Size- and density-dependent acoustic differential bioassembly of spatially-defined heterocellular architecture.

Emerging acoustic bioassembly represents an attractive strategy to build cellular closely-packed organotypic constructs in a tunable manner for biofabrication. However, simultaneously assemble heterogeneous cell types into heterocellular functional units with spatially-defined cell arrangements, such as complementary and sandwich cytoarchitectures, remains a long-lasting challenge. To overcome this challenge, herein we present an acoustic differential bioassembly technique to assemble different cell types at the distinct positions of the acoustic field based on their inherent physical characteristics including cellular size and buoyant density. Specifically, different cell types can be differentially assembled beneath the nodal or the antinode regions of the Faraday wave to form complementary cytoarchitectures, or be selectively positioned at the center or edge area beneath either the nodal or the antinode regions to form sandwich cytoarchitectures. Using this technique, we assemble human induced pluripotent stem cell-derived liver spheroids and endothelial cells into hexagonal cytoarchitecturesin vitroto mimic the cord and sinusoid structures in the hepatic lobules. This hepatic lobule model reconstitutes liver metabolic and synthetic functions, such as albumin secretion and urea production. Overall, the acoustic differential bioassembly technique facilitates the construction of human relevantin vitroorganotypic models with spatially-defined heterocellular architectures, and can potentially find wide applications in tissue engineering and regenerative medicine.

Development of a high-throughput micropatterned agarose scaffold for consistent and reproducible hPSC-derived liver organoids.

Liver organoids represent emerging human-relevantin vitroliver models that have a wide range of biomedical applications in basic medical studies and preclinical drug discovery. However, the generation of liver organoids currently relies on the conventional Matrigel dome method, which lacks precise microenvironmental control over organoid growth and results in significant heterogeneity of the formed liver organoids. Here, we demonstrate a novel high-throughput culture method to generate uniform liver organoids from human pluripotent stem cell-derived foregut stem cells in micropatterned agarose scaffold. By using this approach, more than 8000 uniformly-sized liver organoids containing liver parenchyma cells, non-parenchymal cells, and a unique stem cell niche could be efficiently and reproducibly generated in a 48-well plate with a size coefficient of variation significance smaller than that in the Matrigel dome. Additionally, the liver organoids highly expressed liver-specific markers, including albumin (ALB), hepatocyte nuclear factor 4 alpha (HNF4α), and alpha-fetoprotein (AFP), and displayed liver functions, such as lipid accumulation, glycogen synthesis, ALB secretion, and urea synthesis. As a proof of concept, we evaluated the acute hepatotoxicity of acetaminophen (APAP) in these organoids and observed APAP-induced liver fibrosis. Overall, we expect that the liver organoids will facilitate wide biomedical applications in hepatotoxicity analysis and liver disease modeling.

High-throughput bioengineering of homogenous and functional human-induced pluripotent stem cells-derived liver organoids via micropatterning technique.

Human pluripotent stem cell-derived liver organoids are emerging as more human-relevant in vitro models for studying liver diseases and hepatotoxicity than traditional hepatocyte cultures and animal models. The generation of liver organoids is based on the Matrigel dome method. However, the organoids constructed by this method display significant heterogeneity in their morphology, size, and maturity. Additionally, the formed organoid is randomly encapsulated in the Matrigel dome, which is not convenient for in situ staining and imaging. Here, we demonstrate an approach to generate a novel type of liver organoids via micropatterning technique. This approach enables the reproducible and high-throughput formation of bioengineered fetal liver organoids with uniform morphology and deterministic size and location in a multiwell plate. The liver organoids constructed by this technique closely recapitulate some critical features of human liver development at the fetal stage, including fetal liver-specific gene and protein expression, glycogen storage, lipid accumulation, and protein secretion. Additionally, the organoids allow whole-mount in-situ staining and imaging. Overall, this new type of liver organoids is compatible with the pharmaceutical industry's widely-used preclinical drug discovery tools and will facilitate liver drug screening and hepatotoxic assessment.

Performance and mechanism of tea waste biochar in enhancing the removal of tetracycline by peroxodisulfate.

In this work, tea waste biochar was prepared and used to activate peroxodisulfate (PDS) for the removal of tetracycline (TC) efficiently. And SEM, XRD, Raman, and FTIR were used to characterize the biochar. The effects of reaction conditions including initial pH, biochar dosage, and PDS concentration on the removal of TC were explored, and the result showed that compared with the biochar prepared at 400 °C and 500 °C, the biochar pyrolyzed at 600 °C (TBC600) had the highest TC removal performance due to its higher sp2 hybrid carbon content, richer defective structure, and stronger electron deliverability. Under the optimal dosage of PDS (4 mM) and TBC600 (0.8 g L-1), the removal efficiency of TC (10 mg L-1) reached 81.65%. After four cycles of TBC600, the removal rate could still reach 75.51%, indicating that TBC600 has excellent stability. In addition, quenching experiments and electron paramagnetic resonance (EPR) verified that the active oxygen including SO4·-, ·OH, O2·-, and singlet oxygen (1O2) was involved, among which 1O2 and OH were the main active substance in the TC removal. Therefore, this work provided a green and efficient persulfate activator and a method for recycling tea waste.

Microplastic pollution characteristic in surface water and freshwater fish of Gehu Lake, China.

Much more attention has been poured into microplastic pollution in freshwater systems recently. In the present study, the pollution of microplastics (MPs) in surface water and freshwater fish (crucian carp, etc.) were investigated from Gehu Lake, which is the second largest lake in southern Jiangsu after Taihu Lake. The result manifested that the average abundance of MPs was respectively 6.33±2.67 n/L for surface water and 10.7 items per individual for freshwater fish. The distribution of MPs in Gehu Lake varied from place to place, with the highest abundance of MPs was observed in the two estuaries of the eastern part of the lake. It was speculated that topographical factors and human factors were the main factors affecting the abundance and distribution of MPs. Transparent fibers were the main type of MPs in water samples, accounting for 69.70% of all detected particles. Meanwhile, most of the MPs ingested by freshwater fish were fibers, and the main colors were transparent and blue. In addition, the dominant size of the MPs was between 0.1 to 0.5 mm in water and fish samples. Moreover, PES, man-made fiber, and PP were the dominant polymer types in the surface water and fish samples. The results of this investigation can provide basic data for the research and management of MPs in freshwater systems.

Enhancing degradation of atrazine by Fe-phenol modified biochar/ferrate(VI) under alkaline conditions: Analysis of the mechanism and intermediate products.

In this study, Fe-phenol modified biochar was prepared to enhance atrazine (AT) degradation by ferrate (Fe(VI)) under alkaline conditions, and the properties, mechanism and transformation pathways were extensively investigated. Degradation experiments showed that Fe-phenol modified biochar was more beneficial for improving the oxidation capacity of Fe(VI) than unmodified biochar, and the biochar with a molar ratio of Fe3+ to phenol of 0.1:5 (BC-2) showed the best promoting effect, and more than 94% of AT was removed at pH = 8 within 30 min. Moreover, the rate of oxidation (kapp) of AT by Fe(VI) increased 1.86 to 4.11 times by the addition of BC-2 in the studied pH range. Fe(Ⅴ)/Fe(Ⅳ) and ·OH were the main active oxidizing species for AT degradation in the Fe(VI)/BC-2 group and contributed to 70% and 24%, respectively, of degradation. The formation of ·OH and Fe(Ⅴ)/Fe(Ⅳ) was mainly due to the persistent free radicals and reducing groups on the surface of BC-2. AT was oxidized to 12 intermediate products in the Fe(VI)/BC-2 group through 5 pathways: alkyl hydroxylation, dealkylation, dichlorination, hydroxylation, alkyl dehydrogenation and dichlorination. Compared with those of the initial solution, the total organic carbon content and toxicity after the reaction decreased by 32.8% and 19.02%, respectively. Therefore, the combination of Fe-phenol modified biochar and Fe(VI) could be a promising method for AT removal.

Investigation of the Adsorption of Sulfamethoxazole by Degradable Microplastics Artificially Aged by Chemical Oxidation.

In this study, three different types of microplastics were aged by the thermal activation K2S2O8 method to investigate the adsorption behavior for sulfamethoxazole (SMX) in aqueous solution. The effects of pH, salinity and humic acid (HA) on adsorption behavior were also investigated. At the same time, the morphology and functional groups of microplastics before and after adsorption were characterized. As the aging time increased, the adsorption capacity of the microplastics also increased significantly. Whether it was pristine or aged, polylactic acid (PLA) had the highest adsorption capacity. The adsorption capacity of microplastics was the largest under acidic conditions, and its adsorption capacity decreased significantly in alkaline solutions. The presence of salinity inhibited the adsorption of SMX on polyethylene terephthalate (PET) and PP, but the adsorption capacity of PLA increases when salinity was above 10‰. The adsorption of SMX on microplastics was promoted by HA. When the concentration of HA was 20 mg/L, the adsorption capacity of PLA and PET decreased. Kinetic and isotherm fits were applied to the adsorption process. The increase in sorption capacity was related to the development of holes and cracks and the enhanced number of surface oxygen-containing functional groups. The adsorption kinetics to pristine microplastics conformed to a pseudo-first-order kinetic model, while the kinetics of the aged microplastics conformed to a pseudo-second-order kinetic model. It implies that the adsorption of SMX by aging microplastics involves multiple processes. The adsorption isothermal adsorption process of SMX by microplastics accorded with Freundlich model, belonging to multi-layer adsorption.

Influence of wastewater treatment process on pollution characteristics and fate of microplastics.

The increasing abundance of microplastics (MPs) in rivers and oceans continues to face major challenges. In particular, MPs with smaller particle sizes are difficult to identify and quantify when they reach the environment. This study investigated four typical wastewater treatment plants (WWTPs), including urban WWTPs and industrial WWTP with different treatment technologies. The results showed that the average abundance of MPs in the influent and effluent was 538.67 ± 22.05 n/L to 1290 ± 65.26 n/L and 20.44 ± 1.19 n/L to 40.67 ± 11.12 n/L. The primary and secondary treatment processes can effectively remove MPs between 51.04% and 72.82% from wastewater. After tertiary treatments, the removal efficiency was further increased to more than 90%. The study aims to explore the removal mechanism of MPs in each stage of the wastewater treatment process and to reveal the fate of MPs in WWTPs, and help to understand their future monitoring to optimize the wastewater treatment process.

Insight into the effect of pH-adjusted acid on thermodynamic properties and crystallization sequence during evaporative-crystallization process of hydrolyzed urine.

The evaporative-crystallization process (ECP) is a frequently used approach for complete nutrient recovery from human urine, and crystallization sequence is related to the selection of seed and the optimization of crystallization process. In this study, three hydrolyzed urine (HU) samples, which were acidified to an initial pH of 4 with HCl, H2SO4, and H3PO4, were used to recover crystallized products by ECP, their crystallization process and thermodynamic properties during ECP were compared, and the detailed crystallization sequence was analyzed using the PHREEQC-2 simulation. The results showed that the pH-adjusted acid has a significant effect on crystal precipitation, and the new crystal in HCl-4-HU, H2SO4-4-HU, and H3PO4-4-HU first appeared at volume concentration factors (CFV) of 19.61, 9.90, and 9.96, respectively. Furthermore, the simulated crystallization process characteristics of HU by PHREEQC-2 have a good fit with the actual experimental data, and crystallization sequence of HCl-4-HU, H2SO4-4-HU, H3PO4-4-HU during ECP were NH4Cl (CFV from 10.25 to 100) / NaCl (CFV from 71.43 to 100), NH4NaSO4 (CFV from 10.25 to 55.56) / NH4Cl (CFV from 20 to 100) / (NH4)2SO4 (CFV from 40.45 to 100), NH4H2PO4 (CFV from 10.25 to 100) / NaH2PO4 (CFV from38.46 to 55.5) / NaCl (CFV from 45.46 to 100), respectively. The present study clearly reveals the crystallization sequence and thermodynamic properties of nutrient elements in acidified HU, which provides an important theoretical basis for the optimization of crystallized products obtained from HU for future study.

Facile synthesis of a novel Ag3PO4/MIL-100(Fe) Z-scheme photocatalyst for enhancing tetracycline degradation under visible light.

In this work, a novel visible light-driven heterostructure Ag3PO4/MIL-100(Fe) composite photocatalyst was successfully synthesized via facile chemical deposition method at room temperature. Especially when the mass ratio of Ag3PO4 was 20% of MIL-100(Fe) (APM-2), it displayed the best photocatalytic performance, for which the degradation rate of tetracycline (TC) in conventional environment was 6.8 times higher than that of bare MIL-100(Fe). In addition, the effects of the initial concentration and pH of the solution on the degradation of tetracycline were also studied, and the results showed that the degradation of tetracycline was more favorable in a weakly alkaline environment. The excellent performance of Ag3PO4/MIL-100(Fe) composites was attributed to the fact that on the basis of having adequate photocatalytic active sites, modifying MIL-100(Fe) with an appropriate amount of Ag3PO4 particles can more effectively separate photogenerated electron-hole pairs. Five cycles of experiments showed that APM-2 has good photostability. Lastly, it was proved through quenching experiments that •O2-, h+, and •OH all played corresponding roles in the degradation process, and a possible Z-scheme heterostructure photocatalytic degradation mechanism was proposed.

In situ hydrothermal fabrication of visible light-driven g-C3N4/SrTiO3 composite for photocatalytic degradation of TC.

A series of g-C3N4/SrTiO3 (CN/SrTiO3) composites with the different mass ratio of g-C3N4 were prepared by facile in situ hydrothermal growth method, which was utilized to degrade tetracycline antibiotics (TC) under the visible light. The obtained samples were characterized by XRD, SEM, XPS, FT-IR, and UV-vis DRS. The photocatalytic performance was also investigated in detail. The obtained 20% CN/SrTiO3 composite is sixfold of the pure SrTiO3 and twofold of the pristine g-C3N4 under the visible light irradiation. This impressive performance of the heterojunction is ascribed to the effective restraint of the charge carrier recombination and expanded light absorption region. Moreover, the stability of the composite is also researched in detail. At last, a possible photocatalytic mechanism and charge carrier transfer pathway were further discussed.

Construction of precious metal-loaded BiOI semiconductor materials with improved photocatalytic activity for microcystin-LR degradation.

The composite photocatalyst of precious metal loaded on BiOI (M/BiOI, M = Pt, Au, Ag) was prepared by photochemical deposition and used for the photocatalytic degradation of microcystins (MC-LR). The material was characterized by X-ray powder diffraction (XRD), field emission scanning electron microscopy (FESEM), ultraviolet visible (UV-vis) diffuse reflectance spectroscopy, X-ray photoelectron spectroscopy (XPS), and photoluminescence spectra (PL). The effect of photodegradation of MC-LR and the possible mechanism were investigated. It turned out that, among precious metals of Pt, Au, and Ag, Ag had the most significant improvement for photocatalytic activity of BiOI and Au was the least. The Ag/BiOI catalyst was illuminated 2 h under the simulated visible-light condition with the optimal load ratio of Ag catalyst (1.0 wt%) and the 2-h illumination under simulated visible-light condition, the degradation rate of MC-LR was 61.26% ± 0.12%. In addition, through the experiment of trapping agent and the analysis of electron spin resonance (ESR), we could conclude that the main active species is O2- in the process of the degradation of MC-LR by three precious metal-loaded BiOI semiconductor materials.

Effects of Elevated Tetracycline Concentrations on Aerobic Composting of Human Feces: Composting Behavior and Microbial Community Succession.

The effects of antibiotics on aerobic composting are investigated by dosing of tetracycline (TC) in fresh human feces with sawdust as biomass carrier. Variability in process parameters such as temperature, pH, water-soluble carbon, germination index (GI) and dehydrogenase activity (DHA) are evaluated at TC dosages of 0, 100, 250 and 500 mg/kg in a 21-day composting. Moreover, microbial community succession is examined by high-throughput 16S rRNA gene sequencing. Findings indicate significant impacts to the process parameters with the increase of TC concentration such as inhibition of temperature increases during aerobic composting, lowering of pH, increasing of water-soluble carbon residue, a decrease of GI, and hindering of DHA. Furthermore, elevated TC concentrations significantly alter the microbial community succession and reduce the community diversity and abundance. Therefore, interference in microbial community structures and a hindrance to biological activity are believed to be the main adverse effects of TC on the composting process and maturity of the composting products.

Antitumor immunostimulatory activity of polysaccharides from Panax japonicus C. A. Mey: Roles of their effects on CD4+ T cells and tumor associated macrophages.

In this study, chemical properties of polysaccharides from rhizomes of Panax japonicus C. A. Mey (PSPJ) were investigated and the antitumor immunostimulatory activity of PSPJ was assessed in mice bearing H22 hepatoma cells. Chemical properties of PSPJ were determined by GC, FT-IR, 1H NMR and 13C NMR analysis. Furthermore, we showed that PSPJ repressed H22 tumor growth in vivo with undetectable toxic effects on tumor-bearing mice. PSPJ upregulated host thymus/spleen indexes and ConA/LPS-induced splenocyte proliferation. Cytotoxic activities of natural killer and CD8+ T cells against H22 hepatoma cells were also elevated. Tumor transplantation led to substantial apoptosis of CD4+ T cells and dysregulation of the cytokine profile secreted by CD4+ T cells. These abnormalities were alleviated by PSPJ in a dose-dependent manner. In tumor-associated macrophages (TAMs), PSPJ reduced the production of immunosuppressive factors such as TGF-ß, IL-10 and PEG2. In addition, M2-like polarization of TAMs was also considerably declined in response to PSPJ. Our findings clearly demonstrated the antitumor immunostimulatory activity of PSPJ and supported considering PSPJ as an adjuvant reagent in clinical treatment of malignant diseases.

A Hybrid Wavelet-Based Method for the Peak Detection of Photoplethysmography Signals.

The noninvasive peripheral oxygen saturation (SpO2) and the pulse rate can be extracted from photoplethysmography (PPG) signals. However, the accuracy of the extraction is directly affected by the quality of the signal obtained and the peak of the signal identified; therefore, a hybrid wavelet-based method is proposed in this study. Firstly, we suppressed the partial motion artifacts and corrected the baseline drift by using a wavelet method based on the principle of wavelet multiresolution. And then, we designed a quadratic spline wavelet modulus maximum algorithm to identify the PPG peaks automatically. To evaluate this hybrid method, a reflective pulse oximeter was used to acquire ten subjects' PPG signals under sitting, raising hand, and gently walking postures, and the peak recognition results on the raw signal and on the corrected signal were compared, respectively. The results showed that the hybrid method not only corrected the morphologies of the signal well but also optimized the peaks identification quality, subsequently elevating the measurement accuracy of SpO2 and the pulse rate. As a result, our hybrid wavelet-based method profoundly optimized the evaluation of respiratory function and heart rate variability analysis.

Effect of initial pH and pH-adjusted acid on nutrient recovery from hydrolysis urine by combining acidification with evaporation-crystallization.

Nutrient recovery from human urine is a promising pretreatment of domestic wastewater and provides a sustainable recyclability of nitrogen (N), phosphorus (P), and potassium (K). In this study, we present a method to recover all nutrients from hydrolysis urine (HU) in the form of solid products by combining acidification with evaporation-crystallization. The effect of initial pH (pHinit.) on N retention was investigated, and the optimal pHinit. was further determined by analysis of N retention efficiency. Additionally, crystallization process and product composition based on different pH-adjusted acids were also compared. The results revealed that pHinit. of HU was the key factor for N retention, and the optimal pHinit. was 4. In addition, compared with HCl and H2SO4, acidification by H3PO4 could effectively reduce energy consumption and improve nutrient content in urine-derived solid products (UDSPs) but increase the acid consumption. The major compositions (mass percentage, %) in UDSPs-Cl, UDSPs-S, and UDSPs-P were salammoniac (80%), lecontite (41%) and ammonium nitrate sulfate (30%), and biphosphammite (84%), respectively. The results also demonstrated that the method of mixing of UDSPs-Cl/UDSPs-S and UDSPs-P and addition of fillers such as calcite, ground limestone, or ground dolomite into them is suitable for improving nutrient balance and fertilizer efficiency.

Isoliensinine induces dephosphorylation of NF-kB p65 subunit at Ser536 via a PP2A-dependent mechanism in hepatocellular carcinoma cells: roles of impairing PP2A/I2PP2A interaction.

Our previous study discovered that isoliensinine (isolie) triggers hepatocellular carcinoma (HCC) cell apoptosis via inducing p65 dephosphorylation at Ser536 and inhibition of NF-κB. Here, we showed that isolie promoted p65/PP2A interaction in vitro and in vivo. Repression of PP2A activity or knockdown of the expression of PP2A-C (the catalytic subunit of PP2A) abrogated isolie-provoked p65 dephosphorylation. I2PP2A is an endogenous PP2A inhibitor. Isolie directly impaired PP2A/I2PP2A interaction. Knockdown of I2PP2A boosted p65/PP2A association and p65 dephosphorylation. Overexpression of I2PP2A restrained isolie-induced p65 dephosphorylation. Untransformed hepatocytes were insensitive to isolie-induced NF-κB inhibition and cell apoptosis. In these cells, basal levels of I2PP2A and p65 phosphorylation at Ser536 were lower than in HCC cells. These findings collectively indicated that isolie suppresses NF-κB in HCC cells through impairing PP2A/I2PP2A interaction and stimulating PP2A-dependent p65 dephosphorylation at Ser536.

Degradation of typical antibiotics during human feces aerobic composting under different temperatures.

Four typical antibiotics were added to human feces for aerobic composting using batch reactors with sawdust as the bulk matrix. Under three composting temperatures (room temperature, 35 ± 2 °C and 55 ± 2 °C), decreases in the extractable concentrations of antibiotics in the compost were monitored for 20 days. As a result, the removals of extractable tetracycline and chlortetracycline were found to be more temperature-dependent than the removals of sulfadiazine and ciprofloxacin. However, more than 90 % of all of the extractable antibiotics were removed at 55 ± 2 °C. Three specific experiments were further conducted to identify the possible actions for antibiotic removal, including self-degradation in aqueous solution, composting with a moist sterile sawdust matrix without adding feces and composting with human feces and moist sterile sawdust. As a result, it was found that the removal of tetracycline and chlortetracycline was mainly due to chemical degradation in water, whereas the removal of sulfadiazine was mainly attributed to adsorption onto sawdust particles. The microbial activity of compost varied with temperature to a certain extent, but the differences were insignificant among different antibiotics. Although microbial action is important for organic matter decomposition, its contribution to antibiotic degradation was small for the investigated antibiotics, except for ciprofloxacin, which was degraded by up to 20 % due to microbial action.

Characteristics of simultaneous ammonium and phosphate adsorption from hydrolysis urine onto natural loess.

Nutrient recovery from human urine is a promising pretreatment of domestic wastewater and provides a sustainable recyclability of N and P. In this study, batch experiments were conducted to identify the characteristics of natural loess (NL) for the adsorption and recovery of ammonium and phosphate from hydrolysis urine (HU). The adsorption mechanisms, the adsorption kinetics and isotherms, as well as the major influencing factors, such as pH and temperature, were investigated. Results revealed that adsorption of ammonium occurred by means of ion exchange and molecule adsorption with the ≡ Si-OH groups, while phosphate adsorption was based on the calcium phosphate precipitation reaction and formation of inner-sphere complexes with ≡ M-OH groups. The adsorption processes of ammonium and phosphate were well described by the pseudo-second-order kinetic model and the Freundlich isotherm model. Adsorption of phosphate was endothermic, while ammonium adsorption was exothermic. Furthermore, the maximum ammonium and phosphate adsorption capacities of NL was 23.24 mg N g(-1) and 4.01 mg P g(-1) at an initial pH of 9 and 10, respectively. Results demonstrated that nutrient-adsorbed NL used as compound fertilizer or conventional fertilizer superaddition was feasible for its high contents of N and P as well as its environmental friendliness.

PEG2000-DPSE-coated quercetin nanoparticles remarkably enhanced anticancer effects through induced programed cell death on C6 glioma cells.

In this study, PEGylated nanoparticles quercetin drug delivery vehicles were investigated as carriers for anticancer drugs induced programed cell death (PCD). PEG2000-DPSE-coated quercetin nanoparticles were prepared and tumor cell killing efficacy was studied on glioma C6 cells and assayed for cell survival, apoptosis, or necrosis. The levels of ROS production and mitochondrial membrane potential (ΔΨm) were determined. Western blot assayed p53, p-p53, cytochrome C, and caspase proteins expression were also studied. Results indicate that PEG2000-DPSE-QUE-NPS showed dose-dependent cytotoxicity to C6 glioma cells and enhanced ROS accumulation induced upregulation of p53 protein, which was accompanied with an increase in cytochrome c and caspase-3 protein levels. These results support the hypothesis that quercetin nanoparticles-coated PEG2000-DPSE remarkably enhanced anticancer effect of induced programed cell death on C6 glioma cells. Overall, PEG2000-DPSE-coated quercetin nanoparticles showed promising potential as a drug carrier for cancer therapy.