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RSC Advances · 2017 ·Vol. 7 ·期 74 ·47091-47098 · IF 3.108

Preparation, characterization and anticancer activities of resveratrol loaded redox-sensitive F127-SS-TOC micelles

Yuling Liu,Longfei Lin,Jizheng Song,Ye Zhao,Zhimao Chao,Hui Li

Resveratrol (RES), a natural polyphenolic compound existing in plants, exhibits anticancer potential in inhibiting growth of various types of human cancers especially breast cancer. However, the poor aqueous solubility and low bioavailability limit its clinical application. Pluronic F127 (F127)-SS-Tocopherol (TOC) polymer is a redox-sensitive conjugate which has been synthesized by our previous study. Due to the amphiphilic properties of block copolymer F127-SS-TOC, RES was encapsulated by the F127-SS-TOC polymer and formed RES-loaded micelles (F127-SS-TOC/RES) in aqueous solution by self-assembly via a solvent evaporation method. The drug loading of F127-SS-TOC/RES micelles was 13.25 ± 2.29%, which remained stable for 7 days at 25 °C. The particle size and zeta potential of the above-mentioned micelles measured by dynamic light scattering (DLS) were 39.50 ± 1.39 nm and −4.55 ± 0.39 mV, respectively. Besides, F127-SS-TOC/RES micelles have significant cytotoxicity in human breast cancer cells MCF-7 and MDA-MB-231 compared to free RES and non-redox-sensitive F127-TOC/RES micelles. The results also showed that redox-sensitive F127-SS-TOC/RES micelles could induce apoptosis and elevate the intracellular reactive oxygen species (ROS) level against MDA-MB-231 cells. Hence, our results indicated that RES loaded F127-SS-TOC micelles hold potential in improving the treatment of breast cancer.

研究领域: 药剂学 · 肿瘤学 · 生物材料学
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JOURNAL OF RARE EARTHS · 2017 · IF 2.429

Evaluation of Ce(III) and Gd(III) adsorption from aqueous solution using CTS-g-(AA-co-SS)/ISC hybrid hydrogel adsorbent

Feng WANG,Wenbo WANG,Yongfeng ZHU,Aiqin WANG

CTS- g -(AA- co -SS)/ISC hybrid hydrogel adsorbent with crosslinked network structure and superior adsorption performance for rare-earth metal ions was successfully synthesized in aqueous solution by a simple one-step free-radical grafting polymerization reaction among acrylic acid (AA), sodium p -styrenesulfonate (SS) and chitosan (CTS) using illite/smectite clay (ISC) as the inorganic additive. The structure of the as-prepared CTS- g -(AA- co -SS)/ISC hydrogel adsorbent was characterized, and the reaction parameters such as AA/SS molar ratio and ISC content were optimized, and the effects of pH values, initial concentration and contact time on the adsorption performance for Ce(III) and Gd(III) were systematically evaluated. It was found that the maximum adsorption capacities of the hydrogel adsorbent toward Ce(III) and Gd(III) reached 174.05 and 223.79 mg/g, respectively, and the adsorption quickly achieved equilibrium within 15–20 min. The adsorbed Ce(III) and Gd(III) could be easily desorbed for recovery, and the used adsorbent was able to be regenerated for reuse. After five adsorption-desorption cycles, the regenerated adsorbent could still retain the adsorption capacities that were close to the initial value. The adsorption process was well described by pseudo-second-order kinetic mode and the Langmuir isotherm model, and the chemical complexation between ions and –COO – was mainly responsible for the high adsorption capacity. As a whole, the hybrid hydrogel adsorbent was potential to be used for the adsorption and recovery of Ce(III) and Gd(III) from water.

研究领域: 环境科学 · 材料科学
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COLLOIDS AND SURFACES B-BIOINTERFACES · 2016 · IF 3.902

Redox-sensitive micelles assembled from amphiphilic mPEG-PCL-SS-DTX conjugates for the delivery of docetaxel

Huiyuan Zhang,Kaiming Wang,Pei Zhang,Wenxiu He,Aixin Song,Yuxia Luan

Docetaxel (DTX) can produce anti-tumor effects by inhibiting cell growth and inducing apoptosis. However, the poor solubility of DTX restricts its application and its clinical formulation has caused serious adverse reaction due to the use of Tween-80. In the present study, DTX was conjugated to an amphiphilic di-block polymer to solve these problems. Methoxy poly(ethylene glycol)-poly(ε-caprolactone) (mPEG-PCL) was selected as the polymer skeleton and a redox sensitive disulfide bond was used as the linker between DTX and mPEG-PCL. The synthesized mPEG-PCL-SS-DTX conjugates were characterized by 1 H-nuclear magnetic resonance ( 1 H NMR) and Fourier transform infrared spectroscopy (FTIR). Interestingly, the mPEG-PCL-SS-DTX conjugates could self-assemble into micelles in aqueous solution. The critical micelle concentration (CMC) of mPEG-PCL-SS-DTX micelles was about 2.3   mg   L −1 determined using pyrene molecule fluorescent probe method while the size of mPEG-PCL-SS-DTX micelles was determined to be ca . 17.6   nm and 116.0   nm with a bimodal distribution by dynamic light scattering (DLS). The in vitro release results indicated that the as-prepared micelles exhibited a sustained release profile with good redox sensitive properties. In particular, the hemolytic toxicity test indicated the as-prepared mPEG-PCL-SS-DTX micelles had negligible hemolytic activity, demonstrating their safety in drug delivery system. Cytotoxicity assay of the mPEG-PCL-SS-DTX micelles verified their highly enhanced cytotoxicity to MCF-7/A and A549 cells. These results thus demonstrated that the present redox-sensitive mPEG-PCL-SS-DTX micelle was an efficient and safe sustained drug delivery system in the biomedical area.

研究领域: 药剂学 · 肿瘤学 · 生物医学工程
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MICROPOROUS AND MESOPOROUS MATERIALS · 2017 · IF 3.615

Synthesis of microfibrous-structured SS-fiber@beta composite by a seed-assisted dry-gel conversion method

Jia Ding,Pengjing Chen,Jian Zhu,Guofeng Zhao,Ye Liu,Yong Lu

Microfibrous-structured SS-fiber@beta composites are synthesized by coupling dip-coating method with a seed-assisted dry-gel conversion method. The beta crystals in zeolite shell are formed by growth on the surface of pre-added beta seeds and TEAOH-induced nucleus. One interesting point is that this approach is working highly effectively and efficiently even at high dry gel SiO 2 /Al 2 O 3 ratio of 200 (corresponding to 207 in the beta zeolite shell). Such SS-fiber@beta composites show great potentials for the heat/mass transfer limited reactions due to their hierarchical porosity , small crystals, controllable acidity as well as our distinctive microfibrous-structured design.

研究领域: 材料科学 · 化学工程
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International Journal of Nanomedicine · 2023 · IF 8

Biodegradable mixed MPEG-SS-2SA/TPGS micelles for triggered intracellular release of paclitaxel and reversing multidrug resistance

Kai Dong,Yan Yan,Pengchong Wang,Xianpeng Shi,Lu Zhang,Ke Wang,Jianfeng Xing,Yalin Dong

In this study, a type of multifunctional mixed micelles were prepared by a novel biodegradable amphiphilic polymer (MPEG-SS-2SA) and a multidrug resistance (MDR) reversal agent (d-α-tocopheryl polyethylene glycol succinate, TPGS). The mixed micelles could achieve rapid intracellular drug release and reversal of MDR. First, the amphiphilic polymer, MPEG-SS-2SA, was synthesized through disulfide bonds between poly (ethylene glycol) monomethyl ether (MPEG) and stearic acid (SA). The structure of the obtained polymer was similar to poly (ethylene glycol)-phosphatidylethanolamine (PEG-PE). Then the mixed micelles, MPEG-SS-2SA/TPGS, were prepared by MPEG-SS-2SA and TPGS through the thin film hydration method and loaded paclitaxel (PTX) as the model drug. The in vitro release study revealed that the mixed micelles could rapidly release PTX within 24 h under a reductive environment because of the breaking of disulfide bonds. In cell experiments, the mixed micelles significantly inhibited the activity of mitochondrial respiratory complex II, also reduced the mitochondrial membrane potential, and the content of adenosine triphosphate, thus effectively inhibiting the efflux of PTX from cells. Moreover, in the confocal laser scanning microscopy, cellular uptake and 3-(4,5-dimethyl-thiazol-2-yl)-2,5-diphenyl-tetrazolium bromide assays, the MPEG-SS-2SA/TPGS micelles achieved faster release and more uptake of PTX in Michigan Cancer Foundation-7/PTX cells and showed better antitumor effects as compared with the insensitive control. In conclusion, the biodegradable mixed micelles, MPEG-SS-2SA/TPGS, could be potential vehicles for delivering hydrophobic chemotherapeutic drugs in MDR cancer therapy.

研究领域: 药剂学 · 肿瘤学 · 生物材料科学
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INTERNATIONAL JOURNAL OF PHARMACEUTICS · 2016 · IF 3.994

Redox-sensitive mPEG-SS-PTX/TPGS mixed micelles: An efficient drug delivery system for overcoming multidrug resistance

Dujuan Zhao,Huiyuan Zhang,Shengfeng Yang,Wenxiu He,Yuxia Luan

The main cause of multidrug resistance (MDR) is overexpression of active efflux transporters, such as P-glycoprotein (P-gp). To reverse MDR and improve the chemotherapy effect of paclitaxel (PTX), we propose a new drug delivery system based on mixed micelles constructed with d -α-tocopheryl poly(ethylene glycol) 1000 succinate (TPGS) and the mPEG-SS-PTX conjugate with consideration that TPGS is a P-gp inhibitor that can block the cancer cell action of pumping drugs outside of cells and can enhance the anticancer effect. mPEG-SS-PTX is synthesized by conjugating hydrophilic mPEG with a hydrophobic drug, PTX, via a redox-sensitive disulfide bond. The mPEG-SS-PTX conjugate is amphiphilic and can self-assemble in water. Mixed micelles formed by the mPEG-SS-PTX conjugate and TPGS have a low critical micelle concentration (CMC, ∼1.05   ×   10 −3   mg/mL) and high drug loading content (∼19.6%). The disulfide bond in the mPEG-SS-PTX conjugate can be broken in cancer cells (a reductive environment) and release PTX to kill cancer cells. In vitro cytotoxicity and cell uptake suggest that mixed micelles can effectively improve the accumulation of PTX in multidrug-resistant MCF-7 cells. Therefore, the present as-prepared mixed micelles very effectively reverse the MDR and enhance the therapeutic effect.

研究领域: 药学 · 纳米技术 · 癌症研究 · 药物递送系统
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CARBOHYDRATE POLYMERS · 2019 · IF 6.044

Redox-responsive chitosan oligosaccharide-SS-Octadecylamine polymeric carrier for efficient anti-Hepatitis B Virus gene therapy

Jing Miao,Xi-qin Yang,Zhe Gao,Qian Li,Ting-ting Meng,Jia-ying Wu,Hong Yuan,Fu-qiang Hu

DrzBC and DrzBS (10-23 DNAzyme) could block the expression of HBV e- and s- gene respectively. But the application of 10-23 DNAzyme was limited owing to the lack of appropriate delivery vehicles. Chitosan oligosaccharide-SS-Octadecylamine (CSSO), a redox-responsive nano-sized polymeric carrier, could self-aggregate and bind with DNA by electrostatic interaction at proper mass ratio. Compared with the traditional commercial carrier Lipo2000, CSSO exhibited lower cytotoxicity, efficient cellular uptake by targeting cells, and rapidly DNA released in cytoplasm after escaping from endosomes. Including the same DNA concentration, Lipo2000/(DrzBC or DrzBS) showed maximum inhibitory rate on HBeAg (47.29 ± 1.86%) and HBsAg (33.58 ± 0.72%) secretion after 48 h incubation, and then both decreased. In contrast, HBeAg secretion inhibition by CSSO/DrzBC and HBsAg secretion inhibition by CSSO/DrzBS were up to 73.86 ± 1.77% and 67.80 ± 2.51% at 48 h, and further increased to 83.83 ± 2.34% and 76.79 ± 2.18% at 72 h, respectively. CSSO is a promising redox-responsive polymeric carrier for efficient anti-Hepatitis B Virus gene therapy.

CAS / MDL: 6066-82-6 129-00-0
研究领域: 药理学 · 病毒学 · 分子生物学 · 生物医学工程
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CONSTRUCTION AND BUILDING MATERIALS · 2022 · IF 7.693

Synthesis of a novel poly-TA-Si nanohybrid with dynamic covalent SS bonds and its effect on the mechanical strength of cement paste

Shuzhen Zheng,Wenxiu Qiao,Jianfeng Ma,Yinwen Li,Shoufang Xu,Qianping Ran

Using organic/inorganic nanocomposites to optimize the microstructures of cement hydration products at the micro/nanometre scale is a promising method for improving the mechanical properties of cement-based materials. One type of novel nanohybrid material modified by the flexible autonomous healing polymer poly-TA (thioctic acid) was synthesized and used as a highly efficient mechanical improvement agent for cement paste. The nanohybrids linear LNTS-1 and bulk CNTS-2 were synthesized from silane-coupled nanosilica and alpha thioctic acid. Due to the existence of hydrogen bonds, coordination bonds and dynamic covalent S S bonds, this type of linear poly-TA with a certain amount of calcium content exhibited good self-healing properties. Linear LNTS-1 can effectively improve the macro flexural strength of cement-based materials without a negative effect on their compressive strength. The flexural strength of cement pastes with 1.0‰ LNTS-1 increased by 11.9%, 15.6%, and 16.9% after curing for 3, 7, and 28 d compared with the control cement paste. The results of adsorption experiments show that nanohybrid LNTS-1 has strong adsorption on calcium ions, which affects the formation of cement hydration products.

研究领域: 材料科学 · 土木工程 · 化学工程
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RSC Advances · 2017 ·Vol. 7 ·期 48 ·30242-30249 · IF 3.108

A dual pH- and reduction-responsive anticancer drug delivery system based on PEG–SS–poly(amino acid) block copolymer

Bingqiang Li,Meng Shan,Xiang Di,Chu Gong,Lihua Zhang,Yanming Wang,Guolin Wu

A pH- and reduction-responsive anticancer drug delivery system was prepared and the triggerable and controllable drug release in response to stimuli was observed. In the first step, methoxy-poly(ethylene glycol) (mPEG) was conjugated with polysuccinimide (PSI) via disulfide linkages, and the PSI segment thereafter, was aminolyzed by 2-diisopropylaminoethylamine (DIPEA) and hydrazine hydrate (Hy). The obtained amphiphilic copolymer could form a bond with the model drug doxorubicin (DOX) at pH 7.4 via acid-labile hydrazone bonds, and more free DOX molecules could be encapsulated via hydrophobic interactions and π–π stacking between the aromatic rings, leading to DOX-loaded micelles formation. These polymers and polymeric micelles then were characterized. The results showed that the polymeric micelles exhibited dual pH- and reduction-responsive disassembly behaviors. Moreover, while the blank copolymers had excellent cytocompatibility, the DOX-loaded micelles showed an enhanced drug release profile and improved cytotoxicity with decrease of pH and/or the addition of glutathione (GSH). These results indicated that the novel nanoparticle based on PEG–SS–poly(amino acid) block copolymer is a promising candidate for a carrier in controllable anti-tumor drug delivery.

CAS / MDL: 56-84-8 7087-68-5
研究领域: 药学 · 纳米技术 · 癌症研究 · 药物递送系统
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JOURNAL OF MEMBRANE SCIENCE · 2020 · IF 7.183

An active electro-Fenton PVDF/SS/PPy cathode membrane can remove contaminant by filtration and mitigate fouling by pairing with sacrificial iron anode

Xiaohui Li,Lifen Liu,Tong Liu,Danfeng Zhang,Changwei An,Fenglin Yang

Cathode membranes can provide innovative solutions for membrane-fouling mitigation and filtration performance enhancement, in combination with electric field in a new electrochemical system. In this research, a novel polyvinylidene fluoride/stainless steel/polypyrrole (PVDF/SS/PPy) cathode membrane was prepared via in situ flow-through electro-polymerization method. The PVDF/SS/PPy membrane exhibited excellent electric catalytic activity for 2-electron ORR (oxygen reduction reaction). A battery system with PVDF/SS/PPy membrane cathode and Fe sacrificial anode was developed for in situ •OH generation. A pH range of 3.5–4.0 is preferred and the area ratio of iron anode to PVDF/SS/PPy cathode membrane was ~1:6 according to the •OH production and iron consumption results. The phenol filtration tests suggested that the PVDF/SS/PPy cathode membrane has improved selectivity for removing small refractory organic pollutant such as phenol, the removal rate increased from 54.7% to 79.3%, while flux decreased from 152 L/(m 2 ·h) to 19 L/(m 2 ·h). The results of filtrating river water and BSA indicated that the PVDF/SS/PPy cathode membrane had excellent anti-fouling performance when the foulants load matches the •OH production.

研究领域: 环境科学 · 材料科学 · 电化学工程
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PHYSICAL CHEMISTRY CHEMICAL PHYSICS · 2023 ·Vol. 25 ·期 17 ·12458-12468 · IF 3.3

Folate modified dual pH/reduction-responsive mixed micelles assembled using FA-PEG-PDEAEMA and PEG-SS-PCL for doxorubicin delivery

Chufen Yang,Delin Wang,Wenyao Liu,Zexiong Yang,Teng He,Fang Chen,Wenjing Lin

Aiming at achieving the concurrent performances of high loading, well controlled release and active targeted delivery, folate (FA) modified dual pH/reduction-responsive mixed polymeric micelles were rationally assembled using FA-PEG-PDEAEMA and PEG-SS-PCL by dissipative particle dynamics (DPD) simulations. The optimized polymers PEG112-PDEAEMA40, FA-PEG112-PDEAEMA40, and PEG112-SS-PCL70 were synthesized and characterized using 1H NMR, FT-IR and GPC, and their mixed micelles were applied for doxorubicin (DOX) delivery. The drug loading capacity (LC) and encapsulation efficiency (EE) values of the MIX1 (FA-PEG112-PDEAEMA40/PEG112-SS-PCL70) at a DOX/polymer feeding ratio of 15 mg/30 mg were 20.22% and 50.69%, which were higher than those of single polymer micelles and MIX2 (PEG112-PDEAEMA40/PEG112-SS-PCL70). Particle size distributions, mesoscopic morphologies, DPD simulations and in vitro drug release profiles all confirmed the well-controlled release performance of the DOX-loaded micelles formed by MIX1: slow DOX release with a cumulative release of 20.46% in the neutral environment and accelerated release with a cumulative release of 74.20% at pH 5.0 + 10 mM DTT within 120 h, which were similar to those of MIX2. Cytotoxicity assay found that both MIX1 and MIX2 blank micelles were biocompatible, and a superior inhibitory effect of the FA-modified DOX-loaded micelles MIX1 on HepG2 cells was found compared to that of free DOX and non-FA-modified DOX-loaded micelles MIX2. All of these confirmed the superiority of MIX1 micelles with high loading capacity, well controlled release, and enhanced inhibitory effects on HepG2 cells, which might be a prospective candidate for anticancer drug delivery.

研究领域: 药学 · 纳米技术 · 癌症研究
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Journal of Environmental Chemical Engineering · 2023 · IF 7.7

Novel application of Fe-Mg-Mt-SS activated persulfate for the disinfection of Escherichia coli in water: Performance and mechanism

Jun Chen,Shangqing Xia,Xiaohong Yang,Xue Li,Zhaoming Chen,Zihui Song,Yutong Wang,Zongsheng Zhan,Jie Jin,Dongliang Shao

New technology is required for the effective disinfection of pathogenic bacteria in water. A novel type of activator material (Fe-Mg-Mt-SS) was prepared using bimetallic iron-magnesium (Fe-Mg), montmorillonite (Mt), and sewage sludge carbon (SS) and applied it for disinfection. The specific surface area of Fe-Mg-Mt-SS was 115.72 m 2 /g, and the spatial structure of Fe-Mg-Mt-SS was orderly and layered. Mt played a role in frame support, and Fe-Mg was integrated into the structure in an orderly manner. Fe-Mg-Mt-SS effectively activated persulfate (PS) to disinfect Escherichia coli ( E. coli ) in water, with a disinfection rate of 7.00 lg of E. coli within 80 min in the PS/Fe-Mg-Mt-SS system, and the high disinfection rate was stable under different pH and elevated temperatures. Fe-Mg-Mt-SS showed broad spectrum disinfectant efficiency against other bacteria ( Staphylococcus aureus, Pseudomonas aeruginosa, and Bacillus subtilis ). Fe-Mg-Mt-SS activated PS killed E. coli mainly by producing hydroxyl and oxygen radicals, which damaged the E. coli cell membrane. Bimetallic activation with Fe and Mg synergistically activated PS, graphitised SS had more orderly spatial and laminar structures, and Mt improved the thermal stability and layer spacing of Fe-Mg-Mt-SS, which facilitated better metal insertion and improved its activation properties. The preparation of Fe-Mg-Mt-SS and activation of PS provide a new technology for the disinfection of pathogenic bacteria in water.

研究领域: 环境科学 · 水处理 · 微生物学 · 材料科学
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