CHINESE JOURNAL OF POLYMER SCIENCE
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2025
·
IF 4
Zhang Jian-Ye,Xu Xin-Yu,Sun Qiao,Liu Ling,Liu Zeng-He,Zhu Yu-Tian
Thermosets are indispensable to our daily life, but their crosslinked structures make them unable to be processed by the melt processing like thermoplastics, which greatly limits their shape designs and applications. Herein, we address this challenge via an in situ self-growing strategy, i.e. utilizing the dynamic imidazole-urea moiety to suck up and integrate epoxy into the materials and making the thermoplastics grow in situ into thermosets. With this strategy, thermosets can be readily processed via hot-melt extrusion molding, including melt spinning and fused deposition modeling 3D printing. More importantly, this strategy simultaneously integrates the flexibility of polyurethane and the robustness of epoxy resin into the resulting thermosets, yielding a mechanical-reinforcing effect to make the material not only strong but also tough (toughness: 99.3 MJ·m −3 , tensile strength: 38.8 MPa). Moreover, the crosslinking density and modulus of the as-prepared thermosets (from 34.1 MPa to 613.7 MPa) can be readily tuned on demand by changing the growth index. Furthermore, these thermosets exhibited excellent thermal stability and chemical resistance.
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Nature Communications
·
2025
·Vol. 16
·期 1
·1-16
·
IF 15.7
Zheng Hongyue,Zhang Ke,Piao Jigang,Mu Chaofeng,Xie Xiaowei,Cheng Mengying,Yue Tianxiang,Sun Jiang,Li Bin,Wei Yinghui,Zheng Hangsheng,Jiang Lai,Habiballah Douae Nihed,Li Fanzhu
Late-stage and advanced colorectal cancer (CRC) often prove to be resistant to current treatment regimens, due to the evolving tumor microenvironment. Chemotherapy-dominated multi-modal therapeutic strategies based on the specific CRC microenvironment open a new horizon for eradicating colorectal tumors. Here, in situ valence-transited arsenic nanosheets are developed as a multi-modal therapeutic platform by responding to the H 2 S-enriched CRC microenvironment. Carrier-free pegylated nanosheets of pentavalent arsenic (As V ), aminooxyacetic acid (AOAA), and copper ion (Cu 2+ ) are innovatively self-assembled via coordination with high loading content and good stability. As V in pegylated arsenic nanosheets (CAA-PEG NSs) is rapidly released and reduced to trivalent arsenic (As III ) to exert its chemotherapy in the local tumor. Furthermore, the immunosuppressive microenvironment is thoroughly remodeled via H 2 S depletion of As V to As III conversion and impairment of H 2 S production by AOAA. Additionally, the in situ produced ultrasmall CuS nanoparticles exhibit photothermal activity against CRC under the guidance of photoacoustic imaging. This multi-modal therapeutic strategy, dominated by chemotherapy, completely inhibits CRC progression and prevents its relapse.
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JOURNAL OF FOOD SCIENCE AND TECHNOLOGY-MYSORE
·
2024
·
IF 2.6
Li Ya,Liang Jianfeng,Liang Lili
Pile fermentation plays a crucial role in the formation of the unique flavor of Liupao tea, which can effectively reduce the bitterness of the tea and promote the formation of red tea soup. In this study, the non-volatiles changes of Liupao tea during pile fermentation processing were fully analyzed by UPLC-QTOF-MS/MS. A total of 271 metabolites with significant differences were identified in Liupao tea during pile fermentation( P < 0.01, VIP > 1), and their trends were grouped into 10 subclasses by K-means analysis. Three differential metabolites Choline Alfoscerate, N1-Methyl-4-pyridone-5-carboxamide, and 2-Aminovalienone were shared among the three different pile fermentation periods. The results provided valuable information for understanding the dynamic changes of non-volatile substances during the pile fermentation process of Liupao tea.
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ACTA PHARMACOLOGICA SINICA
·
2024
·
IF 6.9
Yang Ya-qi,Liu Yi-jun,Qiao Wen-xuan,Jin Wei,Zhu Shun-wei,Yan Yu-xi,Luo Qiong,Xu Qiang
Primary Sjögren’s syndrome (pSS) is a chronic inflammatory autoimmune disease with an unclear pathogenesis, and there is currently no approved drug for the treatment of this disease. Iguratimod, as a novel clinical anti-rheumatic drug in China and Japan, has shown remarkable efficacy in improving the symptoms of patients with pSS in clinical studies. In this study we investigated the mechanisms underlying the therapeutic effect of iguratimod in the treatment of pSS. Experimental Sjögren’s syndrome (ESS) model was established in female mice by immunizing with salivary gland protein. After immunization, ESS mice were orally treated with iguratimod (10, 30, 100 mg·kg −1 ·d −1 ) or hydroxychloroquine (50 mg·kg −1 ·d −1 ) for 70 days. We showed that iguratimod administration dose-dependently increased saliva secretion, and ameliorated ESS development by predominantly inhibiting B cells activation and plasma cell differentiation. Iguratimod (30 and 100 mg·kg −1 ·d −1 ) was more effective than hydroxychloroquine (50 mg·kg −1 ·d −1 ). When the potential target of iguratimod was searched, we found that iguratimod bound to TEC kinase and promoted its degradation through the autophagy-lysosome pathway in BAFF-activated B cells, thereby directly inhibiting TEC-regulated B cells function, suggesting that the action mode of iguratimod on TEC was different from that of conventional kinase inhibitors. In addition, we found a crucial role of TEC overexpression in plasma cells of patients with pSS. Together, we demonstrate that iguratimod effectively ameliorates ESS via its unique suppression of TEC function, which will be helpful for its clinical application. Targeting TEC kinase, a new regulatory factor for B cells, may be a promising therapeutic option.
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JOURNAL OF NANOBIOTECHNOLOGY
·
2024
·Vol. 22
·期 1
·1-21
·
IF 10.6
Zhou Hao,Wang Wei,Cai Zedong,Jia Zhou-Yan,Li Yu-Yao,He Wei,Li Chen,Zhang Bang-Le
Chemotherapy and immunotherapy have shown no significant outcome for unresectable pancreatic ductal adenocarcinoma (PDAC). Multi-drug combination therapy has become a consensus in clinical trials to explore how to arouse anti-tumor immunity and meanwhile overcome the poorly tumoricidal effect and the stroma barrier that greatly hinders drug penetration. To address this challenge, a comprehensive strategy is proposed to fully utilize both the ferroptotic vulnerability of PDAC to potently irritate anti-tumor immunity and the desmoplasia-associated focal adhesion kinase (FAK) to wholly improve the immunosuppressive microenvironment via sustained release of drugs in an injectable hydrogel for increasing drug penetration in tumor location and averting systematic toxicity. The injectable hydrogel ED-M@CS/MC is hybridized with micelles loaded with erastin that exclusively induces ferroptosis and a FAK inhibitor defactinib for inhibiting stroma formation, and achieves sustained release of the drugs for up to 12 days. With only a single intratumoral injection, the combination treatment with erastin and defactinib produces further anti-tumor performance both in xenograft and Kras G12D -engineered primary PDAC mice and synergistically promotes the infiltration of CD8 + cytotoxic T cells and the reduction of type II macrophages. The findings may provide a novel promising strategy for the clinical treatment of PDAC.
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Nano-Micro Letters
·
2024
·Vol. 16
·期 1
·1-22
·
IF 31.6
Hu Jiawang,Qian Hao,Han Sanyang,Zhang Ping,Lu Yuan
Photoresponsive black phosphorus (BP)/Ti 3 C 2 T x composites were synthesized by a self-assembly strategy.
Enhanced gas sensitive property was achieved by visible light modulation.
Light activated virtual sensor array was fabricated based on BP/Ti 3 C 2 T x composite.
Diagnosis of coronary heart disease was achieved with the help of machine learning.
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CHINESE JOURNAL OF POLYMER SCIENCE
·
2024
·Vol. 42
·期 10
·1495-1504
·
IF 4.1
Wu Shi-Long,Yang Huan-Huan,Chen Quan
In this study, we synthesized a series of ABA-type vitrimers by crosslinking the short A moieties of precursors with a bifunctional crosslinker and evaporating the small molecular byproduct. The vitrimer samples thus prepared exhibit linear viscoelasticity dependent on the length of A moiety as well as the content of the crosslinks. When the average number of A monomers per end moiety m =1.1, the crosslinker can only extend the chain but not crosslink the chain. When m becomes 2.8 or higher, introducing a crosslinker first leads to the gelation, whereas excess in crosslinker molecules leads opening of the crosslinking sites and accordingly reentry into the sol regime. Surprisingly, a further increase in the length of the A moieties increases the relaxation time much weaker than the exponential increase seen for the physically crosslinked ABA-type ionomers. We attribute this difference to the distinct relaxation mechanisms: the relaxation of the vitrimer samples is based on relatively independent exchange reactions, which contrasts with the ABA-type ionomers that relax through the collective hopping of connected ionic groups from one ion aggregate to another.
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Nature Communications
·
2024
·Vol. 15
·期 1
·1-14
·
IF 14.7
He Xiaoli,Gu Hongri,Ma Yanmei,Cai Yuhang,Jiang Huaide,Zhang Yi,Xie Hanhan,Yang Ming,Fan Xinjian,Guo Liang,Yang Zhan,Hu Chengzhi
Optical patterning of colloidal particles is a scalable and cost-effective approach for creating multiscale functional structures. Existing methods often use high-intensity light sources and customized optical setups, making them less feasible for large-scale microfabrication processes. Here, we report an optical patterning method for semiconductor nanoparticles by light-triggered modulation of their surface charge. Rather than using light as the primary energy source, this method utilizes UV-induced cleavage of surface ligands to modify surface charges, thereby facilitating the self-assembly of nanoparticles on a charged substrate via electrostatic interactions. By using citrate-treated ZnO nanoparticles, uniform ZnO patterns with variable thicknesses can be achieved. These multilayered ZnO patterns are fabricated into a UV detector with an on/off ratio exceeding 10 4 . Our results demonstrate a simple yet effective way to pattern semiconductor nanoparticles, facilitating the large-scale integration of functional nanomaterials into emerging flexible and robotic microdevices.
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Nano-Micro Letters
·
2025
·Vol. 17
·期 1
·1-15
·
IF 36.3
Dong Kailian,Jiang Tao,Chen Guoyi,Cui Hongsen,Wang Shuxin,Zhou Shun,Wang Chen,Yang Yi,Yao Fang,Tao Chen,Ke Weijun,Fang Guojia
The light management strategy is introduced into two-dimensional Dion-Jacobson (2D DJ) perovskite and subsequently elucidated both experimentally and theoretically.
The synthesis of surface-patterned BDAPbBr 4 microplates with high crystalline quality demonstrates the first reported instance of growing such 2D DJ-type perovskite microplates.
The optimized device exhibits excellent photodetection performance under UV region. Moreover, this work represents the successful demonstration of BDAPbBr 4 perovskite for UV weak-light communication, imaging, and polarized light detection.
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Nature Communications
·
2025
·Vol. 16
·期 1
·1-15
·
IF 15.7
Zhong Yuan,Wang Xue,Huang Zhou,Wei Yao,Tang Qing,Gu Songqi,Li Tingting,Dong Weinan,Jiang Feng,Zhu Haifeng,Shi Yujia,Zhou Zhi,Zhang Yu,Bai Xue,Wu Zhennan
The modulation of traps has found attractive attention to optimize the performance of luminescent materials, while the understanding of trap-involved photoluminescence management of metal nanoclusters greatly lags behind, thus extensively impeding their increasing acceptance as the promising chromophores. Here, we report an efficient passivation of the structural oxygen vacancies in AuAg nanoclusters by leveraging the H 2 O molecules, achieving a sensitive color tuning from 536 to 480 nm and remarkably boosting photoluminescence quantum yield from 5.3% (trap-state emission) to 91.6% (native-state emission). In detail, favored electron transfer relevant to the structural oxygen vacancies of AuAg nanoclusters contributes to the weak trap-state emission, which is capable of being restrained by the H 2 O molecules by taking Au-O and Ag-O bonds. This scenario allows the dominated native-state emission with a faster radiative rate. In parallel, the H 2 O molecules can rigidify the landscape of AuAg nanoclusters leveraging on the hydrogen bonding, thus enabling an efficient suppression of electron-optical phonon coupling with a decelerated non-radiative rate. The presented study deepens the understanding of tailoring the photoluminescence properties of metal nanoclusters by manipulating surface trap chemistry and electron relaxation dynamics, which would shed new light on luminescent metal nanoclusters with customizable performance.
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Scientific Reports
·
2025
·Vol. 15
·期 1
·1-12
·
IF 3.9
Tang Zhouzhou,Li Zhihao,Wu Guofeng,Li Jianjun,Tan Jianye,Zhu Lixin
Osteosarcoma (OS) is the most common primary malignant bone tumor. Recent evidence suggests that the novel long noncoding RNA DHRS4 antisense RNA 1 (DHRS4-AS1) serves an important role in cancer progression and metastasis. However, its function and molecular mechanism in OS remain largely unknown. In the present study, DHRS4-AS1 expression was detected in OS cells by quantitative PCR. Gain- and loss-of-function experiments were conducted to study the effects of DHRS4-AS1 on the proliferation and apoptosis of OS cells. The potential mechanism of DHRS4-AS1 was examined through bioinformatics analysis and rescue experiments. DHRS4-AS1 was downregulated in OS cell lines. DHRS4-AS1 depletion promoted proliferation and inhibited apoptosis in OS cells, whereas DHRS4-AS1 overexpression had the opposite effects. Further research suggested that DHRS4-AS1 inhibited OS progression by regulating the microRNA-362-5p/aminopeptidase puromycin sensitive axis. The present findings suggested that DHRS4-AS1 may serve as a potential therapeutic target for OS.
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AAPS PHARMSCITECH
·
2024
·Vol. 25
·期 8
·1-12
·
IF 3.4
Li Bo,Zhao Qianhui,Yang Hanyu,Wang Xueyuying,Zhang Zhijun,Gong Yanling,Wan Xu
Osteosarcoma (OS) is one of the most common primary bone sarcoma with high malignant degree and poor prognosis, for which there is an urgent need to develop novel therapeutic approaches. Recent research has revealed that mifamurtide significantly improved the outcome of OS patients when combined with adjuvant chemotherapy drugs including cisplatin (DDP). The present study aimed to construct a drug delivery system co-loading DDP and mifamurtide. Long-circulating targeted liposomes co-loading DDP and mifamurtide were constructed with Soy lecithin (SPC), cholesterol (Chol) and 1,2-distearoylglycero-3-phosphoethanolamine-n-[poly(ethyleneglycol)] (DSPE-PEG), modified with MMP14 targeting peptide BCY-B in the surface of liposomes. In addition to characterization, the cellular uptake, endocytosis pathway and inhibition on cell viability, migration, invasion and cell apoptosis of MG-63 cells were explored. The constructed liposomal delivery possessed the basic characteristics of liposomes and showed high affinity to MG-63 cells, resulting in high uptake efficiency in MG-63 cells. The endocytosis might be involved in multiple pathways including caveolae-mediated endocytosis, clathrin-mediated endocytosis and macropinocytosis, dependently on energy. The constructed long-circulating targeted liposomes co-loading DDP and mifamurtide significantly inhibited the cell viability, migration, invasion and cell apoptosis of MG-63 cells, improving the antitumor effect of DDP and mifamurtide in vitro . The constructed liposomal delivery system is suitable for co-loading DDP and mifamurtide to achieve active tumor targeting, supplying a new strategy for the treatment of OS. Graphical Abstract
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