Core-shell Structure Research Articles

Facile constructing core-shell F–CIP@O/N-SWCNHs composites for high-performance microwave absorption and anti-corrosion

The development of electromagnetic wave-absorbing materials (EWAMs) with good environmental adaptability has emerged as a focal point of research in the realm of electromagnetic protection. Herein, a core-shell structure composite EWAMs, in which flake carbonyl iron powders and O, N co-doped single-walled carbon nanohorns are respectively a core and a shell (F–CIP@O/N-SWCNHs), has been prepared by a simple electrostatic adsorption method. The high-shape anisotropy of the F–CIP core exhibits strong specific saturation magnetization (160.47 emu/g) and excellent magnetic loss capacity. The tunable O/N-SWCNHs shell effectively enhances the dielectric properties and improves impedance matching, while the oxygen and nitrogen doping strengthens the dipole polarization. The surface protection provided by O/N-SWCNHs imparts favorable corrosion resistance and anti-oxidation properties to the F-CIP@O/N-SWCNHs. Moreover, F–CIP@O/N-SWCNHs exhibit excellent wave absorption performance. When the sample thickness is 1.53 mm, the minimum reflection loss reaches −74.8 dB. This study provides a feasible approach for the preparation of efficient EWAMs with strong environmental adaptability for the practical application of composite-absorbing materials.

Air-stable and UV-NIR broadband photodetectors utilizing graphene and core/shell quantum dots hybrid heterostructure

Photodetectors based on PbSe quantum dots (QDs) are commonly used for light detection in the near-infrared (NIR) region. Nevertheless, the performance of photodetectors based on PbSe QDs is constrained by ineffective carrier transfer and poor photo and thermal stabilities. Herein, a promising strategy that harnesses PbSe/PbS core/shell QDs structures is developed and demonstrated to enhance the long-term stability of photodetectors, further combining with graphene to form hybrid heterojunctions that effectively promote carrier transfer. As a result, the devices exhibit a broad photoresponse to the incident light at range of 365–1250 nm, and also possess a high photosensitivity of 1.5 × 104 A/W and a high detectivity of 4.0 × 1013 Jones. Moreover, the lifetime of graphene-PbSe/PbS core/shell QDs hybrid photodetector was 9 times greater than that of uncoated QDs devices. The enormous boost might be attributed to the passivation and protection provided by the core–shell structure, and graphene’s efficient extraction of charge carriers.

Hierarchical ferrous medium entropy with heterogeneous precipitates embedded in core-shell grain structure for superior mechanical properties

Superalloys designed for high-temperature applications, featuring a face-centered cubic matrix and L12 precipitates, have shown excellent tensile properties at both room and elevated temperatures. However, the substantial Ni and Co, necessary for generating a high fraction of the ordered L12 phase within the matrix, results in high mass density and cost, subsequently limiting their widespread industrial application. It is important to increase Fe content over Ni and Co while preserving outstanding mechanical properties at ambient and high temperatures. In this study, we propose a novel approach to introduce a hierarchical structure in a 60-at%-Fe-based medium entropy alloy. The heterogeneous nano-precipitates embedded in harmonic (core-shell) grain structure reinforce mechanical contrast between soft and hard domains, achieving an excellent heterostructure. The present alloy incorporates hierarchical heterogeneity at multi-scales, combining heterogeneous grain at micrometers, precipitates at tens of nanometers, and elemental fluctuation at nanometers. This hierarchical structure shows superior mechanical properties at room and high temperatures comparable to those of conventional superalloys. Further, the high content of Fe in this alloy system shows excellent performance in alloy cost and mass density. This work suggests the unique hierarchical heterostructure to overcome the trade-off dilemma in alloy cost, mass density, and mechanical properties in room/elevated temperatures.

Novel biopolymeric chitosan-urea-based core-shell hydrogel for use in sustainable agriculture

Agricultural sustainability is a major issue in recent times, deficiency of water as well as insufficient fertilizer to the crop is a main reason for it. This work is focused on core-shell hydrogel aiming to overcome the agricultural issues of water as well as deficiency of fertilizer to the plant. The core-shell hydrogel was prepared by incorporating urea in κ-carrageenan to be part of the controlled release mechanism of the core of the hydrogel. Chitosan was used for the shell structure to prepare over the core and cross-linked by the cations of the salts. The prepared hydrogel was termed as Chitosan-κ-carrageenan-Urea (CK-CU). Four different types of hydrogels were prepared with the different compositions named as CK-CU 2, CK-CU 5, CK-CU 7.5 and CK-CU 10 as varying with the ratio of 2 %, 5 %, 7.5 % and 10 % of urea respectively. The core-shell morphology structure was verified with Scanning electron microscopy (SEM) in which the complete coverage of the κ-carrageenan core by a consistent chitosan shell has been verified. Fourier transform infrared spectroscopy (FTIR) was utilized to confirm the composition of the hydrogel. Thermo-gravimetric analysis (TGA) was also performed for checking the thermal endurance of the hydrogel. The release rate of the urea was determined under Ultraviolet Visible spectroscopy. The swelling index, dewatering, and urea release rate of optimized CK-CU 10 hydrogel were found to 121 %, 21.22 %, and 70.4 % respectively. The developed Core-Shell hydrogel exhibits significant promise as a vehicle for fertilizer and as a soil conditioner in agricultural applications especially in arid and semi-arid areas.

Interface engineering of laminated redox-copolymers for electrochemical remediation of perfluoroalkyl substances

Redox polymers now show promise for selective removal of perfluoroalkyl substances from a complex aqueous matrix at high energy efficiency and no secondary pollution. However, self-agglomeration of redox polymers is a dominating barrier to constructing a low-cost, stable system in practical applications. Herein, we introduce polymer interface engineering strategy to enhance the activity of amine functionalities and nitrous oxide radicals in copolymers composed of 4-methacryloyloxy-2,2,6,6-tetramethylpiperidin-1-oxyl and 4-methacryloyloxy-2,2,6,6-tetramethylpiperidine. The grafted laminated redox polymer on multi-walled carbon nanotubes (termed MWCNT-g-P(TMPMA-co-TMA)) via free-radical polymerization demonstrated a 19.1–59.9 % increase in the electrosorption capacity with a maximum value (Qm) of 725.09 mg g−1 and a pseudo-first-order rate constant k1 = 1.46 min−1 and sustainable regeneration efficiency at ∼80 %. The core–shell structure of MWCNT-g-P(TMPMA-co-TMA) with a laminated redox polymer layer of ∼5 nm processed a low charge transfer resistance, which is expected to contribute to the enhanced capture performance and stability. An integrated system consisting of a MWCNT-g-P(TMPMA-co-TMA) electrode and a boron-doped diamond electrode can efficiently separate and degrade trace-concentration PFOA from industrial wastewater at high mineralization efficiency. This work provides insight into the design and optimization of redox active materials for water purification and beyond.

Effect of degree of substitution of octenyl succinate on starch micelles for synthesis and stability of selenium nanoparticles: Towards selenium supplements

To develop a promising selenium supplement that overcomes the instability and poor water dispersibility of selenium nanoparticles (SeNPs), we synthesized a series of amphiphilic octenyl succinic anhydride starch (OSAS) through esterification. As the degree of substitution (DS) increased, the particle size of OSAS micelles and the critical micelle concentration (CMC) decreased. FTIR and XRD analysis confirmed the successful introduction of octenyl succinic anhydride groups onto starch. Subsequently, OSAS micelles were used as carriers to synthesize SeNPs via in situ chemical reduction, forming SeNPs-loaded self-assembled starch nano-micelles (OSAS-SeNPs). The OSAS-SeNPs exhibited spherical dispersion in water with an average diameter of 116.1 ± 2.3 nm, contributed to enhanced hydrophobic interactions. TEM images showed a core-shell structure with SeNPs as the core and OSAS as the shell. FTIR results indicated hydrogen bonding interactions between OSAS and SeNPs. Due to the negatively charged OSAS shell and hydrogen bonding (OH⋯Se), OSAS-SeNPs remained non-aggregated for one month at room temperature, demonstrating remarkable stability. This study suggests that using OSAS can address the synthesis and stability issues of SeNPs, making it a potential selenium supplement candidate for further evaluation as an anticancer agent.

Signal-enhanced electrochemical sensor employing MWCNTs/CMK-3/AuNPs and Au@Pd core-shell structure for sensitive determinationof AFB1 in complex matrix.

A sandwich electrochemical sensor was fabricated based on multi-walled carbon nanotubes/ordered mesoporous carbon/AuNP (MWCNTs/CMK-3/AuNP) nanocomposites and porous core-shell nanoparticles Au@PdNPs to achieve rapid and sensitive detection of AFB1 in complex matrices. MWCNTs/CMK-3/AuNP nanocomposite, which was prepared by self-assembly method, served as a substrate material to increase the aptamer loading and improve the conductivity and electrocatalytic activity of the electrode for the first signal amplification. Then, Au@PdNPs, which were synthesized by one-pot aqueous phase method, were applied as nanocarriers loaded with plenty of capture probe antibody (Ab) and signal molecule toluidine blue (Tb) to form the Au@PdNPs-Ab-Tb bioconjugates for secondary signal amplification. The sensing system could still significantly improve the signal output intensity even in the presence of ultra-low concentration target compounddue to the dual signal amplification of MWCNTs/CMK-3/AuNP nanocomposites and Au@PdNPs-Ab-Tb. The method exhibited high selectivity, low detection limit (9.13fg/mL), and strong stability to differentiate AFB1 from other mycotoxins. Furthermore, the sensor has been successfully applied to the quantitative determination of AFB1 in corn, malt, and six herbs, which has potential applications in food safety, quality control, and environmental monitoring.

Dramatic Impact of Materials Combinations on the Chemical Organization of Core-Shell Nanocrystals: Boosting the Tm3+ Emission above 1600 nm.

This article represents the first foray into investigating the consequences of various material combinations on the short-wave infrared (SWIR, 1000-2000 nm) performance of Tm-based core-shell nanocrystals (NCs) above 1600 nm. In total, six different material combinations involving two different types of SWIR-emitting core NCs (α-NaTmF4 and LiTmF4) combined with three different protecting shell materials (α-NaYF4, CaF2, and LiYF4) have been synthesized. All corresponding homo- and heterostructured NCs have been meticulously characterized by powder X-ray diffraction and electron microscopy techniques. The latter revealed that out of the six investigated combinations, only one led to the formation of a true core-shell structure with well-segregated core and shell domains. The direct correlation between the downshifting performance and the spatial localization of Tm3+ ions within the final homo- and heterostructured NCs is established. Interestingly, to achieve the best SWIR performance, the formation of an abrupt interface is not a prerequisite, while the existence of a pure (even thin) protective shell is vital. Remarkably, although all homo- and heterostructured NCs have been synthesized under the exact same experimental conditions, Tm3+ SWIR emission is either fully quenched or highly efficient depending on the type of material combination. The most efficient combination (LiTmF4/LiYF4) achieved a high photoluminescence quantum yield of 39% for SWIR emission above 1600 nm (excitation power density in the range 0.5-3 W/cm2) despite significant intermixing. From now on, highly efficient SWIR-emitting probes with an emission above 1600 nm are within reach to unlock the full potential of in vivo SWIR imaging.

Magnetohydrodynamic double diffusion natural convection of power-law Non-Newtonian Nano-Encapsulated phase change materials in a trapezoidal enclosure

PurposeThe present numerical investigation examines the magnetohydrodynamic (MHD) double diffusion natural convection of power-law non-Newtonian nano-encapsulated phase change materials (NEPCMs) in a trapezoidal cavity.Design/methodology/approachThe governing Navier-Stokes, energy and concentration equations based on the Cartesian curvilinear coordinates are solved using the collocated grid arrangement’s finite volume method. The in-house FORTRAN code is validated with the different benchmark problems. The NEPCM nanoparticles consist of a core-shell structure with Phase Change Material (PCM) at the core. The enclosure, shaped as a trapezoidal hollow, features a warmed (Th) left wall and a cold (Tc) right wall. Various parameters are considered, including the power law index (0.6 ≤ n ≤ 1.4), Hartmann number (0 ≤ Ha ≤ 30), Rayleigh number (104 ≤ Ra ≤ 105) and fixed variables such as buoyancy ratio (Br = 0.8), Prandtl number (Pr = 6.2), Lewis number (Le = 5), fusion temperature (Θf = 0.5) and volume fraction (ϕ = 0.04).FindingsThe findings indicate a decrease in local Nusselt (Nu) and Sherwood (Sh) numbers with increasing Hartmann numbers (Ha). Additionally, for a shear-thinning fluid (n = 0.6) results in the maximum local Nu and Sh values. As the Rayleigh number (Ra) increases from 104 to 105, the structured vortex in the streamline pattern is disturbed. Furthermore, for different Ra values, an increase in n from 0.6 to 1.4 leads to a 67.43% to 76.88% decrease in average Nu and a 70% to 77% decrease in average Sh.Research limitations/implicationsThis research is for two-dimensioal laminar flow only.Practical implicationsPCMs represent a class of practical substances that behave as a function of temperature and have the innate ability to absorb, release and store heated energy in the form of hidden fusion enthalpy, or heat. They are valuable in these systems as they can store significant energy at a relatively constant temperature through their latent heat phase change.Originality/valueAs per the literature review and the authors’ understanding, an examination has never been conducted on MHD double diffusion natural convection of power-law non-Newtonian NEPCMs within a trapezoidal enclosure. The current work is innovative since it combines NEPCMs with the effect of magnetic field Double diffusion Natural Convection of power-law non-Newtonian NEPCMs in a Trapezoidal enclosure. This outcome can be used to improve thermal management in energy storage systems, increasing safety and effectiveness.

Influence of nitrogen exchange in the core-shell structure of naphthalenediimide molecules on the advancement of quantum electronic properties

This study explores how nitrogen substitution and gold electrodes collectively influence the electronic characteristics of naphthalenediimide (NDI) molecules (M = 1, 2, and 3) through theoretical analysis. Utilizing ELF, LOL, QTAIM, and NCI analyses, we reveal significant alterations in NDI's electronic structure and interactions upon bonding with gold electrodes (Au-M-Au). Both ELF and LOL analyses demonstrate increased electron localization and delocalization on the NDI surface due to gold electrodes, with a stronger effect on nitrogen-doped molecules (M = 2, 3). QTAIM analysis confirms favorable non-covalent interactions, including evident hydrogen bonding, between NDI molecules and gold electrodes, notably intensified in doped molecules, especially the Au…O interaction. NCI analysis provides insight into the diverse interactions within the molecular system. Overall, this research highlights the crucial role of gold electrodes and nitrogen substitution in fine-tuning NDI molecules' electronic properties. The observed modulation of electron behavior and formation of beneficial interactions with gold electrodes hint at promising applications for doped NDI-gold systems requiring efficient charge transport mechanisms.

Insight into the Influence of Carbon on Core–Shell Structured Co-Z@TiO2 Catalysts for Fischer–Tropsch Synthesis

Insight into the Influence of Carbon on Core–Shell Structured Co-Z@TiO₂ Catalysts for Fischer–Tropsch Synthesis

AuNPs@MoS2 functionalized copper metal organic framework for boosting electrocatalytic glucose oxidation

A novel non-enzyme glucose sensor based on functionalized copper metal–organic framework composite material, AuNPs@MoS2/Cu-MOF, was developed for rapid glucose analysis. Cu-MOF nanomaterial was prepared via a hydrothermal method, followed by the surface loading of core–shell structured AuNPs@MoS2 to synthesize AuNPs@MoS2/Cu-MOF composite material. Consequently, a novel gold nanoparticle @ molybdenum disulfide/copper metal–organic framework (AuNPs@MoS2/Cu-MOF/GCE) non-enzyme glucose sensor was constructed. Scanning electron microscopy (SEM), energy dispersive spectrometer (EDS) and X-ray powder Diffraction (XRD) was used to verify that the non-enzyme glucose sensor had been constructed effectively. Traditional electrochemical characterization methods were employed to study the electrocatalytic performance of the AuNPs@MoS2/Cu-MOF/GCE sensor and its catalytic oxidation of glucose. The experimental results demonstrated a good linear correlation between the concentration of glucose and the peak current within the range of 0.05–14.85 mM, with a detection limit of 16.7 μM. The AuNPs@MoS2/Cu-MOF/GCE sensor exhibited rapid electrochemical response to glucose (within 0.5 s), along with long-term stability and excellent selectivity. This is because Cu(II) in Cu-MOF can serve as active sites for the electrocatalytic oxidation of glucose, while the core–shell structure of AuNPs@MoS2 with excellent conductivity can lower the energy barrier in the reaction, further accelerating this catalytic reaction. The AuNPs@MoS2/Cu-MOF/GCE sensor is cost-effective, easy to operate, and suitable for accurate rapid quantification of glucose.

Core-shell Ru@Co2P synergistic catalyst as polysulfides adsorption-catalytic conversion mediator with enhanced redox kinetics in lithium-sulfur batteries

Lithium-sulfur batteries (LSBs) have emerged as the research hotspot due to their compelling merits, including high specific capacity (1675 mAh g−1), theoretical energy density (2600 Wh kg−1), environmental friendliness, and economic advantages. However, challenges still exist for further application due to their inherent issues such as the natural insulation, shuttle effect, and volume expansion of sulfur cathode during the continuous cycle processes. These factors obstruct the lithium ions (Li+) transfer process and sulfur utilization, resulting in significant impedance and inducing inferior battery performance. Herein, the core–shell nanocube anchoring ruthenium atoms and dicobalt phosphate (Ru@Co2P@NC) were fabricated as the effective catalyst and inhibited barrier for LSBs. On the one hand, the core–shell structure offers numerous channels to expedite Li+ diffusion. On the other hand, ruthenium (Ru) and dicobalt phosphate (Co2P) active sites facilitate the chemical capture of lithium polysulfides (LiPSs), accelerating sluggish kinetics. Ru@Co2P@NC modified cells not only exhibited a high initial specific capacity (1609.35 mAh g−1) at 0.5C and enduring stability with high specific capacity retention of 906.60 mAh g−1 at 0.5C after 400 cycles but also possessed low capacity attenuation rate of 0.07 % per cycle after 600 cycles (1C, Sulfur loading: 1.2 mg). Interestingly, the modified cells demonstrated a high specific capacity and long-cycle stability with high sulfur loading (from 1.984 to 3.137 mg), which provides a promising research approach for high-performance LSBs.

Moisture sorption and mechanical properties of polymer-cement waterproofing membranes investigated by LF NMR

This study investigates the impacts of environmental humidity on moisture absorption and mechanical properties of polymer-based waterproofing membranes. Membranes of polymer-CaCO3, polymer-white cement composites and pure polymer were used for measurements after treated in different relative humidities (RHs). Results indicate that the humidity treatment greatly changes the mechanical properties of the membranes and increasing RH from 0 % to 100 % leads to reduction of tensile strength by 60–80 %, which is believed to originate from the plasticizing effect of the absorbed moisture. LF NMR (Low field NMR) enables quantification of moisture distribution in the polymer-filler composites and three types of water, i.e. the water stored inside polymer matrix (O/O water), the water located in interfacial regions between polymer phase and fillers (I/O water), and the free water in air voids are detected with increasing T2 values. The absorbed moisture majorly accumulates in the O/O interfacial region during the humidity treatments with RH of 0∼80 %, which is because of the larger O/O interfacial area compared with the I/O interface. A large amount of free water appears only at RH of 100 %. A core-shell structure of the polymer domains with dry core and moisturized shell, is interestingly found during the moisture absorption process of the membranes, based on the LF NMR measurements using MSE sequence. It is surprisingly found that the drop of tensile strength of the membranes upon moisture absorption is majorly related to the growing shell thickness of the polymer domains whereas the moisture accumulated in the I/O interfacial region plays a minor role.

Microstructure characteristics for improved thermal shock reliability of sintered Ag[sbnd]Al paste in SiC power module

To meet the harsh thermal shock (−50–250 °C) requirements of power device packaging, a novel sintered Ag-based die attach material based on the sustained release effect of Al was proposed. In this study, Al particles with natural core-shell structure covered with Al2O3 layer were selected as the ideal doping-phase, and micron Al particles doped sintered Ag composite paste (AgAl) was prepared. First, the microstructural evolution of sintered AgAl joints during thermal shock was studied. The results showed that Al particles effectively suppressed the cracks generation, which attributed to the sustained release effect of Al element. To clarify sustained release mechanism of Al, the interfaces evolution between Ag and Al particles was investigated. In the initial stage, Al was covered by the Al2O3 layer, preventing inter-diffusion between Ag and Al. As the thermal shock proceeds, the Al2O3 film was fractured, achieving direct contact between metal Al and Ag. Diffusion thus takes place. For the sintered Ag5Al joint, the shear strength was 17.3 MPa after 1000 cycles, which is 1.57 times that of pure sintered Ag joint. These results indicate the successful development of low-cost, high-reliability die attachment materials for use in harsh thermal shock environments.

Injectable Mechanophore Nanoparticles for Deep-Tissue Mechanochemical Dynamic Therapy.

Photodynamic therapy (PDT) and sonodynamic therapy (SDT), using nonionizing light and ultrasound to generate reactive oxygen species, offer promising localized treatments for cancers. However, the effectiveness of PDT is hampered by inadequate tissue penetration, and SDT largely relies on pyrolysis and sonoluminescence, which may cause tissue injury and imprecise targeting. To address these issues, we have proposed a mechanochemical dynamic therapy (MDT) that uses free radicals generated from mechanophore-embedded polymers under mechanical stress to produce reactive oxygen species for cancer treatment. Yet, their application in vivo is constrained by the bulk form of the polymer and the need for high ultrasound intensities for activation. In this study, we developed injectable, nanoscale mechanophore particles with enhanced ultrasound sensitivity by leveraging a core-shell structure comprising silica nanoparticles (NPs) whose interfaces are linked to polymer brushes by an azo mechanophore moiety. Upon focused ultrasound (FUS) treatment, this injectable NP generates reactive oxygen species (ROS), demonstrating promising results in both an in vitro 4T1 cell model and an in vivo mouse model of orthotopic breast cancers. This research offers an alternative therapy technique, integrating force-responsive azo mechanophores and FUS under biocompatible conditions.

Exploring the Cutting Process of Coaxial Phase Change Fibers under Optical Characterization Tests

Urban heat islands (UHI) are a growing issue due to urbanization, causing citizens to suffer from the inadequate thermal properties of building materials. Therefore, the need for climate-resistant infrastructure is crucial for quality of life. Phase change materials (PCMs) offer a solution by being incorporated into construction materials for thermoregulation. PCMs store and release heat as latent heat, adjusting temperatures through phase changes. Polymeric phase change fibers (PCFs) are an innovative technology for encapsulating PCMs and preventing leaks. This study produced PCFs via wet-spinning, using commercial cellulose acetate (CA, Mn 50,000) as the sheath and polyethylene glycol (PEG 2000) as the core. The PCFs were cut using a hot-cutting method at three different temperatures and washed with distilled water. Morphological analysis was conducted with a bright-field microscope, and chemical analysis was performed using Fourier transform infrared spectroscopy (FTIR) before and after controlled washing. Additionally, the washing baths were analyzed by UV-visible spectroscopy to detect PEG. The PCFs displayed a well-defined core-shell structure. Although some PEG 2000 leakage occurred in unsuccessful cuts, cuts at 50 °C showed sealed ends and less material in the baths, making it viable for civil engineering materials.

In Situ and Rapid Toxicity Assessment of Air Pollution by Self-Assembly Passive Colonization Hydrogel.

Air pollution is a leading environmental health risk factor, and in situ toxicity assessment is urgently needed. Bacteria-based bioassays offer cost-effective and rapid toxicity assessments. However, the application of these bioassays for air toxicity assessment has been challenging, due to the instability of bacterial survival and functionality when directly exposed to air pollutants. Here, we developed an approach employing self-assembly passive colonization hydrogel (SAPCH) for in situ air toxicity assessment. The SAPCH features a core-shell structure, enabling the quantitatively immobilization of bacteria on its shell while continuously provides nutrients from its core. An antimicrobial polyelectrolyte layer between the core and shell confines bacteria to the air-liquid interface, synchronizing bacterial survival with exposure to air pollutants. The SAPCH immobilized a battery of natural and recombinant luminescent bacteria, enabling simultaneous detection of various toxicological endpoints (cytotoxicity, genotoxicity and oxidative stress) of air pollutants within 2 h. Its sensitivity was 3-5 orders of magnitude greater than that of traditional liquid-phase toxicity testing, and successfully evaluating the toxicity of volatile organic compounds and combustion smoke. This study presents a method for in situ, rapid, and economical toxicity assessment of air pollution, making a significant contribution to future air quality monitoring and control.

Timescale dependent homogeneous assembly of lipid-polymer hybrid nanoparticles in laminar mixing for enhanced lung cancer treatment

The homogeneity of core–shell structure lipid-polymer hybrid nanoparticles (HNPs) is crucial for efficient intracellular cargo delivery. While microfluidic techniques have been recognized for their capabilities in precisely controlling the size and drug encapsulation efficiency, there is little research exploring the impact of mass transfer behavior within microchannels on the homogeneous assembly process of HNPs. Here, we manipulated the laminar flow state within TrM device to achieve controlled assembly of HNPs and explored a timescale dependent assembly technique to ensure the homogeneity of folate modified HNPs (FHNPs). Our founding indicate that this method enabled the control over the growth kinetics of PLGA cores within a timescale (τgrow) of 1–15 ms. The homogeneous ligand assembly on the surface of FHNPs can only be achieved when τgrow exceeds the timescale of functional lipid coating (τcoating). Compared to conventional bulk mixing methods, this strategy significantly reduces the risk of heterogeneous assembly in FHNPs fabrication and ensures consistent reproducibility across batches. The homogeneous FHNPs (HFHNPs) fabricated through this method exhibit precise control over particle size (ranging from 75 nm to 150 nm), low polydispersity index, and consistent core–shell structure. Furthermore, this strategy enhances the density of available folate ligands on the surface of FHNPs. In subsequent in vitro and in vivo anti-tumor assays, the icariside Ⅱ (IS) loaded HFHNPs (IS@HFHNPs) exhibited enhanced cellular uptake and tumor accumulation behavior. the timescale dependent homogeneous assembly method for HNPs developed in this research presents a promising avenue for maintaining quality in the synthesis of self-assembly composite nanomecidine.

Tea saponin-Zein binary complex as a quercetin delivery vehicle: preparation, characterization, and functional evaluation

In this study, in order to solve the application problems of poor water solubility and low bioavailability of quercetin, we prepared a nano-delivery system with core-shell structure by anti-solvent method, including a hydrophilic shell composed of tea saponin and a hydrophobic core composed of Zein, which was used to improve the delivery efficiency and biological activity of quercetin. Through the optimal experiments, the loading rate and encapsulation rate of nanoparticles reached 89.41 % and 7.94 % respectively. And the water solubility of quercetin is improved by 30.16 times. At the same time, the quercetin acted with Zein through non-covalent interaction and destroyed its spatial network through structural characterization, while tea saponin covered the surface of Zein through electrostatic interaction, making it change into amorphous state. In addition, the addition of tea saponin makes the nanoparticles remain stable under the changes of external environment. During simulating gastrointestinal digestion procedure, ZQTNPs has higher release rate and bioavailability than free quercetin. Importantly, ZQTNPs can overcome the limitations of a single substance through synergy. These results will promote the innovative development of quercetin precision nutrition delivery system.