Preparation Of Nanoparticles Research Articles

Bio-friendly preparation and characterization of silver nanoparticles from eggshell powder extract: an exploration into their antibacterial and anticancer potential

Bio-friendly preparation and characterization of silver nanoparticles from eggshell powder extract: an exploration into their antibacterial and anticancer potential

Enzymatically and chemically starch nanoparticles preparation using ultrasonication, precipitation and lyophilization post-treatments: Screening and characterization

Starch nanoparticles (SNPs) have been used in food emulsions as natural stabilizer and emulsifier. SNPs in colloidal form were produced using enzymatically, acidic and alkaline hydrolyses in combination to ultrasonication and precipitation methods. X-Ray diffraction test for produced SNPs indicated that enzymatically and acidic prepared SNPs had amorphous structure while, the resulted SNPs using alkaline hydrolysis had lower relatively crystallinity. Results indicated that, enzymatically prepared SNPs, had minimum particle size (225 ± 10 nm) and polydispersity index (0.472 ± 0.05), and maximum zeta potential (−26.3 ± 1 mV), antioxidant activity (3.36 ± 0.05 %) and specific surface area (1.8 ± 0.1 m2g−1). Transmission electron microscopy revealed that prepared SNPs had spherical shape and enzymatically prepared SNPs had mean particle size of <100 nm. SNPs in powder form were prepared using freeze drying (pressure and temperature of 100 Pa and − 70 °C). Atomic force microscopy results demonstrated that starch granules had smooth surface, with polyhedral shape and particle size ranging 5 to 25 μm, and after hydrolysis, SNPs had particle size in nanometer scale. Emulsion ability test indicated that oil separation time from the prepared emulsions containing 10 % (W/V) starch, and enzymatically, acidic and alkaline prepared SNPs powder were 41, 70, 82 and 101 s, respectively.

Single-nanoparticle electrophoretic mobility determination and trapping using active-feedback 3D tracking.

Nanoparticles (NP) are versatile materials with widespread applications across medicine and engineering. Despite rapid incorporation into drug delivery, therapeutics, and many more areas of research and development, there is a lack of robust characterization methods. Light scattering techniques such as dynamic light scattering (DLS) and electrophoretic light scattering (ELS) use an ensemble-averaged approach to the characterization of nanoparticle size and electrophoretic mobility (EM), leading to inaccuracies when applied to polydisperse or heterogeneous populations. To address this lack of single-nanoparticle characterization, this work applies 3D Single-Molecule Active Real-time Tracking (3D-SMART) to simultaneously determine NP size and EM on a per-particle basis. Single-nanoparticle EM is determined by using active feedback to "lock on" to a single particle and apply an oscillating electric field along one axis. A maximum likelihood approach is applied to extract the single-particle EM from the oscillating nanoparticle position along the field-actuated axis, while mean squared displacement is used along the non-actuated axes to determine size. Unfunctionalized and carboxyl-functionalized polystyrene NPs are found to have unique EM based on their individual size and surface characteristics, and it is demonstrated that single-nanoparticle EM is a more precise tool for distinguishing unique NP preparations than diffusion alone, able to determine the charge number of individual NPs to an uncertainty of less than 30. This method also explored individual nanoparticle EM in various ionic strengths (0.25-5 mM) and found decreased EM as a function of increasing ionic strength, in agreement with results determined via bulk characterization methods. Finally, it is demonstrated that the electric field can be manipulated in real time in response to particle position, resulting in one-dimensional electrokinetic trapping. Critically, this new single-nanoparticle EM determination and trapping method does not require microfluidics, opening the possibility for the exploration of single-nanoparticle EM in live tissue and more comprehensive characterization of nanoparticles in biologically relevant environments.

Selective oxidation of glycerol mediated by surface plasmon of gold nanoparticles deposited on titanium dioxide nanowires

This paper describes an alternative method for the in situ synthesis of gold nanoparticles (AuNPs) with a particle size of less than 3 nm, using nanoreactors formed by reverse micelles of 1,4-bis-(2-ethylhexyl) sulfosuccinate sodium (AOT) and nanoparticle stabilization with l-cysteine, which favor the preparation of nanoparticles with size and shape control, which are homogeneously dispersed (1% by weight) on the support of titanium dioxide nanowires (TNWs). To study the activity and selectivity of the prepared catalyst (AuNPs@TNWs), an aqueous solution of 40 mM glycerol was irradiated with a green laser (λ = 530 nm, power = 100 mW) in the presence of the catalyst and O2 as an oxidant at 22 °C for 6 h, obtaining a glycerol conversion of 86% with a selectivity towards hydroxypyruvic acid (HA) of more than 90%. From the control and reactions, we concluded that the Ti–OH groups promote the glycerol adsorption on the nanowires surface and the surface plasmon of the gold nanoparticles favors the selectivity of the reaction towards the hydroxypyruvic acid.

Engineering Platelet Membrane Imitating Nanoparticles for Targeted Therapeutic Delivery.

Platelet Membrane Imitating Nanoparticles (PMINs) is a novel drug delivery system that imitates the structure and functionality of platelet membranes. PMINs imitate surface markers of platelets to target specific cells and transport therapeutic cargo. PMINs are engineered by incorporating the drug into the platelet membrane and encapsulating it in a nanoparticle scaffold. This allows PMINs to circulate in the bloodstream and bind to target cells with high specificity, reducing off-target effects and improving therapeutic efficacy. The engineering of PMINs entails several stages, including the separation and purification of platelet membranes, the integration of therapeutic cargo into the membrane, and the encapsulation of the membrane in a nanoparticle scaffold. In addition to being involved in a few pathological conditions including cancer, atherosclerosis, and rheumatoid arthritis, platelets are crucial to the body's physiological processes. This study includes the preparation and characterization of platelet membrane-like nanoparticles and focuses on their most recent advancements in targeted therapy for conditions, including cancer, immunological disorders, atherosclerosis, phototherapy, etc. PMINs are a potential drug delivery system that combines the advantages of platelet membranes with nanoparticles. The capacity to create PMMNs with particular therapeutic cargo and surface markers provides new possibilities for targeted medication administration and might completely change the way that medicine is practiced. Despite the need for more studies to optimize the engineering process and evaluate the effectiveness and safety of PMINs in clinical trials, this technology has a lot of potential.

Folic-Acid-Conjugated Poly (Lactic-Co-Glycolic Acid) Nanoparticles Loaded with Gallic Acid Induce Glioblastoma Cell Death by Reactive-Oxygen-Species-Induced Stress.

Glioblastoma (GBM) conventional treatment is not curative, and it is associated with severe toxicity. Thus, natural compounds with anti-cancer properties and lower systemic toxicity, such as gallic acid (GA), have been explored as alternatives. However, GA's therapeutic effects are limited due to its rapid metabolism, low bioavailability, and low permeability across the blood-brain barrier (BBB). This work aimed to develop poly (lactic-co-glycolic acid) (PLGA) nanoparticles (NPs) modified with folic acid (FA), as its receptor is overexpressed in BBB and GBM cells, for GA delivery to enhance its therapeutic efficacy. The preparation of NPs was optimized by a central composite design (CCD). The obtained NPs showed physicochemical features suitable for drug internalization in BBB and tumor cells (sizes below 200 nm, monodispersity, and negative surface charge) and the ability to maintain a slow and sustained release for 40 days. In vitro studies using a human GBM cell line (U215) revealed the NPs' ability to accumulate in the target cells, further promoting GA antiproliferative activity by inducing the production of intracellular reactive oxygen species (ROS). Furthermore, GA encapsulation in the developed nanosystems conferred higher protection to healthy cells.

Preparation of Mn3O4 nanoparticles on Al-substrate for degradation of Rhodamine B under solar light

Preparation of Mn3O4 nanoparticles on Al-substrate for degradation of Rhodamine B under solar light

Sustained-release, antibacterial, adhesive gelatin composite hydrogel with AgNPs double-capped with curdlan derivatives

In this work, carboxymethylated curdlan (CMCD) was utilized as a capping and stabilizing agent for the green synthesis of silver nanoparticles. Subsequently, quaternized curdlan (QCD) was introduced as the second capping layer through electrostatic attraction, leading to the preparation of double-capped silver nanoparticles (AgNPs@CQ). The successful synthesis of silver nanoparticles was characterized using UV–vis, FTIR, XRD, TEM, and DLS. AgNPs@CQ were incorporated into gelatin and a AgNPs@CQ/Gel composite hydrogel was obtained. The incorporation of AgNPs@CQ imparts excellent antibacterial properties to the composite hydrogel, thereby enhancing its antimicrobial efficacy. The presence of double-capping layers significantly retards the release rate of silver, contributing to prolonged antimicrobial activity. The MTT and live/dead fluorescence staining results demonstrate that the gelatin hydrogel incorporating double-capped AgNPs exhibits enhanced cell viability compared to the one incorporating single-capped AgNPs. Additionally, the composite hydrogel exhibits remarkable mechanical strength and adhesive performance. The AgNPs@CQ/Gel composite hydrogel demonstrates a cost-effective and facile preparation, showing significant potential in the field of dressings.

Preparation and Characterization of Zinc Oxide Nanoparticles by Co-Precipitation Method and Evaluation of Theirs Antifungal Activity in Spore Germination of Dermatophytes

Preparation and Characterization of Zinc Oxide Nanoparticles by Co-Precipitation Method and Evaluation of Theirs Antifungal Activity in Spore Germination of Dermatophytes

MOF-derived SnO2 nanoparticles for realization of ultrasensitive and highly selective NO2 gas sensing

Herein, SnO2 nanoparticles (NPs) were synthesized from a Sn-metal organic framework (MOF) through a hydrothermal synthesis approach for NO2 sensing studies. The expected phase, morphology and composition of the SnO2 NPs were demonstrated via different characterizations. The individual sizes of SnO2 NPs were ∼20–30 nm, and they had a high surface area (185.31 m2/g). The sensing properties were measured at various temperatures towards NO2 gas. It showed very high responses of 240.60 and 3984.98–10 and 100 ppm NO2, respectively, at 200°C. Also, it still displayed a high response of 47.11–100 ppm NO2 gas at 25°C. Enhanced response of MOF-derived SnO2 NPs gas sensor was owing to the high surface area of the SnO2 NPs, the presence of oxygen vacancies, formation of plenty of SnO2-SnO2 homojunctions and the creation of SnO/SnO2 heterojunctions. The synthesis method employed in this study led to the preparation of high surface area SnO2 NPs that can be used for preparing other metal oxides for the development of sensors.

Preparation of BN Nanoparticle with High Sintering Activity and Its Formation Mechanism.

Hexagonal boron nitride (h-BN) nanoparticles have attracted increasing attention due to their unique structure and properties. However, it is difficult to synthesize h-BN nanoparticles with uniform spherical morphology due to their crystal characteristic. The morphology control by tuning their precursor synthesis is a promising and effective strategy to solve this problem. Especially, the treatment temperature of precursors plays an important role in the morphology and surface area of h-BN nanoparticles. Herein, h-BN nanoparticles with different morphologies were synthesized via regulating the treatment temperature of precursors. The result shows that treatment temperature will affect the microstructure and state of precursor and further influence the morphology of h-BN products. Benefiting from the unique structure, the h-BN obtained using 250 °C precursors shows higher specific surface area (61.1 m2 g-1) than that of 85 °C (36.5 m2 g-1) and 145 °C (27.9 m2 g-1). h-BN products obtained using 250 °C precursors show higher specific surface area than that of 85 °C and 145 °C. The optimal condition for obtaining high-quality spherical h-BN is the pretreatment temperature of 250 °C and sintering temperature of 1300 °C. Importantly, compared with commercial h-BN nanoparticles, the synthesized h-BN nanoparticles show more uniform structure and larger specific surface area, indicating that sintering activity will be greatly improved. Furthermore, the reaction pathway and formation mechanism of h-BN was revealed by DFT calculations. The result shows that the five stationary states and five transition states exist in the reaction pathway, and the energy barrier can be overcome at high temperatures to form a ring h-BN. In view of its simplicity and efficiency, this work is promising for designing and guiding the synthesis of h-BN nanoparticles with uniform morphology.

Seaweed assisted preparation of Fe2O3 nanoparticles and their antiviral studies against White Spot Syndrome Virus (WSSV): In vitro and in silico approach.

In the present study, preparation of Fe2O3 nanoparticles using seaweed Sargassum swartzii extract and characterized using XRD, FTIR, and FE-SEM with EDAX analysis. The crystalline nature of γ-Fe2O3 nanoparticles (hematite powders) were confirmed using XRD. In FT-IR spectra of the Fe2O3 nanoparticles, the major bands at 594 cm−1 and 461 cm−1 observed correspond to the metal‑oxygen (FeO) vibrational modes. The surface morphology of Fe2O3 nanoparticles has been studied by FE-SEM. In vitro toxicity and anti-WSSV activity of Fe2O3 nanoparticles were carried out using the shrimp-insect hybrid cell line (PmLyo-Sf9). The bioactivity of Fe2O3 nanoparticles against the WSSV infected with the PmLyo-SF9 cell line was analyzed through dose-dependent attachment inhibition and virucidal activity at an optimum concentration of 320 μg/mL and confirmed by the expression of viral envelope protein VP28. Further, the computational approach of VP28 envelope protein and Fe2O3 binding affinity was confirmed using molecular docking studies. Hence, the Fe2O3 nanoparticles can be formulated as an anti-viral agent against the aquaculture pathogens in efficient disease control.

One-Step Formation Method of Plasmid DNA-Loaded, Extracellular Vesicles-Mimicking Lipid Nanoparticles Based on Nucleic Acids Dilution-Induced Assembly.

We propose a nucleic acids dilution-induced assembly (NADIA) method for the preparation of lipid nanoparticles. In the conventional method, water-soluble polymers such as nucleic acids and proteins are mixed in the aqueous phase. In contrast, the NADIA method, in which self-assembly is triggered upon dilution, requires dispersion in an alcohol phase without precipitation. We then investigated several alcohols and discovered that propylene glycol combined with sodium chloride enabled the dispersion of plasmid DNA and protamine sulfate in the alcohol phase. The streamlined characteristics of the NADIA method enable the preparation of extracellular vesicles-mimicking lipid nanoparticles (ELNPs). Among the mixing methods using a micropipette, a syringe pump, and a microfluidic device, the lattermost was the best for decreasing batch-to-batch differences in size, polydispersity index, and transfection efficiency in HepG2 cells. Although ELNPs possessed negative ζ-potentials and did not have surface antigens, their transfection efficiency was comparable to that of cationic lipoplexes. We observed that lipid raft-mediated endocytosis and macropinocytosis contributed to the transfection of ELNPs. Our strategy may overcome the hurdles linked to supply and quality owing to the low abundance and heterogeneity in cell-based extracellular vesicles production, making it a reliable and scalable method for the pharmaceutical manufacture of such complex formulations.

Effect of “corona-core” structuring of poly(1-vinyl-1,2,4-triazole)–poly(acrylic acid)-Ag(I) interpolymer complexes on the radiation-induced preparation and stability of silver nanoparticles

Interpolymer complexes (IPC) of water-soluble polymers can be promising matrices for the synthesis of metal colloids. In this work, silver nanoparticles were obtained via radiation-induced reduction (under X-ray irradiation) of complexes based on poly (1-vinyl-1,2,4-triazole) (PVT) and poly (acrylic acid) (PAA) containing Ag+ ions. Particular attention was paid to the role of the supramolecular structure in the formation of nanoparticles. Combined dynamic light scattering and electrophoretic mobility measurements have revealed that, in pH range 5.5–7, micro-scale aggregates of the initial PVT-PAA-Ag(I) IPC transform into nano-sized particles consisting of a PVT-Ag(I) core electrostatically stabilized by PAA loops and tails forming a corona. It was explicitly demonstrated for the first time that such transformation of IPC aggregates can significantly enhance the efficiency of AgNPs formation. In particular, using UV-VIS spectroscopy and transmission electron microscopy, we have shown that at pH 7.0 the core of the “corona-like” form of the PVT-PAA-Ag(I) complex ensures the radiation-induced generation of AgNPs with a narrow size distribution due to the strong affinity of triazole groups to the metal surface. At the same time, the localization of the excessive negatively charged carboxylate groups in the outer part of the complex provides a long-term colloidal stability of the prepared AgNPs.

Methotrexate-Loaded Surface-Modified Solid Lipid Nanoparticles Targeting Cancer Expressing COX-2 Enzyme.

Cancer is a major public health problem worldwide, and it is the second leading cause of death of humans in the world. The present study has been directed toward the preparation of methotrexate-loaded surface-modified solid lipid nanoparticles (SLNs) for potential use as a chemotherapeutic formulation for cancer therapy. A lipid (C14-AAP) derived from myristic acid (C14H30O2) and acetaminophen (AAP) was employed as a targeting ligand for human breast and lung cancer cells that overexpress the cyclooxygenases-2 (COX-2) enzyme. The SLNs consisting of stearic acid and C14-AAP were characterized by several methods, including dynamic light scattering (DLS), differential scanning calorimetry (DSC), powder X-ray diffraction (PXRD), ultraviolet-visible (UV-vis) spectroscopy, high-resolution transmission electron microscopy (HRTEM), and field emission scanning electron microscopy (FESEM) techniques. An in vitro cell cytotoxicity study was done by carrying out an MTT assay and flow cytometry study in the human breast cancer (MCF7) and human lung cancer cell line (A549). The expression level of COX-2 enzyme in MCF7 and A549 cell lines was examined by reverse transcription polymerase chain reaction (RT-PCR). A high level of COX-2 expression was observed in both cell lines. In vitro cell cytotoxicity study in MC7 and A549 cell lines showed the surface-modified, methotrexate-loaded SLN is more effective in cell killing and induction of apoptotic death in both the cell lines than free methotrexate in MTT, flow cytometry, clonogenic assay, and Western blot studies. The surface-modified SLN was radiolabeled with 99mTc with %RCP greater than 95%. In vivo biodistribution study of the 99mTc-labeled SLN in melanoma tumor-bearing C57BL6 mice showed moderate tumor uptake of the radiotracer at 3 h post injection. The SPECT/CT image aligns with the biodistribution results. This study shows that AAP-modified SLNs could be a potential chemotherapeutic formulation for cancer therapy.

One-step electrochemical preparation of platinum nanoparticle decorated self-healing reduced graphene oxide three-dimensional nanoarray for portable detection of bisphenol A

Highly selective and sensitive analysis of bisphenol A (BPA) in many plastic products remains its significance. We explored a simple, highly sensitive, and inexpensive electrochemical sensor based on a self-healing three-dimensional nanoarray (3DN) via a single-step electrochemical preparation of both platinum nanoparticles (PtNPs) and reduced graphene oxide (rGO) on a glassy carbon electrode for the portable detection of bisphenol (BPA) in plastic bottled waters. The structure of PtNPs/3DNrGO was confirmed by electron microscope and spectroscopic characterization. Electrochemical characteristics indicated that PtNPs/3DNrGO could decrease the oxidation overpotential due to the self-healing effect of the physical interaction between PtNPs and hydroxyl groups of rGO with an increase in the active surface area. The PtNPs/3DNrGO exhibited remarkably efficient electrocatalytic performance for the oxidation of BPA. The PtNPs/3DNrGO sensor for BPA demonstrated a wide linear range from 0.7 to 20 µM with a low limit of detection of 6 nM (S/N = 3) and effective performance including high sensitivity, high repeatability, and excellent selectivity. The developed sensor had been effectively implemented to assess BPA in plastic samples with desirable impacts. The interaction mechanism of both PtNPs and rGO was inferred by density functional theory. The proposed electrochemical sensor enabled the development of a portable, low-cost, and user-friendly monitoring of water quality, which will offer theoretical support for environmental monitoring.

Preparation of nanoparticle and nanoemulsion formulations containing repaglinide and determination of pharmacokinetic parameters in rats

Repaglinide (RPG) belongs to the class of drugs known as meglitinides and is used for improving and maintaining glycemic control in the treatment of patients with Type 2 diabetes. RPG is a Class II drug (BCS) because of its high permeability and low water solubility. It also undergoes hepatic first-pass metabolism. The oral bioavailability of RPG is low (about 56 %) due to these drawbacks. Our aim in this study is to prepare two different nano-sized drug carrier systems containing RPG (nanoparticle: RPG-PLGA-Zein-NPs or nanoemulsion: RPG-NE) and to carry out a pharmacokinetic study for these formulations. We prepared NPs using PLGA and Zein. In addition, a single NE formulation was developed using Tween 80 and Pluronic F68 as surfactants and Labrasol as co-surfactant. The droplet size values of the blank-NE and RPG-NE formulations were found to be less than 120 nm. The mean particle sizes of blank-Zein-PLGA-NPs and RPG-Zein-PLGA-NPs were less than 260 nm. The Cmax and tmax values of RPG-Zein-PLGA-NPs and RPG-NE (523 ± 65 ng/mL and 770 ± 91 ng/mL; 1.41 ± 0.46 h and 1.61 ± 0.37 h, respectively) were meaningfully higher than those of free RPG (280 ± 33 ng/mL; 0.72 ± 0.28 h) (p < 0.05). The AUC0-∞ values calculated for RPG-Zein-PLGA-NPs and RPG-NE were approximately 4.04 and 5.05 times higher than that calculated for free RPG. These nanosized drug delivery systems were useful in increasing the oral bioavailability of RPG. Moreover, the NE formulation was more effective than the NP formulation in improving the oral bioavailability of RPG (p < 0.05).

Biosynthesis of gold nanoparticles by using gelatin as reducing and stabilizing agent under ultrasound irradiation: Application of its catalytic activity and for ameliorating motor recovery after spinal cord injury in the Wistar rat’s model

The current project describes the facile preparation of Au nanoparticles mediated by gelatin as a natural capping and reducing agent in mild condition. The formation of Au nanoparticles stabilized by gelatin (Au NPs/Gelatin) and structural characteristics were studied via UV–Vis, FT-IR, TEM, FE-SEM, EDX and elemental mapping techniques. The evidence shown that gelatin-capped gold nanoparticles resulted in the lowest average particle sizes of 15–25 nm and spherical shapes nanoparticles. Further, newly synthesized Au NPs/Gelatin are used as a nanocatalyst for the reduction of 4-nitrophenol (4-NP) dyes. A UV–Vis spectrophotometer is employed to track the effectiveness of the reduction process. Recyclability in six further degradation cycles is used to assess the sustainability of this catalyst, and the results show a steady and notable degradation activity. In the in vivo experiment, 60 male rats were classified into four groups: control, intact, sham, and Au NPs/Gelatin nanocatalyst (20 µg/kg) groups. The Hematoxylin and eosin staining was conducted to examine the post-injury lesions. Additionally, somatosensory evoked potential experiments were conducted to assess the recovery of neural conduction. The expression of GFAP was evaluated to determine the extent of astrogliosis. Furthermore, the behavioral outcomes of the rats were evaluated using the BBB scores on a weekly basis after the spinal cord injury onset. The results of the research demonstrated that the neuroprotective effects of Au NPs/Gelatin nanocatalyst led to an amelioration in the rat’s model. Electromyography (EMG) data revealed a remarkable amelioration in hindlimb function in the Au NPs/Gelatin nanocatalyst (20 µg/kg) group. The ventral motor neurons number significantly raised, while the cavity areas significantly decreased in the Au NPs/Gelatin group. Moreover, the expression of GFAP was notably reduced in the Au NPs/Gelatin nanocatalyst group. The Au NPs/Gelatin nanocatalyst group exhibited a significant reduction in delayed responses and a significant increase in BBB scores during sensory tests.

Preparation of Hollow Silica Nanoparticles with Polyacrylic Acid and Their Moisture Sorption Properties

Hollow silica nanoparticles (HSNPs) have hygroscopic properties because of their high specific surface area and surface hydroxyl groups. However, compared with other hygroscopic materials, their hygroscopic properties are relatively weak, which limits the further application of HSNPs. One feasible method to enhance their hygroscopic properties is by combining highly hygroscopic materials with hollow silica nanoparticles. To take advantage of the high hygroscopicity of polyacrylic acid (PAA) when combined with the high specific surface area of the hollow particles, PAA was coated on the inner and outer surfaces of the silica shell of the nanoparticles in this study to prepare hollow nanoparticles with a PAA/silica/PAA multilayer structure. The size of the PAA/silica/PAA multi-layer nanoparticles is about 85 nm, and the shell thickness is 25 nm. The specific surface area of the multi-layer nanoparticles is 58 m2/g. The water vapor adsorption capacity of multi-layer structure hollow nanoparticles was increased by 160% compared with the HSNPs (increased from 45.9 cm3/m2 to 109.1 cm3/m2). Meanwhile, at the same content of PAA, the PAA/silica/PAA-structured particles will adsorb 9% more water vapor than the PAA/silica-structured particles. This indicates that the high specific surface area structure of the hollow particles will enhance the adsorption ability of PAA toward water vapor. This novel structure of PAA-HSNPs is expected to be used as a humidity-regulating material for filler in environmental and architectural applications.

Development of multifunctional chitosan-based composite film loaded with tea polyphenol nanoparticles for strawberry preservation

Incorporating polysaccharide-based composite films with nanobiotechnology offers a new strategy for food preservation. This study initially focuses on the preparation of tea polyphenol nanoparticles (TPNP), novel and derived from natural antibacterial agents, which serve to improve stability. Afterwards chitosan-based composite films loaded with TPNP (CTN film) were developed using solution casting method. The incorporation of TPNP significantly improved the UV/water/oxygen barrier properties, mechanical properties and thermal stability, alongside notable physical properties including water contact angle (93.65 ± 0.04°), low water vapor permeability (33.72 ± 3.32 g/m2h) and oxygen permeability (0.11 ± 0.02 g/m2h), tensile strength (61.83 ± 0.70 %), and elongation at break (31.60 ± 6.12 %). The CTN film not only exhibited exceptional biodegradability and nontoxicity, but also demonstrated remarkable antimicrobial efficacy against Escherichia coli and Bacillus subtilis. Additionally, it showcased potent antioxidant activity, boasting DPPH and ABTS radical scavenging rates up to 89.25 ± 0.18 % and 93.84 ± 0.42 %. The CTN film was successfully formed on the surface of strawberries through dip-coating process and their shelf life was extended from 4 to 6 days at 20 °C without side-effect on the weight loss, harness, pH and total soluble solids, illustrating its potential for enhancing food preservation.