Zeta Potential Research Articles

Preparation and evaluation of Puerarin-loaded PLGA nanoparticles for improving oral bioavailability in SD rats

BackgroundPuerarin (Pue) is an isoflavone compound with significant therapeutic effect on cardiovascular diseases, but its poor water solubility and low oral bioavailability limit clinical application. MethodsIn this study, Pue was prepared into PLGA nanoparticles (Pue-PLGA NPs) by emulsion solvent volatilization method. The morphology, particle size, Zeta potential, X-ray diffraction (XRD), and fourier transform infrared (FTIR) of the NPs were characterized. Additionally, their stability and in vitro release were evaluated. SD rats were orally administered wtih Pue and Pue-PLGA NPs, and a high performance liquid chromatography-tandem mass spectrometry (LC-MS/MS) method was established to determine the concentration of blood samples and to investigate the pharmacokinetic behaviour of Pue and Pue-PLGA NPs in rats. ResultsThe NPs were observed by transmission electron microscopy (TEM) as regular spheroids and uniformly dispersed. The average particle size of the NPs was (167.1±5.26）nm, the Zeta potential was (-29.88±2.46)mV, the encapsulation rate was (83.12 %±4.73 %) and the drug loading capacity was (7.75 %±1.81 %). The results of in vitro release showed that the drug was released slowly and continuously from the NPs, reaching the release platform in 24 h, and the cumulative release amount was (88.55±2.86) %. The pharmacokinetic results showed that the AUC0–24, AUC0-∞, Cmax, Tmax, t1/2, MRT0–24 and MRT0-∞ of Pue-PLGA NPs were 2.196, 1.978, 1.327, 1.5, 1.385, 3.915 and 3.140 times of Pue, respectively. The relative bioavailability was (197.82±25.28) %. ConclusionThese results indicated that the prepared nanoparticles had small particle size, high encapsulation rate, drug loading capacity and good slow-release effect, and could significantly improve the oral bioavailability of Pue in rats.

Understanding the role of sodium lignosulphonate on obstructing the aggregation of fine serpentine particles on to the hydrophobized pyrite surface

The slime coatings of serpentine via its hydrophobic Si-O layers significantly weaken the floatability of the hydrophobized sulfide minerals. In this paper, sodium lignosulphonate (SLS) was adopted to avoid the aggregation of fine serpentine particles on to the hydrophobized pyrite surface. The micro-flotation findings indicated that for the artificial mixture of pyrite and serpentine (2:1 mass ratio), 1.0 × 10-4 mol/L sodium isobutyl xanthate (SIBX) only floated out ∼22% pyrite at pH ∼9.0, while, after extra addition of 70 mg/L SLS, the floatability of pyrite was restored and its recovery reached ∼90%. In situ AFM (Atomic Force Microscope), contact angle, zeta potential, fourier transform infrared spectrometer (FTIR) and optical microscope deduced that the strong affinity of SIBX to pyrite rendered it replace the most part of the pre-aggregated SLS from pyrite surface, thus to restore the hydrophobicity of pyrite and further decrease the zeta potential. In addition, SLS attached on the positively-charged Mg sites of serpentine through its carboxyl and phenolic hydroxyl groups reduce the hydrophobicity and zeta potential of serpentine. While, the hard base O atom/anion exhibited much stronger affinity to hard acid Mg cation than that of the soft base S atom/anion, SIBX hardly replaced the adsorbed SLS from serpentine surface. Therefore, the increased electrostatic repulsion and weakened hydrophobic attraction between the SLS-adsorbed serpentine and SIBX-hydrophobized pyrite avoided their aggregation. The combination of SLS and SIBX realized the selective flotation separation of pyrite from serpentine.

Application of some cationic pullulan and curdlan derivatives as flocculants in fungicides-containing wastewater purification

The ability of some cationic pullulan (TMAPx-P) and curdlan (TMAP0.4-C) derivative to remove different fungicide particles from synthetic wastewater has been studied. Commercial fungicides formulations of different type, Bordeaux mixture (BM), Dithan M45 (Dt) and Melody Compact49 WG (MC) have been used. The influence of some parameters related to the dispersion characteristics (suspension pH and salinity) and the polysaccharide derivatives (polymer dose, the ionic groups content, flexibility) on the separation process have been assessed. All the polysaccharide samples revealed a good removal efficiency (RE%) for the fungicide formulations prepared in saltless aqueous solutions, namely between 94 and 98 % for BM, 81.5–85 % for Dt, 88–91 % for MC. Slightly higher residual fungicides absorbance percent values for the suspensions prepared in the presence of salts (up to 7 %) than those prepared in water have been noticed. Less amount of BM and MC particles were removed in acidic pH than in water and basic pH, while contrary results were recorded in case of Dt ones, irrespective of the flocculant used. However, the RE% values were located between 79 % and 98 % over the entirely suspension pH investigated. Both zeta potential and floc size measurements indicated the charge patch flocculation mechanism for the fungicide particles separation.

Azelaic acid-based lyotropic liquid crystals gel for acne vulgaris: Formulation optimization, antimicrobial activity and dermatopharmacokinetic study

The proposed study aimed to develop a topical gel containing azelaic acid (AZA)-based lyotropic liquid crystals (LLCs) for the treatment of acne vulgaris. AZA-based LLCs were optimized by varying Poloxamer-407 and polyvinyl alcohol concentration using a central composite design, which showed that both independent variables had a significant effect on the formulation. The highest desirable trial of AZA-based LLCs (Batch-7) containing 300 mg poloxamer-407 and 100 mg polyvinyl alcohol depicted the particle size, zeta potential, and entrapment efficiency of 184.2 nm, −16.1 mV, and 79.96 %, respectively. TEM images confirmed the globular vesicles of LLCs, and ATR-FTIR and DSC results confirmed the compatibility of formulation excipients. In vitro, the release of AZA, AZA-based LLCs, AZA-based LLC gel, and marketed gel showed a release of 23.29, 95.24, 91.07 and 59.88 %, respectively, after 24 h in phosphate buffer pH 6.8. Ex vivo release of AZA-based LLC gel displayed an 86.56 % release after 24 h. The antimicrobial activity of AZA-based LLC gel exhibited a comparable efficacy with marketed gel against Cutibacterium acnes, Staphylococcus epidermis and Staphylococcus aureus. The acute dermal irritation study indicated excellent safety and skin compatibility of AZA-based LLC gel without any erythema and edema. The dermatopharmacokinetic study displayed an enhanced drug retention for AZA-based LLC gel (146.121 ± 21.13 µg/cm2) than marketed gel (58.58 ± 15.95 µg/cm2) in the dermal layer, which would improve its therapeutic effect. These outcomes proved that AZA-based LLC gel has the potential to enhance skin penetration and retention for effective management of acne vulgaris.

Addition of Ostrea rivularis polysaccharides in microneedle loaded with 3-acetylaconitine liposomes enhance analgesic activities and drug delivery properties.

3-Acetylaconitine (AAC) is a natural compound with strong anti-inflammatory and analgesic properties, but the severely narrow safety range limited its clinical application. Two dissolvable microneedle (MN) systems, AAC-ORP-MN and AAC-MN, loaded with AAC liposomes (AAC-Lips) either mixed with or without Ostrea rivularis polysaccharide (ORP) were developed. The size, zeta potential and encapsulation efficiency of AAC-Lips were 112.9±0.5nm, -31.3±0.5mV and 95.7±1.2%. AAC-ORP-MN demonstrated higher mechanical strength and faster initial drug release rate compared to AAC-MN. The results in the spared nerve injury (SNI) model showed that AAC-ORP-MN and AAC-MN both could significantly increase the mechanical pain threshold on the operated side of the rats, and gradually decrease the difference between the equilibrium pain thresholds of both feet, but AAC-ORP-MN showed a faster onset of action. In addition, AAC-ORP-MN significantly reduced inflammatory factors and improved pathological damage in the spinal cord better than AAC-MN, which might be due to the anti-inflammatory activity of ORP. Overall, the above results supported that AAC-ORP-MN showed promise as a clinical option for analgesia, which had anti-inflammatory and analgesic properties, meanwhile it could effectively deliver poorly water-soluble AAC and improve its safety and availability.

Cubosomes hydrogel containing silver based organometallic compounds for enhanced wound healing of burns: In vitro and in vivo studies

The aim of this study is to investigate the treatment of burn wounds and bacterial infections, specifically focusing on silver(I) N-heterocyclic carbene (Ag-NHC) loaded into cubosomes. Ag-NHC is an organometallic complex of silver (Ag) and can be considered an active pharmaceutical ingredient for the topical treatment of burns. A novel nanoparticle system, cubosome dispersions, was formulated using high pressure homogenization methods with different concentrations of lipid phase glyceryl monooleate (GMO), surfactants such as poloxamer 407 (F-127), and polyvinyl alcohol (PVA). The optimized formulation (U6) was characterized by in vitro drug release profile (90.54 ± 1.17 %), particle size (126.7 ± 0.98 nm), zeta potential (−21.6 ± 6.83 mV), entrapment efficiency (89.30 ± 1.46 %), and morphology as observed by transmission electron microscopy (TEM). The U6 formulation was incorporated into a hydrogel containing Carbopol 940 to form a cubosomal hydrogel (cubogel). The cubogel was characterized by the in vitro release of Ag-NHC (92 %), entrapment efficiency (>90 %), pH (5.3), viscosity (1.2 cP), spreadability, and TEM. From the in vitro drug release pattern, it was concluded that the U6 formulation showed slow and sustained drug release over 24 h, and demonstrated superior burn healing compared to marketed products. The in vivo wound healing study revealed that the cubogel demonstrated a superior burn healing rate compared to commercially available products (Quench® and Clotrimazole®). The in vivo histopathological results showed that the prepared cubogel was effective in treating second-degree burns, with no side effects or skin irritation, compared to commercial products. Additionally, Ag-NHC-loaded cubogel facilitated sustained release for treating burn wounds without any bacterial infections. The current findings provide a strong basis for the initiating phase 0 clinal trials, highlighting significant potential for the further research to benefit the pharmaceutical industry.

High-performance copper terephthalic acid metal-organic framework/gum Arabic/carrageenan composite beads for efficient lead(II) removal from aqueous solutions

Lead (Pb(II)) contamination poses a significant threat to human health and the environment. This study investigates a new approach for Pb(II) removal from polluted water using copper terephthalic acid metal-organic framework/gum Arabic/potassium carrageenan (MGC) composite beads. We synthesized copper terephthalic acid MOF, potassium carrageenan beads, and MGC composite beads to evaluate their adsorption potential. Characterization of the synthesized adsorbents was performed using TGA, nitrogen adsorption/desorption, ATR-FTIR, zeta potential, SEM, and TEM analyses, revealing that MOF > MGC > KG in thermal stability. The MGC composite exhibited a high specific surface area (398.03 m2/g) with mesopores and diverse functional groups, alongside a pH of zero point charge (pHpzc) of 6.8 and a small particle size (20 nm). The maximum Langmuir adsorption capacity for Pb(II) removal by MGC reached 374.7 mg/g under optimized conditions (20 °C, pH 5, 60 min shaking time, 3.0 g/L adsorbent dosage). The adsorption data fit well with the Pseudo-First-Order kinetic model and Langmuir and Dubinin-Radushkevich isotherm models. The adsorption process was physical, favorable, and endothermic. EDTA was used as a desorption agent, showing that the composite beads retained 97 % efficiency after ten cycles, highlighting MGC's potential as a sustainable strategy for Pb(II) remediation.

Chitosan/siRNA nanoparticles targeting PARP-1 attenuate Neuroinflammation and apoptosis in hyperglycemia-induced oxidative stress in Neuro2a cells

Hyperglycemia induces an excessive production of superoxide by the mitochondria's electron-transport chain triggers several pathways of injury contributing to the development of diabetic complications. This increase in oxidative and nitrosative stress triggers the activation of PARP-1, a nuclear enzyme, through mechanisms such as DNA damage. siRNA-chitosan nanoparticles were formed based on electrostatic interaction, their particle size, zeta potential, STEM, and cellular uptake were characterized. Neuro2a cells were treated with low glucose (LG) and high glucose (HG) for 24 and 48 h. Neuro2a cells were pre-treated with negative siRNA, naked siRNA, siRNA-Lipofectamine™300, and ChNPs-5. qRT-PCR was used to analyze the expression of regulatory, inflammatory, and apoptotic biomarkers. The siRNA-chitosan complex at the weight ratio 1:3000 were approximately uniform spheres with particle size 150.5 nm and a positive zeta potential of about +41.5 mV. The uptake of FITC-labeled nanoparticles into Neuro2a cells was visualized using fluorescence microscopy with no significant cytotoxicity compared to the control cells. High glucose stimulation of Neuro2a cells increased PARP1 expression, and with siRNA-ChNP (1:3000) treatment, significant inhibition of PARP1 expression is observed that consequently reversed the expression of regulatory genes like SIRT1, FOXO1, FOXO3, and p53. PARP-1 inhibition reduced HG-induced inflammatory response, including NF-kB, IL6, IL1β, TNFα, iNOS, and TGF-β expression, and HG-induced apoptosis response, such as Cas-3, Cas-9, BAK, BAX, and AIF expression. This study highlights the crucial role of siRNA delivery via ChNPs and PARP-1 inhibition in hyperglycemia-induced oxidative stress in Neuro2a cells and PARP-1 inhibition may be a feasible strategy for the treatment of hyperglycemia-induced oxidative stress.

Hybrid Nanoparticle for Co-delivering Paclitaxel and Dihydroartemisinin to Exhibit Synergic Anticancer Therapeutics.

Anticancer treatment is required to provide effective and safe patient medicines. This research aided in developing and applying nanoparticles (NPs) for cancer treatment. The poor solubility of paclitaxel (PTX) restricts its therapeutic efficacy because of allergic side effects caused by formulation excipients. To overcome this, PTX was coupled with artemisinin derivatives and loaded into an NP drug delivery system to enhance its effects while addressing its low solubility. This study prepared and characterized a hybrid PLGA-lecithin NP containing dihydroartemisinin (DHA) and PTX for synergic anticancer therapy. A lyophilization study improved the stability of the NP drug formulations. Dual PTX- and DHA-loaded PLGA- and lecithin-based NPs were prepared using a single-step solvent evaporation method. The NP suspensions were lyophilized, and the types and ratios of cryoprotectants were investigated. The physicochemical properties of NPs and lyophilized cakes (Lyo-NPs) were characterized. The stability of the Lyo-NPs was investigated at 2-8°C and room conditions. The anticancer effects of the drug combination, NP suspension, and lyophilized powder were analyzed using an in vitro cytotoxicity assay and an in vivo model. The optimal PTX-DHA loaded PLGA-lecithin-NP was formulated (200 nm, PDI: 0.248 ± 0.003, Zeta potential: -33.60 ± 3.39 mV). Mannitol was selected for lyophilization. Lyo-NPs improved the stability of the NPs (1 year), wherein the physicochemical properties of the NPs were maintained (RDI was close to 1.0). An in-vitro cytotoxicity assay of PTX combined with DHA showed a synergistic anticancer effect (CI <1.0). The suppressive effects of Lyo-NPs on tumor growth in vivo were dose-dependent. While the cocktail of free drugs showed high toxicity (7.5 mg PTX-15 mg DHA/kg) in-vivo, Lyo-NPs showed no statistical differences in hematological and biochemical parameters compared to the control. Dual-drug-loaded hybrid PLGA-lecithin NP is a potential system to minimize severe side effects while enhancing antitumor efficacy, in which lyophilization is a key process to increase stability.

Development of Novel Women's Friendly Antifungal Microemulsion Loaded Gel for Vulvovaginal Infections

Aim: The research was carried out to develop the microemulsion-loaded gel of curcu-min, alkylpolyglucoside, and tea tree oil to treat vulvovaginal candidiasis infection. Methods: Screening of oils, surfactants, and co-surfactants was done based on solubility studies and the construction of pseudo-ternary phase diagrams with curcumin. The microemulsion was characterized for globule size, zeta potential, viscosity, and thermodynamic stability. Ex-vivo studies were carried out using Franz diffusion cells. The antifungal activity of microemulsion-loaded hydrogel was evaluated using the cup plate method using Candida albicans ATCC 10231 in glucose yeast agar medium. Results: The selected micro-emulsion consisted of curcumin 35μg/mL, IPM+TTO (1:1) 0.1 mL, Milcoside 100 + Acconon MC 8-2 EP NF 0.6-0.3 mL, phosphate buffer pH 4 160 mL showed maximum thermodynamic stability and exhibited lowest particle size and highest intensity. The viscosity of microemulsion-loaded gel was 11.2 pa.s. The surface tension of the microemulsion was measured by tensiometer and was found to be 26.07 mN/m. Antimicrobial susceptibility test-ing assay was done according to NCCLs assay protocol, and the EC50 value of our formulation was found to be 0.4465 μg/mL. In-vitro drug release and ex-vivo permeation studies showed 67.9% release in 420 minutes and 83.02% release in 360 minutes, respectively. An in-vitro irrita-tion study concluded that there was no redness or irritation on goat mucosa. Conclusion: The texture analysis test showed adhesiveness at -172.46 g s at - 4.60 adhesive force, and the peak load was 13.40 g. The microemulsion-loaded gel formulation can be a promis-ing alternative to the marketed formulations available for vaginal yeast infections.

Characterization of Ceria Powders as a Continuous Search for New Rare-earth Based Materials for Radiation Dosimetry

Background: Ceria (CeO2) belongs to rare-earth series and due to its profitable properties, presents a wide commercial use such as catalysis, energy, biological, biomedical, and pharmaceutical. The features of the starting materials in the form of free powders influence notably the processing, formation, as well as characteristics of the final structures\bodies obtained by colloidal processing. This study aims to characterize CeO2 powders. The results obtained are worthwhile data to advance toward new rare-earth based materials for radiation dosimetry. Methods: CeO2 powders were evaluated by the following techniques: PCS, SEM, XRD, FT-IR, EPR, IPC, and pycnometric density (ρ). The stability of particles in aqueous solvent was evaluated by zeta potential (ζ) determination. Results: CeO2 powders exhibited cubic C-type form, Fm-3m space group, a mean particle size (d50) of 19.3nm, and a pycnometric density (ρ) of 7.01g.cm-3. Based on the results of zeta potential determination, CeO2 powders exhibited high stability at pH 6.4 with ζ- value of |34.0|mV. Conclusion: The evaluation of CeO2 powders was reported. The results presented and discussed in this study contribute to advance in the search of new rare-earth based materials for radiation dosimetry.

Enhancement of Mo-Pb flotation separation using gallic acid as a molybdenite depressant: Investigating flotation behavior and mechanism

In the flotation separation of Mo-Pb bulk concentrate and the purification process of Pb-containing molybdenite concentrate, depressants are typically added to depress galena or molybdenite, aiming to obtain high-quality flotation products. Previous studies have focused on the depression of galena. In this study, gallic acid (GA) was utilized as a molybdenite depressant during Mo-Pb flotation separation. Single mineral flotation experiments showed that pH notably influenced galena and molybdenite flotation with GA, particularly at pH 10, displaying the most substantial recovery difference. Mixed mineral flotation experiments revealed GA’s selective depression on molybdenite. At the optimal dosage of GA, the Mo recovery was reduced by 76.62 percentage points, while the Pb recovery remained unaffected. The depression and separation mechanisms of GA were investigated using contact angle, infrared spectroscopy, Zeta potential, inductively coupled plasma optical emission spectrometer (ICP-OES), X-ray photoelectron spectroscopy (XPS) analysis, first-principles calculations analysis, and interface interaction free energy calculations. The results indicate that GA treatment significantly reduces the hydrophobicity of molybdenite surfaces; however, it slightly enhances the hydrophobicity of galena surfaces. At pH 10, the primary species in GA solution is HGA3-. It adsorbs on PbO species of the galena surface as Pb-GA complexes and tends to detach from the surface at high adsorption capacity, resulting in galena not being depressed by GA. Differently, GA adsorbs on the molybdenite surface through hydrophobic attraction force, rendering it hydrophilic. Additionally, after treatment with potassium butyl xanthate (PBX), the hydrophobicity of GA-treated galena is significantly enhanced, while the hydrophobicity of GA-treated molybdenite is not restored. This is because PBX can adsorb stably on GA-treated galena, but its adsorption on GA-treated molybdenite is hindered by the pre-adsorbed GA.

Designing an active green packaging material based on black chickpea protein isolate electrospun nanofibers containing citral nanoliposomes

Active green packaging with a sustainability perspective is one of the trending fields in the food industry. In this regard, we designed an eco-friendly packaging material based on black chickpea protein isolate (BCPI) electrospun nanofibers (NFs) containing citral-loaded nanoliposomes (NLPs). The particle size, PDI, zeta potential, and encapsulation efficiency of the produced citral-loaded NLPs were 145 nm, 0.27, -37 mV, and 88%, respectively. BCPI was successfully extracted and used to produce electrospun NFs. The NLPs were incorporated into BCPINFs at 0, 0.25, 0.5, and 1% w/w concentrations. All samples displayed a narrow, strip-like morphology. However, the incorporation of NLPs significantly (p<0.05) increased the average fiber diameter (400–600 nm). The chemical structure of NFs was investigated, revealing the formation of new interactions among components. The thermal stability and crystalline structure of BCPI-based NFs showed no significant change with the addition of NLPs. However, NLPs concentrations higher than 0.25% enhanced the tensile strength and surface hydrophobicity of NFs. In addition, incorporating citral-loaded NLPs into NFs at concentrations higher than 0.25% provided antioxidant and antibacterial activities. Based on the obtained results, the activated BCPI-based NFs with 0.5% w/w of citral-loaded NLPs was selected as the optimal NFs sample.

Preparation, characterization, and ex vivo evaluation of isoxanthohumol nanosuspension

This study assessed the equilibrium solubility, oil–water distribution coefficient, and dissociation constant of Isoxanthohumol (IXN), and formulated IXN nanoparticles (IXN-Nps) using a micro media grinding method. The research characterized the particle size, polydispersity index, zeta potential, morphology, and structure of the nanoparticles, and evaluated the optimal cryoprotectant. Additionally, the study examined the toxicity and in vitro and in vivo release of IXN on HT-29 cells. IXN is classified as a Biopharmaceutical Classification System (BCS) II class drug with weak acidity. The average particle size of IXN-Nps is 249.500 nm, with a polydispersity index (PDI) of 0.149 and a zeta potential of −25.210 mV. The research identified 5 % mannitol as the optimal cryoprotectant. Compared to IXN, the half-maximal inhibitory concentration of IXN-Nps decreased to one-third, demonstrating a significant inhibitory effect on HT-29 colon cancer cells. The in vitro cumulative release rate of IXN-Nps within 24 h was 3.5 times higher than that of the IXN solution. In vivo pharmacokinetic results revealed that the oral bioavailability of IXN-Nps increased significantly by 2.8 times compared to the IXN solution. The correlation coefficient (r = 0.9227) exceeded the critical value for significance at the 0.01 (r = 0.834) level, indicating a strong correlation between in vivo and in vitro results. Consequently, the nanosuspension overcame the low solubility limitation of IXN and proved to be an effective method for enhancing the oral bioavailability of IXN

Hansen parameters and GastroPlus assisted optimized topical elastic liposomes to treat breast cancer using a novel isatin derivative

Breast cancer treatment is a global health challenge using conventional toxic chemotherapeutic agents. A novel isatin could be a promising alternative. An isatin derivative (TM-19) was synthesized and characterized using NMR (nuclear magnetic resonance), mass spectrometry, Fourier transform infrared (FTIR), and differential scanning calorimetry (DSC). HSPiP and GastroPlus predictive software were used to predict suitable solvents for solubility and in vivo oral pharmacokinetics in humans (fasted condition), respectively. Based on predictive findings, topical elastic liposomes (phosphatidylcholine as PC and span 80 by film hydration method) was prepared, characterized, and optimized using QbD (quality by design). QbD identified the impact of composition on response variables (Y1 for size, Y2 for polydispersity index, Y3 for zeta potential, and Y4 for %EE). In vitro cytotoxicity study was carried out against MCF-7 cell lines. Low molecular weight and lipophilic TM-19 was crystalline in nature (255 g/mol). GastroPlus program predicted limited in vivo dissolution and poor oral absorption (10.4 %). Results confirmed the highest TM-19 solubility in DMSO (dimethyl sulfoxide) ˃ chloroform ˃ PEG 400 (polyethylene glycol 400). Considering experimental and predicted data, topical delivery of TM-19 using optimized (desirability parameter value = 0.97) elastic liposomes (TF1) was quite promising due to optimal size (344 nm), high %EE (61.7 %), low PDI (0.45), and optimal zeta potential (− 12.34 mV). TM-19 loaded TF1 elicited concentration dependent cytotoxic effect (˃ 90 % at 10 µM) against MCF-7 as compared to TM-19 suspension.

Ultrasound-assisted enzymatic extraction of jujube (Ziziphus jujuba Mill.) polysaccharides: Extraction efficiency, antioxidant activity, and structure features

This study investigated the effect of ultrasound-assisted enzymatic extraction (UAEE) on the extraction efficiency, antioxidant activity, and structural properties of jujube polysaccharide (JPS), with hot water extraction (HWE), ultrasound-assisted extraction (UAE), and enzymatic-assisted extraction (EAE) serving as controls. Optimal extraction conditions were determined through a multi-index weighted scoring method that comprehensively accounted for yield, duration, and antioxidant activity. Results demonstrated that the JPS yield obtained by UAEE at 22/33 kHz was 10.5 % to 16.3 % higher than those achieved by the other methods, significantly enhancing antioxidant activity. Monosaccharide composition analysis revealed that UAEE increased the content of key mono-sugars in JPS. Additionally, assessments of molecular weight distribution, zeta potential, and rheological properties showed that UAEE reduced the molecular weight and apparent viscosity of JPS, resulting in a looser structural configuration. These structural modifications were observed in scanning electron microscope (SEM) images, which revealed a filamentous branched morphology in JPS obtained through UAEE. Further observations using the atomic force microscope (AFM) indicated that the polysaccharide chains extracted by UAEE were shorter in length, lower in height, and free from aggregation

Molecularly imprinting polymethacrylamide onto Cu-based metal-organic framework as a pH-sensitive core-shell nanocarrier for potential anti-cancer drug delivery.

Surface molecularly imprinted polymers (MIPs) are an efficient and rapidly advancing approach, increasingly being utilized in drug delivery systems (DDSs). This research involved synthesizing a core-shell structure, consisting of a metal-organic framework (MOF) core and a doxorubicin (DOX) imprinted polymethacrylamide shell, prepared via precipitation polymerization method in green media. The resulting MOF@MIP was utilized as a nanocarrier for DOX delivery, exhibiting high drug loading capacity and pH responsiveness delivery. The materials were characterized using different techniques such as X-ray diffraction (XRD), scanning electron microscopy (SEM), fourier transform infrared (FTIR), transmission electron microscopy (TEM), dynamic light scattering (DLS), thermal gravimetric analysis (TGA), and zeta potential (ZP). In vitro studies on DOX loading and release demonstrated that a higher amount of DOX was released in a sustained manner under tumor tissue conditions (pH 5, 41 °C) compared to normal physiological conditions (pH 7.4, 37 °C). Additionally, cytotoxicity evaluations revealed significant cytotoxic effects of DOX-loaded MOF@MIP on MCF-7 cells (IC50: 2 μg/mL). Based on these findings, the synthesized MOF@MIP shows promise as a potential candidate for the development of anticancer therapeutic delivery platforms.

Effects of interaction between wheat bran dietary fiber and gluten protein on gluten protein aggregation behavior.

Effects of wheat bran dietary fiber (WBDF) as a nutritional additive on flour products quality mainly depends on the interaction between WBDF and gluten protein. In this study, the effects and mechanisms of WBDF with different particle sizes and additive amounts on gluten protein aggregation behavior were investigated. The results showed that the addition of WBDF led to a decrease in free sulfhydryl content, particle size, molecular weight and gluten macromer (GMP) content, an increase in zeta potential and SDS-extractable protein content, and a deterioration in the gluten network morphology compared to the control group, suggesting that the aggregation behavior of gluten protein was inhibited. When WBDF was added at 3 % and 6 %, dilution effect, mechanical shear, steric hindrance, and non-covalent binding were the main mechanisms leading to depolymerization. Further addition of WBDF (9 %, 12 %) inhibited the depolymerization of gluten protein due to competitive hydration and non-covalent binding. However, when WBDF was added at 15 %, the dilution effect, mechanical shear and steric hindrance of WBDF (88 μm < particle size<150 μm) dominated, and their inhibitory of aggregation induced the formation of a loose gluten network structure. In contrast, the weaker mechanical shear and steric hindrance effects of WBDF (particle size<88 μm) mitigated the degradation of gluten network structures by WBDF.

Implementation of Silver Nanoparticles Green Synthesized with Leaf Extract of Coccinia grandis as Antimicrobial Agents Against Head and Neck Infection MDR Pathogens.

Head and neck infections (HNI) associated with multidrug resistance (MDR) offer several health issues on a global scale due to inaccurate diagnosis. This study aimed to identify the bacteria and Candidal isolates and implement the silver nanoparticles green synthesized with leaf extract of Coccinia grandis (Cg-AgNPs) as a therapeutic approach against HNI pathogens. The Cg-AgNPs were characterized by the UV-visible spectrophotometer, FT-IR analysis, Zeta particle size, Zeta potential, and field emission scanning electron microscope (FESEM) analysis to validate the synthesis of nanoparticles. Additionally, the antimicrobial activity of Cg-AgNPs was presented by the zone of inhibition (ZOI), minimum inhibitory concentration (MIC), minimum bactericidal/fungicidal concentration (MBC/MFC), and antibiofilm assay. Moreover, the cell wall rupture assay was visualized on SEM for the morphological study of antimicrobial activities, and the in-vivo toxicity was performed in a swiss mice model to evaluate the impact of Cg-AgNPs on various biological parameters. Different bacterial strains (Staphylococcus aureus, Acinetobacter baumannii, Klebsiella pneumoniae, and Pseudomonas aeruginosa) and Candida sp. (Candida albicans, Candida tropicalis, Candida orthopsilosis, and Candida glabrata) were identified. The MIC, MBC, and antibiofilm potential of Cg-AgNPs were found to be highest against A. baumannii: 1.25 μg/ml, 5 μg/ml, and 85.01±5.19% respectively. However, C. albicans and C. orthopsilosis revealed 23 mm and 21 mm of ZOI. Subsequently, the micromorphology of the cell wall rupture assay confirmed the efficacy of Cg-AgNPs, and no significant alterations were seen in biochemical and hematological parameters on the swiss mice model in both acute and subacute toxicity studies. The green synthesized Cg-AgNPs have multifunctional activities like antibacterial, anticandidal, and antibiofilm activity with no toxicity and can be introduced against the HNI pathogens.

Thermophysical and Corrosion Inhibitor Evaluation of Graphene, Aluminum Nitride and Barium Titanate Nanolubricants

A newly developed kind of fluid known as nanolubricant is produced by dispersing nanometer-sized materials in base oil. The main issue with nanolubricant is particle stability, which occurs when nanoparticles aggregate due to van der Waals forces. The aim of the study is to evaluate the performance of graphene (GR), aluminium nitride (AlN), and barium titanate (BTO) nanolubricants at 0.05 and 0.1 vol. % concentrations. The stability was identified by using sedimentation photograph capturing method and zeta potential analysis, while KD2 Pro Analyzer was used to measure the thermal conductivity, and the effect of corrosion inhibitor evaluation was measured according to ASTM D130-19. The nanolubricants are prepared by two-step method and undergo ultrasonication process to ensure the nanoparticles are well dispersed in base oil. The results showed that nanolubricants containing 0.05 vol. % nanoparticles are more stable than 0.1 vol. % nanolubricants. Nanolubricants with 0.1 vol. % showed signs of instability based on low zeta potential values. This is due to the fact that the higher the concentration of nanoparticles, the closer the nanoparticles are to one another. This increased van der Waals attraction and potentially causing nanoparticle agglomeration. Improvement in thermal conductivity was obtained with high volume concentration of GR, AlN and BTO nanoparticles. All nanolubricants achieved an ASTM Standard D130 classification of 1a based on the Copper Strip Corrosion Test Standard (slight tarnish, slight colour change). As a result, it was discovered that all prepared samples are effective anticorrosion lubricating oil additives.