BIOMEDICINE & PHARMACOTHERAPY
·
2024
·
IF 6.9
Junyu Wang,Chaojie Yang,Zhixin Liang,Junping Sun,Mingyue Zhang,Shaofu Qiu,Xinying Du,Xi He,Xiaoying Pang,Xidong Ma,Mei Xie,Xinjie Han,Ru Fan,Enlu Zhou,Hairong Yu,Danyang She,Hongbin Song,Jianxin Wang
Human adenovirus (HAdV) infection is a major cause of respiratory disease, yet no antiviral drugs have been approved for its treatment. Herein, we evaluated the antiviral and anti-inflammatory effects of cyclin-dependent protein kinase (CDK) inhibitor indirubin-3′-monoxime (IM) against HAdV infection in cells and a transgenic mouse model. After evaluating its cytotoxicity, cytopathic effect reduction, antiviral replication kinetics, and viral yield reduction assays were performed to assess the anti-HAdV activity of IM. Quantitative real-time polymerase chain reaction (qPCR), quantitative reverse transcription PCR (qRT-PCR), and western blotting were used to assess the effects of IM on HAdV DNA replication, transcription, and protein expression, respectively. IM significantly inhibited HAdV DNA replication as well as E1A and Hexon transcription, in addition to significantly suppressing the phosphorylation of the RNA polymerase II C-terminal domain (CTD). IM mitigated body weight loss, reduced viral burden, and lung injury, decreasing cytokine and chemokine secretion to a greater extent than cidofovir. Altogether, IM inhibits HAdV replication by downregulating CTD phosphorylation to suppress viral infection and corresponding innate immune reactions as a promising therapeutic agent.
研究领域:
病毒学
·
药理学
·
免疫学
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DOI
PubMed
高影响因子
SENSORS
·
2022
·Vol. 22
·期 12
·4476
·
IF 3.847
Yiwen Kuang,Mengxue Li,Shiyu Hu,Lu Yang,Zhanning Liang,Jiaqi Wang,Hongmei Jiang,Xiaoyun Zhou,Zhaohong Su
A sensitive simultaneous electroanalysis of phytohormones indole-3-acetic acid (IAA) and salicylic acid (SA) based on a novel copper nanoparticles-chitosan film-carbon nanoparticles-multiwalled carbon nanotubes (CuNPs-CSF-CNPs-MWCNTs) composite was reported. CNPs were prepared by hydrothermal reaction of chitosan. Then the CuNPs-CSF-CNPs-MWCNTs composite was facilely prepared by one-step co-electrodeposition of CuNPs and CNPs fixed chitosan residues on modified electrode. Scanning electron microscope (SEM), transmission electron microscopy (TEM), selected area electron diffraction (SAED), energy dispersive spectroscopy (EDS), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), and linear sweep voltammetry (LSV) were used to characterize the properties of the composite. Under optimal conditions, the composite modified electrode had a good linear relationship with IAA in the range of 0.01–50 μM, and a good linear relationship with SA in the range of 4–30 μM. The detection limits were 0.0086 μM and 0.7 μM (S/N= 3), respectively. In addition, the sensor could also be used for the simultaneous detection of IAA and SA in real leaf samples with satisfactory recovery.
研究领域:
植物学
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材料科学
·
分析化学
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DOI
高影响因子
LABORATORY INVESTIGATION
·
2018
·Vol. 98
·期 12
·1642-1656
·
IF 4.263
Cao Zhanqi,Hao Zhaojun,Xin Ming,Yu Lugang,Wang Lei,Zhang Ying,Zhang Xinke,Guo Xiuli
Tumor cell-endothelial adhesion is one of the key steps in tumor cell haematogenous dissemination in metastasis and was previously shown to be mediated by interaction of galectin-3 with the transmembrane mucin protein MUC1. In this study, the effect of exogenous as well as endogenous galectin-3 on adhesion of two cell lines (low MUC1-expressing human prostate cancer PC-3M cells and non-small-cell lung cancer A549 cells) to monolayer of umbilical vein endothelial cells (HUVECs) was investigated. We found that suppression of endogenous galectin-3 expression reduced tumor cell adhesion to HUVECs and also decreased cell invasion and migration. Exogenous galectin-3 promoted tumor cell adhesion to HUVECs by entering cells. Both exogenous and endogenous galectin-3 upregulated the expression of β-catenin and increased β-catenin nuclear accumulation, and subsequently upregulated the expression of N-cadherin and CD44. We deduced that both exogenous as well as endogenous galectin-3 promoted low MUC1-expressing cancer cell adhesion to HUVECs by increasing the expression of N-cadherin and CD44 via an increase of nuclear β-catenin accumulation. These results were confirmed further by using a β-catenin/TCF transcriptional activity inhibitor, N-cadherin or CD44 siRNAs. Taken together, our results suggest a new molecular mechanism of galectin-3-mediated cell adhesion in cancer metastasis.
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产品关联
DOI
PubMed
高影响因子
TALANTA
·
2019
·
IF 4.916
Chengxin Wu,Yuanyuan Sun,Yuanhang Wang,Wenzhen Duan,Jiangyue Hu,Lei Zhou,Qiaosheng Pu
Diode lasers, especially 405 nm diode laser, as excitation sources offer new opportunities for laser-induced fluorescence (LIF) detection, but the lack of available derivatization reagents limits their widespread applications. Herein, a commercial fluorescent dye , 7-(diethylamino)coumarin-3-carboxylic acid (DEAC-C) was introduced as derivatization reagent and corresponding derivatization strategy for DEAC-C labeling sulfonamides was developed for 405 nm LIF detection. After systematic optimization, three sulfonamides including hydrochlorothiazide (HCTZ), chlorothiazide (CTZ) and chlortalidone (CTD) could be efficiently labeled by DEAC-C in the presence of cyanuric chloride and triethylamine (1.5%) in acetonitrile at 50 °C for 180 min. Based on the laboratory-built capillary electrophoresis-LIF system, a robust method was then proposed for the separation of DEAC-C labeled sulfonamides by micellar electrokinetic chromatography (MEKC) using the classic borax-SDS system. Under the optimized conditions, a baseline separation of three sulfonamides was achieved within 15 min, and the detection limits were determined to be 0.24, 0.29, and 0.23 nM for HCTZ, CTZ, and CTD, respectively. Furthermore, the developed MEKC-LIF method was validated using sulfonamide standards and spiked human urine sample and successfully applied for the analysis of three sulfonamides in complex pharmaceutical and physiological samples.
研究领域:
分析化学
·
药学
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DOI
高影响因子
Journal of Information Display
·
2019
·
IF 0
Xiaoliang Pang,Xuejie Zhang,Bingfu Lei,Haoran Zhang
Embedding CsPbX3 (X = Cl, Br, I) perovskites QDs in inorganic glass matrix via in-situ crystallization has been regarded as a feasible strategy to improve their stability against water, heat, and light irradiation. However, the tunable-emission range of these CsPbX3-nanocrystals-embedded glasses is still narrow, insufficient to cover a wide color gamut. Herein, a simple synthetic method was developed in this study to obtain the tunable-emission CsPb(Cl/Br)3 quantum dots (QDs) in boro-germanate glass (CsPb(Cl/Br)3 QDs@glass) by controlling the molar ratio of PbBr2/PbCl2. With the increase of the PbBr2 concentration from 1.6 to 3.2 mol%, the emission wavelength of CsPb(Cl/Br)3 QDs@glasses can be shifted from 448 to 485 nm, and the corresponding photoluminescence quantum yield (PLQY) increases from 0.61 to 24.43%. In addition, the CsPb(Cl/Br)3 QDs@glass exhibits impressing promotion of thermal stability, photostability, and water resistance due to the excellent protective function of the glass matrix. As a proof-of-concept experiment, a LED device was fabricated by employing the optimal CsPb(Cl/Br)3 QDs@glass with a commercial 375 nm UV chip, yielding an intense cyan light. All the results indicate that the investigated CsPb(Cl/Br)3 QDs@glasses may find promising applications as color convertors in wide-color-gamut liquid crystal displays (LCDs).
研究领域:
材料科学
·
光电技术
·
纳米技术
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DOI
JOURNAL OF THE AMERICAN CERAMIC SOCIETY
·
2018
·Vol. 102
·期 7
·4092-4102
·
IF 2.956
Yunhui Zhang,Haitao Wu
La 2 (Zr 1− x Ti x ) 3 (MoO 4 ) 9 (0 ≤ x ≤ 0.1) ceramics were prepared by the traditional solid-state reaction method. XRD analysis showed that La 2 (Zr 1− x Ti x ) 3 (MoO 4 ) 9 (0 ≤ x ≤ 0.1) ceramics belonged to a trigonal system. Based on the chemical bond theory, the consequences of bond energy, bond ionicity, lattice energy, and thermal expansion coefficient of ceramics on microwave dielectric properties were discussed. As Ti 4+ addition was increased, the reduction in dielectric constant was ascribed to the fact that the polarizability of Ti 4+ is smaller than Zr 4+ , and the downward trend was related to the bond ionicity. Besides, the tendency of Q·f value depended on the packing fraction and the lattice energy. The improvement in τ f value, the increase in bond energy, and the decrease in the coefficient of thermal expansion were all correlated. The far-infrared spectra implied that the absorptions of structural phonon oscillation were the main reason for the maximum polarization contribution. La 2 (Zr 0.92 Ti 0.08 ) 3 (MoO 4 ) 9 ceramics sintered at 750°C for 4 hours exhibited the best dielectric properties ( ε r = 10.33, Q·f = 80 658 GHz, and τ f = 3.48 ppm/°C).
研究领域:
材料科学
·
陶瓷工程
·
电气工程
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DOI
高影响因子
INORGANIC CHEMISTRY
·
2022
·
IF 5.436
Zhiyong Bai,Lehui Liu,Zhoubin Lin,Kang Min Ok
A novel guanidinium-templated ultraviolet (UV) nonlinear optical zinc carbonate crystal, [C(NH2)3]2Zn(CO3)2 (GZCO), has been synthesized in a closed system at low temperatures. GZCO crystallizing in the tetragonal noncentrosymmetric nonpolar space group, P41212 exhibits a three-dimensional anionic framework constructed by interconnected [Zn6C6O32] 12-membered ring channels with inorganic CO3 triangles and ZnO4 tetrahedra. Notably, the anhydrous GZCO shows a very high thermal stability among guanidine-based hybrid NLO materials benefiting from the confinement effect of the organic cations within inorganic channels. The UV–visible transmittance spectrum reveals that GZCO has a short UV cutoff edge of 210 nm, corresponding to the large band gap of 5.9 eV. GZCO exhibits a mild second-harmonic generation efficiency of 0.5 × KH2PO4 with type-I phase-matching behavior.
研究领域:
材料科学
·
光学
·
化学
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DOI
高影响因子
JOURNAL OF MOLECULAR LIQUIDS
·
2023
·
IF 6
Zihao Dong,Yajuan Qu,Yuyang Jiao,Ke Xue,Wenguang Zhu,Hai Liu,Jianguang Qi,Yinglong Wang
A series of poly(1-vinyl-3-methylimidazole dimethyl phosphate- co -N-isopropylacrylamide) oligomers was synthesized by reversible addition-fragmentation chain transfer polymerization. The co-oligomers exhibited a pH-tunable lower critical solution temperature (LCST) phase transition in aqueous solutions. By changing the pH of the aqueous solution (HCI), the hydrogen bonding between the internal molecules of the co-oligomers and water molecules was weakened, which effectively reduced the cloud-point temperature. Poly(1-vinyl-3-methylimidazole dimethyl phosphate- co - N -isopropylacrylamide) oligomers exhibit an upper critical solution temperature (UCST) type of phase transition in an ester solution, which is associated with the formation and breaking of hydrogen bonds within the co-oligomers molecules. FT-IR analysis revealed the effect of temperature on hydrogen bonding between the functional groups. Energy decomposition, Electrostatic Potential (ESP), Atoms-in-Molecules (AIM), and Interaction region indicator (IRI) analyses demonstrated the presence of hydrogen bond donors N–H and imidazole ring C–H, and hydrogen bond acceptors C = O and P = O in the co-oligomers. The sites of hydrogen bonding between the co-oligomers and the solvent molecules as well as intermolecular forces were found to be the main factors contributing to the LCST/UCST-type phase transition.
研究领域:
高分子化学
·
物理化学
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DOI
高影响因子
JOURNAL OF RARE EARTHS
·
2012
·
IF 0.901
Xiaoming PENG,Yufeng HU,Chuanwei JIN,Zhixin WANG,Chao MIAO,Zheyu LI
Viscosities were measured for the ternary systems Y(NO 3 ) 3 +La(NO 3 ) 3 +H 2 O, La(NO 3 ) 3 +Ce(NO 3 ) 3 +H 2 O, and La(NO 3 ) 3 +Nd(NO 3 ) 3 + H 2 O and their binary subsystems Y(NO 3 ) 3 +H 2 O, La(NO 3 ) 3 +H 2 O, Ce(NO 3 ) 3 +H 2 O, and Nd(NO 3 ) 3 +H 2 O at 293.15, 298.15 and 308.15 K. The results were used to test the applicability of simple equations for the viscosity of the mixed solutions. The predictions agreed well with measured values, implying that the viscosities of the examined electrolyte solutions could be related to those of their constituent binary solutions using these simple equations.
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产品关联
DOI
高影响因子
SENSORS AND ACTUATORS B-CHEMICAL
·
2017
·
IF 5.401
Xiao Wang,Ying Zheng,Lan Xu
An electrochemical strategy for adenine detection was described. In order to generate a 3D net-work composite film, gold nanoparticles (Au NPs) capped with 3-thiophene acetic acid (3-TAA) were used to couple with molecular imprinting technique (MIT). In the presence of the 3-TAA capping Au NPs (Au NPs-T), the electrode-surface-tethered 3-TAAs were polymerized to form a homogeneous conductive material immobilized into the electrode. Through this sensor fabrication, Au NPs-T associating with the Au electrode resulted in enhanced sensitivity and MIT contributed to the specificity.
研究领域:
电化学
·
生物传感器
·
纳米技术
·
分析化学
·
分子印迹
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DOI
高影响因子
MICROCHIMICA ACTA
·
2017
·Vol. 184
·期 7
·2325-2331
·
IF 4.58
Huang Xinan,Jiang Hong,Li Yongxin,Sang Lijia,Zhou Huipeng,Shahzad Sohail Anjum,Ibupoto Zafar Hussain,Yu Cong
A sensitive and selective luminescent nanoprobe (referred to as DEPN) is designed for the determination of Cu(II) ions. DEPN shows two emission peaks, one at 602 nm and caused by [Ru(bpy) 3 ] 2+ , the other (peaking at 500 nm) caused by silver nanoclusters (AgNCs). The luminescence of the ruthenium complex is inert and acts as the internal reference signal, while that of the AgNCs is quenched by Cu(II) ions. Under 350 nm photoexcitation, a linear relationship is found between the ratio of emission intensity (I 500 /I 602 ) and the concentration of Cu(II) ions in the 0.1–16 μM range. The detection limit of Cu(II) ions is estimated to be 50 nM. The DEPN was applied to the determination of Cu(II) ions in (spiked) water samples, and to intracellular imaging of Cu(II) in HeLa cells using confocal fluorescence microscopy.
Schematic presentation of a dual-emission photoluminescence nanoprobe for selective Cu 2+ sensing. The emission of the Ag nanoclusters (at 500 nm) is quenched by Cu 2+ , while that of the Ru(bpy) 3
2+ -doped silica nanoparticles (at 602 nm) remains unchanged and serves as a reference.
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产品关联
DOI
高影响因子
SENSORS AND ACTUATORS B-CHEMICAL
·
2022
·
IF 9.221
Xiao-Fan Wu,Qingmei Ge,Nan Jiang,Mao Liu,Hang Cong,Zhu Tao
Utilizing a novel concept of chiral amplification induced by host-guest interactions, a new macrocyclic compound , benzo[3]uril (BU[3]), was formed in a chiral microenvironment via the encapsulation of L -cysteine∙H + (L-Cys∙H), and the electrochemiluminescence properties of BU[3] were sensibilized with the formation of a supramolecular complex . Based on this principle, an ultra-sensitive chiral electrochemiluminescence sensor was constructed to recognize the enantiomer of penicillamine (PA). This sensor exhibited high selectivity and sensitivity for L -PA compared to other reported values, with a detection limit of 10 -12 mol·L -1 within a linear range of 10 -5 –10 -10 mol·L -1 , and no obvious electrochemiluminescence response to D -PA. The sensor presents high stability, good reproducibility, strong anti-interference ability, and acceptable recovery, which suggests an ability to quantitatively detect L -PA in an aqueous environment.
研究领域:
分析化学
·
材料科学
·
电化学
·
手性和超分子化学
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DOI
高影响因子
危险品化学品经营许可证（带存储）