SCIENCE OF THE TOTAL ENVIRONMENT
·
2023
·
IF 9.8
Chanlin Fang,Liya Fang,Shanshan Di,Yundong Yu,Xinquan Wang,Caihong Wang,Yuanxiang Jin
N-(1,3-dimethylbutyl)- N ′-phenyl- p -phenylenediamine (6PPD) is a type of p -phenylenediamine (PPD), which is widely used in the manufacture of rubber tires owing to its excellent antiozonant properties. In this study, the developmental cardiotoxicity of 6PPD was evaluated in zebrafish larvae, and the LC50 was approximately 737 μg/L for the larvae at 96 h post fertilization (hpf). In the 6PPD treatment of 100 μg/L, the accumulation concentrations of 6PPD were up to 2658 ng/g in zebrafish larvae, and 6PPD induced significant oxidative stress and cell apoptosis in the early developmental stages of zebrafish. Transcriptome analysis showed that 6PPD exposure could potentially cause cardiotoxicity in larval zebrafish by affecting the transcription of the genes related to the calcium signal pathway and cardiac muscle contraction. The genes related to calcium signaling pathway ( slc8a2b , cacna1ab , cacna1da , and pln ) were verified by qRT-PCR, which were significantly downregulated in larval zebrafish after exposing to 100 μg/L of 6PPD. Simultaneously, the mRNA levels of the genes related to cardiac functions ( myl7 , sox9 , bmp10 , and myh71 ) also respond accordingly. H&E staining and heart morphology investigation indicated that cardiac malformation occurred in zebrafish larvae exposed to 100 μg/L of 6PPD. Furthermore, the phenotypic observation of transgenic Tg (myl7: EGFP) zebrafish also confirmed that 100 μg/L of 6PPD exposure could change the distance of atria and ventricles of the heart and inhibit some key genes ( cacnb3a , ATP2a1l , ryr1b ) related to cardiac function in larval zebrafish. These results revealed the toxic effects of 6PPD on the cardiac system of zebrafish larvae.
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Journal of Materials Chemistry A
·
2018
·Vol. 6
·期 45
·22580-22589
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IF 9.931
Xiu-Qing Qiao,Zhen-Wei Zhang,Qiu-Hao Li,Dongfang Hou,Qichun Zhang,Jian Zhang,Dong-Sheng Li,Pingyun Feng,Xianhui Bu
Exploiting novel photocatalysts with high efficiency and durability for reduction of hexavalent chromium (Cr(VI)) has gained attention from fundamental science and industrial research. In this work, we synthesized novel two-dimensional (2D) n–n Bi2MoO6 & Bi2S3 heterojunctions by a facile in situ anion exchange process for remarkably efficient removal of Cr(VI). Results show that Bi2MoO6 & Bi2S3 heterojunctions with core–shell structures are formed through the intimate contact of Bi2MoO6 core and Bi2S3 shell. The prepared Bi2MoO6 & Bi2S3 heterojunctions exhibit unprecedented photocatalytic activity for reduction of Cr(VI) under visible light irradiation. The optimized BMO-S1 heterojunction displays the highest reduction efficiency (κapp = 0.164 min−1) for Cr(VI) reduction. To the best of our knowledge, it is one of the highest reduction rate achieved among reported photocatalysts for Cr(VI) reduction under visible-light irradiation. Detailed studies show that strong selective adsorption for Cr(VI) enhances this unprecedented photocatalytic activity. Moreover, the intimate heterojunction between Bi2MoO6 core and Bi2S3 shell can efficiently deteriorate the charge carrier recombination and Bi2S3 content can boost visible light harvesting, thereby contributing to the remarkable photocatalytic catalytic activity, which were proven by PL, EIS and transient photocurrent responses. Characterization of Mott–Schottky plots and DRS prove that the Bi2MoO6 & Bi2S3 heterojunctions established a type-II band alignment with intimate contact, accounting for the efficient transfer and separation of photogenerated carriers. This work provides a simple route for facial synthesis of heterojunction photocatalysts for Cr(VI) reduction in industrial applications.
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ANNALS OF MICROBIOLOGY
·
2017
·Vol. 68
·期 1
·27-34
·
IF 1.122
Xiao Yaqing,Li Peijun,Xu Mei,Wang Wu,Chen Conggui
The objective of this study was to evaluate the ability of five strains of meat-borne bacteria to decrease N-nitrosodimethylamine (NDMA) and N-nitrosodiethylamine (NDEA) and to elucidate the mechanism in Mann-Rogosa-Sharp (MRS) broth. Lactobacillus pentosus R3 was found to be the most effective in decreasing the concentration of the two N-nitrosamines (NAs) in MRS broth, with a rate of 22.05% for NDMA and 23.31% for NDEA. The concentration of the two NAs could not be reduced by either extracellular metabolites or intracellular extracts of Lb. pentosus R3 (P > 0.05), and proteinaceous substances in the cell debris were found to be responsible for the decrease. These were surface-layer proteins (SLPs) located on the cell wall. Therefore, the decrease in NDMA and NDEA by Lb. pentosus R3 is associated with its SLPs. Lb. pentosus R3 may be developed as a starter culture in the production of fermented foods with lower NAs.
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Journal of Energy Storage
·
2024
·
IF 8.9
Jing Huang,Jiang Peng,Junqing Zeng,Liping Zheng,Huajie Chen
Despite the important advances on B/N co-doped porous carbons (BNCs), integrating high B/N-doping content and hierarchical porosity into carbon nanosheets remains a challenging task for supercapacitor application. Herein, we report a novel BNC nanosheet with both expected properties through one-step H 3 BO 3 -mediated carbonization/activation of a newly-developed N/O-rich polymer (DPP). In such a mixture system, an in-suit crossing-linked DPP@H 3 BO 3 composite is formed due to the formation of multiple intermolecular hydrogen bonds between the H 3 BO 3 and the ester groups of DPP. The improved thermal stability for such a composite enables the fixation of more B-/N-bearing species in the carbon skeleton during carbonization. Particularly the nanosheet-like BNC-850 shows a rather high B/N content (6.63/7.27 at.%), a large S BET value (766.5 m 2 g −1 ), and a hierarchical porosity, all of which are in favor of electrochemical performance in both aqueous supercapacitors and zinc-ion capacitors (ZICs). In 6 M KOH electrolyte, the BNC-850 electrodes deliver an impressive capacitance of 341.5 F g −1 at 0.5 A g −1 , a high capacitance retention of 79.2 % at 20 A g −1 , and a good cycling stability (95 % capacitance retention over 10,000 cycles at 5 A g −1 ). The energy density of BNC-850-based ZICs is as high as 126.0 Wh kg −1 at 459.0 W kg −1 , exhibiting an outstanding superiority compared to the reported carbon-based ZICs. This work offers a facile strategy for accessing BNCs with high B/N-doping contents, and highlights the importance of such materials in high-energy-density ZICs.
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JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY
·
2024
·
IF 5.7
Chengqiang Li,Zhuoning Cao,Hong Jiang,Francesco Secundo,Xiangzhao Mao
β-N-Acetylhexosaminidases have attracted much attention in the enzymatic synthesis of lacto-N-triose II (LNT2) as a backbone precursor of human milk oligosaccharides (HMOs). In this study, a novel glycoside hydrolase (GH) 20 family β-N-acetylhexosaminidase, FlaNag2353, from Flavobacterium algicola was biochemically characterized and applied to synthesize LNT2. FlaNag2353 displayed optimal activity to p-nitrophenyl N-acetyl-β-d-glucosaminide (pNP-GlcNAc) at 40 °C and pH 8.0. In addition to its excellent hydrolysis activity toward pNP-GlcNAc and chitooligosaccharides, FlaNag2353 showed trans-glycosylation activity. Under conditions of pH 9.0 and 55 °C for 2 h and utilizing 200 mM lactose and 10 mM pNP-GlcNAc, FlaNag2353 synthesized LNT2 with a conversion ratio of 4.15% calculated from pNP-GlcNAc. Moreover, when applied to LNT2 synthesis with 10 mM pNP-GlcNAc and 9.7% (w/v) industrial waste whey powder, FlaNag2353 achieved a conversion ratio of 2.39%. This study has significant implications for broadening the applications of GH20 β-N-acetylhexosaminidases and promoting the high-value utilization of whey powder.
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APPLIED CATALYSIS B-ENVIRONMENTAL
·
2024
·
IF 20.2
Qingqing Li,Zhiwei Sun,Yilin Wei,Zixu Ma,Liucheng Wang,Renfeng Nie
Reversible hydrogen storage via Liquid organic hydrogen carriers (LOHCs) is one of the key technologies for efficient utilization of hydrogen energy. How to construct efficient dehydrogenation/hydrogenation catalysts that enable low-temperature catalysis still remains challenging. Herein, we present the design and construction of single-atom Co-N-C(x) catalysts allowing significantly improved acceptorless dehydrogenation of 1,2,3,4-tetrahydroquinoline (THQ). By varying the ligand/Co ratio, the optimal Co-N-C(1.5) can achieve 97.5% dehydrogenated product and 0.82 h −1 TOF value at ambient temperature, overperforming many reported non-noble metal even noble metal catalysts. This catalyst exhibits good recyclability and substrate versatility, enabling ambient temperature dehydrogenation of various N-heterocycles and efficient reverse hydrogenation of aromatic N-heterocycles, thus achieving the loop of reversible hydrogen storage. The active catalyst centers consist of specific Co-N x moieties and nitrogen species within the carbon support. Controlled experiments reveal that the different performance of Co-N-C(x) is determined by density of the Co-N x , and the rate-determining step of THQ dehydrogenation is correlated with the bond cleavages in surface-bound THQ. This work offers a promising pathway for energy-efficient and cost-effective hydrogen energy utilization under practical conditions.
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RSC Advances
·
2017
·Vol. 7
·期 15
·9381-9392
·
IF 3.108
Qiao Wang,Chandra Sekhar Biswas,Massimiliano Galluzzi,Yuhang Wu,Bing Du,Florian. J. Stadler
Random copolymer gels of N-isopropylacrylamide (NIPAM) and N-ethylacrylamide (NEAM) were synthesized using a 1 : 1 monomer molar ratio in different methanol–water (xm = 0, 0.06, 0.13, 0.21, 0.31 0.43, 0.57, 0.76, where xm = mole fraction of methanol) mixtures. The samples were characterized using different techniques like Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), swelling ratio measurements, deswelling kinetics study, atomic force microscopy (AFM), and rheology. We found that, with the variation of the solvent composition (methanol–water mixtures) the properties of the gels varied significantly. These results can be explained on the basis of the interactions of the two different kinds of monomers with different methanol–water mixtures, their different kinds of thermoresponsiveness and hydrophilicity, and their different cononsolvent properties toward methanol–water mixtures.
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Journal of Environmental Sciences
·
2016
·
IF 2.208
Xingdu Chen,Chengjian Yang,Weiwei Wang,Bizhou Ge,Jun Zhang,Yucan Liu,Yaping Nan
The biodegradation characteristic and potential metabolic pathway for removal of environmental N,N-dimethylacetamide (DMAC) by Rhodococcus sp. strain B83 was studied. Rhodococcus sp. strain B83 was isolated from the rhizosphere of a pagoda tree and proved capable of utilizing DMAC as sole source of carbon and nitrogen. Batch culture studies showed that strain B83 could tolerate up to 25 g/L DMAC and showed distinct growth on possible catabolic intermediates except for acetate. The nitrogen balance analysis revealed that approximately 71% of the initial nitrogen was converted to organic nitrogen. DMAC degradation has led to accumulation of acetate and organic nitrogen, meanwhile traces of nitrate and ammonia was build-up but without nitrite. The growth of strain B83 could be inhibited by adding exogenous acetate. By means of the assay of enzymatic degradation of DMAC, several catabolic intermediates at different intervals were observed and identified. Based on the results obtained from culture solution and enzymatic degradation assay, a detailed pathway is proposed for DMAC biodegradation.
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高影响因子
JOURNAL OF PHARMACEUTICAL SCIENCES
·
2016
·
IF 2.641
Hongyan Zhu,Jie Cao,Sisi Cui,Zhiyu Qian,Yueqing Gu
ABSTRACT 10-Hydroxycamptothecin (HCPT) is an effective anticancer drug against various types of solid tumors . But the antitumor efficacy of HCPT is far from satisfactory because of its poor physicochemical properties, short circulating half-life, low stability, and nonspecific toxicity to normal tissues. Therefore, a targeted delivery strategy for HCPT to pathological sites is eagerly needed to overcome these limitations. The folate-modified N-succinyl-N′-octyl chitosan (folate-SOC) micelle was chosen in this study and served as the targeted delivery system for HCPT to improve the antitumor efficacy. The water-insoluble anticancer drug HCPT was encapsulated into the folate-SOC micelles by the dialysis method. The near- spherical HCPT-loaded folate-SOC (HCPT/folate-SOC) micelles were formed in aqueous media with diameter of about 100-200 nm. The HCPT/folate-SOC micelles displayed a good stability, reasonable drug-loading content (about 10%), and sustained release behavior for the water- insoluble HCPT. Compared with free HCPT, HCPT/folate-SOC micelles exhibited a significant enhancement of cellular uptake, higher cytotoxicity against folate receptor positive tumor cell (Bel-7402), excellent tumor-targeting capability and substantially better antitumor efficacy on the nude mice bearing Bel-7402 xenografts. These results demonstrate the potential of folate- SOC micelles as long-term stable and effective drug delivery systems in cancer therapy.
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AGRICULTURE ECOSYSTEMS & ENVIRONMENT
·
2017
·
IF 4.099
Congyan Wang,Jiawei Zhou,Jun Liu,Kun Jiang,Daolin Du
Soil N-fixing bacteria communities (SNB) can increase soil N availability, which can facilitate invasions of many kinds of invasive plant species. Meanwhile, variability in the forms of anthropogenic N deposition can mediate obvious shifts in both soil physicochemical properties and soil microbial communities (especially SNB). This can alter the soil micro-ecological mechanisms of plant invasions via changes in soil characteristics and soil microbial communities, especially SNB. This study uses next-generation high throughput sequencing technology to provide insight into the effects of invasion by Amaranthus retroflexus L. on the structure and diversity of SNB under different forms of simulated N deposition (SND). Soil pH under A. retroflexus invasion under various forms of SND was 8.08% lower than controls under a NH 4 -N treatment ( P < 0.05), 15.15% lower than controls under a NO 3 -N treatment ( P < 0.05), and 6.57% lower than controls under CO(NH 2 ) 2 -N and Mix-N treatments ( P < 0.05). Meanwhile, soil pH was one of the most important environmental variables explaining changes in the structure and diversity of SNB. The total number of species of SNB under A. retroflexus invasion was approximately 13.13% higher than controls for the NH 4 -N treatment ( P > 0.05), 11.00% higher than controls for the NO 3 -N treatment ( P > 0.05), 39.42% higher than controls for the CO(NH 2 ) 2 -N treatment ( P < 0.05), and 27.67 higher than controls for the Mix-N treatment ( P < 0.05). The positive effects mediated by the combined treatments of A. retroflexus invasion and SND may be ascribed to enhanced soil nutrient content (especially N), which can enhance the abundance of the nifH gene. The effects of A. retroflexus invasion on the total number of species of SNB under organic and mixed-N addition were greater than under inorganic N addition. This may be a consequence of a disturbance of the balance of inorganic to organic N for SND, as a result of the addition of a single form of inorganic N, which can diminish the stimulatory effects of soil nutrient content on SNB under inorganic N. Another potential cause of this pattern may be stronger acidification under inorganic N addition, which can exert more pronounced effects on SNB. LEfSe analysis showed that some species changed significantly under A. retroflexus invasion in the presence of SND (i.e., Rhodobacteraceae under NH 4 -N and Proteobacteria under CO(NH 2 ) 2 -N). Thus, A. retroflexus invasion in the presence of SND caused obvious shifts in certain species of SNB and increased the total number of species of SNB in particular, to facilitate its further invasion.
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JOURNAL OF APPLIED POLYMER SCIENCE
·
2014
·Vol. 131
·期 17
·
IF 1.64
Hongming Yuan,Zaochuan Ge,Shaojun Chen,Shiguo Chen,Haipeng Yang,Haitao Zhuo
This article demonstrates a comparative investigation about the effect of diisocyanate on pyridine containing shape memory polyurethanes (Py-SMPUs), which are synthesized with N , N -bis(2-hydroxylethyl)isonicotinamide (BINA) and four different diisocyanates: 1,6-hexanediisocyante (HDI), isophorone diisocyanate (IPDI), methylene diphenyl diisocyanate (MDI), and tolylene diisocyanate (TDI). Results show that all BINA–SMPU systems have amorphous reversible phase. Comparatively, the MDI–BINA and TDI–BINA systems show higher T g ; and the HDI–BINA and IPDI–BINA systems show better thermal stability. In addition, the HDI–BINA and the IPDI–BINA systems exhibit good thermal-induced shape memory effect and good moisture-sensitive shape memory effect due to their better moisture absorption properties. Particularly, the HDI–BINA system has better response speed and better shape recovery. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131 , 40721.
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EUROPEAN POLYMER JOURNAL
·
2013
·
IF 2.562
Xiaohong Wang,Guohua Jiang,Zhen Wei,Xia Li,Bolin Tang
The CO 2 stimulus-sensitive nanoparticles based on poly( N , N -dimethylaminoethyl methacrylate)- b -poly styrene (PDMAEMA- b -PS) were prepared via surfactant-free miniemulsion reversible addition–fragmentation chain transfer (RAFT) polymerization. The as-prepared nanoparticles exhibited core–shell structure with about 120 nm in diameter. Their dispersion/aggregation in water can be adjusted by alternatively bubbling of CO 2 and N 2 . Drug release from these nanoparticles can be accelerated (or delayed) by bubbling (or removing) of CO 2 .
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危险品化学品经营许可证（带存储）