CERAMICS INTERNATIONAL
·
2024
·
IF 5.1
Yaochen Si,Lingfeng Li,Ruida Wang,Songting Zhang,Yingnan Cao,Hongyu Li,Shixian Zhao,Hongxia Li,Jing Feng
With the development of high power and high thrust-weight ratio aeronautics and astronautics, aircraft engines and gas turbine technology, the development of thermal barrier coating (TBCs) material is an enormous challenge, which requires both high temperature stability and resistance to molten calcium-magnesium-aluminosilicate (CMAS) corrosion. In this study, five high-entropy rare-earth tantalate (5RE 0.2 )TaO 4 (Re=Y, Gd, Dy, Ce, Sm, La, Yb) ceramics were prepared by high temperature solid state reaction. The phase composition, microstructure, thermophysical and mechanical properties and CMAS corrosion resistance of the obtained high-entropy (5RE 0.2 )TaO 4 ceramics were systematically investigated. The as-prepared five high-entropy rare-earth tantalate (5RE 0.2 )TaO 4 ceramics had monoclinic structure and uniform composition. The five (5RE 0.2 )TaO 4 ceramics all had lower Young’s modulus (135.06∼158.63 GPa), Vickers hardness (3.7∼6.2 GPa), fracture toughness (2.30-2.80 MPa·m 1/2 ) and brittleness index (1.45-2.53 μm –1/2 ) than that of YSZ. The thermal expansion rate and thermal expansion coefficients of the five (5RE 0.2 )TaO 4 ceramics were close to each other but showed higher value than that of single RETaO 4 (RE= Gd, Dy, Sm or Y) and lower value than that of YSZ. The thermal diffusivities and thermal conductivity of the five (5RE 0.2 )TaO 4 ceramics were lower than that of YSZ, YTaO 4 and GdTaO 4 at all temperature. During molten CMAS corrosion, CMAS melt diffused into the (5RE 0.2 )TaO 4 ceramics and then corroded (5RE 0.2 )TaO 4 grains, thereby forming a corrosion area composed of reaction layer and penetration layer. The CaO in penetrated CMAS melt could react with Ta element in (5RE 0.2 )TaO 4 ceramics to generate Ca 2 Ta 2 O 7 in the reaction layer and reduce the content of CaO in the penetrated CMAS melt, which increased the viscosity of the CMAS melt and inhibited the further penetration of CMAS into the ceramics. Based on the obtained results, the CMAS corrosion of (5RE 0.2 )TaO 4 ceramics was primarily controlled by the Ca 2 Ta 2 O 7 formation and the CMAS penetration.
研究领域:
材料科学
·
航空工程
✓ 已验证
产品关联
DOI
高影响因子
JOURNAL OF THE AMERICAN CERAMIC SOCIETY
·
2013
·Vol. 97
·期 3
·990-995
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IF 2.107
Kuo Jiang,Songbai Liu,Yuan Li,Yaofei Li
Powders of zirconia doped with 8 mol% REO 1.5 (RE = Yb, Y, Gd, and Nd) were synthesized by using the sol–spray pyrolysis method. The effects of RE 3+ ionic radius on monoclinic (m) phase content of powders were investigated. The XRD results showed that the metastable tetragonal (t′) phase underwent a complete phase change to form m and cubic (c) phases after a heat treatment of 50–100 h at 1450°C. A cation size-dependent reduction in the m phase content of the REO 1.5 partially stabilized ZrO 2 powders was observed. The SEM–EDS analysis of the powders revealed that the RE 3+ concentrations in the c phases decreased with decreasing the RE 3+ ionic radius. These results indicate that the stabilizer concentration of the c phase can be attributed to RE 3+ ionic radii, resulting in different m phase contents. Compared to the REO 1.5 single doped ZrO 2 , the m phase contents of 8 mol% (RE 0.5 Yb 0.5 )–ZrO 2 (RE = Y, Gd, and Nd) powders were significantly reduced. The results prove that the stabilizer with a lower RE 3+ size is effective in reducing the m phase content of partially stabilized ZrO 2 after annealing at high temperatures.
研究领域:
材料科学
·
陶瓷学
✓ 已验证
DOI
高影响因子
Nanoscale
·
2018
·Vol. 10
·期 20
·9707-9719
·
IF 7.233
Jia Zhou,Tianliang Li,Chunlei Zhang,Junyuan Xiao,Daxiang Cui,Yingsheng Cheng
Multifunctional nanoplatforms have been developed into advanced drug delivery systems for cancer therapy. In this study, we report a charge-switchable nanocapsule with multistage pH-responsive behaviors. First, DOX-encapsulated and oleylamine-embedded hollow structures with a diameter of 132 ± 21 nm are prepared via the double emulsion method. Subsequently, the hollow structures are encompassed by Gd-DTPA-, chlorin e6 (Ce6)-, and folate (FA)-modified BSA to form tumour-targeted, dual NIR/MR imaging-guided and chemo–photodynamic therapeutic nanoplatforms. Importantly, the nanocapsule can intelligently switch its surface charge to positive under mildly acidic conditions (pH 6.5) with no release of Ce6 and DOX, which is confirmed by ξ-potential and cumulative release measurements. Moreover, confocal imaging pictures demonstrate that acid-sensitive DOX sealed in nanocapsules is progressively released into the nuclei of MGC-803 cells. These advantages as well as FA-targeting facilitate effective endocytosis and synergistic therapeutic efficacy. Selective tumour accumulation and long tumour retention time are further indicated by NIR/MR in vivo imaging. In addition, excellent therapeutic efficacy combined with chemotherapy (DOX) and photodynamic therapy (PDT) is observed with the tumour eventually ablating at the 15th day. All results demonstrate that the as-prepared nanocapsules hold great potential for clinical cancer theranostics.
研究领域:
癌症治疗
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药物递送系统
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纳米技术
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成像技术
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材料科学
✓ 已验证
产品关联
DOI
PubMed
高影响因子
CHEMICAL ENGINEERING JOURNAL
·
2020
·
IF 10.652
Junjie Liu,Wenyan Yu,Mingxu Han,Wei Liu,Zhenzhong Zhang,Kaixiang Zhang,Jinjin Shi
Magnetic resonance imaging (MRI) contrast agents (CAs) are a powerful tool for disease diagnosis. However, the “always on” state of clinically used CAs affects the specificity of tumor MR imaging in vivo . Herein, we constructed a tumor microenvironment “switch-on” type nanoprobe (TSN) with a distance-dominated property for specific tumor MR imaging, by employed a superparamagnetic hollow mesoporous iron oxide nanoparticle (HMIN) as the carrier to encapsulate T 1 -field CA (Gd), followed by blocking of the mesoporous channel with biocompatible hyaluronic acid (HA). In normal tissues with low-level hyaluronidase (HAase), Gd was restricted inside the HMIN, the distance between the two substances became quite close, and the magnetic field of Gd was interfered by the superparamagnetic HMIN, turning “off” the T 1 -field signal is “turned off”; in contrast, in tumor tissues with high-level HAase, Gd was rapidly released from the HMIN by specifically responding to overexpressed HAase, the distance between the two substances became significantly enlarged, and the magnetic field of Gd was not interfered, thus turning “on” the T 1 -field signal to achieve tumor-specific “switch on” MR imaging in a distance-controlled manner. The tumor/normal T 1 -field signal ratio after TSN treatment increased by 1.9-fold compared with free Gd-DTPA, because of its high Gd loading content, tumor-targeting ability of HA and the tumor-specific property. This distance-controlled switchable nanoprobe provides an alternative strategy for high-resolution tumor imaging with high specificity.
研究领域:
医学成像
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纳米技术
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生物医学工程
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癌症诊断
✓ 已验证
产品关联
DOI
高影响因子
COMPOSITES SCIENCE AND TECHNOLOGY
·
2022
·
IF 9.879
Jin-Ke Wu,Wei-Wei Zhang,Jian-Jun Wang,Jiang-Tao Zhu,Yu-Hang Zhang,Yi-Xuan Li,Ya-Jun Luo,Ya-Fei Zhang,Li-Xing Dai,Chuan-Xiang Qin,Jun Sun,Jia-Jia Chen
In this work, Gd 3+ ionic nano-aggregate clusters were introduced into metallo-polyelectrolytes to balance the conflicts between high mechanical robustness and X-ray attenuation of flexible shielding materials. The segmented polyurethanes (PUs) containing main-chain bisferrocene and pendant sulfonates in hard segments is applied as a macromolecular template for the subsequent self-assembly with Gd 3+ . Rare earths aggregate into dynamic clusters about 2.2 nm, which is beneficial to improve the radiation attenuation ability and mechanical properties of materials. The hierarchical noncovalent interactions (ionic interactions, coordination interactions, hydrogen bonds , and ferrocene-metal interactions, etc.) in the aggregate PUs enable the co-existence of high mechanical strength , large stretchability, and fast radiation dissipation. As a result, this Gd 3+ hybrid bisferrocene-based PU demonstrates extremely high tensile properties (breaking stress = 27.8 ± 0.2 MPa, breaking strain = 576 ± 7%) as well as super atomic shielding efficiency (14.39 cm 2 g −1 ) at 65 keV.
研究领域:
材料科学
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辐射防护
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聚合物化学
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纳米技术
✓ 已验证
产品关联
DOI
高影响因子
ACS Applied Materials & Interfaces
·
2019
·
IF 8.456
Yeneng Dai,Jinzhong Su,Kun Wu,Wenkang Ma,Bing Wang,Meixing Li,Pengfei Sun,Qingming Shen,Qi Wang,Quli Fan
Multifunctional theranostic nanoplatforms (NPs) in response to environment stimulations for on-demand drug release are highly desirable. Herein, the near-infrared (NIR)-absorbing dye, indocyanine green (ICG), and the antitumor drug, doxorubicin (DOX), were efficiently coencapsulated into the thermosensitive liposomes based on natural phase-change material. Folate and conjugated gadolinium (Gd) chelate-modified liposome shells enhance active targeting and magnetic resonance performance of the NPs while maintaining the size of the NPs. The ICG/DOX-loaded and gadolinium chelate conjugated temperature-sensitive liposome nanoplatforms (ID@TSL-Gd NPs) exhibited NIR-triggered drug release and prominent chemo-, photothermal, and photodynamic therapy properties. With the coencapsulated ICG, DOX, and the conjugated gadolinium chelates, the ID@TSL-Gd NPs can be used for triple-modal imaging (fluorescence/photoacoustic/magnetic resonance imaging)-guided combination tumor therapy (chemotherapy, photothermotherapy, and photodynamic therapy). After tail vein injection, the ID@TSL-Gd NPs accumulated effectively in subcutaneous HeLa tumor of mice. The tumor was effectively suppressed by accurate imaging-guided NIR-triggered phototherapy and chemotherapy, and no tumor regression and side effects were observed. In summary, the prepared ID@TSL-Gd NPs achieved multimodal imaging-guided cancer combination therapy, providing a promising platform for improving diagnosis and treatment of cancer.
研究领域:
癌症治疗
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纳米技术
·
生物医学工程
·
药学
·
医学成像
✓ 已验证
产品关联
DOI
PubMed
高影响因子
Materials Today Bio
·
2024
·
IF 8.7
Mengyang Zhou,Yifei Wang,Yaning Xia,Yinhua Li,Jianfeng Bao,Yong Zhang,Jingliang Cheng,Yupeng Shi
Nanotechnology for tumor diagnosis and optical therapy has attracted widespread interest due to its low toxicity and convenience but is severely limited due to uncontrollable tumor targeting. In this work, homologous cancer cell membrane-camouflaged multifunctional hybrid metal coordination nanoparticles (DRu/Gd@CM) were prepared for MRI-guided photodynamic therapy (PDT) and photothermal therapy (PTT) of tumors. Bimetallic coordination nanoparticles are composed of three functional modules: dopamine, Ru(dcbpy) 3 Cl 2 and GdCl 3 , which are connected through 1,4-Bis[(1H-imidazole-1-yl)methyl]benzene (BIX). Their morphology can be easily controlled by adjusting the ratio of precursors. Optimistically, the intrinsic properties of the precursors, including the photothermal properties of polydopamine (PDA), the magnetic resonance (MR) response of Gd 3+ , and the singlet oxygen generation of Ru(dcbpy) 3 Cl 2 , are well preserved in the hybrid metal nanoparticles. Furthermore, the targeting of homologous cancer cell membranes enables these coordinated nanoparticles to precisely target tumor cells. The MR imaging capabilities and the combination of PDT and PTT were demonstrated in in vitro experiments. In addition, in vivo experiments indicated that the nanoplatform showed excellent tumor accumulation and therapeutic effects on mice with subcutaneous tumors, and could effectively eliminate tumors within 14 days. Therefore, it expanded the new horizon for the preparation of modular nanoplatform and imaging-guided optical therapy of tumors.
研究领域:
纳米技术
·
生物医学工程
·
癌症治疗
·
分子成像
✓ 已验证
产品关联
DOI
PubMed
高影响因子
Advanced Science
·
2020
·Vol. 7
·期 17
·1903341
·
IF 15.84
Qing You,Kaiyue Zhang,Jingyi Liu,Changliang Liu,Huayi Wang,Mengting Wang,Siyuan Ye,Houqian Gao,Letian Lv,Chen Wang,Ling Zhu,Yanlian Yang
Multifunctional nanoplatforms for imaging-guided synergistic antitumor treatment are highly desirable in biomedical applications. However, anticancer treatment is largely affected by the pre-existing hypoxic tumor microenvironment (TME), which not only causes the resistance of the tumors to photodynamic therapy (PDT), but also promotes tumorigenesis and tumor progression. Here, a continuous O 2 self-enriched nanoplatform is constructed for multimodal imaging-guided synergistic phototherapy based on octahedral gold nanoshells (GNSs), which are constructed by a more facile and straightforward one-step method using platinum (Pt) nanozyme-decorated metal–organic frameworks (MOF) as the inner template. The Pt-decorated MOF@GNSs (PtMGs) are further functionalized with human serum albumin-chelated gadolinium (HSA-Gd, HGd) and loaded with indocyanine green (ICG) (ICG-PtMGs@HGd) to achieve a synergistic PDT/PTT effect and fluorescence (FL)/multispectral optoacoustic tomography (MSOT)/X-ray computed tomography (CT)/magnetic resonance (MR) imaging. The Pt-decorated nanoplatform endows remarkable catalase-like behavior and facilitates the continuous decomposition of the endogenous H 2 O 2 into O 2 to enhance the PDT effect under hypoxic TME. HSA modification enhances the biocompatibility and tumor-targeting ability of the nanocomposites. This TME-responsive and O 2 self-supplement nanoparticle holds great potential as a multifunctional theranostic nanoplatform for the multimodal imaging-guided synergistic phototherapy of solid tumors.
研究领域:
生物医学工程
·
纳米技术
·
癌症治疗
·
医学成像
·
材料科学
✓ 已验证
DOI
PubMed
高影响因子
危险品化学品经营许可证（带存储）