Molecular Weight Distribution Research Articles

Structural identification, stability and combination mechanism of calcium-chelating wheat gluten peptides

Abstract In order to explore the structures and combination mechanism of wheat gluten peptides-calcium chelate (WOP-Ca) in depth, WOP-Ca were prepared by chelating wheat gluten peptides (WOP) with calcium. The yield of WOP-Ca was determined to be 51.2 ± 2.12 %, and it exhibited a calcium-chelating rate of 58.96 ± 1.38 %. The structural differences between WOP-Ca and WOP were characterized using various analytical techniques, and the results revealed that WOP-Ca and WOP differed in their microstructure, characteristic group absorption peaks, changes in electron cloud distribution, and thermal stability. WOP-Ca demonstrated remarkable stability and resistance to changes in pH, temperature, and in vitro digestion with gastric protease. After undergoing various treatments, the molecular weight distribution in each interval changed very little. Identification of the peptides in WOP-Ca was achieved by utilizing a mass spectrometer, and a total of 39 peptides were identified in WOP-Ca. Among these, 14 peptides with Score ≥ 30 and Coverage ≥ 20 showed bioavailability percentages exceeding 30 %, with half surpassing 50 %. The binding mode between the 14 peptides and Ca2+ was determined to be α linkage. The Ca–O bond lengths ranged from 2.40 to 3.20 Å, indicating the formation of structurally stable complexes. The carboxyl oxygen atoms played a crucial role in binding with Ca2+, with bond lengths ranging from 2.41 to 2.49 Å and 2.43 to 2.46 Å, respectively. The finding suggested that WOP-Ca prepared by chelation may be used as a calcium supplement that could serve as food additives, dietary nutrients, and pharmaceutical agents.

Liquid-Liquid equilibrium measurements analysis of synthetic multicomponent solvent (n-Pentane, n-Hexane, n-Heptane, Cyclo-Hexane, Toluene)/Bitumen System: Implications for solvent-aided in-situ bitumen extraction

Understanding the Liquid-Liquid Equilibrium (LLE) of multicomponent solvent/bitumen systems is pivotal in optimizing in-situ bitumen extraction. While Vapor-Liquid Equilibria (VLE) of solvent-bitumen systems has been extensively studied, LLE data and predictive models for these mixtures, especially those involving synthetic multicomponent solvents, are scarce. This study provides comprehensive LLE measurements of bitumen and a multicomponent synthetic solvent (n-pentane + n-hexane + n-heptane + cyclo-hexane + toluene) conducted under controlled equilibrium conditions at temperatures of 295 to 352 K, solvent concentrations up to 70 wt% at 1.291 MPa. Application of common correlation used in the construction of solvent-aided process fluid models exhibited average absolute relative deviations (AARDs) of 0.37 % for density and 8.87 % for viscosity. We identified the boundaries marking the shift from homogenous single-phase liquid to two-phase (LLE) states, which occurs within the synthetic multicomponent solvent concentration range of 50 to 60 wt%. We also successfully constructed calibration curves to measure solvent concentrations in both phase regions. The molecular weight distribution and saturates, aromatics, resins, and asphaltene (SARA) fractionation of both liquid phases were determined, highlighting that the heavy liquid phase is primarily asphaltene (∼46 wt%). The insights gained from the measurements and analysis find applications in designing and optimizing solvent-assisted thermal recovery processes for bitumen extraction.

Brown rice protein–dietary fibre conjugate improves bioaccessibility of minerals via modifying gelling structure of yoghurt

SummaryThe present study aims to provide an overview of the impact of brown rice protein (BRP) conjugated with microcrystalline cellulose via the Maillard reaction on characteristic features of yoghurt and the bioaccessibility of essential minerals in this dairy product. The confirmation of conjugation was conducted using FTIR spectroscopy. Adding BRP or Maillard conjugate (MC) proved beneficial in enhancing the water‐holding capacity and decreasing the syneresis of samples. Additionally, yoghurt (MCY) containing the Maillard conjugate demonstrated superior performance in these properties. A lower number of pores and a stronger gel network (structural integrity) were identified in MCY compared to the other samples (BRPY: yoghurt containing BRP and PY: plain yoghurt). On the other hand, in general, supplementation of BRP and MC led to slight alteration in the concentration of aroma compounds. Similarly, the impact of BRP and MC on changes in the molecular weight distribution of proteins during in vitro gastrointestinal digestion was negligible. Bioaccessibility values of Ca and Mg in PY were 53.72% and 10.72%, respectively. The improvement in these values was observed in BRPY (Ca: 57.33% and Mg: 15.60%). Moreover, adding MC to yoghurt led to a tighter interface structure (indicating rigid gel), which allowed more minerals to bind, increasing mineral bioaccessibility (Ca: 64.40% and Mg: 31.14%). A higher general acceptability in sensory evaluation was scored for PY followed by MCY and BRPY. Ultimately, the positive effect of ingredients (especially MC) on yoghurt quality was obvious.

Properties of high cis-1,4 content hydroxyl-terminated polybutadiene and its application in composite solid propellants

In this paper, high cis-1,4 content hydroxyl-terminated polybutadiene (cis-HTPB) with different molecular weights was prepared through the oxidative cracking process using cis-butadiene rubber as raw material. Firstly, this article comprehensively compared the differences between cis-HTPB and conventional I-HTPB in terms of molecular weight distribution, functionality, viscosity, molecular polarity, and other physicochemical properties, which provided effective data support for its subsequent application. In addition, the reaction kinetics study showed that cis-HTPB with isocyanate curing agent has high reactivity, allowing it to be rapidly cured at low temperatures, and the cured elastomers had excellent mechanical properties, with tensile strength and elongation up to 1.89 MPa and 1100%, respectively. It was also found that cis-HTPB has extremely excellent low-temperature resistance, and the glass transition temperature (Tg) of its cured elastomer is as low as −101 °C. Based on the above studies, cis-HTPB is applied as a binder in composite solid propellants for the first time to investigate its practical performance, and the results indicated that cis-HTPB-based propellants have excellent process and mechanical properties.

Multiple mechanical recycling of a post-industrial flexible polypropylene and its nanocomposite with clay: Impact on properties for food packaging applications

The development of polymer nanocomposites for food packaging has been increasing, but there is a lack of studies on their recyclability. The modification of the physical-mechanical properties and overall migration of post-industrial flexible recycled polypropylene (PIPP) and PIPP/compatibilizer/NI.44P clay nanocomposite with the simulated repetitive mechanical recycling were comparatively studied. The structure, thermal properties, crystallinity, and water vapor permeability of the nanocomposite were not significantly affected by multiple recycling (three re-extrsuion cyles). Among the mean findings, the melt flow rate of the polymer was the parameter more affected by the reprocessing, especially in the nanocomposite. PIPP and PIPP nanocomposite tended to molar mass reduction by repetitive reprocessing. However, a narrower molar mass distribution was obtained according to the rheological analysis. Clay addition significantly reduced the ductility of the films in the first reprocessing cycle but interestingly, the tensile properties for PIPP and nanocomposite were similar in the fourth cycle. Prominently, overall migration of the nanocomposite to olive oil diminished by reprocessing cycles, while the opposite was found for the PIPP without clay. Nonetheless, in all cases, the overall migration values to ethanol 10% and olive oil were below the maximum limit permitted for food packaging.

Zwitterionic ring expansion polymerization of tert‐butyl glycidyl ether with B(C6F5)3 towards the generation of cyclic chains

AbstractThe synthesis of cyclic polymers via zwitterionic ring expansion polymerization is limited to a few number of monomer and catalyst pairs. Herein we report the synthesis of cyclic poly(tert‐butyl glycidyl ether) through the polymerization of tert‐butyl glycidyl ether (tBGE) with B(C6F5)3 in different reaction conditions that include different solvents, monomer to initiator ratio, monomer concentration and temperature. We found that bimodal molecular weight distribution is formed in almost all reaction conditions caused by cyclization of short chains. Subsequent chain elongation leads to the formation of cycles of higher molecular weight, particularly in cyclohexane and under bulk conditions. The formation of non‐cyclic byproducts is common in all the systems investigated. Low molecular weight cyclic chains (Mn = 0.7 kDa, Ð = 1.1) of high topological purity were successfully isolated by preparative gel permeation chromatography. By using a click scavenging protocol, the non‐cyclic byproducts were eliminated from the high molecular weight fraction (Mn = 3 kDa, Ð = 1.3) generating pure cyclic chains. Mechanistic investigation using density functional theory calculations was performed on the formation of zwitterionic intermediates and the transfer reaction to the monomer, which notably affects chain growth by the attack of the glycidyl oxygen of the monomer on the growing chain.

A new radical initiation for the ring-opening polymerization of tetrahydrofuran with a radical substitution mechanism

A new radical-Lewis acid system has been discovered to achieve the ring-opening polymerization of tetrahydrofuran. Different types of reaction mechanisms were discovered for the initiation and polymerization processes. The proposed initiation mechanism was studied by MALDI-TOF and ESI-MS as a radical substitution mechanism and polymerization was a coordination-insertion mechanism. And polytetrahydrofuran with high molecular weight (Mn = 14.6 × 104 g mol−1) and narrow molecular weight distribution (PDI = 1.44) could be obtained.

Equibiaxial elongation of entangled polyisobutylene melts: Experiments and theoretical predictions

Equibiaxial elongational deformations are omnipresent in polymer processing technologies. The challenge of generating well-controlled equibiaxial elongational deformations in the laboratory has, however, severely inhibited progress on understanding the rheology of polymeric liquids and other complex fluids in this flow. More recently, a novel technique known as continuous lubricated squeezing flow has been developed that allows for rheological measurements in equibiaxial elongational deformations. In the present study, we examine the rheological behavior of two entangled polyisobutylene (PIB) melts with different molecular weight distributions in constant strain rate equibiaxial elongation flows. These new data are compared with predictions from two molecular models for entangled polymer melts inspired by the idea that entanglements dominate the relaxation dynamics. One model is the discrete slip-link model (DSM), and the other is known as the Rolie Double Poly (RDP) model. For the PIB with a relatively narrow molecular weight distribution, the predictions of both models are in good agreement with experiments and the DSM gives nearly quantitative agreement. For the broad molecular weight distribution PIB, both the DSM and RDP model predict strain hardening, which is not observed in the experiments.

Reverse Engineering of Radical Polymerizations by Multi-Objective Optimization.

Reverse engineering is applied to identify optimum polymerization conditions for the synthesis of polymers with pre-defined properties. The proposed approach uses multi-objective optimization (MOO) and provides multiple candidate polymerization procedures to achieve the targeted polymer property. The objectives for optimization include the maximal similarity of molar mass distributions (MMDs) compared to the target MMDs, a minimal reaction time, and maximal monomer conversion. The method is tested for vinyl acetate radical polymerizations and can be adopted to other monomers. The data for the optimization procedure are generated by an in-house-developed kinetic Monte-Carlo (kMC) simulator for a selected recipe search space. The proposed reverse engineering algorithm comprises several steps: kMC simulations for the selected recipe search space to derive initial data, performing MOO for a targeted MMD, and the identification of the Pareto optimal space. The last step uses a weighted sum optimization function to calculate the weighted score of each candidate polymerization condition. To decrease the execution time, clustering of the search space based on MMDs is applied. The performance of the proposed approach is tested for various target MMDs. The suggested MOO-based reverse engineering provides multiple recipe candidates depending on competing objectives.

Recent advances in green cationic polymerization

AbstractTraditional living/controlled cationic polymerization provides a simple synthetic route for the preparation of various polymers with set molecular weight, narrow molecular weight distribution, and clear structure. Nowadays, under the requirements of sustainable development, it is very important to explore the green chemical technology in depth. This review offers an overview of initiation systems, reaction media, polymerization techniques, and monomers, with the aim of summarizing environmentally friendly methods utilized in the field of cationic polymerization over the past 15 years. It covers a variety of directions from traditional initiation systems to green initiators, from corrosive solvents to environmentally friendly solvents, from drop initiation to external stimulation initiation, from petroleum fractionated monomers to bio‐based monomers. These methods and Techniques aim to develop advanced high‐quality polymer products using cationic polymerization, and achieving efficient energy savings and reducing emissions. The ongoing exploration of green‐controlled cationic polymerization holds promise for opening up new avenues and novel technology for high‐performance polyolefin materials.

Structure dependent fermentation kinetics of dietary carrot rhamnogalacturonan-I in an in vitro gut model

Plant derived dietary polysaccharides are important for gut health and have the potential to modulate the gut microbial community. Dietary rhamnogalacturonan-I obtained by enzymatic treatment of carrot pomace has shown prebiotic properties. In the present study, fermentability of carrot rhamnogalacturonan-I (cRG-I) by faecal microbiota of four donors was studied in an adapted M-SHIME® intestinal model. Despite its complex structure, cRG-I was degraded rapidly in the proximal colon compartment and fermentation became quicker and more complete during three weeks of repeated supplementation. Tracking the change in the molecular weight distribution pattern of cRG-I during the supplementation showed two main donor-dependent gut microbial fermentation strategies designated as either the general or preferential pathway. In the general fermentation pathway, different cRG-I structures were hydrolysed concomitantly, while in the preferential pathway discrete structures were sequentially fermented in a selective manner. Especially arabinan sidechains were utilized before the RG-I backbone, which correlated with an increase in Bifidobacterium longum absolute abundance over the three weeks period. MALDI-TOF MS confirmed that arabinan-, galactan- and arabinogalactan-sidechains were first to be released and degraded. Donor specific production of all SCFA increased over time with a general trend of higher levels of acetate and propionate than butyrate. Strikingly, although the host's baseline gut microbiota composition led to distinct cRG-I hydrolysis routes, the final RG-I consumption was almost complete for both routes, leading to similar metabolic profiles at the end of the three weeks treatment period.

Low-cost protein extracts and hydrolysates from plant-based agro-industrial waste: Inputs of interest for cultured meat

The main challenge in large-scale cultured meat production is replacing fetal bovine serum (FBS), an expensive, animal-derived component in the cell culture medium. This study explored the use of plant-based agro-industrial waste as an economical and nutritionally beneficial alternative to FBS. Soybean and peanut bran were processed to obtain extracts and protein hydrolysates rich in proteins, low molecular weight peptides, and amino acids. The results confirmed the presence of essential nutritional factors conducive to the growth and viability of animal cells in vitro. Protein extracts formed mainly by globulins and albumins resemble the composition of FBS. The hydrolysates contained a protein content similar to FBS and were particularly abundant in leucine and proline. The molecular weight distribution of the peptides indicated a high degree of hydrolysis. Cost analysis revealed that utilizing plant waste for protein inputs could be a favorable approach to reducing cultured meat production costs.

Formation of casein micelles from bovine caseins simulating human casein phosphorylation patterns: Micellar structure and in vitro infant gastrointestinal digestion

This study investigated the micellar structure and in vitro infant gastrointestinal digestion of formed casein micelles simulating human casein composition and phosphorylation patterns. Caseins were fractionated from bovine caseins and formulated according to human casein composition, i.e., β-, κ- and αs1-caseins with a ratio of 68:20:12. The formulated caseins were dephosphorylated for different times and were mixed to obtain mixed phosphorylation patterns (FC-MP) for β-casein, showing 0–5 phosphate groups comparable to human β-casein. The formulated caseins without dephosphorylation and with high dephosphorylation, showing 5 phosphate groups and 0–2 phosphate groups for β-casein, respectively, were categorized as high (FC-HP) and low phosphorylated (FC-LP). With the average mineral concentrations found in human milk, CaCl2, MgCl2, citrate and inorganic phosphate were added into the different formulated casein dispersions to obtain casein micelles (FM-HP, FM-MP and FM-LP). Compared to FM-HP, FM-MP was closer to human micelles in relation to particle size, micellar hydration, molar ratio of Ca:casein, morphology and internal structure, whereas FM-LP showed did not show a characteristic micellar structure and had a larger size and lower molar ratio of Ca:casein. For gastrointestinal digestion, FM-MP was closer to human micelles in terms of the gastric flocs, casein degradation rate, free amino groups, and molecular weight distribution of peptides compared to FM-HP, whereas FM-LP showed larger flocs and lower casein degradation rate. These results show the significance of post-translational phosphorylation in facilitating the assembly of caseins into micellar structures, indicating the potential to form human-like micelles for application in infant formulae.

Polyhydroxybutyrate (PHB)-Based sustainable bioplastic derived from Bacillus sp. KE4 isolated from kitchen waste effluent

Petrochemical-derived plastics pose a major threat to the biosphere and the environment due to their acute or long-term toxicity. Therefore, to ensure sustainability, it is essential to find an effective replacement for synthetic plastics with natural and ecofriendly biomaterial. In this context, production of polyhydroxybutyrate (PHB) was produced by the Bacillus sp. KE4 using glucose as the carbon source, and a maximum dry cell weight (DCW) of 4.4 g/l with a PHB concentration of 3.1 g/l, PHB yield of 0.15 g/g was obtained, and the PHB content was 70.4% of the DCW. The extracted biopolymer was characterized using FTIR, GC-MS, 1H NMR, and 13C NMR which confirmed the structure of the biopolymer as PHB. The findings of TGA, DTG, DTA and DSC studies corresponded to PHB's excellent thermal stability. PHB biopolymer has a melting temperature of 168.7 °C and a maximum degradation temperature of 273 °C. The weight average molar mass (Mw), number average molar mass (Mn), and polydispersity index (PDI) of the extracted PHB was 1,55,436 g mol−1; 1,43,258 g mol−1; and 1.08, respectively. The XRD analysis validated the material's partly crystalline nature. FESEM-EDS and XPS were employed to determine the elemental composition of the purified PHB film. The Young's modulus, tensile strength and elongation at break showed rigid and brittle nature of PHB. Using open windrow composting method, the extracted PHB biopolymer film was assessed to determine its biodegradability. Within 28 days of soil burial, it was found that the biopolymer film had degraded by 61.34%. Cytotoxicity assessment in HepG2 cells indicated that PHB is non-cytotoxic in nature. The results have showed that the biomaterial is environmentally benign, biodegradable, and biocompatible; therefore, it may find its diverse application covering packaging, medicine, agriculture and allied fields.

Structure – property relationships of different natural rubber grades

The effects of various natural rubber (NR) grades, namely RSS 3, STR 5L, STR 10, STR 20 and STR 20CV, towards their final properties were investigated. The molecular characteristics of these NR grades were assessed by gel permeation chromatography and by determining protein contents. The highest molecular weight was found for RSS 3, while STR 20CV had the lowest molecular weight. No relationship between molecular weight and protein content was seen in this study. A higher molecular weight rubber provided greater maximum torque and torque difference, and a better resistance to degradation during processing. However, no significant difference was found among molecular weights higher than 1.25 × 106 g/mol. The final torque during processing and the Mooney viscosity of rubber increased with molecular weight due to tie chain entanglements, as later confirmed by a dynamic mechanical analyzer. Thermo-stability and stress relaxation of the various NR grades were also largely governed by their molecular weights. Stability of rubber at an elevated temperature improved with molecular weight. Also, the tensile properties and the strain-induced crystallization varied with the molecular weight. The tensile strength of various NR grades varied from 15 to 18 MPa while the elongation at break was 600%–800%. The molecular weight of NR was found to have a great effect on the processing, thermomechanical, dynamic, and mechanical properties of the vulcanizates. In addition, a narrow molecular weight distribution also affected the mechanical properties. The crystallinities of the NRs during stretching were closely related to their tensile behavior, and the alignment of crystal structures during stretching was almost parallel to the stretching direction in all NR samples. The molecular weight of NR appears to be a key factor associated with the mechanical properties and reinforcement behavior of vulcanizates.

Simulation approach to study kinetic heterogeneity of gadolinium catalytic system in the 1,4-cis-polyisoprene production

Abstract This article presents a novel simulation approach for solving the inverse problem of kinetic heterogeneity in polymerization processes, specifically focusing on the production of polyisoprene using a gadolinium chloride solvate-based catalytic system. The proposed method is based on the assumption that the distribution of active centers (ACs) can be described by model distributions. By utilizing primary physicochemical data, such as the polymerization rate and molecular weight distribution, the simulation approach automatically identifies the kinetic parameters, determining the Frenkel statistical parameter and solving the problem of kinetic heterogeneity. The experimental results revealed the presence of at least three distinct types of ACs, each contributing different proportions to the polymerization process. The simulation approach offers valuable insights into the complexities of catalytic systems and their role in polymerization, paving the way for optimizing reaction conditions and advancing industrial polymer synthesis processes. This study marks a significant step forward in understanding and controlling polymerization reactions, with potential implications for the development of innovative materials and industrial applications.

The hidden secrets of the average number of radicals per particle ([formula omitted]) and their implications in control of emulsion polymerization reactors

Emulsion polymerization is the method of choice to produce waterborne polymers but is susceptible to run-to-run variations. This variability is hard to avoid because on-line measurement of many of the characteristics of interest, in particular the molar mass distribution (MMD) of non-linear polymers, is not possible. This work offers a way to solve this problem. First, it is shown that the average number of radicals per particle (n¯), a value that can easily be obtained from kinetic measurements, contains sufficient information to directly determine the distribution of particles with n radicals. It is then demonstrated that for a given measured MMD, knowledge of the distribution of radicals per particle allows solving the long standing problem of the accurate estimation of the effective termination rate coefficient in emulsion polymerization. Combining this knowledge, it is shown the value of n¯ alone (a value that can be obtained experimentally by calorimetric measurements) can be used to develop a soft sensor able to estimate on-line the molar mass distribution of highly non-linear polymers. This, for the first time, offers the possibility of on-line control of the MMD of non-linear emulsion polymers.

Lignin structure dynamics: Advanced real-time molecular sensing strategies

Lignin, with its abundant and high energy density, offers potential for sustainable biofuels and chemicals. However, current research faces two primary challenges: limited experimental sampling frequency, impeding the real-time analysis and a lack of theoretical activation energies to elucidate thermodynamic and kinetic properties associated with structural changes under various processing conditions including reaction temperature (343 to 363 K), time (15 to 30 min), and chip size (1.0 to 5.0 mm). To address these challenges, we introduce the “real-time molecular-level sensing approach,” which considers delignification, redeposition, and de/repolymerization over time and various scales, leveraging sparse experimental data and theoretical activation energies. Our approach combines density functional theory, ab-initio molecular dynamics, and kinetic Monte Carlo simulations to deeply explore dynamic nature of lignin. Specifically, we gain insights into lignin content within biomass, molecular weight distribution, and monolignol ratio, improving lignin’s utilization during processing. This work establishes a new standard for comprehensive lignin analysis, fostering efficient lignin utilization by tracking their properties at the molecular level in the real-time manner.

Mesoionic N-Heterocyclic Olefins as Initiators for the Lewis Pair Polymerization of Epoxides.

Mesoionic N-heterocyclic olefins (mNHOs) have recently emerged as a novel class of highly nucleophilic and super-basic σ-donor compounds. Making use of these properties in synthetic polymer chemistry, it is shown that a combination of a specific mNHO and a Mg-based Lewis acid (magnesium bis(hexamethyldisilazide), Mg(HMDS)2) delivers poly(propylene oxide) in quantitative yields from the polymerization of the corresponding epoxide (0.1mol% mNHO loading). The initiation mechanism involves monomer activation by the Lewis acid and direct ring-opening of the monomer by nucleophilic attack of the mNHO, forming a zwitterionic propagating species. Modulation of the mNHO properties is thereby a direct tool to impact initiation efficiency, revealing a sterically unencumbered triazole-derivative as particularly useful. The joint application of mNHOs together with borane-type Lewis acids is also outlined, resulting in high conversions and fast polymerization kinetics. Importantly, while molar mass distributions remain relatively broad, indicating faster propagation than initiation, the overall molar masses are significantly lower than found in the case of regular NHOs, underlining the increased nucleophilicity and ensuing improved initiation efficiency of mNHOs.

Extraction, identification, and molecular mechanisms of α-glucosidase inhibitory peptides from defatted Antarctic krill (Euphausia superba) powder hydrolysates

The objective of this study was to explore the potential of Antarctic krill-derived peptides as α-glucosidase inhibitors for the treatment of type 2 diabetes. The enzymolysis conditions of α-glucosidase inhibitory peptides were optimized by response surface methodology (RSM), a statistical method that efficiently determines optimal conditions with a limited number of experiments. Gel chromatography and LC-MS/MS techniques were utilized to determine the molecular weight (Mw) distribution and sequences of the hydrolysates. The identification and analysis of the mechanism behind α-glucosidase inhibitory peptides were conducted through conventional and computer-assisted techniques. The binding affinities between peptides and α-glucosidase were further validated using BLI (biolayer interferometry) assay. The results revealed that hydrolysates generated by neutrase exhibited the highest α-glucosidase inhibition rate. Optimal conditions for hydrolysis were determined to be an enzyme concentration of 6 × 103 U/g, hydrolysis time of 5.4 h, and hydrolysis temperature of 45 °C. Four peptides (LPFQR, PSFD, PSFDF, VPFPR) with strong binding affinities to the active site of α-glucosidase, primarily through hydrogen bonding and hydrophobic interactions. This study highlights the prospective utility of Antarctic krill-derived peptides in curtailing α-glucosidase activity, offering a theoretical foundation for the development of novel α-glucosidase inhibitors and related functional foods to enhance diabetes management.