Particle Size Values Research Articles

FORMULATION AND IN VITRO TESTS OF KETOPROFEN NANOSUSPENSION USING THE MILLING METHOD WITH POLYMER VARIATIONS

Objective: The aim of this research was to formulate ketoprofen nanosuspension with a variety of polymers and to compare the dissolution rate of the nanosuspensions with ketoprofen suspension. Methods: Ketoprofen nanosuspension was formulated by milling method using a different polymer such as Polyvinyl Pyrrolidone (PVP) K-30 (F1), Polyvinyl Alcohol (PVA) (F2) and Hydroxy Propyl Methyl Cellulose (HPMC) (F3). Nanosuspensions were prepared and characterized, including organoleptic, pH, particle size, zeta potential, Polydispersity Index (PI), specific gravity, crystalline state determination, physical stability at room temperature for 3 mo, and in vitro dissolution test compared with ketoprofen suspension. Results: The ketoprofen nanosuspensions with PVP K-30 and PVA showed stable preparations, while those with HPMC showed less stability, as indicated by sedimentation during storage. The particle size values of PVP K-30 and PVA were 10.004±0.03 nm; and 9.560±0.01 nm; zeta potential and polydispersity index values met the test requirements. The dissolution rate of the ketoprofen nanosuspensions was higher with a cumulative of F1, F2, and F3 were 83.35%; 85.00%, and 81.09% after 60 min, while the ketoprofen suspension was only 7.62%. Conclusion: The milling method of ketoprofen nanosuspensions with PVP and PVA has more stable physical characteristics than nanosuspension with HPMC. The ketoprofen nanosuspensions have a higher dissolution rate than the ketoprofen suspension.

Vesicular Carriers for Improved Oral Anticoagulation Competence of Rivaroxaban: In Vitro and In Vivo Investigation

Rivaroxaban is an anticoagulant for avoidance and therapy of thromboembolic disorders. Unfortunately, oral bioavailability of rivaroxaban is compromised with dose increments. Accordingly, the aim was to test nano-vesicular lipid systems for improved oral anticoagulation activity of rivaroxaban. Rivaroxaban loaded niosomes, bilosomes and spanlastic formulations were prepared. The prepared systems were assessed in terms of particle size, zeta potential, transition electron microscopic features (TEM), entrapment efficiency, in-vitro drug release, and in-vivo anticoagulation performance in rats. The prepared vesicular systems exposed spherical negatively charged vesicles with mean particle size values between 136.6 nm to 387.9 nm depending on the composition. Rivaroxaban was efficiently entrapped in the vesicular systems with entrapment efficiency values ranging from 92.4% to 94.0%. Rivaroxaban underwent sustained release from the fabricated vesicular systems. The in vivo performance of the tested preparation revealed significant enhancement of the anticoagulation parameters. This was manifested from the prolonged clotting time, and prothrombin time. Moreover, the cut tails of the examined rats receiving the formulated nano-systems exposed a lengthy tail bleeding time compared to those receiving the un-processed rivaroxaban aqueous dispersion. In Conclusion, niosomes, bilosomes and spanlastic nano-dispersions have a potential to overwhelm the oral anticoagulation efficiency of rivaroxaban with spanlastic ranked as best.Graphical

Non-destructive measurement of the dispersion of High-density polyethylene/Polystyrene blends using near-infrared diffuse reflectance spectroscopy based on deep learning

The dispersion of polymer blends significantly influences their overall performance. However, current methods for characterizing dispersion are destructive and time-consuming. In this study, a near-infrared (NIR) regression model was first developed for the measurement of cumulative particle size distribution function (CDF) of dispersed particles in polymer blends, thus indirectly and quantitively characterizing dispersion. High-density Polyethylene/Polystyrene (HDPE/PS) with varying dispersed particle sizes were prepared by adjusting the content of PS, flow field intensity during processing, and viscosity ratio between HDPE and PS. Scanning electron microscopy (SEM) was used to provide reference particle size values for calibrating the NIR data. Deep-learning methods were used for the model building. Compared to traditional partial least-square regression, deep learning methods demonstrated superior fitting ability, The best-performing model, an MLP with three hidden layers, achieved an coefficient of determination (R2) of approximately 0.93 on the independent test set. The predicted CDFs closely matched the actual values, with no significant deviations observed. This study provides a non-destructive and time-saving new method for characterizing the dispersion of polymer blends.

Formulation of Polyethylene Glycol Based Ibuprofen Nanosuppository Preparations and Assesment of Dissolution

Ibuprofen is widely formulated in oral and rectal dosage forms. Ibuprofen in the rectal route shows c max and t max longer than syrup preparations, this is due to the low solubility of ibuprofen. Nanoparticles are one of the technologies that are widely used to increase the solubility of an active substance. Nanoscale particle size, can increase the solubility of ibuprofen and allow dose reduction. This study aims to formulate ibuprofen nanosuppository preparations, and test the percent dissolution of nanosuppositories compared to conventional suppositories. The ibuprofen nanosuppository formulation consists of ibuprofen lipid component and PEG mix component (PEG 4000: PEG 6000). The ibuprofen lipid component consisted of ibuprofen VCO oil, tween 80 and propylenglycol. This lipid component was then tested for physical characteristics, transmittance, particle size and zeta potential, then the lipid was added to the suppository base component. The responses observed were disintegration time, hardness, and non-intrinsic dissolution efficiency. The test results showed transmittance values of 91.98%, 92.99%, 93.26%. Particle size and potential zeta values of FI = 107, 5 nm, FII 102 nm and FIII 103 nm. The zeta potential were -16.19 mV, -12.44 and -13.25 mV in the lipid component. The test results of the disintegration time of F1, F2, F3 nanosuppositories were 12 minutes, 11 minutes and 10 minutes. The hardness of F1, F2, and F3 were 1.53 kg, 1.43 kg and 1.26 kg and the dissolution efficiency value was higher than conventional suppositories. Modification of ibuprofen nanosuppositories had a significant effect on the percent dissolution of ibuprofen.

Synthesis, Structural, Morphology and Magnetic Properties: Effect of La on Multiferroic Nature of BiFeO3 Nanoparticles

Objectives: The present study focuses on developing La-doped BiFeO3 multiferroic materials for dielectric absorber applications. Methods: The samples are characterized by X-ray Diffractometer (XRD). Further, the morphology is examined using field emission electron microscopy (FESEM) and Transmission Electron Microscopy (TEM). The dielectric parameters and ac-electrical parameters are carried out by impedance spectroscopy. The magnetic properties are studied using a vibrating sample magnetometer VSM, P-E loop. Findings: XRD confirms the rhombohedral (trigonal) structure of BLFO nanoparticles. The grain and particle size values are determined by SEM and TEM, respectively. The dielectric and ac-electrical parameters for all the samples are thoroughly discussed at room temperature. The Maxwell-Wagner or interfacial polarization is noticed at low input field frequencies for x=0.2-0.8. The impedance analysis shows the contribution of grain and its boundary in the electrical conduction mechanism. The multiferroic behavior is examined using M-H loops, P-E loops, and μi-f plots. Novelty: The samples are synthesized by the hydrothermal process to prepare La-doped BiFeO3 nanomaterials. Keywords: Nanoparticles, Electron Microscopy, Multiferroic, Magnetization, Polarization, Permeability

Unlocking the wound healing potential of Anastatica hierochuntica L. (Kaff Maryam) Extract's nanosuspension: UPLC-MS/MS metabolic profiling, formulation development and statistical optimization

BackgroundAnastatica hierochuntica L. (Kaff Maryam) is a desert plant with documented therapeutic applications. Various medicinal uses have been reported for the plant extract such as antioxidant, anti-inflammatory, antifungal, antimicrobial, hypoglycemic, hypolipidemic, and hepatoprotective activities. The abundant plants constituents are promising and encourage the investigation of novel therapeutic uses. The principal objective of this study was to identify the bioactive constituents of A. hierochuntica (AH) by phytochemical profiling of its ethanolic extract, alongside an investigation of its wound healing efficacy after being formulated into nanosuspension for topical localized wound treatment. MethodA comprehensive metabolomics study of the ethanolic extract of A. hierochuntica aerial parts was assessed using UPLC MS/MS technique. Additionally, the preparation of AH nanosuspension was executed utilizing the antisolvent-precipitation method. A D-optimal experimental design was adopted to investigate the influence of variables such as: stabilizer ratio, antisolvent: solvent ratio, and stabilizer type on particle size (PS), polydispersity index (PDI), and zeta potential (ZP). The design also was employed in the optimization process. The selected optimal formula was further assessed for size characteristics, morphological identification by TEM, storage stability, FTIR, cytocompatibility with human skin fibroblast (HSF), and scratch assay on HSF to assess wound healing aptitude. ResultsChemical profiling of the aerial parts revealed an abundance of glucosinolates, flavonoids, flavolignans, and fatty acids. The optimized AH-nanosuspension showed small particle size (128.87 ± 26 nm), small PDI (0.136 ± 0.05), and high ZP absolute value (−37.53 ± 0.52 mV). Furthermore, TEM photography of the optimal nanosuspension formula exhibited circular non-aggregating nanosized particles. FTIR confirmed the successful formulation of the AH ethanolic extract into nanosuspension with no physicochemical interactions. Additionally, AH-nanosuspension demonstrated cytocompatibility with HSF with IC50 = 58.317 μg/mL. Moreover, both AH pure extract and AH-nanosuspension exhibited a remarkable cell migration rate and wound closure % which propounds an auspicious wound healing potential. ConclusionThe study accentuates the supremacy of the nanosized delivery approach of AH aerial parts ethanolic extract and warrants further in-vivo investigations to establish its clinical utility for wound management.

Enhancing Herbal Efficacy: Synthesis and Evaluation of Nanosuspension from Withania somnifera Root Extract

Background: Ayurveda emphasizes the balance of mind, body, and spirit, drawing on ancient texts that highlight the medicinal properties of herbs like Withania somnifera, known for its wide range of therapeutic applications and pharmacological benefits. Commonly referred to as Indian ginseng or Ashwagandha, Withania somnifera, demonstrates a variety of therapeutic effect , including anti-inflammatory, antitumor, sedative, hypnotic, deobstruent effects, narcotic, antioxidant, tonic, antistress, diuretic, aphrodisiac, immunomodulatory, and rejuvenating properties. Nanotechnology, particularly through the development of nanosuspensions, offers a significant advancement in medicine, addressing challenges like poor solubility and low bioavailability of lipophilic drugs. Nanosuspensions can enhance drug safety and efficacy by improving solubility and altering pharmacokinetics. Methods: This study focuses on formulating and characterizing a nanosuspension using an ethanolic extract of Withania somnifera roots. The nanosuspension (NSWS) underwent comprehensive characterization, utilizing techniques such as FT-IR spectroscopy, particle size analysis, zeta potential measurement, polydispersity index (PDI) assessment, Field emission scanning electron microscopy (FESEM), X-ray diffraction analysis, pH measurement, and stability testing. This study seeks to explore the potential of nanosuspensions, aiming to integrate nanotechnology with herbal medicine to improve the safety and efficacy of herbal formulations. Results: The nanosuspension (NSWS) shown particle size about 133.09 nm, and its uniform particle distribution was indicated by a Polydispersity Index (PDI) about 0.27. Stability and uniformity were further supported by the zeta potential, particle size, and PDI values. Conclusion: Nanosuspension formulations represents a versatile strategy to improve the therapeutic efficacy of hydrophobic drugs across various routes of administration. Keywords: Withania somnifera, Nanosuspension, Characterization, FT-IR, PDI, FESEM

Mechanism study on the improvement of egg white emulsifying characteristic by ultrasound synergized citral: Physicochemical properties, molecular flexibility, protein structure

As a natural emulsifier, egg white protein (EWP) has great interfacial characteristics and high security, and has broad development prospects. This study explored the impact of ultrasound synergized citral (CI) treatment on the microstructure, molecular flexibility and emulsifying property of EWP, and predicted the interaction between CI and ovalbumin (the main protein in EWP) through molecular docking. The decrease in free amino content and the growth in molecular weight of EWP suggested that CI and proteins were successfully grafted. The results of physicochemical properties revealed that UCEWP (ultrasound synergized citral-treated EWP) had smaller particle size and larger ζ-potential absolute value, which meant that the stability of UCEWP system was enhanced. From the perspective of interfacial characteristics, UCEWP had lower interfacial tension, which remarkably improved its emulsifying property. The emulsifying activity index (EAI) and emulsifying stability index (ESI) of UCEWP were 1.99 times and 3.19 times higher than that of natural EWP (NEWP). Analysis of Fourier transform infrared spectroscopy (FT-IR) and fluorescence spectroscopy illustrated that the secondary and tertiary structures of UCEWP were more disordered and stretched than those of EWPs. Protein microstructure demonstrated that UCEWP presented loose small particle distribution, and correlation analysis reflected that the improvement of molecular flexibility was positively correlated with the enhancement of emulsifying property. These results elucidated that ultrasound synergized CI treatment is an effective mean to improve the molecular flexibility and emulsifying property of EWP, which provides a valuable reference for further application of EWP.

Ultrasonic-Assisted Marine Antifouling Strategy on Gel-like Epoxy Primer

Ultrasonic technology has drawn extensive interests for its great potential in marine antifouling applications. However, its effects on the adhesion behavior of marine fouling organisms on marine structures remain underexplored. This work investigated how ultrasonic treatment impacted the adhesion of Pseudoalteromonas on a gel-like marine epoxy primer. And the process parameters for ultrasonic treatment were optimized using response surface analysis with Design-Expert software 11. The results revealed that ultrasonic treatment disrupted the cellular structure of Pseudoalteromonas, causing the deformation and fragmentation of the cell membrane, leading to bacterial death. Additionally, ultrasonic treatment reduced the particle size and Zeta potential value of Pseudoalteromonas, which disrupted the stability of bacterial suspensions. It also increased the relative surface hydrophobicity of Pseudoalteromonas cells, resulting in a reduction in adhesion to the gel-like marine epoxy primer. This study demonstrated that ultrasonic treatment significantly disturbed the adhesion behavior of microorganisms like Pseudoalteromonas on the gel-like marine epoxy primer, which provided an effective approach for controlling marine biofouling.

Study on Preparation and Properties of Pickering Emulsions Prepared by Carboxymethyl Starch‐Xanthan Gum Nanoparticles

AbstractIn this work, carboxymethyl starch‐xanthan gum nanoparticles (CXN) with different ratios are prepared by ethanol precipitation method. The effects of different ratios, NaCl content, and pH on the particle size and zeta potential of the nanoparticles are investigated, as well as the rheological properties and stability of the CXN emulsions. The results show that with the increase of xanthan gum (XG), the particle size, and zeta potential of the nanoparticles decrease and the prepared emulsions have higher shear stress and viscosity, as well as greater thermal and storage stability. Changes in pH and NaCl concentration significantly affect the particle size and zeta potential values of the nanoparticles. Excess acids or bases increase the viscosity of the emulsions. At low salt concentrations (0.05 M), the emulsion viscosity increases significantly, after which the emulsion viscosity decreases with increasing salt concentration. Neutral pH conditions at room temperature are not conducive to the stability of the emulsions. At high temperatures (100 °C), high salt concentrations, excessive acids or bases can destabilize emulsions. This study provides a new way to reduce the particle size of nanoparticles and a feasible strategy for developing long‐term stable Pickering emulsion.

Simulation study on mitigating permeate flux decline with electroosmotic flux in dead-end ultrafiltration process

Piezoelectric membranes establish electrokinetic phenomena, including electroosmotic flow, to mitigate membrane fouling in the ultrafiltration process. This study employs numerical simulations to evaluate the role and impact of the electroosmotic flux effect on permeate flux decline and fouling mechanisms in the dead-end filtration process for silicon dioxide particles. This research demonstrates that electroosmotic flux significantly alleviates flux decline across varying values of surface zeta potential, membrane porosity, particle size and inlet concentration. Specifically, the electroosmotic flux effect is most pronounced in reducing flux decline when the surface zeta potential is higher and the membrane structure is more porous. This reduction in flux decline is attributed to the enhanced lift and drag forces generated by electroosmotic flux near the electrical double layer, which prevents rapid initial adhesion and subsequent fouling, such as internal blocking and cake layer formation. Additionally, the electroosmotic flux effect is most effective with smaller particle sizes and higher feed concentrations, helping to mitigate flux decline that would otherwise occur in the absence of electroosmotic flux. Compared to experimental and modelling investigations, the electroosmotic flux effect is shown to complement a reduction in permeate flux drop to facilitate the longevity of membranes in the ultrafiltration process.

Investigation on the influence of particle size and porosity on solid phase fluidization and heat transfer in carbon fibre porous media

AbstractIn this paper, the 3D pore structure was reconstructed and solid phase fluidization in porous media was investigated. Based on the two fluid model, a computational fluid dynamics (CFD) model of gas–solid fluidization was established and the influence of particle size and porosity were investigated. When porosity was constant, during the fluidization process, the particle velocity and solid concentration standard deviation gradually decreased, and the bed height increased. At the same time, the smaller the particle size was, the smaller the solid concentration standard deviation was, the faster the bed height increased, and the more the particle temperature decreased. Based on the fixed value of particle size, when studying the effect of porosity on fluidization, it was found that with the enhancement of solid‐phase fluidization, particle velocity, solid concentration standard deviation, and particle temperature decreased, and bed height increased. Moreover, when porosity was large, particle velocity decreased rapidly, and solid concentration standard deviation reached a smaller minimum value, which took a longer time. Within the same time, the particle temperature also decreased less.

Development of vitamin D3 and Spirulina platensis protein hydrolysates co-loaded nanoliposomes and coated by sodium caseinate

The objective of this study was to investigate the co-loading of vitamin D3 (VitD3) and Spirulina platensis protein hydrolysates (SPH) within coated nanoliposomes (NLPs) by sodium caseinate, with the intention of developing a novel nutritional supplement. The coated NLPs exhibited particle size, PDI, and zeta potential values of 185.30 ± 29.62 nm, 0.22±0.04, and +18.70 ± 3.44 mV, respectively. Moreover, the encapsulation efficiencies of the coated NLPs for VitD3 and SPH were 83.24 ± 4.22 % and 89.41 ± 4.36 %, respectively. The improving effect of the surface coating by sodium caseinate on the stability and function of the NLPs was exhibited through analysis of chemical structure, thermal stability, and crystalline structure. The transmission electron microscopy pictures of the developed NLPs revealed a spherical morphology with a thin layer around the vesicle. The loaded VitD3 and SPH in the coated NLPs showed controlled release profiles during incubation in the simulated gastrointestinal condition. Moreover, the VitD3/SPH co-loaded NLPs and their coated form had no considerable cell toxicity. To conclude, the developed nanosystem demonstrated the suitable characteristics of a nanocarrier for reaping the nutritional benefits of VitD3 and SPH.

Evaluation of protein-polysaccharide interactions through ζ-potential and particle size measurements to assess their functionality in wine.

Protein-polysaccharide-tannin interactions are important in every aspect of red wine production from physical stability to color, astringency, and body. For this model study, bovine serum albumin (BSA) was selected as the protein, while carboxymethyl cellulose (CMC), mannoproteins, and pectin were the model polysaccharides. Each protein-polysaccharide combination was analyzed for zeta (ζ) potential and particle size at neutral pH and within the wine-like solution. Mixtures were assessed regarding their protective, affinitive, and aggregative behaviors. Based on their individual ζ-potentials, pectin and mannoprotein were most stable at lower concentrations. At higher concentrations, they reduced the suspension's stability and increased the aggregate sizes. CMC consistently increased the stability of any solution under neutral pH conditions. However, with increasing concentrations, these large aggregates are expected to precipitate. Fruit pectin (FP) and BSA interactions seemed to be the main factors in the formation of visible precipitates at neutral pH. FP and the mannoprotein decreased stability enough to cause precipitation without haze formation. The mannoprotein decreased particle sizes, in both the suspension and precipitation, which may indicate greater selectivity toward proteins. FP also decreased the suspended particle sizes under wine conditions. These findings demonstrate the use of ζ-potential and particle size values to characterize macromolecular interactions in model systems and can also be used to indicate effective fining agents. PRACTICAL APPLICATION: This work demonstrates the capabilities of ζ-potential analysis paired with size particle measurements to predict and characterize the interactions between macromolecules in complex systems. The interactions between model wine macromolecules can be evaluated with this technology at a level that cannot be reached with any other analytical technique.

Comparison of free vs. liposomal naringenin in white adipose tissue browning in C57BL/6j mice

Naringenin may play a role in browning by increasing thermogenic gene expression. In this study, we encapsulated naringenin using a liposomal formulation and examined the effects of both free and liposomal naringenin on white adipose tissue browning in C57BL6/J mice. In the first phase of the study, naringenin was encapsulated by the liposome method, which is biocompatible and biodegradable. The physical and chemical properties of liposomal naringenin were tested. In the second phase, a total of 48 six-week-old mice were divided into two main groups: prevention and recovery. Each main group was divided into four subgroups: nano-naringenin, void, free-naringenin, and control. The prevention group received a high-fat diet for 10 weeks along with weekly intravenous injections of 20 µM naringenin. On the other hand, the recovery group was first subjected to a high-fat diet for 10 weeks, followed by an additional 10 weeks of the same diet, along with weekly intravenous injections of 20 µM naringenin. Body weight was measured once per week, and brown adipose tissue, inguinal white adipose tissue, and serum samples were collected from each mouse. The mean particle size, polydispersity index and zeta potential values of liposomal naringenin were ∼207 nm, 0.35, and −27 mV, respectively. The encapsulation and loading efficiencies of liposomal naringenin were 94.6 and 19.2%, respectively. Liposomal naringenin exhibited sustained-release behavior, while free naringenin showed a burst-release profile. Liposomal naringenin showed the best physical stability in light and at 4 °C, while free naringenin was more chemically stable in light and at 4 and 22 °C. Free and liposomal naringenin did not significantly reduce weight gain. In the prevention group, liposomal naringenin increased PRDM16 gene expression in inguinal white adipose tissue 4.29 times more than free naringenin (p = 0.010). However, neither formulation significantly altered the expression levels of other browning or adipogenesis markers in the tissues. The results suggest that free naringenin can be efficiently encapsulated in biocompatible and biodegradable nanoparticles. Further research is needed to better understand the physiological effects of liposomal naringenin.

Exosomal fragment enclosed polyamine-salt nano-complex for co-delivery of docetaxel and mir-34a exhibits higher cytotoxicity and apoptosis in breast cancer cells

A novel core–shell nanocarrier system has been designed for co-delivery of a small anticancer drug, docetaxel (DTX) and tumor suppressor (TS) miR-34a named as Exo(PAN34a+DTX). The core is formed by pH dependent polyamine salt aggregates (PSA) containing both the payloads and the shell is formed by RAW 264.7 cell derived exosomal fragments. Herein, phosphate driven polyallylamine hydrochloride (PAH, MW:17,500 Da) PSA was formed in presence of miR-34a and DTX to form PAN34a+DTX. The formulation exhibited pH dependent DTX release with only 33.55 ± 2.12% DTX release at pH 7.2 and 75.21 ± 1.8% DTX release till 144 h at pH 5.5. At 1.21 molar ratio of phosphate to the amine (known as R value), efficient complexation of miR-34a (3.6 μM) in the PAN particles was obtained. PAN34a+DTX demonstrated particle size (163.86 ± 12.89 nm) and zeta-potential value of 17.53 ± 5.10 mV which upon exosomal fragment layering changed to − 7.23 ± 2.75 mV which is similar to the zeta-potential of the exosomal fragments, i.e., − 8.40 ± 1.79 mV. The final formulation Exo(PAN34a+DTX), loaded with 40 ng/mL DTX and 50 nM miR-34a exhibited 48.20 ± 4.59% cytotoxicity in triple negative breast cancer (TNBC) cells, 4T1. Co-localization of CM-DiI (red fluorescence) stained exosomal fragments and FAM-siRNA (green fluorescence) in the cytoplasm of 4T1 cells after 6 h of Exo(PANFAM) treatment confirmed the efficiency of the designed system to co-deliver two actives. Exo(PAN34a+DTX) also reduced BCL-2 expression (target gene for miR-34a) by 8.98 folds in comparison to free DTX confirming promising co-delivery and apoptosis inducing effect of Exo(PAN34a+DTX) in 4T1.

Ultrasound effect on a biorefinery lignin-cellulose mixture

Forest biorefineries provide multiple new avenues for applied research. The main concept lies in the malleability of the processes and their stepwise organization. The core element of the biorefinery concept addressed in the present study is the pretreatment step; here, wood biomass is converted into free hemicellulosic sugars, lignin and cellulose. In traditional approaches, the pretreatment step is a starting point for isolating and separating lignin or cellulose through different processes. In this study, instead of performing any separation, a lignin-cellulose mixture was used as its own material, and the effects of ultrasound treatment with a probe system at 20 kHz, with various amplitude, sonication time and dry matter content were investigated with the aim of assessing the formation of a nanocellulose structure with a high lignin content (>30 %) and investigating the stability of the lignin-cellulose mixture under aqueous conditions. We demonstrated the importance of dry matter content for the specific particle size and water retention values for this mixture. US treatment of lignin-cellulose mixtures <4 % dry matter formed a gel-like material, with low particle size (90 % below 30 μm and smallest at nanoscale). Low dry matter loading led to better US transfer and higher conversion of cellulose to <100 nm nanoparticles. Our study can serve as a baseline for future developments in the field of stable emulsions, filtering materials or inputs for material synthesis.

Optimization of the Encapsulation of Vitamin D3 in Oil in Water Nanoemulsions: Preliminary Application in a Functional Meat Model System.

Meat products containing Vitamin D3 (VD3) are an innovative option that could contribute to reducing deficiencies in this micronutrient. Designing nanoemulsions that carry VD3 is the first step in developing functional meat products. Thereby, this study investigated the impact of food components on the nanoemulsion properties. A central composite design was used to study the effects of pea protein (PP, 0.5-2.5%), safflower oil (SO, 5-15%), and salt (0-0.5%) on the nanoemulsion stability (ζ-potential and particle size) and the VD3 retention. Also, the optimized nanoemulsion carrying VD3 was incorporated into a meat matrix to study its retention after cooking. The combination of food components in the optimized nanoemulsion were SO = 9.12%, PP = 1.54%, and salt content = 0.4%, resulting in the predicted values of ζ-potential, particle size, and VD3 retention of -37.76 mV, 485 nm, and 55.1%, respectively. The VD3 that was nanoencapsulated and included in a meat product remained more stable after cooking than the VD3 that was not encapsulated. If a meat product is formulated with 5 or 10% safflower oil, the stability of the nanoencapsulated VD3 is reduced. This research contributes to developing functional meat products carrying nanoencapsulated vitamin D3 in natural food-grade components.

Bioavailability of Liposomal Vitamin C in Powder Form: A Randomized, Double-Blind, Cross-Over Trial

The purpose of this study was to evaluate the properties and pharmacokinetics of liposomal vitamin C in powder form obtained by a method devoid of organic solvents. The powder and liposome morphology were analyzed using scanning electron microscopy (SEM) and cryogenic transmission electron microscopy (cryo-TEM), respectively. Additionally, the carrier particle size, size distribution (STEP-Technology®; L.U.M. GmbH, Berlin, Germany), and zeta potential value were determined. The pharmacokinetic parameters of liposomal and non-liposomal vitamin C (AUC, Cmax, C10h, and C24h) were compared in a randomized, single-dose, double-blind, cross-over trial (ClinicalTrials.gov ID: NCT05843617) involving healthy adult volunteers (n = 10, 1000 mg dose). The process of spray drying used to transform liquid suspensions of the liposomes into powder form did not adversely affect the quality of the carrier particles obtained. Compared to non-encapsulated vitamin C, oral administration of the liposomal formulation resulted in significantly better absorption of ascorbic acid into the bloodstream, which equated to a higher bioavailability of the liposomal product (30% increase in AUC, p &lt; 0.05). The duration of elevated vitamin C blood levels was also longer (C24h increase of 30%, p &lt; 0.05). Although the results obtained are promising and suggest higher bioavailability for the liposomal form of vitamin C, the limited sample size necessitates further research with a larger cohort to confirm these findings.

Modified release, enriched biocompatibility, and enhanced oral bioavailability as precious features of nitrofurantoin-loaded polymeric nanoparticles

Nitrofurantoin (NTF) is a first-line therapy for treating urinary tract infections. However, gastric upset, short half-life, and poor bioavailability of NTF are major challenges for clinical use. Hence, the current work incorporated NTF in polymeric nanoparticles (NPs).NTF-loaded NPs (NTF-NPs) were prepared using Eudragit RS100 (RS100), DL-lactide/glycolide copolymer (PLGA), and their mixture at a ratio of 1:1 w/w (RS100/PLGA) as polymers. Pluronic F68, Tween 80, and polyvinyl alcohol (PVA) were applied as stabilizers. The particle size (PS), polydispersity index (PDI), zeta potential (ZP), and entrapment efficiency were determined. Three optimized formulations of NPs; F3, F13, and F29 were selected for further coating with Eudragit L100 (L100) and Eudragit S100 (S100). The optimized NPs and the corresponding coated ones were evaluated for solid-state characterization, morphology, and in vitro release. L100-coated F13 (LCF13) was further investigated for biocompatibility with normal oral epithelial cell (OEC) and Vero cell lines. A pharmacokinetic study using a rat model was also conducted.The results revealed that Tween 80 and PVA-stabilized NPs accomplished a nano-sized range with polymer- and stabilizer-dependent PDI and ZP. Optimized formulations: F3, F13, and F29 were selected for further coating where PS and PDI values not exceeding 260 nm and 0.502, respectively. The coated NPs had negative ZP ranging from −11.00 ± 2.70 to −40.20 ± 1.40 mV, attributable to the L100 or S100 coating. The solid-state characterization confirmed a transition of NTF to amorphousness. The spherical shape with the distinctive halo-like appearance of the coated NPs was proved. Additionally, the coating warranted a prolonged release of NTF especially for LCF13 avoiding the burst effect. Allowing enriched biocompatibility, LCF13 showed an IC50 value of 224.00 ± 9.20 μM for the OEC cell line, whereas a greater IC50 exceeding 300 μM was recognized for the LCF13-treated Vero cell line. After a single oral dose, LCF13 could provide a discernible increase in the extent of absorption (Du∞ = 863.31 ± 73.71 μg) with a significant extension of the absorption rate (tmax and t1/2 of 3 and 2.51 ± 0.317 h, respectively).LCF13 could be considered a controlled and safe nanocarrier that delivered significantly higher levels of NTF for a longer duration than NTF dispersion.