Differential Scanning Calorimetry Results Research Articles

Novel kraft-lignin-based adhesives for the production of particleboards

Lignin is produced worldwide in pulp mills and is currently mainly used for energy recovery. Because of its chemical properties, one possible utilisation is the production of lignin-based materials. Currently, developed lignin-based adhesives are based mainly on lignosulfonate instead of kraft lignin since lignosulfonate is more reactive than kraft lignin. However, worldwide substantially more kraft lignin is produced. The presented research deals with the development of resin chemically modified with kraft lignin up to 40% (w/w) content of kraft lignin. The synthesis of adhesives is described, and developed adhesives are characterised. Namely, viscosity, mechanical properties of resins and results of differential scanning calorimetry are presented. Furthermore, the developed kraft-lignin-based adhesives were used for the production of particleboards. Pre-pressing in a cold press followed by hot pressing in a laboratory press was used for the production of particleboards. The physical (thickness swelling, moisture uptake, vertical density profile), as well as mechanical (internal bonding, modulus of rupture, modulus of elasticity in three-point bending) properties of particleboards, were evaluated. The results clearly show that kraft lignin can be used for the production of lignin-based adhesives for the production of particleboards.

Insight into in situ enzymatic transesterification modification of polyethylene terephthalate fibers with polyethylene glycol

Polyethylene terephthalate (PET) fabric was enzymatically modified with polyethylene glycol (PEG). Lipase from Aspergillus oryzae was used as a catalyst. The wetting behavior of the modified PET fabric was characterized by the water contact angle, water adsorption dynamics and moisture regain. The initial water contact angle of the modified fabric decreased from 129.3° to 74.9°. The water absorption dynamics results indicated that the equilibrium water absorption amount of the modified fabric was approximately 10 times greater than that of the untreated sample. The initial absorption rate (Vinit) of the modified fabric was almost 30 times higher than that of the untreated fabric. The moisture regain reached 3.52% after modification. Scanning electron microscopy revealed granular and sheet coatings on the surface of the modified fabric. Chemical linkage of PEG onto the PET fibers was confirmed by attenuated total reflection–Fourier transform infrared spectroscopy. The modification had no significant effect on the thermal properties of the PET fabrics according to the thermogravimetric curve and differential scanning calorimetry results. The mechanical properties of the modified fabric were slightly improved. Therefore, in situ enzymatic transesterification between PET and PEG could be a potential novel modification approach for adding value to PET fiber textiles.

Euglena gracilis Protein: Effects of Different Acidic and Alkaline Environments on Structural Characteristics and Functional Properties.

Due to the growing demand for human-edible protein sources, microalgae are recognized as an economically viable alternative source of proteins. The investigation into the structural characteristics and functional properties of microalgin is highly significant for its potential application in the food industry as an alternative source of protein. In this research, we extracted protein from Euglena gracilis by using alkaline extraction and acid precipitation and investigated its structural characteristics and functional properties in different acidic and alkaline environments. The molecular weight distribution of Euglena gracilis protein (EGP), as revealed by the size exclusion chromatography results, ranges from 152 to 5.7 kDa. EGP was found to be rich in hydrophobic amino acids and essential amino acids. Fourier infrared analysis revealed that EGP exhibited higher α-helix structure content and lower β-sheet structure content in alkaline environments compared with acidic ones. EGP exhibited higher foaming properties, emulsifying activity index, solubility, free sulfhydryl, and total sulfhydryl in pH environments far from its isoelectric point, and lower fluorescence intensity (2325 A.U.), lower surface hydrophobicity, larger average particle size (25.13 µm), higher emulsifying stability index, and water-holding capacity in pH environments near its isoelectric point. In addition, X-ray diffraction (XRD) patterns indicated that different acidic and alkaline environments lead to reductions in the crystal size and crystallinity of EGP. EGP exhibited high denaturation temperature (Td; 99.32 °C) and high enthalpy (ΔH; 146.33 J/g) at pH 11.0, as shown by the differential scanning calorimetry (DSC) results. The findings from our studies on EGP in different acidic and alkaline environments provide a data basis for its potential commercial utilization as a food ingredient in products such as emulsions, gels, and foams.

Glycidyl methacrylate co-polymer emulsion-based heat and water-resistant wood adhesive

This work aims to add an epoxy-ended co-monomer to polyvinyl acetate (PVAc) emulsion adhesive-based wood adhesive to improve its resistance to heat and moisture. Here, glycidyl methacrylate (GMA), vinyl neodecanoate (VeoVa), and vinyl acetate (VAc) emulsion copolymers have been created and evaluated as wood adhesives. To prepare the emulsion-based adhesive samples, a polyvinyl alcohol (PVA) solution, aluminium chloride solution, preservatives, and a plasticizer are added. Following that, the poly(VAc–VeoVa–GMA) based adhesive sample is compared with the VAc, VeoVa, and methyl methacrylate (MMA) (poly(VAc-VeoVa-MMA)) co-polymer-based adhesive. Tensile shear strength of wood joints under dry and wet conditions was tested in compliance with EN 204-205 standard to assess the adhesives’ performance. The EN 14257 standard, which defines the shear stress of wood joints at 80 °C, was used to assess the heat resistance of the wood adhesives. Tests on the hardness of films confirmed the results of differential scanning calorimetry, which indicated that the glass transition temperature in the GMA-based adhesive was significantly higher than in the MMA-based adhesive. After 6 h of bonding, EN 204 shows that the tensile shear strength of a GMA-based adhesive increased by 15.56% in a dry environment, by 16.67% in a wet environment and 37.84% heat resistance when compared to a co-polymer-based adhesive based on MMA. The approach that was developed provides a simple and useful way of developing adhesives with enhanced heat, water, and bonding strength resistance.

Analytical Aspects of ANSA-BSA Association: A Thermodynamic and Conformational Approach.

Many studies have demonstrated the manner in which ANS interacts with bovine serum albumin (BSA), although they are limited by the extremely low solubility of dye. The present study demonstrates the binding of ANSA dye with BSA, and since this dye can easily replace ANS, it not only simplifies research but also improves sensor accuracy for serum albumin. A combination of calorimetry and spectroscopy has been employed to establish the thermodynamic signatures associated with the interaction of ANSA with the protein and the consequent conformational changes in the latter. The results of differential scanning calorimetry reveal that when the concentration of ANSA in solution is increased, the thermal stability of the protein increases substantially. The fluorescence data demonstrated a decrease in the binding affinity of ANSA with the protein when pH increased but was unable to identify a change in the mode of interaction of the ligand. ITC has demonstrated that the mode of interaction between ANSA and the protein varies from a single set of binding sites at pH 5 and 7.4 to a sequential binding site at pH 10, emphasizing the potential relevance of protein conformational changes. TCSPC experiments suggested a dynamic type in the presence of ANSA. Molecular docking studies suggest that ANSA molecules are able to find ionic centers in the hydrophobic pockets of BSA. The findings further imply that given its ease of use in experiments, ANSA may be a useful probe for tracking the presence of serum albumin and partially folded protein states.

Potential of polyphenols from Ligustrum robustum (Rxob.) Blume on enhancing the quality of starchy food during frying.

The increasing concerns about health have led to a growing demand for high-quality fried foods. The potential uses of Ligustrum robustum (Rxob.) Blume, a traditional tea in China, as natural additives to enhance the quality of starchy food during frying was studied. Results indicated that L. robustum polyphenols extract (LREs) could improve the quality of fried starchy food, according to the tests of color, moisture content, oil content, texture property, and volatile flavor. The in vitro digestion results demonstrated that LRE reduced the final glucose content from 11.35±0.17 to 10.80±0.70mmol/L and increased the phenolic content of fried starch foods from 1.23±0.04 to 3.76±0.14mg/g. The appearance and polarizing microscopy results showed that LRE promoted large starch bulges on the surface of fried starchy foods. Meanwhile, X-ray diffraction results showed that LRE increased the intensity of characteristic diffraction peak of fried starch with a range of 21.8%-28%, and Fourier transform infrared results showed that LRE reduced the damage to short-range order structure of starch caused by the frying process. In addition, LRE increased the aggregation of starch granules according to the SEM observation and decreased the enthalpy of starch gelatinization based on the differential scanning calorimetry results. The present results suggest that LREs have the potential to be utilized as a natural additive for regulating the quality of fried starchy food in food industries. PRACTICAL APPLICATION: The enhancement of L. robustum polyphenols on the quality of starchy food during frying was found, and its mechanisms were also explored. This work indicated that L. robustum might be used as a novel economic natural additive for producing high-quality fried foods.

Thermally induced phase separation of UHMWPE mixture with dioctyl adipate: Competition of liquid–liquid phase separation and polymer crystallization

The thermal behavior of ultra-high molecular weight polyethylene (UHMWPE) with dioctyl adipate (DOA) was investigated by the differential scanning calorimetry (DSC) method. Capillary-porous bodies were obtained via thermally induced phase separation of DOA mixtures with polyethylenes of different molecular weight at different cooling rates. Analysis of the morphology of the prepared porous bodies together with DSC data and results of cloud point estimation revealed an unexpected effect of a cooling rate on the type of phase separation occurring in the mixture during its cooling from homogeneous state. Particularly it was shown that increase in the cooling rate reduces the probability of realization of liquid – liquid phase separation in the mixture. It was argued that such behavior, different from the standard semicrystalline polymers, is a result of kinetic hindrance of liquid – liquid phase separation in mixtures containing a polymer with such a high molecular weight.

Effect of Heat Treatment on Some Thermodynamics Analysis, Crystal and Microstructures of Cu-Al-X (X: Nb, Hf) Shape Memory Alloy

Heat treatment is an important technique that can improve the properties of shape memory alloys. In this study the effect of heat treatment at three different temperatures (973 K, 1073 K and 1173 K) on some thermodynamics parameters, crystal structure, and microstructure of Cu_86 Al_12 Nb_2 and Cu_86 Al_12 Hf_2 (mass %) Shape Memory Alloy has been investigated. After heat treatment, the change in the thermal properties of the samples was determined using Differential Scanning calorimetry (DSC). The effect of heat treatment on the crystal and microstructure of the alloy samples were determined at room temperature using X-ray diffraction (XRD), Scanning Electron microscopy (SEM) device. The DSC result showed that in both samples the temperature hysteresis was decreased after heat treatment. Also grain size was decreased by increasing the treatment temperature in both samples. And finally, optical images represented that Hafnium (Hf) is more dissolved in the alloy compared to Niobium (Nb).

Expanding the Frontiers of nail product evaluation: Novel application of differential scanning calorimetry (DSC) for assessing crosslinking density and predicting nail brittleness and flexibility.

While modern industry advancements have expanded nail beautification options, scientific literature primarily focuses on nail biology and medicine, with limited attention on cosmetic treatments. This study aimed to investigate human nail denaturation properties, including gender impact, blending nails to enlarge the sample pool, nail sensitization through bleaching, and active effectiveness testing. The objective was to understand the DSC and bending fatigue relationship, and define the consumer relevance of the DSC test. Nail clippings were collected from adult female and male volunteers. The wet DSC was employed to validate sample preparation, explore the effects of gender, and assess the potential of using blended nails for claims substantiation testing. Nails were sensitized through bleaching using hydrogen peroxide. The effects were confirmed through DSC and nail flexure tests. Furthermore, the ability of actives to address concerns related to nail softness and brittleness was assessed using these techniques. The results confirmed the viability of equilibrating nails in water for up to 14 h as a standardized testing method. The denaturation temperature results were independent of gender and suitable for claims substantiation testing. Blending nails from different sources did not yield significant variations in denaturation properties. A preliminary study suggested that cadaver nails should be used with caution because they exhibited differences in denaturation temperature, influenced by the sampling location. Bending fatigue tests highlighted the significance of humidity, with higher humidity conditions (80%) enhancing nail flexibility and providing better resolution for claims substantiation. Sensitizing the nails with hydrogen peroxide induced alterations in both DSC and bending fatigue results. Proof-of-principle studies demonstrated an elevation in denaturation temperature and a decrease in the number of cycles to break, indicating a nail-hardening effect when formaldehyde was applied. The use of a nail softener led to an enhancement in nail fatigue resistance due to a notable reduction in nail crosslinking density. The measurement of crosslinking density proved to be a sensitive tool for assessing the effects of cosmetic treatments on nails, particularly in predicting outcomes related to nail brittleness and flexibility.

Terahertz Spectroscopic Insight into the Hydrogelation of Copper Ion-Coordinated Poly(vinyl alcohol).

Metal-coordinated hydrogels are becoming increasingly popular in the biomedical field due to their unique properties. However, the mechanism behind gel forming involving metal ions is not yet fully understood. In this work, terahertz spectroscopy was used to investigate the role of interfacial water in the gelation process of copper ion-coordinated poly(vinyl alcohol) hydrogels. The results showed that the binding of copper ions could alter the interfacial hydration dynamics of the poly(vinyl alcohol) polymers. Combined with the results of differential scanning calorimetry (DSC), we propose a possible hydration layer-mediated mechanism for the formation of cooper ion-coordinated hydrogel during the freeze-thaw cycle. These results highlight the value of terahertz spectroscopy as a sensor for studying the hydration process in hydrogels and provide an important clue for understanding the mechanism of hydrogelation in ion-coordinated hydrogels.

Thermal annealing gradient tailoring on ammonium nitrate-capped CdS nanospheres synthesized via green precipitation

This study explores the impact of thermal annealing gradients on the physical properties and structural evolution of cadmium sulphide (CdS) nanospheres capped with ammonium nitrate as a modifier, which were fabricated through precipitation and subsequent annealing within 160–480 °C temperature range. The properties were characterized using X-ray diffraction (XRD), ultraviolet–visible (UV–Vis), Fourier transform infrared (FTIR), scanning electron microscopy (SEM), thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC) techniques The XRD results show that the present CdS exhibits superior crystallinity compared to pure CdS without capping, transitions from a cubic to a hexagonal phase structure, and increases in crystallite size and crystallinity with increasing temperature. The FTIR spectra postulate that a vibrational band presence evidences ammonium nitrate capping on CdS, with another distinct band that represents CdS in the lower wavenumber region, both intensifying at elevated temperatures. The UV–Vis analysis reveals that CdS exhibits strong ultraviolet (UV) absorption suitable for effective photoreaction under UV light and has a broader band gap compared to bulk CdS. SEM images show an extensive distribution of homogeneous nanospheres over the surface, with increased growth in size when capped with ammonium nitrate and at higher temperatures. As validated by TGA and DSC results, CdS with a smaller crystallite size improves thermal stability and energy transfer, as evidenced by reduced weight loss and a lower endothermic temperature, respectively. Varying the annealing temperature with ammonium nitrate capping can improve the structural and physical properties of CdS, which are beneficial for varied applications such as optoelectronics, energy storage, and photocatalysts.

Stability mechanism of Monascus pigment-soy protein isolate-maltodextrin complex.

Monascus pigment (MP) is a natural food coloring with vital physiological functions but prone to degradation and color fading under light conditions. This study investigated the effect of complex formation of soybean protein isolate (SPI), maltodextrin (MD), and MP on the photostability of MP. Light stability was assessed through retention rate and color difference. Fluorescence spectroscopy (FS), circular dichroism (CD), Fourier-transform infrared (FTIR) spectroscopy, and X-ray diffraction (XRD) explored MP, SPI, and MD interactions, clarifying the MP-SPI-MD complex mechanism on the light stability of MP. Microstructure and differential scanning calorimetry (DSC) analyzed the morphology and thermal properties. The retention rate of MP increased to approximately 80%, and minimal color difference was observed when adding SPI and MD simultaneously. FS revealed hydrophobic interaction between MP and SPI. FTIR analysis showed intensity changes and peak shifts in amide I band and amide II band, which proved the hydrophobic interaction. CD showed a decrease in α-helix content and an increase in β-sheet content after complex formation, indicating strengthened hydrogen bonding interactions. Scanning electron microscopy (SEM) analysis demonstrated that MP was attached to the surface and interior of complexes. XRD showed MP as crystalline, while SPI and MD were amorphous, complexes exhibited weakened or absent peaks, suggesting MP encapsulation. The results of DSC were consistent with XRD. SPI and MD enveloped MP through hydrogen bonding and hydrophobic interaction, ultimately enhancing its light stability and providing insights for pigment-protein-polysaccharide interactions and improving pigment stability in the food industry. © 2024 Society of Chemical Industry.

Development of Monoethanolamine Chloride-Ethylene Diamine Deep Eutectic Solvent for Ffficient Carbon Dioxide Capture

Deep eutectic solvents (DES) emerge as a compelling class of ionic liquids, with distinct advantages over traditional solvents, particularly in the realm of CO2 capture. In the present study, [MEACl][EDA] is synthesized across various molar ratios (1:3 to 1:10) and combined with the results of Differential Scanning Calorimetry (DSC) to identify DESs. The DESs are further characterized using Fourier Transform Infrared Spectroscopy (FTIR), and the properties and performance of the DESs with diverse water contents (30–60 wt%) are systematically studied for CO2 capture. The optimal aqueous solution is identified based on the CO2 uptake and viscosity, followed by the evaluation of the cyclic absorption experiments. Results demonstrate that 40 wt% of [MEACl][EDA] DES with (1:5) molar ratio exhibits higher CO2 uptake (22.09 wt%) and comparable viscosity (4.401 mPa·s before and 13.330 mPa·s after CO2 capture at 25 °C) compared to aqueous 40 wt% MEA (15.74 wt% CO2 capture capacity, viscosity of 3.318 mPa·s before and 8.413 mPa·s after CO2 capture), and its absorption rate is also more favorable than the aqueous MEA. Furthermore, recycling studies reveal ∼ 88 % regeneration of the aqueous DES solution at 100 °C.

Optimizing clozapine-loaded nanostructured lipid carriers through central composite design for enhance bioavailability in antipsychotic therapy

Clozapine (CLZ), a tricyclic dibenzodiazepine antipsychotic drug employed for the treatment of Schizophrenia. However, CLZ's significant first-pass effect, poor water solubility, and low oral bioavailability (27%) limit its potential for therapeutic use. The present investigation aimed to prepare CLZ-loaded nanostructured lipid carriers (NLCs) to improve its solubility, bioavailability, and therapeutic efficacy. The NLCs were prepared using an ultrasonic probe sonication technique using selected solid lipids (Gelucire 44/14), liquid lipids (Labrafil M 1944), and surfactants (Monoemul 80). A central composite design approach was adopted to optimize the NLCs. The optimized CLZ-loaded NLCs were evaluated in terms of particle size, zeta potential, surface morphology, crystallinity, drug loading, and in-vitro CLZ release studies. The optimized CLZ-loaded NLCs showed a particle size, zeta potential, and entrapment efficiency of 115.1 ± 2.48 nm, −17 mV and 96.74 ±1.82%, respectively. The morphology revealed the coarsely spherical shape of NLCs. Fourier transform infrared spectroscopy indicated the physical interaction between the CLZ and lipids rather than chemical interaction. The results of powder X-ray diffraction and differential scanning calorimetry showed the conversion of crystalline to amorphous form of CLZ and distributed molecular level in lipid matrix. In the in-vitro release study, pure CLZ showed 14±1.86% release, whereas CLZ-loaded NLC showed initial burst release (20.0±0.56%) followed by sustained release (69.0±1.03%) up to 24 hours. Collectively, results revealed that the developed novel CLZ-loaded NLCs could be a potential formulation to improve efficacy by increasing solubility and prolonging CLZ release and bioavailability with enhanced patient compliance and reduced side effects.

Preparation and characterization of double-shell phase change material microcapsules with flame retardancy and temperature regulation capability as low-emission building fillers

The building application of phase change materials (PCMs) has attracted widespread attention due to energy conservation and emission reduction. In this study, designed and prepared by two-step polymerization poly melamine tetramethylene phosphonium sulfate (PMTMPS) coating the raw phase change materials microcapsules (MPCMs), which were novel double-shell microcapsules (D-MPCMs). D-MPCMs further achieved low smoke and low toxicity in the fire based on enhancing the temperature regulation performance of MPCMs. The chemical structure of D-MPCMs was characterized by Fourier transform infrared (FTIR) spectroscopy, and 13C solid-state nuclear magnetic resonance (NMR). Transmission electron microscope (TEM) confirmed that D-MPCMs were successfully prepared, whose shapes were regular spherical. The results of differential scanning calorimetry (DSC) showed that D-MPCMs revealed excellent phase transition enthalpy (80.51 J/g). Then, the resultant D-MPCMs had good thermal reliability and stability from the thermogravimetric analysis (TGA), characterized by a residual mass of D-MPCMs was 17 % more than that of MPCMs. In the cone calorimeter test (CCT), we confirmed that the coated PMTMPS significantly reduced the fire risk parameters of the rigid polyurethane foam (RPUF) containing D-MPCMs (D-MPCM/RPUF) referring to the heat release rate (HRR), total heat release (THR), and total smoke production (TSP). D-MPCM/RPUF exhibited the lowest peak values of HRR and TSP, which were 400.115 kW/m2 and 10.512 m2, respectively. In addition, the PMTMPS shell significantly enhanced the solar photo-thermal conversion performance of the D-MPCMs. To sum up, D-MPCMs have great potential to improve flame retardancy, environmental protection, and temperature regulation capability for building thermal insulation materials.

Synthesis of shape memory bio-based crosslinked polymer: Poly(arbutin)-co-poly(tosyl arbutin)-co-poly(ethylene glycol)

Oxidative copolymerization of arbutin (Arb) with 6-O-tosyl-Arb (TArb) was performed in water media in the presence of a di-μ-hydroxo-bis[(N,N,N′,N′-tetramethylethylenediamine)copper(II)] chloride (Cu[tmeda]) catalyst under oxygen to produce the corresponding copolymer PArbxPTArby (where, x and y indicate the molar ratio) with a number-average molecular weight (Mn) ranging from 4.2 to 9.3 kDa depending on the polymerization temperature and the time. This copolymer was further reacted with poly(ethylene glycol) (PEG) with amino groups at the terminals (Mn = 8.0 kDa) (PEG8.0k2NH2) in a silicone mould at 100 °C for 24 h to give the bio-based PArbxPTArbyPEGz crosslinked copolymer (z indicates the molar equivalent of the NH2 functions in the PEG to TArb units). The results of differential scanning calorimetry, wide-angle X-ray analysis and polarizing optical microscope image measurements determined that the PEG domain was homogeneously dispersed within the film. The degree of crystallization of the PEG domain was calculated to be 59%–78% and the film swelled over 2100 vol% after immersion in water for 12 h. This bio-based film showed good shape memory after being moulded at 80 °C, maintaining its shape at 20 °C and quickly recovering its original shape upon reheating.

Formulation and optimization of electrospun nanofiber films for ultrafast delivery of domperidone: In vitro and in-vivo characterization

Nanotechnology has significantly transformed drug delivery approaches by providing precise control of drug release kinetics and enhancing therapeutic effectiveness. Electrospun nanofiber films have unique features, including a significant surface-to-volume ratio and substantial porosity, resulting in enhanced patient adherence. The study was aimed at developing electrospun nanofiber films of domperidone for ultrafast release using polyvinyl alcohol (PVA). The nanofibers were prepared by electrospinning method and optimized using 32 factorial design. Electrospinning process parameters like feed rate, applied electric voltage, and tip-to-collector distance were optimized. The prepared nanofiber film was characterized using scanning electron microscopy, differential scanning calorimetry (DSC), Fourier transform infrared microscopy (FTIR), X ray diffraction (XRD), in-vitro diffusion, and permeation studies. The resultant domperidone-loaded nanofibers (diameters 280–565 nm) exhibited a uniform and highly porous structure. With an increase in applied voltage from 11 to 13 kV, entrapment efficiency increased, and fiber diameter decreased. DSC and XRD results confirmed the amorphous nature of the domperidone. The FTIR study confirmed the compatibility between domperidone and PVA. The wetting and disintegration times of nanofibers were 8 and 4 s, respectively. Due to their nanosize, small particles with an increased surface area resulted in improved drug delivery through nanofibers (93.36% release within 10 min). The nanofiber film had a higher Cmax (398.8 ng/mL) and AUC (2078.593 ± 17.71 ng/mL.h) than the commercial tablet formulation (186.6 ng/mL and 1875.619 ± 10.38). Thus, domperidone nanofibers would be a promising approach for enhancing therapeutic and biopharmaceutical properties by providing ultra-fast delivery.

Enhanced antichemobrain activity of amino acid assisted ferulic acid solid dispersion in adult zebrafish (Danio rerio).

Chemotherapy-induced cognitive impairment (CICI), also known as "chemobrain," is a common side effect of breast cancer therapy which causes oxidative stress and generation of reactive oxygen species (ROS). Ferulic acid (FA), a natural polyphenol, belongs to BCS class II is confirmed to have nootropic, neuroprotective and antioxidant effects. Here, we have developed FA solid dispersion (SD) in order to enhance its therapeutic potential against chemobrain. An amorphous ferulic acid loaded leucin solid dispersion (FA-Leu SD) was prepared by utilizing amino acid through spray-drying technique. The solid-state characterization was carried out via Fourier-transform infrared spectroscopy (FT-IR), differential scanning calorimetry (DSC), X-ray diffraction (XRD), and field emission scanning electron microscopy (FE-SEM). Additionally, in-vitro release studies and antioxidant assay were also performed along with in-vivo locomotor, biochemical and histopathological analysis. The physical properties showed that FA-Leu SD so formed exhibited spherical, irregular surface hollow cavity of along with broad melting endotherm as observed from FE-SEM and DSC results. The XRD spectra demonstrated absence of sharp and intense peaks in FA-Leu SD which evidenced for complete encapsulation of drug into carrier. Moreover, in-vitro drug release studies over a period of 5h in PBS (pH 7.4) displayed a significant enhanced release in the first hr (68. 49 ± 5.39%) and in-vitro DPPH assay displayed greater antioxidant potential of FA in FA-Leu SD. Furthermore, the in-vivo behavioral findings of FA-Leu SD (equivalent to 150mg/kg of free FA) exhibited positive results accompanied by in-vivo biochemical and molecular TNF-α showed a significant difference (p < 0.001) vis-à-vis DOX treated group upon DOX + FA-Leu SD. Additionally, histopathological analysis revealed neuroprotective effects of FA-Leu SD together with declined oxidative stress due to antioxidant potential of FA which was induced by anticancer drug doxorubicin (DOX). Overall, the above findings concluded that spray-dried FA-Leu SD could be useful for the treatment of chemotherapy induced cognitive impairment.

Form-stable oleic acid based polyHIPE/nanoclay framework supported composite phase change materials for low‐temperature latent heat storage

Latent heat storage, one of the promising methods in energy storage, is an important option for the sustainable use of energy and is attracting more attention day by day. Phase change materials (PCMs) produced for this purpose allow the storage/release of latent heat due to the temperature of the medium and can be obtained using various methods. In this work, the preparation of a new fatty acid based composite phase change material was accomplished by applying simple two-step approach. Here, oleic acid (OA) was employed as PCM, and emulsion templated macroporous polymers (polyHIPEs) as supporting matrices. Furthermore, macroporous supports were also fabricated in the presence of surface modified montmorillonite nanoclay to enhance thermal properties of the targeted composite PCMs. In this respect, a neat macroporous support and surface modified nanoclay enhanced macroporous support were synthesized. Then, the composite PCMs were prepared by filling the macropores of the obtained polymer foams with OA via a solvent-assisted impregnation approach for cold energy storage. The examinations on the thermal characteristics of the composite PCMs were performed through Differential Scanning Calorimetry (DSC), while the chemical structure was analyzed with FT-IR. Besides, polarizing optical microscopy (POM) was used to monitor the loading of OA to macroporous polymer supports. Additionally, the thermal behaviors of composite PCMs were investigated by the temperature-history (T-history) method and the findings were also found to be compatible with DSC. Furthermore, thermal stability of the composite PCMs was investigated through thermogravimetric analysis (TGA). According to DSC results, the prepared composite PCMs are candidates for utilizing cold thermal energy storage such as building cooling, cold protection and cold chain transportation applications with their proper melting temperatures (7.08 °C and 7.40 °C) and moderate latent heat capacities.

Identification and isolation of a novel antifreeze peptide from crayfish shells

In this study, a novel antifreeze peptide was isolated from crayfish shells and its antifreeze mechanism and activity were investigated. Firstly, the crayfish shells peptides (CSPs) were prepared by Enzymatic Hydrolysis Technology (alkaline protease and trypsin) and the CSPs could significantly enhance the survival rate of Saccharomyces cerevisiae from 12.5% to 88.5% after 24h freeze-thaw cycle. Then, a total 1004 peptides were identified from CSPs by liquid chromatography/tandem mass spectrometry (LC-MS/MS), among those peptides, two peptide sequences YWDHPIRDGFAPH (AFP1) and GPPGKPGIPDIVDW (AFP1) were selected as potential antifreeze polypeptides (AFPs) according the physicochemical properties: instability index, hydrophilicity, and confidence level. Furthermore, the antifreeze activity and mechanism of AFP1 and AFP2 were studied through molecular dynamics simulation, revealing that the AFP1 and AFP2 could adsorb to ice surface with 7 and 14 hydrogen bonds, respectively. Moreover, AFP2 has a more stable binding capacity and could interact with 33 water molecules. At last, the results of differential scanning calorimetry (DSC) and cold-stage polarization microscope indicated that the thermal hysteresis (TH) values of AFP2 were 1.62–2.09 °C and could inhibit ice recrystallization. Therefore, this study provides a theoretical basis for developing safe peptide-based cryoprotectants which will improve the quality of frozen foods.