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环境毒理学
Arabian Journal of Chemistry · 2021 ·Vol. 14 ·期 10 ·103351 · IF 5.165

An amphiphilic fluorogen with aggregation-induced emission characteristic for highly sensitive and selective detection of Cu2+ in aqueous solution and biological system

Deqiang Wang,Xin Zhou,Chong Ma,Meiying Liu,Hongye Huang,Xiaoyong Zhang,Yen Wei

Fluorescent sensor has demonstrated to be a facile and effective method to detect heavy metal ions owing to its unique characteristics such as simplicity, ease of operation and cost-effectiveness. In this work, a novel fluorescent probe with aggregation-induced emission (AIE) feature that contains an amide ligand base on the tetraphenylethylene (TPE) dye was designed and successfully synthesized. The utilization of the AIE-active fluorescent probe (named as FDPA) for detection of Cu 2+ in aqueous solution has also been examined. We demonstrated that the resultant AIE-active molecule displays amphiphilic property and can self-assemble in aqueous solution with remarkable enhancement of fluorescent intensity owing to its AIE feature. The detection limit of probe for Cu 2+ determination is 6.11 × 10 −9 M and shows excellent selectivity in the presence of competitive ions. This work provides a useful route to overcome the fluorescence quenching of conventional fluorescent probes in aqueous solution and an elegant way to prepare fluorescent probes with better fluorescence properties.

研究领域: 分析化学 · 生物医学工程 · 分子影像 · 环境毒理学 · 化学生物学 · 药物分析 · 纳米医学
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Journal of Analytical Science and Technology · 2021 ·Vol. 12 ·期 1 ·18 · IF 2.769

A highly sensitive fluorescent probe for ozone based on coumarin-benzothiazole derivative

Chen Kangni,Li Yanbo,Shang Jinyan,Zhao Chao,Li Heping

Ozone is widely used in daily life, but studies have shown that O 3 can damage human trachea and lungs, leading to diseases such as asthma, emphysema, and bronchitis. Therefore, it is of great significance to develop a simple and efficient detection method for monitoring O 3 in living cells. In this study, 3-(but-3-en-1-yl)-2-(7-(but-3-en-1-yloxy)-2-oxo-2H-chromen-3-yl)benzo[d]thiazol-3-ium (BCT) as a new type of water-soluble fluorescent probe was synthesized by substitution reaction of 4-bromo-1-butene and hydroxycoumarin-benzothiazole derivatives, which can specifically detect ozone in aqueous solution. The interaction of ozone on the probe can be completed within 20 min, the fluorescence intensity is significantly enhanced, and it has the advantages of high sensitivity (detection limit LOD = 43 nM). The influence of pH on the fluorescent performance of BCT shows that the probe with super stability under weak alkali and acidic environment, which provides the necessary conditions for its detection of ozone in physiological system detection. Therefore, BCT is expected to become an effective tool for detecting ozone in cellular organisms.

研究领域: 分析化学 · 分子生物学 · 环境毒理学 · 生物医学工程 · 细胞生物学
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Food Analytical Methods · 2015 ·Vol. 9 ·期 7 ·2026-2035 · IF 1.956

A Novel Molecularly Imprinted Polymer Based on Carbon Nanotubes for Selective Determination of Dioctyl Phthalate from Beverage Samples Coupled with GC/MS

Du Jiaojiao,Gao Ruixia,Mu Hui

Phthalates represent a potential risk for humans, since they are ubiquitous environmental contaminants. Efficient extraction and purification procedures are demanded for the detection of low concentration levels of phthalates. In this work, a novel type of molecularly imprinted polymers coated onto the surface of vinyl functionalized multi-walled carbon nanotubes was synthesized and coupled with gas chromatography–mass spectrometry (GC/MS) for the selective separation and determination of dioctyl phthalate (DOP) in beverage samples. The morphology, structure property, and thermostability of the resultant polymers were characterized by transmission electron microscopy, Fourier transform infrared spectroscopy, and thermogravimetric analysis. The adsorption properties of the prepared polymers were investigated by equilibrium rebinding and competitive experiments. The resultant imprinted nanomaterials exhibited high capacity and favorable selectivity. In addition, the feasibility of the developed method using the obtained imprinted polymers as a solid-phase sorbent coupled with GC/MS for the selective isolation and determination of DOP in different beverage samples was demonstrated. Under optimal conditions, the limit of detection of the proposed method for DOP was 2.3 ng L −1 . DOP spiked at three levels of concentration in beverage samples was extracted and determined through the application of the present method, with recoveries ranging from 88.6 to 93.0 % with relative standard deviations less than 5.6 %.

研究领域: 分析化学 · 环境毒理学 · 食品安全 · 分子识别 · 材料科学 · 色谱分析
✓ 已验证 DOI 高影响因子
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INORGANIC CHEMISTRY · 2019 · IF 4.85

Hexadentate β-Dicarbonyl(bis-catecholamine) Ligands for Efficient Uranyl Cation Decorporation: Thermodynamic and Antioxidant Activity Studies

Qingchun Zhang,Bo Jin,Tian Zheng,Xingyan Tang,Zhicheng Guo,Rufang Peng

The special linear dioxo cation structure of the uranyl cation, which relegates ligand coordination to an equatorial plane perpendicular to the O═U═O vector, poses an unusual challenge for the rational design of efficient chelating agents. Therefore, the planar hexadentate ligand rational design employed in this work incorporates two bidentate catecholamine (CAM) chelating moieties and a flexible linker with a β-dicarbonyl chelating moiety (β-dicarbonyl(CAM)2 ligands). The solution thermodynamics of β-dicarbonyl(CAM)2 with a uranyl cation was investigated by potentiometric and spectrophotometric titrations. The results demonstrated that the pUO22+ values are significantly higher than for the previously reported TMA(2Li-1,2-HOPO)2, and efficient chelation of the uranyl cation was realized by the planar hexadentate β-dicarbonyl(CAM)2. The efficient chelating ability of β-dicarbonyl(CAM)2 was attributed to the presence of the more flexible β-dicarbonyl chelating linker and planar hexadentate structure, which favors the geometric arrangement between ligand and uranyl coordinative preference. Meanwhile, β-dicarbonyl(CAM)2 also exhibits higher antiradical efficiency in comparison to butylated hydroxyanisole. These results indicated that β-dicarbonyl(CAM)2 has potential application prospects as a chelating agent for efficient chelation of a uranyl cation.

研究领域: 无机化学 · 放射化学 · 配位化学 · 药物化学 · 环境毒理学
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POLYMER TESTING · 2022 · IF 4.931

Preparation and properties of a fast curing carboxymethyl chitosan hydrogel for skin care

Yang-he Mo,Hui Wang,Shao-hua Jin,Ke-lin Peng,Zi-ming Yang,Pu-wang Li,Yu Chen

Fast curing hydrogels are highly valuable in the skin care industry. Multi-arm polyethylene glycol (PEG) is a commonly used crosslinking agent for the preparation of fast curing hydrogels. However, the hydrogel preparation using multi-arm PEG crosslinking agents usually requires the end group modifications of reactants, which makes the preparation process complicated and produces hydrogels with low curing rates. In the present study, a fast in situ curing hydrogel, 4-arm-PEG-succinimidyl carbonate/carboxymethyl chitosan (PEG-SC/CMCS), was prepared using 4-arm-PEG-SC as the crosslinking agent and carboxymethyl chitosan (CMCS), a derivative of natural polysaccharide with excellent comprehensive properties, as the framework without any end groups modified. The structure and properties of the prepared hydrogel were characterized by FTIR, XRD, SEM, rheology and swelling kinetics. The effects of reaction conditions on the structure and properties of hydrogel were investigated. The PEG-SC/CMCS hydrogel exhibited pH-sensitive swelling behaviors. Its application potential in skin care products is demonstrated with its excellent sustained-release performance of Vitamin C, a model drug for skin treatment, and high adsorption capacity of heavy metal ions that are easily deposited on skin surface. Our work has provided a new strategy for building multifunctional gel materials for skin care and offered a PEG-SC/CMCS hydrogel with great application potentials.

研究领域: 生物材料 · 高分子化学 · 药剂学 · 皮肤科学 · 组织工程 · 药物递送系统 · 环境毒理学
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CHROMATOGRAPHIA · 2018 ·Vol. 82 ·期 3 ·683-693 · IF 1.401

Hollow Fiber Stir Bar Sorptive Extraction Combined with GC–MS for the Determination of Phthalate Esters from Children’s Food

Shen Chen,Wu Tong,Zang Xiaohuan

In this work, a zeolitic imidazolate framework-based graphene oxide composite (ZIF-8@GO) was prepared and used as the adsorbent in hollow fiber stir bar sorptive extraction. The stir bar was constructed of a small section of hollow fiber filled with 5 mg ZIF-8@GO and a thin stainless wire of 1.5 cm long in its lumen, and used to extract the trace levels of phthalate esters from children’s food samples prior to gas chromatography–mass spectrometric detection. The ZIF-8@GO showed a high adsorption efficiency for the compounds containing aromatic rings. The main experimental parameters that can impact the extraction efficiency including extraction temperature, extraction time, stirring rate, sample salinity, and desorption conditions were investigated. Under the optimized conditions, the limits of detection (LODs) for the five phthalate esters (diethyl phthalate, dipropyl phthalate, diisobutyl phthalate, butylbenzyl phthalate, and di(2-ethylhexyl) phthalate) were 0.15–0.6 µg L −1 for CiCi beverage and pear juice samples, and 0.75–2.2 µg kg −1 for jam samples. The limits of quantitation (LOQs) were 0.5–2.0 µg L −1 for CiCi beverage and pear juice samples, and 2.5–7.5 µg kg −1 for jam samples. Wide linear ranges of 0.5–500.0 µg L −1 and 2.5–2000 µg kg −1 were obtained for CiCi beverage, pear juice samples and jam samples, respectively, with good repeatability (RSD < 11%) and high method recoveries (72%–100%). The lifetime test results showed that the ZIF-8@GO-based hollow fiber stir bar can be reused for 120 extraction cycles without a significant loss of extraction efficiency, indicating its high durability and stability. The established method was applied successfully for the determination of the phthalate esters (PAEs) in children’s food samples. Graphical abstract

研究领域: 分析化学 · 食品安全 · 环境毒理学 · 暴露科学 · 食品化学 · 污染物检测
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JOURNAL OF SOILS AND SEDIMENTS · 2016 ·Vol. 17 ·期 2 ·536-542 · IF 2.206

The effect of different TiO2 nanoparticles on the release and transformation of mercury in sediment

Zhang Jinyang,Li Chuxian,Wang Dingyong,Zhang Cheng,Liang Li,Zhou Xiong

Purpose The environmental safety of both nano-TiO 2 particles and mercury (Hg) pollution has been of widespread concern. Soils and sediments were the main receiving environments of nano-TiO 2 and Hg. There was a strong association between nano-TiO 2 with Hg compounds. Very limited research has been carried out on the impact of nano-TiO 2 on the environmental behavior of Hg in sediments. The objective of this study was to investigate the effects of nano-TiO 2 on the release and transformation of Hg in sediments. Materials and methods Two types of TiO 2 nanoparticles were employed. Sediment samples were collected in the water level fluctuating zone of the Three Gorges Reservoir, China. Sediment samples spiked with HgCl 2 solution were taken as Hg-contaminated sediments. The flooding experiments were conducted using capped borosilicate glass bottles containing 300 ml TiO 2 suspensions (0.2 g L −1 and 0.4 g L −1 ) and 30 g original or Hg-contaminated sediment samples outdoors. All experiments were conducted in triplicate. Water samples were collected at determined interval times over a 60-day period. Sediments were collected on the 60th day. Total Hg (THg) and methylmercury (MHg) in both water and sediment samples and Hg speciation just in sediment samples were determined. A series of control samples without TiO 2 addition were also prepared. Results and discussion The results showed that nano-TiO 2 particles at high content (4 g kg −1 ) promoted the release of Hg in sediments, and the anatase particles showed a stronger effect. Methyl Hg concentrations in waters of nano-TiO 2 treatments significantly decreased by the 10th day. The effect of nano-TiO 2 greatly depended on anatase and rutile particles. After that, methyl Hg concentrations had no significant difference between nano-TiO 2 treatments and the control, except 2 g kg −1 rutile treatment by the 20th day. The changes of Hg speciation in sediments demonstrated that nano-TiO 2 inhibited the transformation of Hg-bound organic matter into the oxidated state, especially upon 2 g kg −1 rutile treatment. This was consistent with the lower MHg concentrations in the 2 g kg −1 rutile treatment. Conclusions Both anatase and rutile nano-TiO 2 were found to affect the release of Hg in sediment. Nano-TiO 2 promoted THg release in sediments and posed an increased risk of Hg contamination in waters, especially for anatase particles. Moreover, nano-TiO 2 inhibited the methylation process of Hg in sediments at the initial stage of flooding and could affect the transformation of Hg speciation in sediments, especially for low-content rutile particles.

研究领域: 环境科学 · 地球化学 · 水体生态学 · 污染控制 · 环境毒理学
✓ 已验证 DOI 高影响因子
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RSC Advances · 2012 ·Vol. 2 ·期 14 ·5983-5989 · IF 0

Medicinal plant acid-treatment for a healthier herb tea and recycling of the spent herb residue

Hong-Wen Gao,Dong-Dong Ma,Gang Xu

Many kinds of medicinal plants are used in the treatment of disease, and a proportion of these plants grow tenaciously in soils contaminated with heavy metals. An example of one such medicinal plant is the herb Thlaspi rotundifolium L., which accumulates selenium (Se), and has anti-oxidation, anti-aging, anti-cancer and immunity-adjusting properties, but also simultaneously hyperaccumulates harmful metals such as Cd and Zn from the soil. An interesting model named ‘digging metals@plant then backfilling’ has been suggested, where the metals are removed from the plant by acid treatment, then the nano-pores imprinted with the heavy metals are backfilled from the drinking water. Experimental studies of this idea indicate that it can remove unwanted substances from the herb itself and also from the drinking water, ensuring the safety of the herb tea. Additionally, the Se normally embedded in the herb was not noticeably lost. Thus, this model provides a sustainable solution for the disposal of heavy metals using metal-accumulating plants.

研究领域: 植物生理学 · 环境毒理学 · 食品科学 · 天然药物化学 · 环境修复 · 生物医学工程 · 农业资源利用
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SCIENCE OF THE TOTAL ENVIRONMENT · 2024 · IF 8.2

A microcosm evaluation of metal cycling in an urbanized contaminated estuary varying with oxic-hypoxic-anoxic-reoxic transition: Behavior, fluxes, and mechanism

Zhenzhen Jia,Qiuxin Liu,Jiatang Hu,Shiyu Li,Hujunjie Chen

Water hypoxia and metal pollution are commonly co-existed in urbanized estuaries. This study focuses on the effect of an extended dissolved oxygen (DO) full-life dynamics (86 days) on metal behavior across the sediment-water interface through laboratory microcosms from two typical zones in Pearl River Estuary. Combining our time-series results of concentrations and fluxes, it showed that Co, Ni, and Zn consistently presented a release-precipitation-release trajectory with an oxic-hypoxic-anoxic-reoxic transition, characterized with highly variable behavior in the hypoxic-anoxic hotmoments. In parallel, changing DO dynamics significantly activated a repartitioning process of Co, Ni, and Zn among several species and elevated their risk in sediments, promoting the formation of more labile species in the 0–10 mm hotspots, where metals sensitively responded. Over DO transition, metal cycling was tightly co-related with Fe, Mn, and S elements. It was found that Mn was dominated in low oxygen-hypoxic period, but switched to S and Fe in anoxic stage, limiting sustained metal liberation to overlying water. Enlarging this experiment to practice, released Zn fluxes from sediments in hypoxic summer could contribute about ∼2.0% to their stocks in water column, while increase to 20% (1 m bottom water) in highly-stratified zones. This study has certain significance in understanding the long-term metal behavior and fate in estuarine regions, even lakes and reservoirs.

研究领域: 环境科学 · 地球化学 · 水生生态学 · 污染生态学 · 生物地球化学 · 环境毒理学 · 河口学
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Biomed Research International · 2017 ·Vol. 2017 ·期 1 ·2564363 · IF 2.476

Analysis of the Metabolites of Indole Degraded by an Isolated Acinetobacter pittii L1

Zuoyi Yang,Junhui Zhou,Yanbin Xu,Yaping Zhang,Haien Luo,KenLin Chang,Yujie Wang

Indole and its derivatives are typical nitrogen heterocyclic compounds and have been of immense concern since they are known for the risk of their toxic, recalcitrant, and carcinogenic properties for human and ecological environment. In this study, a Gram-negative bacterial strain of eliminating indole was isolated from a coking wastewater. The strain was confirmed as Acinetobacter pittii L1 based on the physiological and biochemical characterization and 16S ribosomal DNA (rDNA) gene sequence homology. 400 mg/L indole could be completely removed within 48 h by the strain on the optimum condition of 37°C, pH 7.4, and 150 rpm. The organic nitrogen was converted to NH 3 -N and then to and the organic carbon was partially transferred to CO 2 during the indole biodegradation. The metabolic pathways were proposed to explain the indole degradation based on the liquid chromatography tandem mass spectrometry (LC-MS/MS) analysis of indigo, 4-(3-Hydroxy-1H-pyrrol-2-yl)-2-oxo-but-3-enoic acid, and isatin. The toxicity of the biodegradation products was evaluated using the Microtox test, which revealed that the metabolites were more toxic than indole. Our research holds promise for the potential application of Acinetobacter pittii L1 for NHCs degradation, production of indigoids, and soil remediation as well as treatment of indole containing wastewater.

研究领域: 环境微生物学 · 生物降解 · 分析化学 · 环境毒理学 · 废水生物处理 · 分子生物学
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ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH · 2023 ·Vol. 30 ·期 58 ·121908-121914 · IF 5.8

Response to gallium (Ga) exposure and its distribution in rice plants

Zhang Dong-Chi,Ullah Abid,Tian Peng,Yu Xiao-Zhang

Root architecture is the temporal and spatial configuration of root system in the heterogeneous matrix of soil that is prone to chemical stresses. Gallium (Ga) is among the emerging chemical pollutants that are mostly associated with high-tech industries, specifically associated with semiconductors. In view of its potential risk and increasing distribution in the environment, this study was designed to evaluate the inhibition rate, Ga distribution in different tissues, and root architecture of rice seedlings under different concentrations of Ga. We observed that 2.59, 46.7, and 168.2 mg Ga/L were minimum (EC 20 ), medium (EC 50 ), and maximum (EC 75 ) effective concentrations for rice plants that corresponded to the 20, 50, and 75% inhibition on the relative growth rate, respectively. Distribution of Ga in rice tissues showed that accumulation of Ga was much higher in roots than shoots of rice seedlings, and it increased with an increase in Ga doses. Evan blue staining technique reveals that the number of damaged/dead cell was dose-dependent on Ga. Moreover, several traits associated with root system architecture demonstrating that rice root system architecture altered in response to Ga stress. Collectively, the results reveal that Ga exposure inhibited the growth and development of rice plants. This study will enhance our understanding that how different concentrations of Ga in the environment can affect plants; however, more comprehensive studies are essential to further determine plant response against Ga stress.

研究领域: 植物生理学 · 环境毒理学 · 土壤生物学 · 重金属污染 · 作物科学
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JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY B-BIOLOGY · 2016 · IF 3.035

Comprehensive spectroscopic probing the interaction and conformation impairment of bovine serum albumin (BSA) by herbicide butachlor

Xiaoyi Liu,Zhaoxing Ling,Xing Zhou,Farooq Ahmad,Ying Zhou

Butachlor is an effective herbicide to deal with undesired weeds selectively and is used at high levels in Asian countries. However, its interaction and impairment effect on BSA was still not clear. In this study, we investigated the interaction between butachlor and bovine serum albumin (BSA) by multi-spectroscopic methods including UV absorption , circular dichroism (CD) spectra, Fourier transform infrared (FTIR) spectra and fluorescence spectra under physiological conditions (pH   =   7.4). The results revealed that there was a static quenching of BSA induced by butachlor stemmed from the formation of complex. Based on thermodynamic data, the interaction of butachlor with BSA was due to happen, and van der Waals force as well as hydrogen bond were the major forces contributed to the interaction. The binding constant K b and number of binding site of butachlor with BSA were 5.158   ×   10 5 and 1.372 at 303   K, respectively. The distance r between donor (BSA) and acceptor (butachlor) was 0.113   nm, obtained according to the Förster theory. The results revealed that butachlor induced conformational changes in BSA but the secondary structure of BSA was still retained. In addition, the microenvironment around chromophore residues of BSA, for example, tryptophan , changed as well, resulting from the formation of more hydrogen bonds.

研究领域: 生物化学 · 分子药理学 · 药物代谢 · 环境毒理学 · 蛋白质科学
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