melting temperature. Therefore, the substitution effect of Na2O by MgO, Al2O3, Li2O, and K2O on the chemical durability and melting properties of sodium aluminosilicate glass (i.e., 80SiO2‒5Al2O3‒15Na2O [mol%]) was examined using a standard hydrolytic resistance test and viscosity measurement. Interestingly, we found that the partial replacement of Na2O by Al2O3, Li2O, and K2O (i.e., 80SiO2‒5Al2O3‒15Na2O → 80SiO2‒6.5Al2O3‒9Li2O‒2.25Na2O‒2.25K2O) makes the glass network with chemical durability and melting properties comparable to those of the commercial borosilicate network, resulting in a low HCl consumption of 0.04 mL/g and working temperature of 1238°C (i.e., temperature at viscosity 104 dPa s). The structural characterizations indicate that the high chemical stability of this glass composition originates from the abundance of SiO4 tetrahedrons with three and four bridging oxygen in the glass network as well as the increase in cationic field strength of mixed alkali ions. These excellent melting properties and superior chemical durability of glass imply the possibility of using the mixed alkali metal oxides aluminosilicate glass together with the commercial borosilicate glass in the markets for numerous practical applications.

Examination of primary aromatic amines content in polylactic acid straws and migration into food simulants using SERS with LC-MS

Polylactic acid (PLA) straws hold eco-friendly potential; however, residual diisocyanates used to enhance the mechanical strength can generate carcinogenic primary aromatic amines (PAAs), posing health risks. Herein, we present a rapid, comprehensive strategy to detecting PAAs in 18 brands of food-grade PLA straws and assessing their migration into diverse food simulants. Surface-enhanced Raman spectroscopy was conducted to rapidly screen straws for PAAs. Subsequently, qualitative determination of migrating PAAs into various food simulants (4 % acetic acid, 10 % ethanol, 50 % ethanol) occurred at 70 °C for 2 h using liquid chromatography-mass spectrometry. Three PAAs including 4,4′-methylenedianiline, 2,4′-methylenedianiline, and 2,4-diaminotoluene were detected in all straws. Specifically, 2,4-diaminotoluene in 50 % ethanol exceeded specific migration limit of 2 μg/kg, raising safety concerns. Notably, PAAs migration to 10 % and 50 % ethanol surpassed that to 4 % acetic acid within a short 2-hour period. Moreover, PLA straws underwent varying degrees of shape changes before and after migration. Straws with poly(butylene succinate) resisted deformation compared to those without, indicating enhanced heat resistance, while poly(butyleneadipate-co-terephthalate) improved hydrolysis resistance. Importantly, swelling study unveiled swelling effect wasn’t the primary factor contributing to the increased PAAs migration in ethanol food simulant, as there was no significant disparity in swelling degrees across different food simulants. FT-IR and DSC analysis revealed higher PAAs content in 50 % ethanol were due to highly concentrated polar ethanol disrupting hydrogen bonds and van der Waal forces holding PLA molecules together. Overall, minimizing contact between PLA straws and alcoholic foods is crucial to avoid potential safety risks posed by PAAs.

The multifactorial phenomenon of enzymatic hydrolysis resistance in unripe banana flour and its starch: A concise review.

Unripe banana flour starch possesses a high degree of resistance to enzymatic hydrolysis, a unique and desirable property that could be exploited in the development of functional food products to regulate blood sugar levels and promote digestive health. However, due to a multifactorial phenomenon in the banana flour matrix-from the molecular to the micro level-there is no consensus regarding the complex mechanisms behind the slow enzymatic hydrolysis of unripe banana flour starch. This work therefore explores factors that influence the enzymatic hydrolysis resistance of raw and modified banana flour and its starch including the proportion and distribution of the amorphous and crystalline phases of the starch granules; granule morphology; amylose-amylopectin ratio; as well as the presence of nonstarch components such as proteins, lipids, and phenolic compounds. Our findings revealed that the relative contributions of these factors to banana starch hydrolytic resistance are apparently dependent on the native or processed state of the starch as well as the cultivar type. The interrelatability of these factors in ensuring amylolytic resistance of unripe banana flour starch was further highlighted as another reason for the multifactorial phenomenon. Knowledge of these factors and their contributions to enzymatic hydrolysis resistance individually and interconnectedly will provide insights into enhanced ways of extraction, processing, and utilization of unripe banana flour and its starch.

Electroauxiliary-Assisted C-C Bond Formations in Lithium Perchlorate / Nitromethane Solution

C-nucleosides have C-C bonds between ribosyl moiety and nucleobase at anomeric carbon. This substitution of covalent bond gives hydrolysis resistance to C-nucleosides. Therefore, C-nucleosides are good candidates for antiviral or antitumor drugs as mimic building blocks of oligonucleotide.To synthesize nucleosides, cation intermediate is used for installing nucleobase on ribosyl moiety. When it comes to generation of cation intermediate, electrochemical methodology is one of the useful tools. In electrochemical method, 1’-arylthioriboses are used as glycosyl donors. They have thioether group as electroauxiliary at anomeric carbon forging O,S-acetal that are activated with anodic oxidation to generate corresponding cation intermediate. Since electrochemically generated cation intermediates have high reactivity enough to react with carbon nucleophiles, this method can be adopted to C-nucleoside synthesis.Previously, electrochemical nucleoside synthesis was reported using cation pool method in combination with electroauxiliary. To avoid undesired oxidation of nucleophile, it is important to pool the cation and/or to lower the oxidation potential of ribose. The low temperature condition such as -78 ~ -50 oC is necessary to pool cation intermediates.In this research, we aimed to achieve electrochemical C-C bond formation at anomeric carbon with ambient temperature condition. In this strategy, we use glycosyl donors with lowered oxidation potential to avoid competitive oxidation with carbon nucleophiles. We also adapt lithium perchlorate/nitromethane system for electrolysis. Figure 1

Toward durable polylactic acid/poly(methyl methacrylate) polyblend fibers with high performance

AbstractPolylactic acid/poly(methyl methacrylate) (PLA/PMMA) composite fibers with high performance were fabricated using melt spinning technique. The crystallization, lamellae orientation and physical properties of composite fibers were investigated systematically. The addition of PMMA (0–20 wt%) has improved the hydrolysis resistance of composite fibers by preventing water molecules from penetrating and diffusing through the fibers, but the strength and heat resistance were reduced at the same time. The stereocomplex crystallites (SC) formed before spinning by introducing poly(D‐lactide) (PDLA) (3 wt%) in poly(L‐lactide) (PLLA) matrix and acted as nucleating agents to enhanced the crystallization and lamellae orientation of PLLA matrix, which improved the physical properties of PLA composite fibers resultful. The tensile strength of PLA fibers with 3 wt% PDLA and 5 wt% PMMA was increased 31% as well as the boiling water shrinkage and the hydrolysis rate were decreased 30% and 33% in relation to PLLA fibers. Finally, the hydrolysis resistance was further enhanced on the basis of realizing high strength and heat resistance, which is of great significance for preparing durable PLA fiber materials and expanding their application.

An Advanced Solvent for the Caustic-Side Solvent Extraction of Cesium from Nuclear Waste: Comparing Lipophilic Guanidines for Improved Hydrolytic Stability

ABSTRACT An advanced solvent has been developed for application in the extraction of cesium from alkaline nuclear waste. Four lipophilic guanidines have been compared to arrive at a more hydrolysis-resistant suppressor component of the solvent. Plans call for deployment of the Next-Generation Caustic Side-Solvent Extraction (NG-CSSX) process at industrial scale for separation of radioactive Cs-137 from the legacy salt waste stored at the US Department of Energy Savannah River Site (SRS). In the solvent used in NG-CSSX, an alkyl guanidine “suppressor” component facilitates efficient stripping of the loaded cesium from the solvent. However, as typical of guanidine compounds, the suppressor previously used in the NG-CSSX solvent, N,N‘,N’’-tri(3,7-dimethyloctyl)guanidine (TiDG), suffers from hydrolytic degradation under process conditions. Recently, the sterically hindered alkyl guanidine N,N’-dicyclohexyl-N’’-(10-nonadecyl)guanidine (DCNDG) has been found to offer 8 to 44 times greater hydrolysis resistance than TiDG. Here, the process performance characteristics of the NG-CSSX solvent incorporating DCNDG are determined in comparison with TiDG and two other guanidine suppressors. The solvent has been adjusted in density to accommodate use in the SRS Salt Waste Processing Facility and tested under aggressive bench-scale conditions intended to increase plant throughput. Experiments include the effect of ageing at normal and off-normal temperatures of the distribution of Cs+ through the NG-CSSX process, the fate and effects of guanidine degradation products, suppressor capacity, coalescence times for aqueous-solvent dispersions, tendency for emulsification, third-phase formation, and degree of protonation of the guanidine in stripping. While the chosen structures of the four compared guanidines mainly effect differences in stability, subtle differences in other system properties such as emulsion formation and suppressor capacity provide insight into the function of this important solvent component. In comparison with TiDG and two other guanidines, DCNDG provides greatly increased stability while not compromising the excellent functional properties of the NG-CSSX solvent.

High Strength UV-Resistant Composite Film of Fe3+-Coordination Lignin/PVA.

The literature on polyvinyl alcohol (PVA) films is extensive, however, these methods often necessitate intricate synthesis processes or the addition of plasticizers to modify the strength and water solubility of the PVA material. A high-strength UV radiation-resistant composite film by chelating Fe3+ with lignin and PVA, which exhibits excellent hydrolysis resistance is developed. This composite film is prepared simply by incorporating a small amount of dealkalized lignin (APPL) and ferric chloride (FeCl3) into PVA through a straightforward composite process. During the scanning test, it is noted that the film exhibits a high density of uniformly dispersed particles, endowing it with efficient ultraviolet absorption capabilities. The infrared and anti-dissolution tests reveal that the coordination of Fe3+ with lignin imparts an outstanding hydrolysis resistance to the film, obviating the need for any extender, curing agent, acid or base. The tensile fracture strength reaches an impressive 187.81Mpa in the tensile test. UV and indicator card tests unequivocally demonstrate that the film achieves a remarkable 100% anti-UV efficiency. This Fe3+ chelated lignin/PVA composite film, with its facile preparation, environmental sustainability, high strength, and outstanding anti-ultraviolet efficiency, can be deployed across diverse applications requiring robust protection against ultraviolet radiation.

Rational design of a novel siloxane-branched waterborne polyurethane coating with waterproof and antifouling performance

Inferior water resistance remains a bottleneck in the development of the waterborne polyurethane (WPU) coatings industry. Herein, a novel strategy for the facile preparation of hydrophobic antifouling WPU coatings is presented in this work. Specifically, a series of siloxane-branched modified polyurethanes (BSi-WPU) was prepared by synergistically introducing diol-hydroxyl single-ended silicone oil (DSSiO) as the branched modified monomer and hydroxylated fluorinated siloxane (HTFSi) as the functional soft-chain segment into the WPU system via a simple polycondensation process. The effects of the introduction of DSSiO on the water resistance and mechanical properties of the BSi-WPU were investigated, and the antifouling and chemical resistance of the modified coatings were also examined. The results demonstrated that the branched DSSiO possessed excellent surface migration efficiency, which effectively improved the water repellence (contact angle up to 109.3°), waterproofness (absorption reduced to 7.5 %), and hydrolysis resistance (minimum 1.6 % loss of strength after water immersion) of the coatings. In addition, owing to thermodynamic immiscibility, the incorporation of HTFSi and appropriate DSSiO amounts enlarged the microphase separation of the polyurethane, whereby the material exhibited improved mechanical properties over ordinary polyurethanes. More importantly, based on the surface enrichment of low-surface-energy silicon and fluorine units, the coatings exhibit excellent repellency to contaminated liquids and corrosive chemical solutions. This approach provided a more applicable alternative idea to the industrial fabrication of hydrophobic and antifouling WPU coatings.