Advanced Composites and Hybrid Materials
·
2025
·Vol. 8
·期 1
·1-10
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IF 21.8
Xie Xinyu,Zhang Yixiao,Qin Yang,Wu Jianbo,Lei Ming,Huang Kai,Wang Ruyue,Du Peng
The incorporation of non-metal dopants can significantly enhance catalytic activity and improve stability. Furthermore, the creation of heterostructures is particularly advantageous to facilitate charge transfer and optimize electronic properties. This study presents an effective bifunctional mixed-valence Ruthenium heterostructure synthesized through a cascading process involving grinding with carbon nitride and subsequent thermal treatment. The catalyst exhibits outstanding electrocatalytic performance with remarkably low overpotentials of 197 mV for the oxygen evolution reaction (OER) and 24.8 mV for the hydrogen evolution reaction (HER), respectively, with the stability exceeding 24 h at a current density of 10 mA cm⁻ 2 in acidic media. Additionally, when employed in an acidic oxygen water splitting (OWS) electrolyzer, the bifunctional catalyst demonstrates excellent activity, achieving an ultralow cell voltage of 1.53 V to sustain 10 mA cm⁻ 2 . Enhanced performance is attributed to efficient charge transfer and increased exposure of active sites, providing valuable insights for the development of effective acidic water-electrolysis catalysts for sustainable hydrogen production.
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ARCHIVES OF MICROBIOLOGY
·
2024
·Vol. 206
·期 5
·1-13
·
IF 2.3
Peng Liang,Yun Hui,Ji Jing,Zhang Wenjie,Xu Ting,Li Si,Wang Zhenfei,Xie Li,Li Xiangkai
Ibuprofen (IBU) and naproxen (NPX), as widely prescribed non-steroidal anti-inflammatory drugs (NSAIDs), are largely produced and consumed globally, leading to frequent and ubiquitous detection in various aqueous environments. Previously, the microbial transformation of them has been given a little attention, especially with the isolated fungus. A yeast-like Apiotrichum sp. IB-1 has been isolated and identified, which could simultaneously transform IBU (5 mg/L) and NPX (2.5 mg/L) with maximum efficiencies of 95.77% and 88.31%, respectively. For mono-substrate, the transformation efficiency of IB-1 was comparable to that of co-removal conditions, higher than most of isolates so far. IBU was oxidized mainly through hydroxylation (m/z of 221, 253) and NPX was detoxified mainly via demethylation (m/z of 215) as shown by UPLC-MS/MS results. Based on transcriptome analysis, the addition of IBU stimulated the basic metabolism like TCA cycle. The transporters and respiration related genes were also up-regulated accompanied with higher expression of several dehydrogenase, carboxylesterase, dioxygenase and oxidoreductase encoding genes, which may be involved in the transformation of IBU. The main functional genes responsible for IBU and NPX transformation for IB-1 should be similar in view of previous studies, which needs further confirmation. This fungus would be useful for potential bioremediation of NSAIDs pollution and accelerate the discovery of functional oxidative genes and enzymes different from those of bacteria.
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JOURNAL OF NANOBIOTECHNOLOGY
·
2025
·Vol. 23
·期 1
·1-20
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IF 12.6
Xiong Sha,Li Zhongjun,Jiao Siwen,Xiao Ting,Wu Yan,Chen Chen,Guo Shiqi,Li Xiaojuan,Pan Zhiyuan,Li Jianqing,Xu Yuehong
Background Androgenetic alopecia (AGA), a chronic and progressive disease, significantly impacts the patients’ social, emotional, and mental well-being. Current treatment for AGA are mainly limited by drug side effects and the stratum corneum (SC) barrier of scalp. Results To address these issues, we developed a microneedle (MN) system loaded with black phosphorus nanosheets (BP) encapsulating baicalin (BA), a natural ingredient, for effective treatment of AGA. We first fabricated BP-BA based on the BP properties of high drug loading capacity and excellent photothermal conversion efficiency. Upon 635 nm laser irradiation, BP-BA demonstrated efficient photothermal conversion to mild thermal of ~ 42 °C. This mild thermal effect controlled BA’s stimuli-responsive release, enhanced cellular uptake, and effectively modulated gene expression in dihydrotestosterone-treated human dermal papilla cells, downregulating negative regulators such as SRD5A2, AR, DKK1, and TGFB1, while upregulating positive regulators like CTNNBIP1 and VEGFA. Furthermore, we encapsulated BP-BA to MN fabricating BP-BA@MNs to overcome the SC barrier. Compared with BP-BA@MNs without laser irradiation, BP-BA@MNs with laser irradiation significantly enhanced drug penetration into the subcutaneous area and accumulation at the follicular site. Importantly, BP-BA@MNs demonstrated synergistic efficacy against testosterone-induced AGA in vivo through combining BA chemotherapy, BP-mediated mild photothermal therapy, and MN delivery, as well as good biocompatibility and biosafety, and the underlying synergistic mechanism was elucidated in terms of follicular microenvironment reconstruction. Conclusions This combining BP mild photothermal and MN system is a promising approach for follicular targeted drug delivery, providing a multifunctional strategy for addressing the clinical needs of anti-AGA. Graphical
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JOURNAL OF NANOBIOTECHNOLOGY
·
2024
·Vol. 22
·期 1
·1-20
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IF 10.6
Zhang Yingjuan,Huang Xianxian,Luo Yicai,Ma Xiangyu,Luo Ling,Liang Ling,Deng Tingting,Qiao Yang,Ye Fanggui,Liao Hongbing
Preserving pulp viability and promoting pulp regeneration in pulpitis have attracted widespread attention. Restricted by the oxidative stress microenvironment of dental pulpitis, excessive reactive oxygen and nitrogen species (RONS) trigger uncontrolled inflammation and exacerbate pulp tissue destruction. However, modulating redox homeostasis in inflamed pulp tissue to promote pulp regeneration remains a great challenge. Herein, this work proposes an effective antioxidative system (C-NZ/GelMA) consisting of carbon dot nanozymes (C-NZ) with gelatin methacryloyl (GelMA) to modulate the pulpitis microenvironment for dental pulp regeneration by utilizing the antioxidant properties of C-NZ and the mechanical support of an injectable GelMA hydrogel. This system effectively scavenges RONS to normalize intracellular redox homeostasis, relieving oxidative stress damage. Impressively, it can dramatically enhance the polarization of regenerative M2 macrophages. This study revealed that the C-NZ/GelMA hydrogel promoted pulp regeneration and dentin repair through its outstanding antioxidant, antiapoptotic, and anti-inflammatory effects, suggesting that the C-NZ/GelMA hydrogel is highly valuable for pulpitis treatment.
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JOURNAL OF NANOBIOTECHNOLOGY
·
2024
·Vol. 22
·期 1
·1-16
·
IF 10.6
Yu Shuo,Shen Huan,Chen Xi,Wang Hong,He Chenyang,Hu Tinghua,Cao Gang,Zhang Lu
Due to the limitations of single-model tumor therapeutic strategies, multimodal combination therapy have become a more favorable option to enhance efficacy by compensating for its deficiencies. However, in nanomaterial-based multimodal therapeutics for tumors, exploiting synergistic interactions and cascade relationships of materials to achieve more effective treatments is still a great challenge. Based on this, we constructed a nanoplatform with a “triple-linkage” effect by cleverly integrating polydopamine (PDA), silver nanoparticles (AgNPs), and glucose oxidase (GOx) to realize enhanced photothermal therapy (PTT) and activatable metal ion therapy (MIT) for hepatocellular carcinoma (HCC) treatment. First, the non-radiative conversion of PDA under light conditions was enhanced by AgNPs, which directly enhanced the photothermal conversion efficiency of PDA. In addition, GOx reduced the synthesis of cellular heat shock proteins by interfering with cellular energy metabolism, thereby enhancing cellular sensitivity to PTT. On the other hand, H 2 O 2 , a by-product of GOx-catalyzed glucose, could be used as an activation source to activate non-toxic AgNPs to release cytotoxic Ag + , achieving activatable Ag + -mediated MIT. In conclusion, this nanosystem achieved efficient PTT and MIT for HCC by exploiting the cascade effect among PDA, AgNPs, and GOx, providing a novel idea for the design of multimodal tumor therapeutic systems with cascade regulation. Graphical abstract
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JOURNAL OF NANOBIOTECHNOLOGY
·
2024
·Vol. 22
·期 1
·1-19
·
IF 10.6
Jiang Mingzhou,Zhu Zhidong,Zhou Ziyu,Yan Zhiqiang,Huang Kai,Jiang Rongrong,Fan Xi,Jieensi Milayi,Pang Liewen,Wang Yiqing,Sun Xiaotian
Background Cardiovascular events secondary to stroke–collectively classified as stroke-heart syndrome–greatly impair the patient’s prognosis, however its underlying mechanism has yet to be determined. To investigate the mechanism of central neuroinflammation and its effects on stroke-heart syndrome, a temperature-ultrasound responsive brain-targeted drug delivery system, DATS/MION-LPE, was synthesized to specifically study neuroinflammation in the mouse middle cerebral artery occlusion (MCAO) model.Results The specific polymer of DATS/MION-LPE can close the nanoparticle pores at 37 °C, restricting drug release in the circulation. After the nanoparticles were targeted to brains, the polymer can be cleaved under external ultrasound irradiation, reopening the nanoparticle pores and allowing drug release, therefore directly managing the neuroinflammation. After a stroke, a significant cerebral inflammation occurred, with elevated IL-1β and pyrin domain-containing 3 (NLRP3) inflammasome. Accordingly, significantly increased histone deacetylase 6 (HDAC6) and decreased sirtuin 1 (SIRT1) were observed. An antagonistic relationship between HDAC6 and SIRT1 was found, which can jointly regulate the cerebral NLRP3 expression. The systemic IL-1β and ATP levels were increased after the stroke, accompanied by a significant heart injury including contractile dysfunction, elevated IL-1β levels, and oxidative stress. Meanwhile, neuroinflammation can trigger sympathetic nervous overexcitation with associated heart damage. DATS/MION-LPE can targetedly effect on ischemic brain, exhibiting cerebral and cardiac protective effects including downregulated cerebral NLRP3 and HDAC6 expressions, upregulated SIRT1 expressions in brain, reduced IL-1β and ATP in circulation, and alleviated cardiac impairment.Conclusion This study introduced the key role of neuroinflammation in stroke-heart syndrome and first investigated the crucial HDAC6/SIRT1-NLRP3 circuit in this process. Heart injury secondary to stroke is mediated by neuroinflammation induced systemic inflammatory responses and sympathoexcitation. DATS/MION-LPE is a unique tool and effective therapeutic agent, which provides new insights into combinational heart and cardiac protection.Graphical Abstract
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JOURNAL OF SOL-GEL SCIENCE AND TECHNOLOGY
·
2024
·
IF 2.3
Xu Peng,Wang Shasha,Dai Wei,Shi Weishan,Xing Gang,Wang Zhaogui,Li Qun,You Chaoqun,Hao Dejun
Abstract Pesticides play a crucial role in modern agriculture, yet their widespread use poses a threat to the ecosystem by causing significant environmental damage. In an effort to address this issue, a novel nanopesticide delivery system was developed, utilizing a tannic acid (TA)-Cu combination deposited onto the surface of dendritic mesoporous silica nanoparticles (DMSNs). This innovative approach aims to enhance the efficiency of pesticide utilization. The process involved incorporating Tebuconazole (Teb) into DMSNs using the one-pot sol-gel method. Subsequently, a coating was applied through the sequential addition of TA and CuCl 2 to an aqueous dispersion of Teb@DMSNs. The resulting nanopesticide, named TA@Teb@DMSNs, exhibited a spherical shape and achieved an impressive Teb loading rate of nearly 26.6%. Kinetic studies on Teb release revealed that TA@Teb@DMSNs demonstrated characteristics conducive to controlled and sustained release. The adhesion quality of TA@Teb@DMSNs on Aesculus chinensis Bunge leaves was confirmed through a comparative study with Teb@DMSNs. Additionally, when compared to Teb suspension, TA@Teb@DMSNs exhibited superior antifungal activity against Fusarium esculenta wilt over an extended period. Consequently, the TA@Teb@DMSNs constructed in this research might be used as an efficient nanopesticide formulation for advancing the sustainable development of agriculture. Graphical Abstract A novel nanopesticide delivery system is prepared by depositing of tannic acid-Cu complex on dendritic mesoporous silica nanoparticles, which effectively improves the adhesion and effective time of pesticide on the leaf.
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高影响因子
JOURNAL OF POLYMER RESEARCH
·
2025
·Vol. 32
·期 4
·1-14
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IF 2.8
Xian Changqing,Deng Tao,Sun Bocun,Yang Wenbo,Li Boyan,Li Youbing,Xia Tian,Yang Chaolong,Yang Yi
Self-healing polyurethanes are garnering attention as a smart material, and has significant application potential in aerospace, biomedical, and electronics fields. In this paper, castor oil is selected as a soft segment in place of petroleum-based polyol to enhance the mechanical properties of polyurethane while improving the mobility of molecular chains. Meanwhile, a polyurethane with good self-healing properties was successfully prepared by selecting 2,2`-Diaminodiphenyl disulfide (DTDA) containing disulfide bonds as a chain extender. As the proportion of DTDA increases, the initial thermal decomposition temperature of polyurethane decreases by 21°C. Cutting and tensile tests confirmed the high mechanical properties and self-healing characteristics of the polyurethane network. And the self-healing efficiency of the polyurethane materials was improved by prolonging the healing time and increasing the healing temperature. As the content of disulfide bonds and hard segments increased, the tensile strength of polyurethane increases progressively, the elongation at break decreased, and the R(stress) and R(strain) of each specimen tended to increase and then decrease. The healing efficiency of the specimen with a disulfide bond content of 13.45% was optimal, with both R(stress) and R(strain) reaching more than 99%.
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Scientific Reports
·
2024
·Vol. 14
·期 1
·1-14
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IF 3.8
Zheng Zihan,Liu YiZhen,Chen Danli,Yang Jianjun,Ren Lingxuan,Jin Zhen,Wang Weirong,Liu Xuyang,He Jianyu,Zheng Nanbo,Lin Rong
Background and purpose: Catalpol (CAT) has diverse pharmacological functions, including cellular homeostasis maintenance and anti-inflammatory effects. Sirtuin 5 (SIRT5) plays a considerable role in regulating cellular homeostasis in cardiac diseases. Our research explores the therapeutic potential of CAT against myocardial injury and its underlying mechanism. Methods: The H9c2 cells were pretreated with different CAT concentrations for 24 h, or CAT for 24 h followed by CoCl 2 stimulation. Cell viability was determined with MTT assay. Biochemical assays, western blotting, and quantitative real-time PCR (qRT-PCR), combined with bioinformatic analysis, were used to examine the impact of CAT on CoCl 2 -induced myocardial injury in H9c2 cells and further explore its molecular mechanisms. Results: CAT ameliorated levels of myocardial enzymes, increased nicotinamide adenine dinucleotide (NAD + /NADH) ratio and adenosine triphosphate (ATP), while inhibited lactic acid (LD), tumor necrosis factor-alpha (TNF-α), interleukin (IL)-1β, and IL-6 in CoCl 2 -induced H9c2 cells. Mechanistically, SIRT5 knockdown inhibited Lin28a expression and negated the effects of CAT on ATP level, LD content, and the expression of inflammatory factors in cells. CAT likely exerted its protective effects on myocardial function through the SIRT5-mediated signaling pathway. Conclusions: CAT regulates energy metabolism and inflammation via the SIRT5-mediated signaling pathway, exerting a protective effect in myocardial injury.
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MOLECULAR MEDICINE
·
2025
·Vol. 31
·期 1
·1-15
·
IF 6.4
Pei Lipeng,Zhu Yan,Li Wenpeng,Xu Bin,Sun Jingli
Background Uterine corpus endometrial carcinoma (UCEC) is one of the most frequent female genital malignant tumors. Targeting DNA damage and cell apoptosis are regarded as effective ways for UCEC therapy. Celastrol is a natural anti-cancer product from the Celastraceae plant family, while its role in UCEC has not been investigated. Methods UCEC cell lines Ishikawa and HEC-1-A were applied and treated with different concentrations of Celastrol. The appropriate and nontoxic concentrations were used for the subsequent experiments. Functional experiments analyzed the cell viability, cell cycle distribution, DNA damage, apoptosis and the expression of related proteins. We determined tumor growth in xenograft nude mice. Bioinformatic analysis, protein coimmunoprecipitation (Co-IP), luciferase assay, cell experiments were performed to reveal the relationship of Celastrol/KAT2B/RBPJ/MCM4 in UCEC. Results Treatment of Celastrol inhibited cell viability in a dose-dependent manner, and caused cell cycle arrest, accompanied by the downregulation of CDK2 and cyclin E expression and the upregulation of p21. Celastrol treatment resulted DNA damage and apoptosis in cultured cells, as demonstrated by increased number of TUNEL-positive cells, activity of caspase-3 and expression of cleaved-caspase-9, cleaved PARP1 and γ-H2AX. In xenograft nude mice, Celastrol also repressed tumor growth. Furthermore, lysine acetyltransferase KAT2B was a putative target of Celastrol, and its expression was upregulated by Celastrol in vitro and in vivo. Overexpression of KAT2B in UCEC inhibited cell proliferation and increased DNA damage and apoptosis. KAT2B knockdown overcame the anti-proliferative and pro-apoptotic roles of Celastrol. Moreover, Co-IP demonstrated that KAT2B bound to RBPJ, a transcriptional repressor, and increased the acetylation of RBPJ. RBPJ could bind to the MCM4 promoter to suppress the luciferase activity. Further functional analysis revealed that the functions of KAT2B in UCEC cell proliferation, DNA damage and apoptosis were mediated by MCM4, and Celastrol enhanced RBPJ acetylation and reduced MCM4 expression. Conclusions These results underscore that Celastrol is a promising anti-cancer agent in UCEC with preferential anti-proliferative, pro-apoptotic and DNA damage effects through the KAT2B/RBPJ/MCM4 axis, and KAT2B is a promising therapeutic target for UCEC. Graphical abstract
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BMC Oral Health
·
2024
·Vol. 24
·期 1
·1-10
·
IF 2.6
Li Shaoping,Jia Cancan,Han Haitong,Yang Yuqing,Xiaowen Yundeng,Chen Zhiyu
Background Polyetheretherketone (PEEK) is well known for its excellent physical–chemical properties and biosafety. The study aimed to open up a new method for clinical application of PEEK to reconstruct large-scale bone defects.Methods A bilayer scaffold for bone regeneration was prepared by combining a sulfonated PEEK barrier framework (SPEEK) with a hydrogel layer loaded with aspirin (ASA) and nano-hydroxyapatite (nHAP) by the wet-bonding of Polydopamine (PDA).Results The hydrogel was successfully adhered to the surface of SPEEK, resulting in significant changes including the introduction of bioactive groups, improved hydrophilicity, and altered surface morphology. Subsequent tests confirmed that the bilayer scaffold exhibited enhanced compression resistance and mechanical compatibility with bone compared to a single hydrogel scaffold. Additionally, the bilayer scaffold showed stable and reliable bonding properties, as well as excellent biosafety verified by cell proliferation and viability experiments using mouse embryo osteoblast precursor (MC3T3-E1) cells.Conclusion The bilayer bone regeneration scaffold prepared in this study showed promising potential in clinical application for bone regeneration.
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Scientific Reports
·
2025
·Vol. 15
·期 1
·1-10
·
IF 3.9
Hu Jian-Xiong,Chen Ying-Kai,Chen Shi-Jun,Lin Yan-Ya,Chen Jun-Nian,Xie Ying,Zhao Cheng-Fei,Chen Cun-Rong
To study the mechanism of calcitonin gene related peptide(CGRP) protecting acute pancreatitis based on metabolomics. 24 adult male rats were randomly divided into control group (Con), acute pancreatitis model group (AP), CGRP treatment group (CGRP + AP, abbreviated as CGRP) and CGRP antagonist(CGRP(8–37)) pretreatment group (preCGRP(8–37) + AP, abbreviated as CGRP37), with 6 rats in each group. After different interventions, pancreases of rats in each group were collected for pathological analysis, and serum was collected for metabolomics analysis. Pathological examination of the pancreas suggested that the inflammation of pancreatitis in AP group was significant, the inflammation of pancreatitis in CGRP group was significantly reduced, and the pancreatitis in CGRP37 group was aggravated. Metabolomics of rat serum suggested that the differences in metabolites in each group were mainly related to amino acid metabolism, coenzyme/vitamin metabolism, carbohydrate metabolism, lipid metabolism, digestive system and other metabolic pathways. According to the trend of metabolite changes, we found 6 differential metabolites that were significantly correlated with CGRP intervention, including L-Valine, 5-Aminopentanoic acid, 4-oxo-L-proline, L-glutamine, L-proline, and Ornithine, all of which were related to amino acid metabolism. CGRP can effectively protect acute pancreatitis, possibly by regulating amino acid metabolism to alleviate acute pancreatitis.
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