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Biomaterials Science · 2020 ·Vol. 8 ·期 17 ·4810-4820 · IF 6.183

Injectable supramolecular gelatin hydrogel loading of resveratrol and histatin-1 for burn wound therapy

Yuanyuan Zheng,Weihao Yuan,Huiling Liu,Shaoshan Huang,Liming Bian,Rui Guo

Prolonged inflammatory response and insufficient vascularization cause delayed and poor wound healing. In this study, we fabricated a supramolecular host–guest gelatin (HGM) hydrogel loaded with resveratrol (Res) and histatin-1 (His-1) to suppress inflammation and promote vascularization at skin burn wound sites. The HGM hydrogel showed good properties of shear-thinning and injectability, thereby allowing easy in situ injection and fast adaption to irregular wounds. Res and His-1 were demonstrated to enhance angiogenesis in vitro using cell migration and tube formation assays based on human umbilical vein endothelial cells (HUVECs). In an established rat burn wound model, HGM/Res/His-1 hydrogel treatment promoted wound healing by inhibiting expression of the pro-inflammatory factors of interleukin 6 (IL-6), interleukin 1β (IL-1β) and tumor necrosis factor α (TNF-α) and increasing the expression of transforming growth factor β1 (TGF-β1) and platelet endothelial cell adhesion molecule-1 (CD31). HGM/Res/His-1 hydrogel treatment showed comparable efficacy with that of the commercial dressing, Tegaderm™, and therefore shows promising potential for clinical translation.

研究领域: 药剂学 · 伤口愈合 · 生物材料 · 炎症 · 血管生成
✓ 已验证 DOI PubMed 高影响因子
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JOURNAL OF POWER SOURCES · 2020 · IF 8.247

High energy-density supercapacitor based on a novel conjugated poly (1, 5-diaminoanthraquinone)/intercalated graphene composite system

Ning An,Zhuhang Shao,Zhen Guo,Jiao Xin,Yuanyuan He,Liwen Lv,Kefeng Xie,Xiuyan Dong,Yang Zhang,Zhongai Hu

In this work, we select a novel multi-redox poly (1, 5-diaminoanthraquinone) (PDAAQ) as electroactive material and Cetyltrimethylammonium bromide (CTAB) modified graphene oxide (CGO) as conductive substrate. Benefit from the excellent dispersion of CGO in organic polymerization medium and the abundant functional groups on the surface of CGO, 1, 5-diaminoanthraquinone (DAAQ) monomers may covalently graft on the conducting substrates and realize the directional growth of PDAAQ via the in-situ chemical oxidative polymerization. In three-electrode system, the optimization of PDAAQ/CGO electrode exhibits a high specific capacitance of 760 F g −1 at 1 A g −1 and superior electrochemical stability of 90.4% after 10 000 cycles. Most importantly, the electrochemical kinetic behavior of PDAAQ/CGO electrode is studied in detail. The result indicates that the energy storage process of PDAAQ/CGO is a synergistic result of diffusion-controlled process and capacitive effects, and the latter one is dominant. According to the simulation calculation of kinetic model , the capacitive contribution ratio of PDAAQ/CGO can be as high as 80.6% at a scan rate of 50 mV s −1 . Finally, the as-fabricated asymmetric supercapacitor (ASC) can deliver an energy density up to 41.1 W h kg −1 at a power density of 1000 W kg −1 , indicating a great potential application in high performance supercapacitors .

研究领域: 材料科学 · 电化学
✓ 已验证 DOI 高影响因子
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MATERIALS SCIENCE FORUM · 2020 · IF 0

Resolution of 1-Methyl-3-Amphetamine by Magnetic Fe3O4-APTES-CS2- Lipase in a Non-Aqueous Solvent

Hong Qian Dai,Yuan Lu,Zhi Hin Ou,Min Xu

Fe3O4-APTES-CS2 was prepared by modification of Fe3O4 with 3-aminopropyltriethoxysilane (APTES) and carbon disulfide (CS2). Lipase was covalently bonded to Fe3O4-APTES-CS2 to obtain the immobilized lipase Fe3O4-APTES-CS2-lipase. The textural characteristic of Fe3O4-APTES-CS2-lipase was assessed by scanning electron microscopy. The optimal immobilization conditions were 2.5 mg/mL lipase, pH 7.0, 35 °C, 3 h. The loading amount of lipase was 119.0 mg/g carrier. The immobilization efficiency reached 57%. (R)-(+)-N-acetyl-1-methyl-3-amphetamine was synthesized by Fe3O4-APTES-CS2-Li- pase. The conversion, enantiomeric excess of (R)-(+)-N-acetyl-1-methyl-3-amphet-a- mine and E value reached 36.8%, 98.5% and 132, respectivel.

研究领域: 化学 · 生物化学 · 材料科学 · 催化
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JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY · 2025 · IF 6.2

1, 8-Cineole Ameliorated Staphylococcus aureus-Induced Pneumonia through Modulation of TRP-KYN and Arginine-NO Reprogramming

Qianwen Cao,Luyao Liu,Xiaoge Ma,Chaomin Zhong,Mengqi Tang,Mengge Liu,Ling-Bo Qu,Bo Wei,Xia Xu

1, 8-Cineole (Cin), a cyclic monoterpenoid derived from tea trees and eucalyptus species, exhibits diverse pharmacological properties. Yet, its therapeutic impact and underlying mechanism against Staphylococcus aureus (S. aureus) pneumonia remain to be elucidated. In this study, metabolomics based on UPLC-MS/MS was integrated with network pharmacology, molecular biology, and molecular docking to investigate the effects of Cin. The findings demonstrated that Cin markedly reduced mortality and lung bacterial load, lessened pulmonary damage while suppressing the levels of proinflammatory factors, including tumor necrosis factor α (TNF-α), interleukin-1β (IL-1β), and interleukin-6 (IL-6) in the bronchoalveolar lavage fluid (BALF) of infected mice. Additionally, 19 metabolites, primarily involved in tryptophan metabolism and arginine biosynthesis, were notably modified by Cin via suppressing the enzymatic activity of indoleamine 2, 3-dioxygenase 1 (IDO1) and inducible nitric oxide synthase (iNOS), thereby attenuating the inflammatory response. Notably, knockdown of IDO1 or iNOS significantly diminished the anti-inflammation effect of Cin. In conclusion, our study validates the therapeutic potential of Cin against S. aureus pneumonia via anti-inflammation by downregulating IDO1 and iNOS. Our results provide a theoretical basis of natural substances applied in bacterial pneumonia treatment.

研究领域: 药理学 · 微生物学 · 免疫学
✓ 已验证 DOI PubMed 高影响因子
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ZEITSCHRIFT FUR KRISTALLOGRAPHIE-NEW CRYSTAL STRUCTURES · 2023 ·Vol. 238 ·期 6 ·1069-1070 · IF 0.3

Crystal structure of polybis(μ 4-3,5-dicarboxylatopyrazol-1-yl)-bis(N,N-dimethylformamide)tri-copper(II)–acetonitrile (1/2), C20H22Cu3N8O10

Yan-Qing Wang,Wen-Qing Yan,Li-Xue Nie,Ping-Ping Luan,Chao-Qun Li

C 20 H 22 Cu 3 N 8 O 10 , monoclinic, C 2/ c (no. 15), a  = 12.0766(11) Å, b  = 16.2778(14) Å, c  = 14.7605(13) Å, β  = 97.8580(10) ∘ , V  = 2874.4(4) Å 3 , Z  = 4, R gt ( F ) = 0.0420, wR ref ( F 2 ) = 0.0988, T  = 298.15 K.

研究领域: 无机化学 · 晶体学
✓ 已验证 DOI 高影响因子
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JOURNAL OF SOLUTION CHEMISTRY · 2022 ·Vol. 52 ·期 1 ·91-104 · IF 2

Liquid–Liquid Equilibrium for Ternary Systems of Ethylene Glycol, 2-Ethyl-1-Hexanol and Different Extractants at 298.2 K and 101.3 kPa

Yu Yingmin,Yi Lingxiao,Wei Jiajun,Guo Hongyue,Li Min

The liquid–liquid equilibrium (LLE) data for ethylene glycol + 2-ethyl-1-hexanol + { n -hexane, 1-hexene, 2-propyl-1-heptanol, and isopropyl ether} were measured at 298.2 K under 101.3 kPa. The distribution constant ( D ) and selectivity ( S ) of 2-ethyl-1-hexanol in the systems were calculated to analyze the extraction ability of the four extractants. The Bachman and Othmer–Tobias equations were chosen to examine the experimental LLE data. The linear correlation coefficient R 2  is greater than 0.98, indicating that the linear fitting of the experimental data is good. The data were regressed by thermodynamic models NRTL and UNIQUAC. The deviation between experimental data and simulated data was calculated by the root mean square deviation (RMSD) and the absolute average deviation (AAD). The RMSD is less than 0.79% and the AAD is less than 0.46%. It indicates that the two models are suitable for the regression of the system.

研究领域: 化学工程 · 热力学
✓ 已验证 DOI 高影响因子
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FARADAY DISCUSSIONS · 2016 ·Vol. 190 ·219-230 · IF 3.544

Immobilization of a rhodium catalyst using a diphosphine-functionalized ionic liquid in RTIL for the efficient and recyclable biphasic hydroformylation of 1-octene

Yong-Qi Li,Huan Liu,Peng Wang,Da Yang,Xiao-Li Zhao,Ye Liu

A highly efficient and stable Rh–P catalytic system in the RTIL of [PEmim]BF4 was developed for the biphasic hydroformylation of 1-octene by using the diphosphine-functionalized ionic liquid (FIL) of 2. While 2-Rh(acac)(CO)2 was immobilized in [PEmim]BF4 (solvent), a typical biphasic catalysis was fulfilled with advantages of facile separation and recycling ability – 9 runs without any loss of activity. It was found that not only the acquired π-acceptor character of 2, but also the synergetic role of the piperidyl group in [PEmim]BF4 as an N-containing donor, cooperatively contributed to the efficient hydroformylation due to the facilitated formation and stability of the Rh-H active species (ν 2045 cm−1). This was supported by the in situ high-pressure FT-IR spectral analysis.

研究领域: 化学工程 · 催化科学
✓ 已验证 DOI PubMed 高影响因子
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Materials Research Express · 2020 ·Vol. 6 ·期 12 ·125376 · IF 1.929

Preparation of 1-dodecanol microcapsules with cellulose nanofibers-modified melamine-formaldehyde resin as a potential phase change material

Sainan Wu,Pan Zhang,Zhilong Xu,Zhang Chen,Yanfeng Gao

A series of microencapsulated phase change materials (microPCMs) are synthesized by encapsulating 1-dodecanol into cellulose nanofibers (CNFs) modified melamine-formaldehyde (MF) resin through in situ polymerization. The chemical structure and crystallography of the microcapsules are characterized by Fourier-transform infrared spectroscopy (FT-IR) and x-ray diffraction (XRD). Scanning electronic microscopy (SEM) images show that the obtained microcapsules are regularly spherical with smooth surface and an average diameter about 1∼3 μm. The cracking ratio test indicates that the addition of CNFs largely enhances the mechanical strength of the microcapsules, and the CNFs/MF-microPCMs (with 3.4 wt% CNFs) have a phase change enthalpy of 100.4 J g−1. Furthermore, the simulation result demonstrates that the indoor temperature modulation ability of CNFs/MF-microPCMs model house is 4.2 °C, which is more than that of model house without microPCMs under room temperature. These results indicate that CNFs/MF-microPCMs are potential candidates for thermoregulating applications.

研究领域: 材料科学 · 能源工程
✓ 已验证 DOI 高影响因子
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JOURNAL OF CHEMICAL SCIENCES · 2024 ·Vol. 136 ·期 3 ·1-11 · IF 1.7

Recycled Pb/C-catalyzed one-pot synthesis of 1-carbonyl-1H-indoles from 2-iodoanilines and calcium carbide

Zhao Zhicai

A series of 1-carbonyl-1 H -indoles were prepared by 2-iodoanilines and calcium carbide in a one-pot reaction catalyzed by recyclable10% Pb/C, resulting in the corresponding substituted indoles in good yields. This protocol offers several advantages, including the utilization of sustainable, low-cost calcium carbide, an easy-to-handle acetylene source, and recyclable Pb/C catalysts. Graphic abstract The synthesis of a series of 1-carbonyl-1 H -indoles were prepared by 2-iodoanilines and calcium carbide in a one-pot reaction catalyzed by 10% Pb/C, resulting in the corresponding substituted indoles in good yields. This protocol offers several advantages, including the utilization of sustainable, low-cost feedstock, an easy-to-handle acetylene source, and recyclable Pb/C catalysts.

研究领域: 有机化学 · 绿色化学
✓ 已验证 DOI 高影响因子
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JOURNAL OF ELECTROANALYTICAL CHEMISTRY · 2024 · IF 4.1

Ultrahigh rate and cycling properties of Li2CuTi3O8 anode derived from HKUST-1 copper source for high-performance lithium-ion batteries

Haoqing Tang,Yulan Wang,Xiaohuan Liu,Tian Tian,Qiang Weng,Xiaotong Liu,Tao Liu

Rational design and preparation of titanium-based anode materials with superior fast charge and discharge are a key focuses of the lithium-ion batteries research. Herein, a novel and facile synthesis of uniformly carbon-coated Li 2 CuTi 3 O 8 (LCuTO) nanoparticles with excellent high-rate lithium storage properties is presented using HKUST-1 with pore structure and active metal sites as a copper source. The well-designed LCuTO@HKUST with carbon bridges between the particles and the carbon layer on the outer surface offers high electronic conductivity for fast charge and discharge. The LCuTO@HKUST exhibits extraordinary lithium storage performance: high capacity (251.8 mAh/g after 1000 cycles at a current density of 1.0 A/g), a superior high-rate capability (160.3 mAh/g after 500 cycles at 3.0 A/g and 138.1 mAh/g after 500 cycles at 5.0 A/g), and excellent cycle reversibility and cycle stability under various current densities. In addition, the lower Li + migration barrier in LCuTO@HKUST demonstrated by density functional theory (DFT) calculations is beneficial to the long-cycle stability and high-rate performance. The proposed preparation method and the strategy of using the MOF as a metal source for lithium-ion battery anode materials provide a new approach for advanced fast charge–discharge energy storage applications.

研究领域: 材料科学 · 能源存储
✓ 已验证 DOI 高影响因子
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JOM · 2020 ·Vol. 72 ·期 11 ·3806-3811 · IF 2.054

Direct Electrochemical Reduction of Solid Lead Oxide in Acetamide-1-Methylimidazolium Trifluoromethylsulfonate Low-Temperature Molten Salt

Li Min,Li Ying

In this work, we report an electrochemical route to directly reduce solid lead oxide (PbO) to lead in an acetamide-1-methylimidazolium trifluoromethylsulfonate (acetamide-MIMTfO) low-temperature molten salt. A cyclic voltammogram recorded using a graphite cavity electrode filled with PbO powder reveals that solid PbO can be directly electrochemically reduced to lead. Constant voltage electrolysis experiments with a PbO pellet cathode and a high-purity graphite anode were performed under different constant voltages (2.2–2.8 V) and at 343 K for different durations (2–6 h). XRD patterns of the electrolysis products confirm that the PbO pellet can be thoroughly reduced to lead after 6 h electrolysis. The present electrochemical route and acetamide-MIMTfO low-temperature molten salt can be used for extracting metals from their oxides at room temperature.

研究领域: 材料科学 · 电化学
✓ 已验证 DOI 高影响因子
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JOURNAL OF HETEROCYCLIC CHEMISTRY · 2023 · IF 2.4

Substrate-controlled chemoselective synthesis of 1-sulfonylquinazoline-2,4(1H,3H)-diones and 2-sulfonamidobenzonitriles

Ping Zhao,Qingle Zeng

We have developed a diversity-oriented, substrate-controlled, chemoselective synthetic method for a variety of structurally diverse 1-sulfonylquinazoline-2,4(1H,3H)-diones and 2-sulfonamidobenzonitriles. This substrate-controlled synthesis is accomplished through the condensation reaction of 2-(sulfonamido)benzamides with or without an N-methyl group on the amides. The reactions are fulfilled within half an hour at room temperature with solid triphosgene as a convenient condensing agent and pyridine as an acid acceptor. This protocol features easily available starting materials, mild reaction conditions, easy experimental operation, and moderate to excellent yields of products.

研究领域: 有机化学 · 药物化学
✓ 已验证 DOI 高影响因子
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