Charged Nanoparticles Research Articles

Hybrid Paul-optical trap with large optical access for levitated optomechanics

We present a hybrid trapping platform that allows us to levitate a charged nanoparticle in high vacuum using either optical fields, radio-frequency fields, or a combination thereof. Our hybrid approach combines an optical dipole trap with a linear Paul trap while maintaining a large numerical aperture (0.77 NA). We detail a controlled transfer procedure that allows us to use the Paul trap as a “safety net” to recover particles lost from the optical trap at high vacuum. The presented hybrid platform adds to the toolbox of levitodynamics and represents an important step towards fully controllable “dark” potentials, providing control in the absence of decoherence because of photon recoil. Published by the American Physical Society 2024

Systematic investigation of nanofluids: impact of nanoparticle charge and temperature on thermophysical properties

Systematic investigation of nanofluids: impact of nanoparticle charge and temperature on thermophysical properties

Fluorocarbon-Functionalized Polymerization-Induced Self-Assembly Nanoparticles Alleviate Hypoxia to Enhance Sonodynamic Cancer Therapy.

Sonodynamic therapy (SDT) is an ultrasound-based, noninvasive cancer treatment that targets tumor cells by triggering reactive oxygen species production. However, the limited accumulation of sonosensitizers and the insufficient supply of O2 to the hypoxic environment at the tumor site greatly limit the effectiveness of SDT. To address these issues, positively charged porphyrin-containing nanoparticles (NPs) from self-assembling of fluorocarbon/polyethylene glycol amphiphilic block copolymer, which is synthesized through reversible addition-fragmentation chain transfer polymerization, are constructed. The NPs with fluorocarbon core and positively charged hydrophilic shells not only stabilize the sonosensitizer and improve its cellular uptake, but also act as an O2 carrier alleviating the hypoxic tumor environment. In vitro and in vivo experiments demonstrate that the NPs effectively deliver O2 to the tumor and supply sufficient O2 to Renca cells after ultrasound treatment. Consequently, the NPs inhibit hypoxia-induced resistance to SDT and significantly produce reactive oxygen species by activated porphyrin moieties, inducing apoptosis in cancer cells. These oxygen-enhanced sonosensitizer NPs hold promise for cancer therapies such as photodynamic therapy, radiotherapy, and chemotherapy by overcoming hypoxia-induced resistance.

Surface-enhanced infrared spectroscopic study of extracellular vesicles using plasmonic gold nanoparticles

Extracellular vesicles (EVs), sub-micrometer lipid-bound particles released by most cells, are considered a novel area in both biology and medicine. Among characterization methods, infrared (IR) spectroscopy, especially attenuated total reflection (ATR), is a rapidly emerging label-free tool for molecular characterization of EVs. The relatively low number of vesicles in biological fluids (~1010 particle/mL), however, and the complex content of the EVs’ milieu (protein aggregates, lipoproteins, buffer molecules) might result in poor signal-to-noise ratio in the IR analysis of EVs. Exploiting the increment of the electromagnetic field at the surface of plasmonic nanomaterials, surface-enhanced infrared spectroscopy (SEIRS) provides an amplification of characteristic IR signals of EV samples. Negatively charged citrate-capped and positively charged cysteamine-capped gold nanoparticles with around 10nm diameter were synthesized and tested with blood-derived EVs. Both types of gold nanoparticles contributed to an enhancement of the EVs’ IR spectroscopic signature. Joint evaluation of UV-Vis and IR spectroscopic results, supported by FF-TEM images, revealed that proper interaction of gold nanoparticles with EVs is crucial, and an aggregation or clustering of gold nanoparticles is necessary to obtain the SEIRS effect. Positively charged gold nanoparticles resulted in higher enhancement, probably due to electrostatic interaction with EVs, commonly negatively charged.

Cysteamine functionalized gold nanoparticles exhibit high efficiency delivery of genetic materials in embryonic stem cells majorly via clathrin mediated endocytosis

Efficient and safe gene delivery is vital for genetic manipulation of stem cells for regenerative medicine. Gold nanoparticles have been used for various biomedical applications in the past, and are currently being researched as transfection agents. In this study, we report a simple one-pot synthesis of positively charged gold nanoparticles functionalized with cysteamine. The nanoparticles exhibit no cytotoxicity and can bind to both plasmid DNA (pDNA) as well as small interference RNA (siRNA). We observed that a five fold lower concentration of pDNA was sufficient for achieving comparable overexpression as that of a commercial transfection agent. We also observed that about 70 % transient silencing of the target gene was achieved with only 25 nM siRNA delivered by our nano-vehicle. To better understand the fate of the nanoparticle, we attempted to identify its uptake mechanism. The results indicate that while all the mechanisms contribute to the uptake, the clathrin-dependent pathway plays a major role. This is the first study on understanding the mechanism of uptake of CA-AuNPs conjugated to pDNA by embryonic stem cells. This is also the first study, where a successful transfection using gold based nanoparticles has been achieved in ESCs at a concentration as low as 0.5 µg/ml for pDNA and 25ƞM siRNA.

Au Nanoparticles-Trisbipyridine Ruthenium(II) Nanoaggregates as Signal-Amplifying SERS Tags for Immunoassay of cTnI.

Acute myocardial infarction (AMI) is one of the leading causes of human mortality worldwide. In the early stages of AMI, the patient's electrocardiogram (ECG) may not change, so the fast, sensitive, and accurate detection of the specific biomarker of cardiac troponin I (cTnI) is of great importance in the early diagnosis of AMI. In this work, for the first time, electrostatic nanoaggregates of negatively charged Au nanoparticles and positively charged trisbipyridine ruthenium(II) ions (i.e., (-)AuNPs|[Ru(bpy)3]2+ ENAs) as novel and signal-amplifying surface-enhanced Raman scattering (SERS) tags were synthesized in an easy and rapid (<3 min) way and applied in the highly sensitive, rapid detection of cTnI in human serum by being combined with an immunochromatographic test strip (ICTS). The synthesized (-)AuNPs|[Ru(bpy)3]2+ ENAs exhibited strong SERS activity due to the multiple Raman-active units (three bpy ligands) carried by each [Ru(bpy)3]2+ complex ion and abundant hotspots in each SERS tag. The developed (-)AuNPs|[Ru(bpy)3]2+ ENAs-based SERS-ICTS has been validated to be applicable in detection of cTnI in human serum with excellent sensing performances, such as fast testing (5 min) and a low detection limit (60 pg/mL). It is envisioned that the developed (-)AuNPs|[Ru(bpy)3]2+ ENAs-based SERS-ICTS sensor may have promising applications in point of care testing of various biomarkers in clinic. Additionally, this work may inspire the finding and the application of new types of Raman reporter molecules based on high valent metal-multi ligand coordination compounds like [Ru(bpy)3]2+.

Size-Dependent Electrostatic Adsorption of Polymer-Grafted Gold Nanoparticles on Polyelectrolyte Brushes.

Designing a functional surface that selectively adsorbs nanoparticles based on their size and shape is essential for developing an advanced adsorption-based, postsynthesis nanoparticle separation device. We demonstrate selective adsorption of larger nanoparticles from solution onto a polyelectrolyte brush by tuning the salt concentration. Specifically, a positively charged polyelectrolyte brush is created by converting pyridine groups of poly(2-vinylpyridine) to n-methylpyridinium groups using methyl iodide. The adsorption kinetics and thermodynamics of poly(ethylene glycol)-grafted, negatively charged gold nanoparticles (diameters of 12 and 20 nm) were monitored as a function of salt concentration. In a salt-free solution, the polyelectrolyte brush adsorbs gold nanoparticles of both sizes. As the salinity increases, the areal number density of adsorbed nanoparticles monotonically decreases and becomes negligible at high salinity. Interestingly, there is an intermediate range of salt concentrations (i.e., 15-20 mM of NaCl) where the decrease in nanoparticle adsorption is more pronounced for smaller particles, leading to size-selective adsorption of the larger nanoparticles. As a further demonstration of selectivity, the polyelectrolyte brush is immersed in a binary mixture of 12 and 20 nm nanoparticles and found to selectively capture larger particles with ∼90% selectivity. In addition, the size distribution of as-synthesized gold nanoparticles, with an average diameter of 12 nm, was reduced by selectively removing larger particles by exposing the solution to polyelectrolyte brush surfaces. This study demonstrates the potential of a polyelectrolyte brush separation device to remove larger nanoparticles by controlling electrostatic interactions between polymer brushes and particles.

Understanding photo-thermal and melting mechanisms in optical charging of nano and micro particles laden organic PCMs

Engineering efficient optical charging process necessitates efficient photo-thermal energy conversion, transfer, as well as storage of the incident solar radiant energy. The present work is a determining step in deciphering, quantifying, and understanding the aforementioned steps involved in the optical charging of PCMs. Herein, the effect of particle size, concentration and thermochromism have been critically investigated. In particular, detailed optical characterization and photo-thermal experimentation pertinent to non-thermochromic nanoparticles laden PCM (referred to as NP-PCM) and thermochromic micro capsules laden PCM (referred to as TMCP-PCM) has been undertaken. Detailed optical analysis points out that opposed to NP-PCM, TMCP-PCM significantly scatter the incident radiations – the diffuse transmittance (at room temperature) in the two cases being approximately 2 % and 39 % respectively. Furthermore, whereas, optical properties of non-thermochromic nanoparticles are nearly invariant to temperature changes; in the case of thermochromic microcapsules, the magnitude of scattering further increases and diffuse transmittance reaches as high as 51 % at elevated temperatures. Although, thermochromism helps in enhancing the penetration depth at elevated temperatures, but, due to significant fraction of scattering, the photo-thermal energy conversion is not that effective. In terms of temperature field, spatial-temporal temperature distribution curves reveal that temperature spread (in the liquid phase) in case of optical charging of non-thermochromic particles (carbon soot nanoparticles) laden PCMs is significantly high (as high as approximately 24 °C) relative to that observed in case of thermochromic particles (microcapsules) laden PCMs (approximately, 4 °C). The magnitude of the temperature spread (being representative of the deviation from thermostatic optical charging) clearly points out that opposed to non-thermochromic laden PCMs, nearly thermostatic optical charging can be achieved in case of thermochromic particles laden PCMs.Furthermore, in case of optical charging without thermochromic assistance, the temperature spread, peak temperatures and the melting rates increase with increase in particles concentration. Whereas, in the latter case, although the temperature spread and peak temperatures are nearly independent; the melting rates do depend on the particles’ concentration. Overall, the present work is a significant step towards accelerated-thermostatic thermal energy storage.

Antibody-Free Glycogen Nanoparticles Engage Human Immune T Cells for Intracellular Delivery of Small Drugs or mRNA.

T cells play a major role in immune defense against viral infections and diseases such as cancer. Accordingly, developing nanoparticle (NP) systems to effectively deliver therapeutics to T cells is of interest. However, NP-mediated delivery of drugs to T cells is challenging because of the nonphagocytic nature of T cells. To engage T cells and induce cellular internalization, NPs are typically decorated with specific receptor-targeting antibodies, often using laborious and costly procedures. Herein, we report that natural glycogen NPs (i.e., nanosugars) with different sizes (20-80 nm) and surface charges (neutral and positively charged) engage Jurkat T cells, undergo intracellular trafficking, and release encapsulated drug without the use of receptor-targeting antibodies. Specifically, glycogen-resveratrol constructs are employed to reactivate HIV-1 latently infected Jurkat T cells (J-Lat A2) and trigger proviral expression. Both neutral and positively charged glycogen NPs engage with J-Lat A2 cells. Large (84 ± 29 nm) and positively charged (23 ± 5 mV) NPs, denoted phytoglycogen-ethylenediamine (PGEDA) NPs, readily associate with the cell membrane and are internalized (60%) in J-Lat A2 cells but remain confined in the endocytic vesicles, with moderate reactivation of latent HIV-1 (4.7 ± 0.5%). Conversely, small (21 ± 5 nm) and positively charged (10 ± 6 mV) NPs, bovine glycogen-EDA (BGEDA) NPs, associate slowly with T cells but show nearly 100% internalization and efficient endosomal escape properties, resulting in 1.5-fold higher reactivation of latent HIV-1 in T cells. PGEDA NPs and BGEDA NPs are also internalized by primary human T cells (>90% cell association) and enable the transfection of mRNA, with BGEDA NPs showing a 2-fold higher transfection than PGEDA NPs. This work highlights the potential of BGEDA NPs for the effective intracellular delivery of small-molecule drugs and mRNA in T cells.

Effect of droplet charge density on stabilization of oil‐in‐dispersion emulsions co‐stabilized by binary mixed surfactants and nanoparticles

AbstractIonic surfactant and similarly charged nanoparticles can co‐stabilize oil‐in‐dispersion (OID) emulsions at extremely low concentrations (0.001 cmc/0.001 wt%), in which particles do not adsorb at the oil/water interface but distribute in the aqueous phase forming a dispersion. In this paper, the effect of droplet charge density on stabilization of the n‐decane‐in‐water OID emulsion was examined by using a cetyl trimethyl ammonium bromide (CTAB)/C12B (dodecyl dimethyl carboxyl betaine) binary mixture at a low fixed total concentration (0.01 mM) with varying molar fractions of CTAB. A model based on the Derjaguin‐Landau‐Verwey‐Overbeek (DLVO) theory is proposed to calculate interaction energies between droplets and between droplets and particles. It is found that the droplet charge density can be well compensated by particle concentration along the stabilization boundary, and the OID emulsion still follows the DLVO stabilization. Particles tend to surround droplets at large distances but may form a monolayer between approaching droplets at shorter distances, which significantly reduces the van der Waals attraction between droplets. In addition, the induced auxiliary droplet–particle repulsion is proportional to the number of particles per unit area of droplet surfaces, which together with the droplet–droplet repulsion ensures a large total repulsion preventing droplets from flocculation and coalescence. This work explains quantitatively the stabilization of OID emulsions, which have potential applications in emulsion products such as foods, cosmetics, pesticides, and various industrial emulsion systems. Moreover, the development of the OID emulsions represents an important advancement in green chemistry as it substantially reduces the required amounts of emulsifiers and their environmental impact after use.

Impact of laterally mobile surface charge on diffusiophoresis of hydrophobic rigid colloids

The diffusiophoresis of charged hydrophobic nanoparticles (NPs) governed by an imposed ionic concentration gradient is analysed. The main objective is to elucidate the impact of the laterally mobile adsorbed surface ions at the interface on the propulsion of the hydrophobic NPs in diffusiophoresis. In addition, the dielectric polarization due to the difference in dielectric constant between the NPs and the suspension medium is also considered. The mobile surface ions create a friction as well as an electric force at the hydrophobic surface, which leads to a modification of the slip velocity condition and the slip length. We obtain an exact numerical solution of the governing electrokinetic equations in their full form by adopting a control volume formulation. The numerical model is supplemented by analytical solutions derived based on the Debye–Hückel linearization. We find that the lateral mobility of the surface ions obstruct the coions to diffuse from the higher concentration side to the lower concentration side, which results in a repulsive force to the particle leading to the occurrence of a negative mobility. Based on the numerical results and analytical solutions, we have shown that for a fully mobile surface charge, the diffusiophoresis of a hydrophobic NP is identical to the diffusiophoresis of a liquid droplet whose viscosity is related to the slip length of the hydrophobic particle. We establish that the dielectric polarization enhances the velocity of a hydrophobic particle, which has potential applications in the practical context.

Stick, Slide, or Bounce: Charge Density Controls Nanoparticle Diffusion.

The diffusion and interaction dynamics of charged nanoparticles (NPs) within charged polymer networks are crucial for understanding various biological and biomedical applications. Using a combination of coarse-grained molecular dynamics simulations and experimental diffusion studies, we investigate the effects of the NP size, relative surface charge density (ζ), and concentration on the NP permeation length and time. We propose a scaling law for the relative diffusion of NPs with respect to concentration and ζ, highlighting how these factors influence the NP movement within the network. The analyses reveal that concentration and ζ significantly affect NP permeation length and time, with ζ being critical, as critical as concentration. This finding is corroborated by controlled release experiments. Further, we categorize NP dynamics into sticking, sliding, and bouncing regimes, demonstrating how variations in ζ, concentration, and NP size control these behaviors. Through normalized attachment time (NAT) analyses, we elucidate the roles of electrostatic interactions, steric hindrance, and hydrodynamic forces in governing NP dynamics. These insights provide guidance for optimizing NP design in targeted drug delivery and advanced material applications, enhancing our understanding of NP behavior in complex environments.

Synergistic bactericidal activity of chlorhexidine loaded on positively charged ionic liquid-protected silver nanoparticles as a root canal disinfectant against Enterococcus faecalis: An ex vivo study

The advancement of nanotechnology and the development of nanocomplexes offer promising solutions to address the limitations in biofilm management within endodontics. Current cleaning and disinfection methods often fail to completely eliminate bacterial biofilms from the complex anatomical structures of root canals, making the invention of new disinfectants or disinfection methods highly relevant. Previously, chlorhexidine-loaded positively charged ionic liquid-protected silver nanoparticles (CHX@AgNPs⁺) were introduced as an innovative root canal irrigation solution, demonstrating significant antibacterial efficacy against Enterococcus faecalis in vitro. This study aimed to further evaluate the antibiofilm activity of CHX@AgNPs⁺ in the root canals of extracted human teeth contaminated with E. faecalis biofilm. Fifty single-rooted human teeth with mature apices were randomly assigned to five experimental groups based on the irrigants used: CHX@AgNPs⁺, AgNPs⁺, 2.5 % NaOCl, 2 % CHX, and normal saline (n = 10 per group). The root canals were contaminated with E. faecalis, and biofilm formation was confirmed. Initial sampling (S1) was performed, followed by mechanical preparation of the root canals using ProTaper F3 files and irrigation with the respective test solutions. Post-instrumentation sampling (S2) was then conducted. The results demonstrated that CHX@AgNPs⁺ exhibited antibiofilm properties comparable to 2.5 % NaOCl, with no significant difference between them. Additionally, CHX@AgNPs⁺ significantly enhanced antimicrobial efficacy compared to CHX alone (P < 0.05), highlighting its potential as an effective root canal disinfectant.

A Multifunctional Nanodrug Increases the Therapeutic Sensitivity of Lenvatinib to Hepatocellular Carcinoma by Inhibiting the Stemness of Hepatic Cancer Stem Cells.

Drug resistance resulting from diverse mechanisms including the presence of cancer stem cells (CSCs) is the main obstacle for improving therapeutic efficacy of lenvatinib in hepatocellular carcinoma (HCC). Herein, a nanomedicine (siCD24-Len-MnO@PLAP) is developed by incorporating manganese oxide (MnO), lenvatinib (Len), and siRNA against CD24 (siCD24) into micelles composed of methoxypolyethylene glycol (mPEG), poly-L-lysine (PLLys), and polyasparagyl(N-(2-Aminoethyl)piperidine) (PAsp(PIP)) triblock copolymer. The nanomedicine can respond to the tumor microenvironment (TME) to release lenvatinib, and produce Mn2+ and O2, accompanied by changes in nanoparticle charge, which facilitates cellular endocytosis of siCD24-loaded nanoparticles. The released siCD24 and lenvatinib synergistically reduces CD24 expression, resulting in a more pronounced inhibition of stemness of CSCs. In the mouse models of HCC using Huh7-derived CSCs and Hepa1-6-derived CSCs, the nanomedicine shows remarkable anti-cancer effect by enhancing the therapeutic effects of lenvatinib against HCC via reducing the expression level of CD24 and decreasing the expression of hypoxia inducible factor-1α (HIF-1α). Moreover, in situ production of paramagnetic Mn2+ from the nanomedicine serves as an excellent contrast agent for magnetic resonance imaging (MRI) to monitor the therapeutic process. This study demonstrates that this multifunctional MRI-visible siCD24- and lenvatinib-loaded nanodrug holds great potential in enhancing therapeutic sensitivity for HCC lenvatinib therapy.

Effect of colloidal magnetite (Fe3O4) nanoparticles on the electrical characteristics of the azolectin bilayer in a static inhomogeneous magnetic field

This work is devoted to the study of the combined effects of applied magnetic field and MNPs on the electrical characteristics of bilayer lipid membranes. We present results of the study of electrical parameters of azolectin membranes in a static inhomogeneous magnetic field at the one-sided addition of positively charged quasi-spherical superparamagnetic magnetite nanoparticles with a diameter of about 4 nm. The magnet was located at different distances from the membrane, and the magnetic field attracted the nanoparticles to the membrane surface with different strengths. We observed three pronounced effects that depended on the external magnetic field. Firstly, after addition of nanoparticles in a magnetic field, the conductance of the membranes increased. A smooth increase in conductance was accompanied in some cases by the appearance of current jumps, which can be associated with the formation of through pores with a radius of no more than 1 nm. The conductance increased with increasing magnetic field gradient. Secondly, at zero command voltage, a negative current through the membrane was observed. Although our experiments did not allow us to unambiguously determine which particles create this current, we believe that this current is associated with the penetration of particles through the membrane. This effect intensified with increasing magnetic field gradient. Thirdly, we observed a sharp change in the nonlinear dependence of capacitance on voltage associated both with the change in the surface potential of the azolectin membrane and with the effect of MNP binding to the membrane surface on the apparent membrane capacitance.

Switching Photoluminescence “On‐Off‐On” for Detection of Chromium (VI) Ion and Ascorbic Acid with N,S‐Codoped Carbon Dots

AbstractA photoluminescent‐based “Turn On → Off → On” technique was adopted for a toxic, heavy metal ion detection, that is, specifically chromium (VI) and a pharmaceutically relevant ascorbic acid molecule. Metal‐free, environmentally benign, and fluorescent carbon dots, a potential vehicle for spectrofluorometric detection, were successfully deployed as sensors. Carbon dots synthesized from citric acid and sulfanilamide conserve the fragments of the precursor molecule on the surface. Zeta potential measurement evidenced the positively charged carbon nanoparticles physically interact with the Cr(VI)/Cr2O72− in acidic pH, resulting in a remarkable quenching in net fluorescence. Thorough studies revealed that the static quenching and inner filter effect were responsible for the reduction in fluorescence intensity. We have demonstrated a new rapid (in seconds) detection platform for Cr(VI) and ascorbic acid.

Precise determination of electric field applied to charged materials in liquid via van der Pauw technique

The electric field is a fundamental physical quantity that determines the characteristics or behavior of charged materials in liquids. The precise characterization of charged materials involving nanoparticles or biomaterials such as cells and extracellular vesicles (EVs) requires a rigorous calculation of the electric field applied to these materials. However, unlike solid-state materials, the precise measurement of the electric field applied in liquids is challenging because of liquid-electrode interface resistance and non-uniform electric-field regions near electrodes. This study proposes a method for determining the precise electric field in liquids using the van der Pauw measurement technique. The conductivity of the liquid was measured using a microfluidic channel with a van der Pauw configuration. The electric field in the liquid was then calculated based on the relationship between the conductivity and current density. The accuracy of the proposed method was verified by measuring the conductivity of standard solutions and phosphate-buffered saline (PBS), followed by determining the electric field applied to the nanoparticles in these solutions. In addition, the proposed method was used to determine the zeta potential of charged nanoparticles. This simple method for determining liquid conductivity and calculating electric fields in liquids could be effectively used for various electrochemical studies.

Oppositely charged polymer-surfactant nanoparticles stabilized by triblock copolymers for enhanced oil loading

When oppositely charged polymers and surfactants combine, they can form a concentrated phase rich in micelles interconnected by polymer chains. Dispersing this concentrated phase as nanoparticles in an aqueous media can be a way to load and deliver hydrophobic ingredients. This study employed triblock copolymers of poly(ethylene oxide)-poly(propylene oxide)-poly(ethylene oxide), EOxPOyEOx, also known as poloxamers or pluronics, to disperse the concentrated phase, forming nanoparticles of aggregated micelles connected by the polyion chains. We showed that nanoparticles formed by hexadecyltrimethylammonium bromide (CTAB), poly(acrylic acid) (PAA), and different EOxPOyEOx copolymers can enhance the loading of oily ingredients compared to pure surfactant micelles. Dispersions with 1.6 wt% of nanoparticles exhibited water-like viscosity and loaded up to 0.48 wt% of oil. Characterization techniques, including dynamic light scattering (DLS), electrophoretic mobility, small-angle X-ray scattering (SAXS), and cryogenic transmission electronic microscopy (cryo-TEM), revealed positively charged spherical 50–180 nm nanoparticles with a core formed by concentrated micelles, that were stable for at least 4 months. Variations in the EO and PO block lengths did not impact morphology, showing that different EOxPOyEOx copolymers were suitable for dispersing the nanoparticles. Increasing EO block length size decreased the diameter of nanoparticles and enhanced stability, providing a means to control their properties. In conclusion, nanoparticles formed by oppositely charged polymer-surfactant mixtures and stabilized by triblock copolymers showed potential for applications, such as sprays, due to their effective oil loading, high stability, and facile preparation.

Hydrophobic and positively charged magnetic nanoparticles for enhanced oil recovery from concentrated emulsion wastewaters

With the development of petroleum industry, a large amount of oil-in-water (O/W) emulsion wastewaters were produced, resulting in serious environmental pollution and resource waste. Up till now, magnetic nanoparticles (MNPs) were frequently reported in emulsion wastewater treatment and mainly focused on the water purification, but little effort was devoted to the facile recovery of oil resource. In the present work, a class of hydrophobic and positively charged MNPs, namely dimethyloctadecyl [3-(trimethoxysilyl) propyl] ammonium chloride (DOTAC)-coated MNPs (M−DOTAC), was carefully synthesized by regulating DOTAC anchoring density on Fe3O4@SiO2, and then employed to treat the concentrated emulsion wastewaters stabilized by anionic sodium dodecyl benzene sulfonate (SDBS) or nonionic Tween-80. M−DOTAC with relatively high DOTAC density (M−DOTAC 1.8) exhibited higher positive charge density and hydrophobicity, and hence could significantly promote the oil droplet coalescence and mergence via the electrostatic attraction and hydrophobic adsorption bridging as well as the hydrophilic-lipophilic transition of interfacial adsorption layer. Accordingly, with addition of moderate dosage of M−DOTAC 1.8, the emulsion was broken and divided into three layers: (1) a continuous oil layer was formed in the upper layer which could be directly recycled; (2) the middle layer was composed of MNPs-tagged oil droplets/flocs; (3) the bottom layer was the clearer water phase. The optimal recovery rate of oil resource reached ∼ 60 % in SDBS stabilized system, and further increased to ∼ 98 % in Tween-80 stabilized system. However, the oil recovery rate was declined at an excessive dosage of M−DOTAC 1.8 due the formation of double emulsion. Besides, M−DOTAC 1.8 exhibited good reusability. These results indicated the fabricated M−DOTAC had great application prospect in treating emulsion wastewaters containing high oil content.

A Strategic Blend of Stabilizing Polymers to Control Particle Surface Charge for Enhanced Mucus Transport and Cell Binding.

Mucus layers, viscoelastic gels abundant in anionic mucin glycoproteins, obstruct therapeutic delivery across all mucosal surfaces. We found that strongly positively charged nanoparticles (NPs) rapidly adsorb a mucin protein corona in mucus, impeding cell binding and uptake. To overcome this, we developed mucus-evading, cell-adhesive (MECS) NPs with variable surface charge using Flash NanoPrecipitation, by blending a neutral poly(ethylene glycol) (PEG) corona for mucus transport with a small amount, 5 wt%, of polycationic dimethylaminoethyl methacrylate (PDMAEMA) for increased cell targeting. In vitro experiments confirmed rapid mucus penetration and binding to epithelial cells by MECS NPs, suggesting a breakthrough in mucosal drug delivery.