Nanomaterials
·
2025
·Vol. 15
·期 12
·897
·
IF 4.3
Haiwei Wu,Jiaming Zhang,Fangbo Zhao,Wei Fan,Song Yang,Jun Ma
In chlorination disinfection treatment, residual iodinated X-ray contrast media (ICMs) are the precursors to iodinated disinfection by-products (I-DBPs). This study employed CoFe2O4nanoparticle catalytic peracetic acid oxidation (CoFe2O4/PAA) to remove iopamidol (IPM) and control I-DBP formation. The experimental results demonstrated that over 90% of the IPM degradation was achieved in 40 min. The metastable intermediate (≡Co(II)-OO(O)CCH3), rather than the alkoxyl radicals, was identified as the dominant oxidation species (ROS). The electron transfer pathways between the metastable intermediate and IPM were oxygen-atom transfer and single-electron transfer. The monoiodoacetic acid formation potential (MIAAFP) was investigated. In ultraviolet-activated ClO−(UV/chlorine), a portion of I−generated through IPM dehalogenation underwent conversion to reactive iodine species (RIS), consequently elevating the MIAAFP. In CoFe2O4/PAA, the MIAAFP was less than 43% of that in UV/chlorine, which can be attributed to the complete conversion of I−into iodate IO3−without generating RIS. CoFe2O4/PAA is thus a promising treatment for removing ICMs and controlling I-DBP formation due to the efficient degradation of ICMs while avoiding the generation of RIS.
✓ 已验证
产品关联
DOI
PubMed
高影响因子
Journal of Cleaner Production
·
2021
·
IF 9.297
Chuankun Yin,Siji Zhou,Keyi Zhang,Jiale Bai,Yangyang Lv,Xuewen Zhang,Xiaoxia Li,Aihua Xu
p-Nitrophenol (PNP) is one of the highly toxic and mutagenic pollutants existed in aquatic environment. In this work, the crednerite CuMnO 2 nanoflake was prepared and used to degrade PNP with peroxymonosulfate (PMS) as the oxidant. It was found that CuMnO 2 exhibited much higher activity than other Cu-based catalysts such as CuO, Cu 2 O, CuFe 2 O 4 and CuFeO 2 , with 90% of PNP degraded after 10 min under mild reaction conditions. The catalyst was also stable during five successive runs. Sulfate and hydroxyl radicals produced from PMS reduction by Cu(I) species, as well as superoxide ions and single oxygen, contribute to the degradation of PNP. More importantly, the interactions between Mn and Cu species in CuMnO 2 were identified by X-ray photoelectron spectroscopy (XPS), fourier transform infrared spectroscopy (FT-IR) and linear sweep voltammetry (LSV), and were further confirmed by the control experiment with the mixture of Cu 2 O + Mn 2 O 3 . The results implied that the high valent Mn(III) species acted as Lewis acids to withdraw electron from PMS, resulting that the Cu(I) species can be easier oxidized to Cu(II) by PMS with the formation of radicals. These findings provide an ideal bimetallic heterogeneous catalyst and a new mechanism for PMS-mediated reaction.
研究领域:
环境科学
·
催化化学
✓ 已验证
DOI
高影响因子
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH
·
2017
·
IF 2.843
Ya-Wen Zhang,Guan Wu,Hui Dang,Kangzhe Ma,Su Chen
Organometal halide perovskites (such as CH3NH3PbX3, X = Cl, Br, I) have received enormous interest due to their strikingly photoelectric properties. Here we develop a facile ligand-assisted reprecipitation method to synthesize NH2CH═NH2PbX3 (NH2CH═NH2+, FA; X = Br and I) perovskite quantum dots (QDs) at room temperature. The FAPbX3 perovskite QDs with uniform monodispersity (sized 4–7 nm) display relatively high photoluminescence quantum yields (PLQYs) of 60–75%. Through manipulating the mixed-organic-cation reactions, we achieve a series of multicolored perovskite QDs with continuously controllable emission wavelengths from 460 to 565 nm. Furthermore, we discuss the influence of ligands (oleic acid and n-octylamine) on PL properties and stabilities of perovskite QDs. Finally, we have successfully designed a white LED via compositing perovskite QDs and poly(methyl methacrylate) (PMMA), which presents a high color rendering index. Considering those remarkable achievements, we believe our work will have great potential to meet various optoelectronic applications.
研究领域:
材料科学
·
光学工程
·
电子工程
✓ 已验证
DOI
高影响因子
LETTERS IN ORGANIC CHEMISTRY
·
2024
·Vol. 22
·期 1
·56-60
·
IF 0.7
Xin-Yu Lin,Guo-Jun Chen,Su-Zhe Wu,Ke-Xuan Xu,Xiao-Tian Zhang,Qi Feng
4-Hydroxyquinoline-2(1H)-ones exhibit multiple biological activities, and studying their synthetic methods is of great significance. In the presence of tetramethylguanidine and silver nitrate, 4-hydroxyquinoline-2(1H)-ones were efficiently synthesized from 2-ethynylanilines and carbon dioxide under atmospheric pressure. The reaction conditions, such as types of silver catalysts and reaction solvents, were optimized, and the applicability of the substrate was preliminarily investigated. This method provides an alternative pathway for the synthesis of 4-hydroxyquinoline-2(1H)-ones and the conversion and utilization of carbon dioxide.
研究领域:
有机化学
·
药物化学
✓ 已验证
DOI
高影响因子
Journal of Physical Chemistry C
·
2013
·
IF 4.814
Lei Huang,Xiuli Wang,Jinhui Yang,Gang Liu,Jingfeng Han,Can Li
The photocatalytic activity and stability of nanocrystals (NCs) are two important issues for their application in photocatalysis. In this work, we report a combined method to promote the photocatalytic activity as well as the stability of CdS NCs for photocatalytic H2 evolution. ZnS shell was grown on CdS NCs forming type I core/shell CdS/ZnS nanocrystals (NCs) to restrain the photocorrosion and passivate the trap states on CdS NCs. Thereafter, dual cocatalysts were loaded to promote the separation and transfer of electrons and holes from the core to outer surface for photocatalytic reactions. It is found that Pt and Ni are effective reduction cocatalysts (RCs) while PdS and PbS are effective oxidation cocatalysts (OCs) for promoting the charge separation and transfer. This strategy was also proved to be effective for other type I core/shell NCs, such as CdTe/CdS/ZnS NCs.
研究领域:
材料科学
·
光催化
✓ 已验证
DOI
高影响因子
EXPERIMENTAL NEUROLOGY
·
2020
·
IF 4.691
Shuai Zhang,Mei-Ling Yan,Lin Yang,Xiao-Bin An,Hong-Mei Zhao,Sheng-Nan Xia,Zhuo Jin,Si-Yu Huang,Yang Qu,Jing Ai
Chronic cerebral hypoperfusion (CCH) promotes the development of Alzheimer's pathology. However, whether and how CCH impairs the synaptic vesicle trafficking is still unclear. In the present study, we found that the hippocampal glutamatergic vesicle trafficking was impaired as indicated by a significant shortened delayed response enhancement (DRE) phase in CA3-CA1 circuit and decreased synapsin I in CCH rats suffering from bilateral common carotid artery occlusion (2VO). Further study showed an upregulated miR-153 in the hippocampus of 2VO rats. In vitro, overexpression of miR-153 downregulated synapsin I by binding the 3′UTRs of SYN1 mRNAs, which was prevented by its antisense AMO-153 and miRNA-masking antisense oligodeoxynucleotides ( SYN1-ODN ). In vivo , the upregulation of miR-153 elicited similar reduced DRE phase and synapsin I deficiency as CCH. Furthermore, miR-153 knockdown rescued the downregulated synapsin I and shortened DRE phase in 2VO rats. Our results demonstrate that CCH impairs hippocampal glutamatergic vesicle trafficking by upregulating miR-153 , which suppresses the expression of synapsin I at the post-transcriptional level. These results will provide important references for drug research and treatment of vascular dementia .
研究领域:
神经科学
·
分子生物学
·
神经退行性疾病
✓ 已验证
DOI
PubMed
高影响因子
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
·
2021
·
IF 3.575
Dequan Kong,Baoying Xie,Yuhang Li,Yaping Xu
Palmitoylethanolamide (PEA) offers a strong protection against BBB disruption and neurological deficits after cerebral ischaemic/reperfusion (I/R) injury. To date, these BBB protective effects of PEA are mainly attributed to PPARα-mediated actions. However, whether PEA protects against BBB disruption through direct regulation of cytoskeletal microfilaments remains unknown. Here, we identified PEA as a Rho-associated protein kinase (ROCK2) inhibitor (IC 50 = 38.4 ± 4.8 μM). In vitro data suggested that PEA reduced the activation of ROCK/MLC signaling and stress fiber formation within microvascular endothelial cells (ECs) after oxygen-glucose deprivation (OGD), and consequently attenuated early (0–4 h) EC barrier disruption. These actions of PEA could not be blocked by the PPARα antagonist GW6471. In summary, the present study described a previously unexplored role of PEA as a ROCK2 inhibitor, and propose a PPARα-independent mechanism for pharmacological effects of PEA.
研究领域:
神经科学
·
药理学
·
细胞生物学
✓ 已验证
DOI
PubMed
高影响因子
Journal of Functional Foods
·
2020
·
IF 3.701
Zhenbang Xiao,Shengtao Yang,Jiali Chen,Chengyong Li,Chunxia Zhou,Pengzhi Hong,Shengli Sun,Zhong-Ji Qian
Ultraviolet radiation B cause photoaging of the skin by enhancing the high expression of matrix metalloproteinases (MMPs) to degrade collagen and inhibit the synthesis of procollagen. Trehalose (TRE), a widely occurring natural disaccharide, has been shown to play a cytoprotective role in many pathological processes. However, few studies have evaluated whether it has anti-photoaging potential. In this study, we investigated the anti-photoaging and mechanism of action of TRE using Human immortalized keratinocytes (HaCaT) cells. The results indicated that TRE pretreatment effectively scavenges reactive oxygen species (ROS) accumulation induced by UVB and increases the content of certain endogenous antioxidant factors in HaCaT cells. TRE suppressed UVB-induced MMP expression by blocking mitogen-activated protein kinases (MAPKs), activator protein 1 (AP-1) and NF-κB signaling. TRE treatment increased procollagen I synthesis via activating transforming growth factor-β (TGF-β)/Smad pathway and demonstrated that TRE may be a potential natural disaccharide for photoaging therapy in the future.
研究领域:
皮肤科
·
细胞生物学
·
药理学
✓ 已验证
DOI
高影响因子
Collagen and Leather
·
2026
·Vol. 8
·期 1
·23
·
IF 10.1
Wei Nannan,Zhang Yuchen,Huang Wenjie,Tian Xinyu,Yao Linyan,Xiao Jianxi
Ultraviolet (UV) irradiation is a major cause of photoaging, driving oxidative stress, inflammation, and extracellular matrix (ECM) degradation. Collagen is central to dermal integrity, yet animal-derived sources pose immunogenic and pathogen risks, while recombinant collagens reported to date often lack the stable triple-helical architecture required for bioactivity. Here, we present a triple-helical recombinant humanized type I collagen (THRCI) that combines native-like conformation with excellent biosafety and regenerative efficacy. THRCI supported fibroblast adhesion, proliferation, migration, and collagen synthesis, while suppressing intracellular reactive oxygen species and pro-inflammatory cytokines. In zebrafish, THRCI reduced oxidative stress and alleviated UV-induced caudal fin atrophy. In a murine model of acute UV photodamage, topical THRCI accelerated epidermal recovery, restored hydration and barrier function, increased dermal density, and promoted collagen fiber remodeling, while downregulating IL-6 , IL-1β , MMP-1 , and MMP-9 . Collectively, these findings indicate that THRCI exhibits effective photodamage-repair properties in our established models and represents a promising animal-free collagen biomaterial for skin regeneration. Graphical The alternative text for this image may have been generated using AI.
✓ 已验证
DOI
高影响因子
JOURNAL OF ALLOYS AND COMPOUNDS
·
2026
·
IF 6.7
Jitang Chen,Qian Li,Chengbing Ma,Yupeng Yuan,Huiquan Li
The rational design of heterojunction photocatalysts is essential for overcoming the persistent challenge of charge recombination in solar water-splitting systems. Herein, a step-scheme (S-scheme) AgI/Bi₇O₉I₃ heterojunction was fabricated using a facile one-pot hydrothermal method, where deliberate interfacial engineering enables efficient charge separation and transfer. The optimized heterojunction demonstrated remarkable photocatalytic oxygen (O₂) evolution activity, achieving a rate of 2046.22 μmol·g⁻¹·h⁻¹ under visible-light irradiation (λ ≥ 420 nm)—3.1 and 1.97 times higher than those of pristine AgI and Bi₇O₉I₃, respectively. Ultraviolet photoelectron spectroscopy (UPS) and electron spin resonance (ESR) analyses collectively revealed that a built-in electric field formed at the interface drives the directional migration of electrons from AgI to Bi₇O₉I₃, following an S-scheme charge transfer pathway. This mechanism not only enhances the separation of photogenerated carriers but also preserves strong redox capabilities for the water oxidation reaction. This study presents an effective interfacial engineering strategy for developing high-performance heterojunction photocatalysts and provides fundamental insights into charge behavior in S-scheme photocatalytic systems.
✓ 已验证
产品关联
DOI
高影响因子
Nanoscale Advances
·
2023
·Vol. 5
·期 3
·830-839
·
IF 4.7
Yazhou Huang,Yunfei Zhang,Junyan Lv,Yinfeng Shao,Dongfang Yang,Yuan Cong
The sensitive detection of cardiac troponin I (cTnI) is of great significance for the early diagnosis of acute myocardial infarction (AMI). Herein, in order to fabricate an electrochemical biosensor for ultrasensitive cTnI detection, atomic layer deposition (ALD) was employed to directly deposit NbS2 nanoflakes (NFs) on carbon fiber paper (CFP). Due to the self-limiting reaction of ALD, NbS2NFs were deposited uniformly and accurately on the surface of carbon fibers by controlling the number of ALD cycles, which ensured ultrasensitive detection. Precise regulation of the nanoscale morphology and electrochemical performance of NbS2 nanoflakes via ALD cycles was observed in depth. Owing to the high surface area and conductivity, an anodic/cathodic current of ∼3.01 mA of NbS2NFs/CFP can be obtained. Subsequently, an electrochemical biosensor based on the excellent performance of NbS2NFs/CFP was fabricated. The ultrasensitive detection of cTnI in a linear range of 1 fM to 0.1 nM with a detection limit of 0.32 fM was achieved.
✓ 已验证
产品关联
DOI
PubMed
高影响因子
JOURNAL OF LUMINESCENCE
·
2022
·
IF 4.171
Shiyu Xiao,Shian Xie,Manbo Zhang,Shengmin Hu,Marc Adape,Jian Wang,Xinhui Zhang,Yongqin Wei,Wei Chen
Here we report two luminescent copper complexes with different structures and luminescent properties, the blue-green [CuI(dmpyHS) (PPh 3 ) 2 ]⸱CH 3 CN (CuPy-PPh 3 ) and the red [Cu 6 (dmpyS) 6 ]⸱H 2 O (CuPy). When the blue-green light (CuPy-PPh 3 ) is heated to above 147 °C, it loses the phosphine-containing ligand, PPh 3 , and turns into CuPy and instead emits red light. Many luminescent complexes show the change of luminescence properties when the temperature is lower than room temperature , while the luminescence change of CuPy-PPh 3 occurs during the heating process above room temperature. Even more interesting, the luminescence wavelength transition span is large, from blue-green light emission at 490 nm to red light at 676 nm. The luminescence of the two copper complexes covers the three primary colors of red, green and blue required for the formation of white light emitting diodes WLEDs, which has potential in the development of non-rare earth phosphor white color displays. The integration of CuPy-PPh 3 and CuPy on a 395 nm near-ultraviolet chip can assemble WLEDs with good white light properties, which provides a new way for the construction of rare earth-free phosphor WLEDs. The synthesis of the two luminescent copper complexes is simple and environmentally friendly. Even though the structures of two copper complexes have been reported, the synthesis methods are different from those in the related literature and the luminescence properties of these complexes have never been described previously. The red emission copper complex CuPy is obtained by the thermal conversion of the blue-green emission copper complex CuPy-PPh 3 , which is a new phenomenon discovered for the first time in this work.
✓ 已验证
产品关联
DOI
高影响因子