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NANOTECHNOLOGY · 2013 ·Vol. 24 ·期 14 ·145101 · IF 3.842

A pH-responsive chitosan-b-poly(p-dioxanone) nanocarrier: formation and efficient antitumor drug delivery

Dao-Lu Tang,Fei Song,Cheng Chen,Xiu-Li Wang,Yu-Zhong Wang

Increasing attention has recently been paid to the fabrication of drug delivery systems with excellent cell internalization and intracellular drug release properties. In this study, an amphiphilic block copolymer of chitosan was synthesized for the first time, which can self-assemble into micelles in a neutral aqueous solution but partially disassemble in an acidic endosomal/lysosomal environment. The antitumor drug, camptothecin (CPT), was encapsulated in the cores of the micelles for tumor cell therapy. In vitro drug release studies demonstrated that the micelles presented a much faster release of CPT at pH 5.0 than at pH 7.4. Blank micelles were found to be nontoxic in preliminary in vitro cytotoxicity assays. Cell experiments showed that the CPT-loaded micelles could be effectively internalized by Hela cells and accomplished a potent antitumor cell efficacy, indicating that the chitosan-based micelles might be an attractive new platform for efficient intracellular drug delivery.

CAS / MDL: 814-68-6
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RESEARCH ON CHEMICAL INTERMEDIATES · 2015 ·Vol. 41 ·期 12 ·10169-10180 · IF 1.221

A novel colorimetric chemosensor for Cu2+ with high selectivity and sensitivity based on Rhodamine B

Li Changjiang,Xiang Kaiqiang,Liu Yunchang,Zheng Yuchuan,Tian Baozhu,Zhang Jinlong

9-formyl-8-hydroxy-2,3,6,7-tetrahydro-1H, 5H-benzo[ij]-quinolizine rhodamine B hydrazone (FHQRH), a novel colorimetric chemosensor for Cu 2+ , was synthesized by a three-step synthetic route. It was found that FHQRH showed a high selectivity for Cu 2+ ions and excellent anti-interference capability toward other metal ions. The FHQRH solution exhibited a visual color change after the addition of Cu 2+ , owing to the open spirocyclic structure via coordination with Cu 2+ . The complexation coefficient of FHQRH toward Cu 2+ was measured to be 1:1. Furthermore, this Cu 2+ chemosensor has a remarkable low detection limit of 0.45 μM, which is 2 % of the toxic level (20 μM) in drinking water as defined by the US Environment Protection Agency (EPA).

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Journal of Materials Chemistry B · 2015 ·Vol. 3 ·期 38 ·7554-7559 · IF 4.726

TiO2-B nanorod based competitive-like non-enzymatic photoelectrochemical sensing platform for noninvasive glucose detection

Shupei Zhang,Guifang Xu,Lingshan Gong,Hong Dai,Yilin Li,Zhensheng Hong,Yanyu Lin

TiO2-B nanorods, with excellent properties including large specific surface area, open structures with significant voids, and continuous channels, were explored for the first time in the photoelectrochemical biosensing field. To reduce the destructive effect of UV light on biomolecules, dopamine was introduced onto the TiO2-B nanorod surface through the coordination of dopamine to the undercoordinated titanium atoms of the TiO2-B nanorods, which makes the complex a promising matrix for subsequent biosensing. Furthermore, concanavalin A as a recognition element was attached onto the TiO2-B nanorod/dopamine modified electrode surface by virtue of covalent interaction between concanavalin A and dopamine. Accordingly, a new competitive-like non-enzymatic photoelectrochemical biosensor was established by using glucose labeled SiO2 nanospheres of fixed concentration as photoelectrochemical signal inhibitors competing with target glucose of various concentrations for reaction with concanavalin A. Moreover, this ultrasensitive biosensor with excellent analytical performance was successful applied to noninvasive glucose determination in human saliva. Promisingly, the successful application of TiO2-B nanorods in this research provides a new consideration in the selection of excellent photoactive materials for photoelectrochemical sensing.

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Polymer Chemistry · 2014 ·Vol. 5 ·期 12 ·3824-3830 · IF 5.368

Folic acid-functionalized AIE Pdots based on amphiphilic PCL-b-PEG for targeted cell imaging

Yan Zhang,Yujue Chen,Xing Li,Jibo Zhang,Jinlong Chen,Bin Xu,Xueqi Fu,Wenjing Tian

Fluorescent block amphiphilic copolymers are one of the most important bioimaging materials which are highly desirable for early stage cancer diagnosis and treatment. However, sometimes the application of the fluorescent block copolymers is severely limited because of the aggregation-caused quenching (ACQ) effect. In this study, new aggregation induced emission polymer dots (AIE Pdots) were prepared through a self-assembly process by using an AIE-conjugated block copolymer containing an AIE fluorophore, 9,10-bis(4-hydroxystyryl)anthracene, hydrophobic poly(ε-caprolactone) segments, hydrophilic poly(ethylene glycol) segments and folate groups. The AIE Pdots are monodispersed in H2O with an average diameter of 15 nm, and possess strong emission and high solid state fluorescence quantum efficiency (Φ = 27.0%). Furthermore, the AIE Pdots show good stability and little toxicity to living cells and thus can be utilized for targeted HeLa cell imaging. Biological imaging investigation indicated that the folic acid functionalized AIE Pdots can be applied for targeted HeLa intracellular imaging.

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JOURNAL OF BIOMATERIALS SCIENCE-POLYMER EDITION · 2014 · IF 1.357

Thermosensitive AB4 four-armed star PNIPAM-b-HTPB multiblock copolymer micelles for camptothecin drug release

Yan-Ling Luo,Jing-Yu Fu,Feng Xu,Ya-Shao Chen,Bin Zhang

Thermo-sensitive poly(N-isoproplacrylamide)m-block-hydroxyl-terminated polybutadiene-block-poly(N-isoproplacrylamide)m (PNIPAMm-b-HTPB-b-PNIPAMm, m = 1 or 2) block copolymers, AB4 four-armed star multiblock and linear triblock copolymers, were synthesized by ATRP with HTPB as central blocks, and characterization was performed by 1H NMR, Fourier transform infrared, and size exclusion chromatography. The multiblock copolymers could spontaneously assemble into more regular spherical core–shell nanoscale micelles than the linear triblock copolymer. The physicochemical properties were detected by a surface tension, nanoparticle analyzer, transmission electron microscope (TEM), dynamic light scattering, and UV–vis measurements. The multiblock copolymer micelles had lower critical micelle concentration than the linear counterpart, TEM size from 100 to 120 nm, and the hydrodynamic diameters below 150 nm. The micelles exhibited thermo-dependent size change, with low critical solution temperature of about 33–35 °C. The characteristic parameters were affected by the composition ratios, length of PNIPAM blocks, and molecular architectures. The camptothecin release demonstrated that the drug release was thermo-responsive, accompanied by the temperature-induced structural changes of the micelles. MTT assays were performed to evaluate the biocompatibility or cytotoxicity of the prepared copolymer micelles.

CAS / MDL: 20769-85-1 79-36-7
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CHEMICAL ENGINEERING JOURNAL · 2013 · IF 3.473

Efficient performance of porous Fe2O3 in heterogeneous activation of peroxymonosulfate for decolorization of Rhodamine B

Fei Ji,Chaolin Li,Xiyu Wei,Jie Yu

Porous Fe 2 O 3 particle was synthesized by the hydrothermal-calcination method and then used to activate peroxymonosulfate (PMS) for Rhodamine B (RhB) decolorization. Several analytical means such as X-ray powder diffraction (XRD), scanning electron microscopy (SEM), and N 2 physisorption were used to determine the characteristics of the catalyst particles. The results of experiments indicated that the catalyst showed a high activity in decolorization of RhB in the presence of PMS. Several key parameters including initial pH, amounts of catalyst, PMS concentration, and temperature were investigated in order to understand their effect on the decolorization efficiency. Furthermore, the catalyst showed good reusability and stability after three recycles. Finally, the free radicals participating in the process were classified by radical quenching studies, and a rational mechanism was proposed based on the results obtained to understand the catalytic process.

CAS / MDL: 7722-76-1
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APPLIED SURFACE SCIENCE · 2014 · IF 2.538

Amorphous TiO2 doped with carbon for visible light photodegradation of rhodamine B and 4-chlorophenol

Penghui Shao,Jiayu Tian,Zhiwei Zhao,Wenxin Shi,Shanshan Gao,Fuyi Cui

Visible light photocatalytic activity of amorphous TiO 2 doped with carbon is prepared by a facile sol-gel route for the first time. The most active sample with mesostructure of amorphous phase, high surface area (273   m 2   g −1 ) and large pore volume (0.33   cm 3   g −1 ) is identified by X-ray diffractometer, Raman spectrometer, transmission electron microscope and N 2 adsorption–desorption isotherms. In addition, the most active sample is characterized by Fourier transform-infrared spectrometer, X-ray photoelectron spectrometer, UV–vis diffuse reflectance spectrometer and luminescence spectrometer. The results show that the most active sample with oxygenic groups has a narrower bandgap and lower recombination of electron–hole, due to the carbon doping and phase of amorphous. Effective photodegradation capability and stability of rhodamine B and colorless 4-chlorophenol are verified by photocatalytic tests under visible light irradiation. A possible mechanism of amorphous TiO 2 doped with carbon for visible light photocatalysis is proposed. The findings of this paper will provide new insights to design visible light-induced photocatalyst based on amorphous TiO 2 for organic removal.

CAS / MDL: 106-48-9 81-88-9
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JOURNAL OF WUHAN UNIVERSITY OF TECHNOLOGY-MATERIALS SCIENCE EDITION · 2024 ·Vol. 39 ·期 4 ·869-876 · IF 1.3

Enhanced Photocatalytic Activity of Z-scheme Meso-BiVO4-Au-CdS for Degradation of Rhodamine B

Zhang Yanwei,Wang Yanze,Li Junguo,Xie Jingjing,Wang Wenxuan,Fu Zhengyi

We synthesized BiVO 4 mesocrystals with ordered assembly structure, and studied the structural order and the relationship between the photodegradation of Rhodamine B. Au nanoparticles (NPs) were successfully loaded onto Meso-BiVO 4 by light-assisted induction, and Cd nanoparticles were further selected to be deposited on Au nanoparticles to form Z-scheme photocatalyst Meso-BiVO 4 -Au-CdS heterostructures. We try and propose to analyze its ordered assembly structure by XRD for the first time. The results show that Meso-BiVO 4 is a mesocrystal with highly exposed (001) plane and directional assembly structure. The charge separation efficiency of all samples was studied by PL spectroscopy. The results show that the Z-scheme Meso-BiVO 4 -Au-CdS can promote the charge separation and obtain the best carrier separation efficiency. Thus, it has the best photocatalytic activity in the experiment of photocatalytic degradation of rhodamine B. The main active species in the degradation process were confirmed by free radical trapping experiment, and the degradation mechanism was put forward.

CAS / MDL: 16961-25-4
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WATER AIR AND SOIL POLLUTION · 2024 ·Vol. 236 ·期 1 ·1-15 · IF 3.8

CS-biochar/ZnO/TiO2 for efficient photocatalytic removal of Rhodamine B: performance and mechanism insights

Li Xiao-fang,Ding Yue,Wang jing,Feng Xiao-qiang

Based on the excellent adsorption, photosensitization and electron transfer ability of biochar, the combination of photocatalyst and biochar is an effective method to improve the overall photocatalytic activity. Hence, a novel efficient CS-biochar/ZnO/TiO 2 photocatalyst with the different content of N-doped porous CS-biochar were constructed and characterized by a variety of testing methods, such as FT-IR, XRD, UV–vis DRS, SEM–EDS, PL, EIS, TPR, LSV. Photocatalytic experiments indicated that all the CS-biochar/ZnO/TiO 2 composites with different CS-biochar content exhibit excellent photocatalytic activity for Rh B degradation. Among them, 63%-CS/ZnO/TiO 2 composite has the best catalytic activity, which 94.5% of Rh B was degraded within 25 min, and the kinetic constant was 0.0993 min −1 , which is about 1.96 and 1.72 times that ZnO (0.0507 min −1 ) and TiO 2 (0.0576 min −1 ), respectively. Moreover, photoelectrochemical experiment results confirmed that CS-biochar/ZnO/TiO 2 greatly enhanced the charge separation process compare with ZnO and TiO 2 . Meanwhile, CS-biochar/ZnO/TiO 2 has excellent stability, and a possible photocatalytic mechanism was put forward.

CAS / MDL: 81-88-9
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Materials Today Communications · 2024 · IF 3.7

Facile synthesis of ultrafine Co3O4/Al2O3 catalysts for superior peroxymonosulfate activation in rhodamine B degradation

Rui Luo,Yuting Huang,Min Wang,Tong Yu,Kexin Tai,Lin Hu,Xiankun Wu

Advanced oxidation processes based on persulfate (PS-AOPs) have emerged as effective strategies for environmental remediation, with cobalt-based oxides serving as prominent catalysts for peroxymonosulfate (PMS) activation. In this study, we developed a highly active Co 3 O 4 /Al 2 O 3 catalyst (Co/AA) featuring ultrafine nanoparticles, synthesized via a facile approach using tannic acid (TA) as a coordinating agent and activated alumina as a robust support. Co/AA-0.1, as the representative catalyst, was characterized and exhibited outstanding performance in degrading rhodamine B (RB) via PMS activation. Our findings highlight TA's critical role in reducing Co 3 O 4 nanoparticle size, thereby increasing the availability of active sites. The degradation mechanism was elucidated through reactive oxygen species (ROS) quenching experiments and electron paramagnetic resonance (EPR) analysis, revealing that sulfate radicals (SO 4 •− ) are the dominant ROS. The high activity of Co/AA-0.1 is confirmed by analyzing X-ray photoelectron spectroscopy, Brunauer-Emmett-Teller surface area and O 2 -temperature programmed desorption data of the samples. We also investigate the effects of various factors, such as anions, reaction temperatures, and PMS dosage, on RB degradation. Higher temperatures for treating the catalyst are found to reduce activity but improve stability. Notably, the catalyst synthesized through EDTA-assisted synthesis showed balanced activity and stability. Furthermore, the versatility of our synthesis method was demonstrated by successfully applying it to other supports, such as SiO 2 and TiO 2 , offering the development of more efficient and stable catalysts for environmental applications.

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Nature Communications · 2025 ·Vol. 16 ·期 1 ·1-11 · IF 15.7

Highly selective upcycling of plastic mixture waste by microwave-assisted catalysis over Zn/b-ZnO

Zhao Jun,Liu Bonan,Xiong Lunqiao,Liu Wenchao,Wang Duanda,Ma Wangjing,Jiang Litong,Yang Jianlong,Wang Ping,Xiao Tiancun,Zhao Sui,Edwards Peter P.,Tang Junwang

7 billion of 9.2 billion tons of plastic produced becomes waste while conventional catalytic plastic recycling methods are vulnerable with degraded performance and intensive energy input. Here, a hybrid Zn/b-ZnO catalyst, together with the specially-designed microwave reaction system, has achieved fast plastic waste upgrading under atmospheric pressure without using H 2 . Bifunctional ZnO acts as a microwave absorber and substrate catalyst, and in-situ formed Zn clusters promote C-C bond cleavage and nearly 100% upcycle landfilled plastic mixtures into lubricant base oil precursors and monomers. Unprecedented turnover number (250 g plastic g −1 catalyst ) of plastic depolymerisation and long-time stability over 50 successive cycles have been demonstrated, together with 8-time higher energy efficiency compared with conventional catalysis, indicating this strategy is an economical approach to efficient upcycling of plastics towards valuable products. Moreover, the catalyst can tolerate high contaminates, even the landfilled plastics can still be converted to lubricant base oil precursors, which has never been reported before.

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JOURNAL OF MATERIALS SCIENCE · 2024 ·Vol. 59 ·期 19 ·8556-8570 · IF 3.5

Highly thermally stable Ti/Si/B modified bisphenol A-phenolic resins with co-continuous structure

Wang Jianwen,Huang Siyu,Shi Fengyue,Yang Yang,Yang Xinjia,Li Jun,Zhao Guangdong

The synthesis of Bisphenol A Glutaraldehyde Phenolic Resin (BPA-GA PF) was carried out under alkaline conditions using Bisphenol, A (BPA) and Glutaraldehyde (GA) as raw materials, with n-butanol serving as the solvent. Based on the aforementioned information, the researchers prepared modified BPA-GA PF resins by incorporating titanium (Ti), silicon (Si), and boron (B) through a polymer derivative method. This process led to the formation of Ti/Si/B-modified PF resins. By manipulating the proportion of elements in the BPA-GA PF, the modified phenolic resin demonstrated improved capacity for design and processing. The characterization of the modified BPA-GA PF involved the analysis of its transformation process and thermal behavior through the utilization of Fourier transform infrared spectroscopy (FT-IR) and thermogravimetric Analysis (TGA). The presence of B, Ti, and Si elements in the system resulted in the formation of Si–O-B and B-O bonds, as determined. The Ti/Si/B -modified PF exhibited a significant increase in yield. Analysis employing X-ray photoelectron spectroscopy (XPS) and scanning electron microscopy (SEM) revealed that, following high-temperature annealing, the materials underwent a transformation into Ti/Si/B-modified PF with a highly cross-linked network structure. Oxidation experiments conducted under static conditions demonstrated that the Ti/Si/B-modified BPA-GA PF exhibited significantly greater high-temperature resistance compared to the BPA-GA PF. Among the various options, the Ti/Si/B-modified PF material with a Ti/Si ratio of 1:2 exhibited the most superior resistance to high-temperatures.

CAS / MDL: 80-05-7 10043-35-3
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