Journal of Materials Chemistry B
·
2015
·Vol. 3
·期 10
·2215-2228
·
IF 4.726
Minghui Xu,Junmin Qian,Aili Suo,Ning Cui,Yu Yao,Weijun Xu,Ting Liu,Hongjie Wang
Combined treatment of chemotherapeutics and small interfering RNAs (siRNAs) is a promising therapy strategy for breast carcinoma via their synergetic effects. In this study, to improve the therapeutic effect of doxorubicin (DOX), novel triblock copolymers, folate/methoxy-poly(ethylene glycol)-block-poly(L-glutamate-hydrazide)-block-poly(N,N-dimethylaminopropyl methacrylamide) (FA/m-PEG-b-P(LG-Hyd)-b-PDMAPMA), were synthesized and used as a vehicle for the co-delivery of DOX and P-glycoprotein (P-gp) siRNA into breast cancer cells. The triblock copolymers were synthesized by a combination of ring-opening polymerization of γ-benzyl-L-glutamate-N-carboxyanhydride using cystamine-terminated heterotelechelic PEG derivatives possessing folate or methoxy end groups (FA/m-PEG-Cys) as initiators and reversible addition–fragmentation chain transfer polymerization of N,N-dimethylaminopropyl methacrylamide followed by hydrazinolysis. The successful synthesis of the copolymers was confirmed by 1H NMR and gel permeation chromatography. DOX was covalently conjugated onto the poly(L-glutamate-hydrazide) blocks via a pH-labile hydrazone linkage, and the DOX-conjugated triblock copolymers could self-assemble into nanoparticles in aqueous solutions. P-glycoprotein (P-gp) siRNA was then bound to the cationic poly(N,N-dimethylaminopropyl methacrylamide) (PDMAPMA) blocks through an electrostatic interaction, resulting in the formation of spherical nanocomplexes with an average diameter of 196.8 nm and a zeta potential of +28.3 mV. The in vitro release behaviors of DOX and siRNA from the nanocomplexes were pH- and reduction-dependent, and the release rates were much faster under a reductive acidic condition (pH 5.0, glutathione: 10 mM) simulating the intracellular endo-lysosomal environment of cancer cells compared to physiological conditions. The fast payload release rates were closely related to both the glutathione-triggered detachment of PEG blocks from the nanocomplex surface and the pH-sensitive cleavage of hydrazone linkages. FA-decorated nanocomplexes showed higher cellular uptake efficiency and cytotoxicity against MCF-7 cells than FA-free nanocomplexes, as confirmed by confocal laser scanning microscopy, transmission electron microscopy, MTT and flow cytometry analyses. Our results demonstrated that the multifunctional triblock copolymer-mediated co-delivery of DOX and P-gp siRNA might be a new promising therapeutic strategy for breast cancer treatment.
✓ 已验证
产品关联
DOI
PubMed
高影响因子
JOURNAL OF POWER SOURCES
·
2015
·
IF 6.217
Yaoming Xiao,Gaoyi Han,Jihuai Wu,Jeng-Yu Lin
A novel bifacial perovskite solar cell (PSC) is devised and prepared by using a highly transparent poly(3,4-ethylenedioxythiophene) (PEDOT) electrode. The PEDOT is used as the p-type hole-transporting material (HTM) due to the well matched band positions for the charge separation and transport. Moreover, the PEDOT layer can play a role of electron blocking layer at the CH 3 NH 3 PbI 3 /PEDOT interface to reduce the electron recombination rate because of its LUMO level is higher than that of the perovskite sensitizer. As a result, the bifacial PSC based on the PEDOT HTM yields front and rear efficiencies of 12.33% and 11.78% respectively, which are higher than those of the PSC without the PEDOT HTM (8.67% and 8.27% of the front and rear efficiencies). And the front efficiency is only decreased by 4.46% to the rear efficiency. These promising results highlight the potential application of the PEDOT in the cost-effective and transparent PSC, which could be used in the bifacial solar cell and tandem solar cell .
✓ 已验证
产品关联
DOI
高影响因子
CHEMICAL RESEARCH IN CHINESE UNIVERSITIES
·
2014
·Vol. 30
·期 5
·731-737
·
IF 1.119
Ma Jingwei,Kan Hong,Ma Yinghui,Men Lihui,Pi Zifeng,Liu Zhiqiang,Liu Zhongying
Ultra performance liquid chromatographic-electrospray ionization-mass spectrometry(UPLC-ESI-MS) was used to investigate the potential interaction between selected ingredients of Aconitum and fritillary. The efflux ratios of 14-benzoylmesaconine(BM), 14-benzoylaconine(BC), 14-benzoylhypaconine(BH), mesaconitine(MA), aconitine( AC) and hypaconitine(HA) was 11.16, 12.53, 11.69, 12.8, 11.03 and 6.15, respectively, and the secretion of them was inhibited by Verapamil, which means they are the substrates of permeability-glycoprotein(P-gp). The transport of Aconitum alkaloids extract through a Caco-2 cell monolayer was determined in the absence and presence of fritillary extract. And the fritillary extract increased the absorption of Aconitum alkaloids. Peimine(PE) and peiminine( PEN) in fritillary increased the absorption of pure Aconitum alkaloids. The transport of digoxin was respectively enhanced by PE and PEN, which means they are the inhibitors of P-gp. PEN showed more effective inhibition than PE at the same concentration. The in vitro data suggest that the compounds such as fritillary present in alkaloids were able to inhibit the P-gp activity and lead modifying the transport of alkaloids.
✓ 已验证
产品关联
DOI
高影响因子
Journal of Materials Chemistry A
·
2016
·Vol. 4
·期 22
·8602-8609
·
IF 8.262
Wei Wan,Qiang Wang,Li Zhang,Hai-Wei Liang,Ping Chen,Shu-Hong Yu
The zinc–air battery is a promising energy device because of its high energy density and high safety. Developing efficient electrocatalysts for the oxygen reduction reaction (ORR) in air electrode is of great importance for high-performance zinc–air batteries. Herein, we first report N, P and Fe-tridoped nanoporous carbon ORR electrocatalysts derived from plant biomass corn silk. It is a cheap, accessible and recyclable biomass, which can offer a good basis for developing catalysts with low-cost and high yield production. The electrocatalysts were prepared by a hydrothermal process and a two step heat treatment process. The Fe element doped in the catalyst mainly came from FeCl3 and the P element came from corn silks. The N was from NH3 and corn silks. The biomass-derived catalyst exhibited a remarkably higher ORR activity, superior stability and tolerance to methanol poisoning effects in alkaline media than Pt/C catalyst. The catalyst also showed higher voltage and higher specific capacity than the Pt/C in a zinc–air battery and it may be an alternative to Pt/C in the practical application of the zinc–air battery. This study showed the possibility for rational design and preparation of high-performance electrocatalysts with a low-cost from a highly available and recyclable plant biomass.
✓ 已验证
产品关联
DOI
高影响因子
Asia-Pacific Journal of Chemical Engineering
·
2016
·Vol. 11
·期 2
·305-313
·
IF 0.728
Xing Li,Lei Bei,Zhi Sun,Kun Liu,Xu Zhang,Xiaozhao Han
The study aimed at investigating the addition effects of P, K, and micronutrient fertilizers on the permeability of N-nutrient fertilizer urea through a representative polymer membrane, which is of great importance in polymer-coated compound fertilizer. Specifically, the permeability of urea through polystyrene membrane was determined experimentally at the nominal temperature of 298 K using the Ussing chamber method for fertilizer solutions of urea–water, urea–NaH 2 PO 4 –water, urea–Ca(H 2 PO 4 ) 2 –water, urea–KCl–water, and urea–NaCl–water. The experimental data showed that the addition effects of NaH 2 PO 4 , KCl, and NaCl on urea permeability were pronounced and could be promotion or suppression depending on the amounts added. The variation of urea permeability with additive concentration could be explained by the ‘solution–diffusion’ model, suggesting that the specific intermolecular and interionic interactions in the permeation solution were an important factor determining the permeability. Using the saturated urea–water solution as basis, the addition of saturated KCl increased the urea permeability by 2.5 times, while the addition of saturated Ca(H 2 PO 4 ) 2 and NaH 2 PO 4 decreased the permeability by 41% and 76%, respectively. © 2016 Curtin University of Technology and John Wiley & Sons, Ltd.
✓ 已验证
产品关联
DOI
高影响因子
MACROMOLECULES
·
2017
·
IF 5.835
Zhen Hu,Qing Shao,Mark G. Moloney,Xirong Xu,Dayu Zhang,Jun Li,Chunhua Zhang,Yudong Huang
A direct and nondestructive strategy for growing polymers from the surface of graphene is demonstrated. The technique involves the covalent attachment of an initiator via one-step cycloaddition of a diarylcarbene, followed by the polymerization of 2-hydroxyethyl methacrylate (HEMA) using atom transfer radical polymerization (ATRP). The functionalization strategy is shown to significantly increase the solubility of the resulting materials (PHEMA-G) and leave the structure of the graphene largely intact. Importantly, the PHEMA-G/poly(p-phenylene benzobisoxazole) (PBO) composite fibers could be obtained by a one-pot polymerization and dry-jet wet spinning process. The nanocomposite fibers exhibited a tensile strength of 3.22 GPa (51.2% higher than PBO) and Young’s modulus of 139.3 GPa (33.7% higher than PBO) at very low PHEMA-G loading (1.0 wt %). This represents an excellent reinforcing efficiency, better than other reports of the graphene/PBO fibers system, and indicates that this material is suitable for applications in composite science.
✓ 已验证
产品关联
DOI
高影响因子
CERAMICS INTERNATIONAL
·
2016
·
IF 2.758
Nuoxin Xu,Xingrong Xiao,Hui Yang,Enjie Yu,Qilong Zhang
In this study, TiO 2 nanowires with various aspect ratios were prepared via a precursor-controlled hydrothermal process. Ternary composite films comprised of P(VDF-HFP) polymer, Ag particles and the as-synthesized TiO 2 nanowires were then fabricated. The results reveal that TiO 2 NWs with high aspect ratios (i.e., pa-TiO 2 ) exhibit superiority in enhancing the dielectric constants of composites in comparison with their low-aspect-ratio counterparts (i.e., pr-TiO 2 ). For instance, the dielectric constant of the Ag/pa-TiO 2 /P(VDF-HFP) composite with 30 vol% TiO 2 NWs reaches 33.4 at 100 Hz, which is 42.1% larger than that of Ag/pr-TiO 2 /P(VDF-HFP) sample and 227% higher than pristine P(VDF-HFP). In addition, TiO 2 nanowires also serve as physical obstacles to avoid aggregation of Ag particles. As a consequence, the ternary composites filled with high-aspect-ratio TiO 2 NWs exhibit suppressed dielectric losses (e.g., 0.023 at 100 Hz) and low conductivities, making them promising candidates for applications in integrated capacitors and energy storage devices.
✓ 已验证
产品关联
DOI
高影响因子
FLUID PHASE EQUILIBRIA
·
2017
·
IF 2.473
Kai Kang,Xiaopo Wang
The experimental measurements for liquid densities of n -decane and p -xylene binary mixtures were performed over the entire composition with a high-pressure vibrating-tube densimeter. The temperature ranges for the present measurement were from 293.15 K to 363.15 K and the pressures were reached to 60 MPa. The experimental uncertainty is estimated to be 0.001 with 0.95 confidence level. Experimental density values were fitted by the modified Tammann–Tait equation. The PC-SAFT equation of state and Cibulka's equation was used to predict the densities of n -decane and p -xylene and its mixtures. In addition, derived volumetric properties, such as the excess molar volumes , the isothermal compressibility , and isobaric thermal expansivity, were calculated from the experimental density data. The effects of pressure and temperature on the derived properties were also discussed.
✓ 已验证
产品关联
DOI
高影响因子
Frontiers of Materials Science
·
2017
·Vol. 11
·期 3
·223-232
·
IF 1.471
Wei Lulu,Lu Beibei,Li Lei,Wu Jianning,Liu Zhiyong,Guo Xuhong
A novel β-cyclodextrin-poly(2-(2-methoxyethoxy)ethyl methacrylate)- co -poly(ethylene glycol) methacrylate (abbreviated as: β-CD-(P(MEO 2 MA- co -PEGMA)) 21 ) was prepared by using the one-step strategy, and then the star-shaped copolymers were used in the atom transfer radical polymerization (ATRP). The structure of star-shaped β-CD-(P(MEO 2 MA- co -PEGMA)) 21 copolymers were studied by FTIR, 1 H NMR and gel permeation chromatography (GPC). The star-shaped copolymers could self-assembled into micelles in aqueous solution owing to the outer amphiphilic β-CD as a core and the hydrophilic P(MEO 2 MA- co -PEGMA) segments as a shell. These thermo-responsive starshaped copolymers micelles exhibited lower critical solution temperature (LCST) in water, which could be finely tuned by changing the feed ratio of MEO 2 MA to PEGMA. The LCST of star-shaped β-CD-(P(MEO 2 MA- co -PEGMA)) 21 copolymer micelles were increased from 35°C to 58°C with the increasing content of PEGMA. The results were investigated by DLS and TEM. When the temperature was higher than corresponding LCSTs, the micelles started to associate and form spherical nanoparticles. Therefore, β-CD-(P(MEO 2 MA- co -PEGMA)) 21 star-shaped copolymer micelles could be potentially applied in nano-carrier, nano-reactor, smart materials and biomedical fields.
✓ 已验证
产品关联
DOI
高影响因子
JOURNAL OF MATERIALS SCIENCE
·
2016
·Vol. 51
·期 23
·10574-10584
·
IF 2.302
Zhao Jie,Xie Yu,Fang Jing,Ling Yun,Gao Yunhua,Liu Xiaoming,Zhang Qiugen,Xu Qiuhua,Xiong Hui
A novel electromagnetic material has been synthesized through P -phenylenediamine-benzoquinone (PB) Schiff base Ag(I) complexes chemically bonded to few-layered graphene (FLG). The structure of the samples was characterized by Fourier transform infrared spectroscopy and X-ray diffraction. The shape and size were observed by scanning electron microscopy and transmission electron microscopy. The conductive properties were tested by a four-probe conductivity tester at room temperature, and the magnetic properties of the samples were tested with the vibrating sample magnetometer. These results show that the PB Schiff base Ag(I) complexes are chemically bonded onto the FLG layers. The conductivity, magnetic saturation, residual magnetization, and coercive force of the composite achieve 5.86 S cm −1 , 1.47 emu g −1 , 0.26 emu g −1 , and 208.3 Oe, respectively. Finally, based on the experimental results, the probable formation, electronic transmission, and magnetic mechanism have also been investigated.
✓ 已验证
产品关联
DOI
高影响因子
JOURNAL OF COLLOID AND INTERFACE SCIENCE
·
2024
·
IF 9.4
Qiuling Chen,Shun Wang,Baoji Miao,Qiuping Chen
The creation of a Z-scheme heterojunction is a sophisticated strategy to enhance photocatalytic efficiency. In our study, we synthesized an In 2 S 3 /MnO 2 /BiOCl dual Z-scheme heterostructure by growing BiOCl nanoplates on the sheets of In 2 S 3 nanoflowers, situated on the surface of MnO 2 nanowires. This synthesis involved a combination of hydrothermal and solution combustion methods. Experiments and density functional theory (DFT) calculations demonstrated that the In 2 S 3 /MnO 2 /BiOCl composite exhibited notable photo reduction performance and photocatalytic stability. This was attributed to the pivotal roles of BiOCl and MnO 2 in the composite, acting as auxiliaries to enhance the electronic structure and facilitate the adsorption/activation capacity of CO 2 and H 2 O. The yield rates of CO, CH 4 , and C 2 H 4 over In 2 S 3 /MnO 2 /BiOCl as the catalyst were 3.94, 5.5, and 3.64 times higher than those of pure In 2 S 3 , respectively. Photoelectrochemical analysis revealed that the dual Z-scheme heterostructure, with its oxygen vacancies and large surface area, enhanced CO 2 absorption and active sites on the nanoflower/nanowire intersurfaces. Consequently, the dual Z-scheme charge transfer pathway provided efficient channels for boosting electron transfer and charge separation, resulting in high C 2 H 4 , CH 4 , and CO yields of formed and exihibits an promising photoreduction rate of CO 2 to CO (51.2 µmol/g.h), CH 4 (42.4 µmol/g.h) and C 2 H 4 (63.2 µmol/g.h), respectively. DFT, in situ Diffuse reflectance infrared fourier transform spectroscopy, and temperature-programmed desorption tests were employed to verify the intermediates pathway. The study proposed a potential photocatalytic mechanism based on these findings.
✓ 已验证
产品关联
DOI
PubMed
高影响因子
INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES
·
2024
·
IF 7.7
Jingjie Gao,Shaowei Bai,Fan Wang,Liangzhen Yang,Yufeng Hu,Yuhuan Yang,Bing Bai,Zuoming Zhang
Enzymatic glycosylation is an efficient and biocompatible approach to enhance natural product bioavailability. Cellobiose phosphorylase, a novel glycosyltransferase, utilizes 1-phospho-glucose (1-p-Glc) as a glycosyl donor for regioselective glycosylation of various natural substrates. However, the high cost of 1-p-Glc limits the economic feasibility of the process. Thus, a dual-enzyme cascade system involving cellulase Ac Cel9A and cellobiose phosphorylase Cb CBP using a co-immobilization strategy was developed to overcome this challenge. The system utilizes low-cost carboxymethyl cellulose (CMC) for continuous 1-p-Glc production, which was then used in the fluorodeoxy glucose (FDG) glycosylation to generate fluorodeoxy cellobiose (FDC), which potentially traces fungal infections. The compartmentalized co-immobilization of the two enzymes within the internal and external regions of a porous zeolitic imidazolate framework-8 (ZIF-8) carrier enhanced the overall stability of the dual-enzyme system. The immobilized enzymes retained approximately 63.3 % activity after seven reuse cycles and 74 % catalytic efficiency after 12 days of storage at room temperature. Therefore, the developed co-immobilized multi-enzyme system holds significant potential for industrial biocatalysis applications.
✓ 已验证
产品关联
DOI
PubMed
高影响因子
危险品化学品经营许可证（带存储）