Large Surface Charge Research Articles

Intracellular Biomacromolecule Delivery by Stimuli-Responsive Protein Vesicles Loaded by Hydrophobic Ion Pairing.

Proteins can perform ideal therapeutic functions. However, their large size and significant surface hydrophilicity and charge prohibit them from reaching intracellular targets. These chemical features also render them poorly encapsulated by nanoparticles used for intracellular delivery. In this work, a novel combination of protein vesicles and hydrophobic ion pairing (HIP) was used to load protein cargo and achieve cytosolic delivery to overcome the limitations of previous protein vesicle properties. Protein vesicles are thermally self-assembling nanoparticles made from elastin-like polypeptide (ELP) fused to an arginine-rich leucine zipper and a globular protein fused to a glutamate-rich leucine zipper. To impart stimuli-responsive disassembly, physiological stability, and small size, the ELP sequence was modified to include histidine and tyrosine residues. HIP was used to load and release protein cargo requiring endosomal escape for cytosolic function. HIP vesicles enabled delivery of cytochrome c, a cytosolically active protein, and a significant reduction in viability in both a traditional two-dimensional (2D) human cancer cell line culture and a biomimetic three-dimensional (3D) organoid model of acute myeloid leukemia. By examining the uptake of positively and negatively charged fluorescent protein cargos loaded by HIP, this work revealed the necessity of HIP for cytosolic cargo delivery and how HIP loading influences protein vesicle self-assembly and disassembly using microscopy, small-angle X-ray scattering, and nanoparticle tracking analysis. HIP protein vesicles have the potential to broaden the use of intracellular proteins as therapeutics for various diseases and extend protein vesicles to deliver other biomacromolecules, as the strategy developed here resulted in the first cytosolic protein cargo delivery using protein vesicles.

Redox potential tuning by calcium ions in a novel c-type cytochrome from an anammox organism.

The electrochemical potentials of redox-active proteins need to be tuned accurately to the correct values for proper biological function. Here we describe a diheme cytochrome c with high heme redox potentials of about +350 mV, despite having a large overall negative charge which typically reduces redox potentials. High resolution crystal structures, spectroelectrochemical measurements and high-end computational methods show how this is achieved: each heme iron has a calcium cation positioned next to it at a distance of only 6.9 Å, raising their redox potentials by several hundred mV through electrostatic interaction. We suggest that this has evolved to provide the protein with a high redox potential despite its large negative surface charge, which it likely requires for interactions with redox partners.

Synthesis, Characterization, Density Functional Theory Study, Antibacterial Activity and Molecular Docking of Zeolitic Imidazolate Framework‐8

ABSTRACTIn this study, Zeolitic Imidazolate Framework‐8 (ZIF‐8) nanomaterials were synthesized using a co‐precipitation one‐pot method that uses ethanol, methanol, and water as solvents for the precursors (2‐methylimidazole and Zinc nitrate hexahydrate), resulting in yields of 66.77%, 73.14%, and 68.12%, respectively. The as‐synthesized ZIF‐8 nanomaterials were thoroughly characterized by X‐ray diffraction analysis, transmission electron microscopy, ultraviolet–visible spectroscopy, and Fourier‐transform infrared spectroscopy. The X‐ray diffraction analysis showed that the crystallite size of ethanol‐based ZIF‐8 (24.76 ± 1.67 nm) was smaller than those synthesized in water (26.92 ± 1.89 nm) and methanol (31.39 ± 1.03 nm). However, methanol‐based ZIF‐8 exhibited lower crystallinity (85.93%) than water‐based ZIF‐8 (91.48%) and ethanol‐based ZIF‐8 (92.71%). Zeta potential studies revealed that ethanol‐based ZIF‐8 had a larger surface charge (+37 mV) than water‐based ZIF‐8 (+35 mV) or methanol‐based ZIF‐8 (+24 mV). Transmission electron microscopy analysis confirmed particle sizes of 54.35 ± 2.11 nm for ethanol‐based ZIF‐8, 57.91 ± 2.26 nm for water‐based ZIF‐8, and 63.25 ± 4.12 nm for methanol‐based ZIF‐8. Thermogravimetric analysis indicated thermal stability up to 800 °C, with mass losses of 55.98% for ethanol‐ZIF‐8, 50.12% for water‐based ZIF‐8, and 65.36% for methanol‐based ZIF‐8 by 600 °C. In antibacterial studies, water‐based ZIF‐8 exhibited the largest zone of growth inhibition (17.30 ± 0.26 mm) against Escherichia coli compared to ethanol‐based ZIF‐8 (15.57 ± 0.32 mm) and methanol‐based ZIF‐8 (14.70 ± 0.20 mm). Pearson's correlation study revealed that zeta potential, crystallinity, and antibacterial activity are positively related. Furthermore, water‐based ZIF‐8, with a minimum inhibitory concentration of 50 μg/100 μL, confirmed evident cell membrane disruption. Molecular docking experiments revealed ZIF‐8's significant binding affinity for the E. coli protein 5AZC, supporting its robust antibacterial activity.

Influence mechanisms of ultraviolet irradiation aging on DC surface discharge properties of silicone rubber in dry and humid air

In the modern DC electrical transmission system, high-energy photons interact with silicone rubber (SIR) chains during long-term ultraviolet (UV) irradiation, it degrades the surface properties and triggers surface discharge (flashover) along the SIR-air interface, threatening the secure operation of the advanced electrical equipment. To further comprehend how UV-aging influences the flashover performance, in this work, the chemical bonds, surface charge transport parameters, and flashover performance of UV-aged SIR samples are characterized, and the influence mechanisms of UV-aging on surface discharge in dry and humid air are comprehensively clarified through the investigation from “molecular-mesoscopic-macroscopic” scales. The results indicate both degradation and oxidization reactions occur during UV-aging. The degraded molecular chains dominate the discharge in dry air, while oxidization reactions determine the discharge in humid environment: The degradation reactions reduce the surface trap depth and increase surface conductivity, leading to large surface leakage current and surface charge dissipation rate, causing flashover voltage in dry air increases and decreases as UV-aging time increasing. The oxidization of the chains introduces –OH and –COOH groups into chains, enhancing permittivity and adsorbing H2O molecules, significantly increasing surface leakage current, causing surface discharge voltage in humid air to decrease as UV-aging time increases.

Novel ultrastable 2D MOF/MXene nanofluidic membrane with ultralow resistance for highly efficient osmotic power harvesting

Two-dimensional (2D) materials have shown great potential in harvesting osmotic power due to their high membrane selectivity, but the high resistance from tortuous pathways of 2D nanofluidic membranes still impedes the further improvement in output performance. Here, we report an innovative 2D MXCT (MXene/Cu-TCPP) lamellar membrane with ultralow resistance for highly efficient osmotic power generation. The incorporation of 2D Ti3C2Tx MXene with rich functional groups not only resolves the water-stability issue of 2D metal-organic framework (MOF) Cu-TCPP, but provides large surface charges for selective ion transport. The orderly sub-2 nm framework channels of Cu-TCPP provide much shorter permeation pathways for fast ion transport, thus endowing the MXCT membrane with ultralow resistance. Consequently, the MXCT membrane reaches an ultrahigh power output of ∼8.29 W/m2 by mixing seawater and river water, which is ∼275 % higher than that of the pristine MXene membrane. Additionally, it outperforms all the reported single-layer 2D nanosheet-based osmotic power generators under the same experimental conditions in terms of output power and internal resistance (9 kΩ). This work presents a reliable strategy for stabilizing 2D Cu-TCPP MOF in electrolytes, opening new avenues for designing promising 2D nanofluidic membranes for efficient blue energy harvesting and ionic devices.

Nanoscale electrohydrodynamic ion transport: Influences of channel geometry and polarization-induced surface charges.

Electrohydrodynamic ion transport has been studied in nanotubes, nanoslits, and nanopores to mimic the advanced functionalities of biological ion channels. However, probing how the intricate interplay between the electrical and mechanical interactions affects ion conduction in asymmetric nanoconduits presents further obstacles. Here, ion transport across a conical nanopore embedded in a polarizable membrane under an electric field and pressure is analyzed by numerically solving a continuum model based on the Poisson, Nernst-Planck, and Navier-Stokes equations. We report an anomalous ionic current depletion, of up to 75%, and an unexpected rise in current rectification when pressure is exerted along the external electric field. Membrane polarization is revealed as the prerequisite to obtain this previously undetected electrohydrodynamic coupling. The electric field induces large surface charges at the pore tip due to its conical shape, creating nonuniform electrical double layers (EDL) with a massive accumulation of electrolyte ions near the orifice. Once applied, the pressure distorts the quasiequilibrium distribution of the EDL ions to influence the nanopore conductivity. Our fundamental approach to inspect the effect of pressure on the channel EDL (and thus ionic conductance) in contrast to its effect on the current arising from the hydrodynamic streaming of ions further explains the pressure-sensitive ion transport in different nanochannels and physical regimes manifested in past experiments, including the hitherto inexplicit mechanism behind the mechanically activated ion transport in carbon nanotubes. This enhances our broad understanding of nanoscale electrohydrodynamic ion transport, yielding a platform to build nanofluidic devices and ionic circuits with more robust and tunable responses to electrical and mechanical stimuli.

Removal of diclofenac sodium from water using a polyacrylonitrile mixed-matrix membrane embedded with MOF-808.

MOF-808, owing to the synergistic effect of its large surface area and surface charge matching, showed a diclofenac sodium (DCF) removal capacity as high as 630 mg g-1, and the ability to adsorb 436 mg g-1 DCF in two hours, outperforming many common Zr-MOFs under the same conditions. Importantly, a series of free-standing mixed-matrix membranes made by combining polyacrylonitrile with MOF-808 were fabricated and exhibited high efficiency of removing DCF from water via an easily accessible filtration method.

Influence of thermal boundary layer on thermophysical properties of construction materials

The paper considers the influence of thermal boundary layer on the thermal conductivity coefficient of building materials. The influence of thermal boundary layer on the thermal characteristics is shown on the example of cellular materials such as foam concrete, gas silicate and vacuum-powder thermal insulation materials.New ideas about regularities and mechanism of action of such factors as pore size, thickness and composition of interstitial partitions on thermal conductivity of porous materials are proposed. The thermal characteristics of porous systems were analyzed using the theory of similarity (calculation of Grasgoff, Rayleigh, and Prandtl criteria). Calculation of these criteria showed that in cellular materials with pore diameter up to 4 mm the convective component does not influence the heat transfer coefficient. The thermal boundary layer, a low-moving thin layer of gas adsorbed on the inner surface of the pore, has a great influence on the heat transfer processes in the pore. The paper considers the structure of the thermal boundary layer from the approach of the electrical surface properties of the pore and the gas in it. It is shown that the structure of the thermal boundary layer depends on the surface charges of the solid phase and gas. In the environment of air or oxygen denser and more homogeneous in structure thermal boundary layer will have materials, which pore walls will have an effective positive charge, and the thermal boundary layer of materials with a large negative surface charge will be loose, inhomogeneous. In hydrogen medium, on the contrary, materials with an effective negative charge will have a denser and more homogeneous thermal boundary layer structure.

Synthesis and Evaluation of Peptide-Manganese Dioxide Nanocomposites as Adsorbents for the Removal of Strontium Ions.

In this study, a novel organic-inorganic hybrid material IIGK@MnO2 (2-naphthalenemethyl-isoleucine-isoleucine-glycine-lysine@manganese dioxide) was designed as a novel adsorbent for the removal of strontium ions (Sr2+). The morphology and structure of IIGK@MnO2 were characterized using TEM, AFM, XRD, and XPS. The results indicate that the large specific surface area and abundant negative surface charges of IIGK@MnO2 make its surface rich in active adsorption sites for Sr2+ adsorption. As expected, IIGK@MnO2 exhibited excellent adsorbing performance for Sr2+. According to the adsorption results, the interaction between Sr2+ and IIGK@MnO2 can be fitted with the Langmuir isotherm and pseudo-second-order equation. Moreover, leaching and desorption experiments were conducted to assess the recycling capacity, demonstrating significant reusability of IIGK@MnO2.

Single-Layer Hexagonal Boron Nitride Nanopores as High-Performance Ionic Gradient Power Generators.

Atomically thin two-dimensional (2D) materials have emerged as promising candidates for efficient energy harvesting from ionic gradients. However, the exploration of robust 2D atomically thin nanopore membranes, which hold sufficient ionic selectivity and high ion permeability, remains challenging. Here, the single-layer hexagonal boron nitride (hBN) nanopores are demonstrated as various high-performance ion-gradient nanopower harvesters. Benefiting from the ultrathin atomic thickness and large surface charge (also a large Dukhin number), the hBN nanopore can realize fast proton transport while maintaining excellent cation selectivity even in highly acidic environments. Therefore, a single hBN nanopore achieves the pure osmosis-driven proton-gradient power up to ≈3nW under 1000-fold ionic gradient. In addition, the robustness of hBN membranes in extreme pH conditions allows the ionic gradient power generation from acid-base neutralization. Utilizing 1m HCl/KOH, the generated power can be promoted to an extraordinarily high level of ≈4.5nW, over one magnitude higher than all existing ionic gradient power generators. The synergistic effects of ultrathin thickness, large surface charge, and excellent chemical inertness of 2D single-layer hBN render it a promising membrane candidate for harvesting ionic gradient powers, even under extreme pH conditions.

Controlled synthesis of transition metal oxide multi-shell structures and in situ study of the energy storage mechanism

Multi-shell transition metal oxide hollow spheres show great potential for applications in energy storage because of their unique multilayered hollow structure with large specific surface area, short electron and charge transport paths, and structural stability. In this paper, the controlled synthesis of NiCo2O4, MnCo2O4, NiMn2O4 multi-shell layer structures was achieved by using the solvothermal method. As the anode materials for Li-ion batteries, the three multi-shell structures maintained good stability after 650 long cycles in the cyclic charge/discharge test. The in situ transmisssion electron microscope characterization combined with cyclic voltammetry tests demonstrated that the three anode materials NiCo2O4, MnCo2O4 and NiMn2O4 have similar charge/discharge transition mechanisms, and the multi-shell structure can effectively buffer the volume expansion and structural collapse during lithium embedding/delithiation to ensure the stability of the electrode structure and cycling performance. The research results can provide effective guidance for the synathesis and charging/discharging mechanism of multi-shell metal oxide lithium-ion battery anode materials.

Polystyrene nanoplastics aggravated dibutyl phthalate-induced blood-testis barrier dysfunction via suppressing autophagy in male mice

Nanoplastics (NPs) frequently cause adverse health effects by transporting organic pollutants such as dibutyl phthalate (DBP) into organisms by utilizing their large specific surface area, large surface charge, and increased hydrophobicity. However, the effects of NPs combined with DBP on the reproductive systems of mammals are still unclear. The present investigation involved the administration of polystyrene NPs (PS-NPs) to BALB/c mice via gavage, with a size of 100 nm and at doses of 5 mg/kg/day or 50 mg/kg/day, along with DBP at a dose of 0.5 mg/kg/day, or a combination of PS-NPs and DBP, for 30 days, to assess their potential for reproductive toxicity. The co-exposure of mice to PS-NPs and DBP resulted in a significant increase in reproductive toxicities compared to exposure to PS-NPs or DBP alone. This was demonstrated by a marked decrease in sperm quality, significant impairment of spermatogenesis, and increased disruption of the blood-testis barrier (BTB). Furthermore, a combination of in vivo and in vitro investigations were conducted to determine that the co-exposure of DBP and PS-NPs resulted in a noteworthy reduction in the expressions of tight junction proteins (ZO-1 and occludin). Moreover, the in vitro findings revealed that monobutyl phthalate (MBP, the active metabolite of DBP, 0.5 μg/mL) and PS-NPs (30 μg/mL or 300 μg/mL) inhibited autophagy in Sertoli cells, thereby increasing the expression of matrix metalloproteinases (MMPs). The study found that PS-NPs and DBP co-exposure caused harmful effects in male reproductive organs by disrupting BTB, which may be alleviated by reactivating autophagy. The paper's conclusions provided innovative perspectives on the collective toxicities of PS-NPs and other emerging pollutants.

Cytotoxicity Evaluation of Photosensitizer-Conjugated Hexagonal Upconverting Nanoparticles.

In this report, we synthesized hexagonal NaYF4:Yb,Er upconverting nanoparticles (UCNPs) of 171 nm in size with a narrow particle size distribution. To address their colloidal stabi-lity in aqueous media and to incorporate a photosensitizer that can produce reactive singlet oxygen (1O2) to kill tumor cells, UCNPs were conjugated with 6-bromohexanoic acid-functionalized Rose Bengal (RB) and coated with PEG-alendronate (PEG-Ale). The particles were thoroughly characterized by transmission electron microscopy, dynamic light scattering, ATR FTIR, X-ray photoelectron spectroscopy, thermogravimetric analysis, and spectrofluorometry, and 1O2 formation was detected using a 9,10-diphenylanthracene spectrophotometric probe. Cytotoxicity determination on rat mesenchymal stem cells by using the MTT assay showed that neutralization of the large positive surface charge of neat UCNPs with PEG-Ale and the bound RB sensitizer significantly reduced the concentration-dependent cytotoxicity. The presented strategy shows great potential for the use of these particles as a novel agent for the photodynamic therapy of tumors.

Pulsating mode in X-ray generators based on the SBN-61 crystal

Currently, pyroelectric crystals are used in the development of new portable sources of X-ray and neutron radiation. Typically, X-rays are produced when pyroelectric crystals are heated or cooled. In this work, in an X-ray generator based on a ferroelectric crystal of barium-strontium niobate Sr0.61Ba0.39Nb2O6, the pulsations of the electron and X-ray flux were registered at a constant temperature when the gas pressure increased in the range 2·10−2–10−1 Torr. The electron flux had the shape of a cross in the crystal plane. The flash duration did not exceed 0.04 seconds. The observed effect is explained by the movement of domain boundaries on the depolarized crystal face in vacuum, resulting in a large surface charge and, accordingly, an electric potential, leading to the formation of a pulsed electron flux.

Formation mechanism and functional properties of walnut protein isolate and soy protein isolate nanoparticles using the pH-cycle technology.

Walnut protein isolate (WPI) is a nutritious protein with poor solubility, which severely limits its application. In this study, composite nanoparticles were prepared from WPI and soy protein isolate (SPI) using the pH-cycle technology. The WPI solubility increased from 12.64 to 88.53% with a WPI: SPI ratio increased from 1: 0.01 to 1: 1. Morphological and structural analyses illustrated that interaction forces with hydrogen bonding as the main effect jointly drive the binding of WPI to SPI and that protein co-folding occurs during the neutralization process, resulting in a hydrophilic rigid structure. In addition, the interfacial characterization showed that the composite nanoparticle with a large surface charge enhanced the affinity with water molecules, prevented protein aggregation, and protected the new hydrophilic structure from damage. All these parameters helped to maintain the stability of the composite nanoparticles in a neutral environment. Amino acid analysis, emulsification capacity, foaming, and stability analysis showed that the prepared WPI-based nanoparticles exhibited good nutritional and functional properties. Overall, this study could provide a technical reference for the value-added use of WPI and an alternative strategy for delivering natural food ingredients.

Fabrication and characterization of CuO nano-needles from thermal decomposition of Cu(II) metal complex: Fluorometric detection of antibiotics, antioxidant, and antimicrobial activities

In the present study, CuO NPs and CuO nano-needles were synthesized using thermal decomposition of Cu(II) complex derived from 2-(4-(trifluoromethoxy)phenylimino)methyl)-6-methoxyphenol (TMPM6MOP) and characterized by UV–vis DRS, PL, FTIR, XRD, and SEM. The monoclinic crystalline nature of the CuO NPs and CuO needles was illustrated by the XRD. The average size of the CuO NPs (30 nm) and CuO needles (diameter 10 nm, length 250 nm) were estimated from XRD and SEM. The prepared CuO needles were used as a fluorescent sensor for the selective and sensitive detection of ciprofloxacin (Cipro) among various antibiotics at diverse pH (4.0–9.0) conditions and the optimized pH = 5.0. The response of Cipro using the CuO needles was linear over the range from 10 to 100 µM L–1. This sensor showed the lowest limit of detection of 0.21 nM and was much lower than the other antibiotic sensors. In addition, the sensor is highly sensitive, selective, and durable in the presence of a range of potentially interfering fluorometric active compounds due to the large surface area and positive surface charge of the CuO needles. Moreover, antimicrobial activities and antioxidant activities were investigated to evaluate the biological potential of the CuO NPs and CuO needles.

Study of the thermal behaviour of a derivative based on a zirconium agent (modified montmorillonite) and determination of the physical characteristics

In this research, untreated Algerian maghnite has been used to develop two types of modified clays: the first one is a homo-ionic sodium clay (Na-Mag) which is a support to develop a montmorillonite by insertion of zirconium hydroxyl cations. The different series of techniques, including thermogravimetric analysis (TGA), differential thermal analysis (DTA), dynamic light scattering (DLS), and zeta potential (ζ), have been used to define the physical characteristics of the clays by studying their particle size distribution as well as the thermal profile. In addition, the pillar-shaped montmorillonite (Maghnite) exhibit a negative charge even when its pH reach 2.8. This large negative surface charge of montmorillonite suggests optimal removal of organic molecule particles present in the aqueous medium. The results obtained by Fourier transform infrared (FT-IR) analysis show that the bands characterizing the presence of intercalating agents are visible. Thermography of the zirconium pillar species shows an improvement in the thermal stability of the silicate structure with two well differentiated zones. Adsorbed organic cations result in a reduction of the surface load, that is, a decrease of its negativity, as well as a cancellation of the charge.

Essence of the Enhanced Osmotic Energy Conversion in a Covalent Organic Framework Monolayer.

Low membrane conductivity originated from a high membrane thickness has long been the "Achilles heel" of the conventional polymeric membrane, greatly hampering the improvement of the output power density in osmotic power generation. Herein, we demonstrate a molecularly-thin two-dimensional (2D) covalent organic framework (COF) monolayer membrane, featured with ultimate thickness, high pore density, and tight pore size distribution, which performs as a highly efficient osmotic power generator. Despite the large pore size up to 3.8 nm and relatively low surface charge density of 2.2 mC m-2, the monolayer COF membrane exhibits a high osmotic current density of 16.7 kA m-2 and an output power density of 102 W m-2 under 50 times the NaCl salinity gradient (0.5 M/0.01 M). This superior power density could be further improved to 170 W m-2 in the real seawater/river water gradient system. When the large pore size and low surface charge density are considered, this superior performance is not expected. Computational studies further reveal that the ultimate membrane permeability originated from the high membrane porosity, rather than ion selectivity, plays a dominant role in the production of high current density, especially under high salinity. This work provides an alternative strategy to realize improved output power density in ultrapermeable membranes.

Tailored construction of Ag/WO3 nanospindles modified SERS substrates: An efficient analytical assay for identification of neonicotinoids on the surface of fruits

The peel of fruits and vegetables contain toxic elements present in pesticide like neonicotinoids, whose presence cause various health issue in humans. In this regard, for the first time, we demonstrate the ultrasensitivity detection of neonicotinoids imidacloprid on the surface of grapes by a modified SERS substrate with microspheres constitution of Ag/WO3 nanospindles. Surface engineering, phase purity, thermal stability, and elemental states of the as developed nanospindles were explored by electron microscopy, XRD, XPS, spectroscopy analysis, and the detection of imidacloprid was studied through SERS. The modified SERS substrate prominently increased the efficiency of the sensing of imidacloprid, an outstanding wide range from 10−1 to 10−11 M, a low detection range of 3 ng/cm2 (S/N = 3) with correlation coefficient R2 = 0.9904, good reproducibility, and strong anti-interference ability compared to reports data. Notably, the improved sensing activity of Ag/WO3 nanospindles can be attributed to the large surface area and charge transfer behavior. Ag nanoparticles served as a high conductivity matrix while preventing WO3 from the synergistic effect as discussed in the reaction mechanism section. Finally, the projected SERS substrate has extreme potential for pesticide detection of on-site analysis which is the upcoming scenario.

The combined toxic effects of polyvinyl chloride microplastics and di(2-ethylhexyl) phthalate on the juvenile zebrafish (Danio rerio)

Microplastics (MPs) have the characteristics of large specific surface area, high hydrophobicity and surface charge, so they are easy to combine with other pollutants and cause toxic effects on aquatic organisms. Here, we prepared a polyvinyl chloride-microplastics (PVC-MPs) fragmentation model to simulate the real microplastic state, and characterized its composition, morphology, particle size and zeta potential. On this basis, we used single and compound exposure of PVC and di(2-ethylhexyl) phthalate (DEHP) to explore their effects on hatchability and mortality of zebrafish (Danio rerio) embryos and toxicity to oxidative stress and cardiac development in zebrafish larvae. Herein, PVC-MPs slowed down the hatching rate of zebrafish embryos and induced the death of zebrafish, while DEHP could slow down the induced of death, it had no effect on hatching rate. The PVC-MPs/DEHP single pollution could induce the reactive oxygen species (ROS) and activated the antioxidant defense signaling pathway, while the compound group showed the level of feedback autoregulation of NF-E2-related factor 2 (Nrf2) signaling pathway. The single pollution also could inhibit the expression of genes related to cardiac development, while the combined pollution showed an antagonistic effect. This study provided a theoretical basis for the ecotoxicology and biomonitoring of MPs in the natural state.