CHEMICAL ENGINEERING JOURNAL
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2019
·
IF 8.355
Yuqi Geng,Jiaqi Li,Wenjuan Lu,Ning Wang,Zeyang Xiang,Yanzhao Yang
In this paper, superparamagnetic Fe 3 O 4 @SiO 2 -NH 2 nanoparticles were applied to adsorb Au(III)/Pd(II)/Pt(IV) in HCl medium. The successful synthesis of Fe 3 O 4 @SiO 2 -NH 2 was characterized through TEM, SEM and FT-IR. Electrostatic interaction between magnetic NPs and metal anions was proposed as the main adsorption mechanism by zeta potential analysis. Maximum adsorption capacities and adsorption behaviors under metal anions concentrations, acidity, NaCl, kinetic and isotherm models were investigated. Notably, the Fe 3 O 4 @SiO 2 -NH 2 shows the excellent acidity and salinity resistance on Au(III), Pd(II) adsorption. The separation routine among Au(III), Pd(II) and Pt(IV) was proposed. As investigated, Pt(IV) could be isolated due to the less adsorption amount onto Fe 3 O 4 @SiO 2 -NH 2 (≤1%). Then, the adsorbed Au(III) was eluted selectively by HCl + N-hexanol alcohol + ethanol + H 2 O 2 mixing solution. Then, the adsorbed Pd(II) was completely eluted by thiourea solution. The recovery efficiencies of Au(III), Pd(II) and Pt(IV) were kept over 92%, 97% and 94% respectively, during 5 turns of cycling separation experiments. Total loss amount of Fe is around 7%. Hence that, the particle demonstrates the good stability and high adsorption capacity, which possess great potential for practical Au(III), Pd(II) and Pt(IV) separation.
研究领域:
化学工程
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材料科学
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环境科学
✓ 已验证
产品关联
DOI
高影响因子
Research
·
2022
·
IF 11.036
Qingfei Zhang,Xiaocheng Wang,Gaizhen Kuang,Yunru Yu,Yuanjin Zhao
Biomedical scaffolds have shown great success in postsurgical tumor treatment; their current efforts are focusing on eradicating residual tumor cells and circulating tumor cells and simultaneously repairing postoperative tissue defects. Herein, we report a novel photopolymerized 3D scaffold with Pt(IV) prodrug initiator to achieve the desired features for tumor comprehensive therapy. The Pt-GelMA scaffold was fabricated from the microfluidic 3D printing of methacrylate gelatin (GelMA) bioinks through a Pt(IV)-induced photocrosslinked process without any other additional photoinitiator and chemotherapeutic drug. Thus, the resultant scaffold displayed efficient cell killing ability against breast cancer cells in vitro and significantly inhibited the local tumor growth and distant metastases on an orthotopic postoperative breast cancer model in vivo. Besides, benefiting from their ordered porous structures and favorable biocompatibility, the scaffolds supported the cell attachment, spreading, and proliferation of normal cells in vitro; could facilitate the nutrient transportation; and induced new tissue ingrowth for repairing tissue defects caused by surgery. These properties indicate that such 3D printing scaffold is a promising candidate for efficient postoperative tumor treatment in the practical application.
研究领域:
生物医学工程
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肿瘤学
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材料科学
✓ 已验证
DOI
高影响因子
RSC Advances
·
2019
·Vol. 9
·期 57
·33302-33309
·
IF 3.049
Yanhua Zhang,Hui Huang,Hao Fu,Meng Zhao,Zhihua Wu,Yang Dong,He Li,Yourong Duan,Ying Sun
As known to all, ovarian cancer ranks the most lethal of the gynecological malignancies. The antitumor drugs based on platinum are first-line chemotherapy drugs for ovarian cancer. However, their therapeutic efficiency is severely limited owing to dose-limiting toxicities of platinum. New theranostic strategies to overcome chemotherapy toxicity is highly desirable. Meanwhile, the real-time treating effect is not visible for doctors. Herein, we constructed PFH/siRNA/Fe3O4@Pt(IV) NPs-cRGD (NPs-cRGD) for precise theranostics against ovarian tumors with real-time imaging. The NPs-cRGD had a good storage stability and resisted the serum-induced aggregation, which was beneficial for drug delivery. Additionally, gel-retardation assay demonstrated that the NPs-cRGD exhibited great protection to siRNA to resist nuclease degradation. In vitro, the NPs-cRGD showed good dual-mode US/MRI imaging and the relative imaging research was also discussed. Moreover, the in vitro experiments indicated that the NPs-cRGD with US exhibited excellent antitumor therapeutic efficiency, resulting from the cRGD ligands and US exposure enhanced the cellular uptake efficiency. Thus, the dual-mode nanoparticles in this work may provide precious insight into the development of various multi-mode nanoplatforms delivering drugs or genes for precise theranostics against various cancer.
研究领域:
癌症治疗
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纳米医学
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医学影像
·
分子生物学
✓ 已验证
产品关联
DOI
PubMed
高影响因子
Bioactive Materials
·
2022
·
IF 16.874
Qingfei Zhang,Xiaocheng Wang,Gaizhen Kuang,Yuanjin Zhao
Multimodal treatment modalities hold great potential for cancer therapy, thus current efforts are focusing on the development of more effective and practical synergistic therapeutic platforms. Herein, we present a novel trans, trans,trans -[Pt(N 3 ) 2 (OH) 2 (py) 2 ] (Pt(IV)) prodrug-initiated hydrogel microparticles (M ICG-Pt ) with indocyanine green (ICG) encapsulation by microfluidics for efficiently synergistic chemo-, photothermal (PTT) and photodynamic therapy (PDT). The employed Pt(IV) could not only serves as an initiator to generate azidyl radical (N 3 • ) for photo-polymerization of methacrylate gelatin (GelMA) matrix, but also be reduced to high cytotoxic platinum(II) (Pt(II)) species for tumor chemotherapy. The laden ICG with highly photothermal heating ability and intrinsic reactive oxygen species (ROS) productivity endows the M ICG-Pt with effective PTT/PDT performances upon near-infrared (NIR) light irradiation. In addition, benefiting from the production of oxygen during the photo-activation process of Pt(IV), the PDT efficacy of ICG-laden M ICG-Pt could be further enhanced. Based on these advantages, we have demonstrated that the M ICG-Pt could significantly eliminate cancer cells in vitro , and remarkably suppressed the tumor growth in vivo via synergistic chemotherapy, PTT, and PDT. These results indicate that such Pt(IV)-initiated hydrogel microparticles are ideal candidates of multimodal treatment platforms, holding great prospects for cancer therapy.
研究领域:
癌症治疗
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药学
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材料科学
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生物医学工程
✓ 已验证
产品关联
DOI
PubMed
高影响因子
JOURNAL OF HAZARDOUS MATERIALS
·
2021
·
IF 10.588
Jinghao Wang,Wenmin Lin,Yuancai Chen,Yongyou Hu,Qijin Luo
Due to the excellent hydrogen affinity and high conductivity, palladium nanoparticles (Pd NPs) were considered as a potential strategy to regulate bacterial electron transfer and energy metabolism. Herein, Citrobacter freundii JH, capable of in-situ biosynthesizing Pd(0) NPs, was employed to promote Pt(IV) reduction. The results showed that the Pt(IV) reduction to Pt(II) was accomplished mainly via the flavins-mediated extracellular electron transfer (EET) process, while Pt(II) reduction to Pt(0) was limit step, and proceeded via two intracellular respiratory chains, including FDH/Hases-based short chain (S-chain) and typical CoQ-involved long respiratory chain ( L -chain). Noteworthily, the incorporation of Pd(0) NPs mainly diverted the electrons to S-chain (as high as 71.7%−73.4%) by improving the hydrogenases (Hases) activity. Furthermore, Pd(0) NPs could stimulate the secreting of flavins and the combination between flavins and cytochrome c (c-Cyt), which converted electron transfer manner of L -chain. Additionally, Pd(0) NPs might also act as alternative proton channels to improve the energy metabolism. These findings provided significant insights into the promotion by Pd(0) NPs in terms of electron generation, electron consumption and proton translocation.
研究领域:
纳米技术
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微生物学
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生物化学
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环境科学
✓ 已验证
产品关联
DOI
PubMed
高影响因子
BIOMATERIALS
·
2015
·
IF 8.557
Xiaoran Deng,Yunlu Dai,Jianhua Liu,Ying Zhou,Ping'an Ma,Ziyong Cheng,Yinyin Chen,Kerong Deng,Xuejiao Li,Zhiyao Hou,Chunxia Li,Jun Lin
Combining the multi-modal medical imaging with cancer therapy in one single system has attracted the great interests for theranostic purpose. In this paper, CaF 2 :Yb 3+ /Er 3+ /Mn 2+ -poly(2-Aminoethyl methacrylate) (UCHNs-PAMA) hybrid microspheres were successfully fabricated. The synthetic route to the nanocomposite based on a facile hydrothermal method for fabrication of hollow upconversion (UC) nanospheres at first and then post-filling the PAMA interiorly through photo-initiated polymerization. The UCHNs showed orange fluorescence under 980 nm near infrared (NIR) laser excitation , which provided the upconverting luminescence (UCL) imaging modality . Meanwhile, the presence of functional Mn 2+ and Yb 3+ offered the enhanced T 1 -weighted magnetic resonance (MR) and computed tomography (CT) imaging, respectively. Thanks to introducing amine groups-containing PAMA inside the hollow nanospheres, the Pt(IV) pro-drug, c,c,t-Pt(NH 3 ) 2 Cl 2 (OOCCH 2 CH 2 COOH) 2 (DSP), can be conveniently bonded on the polymer network to construct a nanoscale anti-cancer drug carrier. The UCHNs-PAMA-Pt(IV) nanocomposite shows effective inhibition for Hela cell line via MTT assay . In contrast, Pt(IV) pro-drug and UCHNs-PAMA microspheres behave little cytotoxicity to Hela cells. This should be attributed the fact that the anti-cancer ability can be recovered only when Pt(IV) pro-drug was reduced to Pt(II)-drug in cellular environment. Furthermore, the in vivo experiments on small mice also confirm that the hybrid microspheres have relatively low toxic side effects and high tumor inhibition rate. These findings show that the multifunctional hybrid microspheres have potential to be used as UCL/MR/CT tri-modal imaging contrast agent and anti-cancer drug carriers.
研究领域:
纳米医学
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生物材料
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癌症治疗
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医学影像学
✓ 已验证
产品关联
DOI
PubMed
高影响因子
SEPARATION AND PURIFICATION TECHNOLOGY
·
2022
·
IF 9.136
Yangyang Wang,Shuwen Chen,Ronghao Liu,Lixin Zhang,Wenfeng Xue,Yanzhao Yang
The development of efficient ionic liquids (ILs) for disposable separation and recovery of various precious metals was of great importance, but still faced difficult challenges. A phase change temperature-controlled system composed of IL and HCl solution was developed for the extraction and separation of Au(III), Pd(II) and Pt(IV) from secondary resources. UCST (upper critical solution temperature)-type IL ([1,4,7-TMTA][Tf 2 N]) possessed outstanding selectivity of precious metals and the property of temperature-controlled phase transition. The ability of ILs to form solvated hydrogen bonds was confirmed by quantum-chemical calculation to be correlated with their corresponding UCST. Different experimental parameters were optimized to explore the extraction behavior of IL. It is noteworthy that homogeneous liquid-liquid extraction system (HLLE) constructed by UCST-type IL could significantly enhance the extraction kinetic of Au(III), Pd(II) and Pt(IV) by decreasing phase interface resistance. For Au(III), Pd(II) and Pt(IV), when the system temperatures were higher than 40 °C, 49 °C and 65 °C, the maximum values were 98.5%, 98.3% and 93.2% at the highest efficiency. In addition, the extraction mechanism of anion exchange was revealed by UV–vis, IR, NMR and LC-MS spectrometry. At last, Au(III), Pd(II) and Pt(IV) could be selectively separated from multi-metal solutions where impurity ions coexist by K 2 C 2 O 4 , NH 3 ·H 2 O and CS(NH 2 ) 2 /HCl, respectively. After 5 cycles, the extraction performance of [1,4,7-TMTA][Tf 2 N] maintained. In summary, this paper overcame the obstacle of slow kinetics of solvent extraction technology, and pointed out a way for polymetallic co-extraction and separation in HLLE system.
研究领域:
材料科学
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环境化学
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分析化学
·
绿色化学
✓ 已验证
产品关联
DOI
高影响因子
COLLOIDS AND SURFACES B-BIOINTERFACES
·
2021
·
IF 5.268
Xiao Kuang,Dongxu Chi,Jinbo Li,Chunlin Guo,Yinxian Yang,Shuang Zhou,Cong Luo,Hongzhuo Liu,Zhonggui He,Yongjun Wang
The platinum-based drugs prevail in the therapy of malignant tumors treatment. However, their clinical outcomes have been heavily restricted by severe systemic toxicities. To ensure biosafety and efficiency, herein, we constructed a disulfide bond inserted Pt(IV) self-assembled nanoplatform that is selectively activated by rich glutathione (GSH) in tumor site. Disulfide bond was introduced into the conjugates of oxaliplatin (IV) and oleic acid (OA) which conferred cascade reduction-responsiveness to nanoassemblies. Disulfide bond cleavage and reduction of Pt(IV) center occur sequentially as a cascade process. In comparison to oxaliplatin solution, Pt(IV) nanoparticles (NPs) achieved prolonged blood circulation and higher maximum tolerated doses. Furthermore, Oxa(IV)-SS-OA prodrug NPs exhibited potent anti-tumor efficiency against 4T1 cells and low toxicities in other normal tissues, which offers a promising nano-platform for potential clinical application.
研究领域:
药学
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纳米技术
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肿瘤学
·
药物递送系统
✓ 已验证
产品关联
DOI
PubMed
高影响因子
Polymer Chemistry
·
2017
·Vol. 8
·期 15
·2410-2422
·
IF 5.375
Zihao Zhang,Yongjing Li,Jiaxun Wan,Peihua Long,Jia Guo,Guosong Chen,Changchun Wang
Cisplatin is a widely-used chemotherapeutic drug in the clinic against a range of cancers. However, its anti-cancer efficacy and bioavailability are severely affected by systemic toxicity as well as drug resistance, which are mainly due to indiscriminate body distribution, low tumor accumulation and glutathione (GSH)-related drug detoxification. In this study, we prepared for the first time a new kind of Pt(IV)-crosslinked polymer nanoparticle with small, uniform size and high loading of cisplatin (60.8%). Such a kind of polymer nanodrug could keep its structural integrity during blood circulation to afford higher tumor accumulation via the EPR effect and receptor-mediated targeting effect, yet rapidly self-disintegrate to release drugs in response to tumor intracellular bio-reducing molecules, such as glutathione (GSH), resulting in efficient cancer cell inhibition and reduced systemic toxicity in vivo. Meanwhile, some of the cellular GSH molecules are depleted and transformed into an oxidized GSSG form to decrease their chelating interaction with platinum drugs, which attenuate their detoxifying effect on the Pt(II) species and may have an advantage for overcoming the tumor resistance to cisplatin induced by GSH. Moreover, the maximum tolerated dose of drug could be greatly enhanced (>3 fold), which improved the bioavailability of the nanodrug at relatively high doses. The present work provides a novel drug self-crosslinked design tactic and might open a new window for clinical cancer treatment.
研究领域:
药学
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纳米技术
·
肿瘤学
·
药物递送系统
✓ 已验证
产品关联
DOI
高影响因子
Inorganic Chemistry Frontiers
·
2020
·Vol. 7
·期 5
·1220-1228
·
IF 5.958
Xiao-Jing Ding,Ran Zhang,Rui-Ping Liu,Xue-Qing Song,Xin Qiao,Cheng-Zhi Xie,Xiu-He Zhao,Jing-Yuan Xu
A series of Pt(IV) compounds comprising a special short-chain fatty acid (a histone deacetylase inhibitor) and 5-FU (a thymidylate synthase inhibitor) were prepared and bio-evaluated for their antiproliferative activity using the MTT assay. The assembled compounds 11–15, as triple-prodrugs, exhibited a potent anti-cancer activity. In particular, compounds 14 and 15 both with valproic acid (VPA) showed higher potent cytotoxicity against the tested cancer cells, whereas lower cytotoxicity toward normal human umbilical vein endothelial cells than the free drugs involved. Compound 14, as a representative for further study, rapidly enhanced the cellular accumulation in a time-dependent manner, significantly induced the DNA-damage, cell cycle blocking at the S phase, and cell apoptosis as well as suppressed migration in HeLa. Most strikingly, compound 14 simultaneously regulated the TS, HDAC and γH2AX factors, suggesting a synergistic action of 5-FU, VPA and CDDP to increase the drug effects.
研究领域:
药理学
·
肿瘤学
·
化学
·
分子生物学
✓ 已验证
产品关联
DOI
高影响因子
CELLULOSE
·
2020
·Vol. 27
·期 17
·10167-10181
·
IF 4.21
Guo Wanghuan,Zhao Zhigang,Yang Fan,Xie Meiying,Shao Zhiheng,Xue Liyan,Zhang Yang,Lin Wanqing,Du Chang,Zhang Yongjian
Abstract The separation and recovery of Au(III), Pd(II), and Pt(IV) is a challenge in hydrometallurgy, and finding good adsorbents is a way to solve this problem. In this work, two novel adsorbents, carboxymethyldiethylammoniumethyl cellulose (CM-n-DEAEC) and carboxymethyl-2-diethylaminoethyl cellulose (CM-o-DEAEC), were synthesized by changing the grafting site of carboxymethyl on diethylaminoethyl cellulose (DEAEC). The structures and morphologies of the adsorbents were examined by NMR, FT-IR, EA, TGA, and SEM analyses. The effects of adsorbents on the separation performance of Au(III), Pd(II), and Pt(IV) at different adsorption conditions were studied. The performances of stripping and recycling were investigated. At a 3 M chloride ion concentration, CM-n-DEAEC's adsorption rates for Pd(II), Au(III), and Pt(IV) were stabilized at 60%, 30%, and 7% in the pH range of 1.0–3.0 and were unaffected by coexisting metal ions. However, at a 0.1 M chloride ion concentration, CM-o-DEAEC separated Pt(IV) before Au(III) and Pd(II) in the pH range from 1.0 to 2.0 without being affected by coexisting metal ions. In addition, the absorbed metal ions can be easily stripped by a 0.1 M thiourea-0.1 M HCl solution, and the adsorption rate only decreased by 3.0% and 1.8% after seven adsorption–desorption cycles. Therefore, it was shown that CM-n-DEAEC and CM-o-DEAEC are excellent adsorbents that can control the adsorption order of precious metals and can selectively and quickly recover Pd(II) or Pt(IV) from wastes containing Au(III). Graphic abstract
研究领域:
化学工程
·
材料科学
·
环境科学
✓ 已验证
产品关联
DOI
高影响因子
Journal of Materials Chemistry B
·
2020
·Vol. 8
·期 27
·5903-5911
·
IF 5.344
Qingfei Zhang,Gaizhen Kuang,Dongfang Zhou,Yanxin Qi,Mingzhe Wang,Xiaoyuan Li,Yubin Huang
Endo/lysosomal escape and the subsequent controllable/precise release of drugs and genes are key challenges for efficient synergistic cancer therapy. Herein, we report a photoactivated polyprodrug nanoparticle system (PPNPsiRNA) centered on effective light-controlled codelivery of Pt(IV) prodrug and siRNA for synergistic cancer therapy. Under green-light irradiation, PPNPsiRNA can sustainedly generate oxygen-independent azidyl radicals to facilitate endo/lysosomal escape through the photochemical internalization (PCI) mechanism. Besides, concurrent Pt(II) release and siRNA unpacking could occur in a controllable manner after the decomposition of Pt(IV), main chain shattering of photoactivated polyprodrug and the PPNPsiRNA disassociation. Based on these innovative features, excellent synergistic therapeutic efficacy of chemo- and RNAi therapies of PPNPsiBcl-2 could be achieved on ovarian cancer cells under light irradiation. The facile synthesized and prepared photoactivatable polyprodrug nanoparticle system provides a new strategy for effective gene/drug codelivery, where controllable endo/lysosomal escape and the subsequent drug/gene release/unpacking play vital roles, which could be adopted as a versatile codelivery nanoplatform for the treatment of various cancers.
研究领域:
纳米技术
·
癌症治疗
·
药物递送系统
·
药学
·
生物医学工程
✓ 已验证
产品关联
DOI
PubMed
高影响因子