RSC Advances
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2025
·Vol. 15
·期 3
·1507-1513
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IF 4.6
Wei Li,Yan Wang,Hongkun Miao,Maohui Yan,Chen Liu,Yu Wang,Jianjun Zhang,Zhiguang Fu
Oral squamous cell carcinoma is one of the most common types of cancer. Surgical resection is one of the most important treatments at present. However, patients often suffer from regional recurrence after surgery. Therefore, new strategies for combination therapy need to be investigated. This work identified a smart injectable hydrogel system co-delivering DOX and sunitinib nanoparticles. The nano drugs are continuously released from the hydrogels and effectively taken up by cells. The nano drugs in the hydrogel can inhibit tumor cell viability and induce cancer cell apoptosis in vitro. The drug-loaded hydrogel could control the recurrence of subcutaneous xenograft tumors, prolong the survival time, and have no obvious toxicity in nude mice. These findings suggest that this smart injectable hydrogel system may provide new ideas for the comprehensive treatment of oral squamous cell carcinoma.
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JOURNAL OF COLLOID AND INTERFACE SCIENCE
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2024
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IF 9.4
Kang Xi,Yongdong Wang,Chengzhe Li,Yue Lei,Xin Xu,Lai Wei,Yunfang Gao
The application of solid-state electrolytes (SSEs) is anticipated to enhance the safety performance of lithium metal batteries (LMBs). However, the progress of SSEs has been hindered by the unstable electrode–electrolyte interfaces (EEIs). In this study, in-situ polymerization of 1,3-dioxolane (DOL) is employed for the preparation of SSEs, with the addition of tributyl borate (TBB) to establish stable EEIs, particularly under high-voltage conditions. On one hand, the addition of TBB promotes the dissociation of lithium salts and increases the concentration of free Li + , resulting in an increase in room temperature ionic conductivity to 1.13 × 10 −4 S cm −1 and an improvement in the Li + transference number to 0.69 for the prepared poly-DOL electrolytes (PDE-TBB). Benefiting from the enhanced Li + transport, the Li/PDE-TBB/Li symmetric cell exhibits a cycle life exceeding 1,000 h with a low polarization voltage as low as 12 mV, and the Li/PDE-TBB/LiFePO 4 cell demonstrates exceptional cyclic stability over 800 cycles at 1C, with a coulombic efficiency exceeding 99.8 % and a capacity retention of 89.6 %. On the other hand, PDE-TBB exhibits improved stability under high-voltage conditions and the capacity to establish robust boron-rich cathode electrolyte interphase (CEI) on the LiNi 0.8 Co 0.1 Mn 0.1 O 2 (NCM811) surface, thereby enhancing the structural stability of cathode materials and ensuring exceptional cycling performance of Li/PDE-TBB/NCM811cell. This work presents a promising strategy for developing novel ether-based SSEs suitable for high-voltage lithium metal batteries.
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BIOCHEMICAL PHARMACOLOGY
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2024
·
IF 5.3
Aijun Qian,Gengmiao Xiao,Zhuang Li,Yunping Mu,Xiaohong Liu,Xue Tian,Jianqin Yang,Allan Z. Zhao,Fanghong Li
The escalating obesity epidemic poses serious public health challenges, requiring the development of effective therapeutic strategies. In this study, we aimed to determine if recombinant glycoprotein hormone β5 (GPHB5) protein, particularly in the hybrid form with glycoprotein hormone α2 (GPHA2) (recombinant corticotroph-derived glycoprotein hormone, rCGH), can alleviate obesity in the genetically obese mice, ob/ob . Six-week-old male ob/ob mice were intraperitoneally injected for four weeks with rCGH (10 mg/kg) treatment. Body weight, fat mass and lean mass as well as energy expenditure were evaluated. Blood samples were collected to assess circulating concentrations of triiodothyronine (T3) and thyroxine (T4). Glucose and insulin tolerance tests were also conducted. rCGH significantly decreased body weight and fat mass, stimulated energy expenditure without alterations in food consumption, induced lipolysis and browning of white adipose tissue (WAT) by activating cyclic adenosine monophosphate (cAMP)/protein kinase A (PKA) signaling pathway. The treatment with the recombinant protein also led to marked reduction in hepatic steatosis, improved glucose tolerance and insulin sensitivity, and reduced triglycerides (TG), and total cholesterol (T-CHO) levels in ob/ob mice. In conclusion, rCGH attenuated obesity and alleviated metabolic syndromes in ob/ob mice, and it may represent a promising polypeptide-based drug candidate in treating obesity and obesity-related complications without interfering energy intake.
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SEPARATION AND PURIFICATION TECHNOLOGY
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2024
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IF 8.1
Qingdi Mu,Lujie Sheng,Shuhui Chen,Yuanfa Liu,Maicun Deng,Jizhong Ren
Defect engineering of metal organic frameworks (MOFs) is an emerging effective approach for manipulating their microporosity structure. They are very promising but challenging to achieve significant gas separation performance improvements for mixed matrix membranes (MMMs) fabrication. Herein, we propose a novel thermal induced in-situ defect engineering strategy of ZIF-8 in MMMs by carefully post controlled annealing (above polyimide matrix T g and below ZIF-8 T d ). Attractively, the thermal-triggered polyimide matrix (P84 HT) crosslinking repairs interfacial voids between ZIF-8 and P84 HT. The resulting advanced MMMs exhibit more gas sorption sites and diffusion pathways owing to the missing Zn-N bond of ZIF-8, while exciting enhancement of H 2 /CH 4 and H 2 /N 2 separation performance is obtained compared with the pristine P84 HT membrane. Furthermore, after in-situ defect engineering at 400 °C, the H 2 permeability of the advanced MMMs with 20 wt% ZIF-8 loading is 123.8 Barrer, 19.4 times higher than the pristine P84 HT membrane (6.4 Barrer), while the H 2 /CH 4 and H 2 /N 2 selectivity almost remains essentially unchanged. More importantly, this facile but very effective method demonstrates a new direction to regulate structure of polyimide/MOFs based MMMs for gas separation.
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Nature Communications
·
2024
·Vol. 15
·期 1
·1-10
·
IF 14.7
Zhang Wencong,Li Fan,Li Yi,Song Anran,Yang Kun,Wu Dongchang,Shang Wen,Yao Zhenpeng,Gao Wenpei,Deng Tao,Wu Jianbo
Intermetallic phases with atomic ordering are highly active and stable in catalysts. However, understanding the atomistic mechanisms of disorder-to-order phase transition, particularly in multi-component systems, remains challenging. Here, we investigate the atom diffusion and phase transition within Pd@Pt-Co cubic nanoparticles during annealing, using in-situ electron microscopy and ex-situ atomic resolution element analysis. We reveal that initial outward diffusing Pd partially substitutes Pt, forming a (Pt, Pd)-Co ternary system in the surface region, enabling the phase transition at a low temperature of 400 °C, followed by shape-preserved inward propagation of the ordered phase. At higher temperatures, excessive interdiffusion across the interface changes the stoichiometric ratio, diminishing the atomic ordering, leading to obvious change in morphology. Calculations indicate that the Pd-substitute in (Pt, Pd)-Co system leads to a significantly lower phase transition temperature compared to that of Pt-Co alloy and thus a lower activation energy for atomic diffusion. These insights into atomistic behavior are crucial for future design of multi-component systems.
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Journal of Functional Foods
·
2025
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IF 4
Lanlan Yang,Nian Yang,Yuanquan Ran,Huan Zhao,Qiong Hu,Yi Hong,Minyi Tian
Herein, the chemical constituents of Pittosporum glabratum leaf essential oil (EO) were analyzed, and its anticancer efficacy was explored in vitro and in vivo . Its primary phytochemicals were α -caryophyllene, ( E )- β -farnesene, and germacrene D. It displayed significant cytotoxicity against cancerous A549 cells and lower cytotoxicity against noncancerous MRC-5 cells. It induced cell cycle arrest in the G1 phase by downregulating CDK2-cyclin E1/2 and CDK4-cyclin D3 complexes and upregulating p21, thereby inhibiting A549 cell proliferation. It triggered A549 cell apoptosis via the mitochondrial pathway, resulting in the ratio increase of Bax/Bcl-2, ΔΨm decrease, Cyt c release, caspase-9 and caspase-3 activation, and PARP cleavage. It blocked migration ability by decreasing MMP-2, MMP-9, and N-cadherin levels. Additionally, it effectively suppressed tumor growth by inducing apoptosis of transplanted tumor cells in nude mice. Hence, P. glabratum leaf EO has remarkable anticancer properties and has great potential as an anticancer drug in the pharmaceutical field.
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International Journal of Nanomedicine
·
2024
·
IF 6.6
Xu Zuo,Yinuo Gu,Xiaoping Guo,Wenxue Zheng,Haoyu Zheng,Yiming An,Caina Xu,Fang Wang
Purpose Inhaled corticosteroids, including budesonide (BUD), are widely employed for the treatment of asthma. However, the frequent use of corticosteroids is associated with numerous adverse effects and poses challenges to ongoing drug therapy and patient adherence. Budesonide liposomal nanoparticles (BUD-LNPs) were developed to improve the bioavailability of the drug and thereby improve the effectiveness of asthma treatment.Methods BUD-LNPs were prepared via thin-film hydration, and the characterizations, stability, and in vitro release of BUD-LNPs were studied. In vitro cellular uptake was observed by laser-scanning confocal microscope (LSCM) and flow cytometry. And the in vitro anti-inflammatory activity of BUD-LNPs was evaluated by measuring the expression of pro-inflammatory cytokines in activated macrophages. Besides, the accumulation time in the lung of drugs delivered via liposomal carriers and free drugs was compared in vivo. And the in vivo therapeutic efficacy of BUD-LNPs was assessed in OVA-induced asthmatic mice. Finally, in vivo biosafety assessment was performed.Results The particle size, PDI, and zeta potential of BUD-LNPs were 127.63±1.33 nm, 0.27±0.02, and 3.33±0.13 mV, respectively. BUD-LNPs exhibited excellent biosafety and anti-inflammatory activity in vitro. Furthermore, compared with the free drugs, the utilization of liposomal nano-vehicles for drugs delivery could effectively extend the duration of drugs accumulation in the pulmonary system. Additionally, treatment with BUD-LNPs alleviated airway hyperresponsiveness, reduced airway mucus secretion, and mitigated pulmonary inflammation in OVA-induced asthmatic mice. And the BUD-LNPs demonstrated superior therapeutic efficacy compared to free BUD.Conclusion BUD-LNPs was successfully prepared with excellent stability and sustained release for 24 h in vitro. The data of anti-inflammatory activity, asthma therapeutic effects and safety studies indicated that drug delivery mediated by liposomal nano-vehicles was a feasible and desirable strategy for medical strategy and showed great promise in the clinical therapy of asthma.
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FOOD CHEMISTRY
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2024
·
IF 8.5
Aminu Shehu Abubakar,Bilal Ahmad,Nabi Ahmad,Liangliang Liu,Bin Liu,Yatong Qu,Jikang Chen,Ping Chen,Haohan Zhao,Jia Chen,Kunmei Chen,Gang Gao,Aiguo Zhu
Luobuma tea is made from the leaves of Apocynum hendersonii (Bt) and A. venetum (Ht) and has been used for a very long time in China and Japan as herbal tea. This study isolated water-soluble polysaccharides from the two species` teas. Physicochemical properties, structural properties, in vitro and in vivo antioxidant and immunomodulatory activities were determined for the first time. The results showed that the Bt and Ht polysaccharides with molecular weights of 31.21 and 49.11 kDa, respectively, composed of arabinose, galactose, rhamnose, glucose, xylose, fucose, and mannose. A dose-dependent nitric oxide production and interleukin-6 inhibitory effects were obtained. Also, they suppressed the expression of cyclooxygenase-2, tumor necrosis factor-α and interleukin-6 mRNA in LPS-induced RAW 264.7 macrophages. Likewise, Bt and Ht have significantly reduced edema in the paws of mice after carrageenan injection. These results suggested that the Luobuma teas polysaccharides can be explored as potential antioxidants and anti-inflammatory agents.
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ACS Nano
·
2024
·
IF 15.8
Jie Lu,Shu Zhang,Jianhua Yao,Ziyang Guo,Markus Osenberg,André Hilger,Henning Markötter,Fabian Wilde,Ingo Manke,Xiao Zhang,Fu Sun,Guanglei Cui
Rechargeable alkali metal–CO2 batteries, which combine high theoretical energy density and environmentally friendly CO2 fixation ability, have attracted worldwide attention. Unfortunately, their electrochemical performances are usually inferior for practical applications. Aiming to reveal the underlying causes, a combinatorial usage of advanced nondestructive and postmortem characterization tools is used to intensively study the failure mechanisms of Li/Na–CO2 batteries. It is found that a porous interphase layer is formed between the separator and the Li/Na anode during the overvoltage rising and battery performance decaying process. A series of control experiments are designed to identify the underlying mechanisms dictating the observed morphological evolution of Li/Na anodes, and it is found that the CO2 synergist facilitates Li/Na chemical corrosion, the process of which is further promoted by the unwanted galvanic corrosion and the electrochemical cycling conditions. A detailed compositional analysis reveals that the as-formed interphase layers under different conditions are similar in species, with the main differences being their inconsistent quantity. Theoretical calculation results not only suggest an inherent intermolecular affinity between the CO2 and the electrolyte solvent but also provide the most thermodynamically favored CO2 reaction pathways. Based on these results, important implications for the further development of rechargeable alkali metal–CO2 batteries are discussed. The current discoveries not only fundamentally enrich our knowledge of the failure mechanisms of rechargeable alkali metal–CO2 batteries but also provide mechanistic directions for protecting metal anodes to build high-reversible alkali metal–CO2 batteries.
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COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS
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2024
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IF 4.9
Mingwei Zhao,Ying Li,Caili Dai,Yingpeng Chen,Xin Sun,Xinyu Ge,Shixu Ma
In this work, a novel three-step method was used to modify the surface of silicon quantum dots to synthesize amphiphilic silicon quantum dots (A-SiQDs) with higher interfacial activity. The particle size of A-SiQDs was only 3.5 nm. By adding a small amount of dodecyl dimethyl betaine (BS-12), the performance of A-SiQDs was further improved. Through particle size and zeta potential testing, it can be seen that the mixed system of A-SiQDs and BS-12 had good temperature and salinity resistance, and can be stable at 120 °C and 50,000 mg/L NaCl. Meanwhile, the mixed system exhibited superior interfacial activity compared with individual A-SiQDs and BS-12. The mixed system can lower the interfacial tension from 32.15 mN/m to 1.82 mN/m and transform the rock surface from an oil-wet to a strong water-wet state. This ensured the excellent imbibition ability of the mixed system, which can increase the oil recovery to 35.7 %. Finally, from the perspective of force, the influence of nanofluids on oil stripping and migration was analyzed to reveal the imbibition mechanism. This paper proposes a facile three-step method for synthesizing A-SiQDs, and also provides a novel nanomaterial for high efficiency imbibition in low-permeability reservoirs.
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Bioengineering-Basel
·
2025
·Vol. 12
·期 1
·34
·
IF 3.7
Fang Chen,Run Guo,Tian Chen,Liping Liu,Fan Ding,Gang Zhao,Bo Zhang
Background: Cholesterol gallstone disease (CGS) is often accompanied by gallbladder contraction dysfunction and chronic inflammation, but effective therapeutic options remain limited. This study investigates whether a low-intensity pulsed ultrasound (LIPUS) treatment can improve gallbladder motility and alleviate chronic inflammation while exploring the underlying mechanisms. Methods: Gallbladder motility was assessed through in vitro and in vivo contraction tests, while bile condition was evaluated by observing bile crystal clearance. Tissue analysis and Western blotting were performed to examine the expression of the cholecystokinin A receptor (CCKAR) and α-smooth muscle actin (α-SMA) as markers of gallbladder smooth muscle health and the inflammatory microenvironment. Blood cholesterol levels were measured via biochemical assays. Results: LIPUS treatment obviously enhanced gallbladder contractility in response to CCK-8 stimulation and accelerated bile crystal clearance. It also reduced inflammatory cell infiltration and tissue edema, and promoted new capillary formation in the gallbladder, mitigating the progression of CGS. Furthermore, LIPUS restored CCKAR expression and improved the thickness of the gallbladder smooth muscle layer, providing a structural basis for increased smooth muscle contractility. Conclusion: LIPUS improves gallbladder motility and reduces chronic inflammation in CGS by enhancing CCKAR expression and smooth muscle integrity. These findings highlight the potential of LIPUS as a non-invasive therapeutic approach for managing CGS.
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MOLECULES
·
2024
·Vol. 29
·期 17
·4073
·
IF 4.2
Beihua Xu,Zhenyu Wang,Huimin Zhang,Xiao Xu,Mengjie Tang,Gang Wang,Zhongpeng Ding,Ruihao Yu,Meihong Ding,Ting Zhang,Senlin Shi
Objective: The aim of this study was to optimize the formulation of a C60-modified self-microemulsifying drug delivery system loaded with triptolide (C60-SMEDDS/TP) and evaluate the cytoprotective effect of the C60-SMEDDS/TP on normal human cells. Results: The C60-SMEDDS/TP exhibited rapid emulsification, an optimal particle size distribution of 50 ± 0.19 nm (PDI 0.211 ± 0.049), and a near-neutral zeta potential of −1.60 mV. The release kinetics of TP from the C60-SMEDDS/TP exhibited a sustained release profile and followed pseudo-first-order release kinetics. Cellular proliferation and apoptosis analysis indicated that the C60-SMEDDS/TP (with a mass ratio of TP: DSPE-PEG-C60 = 1:10) exhibited lower toxicity towards L02 and GES-1 cells. This was demonstrated by a higher IC50 (40.88 nM on L02 cells and 17.22 nM on GES-1 cells) compared to free TP (21.3 nM and 11.1 nM), and a lower apoptosis rate (20.8% on L02 cells and 26.3% on GES-1 cells, respectively) compared to free TP (50.5% and 47.0%) at a concentration of 50 nM. In comparison to the free TP group, L02 cells and GES-1 cells exposed to the C60-SMEDDS/TP exhibited a significant decrease in intracellular ROS and an increase in mitochondrial membrane potential (ΔψM). On the other hand, the C60-SMEDDS/TP demonstrated a similar inhibitory effect on BEL-7402 cells (IC50 = 28.9 nM) and HepG2 cells (IC50 = 107.6 nM), comparable to that of the free TP (27.2 nM and 90.4 nM). The C60-SMEDDS/TP group also exhibited a similar intracellular level of ROS and mitochondrial membrane potential compared to the SMEDDS/TP and free TP groups. Method: Fullerenol-Grafted Distearoyl Phosphatidylethanolamine-Polyethylene Glycol (DSPE-PEG-C60) was synthesized and applied in the self-microemulsifying drug delivery system. The C60-SMEDDS/TP was formulated using Cremophor EL, medium-chain triglycerides (MCT), PEG-400, and DSPE-PEG-C60, and loaded with triptolide (TP). The toxicity and bioactivity of the C60-SMEDDS/TP were assessed using normal human liver cell lines (L02 cells), normal human gastric mucosal epithelial cell lines (GES-1 cells), and liver cancer cell lines (BEL-7402 cells and HepG2 cells). The production of reactive oxygen species (ROS) after the C60-SMEDDS/TP treatment was assessed using 2′,7′-dichlorofluorescein diacetate (DCFDA) staining. The alterations in mitochondrial membrane potential (ΔψM) were assessed by measuring JC-1 fluorescence. Conclusions: The cytoprotection provided by the C60-SMEDDS/TP favored normal cells (L02 and GES-1) over tumor cells (BEL-7402 and HepG2 cells) in vitro. This suggests a promising approach for the safe and effective treatment of TP.
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