MICROCHEMICAL JOURNAL
·
2022
·
IF 5.304
Yuan Peng,Si-Yuan He,Fang-Huan Wang,Hao-Bo Zheng,Zhe Meng
In this work, a magnetic mesoporous molybdenum disulfide/graphite nanosheets (mm-MoS 2 /GN) was successfully synthesized and applied to magnetic solid phase extraction (MSPE) of 13 polycyclic aromatic hydrocarbons (PAHs) from edible oil samples. The prepared mm-MoS 2 /GN was characterized by FT-IR, XRD, VSM, BET, SEM and TEM. The influence of various parameters such as the adsorbent mass, adsorption/desorption time, and elution solvent through response surface methodology in MSPE was investigated. The porous and fluffy structure with rich active sites (π interactions, electrostatics, hydrogen bonds) and amphiphilicity properties of mm-MoS 2 /GN make it an ideal material for the separation and enrichment of trace PAHs in edible oils. Under optimal MSPE and GC-MS conditions, the linearity ranges of the proposed method were 1.0–100.0 μg·kg −1 with a satisfactory correlation coefficient above 0.9907. The limits of detection and quantification for 13 PAHs were 0.10–2.50 μg·kg −1 and 0.85–5.00 μg·kg −1 , respectively. The intra- and inter-day precisions were less than 3.0 % and 3.6 %, respectively. The recoveries for spiked edible oil samples ranged from 70.2 % to 112.6 % with RSDs of less than 5.8 %. In this work, a novel, rapid, economic and effective method was proposed, and successfully applied to detect polycyclic aromatic hydrocarbons in several oil samples from local market.
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JOURNAL OF HAZARDOUS MATERIALS
·
2022
·
IF 14.224
Xian Cao,Chong Zhang,Shuai Zhang,Takashi Sakamaki,Hui Wang,Xian-Ning Li
In the water environment such as lakes, there is a phenomenon that the sediment and overlying water are polluted at the same time. In this study, A microbial electrochemical system with an embedded active electrode was developed for simultaneous removal of polycyclic aromatic hydrocarbons in sediment and antibiotics in overlying water by in-situ utilization of electrons. In the closed-circuit group, the pyrene concentration in sediment decreased from 9.94 to 2.08 mg/L in 96 d, and the sulfamethoxazole concentration in water decreased from 5.12 to 1.12 mg/L in 168 h. These values were 18.71 % and 31.21 % higher, respectively, than those of the open-circuit group. The pyrene degradation pathway may be from polycyclic aromatic substances to low-cyclic aromatic hydrocarbons via successive breakdown of benzene rings. Multiple metabolites produced by reduction verified that SMX or its intermediates were reductively degraded in water. On the active electrode, the relative abundances of Acetobacterium and Piscinibacte r, which were genera related to SMX degradation, was promoted, while the electricity-producing genus Pseudomonas was inhibited. ccdA , pksS , torC , and acsE genes related to extracellular electron transport may accelerate electron transport. Electrons could be transferred to SMX under the influence of proteins involved in extracellular electron transport, and SMX could be degraded reductively as an electron acceptor by microbes. Generation of electrons and in-situ utilization for simultaneous removal of solid-liquid two-phase pollutants will provide mechanistic insight into pollutant biodegradation by microbial electrochemistry and promote the development of sustainable bioremediation strategies for surface water.
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ANALYTICAL CHEMISTRY
·
2022
·
IF 8.008
Fengjian Chu,Gaosheng Zhao,Wangyu Li,Wei Wei,Weiwei Chen,Zihan Ma,Zhan Gao,Nazifi Sani Shuaibu,Jikui Luo,Bingwen Yu,Hongru Feng,Yuanjiang Pan,Xiaozhi Wang
The atmospheric oxidation of chemicals has produced many new unpredicted pollutants. A microwave plasma torch-based ion/molecular reactor (MPTIR) interfacing an online mass spectrometer has been developed for creating and monitoring rapid oxidation reactions. Oxygen in the air is activated by the plasma into highly reactive oxygen radicals, thereby achieving oxidation of thioethers, alcohols, and various environmental pollutants on a millisecond scale without the addition of external oxidants or catalysts (6 orders of magnitude faster than bulk). The direct and real-time oxidation products of polycyclic aromatic hydrocarbons and p-phenylenediamines from the MPTIR match those of the long-term multistep environmental oxidative process. Meanwhile, two unreported environmental compounds were identified with an MPTIR and measured in the actual water samples, which demonstrates the considerable significance of the proposed device for both predicting the environmental pollutants (non-target screening) and studying the mechanism of atmospheric oxidative processes.
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SCIENCE OF THE TOTAL ENVIRONMENT
·
2022
·
IF 10.753
Taiguang Li,Mingyong Wang,Yongmei Hao
A novel magnetic core-shell Fe 3 O 4 @SiO 2 @CdS embedded graphene oxide (GO) composite was prepared for the visible-light-driven photodegradation of high ring number polycyclic aromatic hydrocarbons (PAHs). The potential application of GO-Fe 3 O 4 @SiO 2 @CdS was evaluated through the photodegradation of phenanthrene and pyrene in deionized water, tap water , and lake water, respectively. It was found that GO-Fe 3 O 4 @SiO 2 @CdS could remove 86.4 % of phenanthrene and 93.4 % of pyrene, suggesting its potential for the degradation of high-ring number PAHs. The density functional theory (DFT) calculations demonstrate that pyrene has more active sites attacked by free radicals. The photoelectrochemical measurement and quenching experiments indicate that GO can transfer photoelectrons efficiently, resulting in the crucial radicals ( O 2 − , OH and 1 O 2 ). More importantly, the photocatalytic activity kept almost constant during five cycles, confirming the significant anti-photocorrosion of GO-Fe 3 O 4 @SiO 2 @CdS. This work provides some new insights into the removal of PAHs with high-ring numbers in the natural water environment.
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Advanced Healthcare Materials
·
2026
·
IF 11
Yixuan Gao,Haonan Wu,Jian Yang,Junyu Meng,Junhua Zhang,Han Zhang,Jian Yang
Acute lung injury (ALI) features vascular endothelial damage, impaired barrier function, and excessive ROS accumulation, which depletes endogenous peroxidases and disrupts redox homeostasis. Transcriptomic comparison between control and ALI model groups verified marked dysregulation of genes linked to oxidative stress, inflammation, and endothelial barrier dysfunction. To date, exogenous enzyme supplementation represents a necessary strategy for treating ALI, yet very few options are available to halt excessive ROS accumulation within the critical therapeutic time window. Here, we developed a nanozyme system (SCP@CD) capable of solving this problem by encapsulating autofluorescent Mn/S-co-doped carbon dots (CDs) into polymer micelles self-assembled via a Schiff base formed by sialic acid-modified chitosan oligosaccharide and protocatechualdehyde. As a targeting ligand, sialic acid enables active targeting of E-selectin on inflamed endothelium, realizing enhanced fluorescence for noninvasive in vivo tracking. Chitosan oligosaccharide linked to sialic acid reduces systemic toxicity, while the Schiff base formed by chitosan oligosaccharide and protocatechualdehyde mediates pH-responsive release via cleavage in acidic inflammatory microenvironments. SCP@CD functions as an exogenous enzyme supplementation via the multi-nanozyme activities of CDs and achieves synergistic anti-inflammatory and endothelial barrier-repairing effects by regulating inflammatory mediators and junctional proteins. This platform offers a novel precision nanomedicine strategy for ALI.
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JOURNAL OF HAZARDOUS MATERIALS
·
2023
·
IF 13.6
Jinghua Li,Yiwen Ou,Lijuan Wang,Yue Zheng,Weiyun Xu,Jianbiao Peng,Xin Zhang,Zhiguo Cao,Junpei Ye
For the bioremediation of mixed-contamination sites, studies on polycyclic aromatic hydrocarbon (PAH) degradation or Cd (II) tolerance in bacteria are commonly implemented in nutrient-rich media. In contrast, in the field, inocula usually encounter harsh oligotrophic habitats. In this study, the environmental strain Paraburkholderia fungorum JT-M8 was used to explore the overlooked Cd (II) defense mechanism during PAH dissipation under P-limited oligotrophic condition. The results showed that the growth and PAH degradation ability of JT-M8 under Cd (II) stress were correlated with phosphate contents and exhibited self-regulating properties. Phosphates mainly affected the Cd (II) content in solution, while the cellular distribution of Cd (II) depended on Cd (II) levels; Cd (II) was mainly located in the cytoplasm when exposed to less Cd (II), and vice versa. The unique Cd (II) detoxification pathways could be classified into three aspects: (i) Cd (II) ionic equilibrium and dose–response effects regulated by environmental matrices (phosphate contents); (ii) bacterial physiological self-regulation, e.g., cell surface-binding, protein secretion and active transport systems; and (iii) specific adaptive responses (flagellum aggregation). This study emphasizes the importance of considering culture conditions when assessing the metal tolerance and provides new insight into the bacterial detoxification process of complex PAH-Cd (II) pollutants.
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JOURNAL OF DRUG DELIVERY SCIENCE AND TECHNOLOGY
·
2023
·
IF 5
Yanan Bu,Hongcai Wang,Ting Wu,Xiuqiong Chen,Siyuan Zhao,Huiqiong Yan,Qiang Lin
Nowadays, self-assembled polymeric micelles from amphiphilic polymer conjugates are urgently needed to enhance drug targeting and release efficiency. On account of the excellent properties of alginate and the redox-responsiveness of disulfide bonds , a redox-sensitive alginate–SS–ibuprofen derivative (LSA–SS–IBU) based anti-tumor target drug delivery system was created by attaching the hydrophobic ibuprofen (IBU) onto the hydrophilic alginate molecular skeleton through disulfide linkages for glutathione (GSH) triggered delivery of doxorubicin hydrochloride (DOX). The structure and self-assembly behavior of the synthesized LSA–SS–IBU was systematically evaluated by FT-IR spectrometer, 1 H NMR spectrometer, fluorescence spectrophotometer (FM), transmission electron microscope (TEM) and dynamic light scattering (DLS). Furthermore, the in vitro release of drugs from the LSA–SS–IBU micelles loaded with DOX was examined, along with the assessment of their cytotoxicity to HeLa cells. The resultant LSA–SS–IBU had a critical micelle concentration (CMC) value of 0.19 mg/mL that was able to self-assemble into the spherical micelles with the particle size and zeta potential of 148.2 ± 4.3 nm (PDI = 0.25) and −47.2 ± 0.4 mV, respectively. At a mass ratio of 3:10 for DOX/LSA–SS–IBU, the LSA–SS–IBU micelles achieved drug loading ratio (DLR) and encapsulation efficiency (EE) values of 12.2 % and 46.3 %, respectively. Furthermore, the in vitro drug release study indicated that the total drug release percentage of the drug-encapsulated LSA–SS–IBU micelles in PBS with the presence of 10 mmol/L GSH for 12 h exceeded 67.0 %, demonstrating a substantial increase compared to that in GSH-free PBS. The in vitro cytotoxicity findings indicated that LSA–SS–IBU had good biocompatibility , while the IC 50 value and the cell viability of DOX-loaded LSA–SS–IBU micelles cultured with HeLa cells for 48 h was 2.2 μg/mL and less than 20.1 %, respectively, which could significantly inhibit the growth of HeLa cells. Therefore, redox-responsive LSA–SS–IBU micelles had potential applications in cancer therapy for hydrophobic anti-tumor drug delivery.
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SENSORS AND ACTUATORS B-CHEMICAL
·
2023
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IF 8.4
Shishi Shao,Jiaqiang Zhao,Wei Wang,Hanbing Nie,Yan Jie Li,Xuepeng Zhang,Cheng Zhi Huang,Peng Fei Gao
Host-guest doping room-temperature phosphorescence (RTP) materials have showed excellent potential for ultra-sensitive detection due to its bright luminescence in presence of trace guests. However, the inherent signal fluctuation of solid-state sensors restricts their widespread applications. Herein we constructed a simple internal standard method to overcome the signal fluctuation problem in RTP spectral analysis. Ultralong organic RTP can be obtained by using 1,4-dichlorobenzene (DCB) as a host and trace gaseous NL as a guest through the host-guest doping strategy. In this study, a dual-emission ratiometric phosphorescent probe pyrene (Py)/pentachloropyridine (PCP)-DCB was constructed by using the Py/PCP system fabricated via melt-casting as the reference afterglow and using the DCB as the stimuli-responsive unit of gaseous NL. This probe can be used for visual identification and content detection of NL in commercial mothballs. The ratio of phosphorescence intensity (I485/I595) was linearly related to the mass of added NL (mNL) within the range of 0.05–1.45 mg in this ratiometric RTP platform, and had a low detection limit of 0.012 mg. Furthermore, the NL content of five commercially available mothballs with different NL content was detected by this Py/PCP-DCB platform, and it had good performance compared to the gas chromatography (GC) analysis results.
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ENVIRONMENTAL SCIENCE & TECHNOLOGY
·
2023
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IF 11.4
Wenzhang Tian,Jun Yang,Wen-Qing Xu,Lin Lian,Xia-Wen Qiu,Xiao Liang,Chen-Chou Wu,Xiangjun Gong,Guangzhao Zhang,Lian-Jun Bao,Eddy Y. Zeng
Chemical transfer across the air–water interface is one of the most important geochemical processes of global significance. Quantifying such a process has remained extremely challenging due to the lack of suitable technologies to measure chemical diffusion across the air–water microlayer. Herein, we present a fluorescence optical system capable of visualizing the formation of the air–water microlayer with a spatial resolution of 10 μm and quantifying air–water diffusion fluxes using pyrene as a target chemical. We show for the first time that the air–water microlayer is composed of the surface microlayer in water (∼290 ± 40 μm) and a diffusion layer in air (∼350 ± 40 μm) with 1 μg L–1 of pyrene. The diffusion flux of pyrene across the air–water interface is derived from its high-resolution concentration profile without any pre-emptive assumption, which is 2 orders of magnitude lower than those from the conventional method. This system can be expanded to visualize diffusion dynamics of other fluorescent chemicals across the air–water interface and provides a powerful tool for furthering our understanding of air–water mass transfer of organic chemicals related to their global cycling.
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MICROCHIMICA ACTA
·
2018
·Vol. 185
·期 9
·1-10
·
IF 5.705
Zhou Xiu-Jie,Zhang Li-Shun,Song Wen-Fang,Huang Yan-Ping,Liu Zhao-Sheng
An inorganic-organic hybrid monolith incorporated with stellated mesoporous silica nanoparticles (SMSNs) was prepared. Using binary solvents, deep eutectic solvents and room temperature ionic liquids, an SMSN-incorporated poly(butyl methacrylate- co -ethylene glycol dimethacrylate) monolith demonstrated uniform structure with good column permeability. A systematic investigation of preparation parameter was performed, including SMSN content, crosslinking monomer content, and the component of binary solvent. The optimized monoliths were characterized by field emission scanning electron microscopy, transmission electron microscopy, area scanning energy dispersive spectrometry, and nitrogen adsorption. Column performance was tested by separating four groups of analytes (alkylbenzenes, anilines, naphthalenes and phenols) by capillary electrochromatography (CEC). Baseline separation of all analytes was obtained with column efficiencies of up to 266,000 plates m −1 . The performance of the resulting monolith was further investigated in detail by separating mixtures of polycyclic aromatic hydrocarbons (PAHs), nonsteroidal antiinflammatory drugs (NSAIDs), and hydroxybenzoic acid isomers. Compared with the corresponding SMSN-free monolith, the CEC performance was improved by about six times. Successful extraction of PAHs and quinolones (QNs) were also performed using this capillary. Improved extraction efficiency (20.2%) for complex samples, lake water, was also found when the material was applied to solid phase microextraction of fluoranthene.
A poly(butyl methacrylate-co-ethylene glycol dimethacrylate) monolith incorporated with stellated mesoporous silica nanoparticles was prepared. It demonstrated column efficiency up to 266,000 plates m −1 in capillary electrochromatography and ability as solid phase microextraction for organic small molecules with good column permeability.
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INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH
·
2021
·
IF 3.764
Yu Chen,Han Han,Mengqiuzi Yin,Xiao Wang,Xiaoman He,Qiwu Zhang
Soil contaminated by polycyclic aromatic hydrocarbons (PAHs) is a common problem in the world. Mechanochemical treatment is a promising technology for remediation of PAH-contaminated soil. This study investigated the feasibility of pyrene degradation with silica by mechanochemical remediation. The effects of ball milling time and rotation speed on the removal efficiency of pyrene in soil were also studied. When the milling time was 3 h and the rotation speed was 500 rpm, the removal efficiency of pyrene in soil was over 98%. The intermediate products detected by gas chromatography–mass spectrometry proved that the hydrogenation reaction and the destruction of benzene rings occurred in the milling process. Both graphite and amorphous carbon were detected by Raman spectra. The main degradation pathway and mechanism of pyrene by mechanochemical treatment should be the destruction of benzene rings caused by free radicals and further carbonization.
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ANALYTICAL LETTERS
·
2023
·
IF 2
Qian Gao,Yang Li,Xinyi Li,Huiqing Wang,Lin Tian,Hao Gong,Cuiping Ma,Chao Shi
A highly ultrafast and sensitive electrochemical sensor based on electrical potential-assisted hybridization was developed for the determination of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). The electrode was modified with multi-walled carbon nanotubes (MWCNTs) and Au nanoparticles (AuNPs) for excellent electrochemical performance. The constant electric field was applied to rapidly and efficiently enrich the capture probes to the electrode surface in 60 s. Meanwhile, pyrene as the backfill reagent resulted in a significant reduction of nonspecific adsorption. The electrochemical properties of the modified electrode were investigated via electrochemical impedance spectroscopy (EIS) and cyclic voltammetry (CV). The analytical response was measured by differential pulse voltammetry (DPV). The sensor achieved the ultrafast hybridization of nucleic acids at the electrode interface within 90 s, substantially reducing the reaction time from hours to minutes. Under optimal conditions, the sensor exhibited a superior detection limit of 60 fM and showed satisfactory specificity toward single-base mismatch. Additionally, the proposed sensor realized sensitive determination of SARS-CoV-2 in throat swabs. The enzyme-free and non-amplification sensing strategy showed promising potential for application in point-of-care testing (POCT).
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