Hydrolytic Behavior Research Articles

Acetylcholinesterase-free colorimetric sensing platform for carbosulfan detection based on hollow PDA/MnO2 nanozyme.

Rapid and accurate detection of carbosulfan residues in vegetables is important for ensuring food safety. Herein, based on the unique hydrolysis behavior of carbosulfan, a nanozyme-based colorimetric sensing platform was proposed for detection of carbosulfan. Hollow polydopamine/MnO2 nanoparticles (H-PDA/MnO2 NPs) with excellent oxidase-like activity were synthesized, which can promote the oxidation of 3,3',5,5'-tetramethylbenzidine (TMB) into blue oxidative product (oxTMB). Under acidic conditions, carbosulfan can be decomposed and produce reductive sulfide species (-SH), which are capable to disintegrate MnO2 NPs, resulting in decreased oxidase-like activity of H-PDA/MnO2 NPs. Based on the inhibitory effect on oxidase activity of H-PDA/MnO2 NPs, an acetylcholinesterase-free colorimetric assay was proposed for detection of carbosulfan with low limit of detection of 0.63ngmL-1. Integrating test swabs with smartphone, a portable colorimetric sensor was constructed, showing great potential for on-site detection. To demonstrate the feasibility of this method, carbosulfan in real vegetable samples were determined.

Computational Explorations of Th4+ First Hydrolysis Reaction Constants: Insights from Ab Initio Molecular Dynamics and Density Functional Theory Calculations.

The fundamental hydrolysis behavior of tetravalent actinide cations (An4+) with a high charge is crucial for understanding their solution chemistry, particularly in nuclear fuel reprocessing and environmental behavior. Using Th4+ as a reference of the An4+ series, this work employed both the periodic model and the cluster model to calculate the first hydrolysis reaction constant (pKa1) of the Th4+ aqua ion and conducted a detailed evaluation of these approaches. In the periodic model, ab initio molecular dynamics (AIMD) simulations of Th4+ in the explicit solvation environment are conducted, using metadynamics and constrained molecular dynamics to calculate pKa1 values. Metadynamics simulations with sufficient sampling yielded a value of 5.02, aligning with the experimental values (4.12-4.97). Moreover, AIMD results reveal further Grotthuss-type proton transfers and changes in the solvent structures, which are important for accurately modeling the hydrolysis process. In the cluster model, density functional theory calculations are performed on isolated hydrate clusters to obtain pKa1 values, describing solvation effects through the cluster-continuum model. Based on insights from the periodic models, particularly regarding further proton transfer, the cluster model was modified and tested using different functionals and similar cations (La3+and Ac3+). The pKa1 values obtained in the cluster model also show good agreement with the experimental values. The current computational approaches provide a comprehensive understanding of Th4+ hydrolysis and a reference framework for studying the hydrolysis of other lanthanide and actinide ions.

Selective colorimetric detection of carbosulfan based on its hydrolysis behavior and Ti3C2/AuPt nanozyme

Carbosulfan (CBS) is a widely used carbamate pesticide in agricultural production, its easy decomposition into hypertoxic carbofuran poses serious threats to human health and food safety. Therefore, sensitive and accurate detection of CBS is of significant importance. Conventional chromatography-based techniques require expensive instruments and complicated sample pretreatment, limiting their application for fast detection. Current electrochemical and colorimetric methods for detection of pesticides based on the cascade catalytic reactions between acetylcholinesterase (AChE) and nanozymes, which exhibit inferior selectivity. Hence, selective, sensitive and fast detection of CBS is still challenging. In this work, an AChE-free colorimetric method was proposed for selective detection of CBS based on its unique hydrolysis behavior and nanozyme. Ti3C2 nanosheets/AuPt nanoparticles (Ti3C2/AuPt NPs) with enhanced peroxidase-like activity were prepared via one-step self-reduction reaction. CBS can be hydrolyzed under acidic condition and produce -SH moieties, which could bond to Pt atoms of Ti3C2/AuPt NPs and shield the active sites of nanozyme, resulting in decreased catalytic activity. Based on the inhibitory effect on the peroxidase-like activity of Ti3C2/AuPt NPs, a colorimetric method was proposed for direct detection of CBS. Under optimal conditions, the method showed wide linear range (0.5ngmL-1-5μgmL-1), low limit of detection (0.342nM), good selectivity and anti-interference ability. The feasibility of this method for practical use was confirmed by analysis of CBS in real lake water samples. This work proposed a simple colorimetric method for selective and fast detection of CBS, which avoided employing AChE and cascade catalytic reactions, significantly lowering the detection cost and improving detection efficiency. The method showed great potential for accurate detection of CBS in actual samples, and provided a new avenue for developing nanozyme-based colorimetric method for detection of other pesticide residues.

Hydrolysis behavior evaluation of sports protein supplements with different composition and dosage forms: In vitro dynamic gastric digestion

Hydrolysis behavior evaluation of sports protein supplements with different composition and dosage forms: In vitro dynamic gastric digestion

Elucidating trends in synthesis and structural periodicity in a series of tetravalent actinide–oxo hexamers

Differences in synthetic conditions and structural systematics in a series of actinide–oxo clusters reflect trends in the hydrolysis behavior of the tetravalent metal ions, Th–Pu.

Effect of Food-Simulating Liquids on Hydrolytic Behavior of Resin Matrix Ceramics.

This study aimed to evaluate the hydrolytic behavior of different computer-aided design/computer-aided manufacturing (CAD/CAM) resin matrix ceramics (RMCs) in different food-simulating liquids (FSLs). Five different CAD/CAM blocks, one from polymer-infiltrated ceramic networks (PICNs; Vita Enamic (EN)) and four from resin-based composites (RBCs; Lava Ultimate (UL), Cerasmart (CER), Brilliant Crios (BR), and Block HC (HC)) were selected. Forty specimens were prepared for each material, and they randomly distributed to each FSLs. The specimens were kept in a desiccator initially, then placed in 5 ml of liquid at 37±1°C for 30 days and weighed at various time intervals. Percentage mass change (Mg%), sorption (SP), percentage of liquid absorbed (SP%), solubility (SL), percentage solubility (SL%), and percentage of liquid absorbed by the polymer matrix (SPpm) water absorption of the specimens were evaluated. Significance was evaluated at p<0.05 levels. Hydrolytic behavior of the materials showed statistical differences in terms of SP, SL, SP%, and SL% values depending on the liquid environment (p=0.001). The highest SP values were obtained from the HC material in saliva, and the lowest values were obtained from the BR in ethanol. The highest SL values were obtained from the CER and EN in heptane, and the lowest values were obtained from the HC in ethanol. However, all results detected in the study remained below the ISO threshold values. All materials tested exhibited clinically acceptable hydrolytic behavior over the time tested. Not only the material content but also many factors can affect the hydrolytic behavior.

Two mixed-valent cerium oxo clusters: synthesis, structure, and self-assembly.

Studies on cerium oxo clusters (CeOCs) are not only significant for understanding the redox and hydrolysis behaviors of Ce(III/IV) ions but also crucial for the rational synthesis of novel clusters and nanoceria with specific Ce(III)/Ce(IV) ratios. Here, two sets of reactions were conducted using cerium nitrate and H2O2-oxidized cerium nitrate, resulting in the formation of two distinct mixed-valent CeOCs [CeIII 4CeIV 10O14(OH)2(PhCO2)22(DMF)6] (Ce14) and [CeIII 2CeIV 22O28(OH)8(PhCO2)30(DMF)4] (Ce24C). These two clusters exhibit different structures and Ce(III)/Ce(IV) ratios, demonstrating the critical role of cerium oxidation states and the occurrence of redox reactions in cluster formation. Ce14 is the first tetradecanuclear CeOC with a novel structure, whereas Ce24C differed in its Ce(III)/Ce(IV) ratio, protonation levels of O atoms, and ligands from previously reported 24-nuclear CeOCs. Furthermore, various techniques were employed to investigate the formation process of these two clusters. X-ray photoelectron spectra (XPS) revealed that the white precipitates formed during the preparation of Ce14 contain Ce(III) ions, while the reddish-brown precipitates formed during the preparation of Ce24C contain a mixture of Ce(III) and Ce(IV) ions. These two precipitations were individually dissolved in N,N-Dimethylformamide (DMF). The evolution of solution color and ultraviolet-visible (UV-Vis) spectra over time revealed the gradual oxidation of partial Ce(III) ions by oxygen in the solution of the white precipitation. As Ce(IV) ions increased in this solution, time-resolved small angle X-ray scattering (SAXS) data demonstrated the self-assembly of the Ce14 clusters after 4days. In contrast, SAXS data and UV-Vis spectra revealed the rapid assembly of Ce24C clusters within 2h due to the initial coexistence of Ce(IV) and Ce(III) ions in the DMF solution of the reddish-brown precipitation. The continued reduction of partial Ce(IV) ions in this solution does not affect Ce24C clusters' formation and stability. Our studies expand the family of CeOCs and enhance our understanding of the effects of cerium's oxidation states on cluster formation.

The role of extraction method to collagen substrates in enzymolysis of type I collagenase

Collagens are ubiquitous biomaterials in animal tissues whose characteristic triple-helical structure can only be hydrolyzed under physiological conditions by a few specific proteases. At present, information on the differences of collagenase hydrolysis behavior to collagen substrate caused by extraction methods is still lacking. Acid-relaxed extracted collagen (ARC) and acetic acid-pepsin extracted collagen (APC) were obtained from bovine hide by acetic acid and acetic acid-pepsin extraction method, respectively. The enzymolysis behavior of type I collagenase on ARC and APC were investigated by means of fluorescence spectra, UV spectra, and determination the release of hydrolysates into the supernatant. The results revealed that APC showed a lower molecular weight, a higher pI (5.59) and denaturation temperature (Td=66.9°C) than that of ARC (pI=4.67, Td=57.8°C). Moreover, APC demonstrated greater resistance to type I collagenase than ARC. The cleavage on the non-helical terminal domains by pepsin might play the role in the better thermal stability, the higher pI, and the more collagenase resistance of APC than ARC. The findings of this work should provide new insights into collagenase hydrolysis behavior and facilitate targeted utilization of collagen extracted by various method.

Surface modified cellulose nanospheres with simultaneous nucleation and degradation-accelerating effects on poly(lactic acid)

Surface modified cellulose nanospheres with simultaneous nucleation and degradation-accelerating effects on poly(lactic acid)

Developing zirconium xerogel coagulants for deep removal of phosphorous

Developing zirconium xerogel coagulants for deep removal of phosphorous

Effect of carbodiimides on the compatibility and hydrolytic behavior of PLA/PBAT blends

Blends of polylactic acid (PLA) and poly(butylene adipate-co-terephthalate) (PBAT) have great potential to replace conventional polyolefin and polyester materials. However, poor compatibility and fast degradation rate limit its development. In this paper, the effects of two monomer-type carbodiimides and one polymerized carbodiimide on the crystalline, thermal stability, hydrolysis properties, and mechanical properties of PLA/PBAT blends are investigated by Fourier transform infrared spectroscopy, scanning electron microscope, differential scanning calorimetry, thermogravimetric analysis, gel permeation chromatography, melt mass-flow rate, terminal carboxyl content, tensile properties, and rotational torque. It is found that all the three carbodiimide additives can improve the compatibility and enhance the mechanical, processing, and thermal stability properties of PLA/PBAT blends except for their reduced crystallization performance. Moreover, regarding the hydrolysis properties, the two monomeric carbodiimides exhibit little effect on the hydrolysis of PLA/PBAT blends, even accelerating the degradation rate under alkaline conditions. However, the antihydrolysis effect of polycarbodiimide is remarkable, which effectively improves the compatibility and antihydrolysis properties of PLA/PBAT blends.

Arc-shaped air layer bioinspired by ginkgo nut to resist high humidity environment for PET fabrics

Arc-shaped air layer bioinspired by ginkgo nut to resist high humidity environment for PET fabrics

Improved hydrolytic resistance of polylactide biocomposite films reinforced by rice husk before and after accelerated aging

AbstractThe enhanced durability of biobased polylactide (PLA) is a critical prerequisite for it to be considered a viable alternative to petroleum‐based polymers for long‐term applications. Leveraging the performance improvements achieved through interface construction, PLA‐biomass composites have garnered considerable interest and have been widely utilized as a completely degradable material. The hydrolytic behavior of PLA biocomposites in photo‐hydrothermal environments was examined in this study in relation to the impact of biomass components and the specifically designed interface. We observed that biomass could act as an effective stabilizer in the composites, leading to a 25.6% reduction in the hydrolysis reaction rate constant. This stabilization occurs as biomass impedes the diffusion of water molecules and the extension of PLA molecular chains across various hydrothermal environments, thereby enhancing the hydrolytic resistance of PLA. The intriguing aspect is that this stabilizing effect of biomass could be moderated by an interface created through surface treatment, which facilitates enhanced transfer of active small molecules during the photolysis‐hydrolysis process. Consequently, this approach presents a novel method for producing PLA biocomposites that offers excellent hydrolytic resistance, an adjustable degradation cycle, and expected potential applications in advanced packaging and agricultural domains.Highlights Biomass significantly enhances the hydrolysis resistance of polylactide (PLA) biocomposites. This stability boosts due to the obstructive and shielding effects of biomass. Effective interface could regulate the usable life of PLA biocomposites. The role that biomass/ interfaces play also applies to PLA photodegradation. Photo‐hydrolysis mechanism is not affected by biomass or designed interface.

Study on the effect of multi-factor compound action on long-term tensile performance of GFRP composite pipe and life prediction analysis

Study on the effect of multi-factor compound action on long-term tensile performance of GFRP composite pipe and life prediction analysis

An improved coking model for simulating reactive transport phenomena and coking behavior in sucrose hydrolysis

An improved coking model for simulating reactive transport phenomena and coking behavior in sucrose hydrolysis

Improved recyclability of the superbase ionic liquid [MTBNH][AcO] used in the lyocell fiber spinning process

In the research of new solvents for cellulose dissolution for textile fiber production, some ionic liquids offer high dissolving capacities making them attractive solvents for lyocell processes. One especially interesting group is superbase carboxylates. However, despite their excellent pulp dissolving abilities and good spinnability properties in a lyocell process, they have been lacking hydrolytic stability, which hinders their recyclability. In this article, a new type of superbase-based ionic liquid, [MTBNH][AcO], is aimed to provide higher hydrolytic stability than its structural relative predecessors. For evaluation of the hydrolysis behavior of [MTBNH][AcO], we have tested the ionic liquid in two sets of recycling experiments. The “blank-experiments” were applied to investigate hydrolytic behavior without the presence of pulp. These values were compared with the results from spinning trials with pulp. It was found that this new ionic liquid is not only more stable than its predecessor [MTBDH][AcO] in terms of hydrolysis but can also dissolve and spin cellulose at lower temperatures. The spun fibers were tested for their textile-physical properties and their performance was comparable to other lyocell fibers.

The Hydrolysis Behavior of Antimony Trichloride and Phase Transformation Mechanism of Hydrolysates with the Effect of Arsenic

The Hydrolysis Behavior of Antimony Trichloride and Phase Transformation Mechanism of Hydrolysates with the Effect of Arsenic

New insights into the destabilization of fat globules in ultra-instantaneous UHT milk induced by added plasmin: Molecular mechanisms and the effect of membrane structure on plasmin action

Residual plasmin activity in whole ultra-instantaneous UHT (UI-UHT) milk causes rapid fat rise during storage, seriously affecting consumers' purchase intentions. In this work, the molecular mechanisms underlying fat destabilization in whole UI-UHT milk by added plasmin were investigated based on the hydrolysis behavior of interfacial proteins. By using SDS-PAGE and peptidomic analysis, we found that the hydrolysis of interfacial proteins by plasmin led to a decrease in the amount and coverage of interfacial proteins and an increase in zeta-potential value, causing the flocculation and coalescence of fat globules. Moreover, the hydrolysis pattern varied in different categories of interfacial proteins by plasmin. In total, 125 peptides in all samples were identified. Plasmin tended to hydrolyze most major milk fat globule membrane (MFGM) proteins into protein fragments (>10 kDa) rather than peptides (<10 kDa). In contrast, peptides derived from caseins were more preferentially identified within a relatively short incubation time. It was the co-hydrolysis of caseins and some major MFGM proteins as anchors that destroyed the stability of MFGM. Furthermore, studies on the effect of trilayer membrane structure remaining at the interface on the hydrolysis rate of major MFGM proteins by plasmin revealed that ADPH and BTN were very sensitive to plasmin action, while PAS 7 was very resistant to plasmin action. Overall, membrane structure reduced the susceptibility of some major MFGM proteins to plasmin and provided protective effects. Therefore, this study provided important insights into the hydrolysis behavior of interfacial proteins in whole UI-UHT milk induced by plasmin.

Hydrolytic degradation behaviors of polylactides/poly(propylene carbonate blends: Monolayers and bulk films

The study investigates the hydrolytic degradation behaviors of blends comprising polylactides (PLA) and poly(propylene carbonate) (PPC) in the form of monolayers and bulk films. PLA is a biodegradable polymer widely used in various applications, while PPC offers unique properties, making it a promising candidate for blend formulations. The research explores the degradation kinetics and mechanical properties under controlled hydrolysis conditions. The finding focuses on the compatibility of PLA and PPC, their degradation mechanisms, and the impact of blend composition on degradation rates. Understanding the hydrolytic behavior of these blends is crucial for designing eco-friendly materials with tailored degradation profiles for diverse applications.

Tuning multiple enzyme-like activities by metal doping for identification and quantitation of antioxidants in cosmetics

Tuning multiple enzyme-like activities by metal doping for identification and quantitation of antioxidants in cosmetics