Average Hydrodynamic Diameter Research Articles

Silver Nanocolloids Loaded with Betulinic Acid with Enhanced Antitumor Potential: Physicochemical Characterization and In Vitro Evaluation.

Betulinic acid (BA), a natural compound with various health benefits including selective antitumor activity, has a limited applicability in vivo due to its poor water solubility and bioavailability. Thus, this study focused on obtaining a BA nano-sized formulation with improved solubility and enhanced antitumor activity using silver nanocolloids (SilCo and PEG_SilCo) as drug carriers. The synthesis was performed using a chemical method and the physicochemical characterization was achieved applying UV-Vis absorption, transmission electron microscopy (TEM), Raman and photon correlation spectroscopy (PCS). The biological evaluation was conducted on two in vitro experimental models—hepatocellular carcinoma (HepG2) and lung cancer (A549) cell lines. The physicochemical characterization showed the following results: an average hydrodynamic diameter of 32 nm for SilCo_BA and 71 nm for PEG_SilCo_BA, a spherical shape, and a loading capacity of 54.1% for SilCo_BA and 61.9% for PEG_SilCo_BA, respectively. The in vitro assessment revealed a cell type- and time-dependent cytotoxic effect characterized by a decrease in cell viability as follows: (i) SilCo_BA (66.44%) < PEG_SilCo_BA (72.05%) < BA_DMSO (75.30%) in HepG2 cells, and (ii) SilCo_BA (75.28%) < PEG_SilCo_BA (86.80%) < BA_DMSO (87.99%) in A549 cells. The novel silver nanocolloids loaded with BA induced an augmented anticancer effect as compared to BA alone.

Hydrophobic insertion-based engineering of tumor cell-derived exosomes for SPECT/NIRF imaging of colon cancer

BackgroundTumor cell-derived exosomes (TEx) have emerged as promising nanocarriers for drug delivery. Noninvasive multimodality imaging for tracing the in vivo trafficking of TEx may accelerate their clinical translation. In this study, we developed a TEx-based nanoprobe via hydrophobic insertion mechanism and evaluated its performance in dual single-photon emission computed tomography (SPECT) and near-infrared fluorescence (NIRF) imaging of colon cancer.ResultsTEx were successfully isolated from HCT116 supernatants, and their membrane vesicle structure was confirmed by TEM. The average hydrodynamic diameter and zeta potential of TEx were 110.87 ± 4.61 nm and –9.20 ± 0.41 mV, respectively. Confocal microscopy and flow cytometry findings confirmed the high tumor binding ability of TEx. The uptake rate of 99mTc-TEx-Cy7 by HCT116 cells increased over time, reaching 14.07 ± 1.31% at 6 h of co-incubation. NIRF and SPECT imaging indicated that the most appropriate imaging time was 18 h after the injection of 99mTc-TEx-Cy7 when the tumor uptake (1.46% ± 0.06% ID/g) and tumor-to-muscle ratio (8.22 ± 0.65) peaked. Compared with radiolabeled adipose stem cell derived exosomes (99mTc-AEx-Cy7), 99mTc-TEx-Cy7 exhibited a significantly higher tumor accumulation in tumor-bearing mice.ConclusionHydrophobic insertion-based engineering of TEx may represent a promising approach to develop and label exosomes for use as nanoprobes in dual SPECT/NIRF imaging. Our findings confirmed that TEx has a higher tumor-targeting ability than AEx and highlight the potential usefulness of exosomes in biomedical applications.

In vitro evaluation of albendazole nanocrystals against Echinococcus granulosus protoscolices.

Echinococcus granulosus is a zoonotic parasite causing hydatidosis in humans and animals. This study has been done in order to investigate the effect of albendazole nanocrystals on the viability of E. granulosus protoscolices. The average size and hydrodynamic diameter of albendazole nanocrystals were 976±218 and 1334±502 nm, respectively. Fertile hydatid cysts were isolated from the liver of slaughtered sheep. The isolated cysts were further identified using morphological and molecular techniques. The nucleotide sequence analysis indicated that the genotype of the protoscolices was E. granulosus sensu stricto with 100% similarity. The parasites were examined precisely for susceptibility to albendazole nanocrystals. The results revealed that albendazole nanocrystals are effective in removing protoscolices. It was observed that 1 μg/ml albendazole nanocrystals and albendazole completely inhibited the viability of the protoscolices within 17 and 23 days, respectively. The results suggested that albendazole nanocrystals can be used as an alternative effective treatment for E. granulosus infection.

Fabrication of core-shell type poly(NIPAm)-encapsulated citral and its application on bamboo as an anti-molding coating.

Bamboo is a widely used renewable and degradable biomass material; however, its sustainable utilisation is hindered by its susceptibility to mold. The current bamboo anti-mold technology is mainly based on organic chemical agents; these agents can easily induce mold resistance in bamboo with long-term use, and can even adversely affect human health. In the present study, the poly(N-isopropyl acrylamide) (PNIPAm)/citral nanohydrogel was prepared by encapsulating the natural antibiotic citral in PNIPAm for the anti-mold treatment of bamboo. The results revealed that this nanohydrogel exhibited a core–shell system with citral as the ‘core’ and PNIPAm as the ‘shell’, an average hydrodynamic diameter of 88.1 nm, and a low critical solution temperature (LCST) of 35.4 °C. After the high-pressure impregnation with the nanohydrogel, the bamboo strips showed excellent control effects toward common bamboo molds. Therefore, the nanohydrogel demonstrated high efficiency and it may become an ideal alternative to organic chemical anti-mold agents, thus showcasing its significant potential in the field of mold prevention for bamboo.

Трипсинолиз полиуретановых частиц на основе циклодекстрина с инкапсулированным моксифлоксацином

Abstract-Moxifloxacin encapsulation in polymer cyclodextrin-based particles with an average hydrodynamic diameter of 150--200 nm has led to the formation of potential delivery systems with a degree of moxifloxacin inclusion of more than 80%. Cross-linking of the moxifloxacin-cyclodextrin complexes caused a pronounced slowdown in the release of the drug molecules in acidic media to less than 10% per day. In the presence of trypsin, the drug release was accelerated by 15--20% within 90 min. It was shown by Fourier-transform infrared spectroscopy that this acceleration was due to the partial enzymatic degradation of the urethane bonds of the polymer matrix near the surface of the particles. The results obtained are important for the development of highly effective oral dosage forms of prolonged action. Key words: fluoroquinolones, cyclodextrins, FTIR spectroscopy, trypsin

Size measurement of silica nanoparticles by Asymmetric Flow Field-Flow Fractionation coupled to Multi-Angle Light Scattering: A comparison exercise between two metrological institutes

In this work we present a comparison exercise between two metrological institutes for size measurement of silica nanoparticles by Asymmetrical Flow Field-Flow Fractionation (AF4) coupled to static light scattering. The work has been performed in the frame of a French inter-laboratory comparison (ILC) exercise organized by the nanoMetrology Club (CnM). The general aim of this multi-technique comparison was to improve the measurement process for each technique, after establishing a well-defined measurement procedure. The results obtained by two national metrological institutes (NMIs), the LNE (France) and the SMD (Belgium) by AF4-UV-DRI-MALS will be presented and discussed. Three different samples were characterized: the reference material ERM®-FD304, which is a suspension of colloidal silica in aqueous solution and two silica bimodal samples consisting of two populations of SiO2 nanoparticles of unknown size in aqueous solution, with different populations’ ratios. The procedure for the preparation of the sample before the analysis, and main separation parameters have been previously defined between the two institutes and will be described. The principals measured parameters were the weight-average (dge_w), number-average (dge_n) and z-average (dge_z) geometric diameter; the average hydrodynamic diameter (dh); and the diameter obtained by external calibration using polystyrene latex standards (dcal). Results between the two NMIs were comparable and coherent with the expected size values of those obtained by other techniques like Scanning Mobility Particle Sizer (SMPS) and Scanning Electron Microscopy (SEM) also involved in this ILC exercise. Where discrepancies are observed, they leave the results compatible within their uncertainties and underpin the challenges in analysing data and reporting results, making AF4 a powerful tool to compare to other measurement techniques.

Coacervate Thermoresponsive Polysaccharide Nanoparticles as Delivery System for Piroxicam.

Low water solubility frequently compromises the therapeutic efficacy of drugs and other biologically active molecules. Here, we report on coacervate polysaccharide nanoparticles (CPNs) that can transport and release a model hydrophobic drug, piroxicam, to the cells in response to changes in temperature. The proposed, temperature-responsive drug delivery system is based on ionic derivatives of natural polysaccharides—curdlan and hydroxypropyl cellulose. Curdlan was modified with trimethylammonium groups, while the anionic derivative of hydroxypropyl cellulose was obtained by the introduction of styrenesulfonate groups. Thermally responsive nanoparticles of spherical shape and average hydrodynamic diameter in the range of 250–300 nm were spontaneously formed in water from the obtained ionic polysaccharides as a result of the coacervation process. Their morphology was visualized using SEM and AFM. The size and the surface charge of the obtained objects could be tailored by adjusting the polycation/polyanion ratio. Piroxicam (PIX) was effectively entrapped inside the nanoparticles. The release profile of the drug from the CPNs-PIX was found to be temperature-dependent in the range relevant for biomedical applications.

Nanocatalytic Medicine of Iron-Based Nanocatalysts

Iron can be found in all mammalian cells and is of critical significance to diverse cellular activities within human bodies. Widespread applications and the underlying chemical and biological funda...

Acid Hydrolysis‐Induced Nanoconversion of Sweet Potato (Ipomoea Batatas) Starch: Effect on Morphological, Rheological, and Thermal Properties

AbstractThe present study aims to prepare starch nanocrystals (SNCs) from sweet potato tuber starch and study their morphological, crystalline, rheological, and thermal properties. The platelet‐like SNCs are obtained using acid hydrolysis of round or polygonal native sweet potato starch granules. The average hydrodynamic diameter of SNCs is 184 nm as measured using the dynamic light scattering technique. The polydispersity index value based upon molecular weight distribution as determined using gel permeation chromatography increases from 1.386 for native starch (NS) to 2.958 for SNCs, indicating the heterogenous molecular weight distribution of acid hydrolyzed starch. The zero value of the radius of gyration for nanocrystals indicates the formation of anisotropic platelet‐like SNCs. The gelatinization temperature and melting enthalpy significantly increased after the nanoconversion of starch granules; thus, SNC's thermal properties are improved after acid hydrolysis of NS. The SNCs exhibit shear‐thinning behavior (lower viscosity) at high concentrations; the visco‐elastic behavior of SNCs dispersions is frequency‐dependent, with elastic character prevalence over viscous at lower frequencies.

Preparation and Ultrasonic Imaging Investigation of Perfluoropentane-Filled Polylactic Acid Nanobubbles As a Novel Targeted Ultrasound Contrast Agent

In the study reported here, polylactic acid (PLLA) polymer was synthesized using stannous octoate (Sn(Oct)2) and N-(t-butoxycarbonyl) ethanolamine (EABoc) as the catalyst and the initiator, respectively. The selected PLLA polymer with proper molecular weight was used to prepare nanobubbles encapsulating with liquid perfluoropentane. Then, lactoferrin (Lf), which has a good affinity with tumor cells, was conjugated to PLLA nanobubbles. The resulting Lf–PLLA nanobubbles were examined from the perspective of appearance, size, zeta potential, and stability in vitro. The average hydrodynamic diameter of the Lf–PLLA nanobubbles was 315.3 ± 4.2 nm, the polydispersity index (PDI) was 0.153 ± 0.020, and the zeta potential was around −11.3 ± 0.2 mV. Under the transmission electron microscope (TEM), Lf–PLLA nanobubbles were highly dispersed and had a spherical shape with a distinct capsule structure. The Lf–PLLA nanobubbles also showed little cytotoxicity and low hemolysis rate and exhibited good stability in vitro. The enhanced ultrasound imaging ability of Lf–PLLA nanobubbles was detected by an ultrasound imaging system. The results of ultrasound studies in vitro showed that the liquid perfluoropentane underwent phase transition under ultrasonic treatment, which proved the Lf–PLLA nanobubbles could enhance the ability of ultrasonic imaging. The studies of ultrasonic imaging in nude mice bearing subcutaneous tumors showed that the ability of enhanced ultrasonic images was apparent after injection of Lf–PLLA nanobubbles. Acoustic behavior in vitro and in vivo showed that the Lf–PLLA nanobubbles were characterized by strong, stabilized, and the ability of tumor-enhanced ultrasound imaging. Thus, the Lf–PLLA nanobubbles are an effective ultrasound contrast agent for contrast-enhanced imaging.

Liposomes Composed by Membrane Lipid Extracts from Macrophage Cell Line as a Delivery of the Trypanocidal N,N'-Squaramide 17 towards Trypanosoma cruzi.

Chagas is a neglected tropical disease caused by Trypanosoma cruzi, and affects about 25 million people worldwide. N, N’-Squaramide 17 (S) is a trypanocidal compound with relevant in vivo effectiveness. Here, we produced, characterized, and evaluated cytotoxic and trypanocidal effects of macrophage-mimetic liposomes from lipids extracted of RAW 264.7 cells to release S. As results, the average hydrodynamic diameter and Zeta potential of mimetic lipid membranes containing S (MLS) was 196.5 ± 11 nm and −61.43 ± 2.3 mV, respectively. Drug entrapment efficiency was 73.35% ± 2.05%. After a 72 h treatment, MLS was observed to be active against epimastigotes in vitro (IC50 = 15.85 ± 4.82 μM) and intracellular amastigotes (IC50 = 24.92 ± 4.80 μM). Also, it induced low cytotoxicity with CC50 of 1199.50 ± 1.22 μM towards VERO cells and of 1973.97 ± 5.98 μM in RAW 264.7. MLS also induced fissures in parasite membrane with a diameter of approximately 200 nm in epimastigotes. MLS showed low cytotoxicity in mammalian cells and high trypanocidal activity revealing this nanostructure a promising candidate for the development of Chagas disease treatment.

Allantoin Yüklü Kitosan Nanopartiküllerinin Hazırlanması ve Kitosanın Moleküler Ağırlığının İlaç Salımı Üzerindeki Etkisi

In this study, allantoin-loaded chitosan nanoparticles were prepared and the effect of molecular weights (low, medium, and high) of chitosan was investigated on the release of allantoin. The allantoin-loaded chitosan nanoparticles were characterized by various methods. The morphology, size, zeta potential, and loading efficiency were affected by the molecular weight of chitosan. The results displayed that the average hydrodynamic diameter of chitosan nanoparticles was in the range of 427–768 nm and the zeta potential values from 5.97 to 5.12 mV was obtained. The allantoin release from chitosan nanoparticles reached the plateau level in 96 hours. Cumulative allantoin release values of low, medium, and high molecular mass chitosan nanoparticles were determined as 43%, 30%, and 27%, respectively. According to the results, the molecular weight of chitosan influenced on allantoin release.

Synthesis of Nanoscale Liposomes via Low-Cost Microfluidic Systems.

We describe the manufacture of low-cost microfluidic systems to produce nanoscale liposomes with highly uniform size distributions (i.e., low polydispersity indexes (PDI)) and acceptable colloidal stability. This was achieved by exploiting a Y-junction device followed by a serpentine micromixer geometry to facilitate the diffusion between the mixing phases (i.e., continuous and dispersed) via advective processes. Two different geometries were studied. In the first one, the microchannels were engraved with a laser cutting machine on a polymethyl methacrylate (PMMA) sheet and covered with another PMMA sheet to form a two-layer device. In the second one, microchannels were not engraved but through-hole cut on a PMMA sheet and encased by a top and a bottom PMMA sheet to form a three-layer device. The devices were tested out by putting in contact lipids dissolved in alcohol as the dispersed phase and water as the continuous phase to self-assemble the liposomes. By fixing the total flow rate (TFR) and varying the flow rate ratio (FRR), we obtained most liposomes with average hydrodynamic diameters ranging from 188 ± 61 to 1312 ± 373 nm and 0.30 ± 0.09 PDI values. Such liposomes were obtained by changing the FRR from 5:1 to 2:1. Our results approached those obtained by conventional bulk synthesis methods such as a thin hydration bilayer and freeze-thaw, which produced liposomes with diameters ranging from 200 ± 38 to 250 ± 38 nm and 0.30 ± 0.05 PDI values. The produced liposomes might find several potential applications in the biomedical field, particularly in encapsulation and drug delivery.

Avoiding the Spherical Particle Assumption: Fractal Particle Density, Size, and Structure Characterization through Combined Sedimentation and Viscometry Measurements.

Physically meaningful characterization of irregularly shaped particles continues to present substantial challenges to the experimentalist. "Equivalent diameters" based on experimental techniques such as static and dynamic light scattering or sedimentation have proliferated to the point that they are often no longer recognized as equivalent. This study demonstrates the use of dual-fluid disk centrifuge photosedimentometry coupled with rheological measurements of viscosity to provide direct insights into both the average mass of a structured particle size distribution and the average hydrodynamic diameter.

Physical Stability and Interfacial Properties of Oil in Water Emulsion Stabilized with Pea Protein and Fish Skin Gelatin

This study aimed to investigate the physical stability and interfacial properties of oil-in-water (O/W) emulsions stabilized with fish skin gelatin (FG) and pea protein (PP) at pH 3. Physico-chemical properties, elemental composition and SDS-PAGE of the proteins were determined in the first part of this work. Emulsions were prepared at different ratio FG: PP (100: 0–75: 25–50: 50–25: 75–0: 100) by mechanical stirring followed by ultrasound treatment. Higher physical stability was observed in the presence of FG (ratio 100: 0), where the O/W were stable ~50 h. An average hydrodynamic diameter < 1 μm was found for all the emulsions except for the ratio 75: 25, where it was 2.8 μm. The presence of the protein on the O/W interface was explored by confocal laser scanning microscopy whereas the thermal properties of the protein ratios were analyzed by differential scanning calorimetry. The lower denaturation temperature was observed for ratio 50: 50, which was founded at ~89 °C, whereas the denaturation temperatures for the others O/W emulsions were in the range of 99 and 108 °C. A predominant viscous behavior was observed for all the ratios while a slight decrease of the surface tension was observed in the presence of PP. The equal mixing of FG with PP showed an increase in the emulsifying properties of PP forming a more stable emulsion with lower particle size.

A new method for single step sonosynthesis and incorporation of ZnO nanoparticles in cotton fabrics for imparting antimicrobial property

An efficient and effective sonosynthesis technique for the synthesis and simultaneous incorporation of Zinc oxide nanoparticles (ZnO NPs) on cotton fabrics is developed. The surface plasmon resonace (SPR) of ZnO NPs was studied using UV–visible spectroscopy and the average hydrodynamic diameter of the particles was determined by dynamic light scattring (DLS). The ZnO NPs incorporated cotton fabrics were characterized by X-ray diffraction (XRD), attenuated total reflectance Fourier transform infrared (ATR-FTIR) spectroscopy and Scanning electron microscopy (SEM). The tensile strength, flexural rigidity, air permeability, and water contact angle of the ZnO NPs deposited cotton fabrics were measured and compared with the pristine cotton. The SEM images showed excllent deposition of the NPs on the cotton yarns. Textile engineering characterization revealed that the inherent properties of cotton fabric remain in acceptable limits after deposition of the NPs. The ZnO NPs deposited cotton fabrics exhibited excellent antibacterial activities against Escherichia coli and Staphylococcus aureus bacteria.

Self-Assembly of Supramolecular Architectures by the Effect of Amino Acid Residues of Quaternary Ammonium Pillar[5]arenes.

Novel water-soluble multifunctional pillar[5]arenes containing amide-ammonium-amino acid moiety were synthesized. The compounds demonstrated a superior ability to bind (1S)-(+)-10-camphorsulfonic acid (S-CSA) and methyl orange dye depending on the nature of the substituent, resulting in the formation one-to-one complexes with both guests. The formation of host-guest complexes was confirmed by ultraviolet (UV), circular dichroism (CD) and 1H NMR spectroscopy. This work demonstrates the first case of using S-CSA as a chiral template for the non-covalent self-assembly of architectures based on pillar[5]arenes. It was shown that pillar[5]arenes with glycine or L-alanine fragments formed aggregates with average hydrodynamic diameters (d) of 165 and 238 nm, respectively. It was established that the addition of S-CSA to the L-alanine-containing derivative led to the formation of micron-sized aggregates with d of 713 nm. This study may advance the design novel stereoselective catalysts and transmembrane amino acid channels.

Green Synthesis of Silver Nanoparticles Using Raw Fruit Extract of Mimusops elengi and their Antimicrobial Study

These days, nanoparticles are being considered as nano-antibiotics because of their execution of antimicrobial activities towards a broad range of microbes. Nanoparticles are used in industrial products, health, food, space, and cosmetics;thus, researchers need for a green, ecofriendly, and low-cost approach to synthesize it. Green synthesis is such an approach of synthesizing NPs using microorganisms and plants, which is free of additional impurities. We used Mimusops elengi Linn. raw fruit extract in water to reduce the silver nitrate salt to produce silver NPs. The samples were characterized using various instrumental techniques. Broadband known as Surface Plasmon Resonance found near 450 nm in the absorption spectrum shows the formation of Ag NPs. NPs with average hydrodynamic diameters in the ranges 20-300 nm were detected from DLS study having negative zeta potential value (varies between - 25.8 to 15.8 mV), which suggests that as NPs surface is charged, it provides colloidal stability to the NPs in a liquid medium. FTIR study reveals that an increase in the intensity of some of the vibrational band with NP-content is due to the adsorption of some molecules on the surface of NPs. XRD pattern shows that NPs have an fcc structure. Samples were tested to have capabilities to kill both bacteria and fungi.

Capsaicin-Loaded Chitosan Nanocapsules for wtCFTR-mRNA Delivery to a Cystic Fibrosis Cell Line.

Cystic fibrosis (CF), a lethal hereditary disease caused by mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene coding for an epithelial chloride channel, is characterized by an imbalanced homeostasis of ion and water transports in secretory epithelia. As the disease is single-gene based, transcript therapy using therapeutic mRNA is a promising concept of treatment in order to correct many aspects of the fatal pathology on a cellular level. Hence, we developed chitosan nanocapsules surface-loaded with wtCFTR-mRNA to restore CFTR function. Furthermore, we loaded the nanocapsules with capsaicin, aiming to enhance the overall efficiency of transcript therapy by reducing sodium hyperabsorption by the epithelial sodium channel (ENaC). Dynamic light scattering with non-invasive back scattering (DLS-NIBS) revealed nanocapsules with an average hydrodynamic diameter of ~200 nm and a Zeta potential of ~+60 mV. The results of DLS-NIBS measurements were confirmed by asymmetric flow field-flow fractionation (AF4) with multidetection, while transmission electron microscopy (TEM) images confirmed the spherical morphology and size range. After stability measurements showed that the nanocapsules were highly stable in cell culture transfection medium, and cytotoxicity was ruled out, transfection experiments were performed with the CF cell line CFBE41o-. Finally, transepithelial measurements with a new state-of-the-art Ussing chamber confirmed successfully restored CFTR function in transfected cells. This study demonstrates that CS nanocapsules as a natural and non-toxic delivery system for mRNA to target cells could effectively replace risky vectors for gene delivery. The nanocapsules are not only suitable as a transcript therapy for treatment of CF, but open aspiring possibilities for safe gene delivery in general.

Extraction of cellulose nanocrystals from microcrystalline cellulose for the stabilization of cetyltrimethylammonium bromide-enhanced Pickering emulsions

The cellulose nanocrystals (CNCs) synthesized by sulfuric acid hydrolysis are highly hydrophilic and prone to form the agglomerations due to the hydrogen bonding, which limit their applications in the formulations of Pickering emulsions. For this reason, we selected microcrystalline cellulose (MCC) as the raw material for the extraction of CNCs through sulfuric acid hydrolysis and hydrogen peroxide oxidation, and then combined the surfactants of cetyltrimethylammonium bromide (CTAB) and CNCs to prepare the (O/W) Pickering emulsions by high-speed shearing method. The physicochemical properties of the resultant CNCs were evaluated by scanning electron microscopy (SEM), atomic force microscope (AFM), transmission electron microscopy (TEM), dynamic light scattering (DLS), Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD) and thermal gravimetric analysis (TGA). The formed emulsions were characterized by fluorescent microscope (FM). And the effects of the CTAB concentration, pH and ionic strength on the stability of the formed Pickering emulsions were also investigated. Experimental results showed that the sulfuric acid hydrolysis of MCC induced the removal of the amorphous components and the cleavage of the crystalline microfibrils, making CNCs exhibit the curled and rod-like shape with the average hydrodynamic diameter of 460.5 nm (PDI = 0.585), zeta potential of -34.1 mV and the crystallinity index (CrI) of 77.3 %, which revealed good colloidal properties. In addition, the optimal emulsification conditions for CTAB concentration, pH and ionic strength were respectively 0.5 CMC, 11 and 20∼60 mmol/L. On the basis of the above results, the Pickering emulsions stabilized by CTAB/CNCs complex may have potential for large applications in foods, cosmetics and medicines.