TRIBOLOGY INTERNATIONAL
·
2025
·
IF 6.9
Shanshan Li,Chuanping Gao,Chunjian Duan,Shengmao Zhang,Pingyu Zhang,Zhijun Zhang
Oil-based superlubricity introduces a novel approach to energy conservation. Facing two main obstacles at present, i.e., higher viscosity of lubricating oil and special tribopairs, a novel solid-liquid combined system is built in this work, which is mainly based on excellent tribological property of oil-soluble dialkyl-dithiophosphoric-modified Cu nanoparticles (DDP-Cu NPs) and superior self-lubricating capability of polymeric tribopairs. In this system, polyetheretherketone (PEEK) is coupled with polytetrafluoroethylene (PTFE) to form a similar/dissimilar tribopair; and neat PAO40 (a real serving lubricating oil with high viscosity in poly-alpha olefin oil family), or PAO40 containing oil-soluble DDP-Cu NPs (PAO40 + Cu), is used as a lubricant during the sliding test. The results show that only dissimilar tribopair, i.e., PEEK-PTFE, can achieve oil-based superlubricity under the selected sliding conditions, which can be attributed to the synergistic effect between PEEK-PTFE tribopair and PAO40/PAO40 + 0.25 Cu. Furthermore, due to lower cohesive energy density (CED), PTFE is more likely to be transferred onto PEEK together with some tribochemical reactions, finally generating a high-performance tribofilm rich in carboxylated PTFE. In addition, it is concluded that, when lubricated with PAO40, the above synergistic effect is a key to achieve superlubricity; and for PAO40 + 0.25 Cu, the carboxylated PTFE and the exposed Cu core will create chelate effect, which can not only further enhance this synergistic effect, but also improve the wear-resistance of the system reaching near-zero wear. This work not only provides a novel idea for designing oil-based superlubricity system, but broadens the type of tribopair materials achieving oil-based superlubricity to some extent.
研究领域:
材料科学
·
摩擦学
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纳米技术
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产品关联
DOI
高影响因子
E-POLYMERS
·
2017
·Vol. 17
·期 6
·463-470
·
IF 0.949
Yongqian Nie,Xuanxi Leng,Yixue Jiang,Shigan Chai,Jinzhi Zhang,Qichao Zou
Unsaturated polyester resins (UPR) were prepared by the melt condensation method based on adipic acid, o-phthalic anhydride, maleic anhydride and ethylene glycol in the presence of PSS-(2,3-propanediol)propoxy-heptaisobutyl substituted (PSS-POSS) or/and 9 wt% [(6-oxide-6H-dibenz(c,e)(1,2)oxaphosphorin-6-yl)methyl]butanedioic (DDP). We synthesized UPR containing DDP (DDP-UPR) and UPR containing both DDP and PSS-POSS (DDP-PSS-POSS-UPR series). The chemical structures of the modified polyesters were characterized and confirmed by Fourier transform infrared (FTIR) and 31 P nuclear magnetic resonance ( 31 P NMR). The thermal stability and flammability behaviors of UPR were evaluated by thermogravimetric analysis (TGA) and limited oxygen index (LOI) and the vertical burning test. The morphology of residual char of UPR was shown by scanning electron microscopy (SEM). The results indicate that the incorporation of PSS-POSS has little influence on the thermal stability of DDP-UPR, but enhances the flame retardance of DDP-UPR, and when the PSS-POSS content reaches 10 wt%, the DDP-PSS-POSS-UPR has better flame retardance.
研究领域:
材料科学
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聚合物化学
·
消防安全工程
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产品关联
DOI
高影响因子
BIOORGANIC CHEMISTRY
·
2021
·
IF 5.275
Lanmei Chen,Jie Wang,Xianhong Cai,Suxiang Chen,Jingjing Zhang,Baojun Li,Weigang Chen,Xinhua Guo,Hui Luo,Jincan Chen
Both ruthenium (Ru) and isoquinoline (IQ) compounds are regarded as potential anticancer drug candidates. Here, we report the synthesis and characterization of three novel cyclometalated Ru(II)-isoquinoline complexes: RuIQ-3 , RuIQ-4 , and RuIQ-5, and evaluation of their in vitro cytotoxicities against a panel of cell lines including A549/DDP, a cisplatin-resistant human lung cancer cell line. A549/DDP 3D multicellular tumor spheroids (MCTSs) were also used to detect the drug resistance reversal effect of Ru(II)-IQ complexes. Our results indicated that the cytotoxic activities against cancer cells of Ru(II)-IQ complexes, especially RuIQ-5 , were superior compared with cisplatin. In addition, RuIQ-5 exhibited low toxicity towards both normal HBE cells in vitro and zebrafish embryos in vivo . Further investigation on cellular mechanism of action indicated that after absorption by A549/DDP cells, RuIQ-5 was mainly distributed in the nucleus, which is different from cisplatin. Besides, RuIQ-5 could induce apoptosis through mitochondrial dysfunction, reactive oxygen species (ROS) accumulation, ROS-mediated DNA damage, and cycle arrest at both S and G2/M phases. Moreover, RuIQ-5 could inhibit the overexpression of Nrf2 through regulation of Akt/GSK-3β/Fyn signaling pathway and hindering the nuclear translocation of Nrf2. Based on these findings, we firmly believe that the studied Ru(II)-IQ complexes hold great promise as anticancer therapeutics with high effectiveness and low toxicity.
研究领域:
药理学
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肿瘤学
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细胞生物学
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化疗
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DOI
PubMed
高影响因子
CHEMICAL RESEARCH IN CHINESE UNIVERSITIES
·
2024
·Vol. 40
·期 3
·499-507
·
IF 3.1
Tao He,Ji Chengshan,Zhang Jian,Yin Yuanyuan,Jia Wenwen,Jiang Xin,Xu Jie,Yang Yulin
The abuse of tetracycline antibiotics has caused great harm to human health and ecosystems. Developing inexpensive, convenient and sensitive methods for the detection of tetracycline antibiotics is highly desirable. Herein, based on the H 4 ddp ligand [H 4 ddp=3-(3,5-dicarboxyphenyl)pyridine-2,6-dicarboxylic acid], two novel zinc-based metal-organic frameworks (MOFs) {[Zn 3 (ddp) 2 (H 2 O) 4 ]·3H 2 O} n (Zn1-ddp) and {[Zn 3 (ddp) 2 (H 2 O) 4 ]·3H 2 O} n (Zn2-ddp) were successfully designed by delicate structural regulation. Both Zn1-ddp and Zn2-ddp exhibited excellent water and chemical stability and showed excellent fluorescence quenching performance for tetracycline antibiotics. Notably, the more advanced framework structure and better fluorescent performance make Zn1-ddp more sensitive than Zn2-ddp in fluorescent detection with a detection limit of 0.29 µmol/L for tetracycline (TC), 0.09 µmol/L for doxycycline (DOX), 0.10 µmol/L for minocycline (MIN) and metacycline (MEL), 0.19 µmol/L for chlortetracycline (CTC), and 0.67 µmol/L for oxytetracycline (OTC) among tetracycline antibiotics. The fluorescence quenching mechanism of Zn1-ddp and Zn2-ddp for tetracycline antibiotics detection was deeply investigated. The reasons for the superior detection performance of Zn1-ddp over Zn2-ddp were also analyzed in depth through Fourier transform infrared spectrophotometry (FTIR), X-ray photoelectron spectroscopy (XPS) analysis and framework structure analysis. The developed method opens up a new perspective for antibiotics detection based on zinc-based MOFs.
研究领域:
分析化学
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环境科学
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生物医学
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产品关联
DOI
高影响因子
CHEMICAL ENGINEERING JOURNAL
·
2025
·
IF 13.2
Qi Jiang,Han Hu,Jinhao Sun,Weihong Cao,Qingyang Luan,Hanxu Zhu,Weiqi Chen,Peng Liang,Jinggang Wang,Jin Zhu
Adhesives have been increasingly utilized in multifaceted applications, such as furniture, electrical appliances, and buildings. Currently, in addition to fundamental requirements for high adhesiveness, there are increasing demands for environmental sustainability, flame retardancy, and high-performance in extreme conditions. (6H-dibenz[c,e][1,2]oxaphosphorin-6-ylmethyl)-p-oxide-butanedioic acid (DDP) is selected to be incorporated into the Poly(butylene adipate-co-terephthalate) (PBAT) backbone, enabling the synthesis of a novel adhesive (poly(butylene adipate-co-terephthalate-co-phosphaphenanthrene) (PBATDn). Due to the π-π stacking of DDP, PBATD 20 exhibits an extremely high adhesion strength of 11 N/cm. Owing to the hydrophobicity of the aromatic ring and the insensitivity of π-π stacking to water, PBATD 20 maintains a high adhesion even after being immersed in water for 15 days, thus meeting the requirements for wet-environment applications. In addition to meeting the demand for adhesives, PBATD 20 has been shown to reduce the potential fire risk. DDP releases phosphorus-oxygen free radicals to capture the ·H or ·OH radicals generated by polymer burning, effectively inhibiting the burning process. PBATD 20 leaves some compact char residues that act as barriers to slow down the transfer of heat, oxygen, and combustible gases, showing excellent flame retardancy. Furthermore, PBATD 20 exhibits a superior biodegradation capacity in Candida antarctica lipase B (CALB) at 37 ℃ compared with PBAT, thus reducing environmental pollution. PBATD 20 is considered highly suitable for diverse applications in daily production and consumer use, including degradable packaging adhesion, electronics assembly, and the bonding of environmentally friendly building materials.
研究领域:
材料科学
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环境科学
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产品关联
DOI
高影响因子
Cancer Management and Research
·
2023
·
IF 3.3
Ping Huang,Shi-Xia Du
Objective The effect of PUE on enhancing the anti-cancerous efficacy of DDP on drug-resistant A549/DDP cancer and the underlying mechanisms were thoroughly investigated.Materials and Methods The cytotoxicity of PUE, DDP, and PUE + DDP to A549 cells and A549/DDP cells, respectively, is determined by cell apoptosis experiments. Anti-proliferation effect of PUE, DDP, and PUE + DDP on A549 cells and A549/DDP cells is evaluated by the cell cloning assay. Qualitative and quantitative analysis of the levels of PUE, DDP, and PUE + DDP of cell proliferation-related genes and proteins expressions in A549/DDP cells are determined by Western blot assay. The levels of VEGF in A549/DDP cells after different treatment strategies are determined by ELISA assay. Qualitative and quantitative determination of VEGF expression in tumor tissues are done by immunohistochemical staining.Results In vitro cellular experiments revealed that co-incubation of A549/DDP cells with PUE and DDP led to a dramatically decreased cell viability and cell survival rate compared with the cells only treated by DDP. Such a stimulating effect of PUE on DDP was further confirmed in vivo with results shown that the A549/DDP cancer-bearing mice treaded by combination therapy achieved the lowest tumor growth rate and longest survival time.Conclusion Taking these results together, we can draw the conclusion that the PUE enhances the anti-tumor effect of DDP on the drug-resistant A549 cancer in vivo and in vitro through activation of the Wnt signaling pathway.
研究领域:
肿瘤学
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药理学
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分子生物学
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产品关联
DOI
PubMed
高影响因子
Advanced Healthcare Materials
·
2024
·
IF 10
Xiali Yin,Yaohua Ke,Ying Liang,Shuxian Zhang,Ziqi Chen,Lixia Yu,Ming Jiang,Qin Liu,Xiaoping Gu
Chemotherapy is the cornerstone of triple-negative breast cancer. The poor effectiveness and severe neuropathic pain caused by it have a significant impact on the immune system. Studies confirmed that immune cells in the tumor microenvironment (TME), have critical roles in tumor immune regulation and prognosis. In this study, it is revealed that the painless administration of Esketamine, combined with Cisplatin (DDP), can exert an anti-tumor effect, which is further boosted by the hydrogel delivery system. It is also discovered that Esketamine combined with DDP co-loaded in Poloxamer Hydrogel (PDEH) induces local immunity by increasing mature Dendritic Cells (mDCs) and activated T cells in PDEH group while the regulatory T cells (Tregs) known as CD4 + CD25 + FoxP3 + decreased significantly. Finally, , CD8 + and CD4 + T cells in the spleen exhibited a significant increase, suggesting a lasting immune impact of PDEH. This study proposes that Esketamine can serve as a painless immune modulator, enhancing an anti-tumor effect while co-loaded in poloxamer hydrogel with DDP. Along with improving immune cells in the microenvironment, it can potentially alleviate anxiety and depression. With its outstanding bio-safety profile, it offers promising new possibilities for painless clinical therapy.
研究领域:
肿瘤学
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药理学
·
免疫学
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产品关联
DOI
PubMed
高影响因子
Cancer Biomarkers
·
2019
·Vol. 24
·期 4
·469-475
·
IF 2.859
Qin Yujing,Li Wenxue,Long Yingli,Zhan Zhijia
OBJECTIVE: This study aims to determine the correlation between p-cofilin expression and cisplatin resistance in patients with ovarian cancer, and also to investigate the role of p-cofilin in prognosis. PATIENTS AND METHODS: The ovarian cancer cell line A2780/DDP resistant to cisplatin was prepared. The cell resistance to cisplatin was measured via MTT assay. The cell invasion capacity was identified via Transwell assay. The mRNA expression and protein level was evaluated via semi-quantitative PCR and Western blot, respectively. The tumor tissues of patients with cisplatin-resistant ovarian cancer were collected. The relationship between prognosis and p-cofilin expression was analyzed. RESULTS: The growth rate of A2780 was similar to that of A2780/DDP. The sensitivity of A2780 to cisplatin was significantly higher than that of A2780/DDP (p< 0.01). The migration capacity of A2780/DDP was significantly increased compared to that of A2780 (p< 0.01), indicating that the cisplatin-resistant cell lines were successfully constructed. Both CFL1 mRNA level and p-cofilin level in A2780/DDP was significantly higher than that in A2780 (p< 0.01). The p-cofilin level in cancer tissues in patients with cisplatin-resistant ovarian cancer was significantly higher than that in patients with cisplatin-sensitive ovarian cancer (p< 0.01). The cisplatin resistance was positively correlated with the p-cofilin expression level (r= 0.802, p= 0.023). The survival time of patients with normal or low level of p-cofilin was significantly longer than that of patients with high expression. CONCLUSION: The cisplatin resistance of ovarian cancer is closely related to the expression level of p-cofilin, which affects the prognosis of patients with ovarian cancer.
研究领域:
肿瘤学
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分子生物学
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癌症研究
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产品关联
DOI
PubMed
高影响因子
JOURNAL OF DRUG TARGETING
·
2023
·
IF 4.5
Wenhui Ye,Huaiyou Lv,Qinxiu Zhang,Jianxiong Zhao,Xin Zhao,Guozhi Zhao,Chongzheng Yan,Fengqin Sun,Zhongxi Zhao,Xiumei Jia
Non-small cell lung cancer (NSCLC) accounting for about 80-85% of all lung cancer cases is one of the fastest-growing malignancies in terms of incidence and mortality worldwide and is commonly treated with cisplatin (DDP). Although treatment may initially be effective, the DDP therapy often leads to the development of chemoresistance and treatment failure. Disulfiram (DSF), an old alcohol-aversion drug, has been revealed to help reverse drug resistance in several cancers. In addition, several studies have shown a close relationship between drug resistance and cancer cell stemness. In this study, DDP and DSF were embedded in hydroxypropyl-β-cyclodextrin (CD) to prepare a co-loaded inclusion complex of DDP and DSF (DDP-DSF/CD) with enhanced solubility and therapeutic effects. The effects and mechanism of DSF on the DDP resistance from the perspective of cancer cell stemness were determined. Our data show that DDP-DSF/CD increased cytotoxicity and apoptosis of DDP-resistant A549 (A549/DDP) cells, inhibited stem cell transcriptional regulatory genes and drug resistance-associated proteins and reversed the DDP resistance in vitro and in vivo. Overall, DDP-DSF/CD could be a promising formulation for the reversal of DDP resistance in NSCLC by inhibiting cancer cell stemness.
研究领域:
肿瘤学
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药学
·
分子生物学
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DOI
PubMed
高影响因子
JOURNAL OF COLLOID AND INTERFACE SCIENCE
·
2023
·
IF 9.9
Xucan Yang,Lulu Cheng,Yile Zhao,Haoran Ma,Haitao Song,Xuanmin Yang,Kang-Nan Wang,Yanrong Zhang
The efficacy of imaging-guided photodynamic therapy (PDT) is compromised by the attenuation of fluorescence and decline in reactive oxygen species (ROS) generation efficiency in the physiological environment of conventional photosensitizers , limited near-infrared (NIR) absorption, and high systemic cytotoxicity. This paper presents the synthesis of two cyclometalated Ir (III) complexes (Ir-thpy and Ir-ppy) by using a triphenylamine derivative (DPTPA) as the primary ligand and their encapsulation into an amphiphilic phospholipid to form nanoparticles (NPs). These complexes exhibit aggregation-induced emission features and remarkably enhanced ROS generation compared to Chlorin e6 (Ce6). Moreover, Ir-thpy NPs possess the unique ability to selectively target mitochondria , leading to depolarization of the mitochondrial membrane potential and ultimately triggering apoptosis. Notably, Ir-thpy NPs exhibit exceptional photocytotoxicity even towards cisplatin-resistant A549/DDP tumor cells. In vivo two-photon imaging verified the robust tumor-targeting efficacy of Ir-thpy NPs. The in vivo results unequivocally demonstrate that Ir-thpy NPs exhibit excellent tumor ablation along with remarkable biocompatibility. This study presents a promising approach for the development of multifunctional Ir-NPs for two-photon imaging-guided PDT and provides novel insights for potential clinical applications in oncology.
研究领域:
材料科学
·
纳米技术
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癌症研究
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生物医学工程
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药学
✓ 已验证
产品关联
DOI
PubMed
高影响因子
JOURNAL OF CONTROLLED RELEASE
·
2025
·
IF 11.5
Xi Wang,Guiquan Liu,Xueyu Pu,Tangjun Ren,Fan Zhang,MengJie Shen,Yan Zhu,Alexander Kros,Jian Yang
Drug resistance to chemotherapy in treating cancers becomes an increasingly serious challenge, which leads to treatment failure and poor patient survival. Drug-resistant cancer cells normally reduce intracellular accumulation of drugs by controlling drug uptake and promoting drug efflux, which severely limits the efficacy of chemotherapy. To overcome this problem, a membrane fused drug delivery system (MF-DDS) was constructed to treat cisplatin (DDP)-resistant lung cancer (A549-DDP) by delivering DDP via membrane fusion using a complementary coiled-coil forming peptides (CP 8 K 4 /CP 8 E 4 ). The lipopeptide CP 8 K 4 was pre-incubated firstly and decorated on the surface of A549-DDP cells, and then the cells interacted with the lipopeptide CP 8 E 4 modified on the lipid bilayer (LB) coated PLGA nanoparticles loading DDP (PLGA-DDP@LB-CP 8 E 4 ), leaded to the direct cytosolic DDP delivery and cancer cell death. Compared with free DDP, this MF-DDS achieved a 13.42-folds reduced IC 50 value of A549-DDP cells in vitro , and tumor size was down-regulated, showing only 1/5.26 of the original weight in vivo . Meanwhile, the anti-drug resistant mechanism was explored, where the MF-DDS inhibited the expression of efflux protein genes, including MRP1, MRP2, and ABCG2, leading to increased intracellular drug accumulations. Altogether, this MF-DDS effectively delivered DDP into DDP-resistant cancer cells, making it a promising and improved pharmacological therapeutic approach for drug-resistant tumor treatment.
研究领域:
肿瘤学
·
药理学
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纳米技术
·
分子生物学
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产品关联
DOI
PubMed
高影响因子
IET Nanobiotechnology
·
2023
·Vol. 17
·期 3
·224-233
·
IF 2.3
Junjie Zhao,Niu Niu,Fan Yang,Haitao Liu,Weibo Qi
Background Multidrug resistance is the biggest barrier on the way to chemotherapy for lung adenocarcinoma (LUAD). For some LUAD patients with cisplatin (DDP) resistance and poor prognoses, the authors put forward RNA nanoparticles (NPs) carrying miR-301b-3p Inhibitor. Methods The NPs were composed of miR-301b-3p, A549 aptamer (A549apt), and Cyanine 5 in a bottom-up manner with a 3-way-junction (3WJ) structure. Diameter, assembly process, and morphology of NPs were observed by Dynamic Light Scattering, Native-Polyacrylamide Gel Electrophoresis, and Atomic Force Microscopy. Cell internalisation, toxicity, proliferation, migration, invasion, and apoptosis were assayed by confocal laser scanning microscope, CCK8, colony formation assay, Transwell, western blot, and flow cytometry. Results 3WJ-apt-miR was evenly distributed, with diameter of 19.61 ± 0.49 nm and triangular branching structures. The accurate delivery of this NP in vivo was ensured by A549 aptamer featuring specific targeting, with smaller side effects than traditional chemotherapy. Such nanomaterials were effectively internalized by cancer cells, with normal cell activity intact. Cancer cell proliferation, invasion, and migration were suppressed, and DDP sensitivity was enhanced, causing DNA damage and facilitating apoptosis of DDP-resistant cells. Conclusion Based on RNA self-assembling, the authors researched the effect of miRNA on DDP sensitivity in LUAD regarding gene regulation. 3WJ-apt-miR paves the way for clinical tumour therapy.
研究领域:
癌症生物学
·
纳米技术
·
分子生物学
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药学
·
基因治疗
✓ 已验证
DOI
PubMed
高影响因子
危险品化学品经营许可证（带存储）