High Zeta Potential Research Articles

Preparation and Optimization of Olanzapine as Transdermal Nanoparticles Delivery System

Background: The treatment of schizophrenia typically involves the use of olanzapine (OLZ), a typical antipsychotic drug that has poor oral bioavailability due to its low solubility and first-pass effect. Objective: To prepare and optimize OLZ as nanoparticles for transdermal delivery to avoid problems with oral administration. Methods: The nanoprecipitation technique was applied for the preparation of eight OLZ nanoparticles by using different polymers with various ratios. Nanoparticles were evaluated using different methods, including particle size, polydispersity index (PDI), entrapment efficiency (EE%), zeta potential and an in vitro release study. The morphology was evaluated by a field emission scanning electron microscope (FESEM) and an atomic force microscope (AFM). We also perform differential scanning calorimetry (DSC). Results: Characterization studies of OLZ nanoparticles showed that OLZ-6 was the best formula with a particle size of 115.76 nm, a PDI of 0.24, a high EE% of 78.4%, and a high zeta potential of -19.01 mV. The in vitro release of OLZ was higher than that of other formulations. FESEM reveals the spherical shape of the nanoparticles, and AFM screening confirms that the OLZ-6 size is comparable to what the Zeta sizer finds. The DSC results confirm the purity of OLZ and the compatibility between the drug and polymer. Conclusions: OLZ-6, as a transdermal delivery system, is a promising formula to overcome the problems associated with oral drug administration and could enhance its bioavailability.

HSPiP and QbD oriented optimized green nanoemulsion to treat chloramphenicol contaminated water

Nanoemulsion is an isotropic and kinetically stable system used for multiple purposes. Exhaustive flow of chloramphenicol (CAMP) in the water systems raised global thereat to aquatic and human lives. Innate cohesive energy of the material is the basis of predictive HSPiP program. We aimed to prepare biocompatible nanoemulsion employing eugenol oil, lecithin, tween 80, and propylene glycol) for the contaminated water treatment. Furthermore, experimental design oriented robust nanoemulsion (OCEN1) investigated the impact of composition, CTime (exposure time), and nanoemulsion characteristics on percent removal efficiency (%RE). Thermodynamic stability study was conducted at different temperatures. Finally, the presence of CAMP in the treated water was negated by ICP-OES (inductively coupled plasma-optical emission spectroscopy). HSP (Hansen solubility parameters) and experimental solubility data were the basis of excipient selection. A blend of tween-80 and lecithin served as surfactant mixture (Smix) to stabilize nanoemulsion. OCEN1 was associated with high desirability (D = 0.93), low size (43 nm), low PDI (0.19), high %RE (90.72 % over period of 17 min of exposure time), optimal viscosity (1.12 cP), and high zeta potential (−25 mV). Experimental design identified significant impact of composition, exposure time (CTime), and nanoemulsion characteristics on %RE as prime factors to consider before wastewater treatment plant installation. Thus, the approach is simple, rapid, ecofriendly, and scalable to treat CAMP contaminated water with high selectivity and efficiency.

Nanostructured lipid carriers loaded with essential oils: a strategy against SARS-CoV-2

This work aimed to investigate the effectiveness of Lippia sidoides and Syzygium aromaticum essential oils (EOs) encapsulated in nanostructured lipid carriers (NLCs) as SARS-CoV-2 inhibitors through virucidal activity assessment. We developed anionic and cationic NLCs loaded with the EOs and assessed their physicochemical properties and SARS-CoV-2 virucidal activity, focusing on the effects of EO type and the NLCs composition. The NLCs exhibited particle sizes of 141.30 to 160.53 nm for anionic and 109.30 to 138.60 nm for cationic types, with PDIs between 0.16 and 0.25. High zeta potentials (>29.0 in modulus) indicated stable formulations. The NLCs effectively encapsulated the EOs, achieving encapsulation efficiencies between 84.6 to 100% w/w of marker compound. The EOs-loaded NLCs reduced the SARS-CoV-2 virion count, exceeding 2 logs over the control. NLCs loaded with Lippia sidoides and Syzygium aromaticum EOs represent an innovative strategy for combating SARS-CoV-2.

Antibacterial and anti-inflammatory Bi-functional carbon dots hydrogel dressing for robust promotion of wound healing

The abuse of antibiotics leading to bacterial resistance has emerged as a significant impediment to wound healing. Consequently, this study developed antibacterial and anti-inflammatory bi-functional carbon dots (AAB-CDs) as the primary active material for the preparation of hydrogel wound dressings, aiming to promote wound healing. The synthesized AAB-CDs exhibited ultra-small size (2.3 nm), abundant surface functional groups, high Zeta potential (30.9 mV), and excellent biocompatibility. The positively charged AAB-CDs with outstanding antibacterial properties, mitigating the risk of bacterial resistance, while the abundant surface functional groups imparted stable antioxidant performance for sustained wound anti-inflammatory effects. Moreover, in vitro experiments demonstrated that the hydrogel dressings exhibited remarkable antibacterial properties against Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus), and significantly promoted the proliferation of L929 fibroblasts. In vivo experiments further substantiated the feasibility of the hydrogel dressings in promoting wound healing and histological analysis revealed the biological mechanisms underlying the promotion of wound healing. In conclusion, AAB-CDs with robust antibacterial and anti-inflammatory properties hold tremendous potential for promoting wound healing, providing practical insights for the biological application of CDs.

Flow synthesis of silver nanoparticles using water in supercritical CO2 emulsion

Rapid and continuous synthesis of metal nanoparticles using green solvent system is still a serious challenge for both fundamental and practical research. In this work, we report a new flow process using water in supercritical CO2 (w/scCO2) emulsion and applied it to the synthesis of silver nanoparticles (AgNPs). To investigate the performance of our system, AgNPs were synthesized by batch, flow and w/scCO2 emulsion flow system at 40 ºC while using AgNO3, NaBH(OAc)3, trisodium citrate and Aerosol-OT as precursor, reducer, stabilizer and emulsifier. As a result, we demonstrated that water droplets in w/scCO2 emulsion significantly contribute to a rise in the size controllability and productivity (product yield). Additionally, w/scCO2 emulsion flow process allowed the control of mean size from 4.0 to 36.6 nm and yield from 25% to 65% by changing the CO2 pressure and Aerosol-OT concentration. Furthermore, synthesized AgNPs successfully gave citrate-modified surface with high zeta potential of –54 mV and the transparent water dispersion with unimodal size distribution, showing promising potential to allow various practical applications.

Linezolid Loaded Nanoparticle for Topical Administration of Diabetic Foot Treatment: Formulation, In Vitro and Ex Vivo Characterization

The aim of this research work was to develop a topical gel formulation containing nanoparticle to diabetic foot ulcer (DFU). In this respect, the nanoparticle formulations were prepared by using spontaneous emulsification technique. The linezolid (LZD) loaded nanoparticle formulation exhibited an low average particle size (PS) of 195.27±5.42 nm, low polydispersity index (PI) of 0.214±0.019, a high zeta potential (ZP) of 20.57±0.35 and high drug entrapment efficiency (EE) of 99.746±0.021%. In order to enhance topical residence time, the LZD-loaded nanoparticles were dispersed in a gel formulation using Methocel TM K4M (HPMC) and Carbopol® 974 P NF. The formulated gels demonstrated favorable characteristics, including an appropriate pH value, suitable mechanical performance, and desirable viscosity and spreadability for topical administration. All formulations displayed pseudoplastic flow and exhibited typical gel-type mechanical spectra at the specified frequency value. Moreover, the developed formulation achieved sustained drug release as intended for these systems. During the ex vivo drug diffusion studies, 0.007±0.004% of LZD was found in receptor phase, and this was an indicator of local effect. The optimum formulation was stable for 6 months. The initial findings suggest that the formulated topical gel containing LZD-loaded nanoparticles holds promise as an effective drug delivery system for DFU management. However, further comprehensive investigations are required to substantiate this hypothesis.

Study on the Interaction of Polymeric Chemical Additives with Phase Change Materials in Air Lime Renders.

The interaction of microencapsulated phase change materials (PCMs) with polymeric chemical additives in an air lime binding matrix was studied. These polymer-based additives included an adhesion booster (derived from starch) and a superplasticizer (polycarboxylate ether). Two different PCMs with melting points of 18 °C and 24 °C were assayed. The microcapsules were composed of melamine, with paraffin-based PCM cores. Measurements of zeta potential, particle size distribution, adsorption isotherms, and viscosity analyses were performed to comprehend the behavior of the polymer-based additives within the air lime matrix and their compatibility with PCMs. Zeta potential experiments pointed to the absence of a strong interaction between the lime particles and the microcapsules of PCMs. At the alkaline pH of the lime mortar, the negative charge resulting from the deprotonation of the melamine shell of the microcapsules was shielded by cations, yielding high positive zeta potential values and stable dispersions of lime with PCMs. The polycarboxylate ether demonstrated the ability to counteract the increase in mixing water demand caused by the PCM addition in the lime matrix. The dispersing action of the superplasticizer on the lime particles was seen to exert a collateral dispersion of the PCMs. Conversely, despite the positive values of zeta potential, the addition of the starch-based additive resulted in the formation of large PCM-lime clumps. Air lime renders incorporating 5, 10, and 20% PCMs by weight with various dosages of these chemical additives were experimented with until the optimal formulation for the specific application of the mortars as renderings was achieved. This fine-tuned formulation effectively tackled issues commonly associated with the addition of PCMs to mortars, such as poor adhesion, crack formation, and reduced fluidity.

Natural Polymer-Based Nanogel for pH-Responsive Delivery of Sorafenib Tosylate in Hemangiosarcoma.

Smart nanomedicinal treatment for cancer manifests a solubility challenge with inherent nanoscale size and nonspecific release with stimuli-responsive potential. This is the limelight in novel chemotherapy to pursue physiochemical differences between the tumor microenvironment (TME) and normal cells, which introduces active groups of nanocarriers responding to various stimuli, endowing them with concise responses to various tumor-related signals. The nanogels were successfully prepared by a modified solvent evaporation technique. Nine batches were formulated by changing the chitosan concentration (12, 14, 16mg/ml) and sonication time (5, 10, 15min). The formulations were optimized for particle size and zeta potential with high percent entrapment efficiency (%EE) through Central Composite Design software. The optimized batch F7 had a 182-nm size and high zeta potential (64.5mV) with 98% EE. The drug release of F7 was higher at pH 6 (97.556%) than at pH 7.4 (45.113%). The pharmacokinetic study shows that the release follows the Hixon plot model (R2 = 0.9334) that shifts to zero order (R2 = 0.9149). The nanogel F7 was observed for stability and showed an absence of color change, phase separation, and opacity for 6months. In the present study, the pH difference between cancer cells and normal cells is the key point of the smart nanogel. This study is promising but challenging depending on the in vivo study. The nanogel was successfully prepared and evaluated for pH-responsive release. As hemangiosarcoma commonly occurs in dogs, this formulation helps to limit the difficulties with administration.

Stabilization of Pickering emulsions with bacterial cellulose nanofibrils (BCNFs) fabricated by electron beam irradiation

Bacterial cellulose (BC) had been considered as a promising Pickering stabilizer for its non-toxicity, high purity, and biocompatibility. The electron beam irradiation (EBI) technology had gained significant attention in the field of cellulose degradation due to its operational convenience and mild reaction conditions. Pickering emulsions using BC degraded by EBI as Pickering stabilizers were successfully prepared. Irradiated bacterial cellulose nanofibers (IBCNFs) exhibited a high aspect ratio(30–80 μm in length and 21–109 nm in width) and high absolute zeta potential (-50 mV). The optimal emulsification performance of IBCNFs was observed at an irradiation dosage of 100 kGy (IBC-100). The emulsions based on IBC-100 achieved an EI value of 96.15 ± 0.19%, while those based on IBC-500 obtained an EI value of 59.93 ± 1.47%. Stable Pickering emulsions were prepared when the concentration of IBC-100 stabilizer exceeded 0.3 wt% with a fixed oil phase of 30%, or when the rapeseed oil phase was below 50% while maintaining a fixed suspension of 0.5 wt% IBCNFs. Confocal laser scanning microscopy (CLSM) demonstrated that IBCNFs facilitated the formation of a dense interfacial layer at the oil-water interface and formed a three-dimensional network within the water phase. Which effectively hindered the aggregation and flocculation between individual oil droplets. Furthermore, rheological findings demonstrated that emulsions possessed primarily exhibited properties of elasticity, and their gel strength could be enhanced by adjusting the irradiation dosages of IBCNFs. Moreover, environmental stability experiments indicated that IBCNFs-based emulsions exhibited exceedingly high temperature (20–80 °C) and pH tolerance (4–12). Flocculation occurred under high acid (pH = 2) conditions and at high ionic levels (≥ 40 mM NaCl), without causing disruption to the emulsion droplet structure. This study provided an innovative approach to preparing cellulose nanofibers with high aspect ratio, which could be utilized as emulsion stabilizers. The study also demonstrated that Pickering emulsions based on IBCNFs exhibit excellent stability and rheological properties. IBCNFs have promising potential to serve as a natural Pickering emulsifier for stabilizing oil-in-water emulsions in various food applications, cosmetic and pharmaceutical formulations.

Metformin Loaded Zein Polymeric Nanoparticles to Augment Antitumor Activity against Ehrlich Carcinoma via Activation of AMPK Pathway: D-Optimal Design Optimization, In Vitro Characterization, and In Vivo Study.

Metformin (MET), an antidiabetic drug, is emerging as a promising anticancer agent. This study was initiated to investigate the antitumor effects and potential molecular targets of MET in mice bearing solid Ehrlich carcinoma (SEC) as a model of breast cancer (BC) and to explore the potential of zein nanoparticles (ZNs) as a carrier for improving the anticancer effect of MET. ZNs were fabricated through ethanol injection followed by probe sonication method. The optimum ZN formulation (ZN8) was spherical and contained 5 mg zein and 30 mg sodium deoxycholate with a small particle size and high entrapment efficiency percentage and zeta potential. A stability study showed that ZN8 was stable for up to three months. In vitro release profiles proved the sustained effect of ZN8 compared to the MET solution. Treatment of SEC-bearing mice with ZN8 produced a more pronounced anticancer effect which was mediated by upregulation of P53 and miRNA-543 as well as downregulation of NF-κB and miRNA-191-5p gene expression. Furthermore, ZN8 produced a marked elevation in pAMPK and caspase-3 levels as well as a significant decrease in cyclin D1, COX-2, and PGE2 levels. The acquired findings verified the potency of MET-loaded ZNs as a treatment approach for BC.

The Synthesis of Broccoli Sprout Extract-loaded Silk Fibroin Nanoparticles as Efficient Drug Delivery Vehicles: Development and Characterization

Targeted drug delivery of biological molecules using the development of biocompatible, non-toxic, and biodegradable nanocarriers can be a promising method for cancer therapy. In this study, silk fibroin protein nanoparticles (SFPNPs) were synthesized as a targeted delivery system for sulforaphane-rich broccoli sprout extract (BSE). The BSE-loaded SFPNPs were conjugated with polyethylene glycol and folic acid, then their physicochemical properties were characterized via UV-Vis, XRD, FTIR, DLS, FE-SEM, and EDX analyses. In vitro release profile, antioxidant and anticancer activities of NPs were also studied. The FE-SEM and DLS analyses indicated stable NPs with an average size of 88.5 nm and high zeta potential (-32 mV). The sulforaphane release profile from NPs was pH-dependent, with the maximum release value (70%) observed in simulated intestinal fluid (pH = 7.4). Encapsulation of BSE also decreased the release rate of sulforaphane from the capsules compared to the free BSE. In vitro cytotoxicity of BSE and NPs on breast cancer cell lines (MCF-7) were concentration-dependent, and IC50 for BSE and NPs were acquired in 54 and 210 μg mL−1, respectively. Moreover, the NPs demonstrated no appreciable cytotoxicity in normal mouse fibroblast (L929) cell lines. These results indicated that biocompatible NPs synthesized as controlled and long-term targeted drug delivery systems can be a potential candidate for breast cancer therapy.

Flexible multiple-stimulus-responsive photonic films based on layer-by-layer assembly of cellulose nanocrystals and deep eutectic solvents

Photonic crystal materials responding to environmental stimuli are important in sensors, intelligent detection, and anti-counterfeiting. However, traditional photonic materials usually lack tunable color and sufficient color suppleness, hindering their practical applications. Here, we report a facile strategy to achieve mechanical and color-tunable photonic films by doping deep eutectic solvents (DES) into cellulose nanocrystals (CNC) using layer-by-layer assembly. The amount of DES and several assembly layers were vital in determining the structure color and mechanical and response properties in the CNC photonic films. The experimental results revealed that DES could endow CNC suspension systems with high zeta potential, high viscoelasticity, and low transmittance. The tiny DES compensated for the insufficient flexibility of the CNC film, resulting in a wide color range, high solvent discrimination ability, and multi-color at several view angles. Moreover, photonic crystal film also played an important role in intelligent display and could be applied to traffic reflective signs to remind pedestrians and drivers of road safety and as smart labels for indoor humidity detection. These characteristics of the CNC photonic films could provide a promising strategy for developing advanced intelligent sensors, detection, and anti-counterfeiting materials.

Halloysite Nanotube (HNT) Dispersion Stability in 10% Ethanol-Water Mixture and Water

This study investigates Halloysite Nanotube (HNT) dispersibility in ethanol-water mixtures – 0% and 10% ethanol at 100, 300, and 500 ppm HNT concentrations. Overall, the study finds that changes in HNT concentration linearly affect the response variables and showed that the 10% ethanol solvent has a higher zeta potential, smaller particle size, higher viscosity, and settling velocity. The enlargement of HNT particles at 10% ethanol while keeping better stability than water solvent is unexpected and can open novel studies about the dispersion of HNT in this solvent system.

Innovative chitosan-polyacrylic acid-MoS2 nanocomposite for enhanced and pH-responsive quercetin delivery

Cancer remains a global health challenge, with current treatments often leading to adverse side effects. Herein, a pH-sensitive, biocompatible nanocomposite composed of chitosan (CS), polyacrylic acid (PAA), and MoS2 nanosheets, loaded with quercetin (QCT) as a model anticancer drug has been synthesized via the water-oil-water (W/O/W) emulsification method, with the aim to be used for targeted breast cancer treatment. Characterization via Fourier-transform infrared spectroscopy (FT-IR) revealed strong interaction between the polymers via hydrogen bonding, and X-ray diffraction (XRD) showed a reduction in the level of crystallinity upon drug loading. Dynamic light scattering (DLS), zeta potential, and field-emission scanning electron microscopy (FE-SEM) tests revealed that the synthesized nanocarriers were spherical in shape and had a hollow structure, with a mean size of 484 nm and a high zeta potential of +44.3 mV, which confirms their high colloidal stability. The addition of MoS2 nanosheets to the polymeric mixture increased drug loading and encapsulation efficiency to 47% and 89%, respectively. The nanocomposite showed high potential as a pH-responsive drug delivery system, releasing 97% and 68% of QCT in acidic and neutral environments, respectively, over 96 hours. The biological performance was investigated using MTT and flow cytometry assays, which confirmed the efficiency of the nanocomposite for tumor cell removal.

Periodic electroosmotic flow of nanofluids with slip-dependent high zeta potential

The time periodic electroosmotic flow of nanofluids is investigated analytically in a hydrophobic microchannel. In this study, we consider the interdependence relationship between the wall electrical potential and slip. According to the non-linear slip-dependent zeta potential, we obtain an analytical solution of electrical potential for arbitrary value of wall electrical potential. Subsequently, we give the analytical integration expression of time periodic electroosmotic velocity of nanofluids. Based on the obtained electrical potential distribution, the oscillating flow velocity and rate are calculated numerically. The flow characteristics are determined by the oscillating frequency of electrical field, the volume fraction of nanoparticles and wall electrical potential. The noteworthy results are that, the oscillating electrical field can result in the oscillation of nanofluids. However, such oscillation is strongly dependent on the electrical field frequency and the flow characteristics are significantly different for various frequencies. Moreover, when the nanoparticles are introduced into the time periodic electroosmotic flow, the oscillation can be restrained. This may be helpful to understand the electrohydrodynamic instability of nanofluids.

Unraveling Water-Based Lubrication with Carbon Dots of Asphaltene Origin.

Despite the lower toxicity of water-based lubricants over nonrenewable petroleum-based analogues, they face challenges in achieving widespread adoption due to low stability and inadequate friction-reduction performance. To address this, a cost-effective nanoadditive is synthesized by expansive oxidation of asphaltenes to create biocompatible asphaltene-derived carbon dots [(ACDs); 5 nm]. These ACDs exhibit excellent water redispersibility, promoting long-term friction reduction and marking the first use of an asphaltene-based system for friction reduction in water or oil. Even at low loadings (0.2-4.0 wt %), ACDs significantly reduce friction on steel surfaces (>54%) with tribofilm stability surpassing pristine carbon dots, typical carbon-based graphene quantum dots, and inorganic nanomaterials (commercial 5 and 20 nm silica). The ACDs' attributes include high negative zeta potential, considerable water uptake, varied functional groups, biocompatibility, and a nanodisc shape conducive to stable tribofilm formation through effective particle stacking. The scalable synthesis, high yield, and impressive water redispersibility of ACDs position them favorably for commercial water-based lubrication.

Preparation and characterisation of silybin nanoemulsions based on complex emulsifiers: stability, in vitro release properties and antioxidant capacity

SummaryThe low solubility of Silybin (Slb) presents a significant obstacle to its further application. In this study, silybin nanoemulsion (Slb‐NE) stabilised by sodium aseinate/glycyrrhetinic acid (NaCas/GA) complex emulsifiers were prepared for effective delivery of Slb. When the NaCas:GA mass ratio was 1:1, Slb‐NE had small particle size (189 nm), low PDI (0.125), and high zeta potential (−27.27 mv). SEM, TEM, and FI‐IR studies indicated that the emulsion system was spherical and homogeneous, and Slb was successfully loaded into Slb‐NE without generating new chemical bonds. Furthermore, the complex emulsifiers improved the stability of Slb‐NE. In vitro release and antioxidant experiments showed that the incorporation of GA strengthened the sustained release and antioxidant capacity of Slb‐NE. NaCas/GA can be used as a natural and green complex emulsifiers for delivery of difficult‐to‐solve ingredients.

Magnetic Lipid-Based hybrid nanosystems: A combined stimuli- responsive nanocarriers for enriched chemotherapeutic potential of L-carnosine in induced breast Ehrlich ascites tumor model

Magnetic Lipid-Based Hybrid Nanosystems (M-LCNPs) is a novel nanoplatform that can respond to magnetic stimulus and are designed for delivering L-carnosine (CN), a challenging dipeptide employed in the treatment of breast cancer. CN exhibits considerable water solubility and undergoes in-vivo degradation, hence restricting its application. Consequently, it is anticipated that the developed M-LCNPs will enhance the effectiveness of CN. To ensure the physical stability of MNPs, they were initially coated with a mixture of oleic acid and oleylamine before being included in pegylated liquid crystalline nanoparticles (PLCNPs). The proposed M-LCNPs exhibited promising in-vitro characteristics, notably a small particle size (143.5 nm ± 1.25) and a high zeta potential (-39.5 mV ± 1.54), together with superparamagnetic behavior. The in-vitro release profile exhibited a prolonged release pattern. The IC50 values of M-LCNPs were 1.57 and 1.59 times lower than these of the CN solution after 24 and 48 hours, respectively. Female BALB/C female mice with an induced breast cancer (Ehrlich Ascites tumor [EAT] model) were used to study the influence of an external magnetic field on the chemotherapeutic activity and toxicity of CN loaded in the developed M-LCNPs.Stimuli-responsive M-LCNPs exhibited no apparent systemic toxicity in addition to enhanced chemotherapeutic efficacy compared to nontargeted M-LCNPs and CN solution, as evidenced by a reduction of % tumor growth (11.7%), VEGF levels (22.95 pg/g tissue), and cyclin D1 levels (27.61 ng/g tissue), and an increase in caspase-3 level (28.9 ng/g tissue). Ultimately, the developed stimuli-responsive CN loaded M-LCNPs presented a promising nanoplatform for breast cancer therapy.

Rosmarinic Acid-Rich Perilla frutescens Extract-Derived Silver Nanoparticles: A Green Synthesis Approach for Multifunctional Biomedical Applications including Antibacterial, Antioxidant, and Anticancer Activities.

This study describes a simple, cost-effective, and eco-friendly method for synthesizing silver nanoparticles using a rosmarinic acid extract from Perilla frutescens (PFRAE) as the bioreduction agent. The resulting nanoparticles, called PFRAE-AgNPs, were characterized using various analytical techniques. The UV-Vis spectrum confirmed the formation of PFRAE-AgNPs, and the FTIR spectrum indicated the participation of rosmarinic acid in their synthesis and stabilization. The XRD pattern revealed the crystal structure of PFRAE-AgNPs, and the TEM analysis showed their spherical morphology with sizes ranging between 20 and 80 nm. The DLS analysis indicated that PFRAE-AgNPs were monodispersed with an average diameter of 44.0 ± 3.2 nm, and the high negative zeta potential (-19.65 mV) indicated their high stability. In the antibacterial assays, the PFRAE-AgNPs showed potent activity against both Gram-positive (Bacillus subtilis and Staphylococcus aureus) and Gram-negative (Escherichia coli and Pseudomonas aeruginosa) bacterial pathogens, suggesting that they could be used as a potential antibacterial agent in the clinical setting. Moreover, the antioxidant activity of PFRAE-AgNPs against DPPH and ABTS radical scavengers highlights their potential in the treatment of various oxidative stress-related diseases. PFRAE-AgNPs also demonstrated significant anticancer activity against a range of cell lines including human colon cancer (COLO205), human prostate carcinoma (PC-3), human lung adenocarcinoma (A549), and human ovarian cancer (SKOV3) cell lines suggesting their potential in cancer therapy. The nanoparticles may also have potential in drug delivery, as their small size and high stability could enable them to cross biological barriers and deliver drugs to specific target sites. In addition to the aforementioned properties, PFRAE-AgNPs were found to be biocompatible towards normal (CHO) cells, which is a crucial characteristic for their application in cancer therapy and drug delivery systems. Their antibacterial, antioxidant, and anticancer properties make them promising candidates for the development of new therapeutic agents. Furthermore, their small size, high stability, and biocompatibility could enable them to be used in drug delivery systems to enhance drug efficacy and reduce side effects.

Formation mechanism of herpetrione self-assembled nanoparticles based on pH-driven method

The self-assembled nanoparticles (SAN) formed during the decoction process of traditional Chinese medicine (TCM) exhibit non-uniform particle sizes and a tendency for aggregation. Our group found that the pH-driven method can improve the self-assembly phenomenon of Herpetospermum caudigerum Wall., and the SAN exhibited uniform particle size and demonstrated good stability. In this paper, we analyzed the interactions between the main active compound, herpetrione (Her), and its main carrier, Herpetospermum caudigerum Wall. polysaccharide (HCWP), along with their self-assembly mechanisms under different pH values. The binding constants of Her and HCWP increase with rising pH, leading to the formation of Her-HCWP SAN with a smaller particle size, higher zeta potential, and improved thermal stability. While the contributions of hydrogen bonding and electrostatic attraction to the formation of Her-HCWP SAN increase with rising pH, the hydrophobic force consistently plays a dominant role. This study enhances our scientific understanding of the self-assembly phenomenon of TCM improved by pH driven method.