APPLIED SPECTROSCOPY
·
2025
·
IF 2.2
XingYi Guo,Chun Zhu,Guoqing Chen,Lei Li,Chaoqun Ma,Taiqun Yang,Anqi Hu,WenHui Yang,YaLi Qian
In this paper, a lanthanide complex-based fluorescent sensor Tb(4-MBA) was developed for the selective recognition of diabetic ketoacidosis (DKA) and the diabetes biomarker β-hydroxybutyric (β-Hb). β-Hb significantly enhanced the fluorescence emission of the Tb(4-MBA) complex at 539 nm. Based on the analysis of the surface electrostatic potential distribution and time-resolved spectra, we speculate that in the reaction system of β-Hb with Tb(4-MBA), β-Hb and Tb(4-MBA) may form a complex through hydrogen bonding interactions, which brings β-Hb closer to Tb3+ and thus reduces the non-radiative energy loss of the solvent molecules to Tb3+ and significantly enhances the Tb(4-MBA) fluorescence intensity. The linear range of Tb(4-MBA) for β-Hb was 2–55 μM, and the limit of detection (LOD) was 50.6 nM. This sensor has high sensitivity and selectivity and shows great potential in the field of screening and diagnosis of diabetes mellitus and DKA.
研究领域:
分析化学
·
生物无机化学
·
荧光传感
·
糖尿病研究
·
材料科学
✓ 已验证
DOI
PubMed
高影响因子
Desalination and Water Treatment
·
2016
·
IF 1.272
Xudong Zheng,Jiangdong Dai,Jianming Pan
In this work, mesoporous attapulgite (mATP) was firstly prepared in the presence of the cetyltrimethylammonium bromide using attapulgite (ATP) as the matrix materials. Then, it was modified by β-cyclodextrin (β-CD) to obtain the β-cyclodextrin/mesoporous attapulgite composites (β-CD/mATP). The characterization of the composites showed that β-CD/mATP composites remained excellent channel structure and the value of the specific surface area was 300.30 m2/g. As-prepared β-CD/mATP was evaluated as sorbents to adsorption of 2,4,6-trichlorophenol (2,4,6-TCP) and 2,4,5-trichlorophenol (2,4,5-TCP). The results of the batch mode experiment revealed that the Langmuir isotherm model fitted the equilibrium data better, while the kinetic data could be described by pseudo-second-order model perfectly. Furthermore, 2,4,5-TCP adsorption onto β-CD/mATP was more affected than that of 2,4,6-TCP in the presence of competitive phenolic compound. In addition, β-CD/mATP possessed excellent regeneration property.
研究领域:
材料科学
·
环境科学
✓ 已验证
DOI
高影响因子
ULTRASONICS SONOCHEMISTRY
·
2020
·
IF 6.513
Rong Zhang,Yanlan Ma,Wenting Lan,Dur E Sameen,Saeed Ahmed,Jianwu Dai,Wen Qin,Suqing Li,Yaowen Liu
Polyacrylonitrile (PAN)/β-cyclodextrin (β-CD) composite nanofibrous membranes immobilized with nano-titanium dioxide (TiO 2 ) and graphene oxide (GO) were prepared by electrospinning and ultrasonic-assisted electrospinning. Scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS), transmission electron microscopy (TEM), and X-ray diffraction (XRD) confirmed that TiO 2 and GO were more evenly dispersed on the surface and inside of the nanofibers after 45 min of ultrasonic treatment. Adding TiO 2 and GO reduced the fiber diameter; the minimum fiber diameter was 84.66 ± 40.58 nm when the mass ratio of TiO 2 -to-GO was 8:2 (PAN/β-CD nanofibrous membranes was 191.10 ± 45.66 nm). Using the anionic dye methyl orange (MO) and the cationic dye methylene blue (MB) as pollutant models, the photocatalytic activity of the nanofibrous membrane under natural sunlight was evaluated. It was found that PAN/β-CD/TiO 2 /GO composite nanofibrous membrane with an 8:2 mass ratio of TiO 2 -to-GO exhibited the best degradation efficiency for the dyes. The degradation efficiency for MB and MO were 93.52 ± 1.83% and 90.92 ± 1.52%, respectively. Meanwhile, the PAN/β-CD/TiO 2 /GO composite nanofibrous membrane also displayed good antibacterial properties and the degradation efficiency for MB and MO remained above 80% after 3 cycles. In general, the PAN/β-CD/TiO 2 /GO nanofibrous membrane is eco-friendly, reusable, and has great potential for the removal of dyes from industrial wastewaters.
研究领域:
环境科学
·
材料科学
✓ 已验证
DOI
高影响因子
ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH
·
2022
·Vol. 29
·期 42
·64244-64251
·
IF 5.19
Zhao Ke-meng,Liu Ze-hua,Zhang Jun,Zhong Shu-shu,Dang Zhi
Arylsulfatase and β-glucuronidase are the two substantial enzymes having a significant role in the cleavage of conjugated natural estrogens (C-NEs). The present study reports that arylsulfatase and β-glucuronidase have been abundantly found in the digestive tracts of Cipangopaludina chinensis ; in which, their corresponding activities were 60 and 5 U/g wet waste, respectively. The arylsulfatase from Cipangopaludina chinensi s could show high activity at low temperatures. Hence, its activity still remained at 53.2% of maximal activity even at an extremely low temperature of 4 ℃; while the corresponding activities of arylsulfatase from Helix pomatia or activated sludge were less than 20% and 10%, respectively. The arylsulfatase and β-glucuronidase from Cipangopaludina chinensis could efficiently cleave C-NEs suggesting that they could be alternative enzymes derived from Helix pomatia that are used for cleavage of conjugated compounds in environmental or biological sample analysis. Meanwhile, they might also be used to enhance the cleavage of C-NEs in municipal wastewater.
研究领域:
环境生物学
·
生物化学
✓ 已验证
DOI
PubMed
高影响因子
ACS Applied Materials & Interfaces
·
2019
·
IF 8.456
Yindian Wang,Yuan Qi,Chuxuan Chen,Changwen Zhao,Yuhong Ma,Wantai Yang
Exploring a suitable immobilization strategy to improve catalytic efficiency and reusability of cellulase is of great importance to lowering the cost and promoting the industrialization of cellulose-derived bioethanol. In this work, a layered structure with a thin PEG hydrogel as the inner layer and sodium polyacrylate (PAANa) brush as the outer layer was fabricated on low density polyethylene (LDPE) film by visible-light-induced graft polymerization. Two enzymes, β-glucosidase (BG) and cellulase, were separately coimmobilized onto this hierarchical film. As supplementary to cellulase for improving catalytic efficiency, BG was in situ entrapped into the inner PEG hydrogel layer during the graft polymerization from the LDPE surface. After graft polymerization of sodium acrylate on the PEG hydrogel layer was reinitiated, cellulase was covalently attached on the outer PAANa brush layer. Owing to the mild reaction condition (visible-light irradiation and room temperature), the immobilized BG could retain a high activity after the graft polymerization. The immobilization did not alter the optimal pH and temperature of BG or the optimal temperature of cellulase. However, the optimal pH of cellulase shifts to 5.0 after immobilization. Compared with the original activity of single cellulase system and isolated BG/cellulase immobilization system, the dual-enzyme system exhibited 82% and 20% increase in catalytic activity, respectively. The dual-enzyme system could maintain 93% of carboxymethylcellulose sodium salt (CMC) activity after repeating 10 cycles of hydrolysis and 89% of filter paper activity after 6 cycles relative to original activity, exhibiting excellent reusability. This layer coimmobilization system of BG and cellulase on the polymer film displays tremendous potential for practical application in a biorefinery.
研究领域:
生物技术
·
材料科学
·
酶工程
✓ 已验证
DOI
PubMed
高影响因子
ACS Applied Nano Materials
·
2022
·
IF 6.14
Le Zhang,Xin Zhou,Shaohua Chai,Jian Guan,Guijun Fan,Wuxinchen Yang,Guojun Ma,Ning Han,Yunfa Chen
There is a high demand to synthesize ozone decomposition catalysts especially in high-space-velocity and high-relative-humidity (RH) environments. Herein, two polymorphs of cobalt hydroxide, α- and β-Co(OH)2, are synthesized and applied for ozone elimination. β-Co(OH)2 shows ∼90% ozone decomposition efficiency under high space velocity (weight hourly space velocity (WHSV) = 1,200,000 mL g–1 h–1, 25 °C, 40 ppm), which is far higher than that of α-Co(OH)2 (∼5%). β-Co(OH)2 has high spin Co(II) in distorted octahedral coordination caused by the Jahn-Teller effect, leading to a higher crystal field splitting energy level and thus contributing to the easier electron transfer between the ozone and catalyst. Moreover, β-Co(OH)2 still shows high performance (∼87%) even in humid conditions (RH ∼50%, 25 °C, 40 ppm, WHSV = 600,000 mL g–1 h–1), which is attributable to its abundant surface non-hydrogen-bonded hydroxyls weakening water molecule adsorption, providing an idea to develop highly efficient catalysts for ozone decomposition in humid environments.
研究领域:
材料科学
·
催化
·
环境科学
✓ 已验证
DOI
高影响因子
Journal of Translational Medicine
·
2025
·Vol. 23
·期 1
·1-18
·
IF 7.5
Dong Rui,Li Meihui,Gu Xiu Feng,Gao Haiting,Wei Ziyi,Qi Houbao,Zhang Jun,Feng Qiang
Background Periodontitis is a chronic inflammatory disease that significantly impacts periodontal bone regeneration, yet the distinct biological features of osteoblasts in this condition remain poorly understood. This study aims to elucidate the cellular and molecular mechanisms underlying osteoblast dysfunction in periodontitis, with a focus on the role of Fusobacterium nucleatum (Fn) and its effector protein, D-galactose-binding periplasmic protein (Gbp).MethodSingle-cell RNA sequencing (scRNA-seq) data from human gingival tissues of periodontitis patients (PD) and healthy controls (HC) were analyzed to identify cellular heterogeneity and molecular pathways. An experimental periodontitis model in mice and primary osteoblast cultures were used to investigate the effects of Fn and Gbp on osteogenic differentiation. Transcriptomic analysis, gene set enrichment analysis (GSEA), and protein-protein interaction (PPI) networks were employed to explore the underlying mechanisms.Results scRNA-seq revealed a reduction in mesenchymal stem cells (MSCs) and osteoblastic lineage cells in PD tissues, with significant downregulation of osteogenic pathways such as Wnt signaling. Fn infection induced alveolar bone destruction in vivo and inhibited osteoblast proliferation, differentiation, and mineralization in vitro. Gbp, an Fn adhesin, similarly impaired osteogenic differentiation by downregulating key osteogenic genes and pathways. Transcriptomic analysis identified shared inflammatory and osteogenic pathways affected by Fn and Gbp, with NF-κB signaling activated and Wnt/β-catenin signaling inhibited. Mechanistically, Gbp interacted with the host protein ANXA2, disrupting the ANXA2/GSK3β complex and inhibiting Wnt/β-catenin signaling, a pivotal route for osteoblast differentiation. ANXA2 knockdown mitigated the Fn/Gbp-induced suppression of osteogenic activity, emphasizing its role in Fn-induced bone loss.Conclusion This study demonstrates that Fn and its effector Gbp disrupt osteogenic differentiation by inactivating the Wnt/β-catenin pathway binding to ANXA2.
研究领域:
微生物学
·
分子生物学
·
口腔健康
·
干细胞研究
✓ 已验证
产品关联
DOI
PubMed
高影响因子
Sustainable Energy & Fuels
·
2022
·Vol. 6
·期 11
·2745-2754
·
IF 6.813
Hua Tan,Xuecheng Li,Hao Ma,Xiaolin Yang,Tong Zhan,Wenyu Xie,Suhua Wang,Jiaping Zhu
Herein, N-doped carbon embedded Ni catalysts were prepared by a co-impregnation method followed by pyrolysis in a N2 atmosphere for transfer hydrogenolysis of lignin β-O-4 alcohol and ketone model compounds using isopropanol as the hydrogen source. It was found that pyrolysis at 800 °C resulted in the formation of graphitic N-doped carbon shell encapsulated Ni nanoparticles (Ni@NC-800). The obtained Ni@NC-800 exhibited higher activity and selectivity to aromatics in the conversion of 2-phenoxy-1-phenylthanol and 2-phenoxyacetophenone, compared with Ni@NC-600 and Ni/NC-800. Moreover, the selectivity to aromatics could be further improved over Ni@NC-800-H, which is Ni@NC-800 after strong acid leaching. However, the presence of Cα–OH in lignin β-O-4 model compounds was essential for their product distributions. The control and characterization experiments suggested that the catalytic reaction occurred on the surface of N-doped carbon shells, because the encapsulated Ni NPs could donate electrons to the outer shells, leading to surface electron enrichment, thus making inert shells the new active sites in Ni@NC-800-H. In addition, Ni@NC-800-H was efficient for the conversion of various lignin β-O-4 alcohol and ketone model compounds with methoxyl groups with high yields of the aromatic products and also possessed high stability during consecutive reaction runs, which is because Ni nanoparticles are physically isolated from the reactive environment.
研究领域:
化学工程
·
催化材料
·
可再生资源转化
✓ 已验证
DOI
高影响因子
ACS Applied Polymer Materials
·
2025
·
IF 4.7
Lingfeng Cui,Jing Qiao,Guanyue Zeng,Yuzhu Xiong,Gege Huang,Daiqiang Li
Developing biobased rubber composites that simultaneously boost tensile strength and elongation at break while integrating self-healing capacity and reprocessability remains a critical challenge in the rubber industry. Inspired by the unique multiple hydrogen bonding structure of spider silk and the dynamic β-hydroxy ester exchange reaction, this study constructed an epoxy polyurethane rubber containing octuple hydrogen bonds and incorporated it into epoxidized natural rubber. Carboxylated silica was utilized as a bridging agent to form β-hydroxy ester reversible covalent bonds at the interface between the filler and the rubber, thereby designing a high-strength, self-repairing, and reprocessable’vitrimer’ biobased elastomer. This design approach endows the material with outstanding mechanical properties (tensile strength of 8.92 MPa, Young’s modulus of 2.71 MPa, toughness of 17.45 MJ/m3), excellent self-healing performance (healing efficiency of 92.1%), and superior processability (tensile strength recovery of 97.6%). These properties are primarily attributed to the presence of reversible noncovalent octet hydrogen bonds and dynamic covalent β-hydroxy ester bonds. Furthermore, this design can be readily implemented across different biobased epoxy polymers and carboxyl-rich nanofillers. The design concepts presented herein can be applied to the development of self-healing and reprocessable’vitrimer’ biobased elastomers, providing valuable insights for the future design of green and sustainable polymers.
研究领域:
材料科学
·
高分子化学
·
绿色化学
✓ 已验证
产品关联
DOI
高影响因子
JOURNAL OF HAZARDOUS MATERIALS
·
2020
·
IF 9.038
Yuancai Lv,Jiachen Ma,Kaiyang Liu,Yanting Jiang,Guifang Yang,Yifan Liu,Chunxiang Lin,Xiaoxia Ye,Yongqian Shi,Minghua Liu,Lihui Chen
A porous β -cyclodextrin modified cellulose nano-fiber membrane (CA-P-CDP) was fabricated and employed to treat the trace bisphenol pollutants (bisphenol A (BPA), bisphenol S (BPS), and bisphenol F (BPF)) in water. The characterization highlighted the porous structure, stable crystal structure, good thermal stability of the obtained CA-P-CDP, as well as abundant functional groups, which could greatly improve the adsorption of bisphenol pollutants and recovery. During the static adsorption process, the adsorbents dosage, temperature and pH showed significant influence on the adsorption performance. At the selected conditions (25 °C, 7.0 of pH and 0.1 g L -1 of CA-P-CDP dosage), the BPA/BPS/BPF adsorption on CA-P-CDP could rapidly reached the equilibrium in 15 min by following the pseudo-second-order kinetic model, and the maximum adsorption capacities were 50.37, 48.52 and 47.25 mg g −1 , respectively, according to Liu isotherm model. The mechanisms between the bisphenol pollutants and CA-P-CDP mainly involved the synergism of hydrophobic effects, hydrogen-bonding interactions and π-π stacking interactions. Besides, the dynamic adsorption data showed that the volume of treated water for CA-P-CDP (0.58 L) was 14.5 times larger than that of pristine cellulose membrane (0.04 L), revealing satisfactory adsorption performance of trace BPA in water. Furthermore, during the treatment of real water samples (lake water and river water) with trace bisphenol pollutants, the complete removal of the pollutants were evidently observed, which strongly verified the possibility of CA-P-CDP for the practical application.
研究领域:
环境科学
·
材料科学
✓ 已验证
DOI
PubMed
高影响因子
CELLULAR AND MOLECULAR BIOLOGY
·
2024
·Vol. 70
·期 3
·95-101
·
IF 1.5
Shanfu Wang,Bing Xu,Heng Yin,Zhen Hua,Yang Shao,Jianwei Wang
Osteoporosis is a common chronic bone disorder in postmenopausal women. Ginsenosides are primary active components in ginseng and the effects of various ginsenoside variants in osteoporosis treatment have been widely revealed. We planned to explore the impact of ginsenoside Rc on bone resorption in an osteoporosis rat model. We used ovariectomized rats to assess the potential impact of ginsenoside Rc on osteoporosis. μ-CT was implemented for analyzing the microstructure of the distal left femur in rats. H&E staining together with Masson staining were applied for bone histomorphometry evaluation. ELISA kits were implemented to detect serum concentrations of TRACP-5b, OCN, CTX, as well as PINP. Ginsenoside Rc treatment lessened the serum levels of TRACP-5b as well as CTX, while increasing serum levels of OCN, and PINP of OVX rats. Moreover, we found that ginsenoside Rc contributed to the synthesis of type I collagen via increasing Col1a1 and Col1a2 levels in femur tissues of ovariectomized rats. Our findings also revealed that ginsenoside Rc activated the TGF-β/Smad pathway by increasing TGF-β as well as phosphorylated Smad2/3 protein levels. Ginsenoside Rc alleviates osteoporosis in rats through promoting the TGF-β/Smad pathway.
研究领域:
药理学
·
骨科
·
内分泌学
·
分子生物学
✓ 已验证
DOI
高影响因子
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY
·
2022
·
IF 5.895
Jianlin Chu,Yani Tian,Qian Li,Gaofei Liu,Qi Yu,Tianyue Jiang,Bingfang He
Levan-type fructooligosaccharides (FOS) exhibit enhanced health-promoting prebiotic effects on gut microbiota. The wild type (WT) of β-fructofuranosidase Fru6 could mainly yield 6-ketose. Semirational design and mutagenesis of Fru6 were exploited to promote the transfructosylating capacity for FOS. The promising variants not only improved the formation of 6-kestose but also newly produced tetrasaccharides of 6,6-nystose and 1,6-nystose (a new type of FOS), and combinatorial mutation boosted the production of 6-kestose and tetrasaccharides (39.9 g/L 6,6-nystose and 4.6 g/L 1,6-nystose). Molecular docking and molecular dynamics (MD) simulation confirmed that the mutated positions reshaped the pocket of Fru6 to accommodate bulky 6-kestose in a reactive conformation with better accessibility for tetrasaccharides formation. Using favored conditions, the variant S165A/H357A could yield 6-kestose up to 335 g/L, and tetrasaccharides (6,6-nystose and 1,6-nystose) reached a high level of 121.1 g/L (134.5 times of the mutant S423A). The β-(2,6)-linked FOS may show the potential application for the prebiotic ingredients.
研究领域:
酶工程
·
食品科学
·
微生物学
·
生物技术
✓ 已验证
DOI
PubMed
高影响因子
危险品化学品经营许可证（带存储）