Journal of Magnesium and Alloys
·
2022
·
IF 11.813
Yongyang Zhu,Mili Liu,liming Zeng,Yin Wang,Daifeng Wu,Rui Li,Qing Zhou,Renheng Tang,Fangming Xiao
The hydrolysis of MgH 2 delivers high hydrogen capacity (15.2 wt%), which is very attractive for real-time hydrogen supply. However, the formation of a surface passivation Mg(OH) 2 layer and the large excess of H 2 O required to ensure complete hydrolysis are two key challenges for the MgH 2 hydrolysis systems. Now, a low-cost method is reported to synthesize MgH 2 @Mg(BH 4 ) 2 composite via ball-milling MgH 2 with cheap and widely available B 2 O 3 (or B(OH) 3 ). By adding small amounts of B 2 O 3 , the in-situ formed Mg(BH 4 ) 2 could significantly promote the hydrolysis of MgH 2 . In particular, the MgH 2 –10 wt% B 2 O 3 composite releases 1330.7 mL·g −1 H 2 (close to 80% theoretical hydrogen generation H 2 ) in H 2 O and 1520.4 mL·g −1 H 2 (about 95%) in 0.5 M MgCl 2 in 60 min at 26 °C with hydrolysis rate of 736.9 mL·g −1 ·min −1 and 960.9 mL·g −1 ·min −1 H 2 during the first minute of the hydrolysis, respectively. In addition, the MgCl 2 solution allows repeated use by filtering and exhibits high cycle stability (20 cycles), therefore leading to much reduced capacity loss caused by the excess H 2 O. We show that by introducing B 2 O 3 and recycling the 0.5 M MgCl 2 solution, the system hydrogen capacity can approach 5.9 wt%, providing a promising hydrogen generation scheme to supply hydrogen to the fuel cells.
研究领域:
材料科学
·
能源化学
·
无机合成
·
氢能技术
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表面工程
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DOI
高影响因子
JOURNAL OF CONTROLLED RELEASE
·
2021
·
IF 9.776
Chi Ming Laurence Lau,Ghodsiehsadat Jahanmir,Yu Yu,Ying Chau
Using hydrogels to control the long-term release of protein remains challenging, especially for in-situ forming formulations. The uncontrollable burst release in the initial phase, the halted release in the subsequent phase, and the undesired drug dumping at the late stage are some obstacles hydrogel-based depots commonly encounter. In this study, we report hydrolyzable dextran-based hydrogels crosslinked by Michael addition to demonstrate a systematic solution to solve these problems. First, the polymer concentration was used as the critical parameter to control the proportion of releasable versus physically trapped protein molecules in the initial hydrogel meshwork. Subsequently, the dynamic change of the hydrogel meshwork was modulated by the crosslinking density and the cleavage rate of ester linkers. To this end, we designed and synthesized a series of ester linkers with hydrolytic half-life ranging from 4 h to 4 months and incorporate them into the hydrogel. Controlled release was demonstrated for model proteins varied in size, including lysozyme (14 kDa), bovine serum albumin (66 kDa), immunoglobulin G (150 kDa), and bevacizumab (149 kDa). In particular, sustained release of IgG ranging from 10 days to 8 months was achieved. Lastly, a tunable multi-phase release profile was made feasible by incorporating multiple ester linkers into one hydrogel formulation. The linker's half-life determined each phase's release duration, and the linkers' mixing ratio determined the corresponding release fraction. The reported hydrogel design engenders a versatile platform to address the needs for long-term and readily adjustable protein release for biomedical applications.
研究领域:
生物材料
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药物递送
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生物医学工程
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产品关联
DOI
PubMed
高影响因子
Materials Today Bio
·
2025
·
IF 10.2
Tingting Li,Nianlu Li,Haoyu Sheng,Luyao Zhang,Qian Luo,Sashuang Liu,Yijing Zhao,Wenqiang Chen,Dexiang Liu,Zhen Wang
Inflammatory bowel disease (IBD) is a kind of chronic non-specific intestinal inflammatory disease, which accompanied by various abnormal psychological states, such as anxiety and depression. Nevertheless, the pathogenesis of IBD with depression is still unclear. Herein, we synthesized an enable a drinkable, liquid in situ-forming hydrogel, which form directly in the stomach through sequential ingestion of a crosslinker solution of CaCl 2 and ε-poly-l-lysine (ε-PL), followed by a drug-containing polymer solution of sodium alginate (SA). Using olsalazine (Olsa) and antioxidant (ellagic acid (EA) and ZnCl 2 ) as small molecule drug (referred as Olsa/EA/Zn), the resulting hydrogel (referred as Olsa/EA/Zn@SA/ε-PL hydrogel) could form rapidly in gastric fluid and exhibit remarkable stability under acidic conditions, unique low swelling properties and a rational release of drug in entering the intestine. We demonstrated that the oral administration of drug-loaded in situ-forming hydrogel with excellent antioxidant, anti-inflammatory activities, cytocompatibility, intestinal retention capacity of the drug, significantly enhanced the IBD therapeutic outcomes, and relieve accompanying depression-like symptoms in colitis mice. Overall, this designed in situ-forming hydrogel oral delivery system will open up new pathway in combined gastrointestinal therapy and psychological comorbidities for IBD patients, especially those with dysphagia.
研究领域:
药剂学
·
神经科学
·
胃肠病学
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产品关联
DOI
PubMed
高影响因子
Energy & Environmental Science
·
2019
·Vol. 12
·期 4
·1404-1412
·
IF 33.25
Jiamin Fu,Pengfei Yu,Nian Zhang,GuoXi Ren,Shun Zheng,Wencheng Huang,Xinghui Long,Hong Li,Xiaosong Liu
Adopting inorganic solid electrolytes (ISEs) is a promising approach to assemble batteries using Li metal anodes because of their superior Li-ion conductivity and high mechanical strength. This approach greatly improves the energy density and the safety of batteries. However, lithium dendrites still can pierce the bare ISE because of inhomogeneous current distributions at interfaces, leading to serious short circuits. This work proposes to reduce the interfacial resistance and prevent lithium dendrite growth simultaneously through in situ formation of interlayers enabled by a conversion reaction of MoS2 layers coated on a bare Li6.5La3Zr1.5Ta0.5O12 (LLZO) pellet. The interfacial resistance is reduced to only 14 Ω cm2, with the overpotential decreasing notably. The critical current density of cells is improved from 0.7 mA cm−2 to 2.2 mA cm−2. Furthermore, short circuits are significantly suppressed above the critical current density with the potential diverging quickly. The cell can be recovered to some extent by applying an inverse potential for a short time. The comparison between XPS and XAS measurements reveals that the nanoscale thin MoS2 layer in contact with the Li anode can be converted into an interlayer composed of Mo and Li2S through the conversion reaction. The sluggish kinetics of the conversion reaction resulting from the poor electronic conductivity makes the in situ-formed interlayer kinetically stable, which can hinder further reaction of MoS2 with Li effectively. Moreover, the in situ reaction could suppress the local tip electric field effect efficiently and make the current distribution more even. This study provides a new strategy to optimize the interface of anodes by screening for more candidates which undergo a conversion reaction.
研究领域:
材料科学
·
电化学
✓ 已验证
DOI
高影响因子
JOURNAL OF APPLIED ELECTROCHEMISTRY
·
2015
·Vol. 46
·期 1
·1-8
·
IF 2.409
Liang Xiaocai,Xiao Mingshu,Xu Minglu,Yang Dazhang,Yan Yuhua,Tian Yanping,Miao Yuqing
This study investigated the simultaneous in situ formation of Ni-based catalysts at the anode and cathode for glycerol oxidation and hydrogen evolution, respectively. The formation of electrocatalysts and their immobilization on the electrode surface occur simultaneously, avoiding the tedious and laborious procedures for the preparation and immobilization of the electrocatalysts. Ni salt in the homogeneous solution was deposited to repair the Ni-based electrocatalysts on the electrode surface, accompanied by the electrolysis of glycerol at the anode and the hydrogen evolution reaction at the cathode, exhibiting good working stability. This technique may find potential applications in the conversion of solar energy into storable fuels via the electrolysis of H 2 O or small molecules to produce hydrogen.
研究领域:
化学工程
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可再生能源
·
电催化
✓ 已验证
产品关联
DOI
高影响因子
ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH
·
2023
·Vol. 30
·期 31
·77488-77498
·
IF 5.8
Lan Bingyan,Hao Chenhui,Zhang Mengze,Yan Xiaomin
Two in situ formed Fe(III) oxyhydroxides (FeO x ) originated from ferrate reduction (designated FeO x –Fe VI ) and ferrous oxidation by H 2 O 2 (designated FeO x –Fe II ) were compared in the aspects of morphology, hydrolyzed species, surface binding mechanism of lead. The theoretical maximum adsorption capacity calculated from the Langmuir model toward Pb(II) was 929.54 and 810.37 mg/g Fe by FeO x –Fe VI and FeO x –Fe II , respectively. At pH 6 and the same Fe/Pb ratio, the kinetic rate of Pb removal by the FeO x –Fe VI process was 8 times faster. FTIR, SEM, and Ferron assay suggest FeO x –Fe VI was associated with a lesser polymerization degree and contained more reactive hydroxyl-Fe polymers than those in the FeO x –Fe II sample. SAXS verified that the particles possessed a smaller, more homogeneous, and open structure when Fe was hydrolyzed by ferrate reduction than ferrous oxidation. XPS coupled with fractal analysis suggests the different sorption capacities of Pb(II) can be ascribed to their distinct growth patterns. Fast cluster agglomeration during FeO x –Fe II fabrication decreased the exposure of effective adsorption sites. In comparison, the incompact assemblies of FeO x –Fe VI clusters facilitated Pb(II) ions to access the interstices of octahedral FeO 6 units and formed an edge-sharing complex. This work provides new insight into mechanisms of particle fabrication and heavy metal removal of Fe(III) formed in situ.
研究领域:
环境科学
·
材料科学
✓ 已验证
DOI
PubMed
高影响因子
JOURNAL OF BIOMATERIALS SCIENCE-POLYMER EDITION
·
2021
·
IF 3.517
Song Yang,Mengya Hu,Wenqing Liu,Nuohan Hou,Kaidi Yin,Chen Shen,Qing Shang
In this study, a novel PLGA in situ forming implants (ISFIs) were fabricated and methods for testing the in vitro release profiles were also developed. The correlations between in vitro release profiles and in vivo performances (in vitro–in vivo correlation, IVIVC) were also studied. PLGA with different molecular weights were selected as the polymeric matrix. Biocompatible N-methy1-2-pyrrolidone (NMP) or glyceryl triacetate (GTA) were used as the solvents with the ratios of NMP/GTA from 60/40 (vol/vol) to 20/80 (vol/vol). Eprinomectin (EPR) was chosen as the model therapeutic. In vitro release profiles of the EPR-loaded PLGA ISFIs were investigated using various methods (i.e. ‘tubule’ sample-and-separate and dialysis method). Sprague–Dawley rats were used to study the in vivo pharmacokinetics of EPR-loaded PLGA ISFIs. The release data obtained via ‘tubule’ sample-separate method had a good IVIVC (Level A, R2 > 0.99). These results showed that the ‘tubule’ sample-separate method was capable of discriminating the EPR-loaded ISFIs which were equivalent in formulation composition with manufacturing differences. Meanwhile, this method could be used to predict the in vivo performances of ISFIs in the investigated animal model.
研究领域:
药剂学
·
生物医学工程
✓ 已验证
产品关联
DOI
PubMed
高影响因子
BIOSENSORS & BIOELECTRONICS
·
2015
·
IF 6.409
Ting Hou,Lianfang Zhang,Xinzhi Sun,Feng Li
Herein, we reported a facile and highly sensitive biphasic photoelectrochemical (PEC) sensing strategy based on enzymatic product-mediated in situ formation of CdS quantum dots (QDs), and assayed the activity and inhibition of acetylcholinesterase (AChE) in its optimal state. Upon the hydrolysis of acetylthiocholine catalyzed by AChE, the product thiocholine stabilizes the in situ formation of CdS QDs in homogenous solution. Due to the electrostatic attraction , the resulting tertiary amino group-functionalized CdS QDs are attached to the surface of the negatively charged indium tin oxide (ITO) electrode, generating significant PEC response upon illumination in the presence of electron donors . By taking full advantage of the in situ formation of CdS QDs in homogenous solution, this strategy is capable of detecting AChE activity and inhibition in its optimal state. A directly measured detection limit of 0.01 mU/mL for AChE activity is obtained, which is superior to those obtained by some fluorescence methods . The inhibition of AChE activity by aldicarb is successfully detected, and the corresponding IC 50 is determined to be 13 μg/L. In addition to high sensitivity and good selectivity, this strategy also exhibits additional advantages of simplicity, low cost and easy operation. To the best of our knowledge, the as-proposed strategy is the first example demonstrating the application of CdS QDs formed in situ for biphasic PEC detection of enzyme activity and inhibition. More significantly, it opens up a new horizon for the development of homogenous PEC sensing platforms, and has great potential in probing many other analytes.
研究领域:
生物化学
·
分析化学
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产品关联
DOI
PubMed
高影响因子
CHEMISTRY-A EUROPEAN JOURNAL
·
2017
·Vol. 23
·期 36
·8712-8718
·
IF 5.317
Si-Yu Liu,Chao-Ying Fan,Han-Chi Wang,Jing-Ping Zhang,Xing-Long Wu
Graphical Anodes go bimetallic : On cycling of as-prepared 3D CoTiO 3 nanofibers, during the first lithiation process, along with the formation of a Li 2 O matrix, Ti IV and Co II species were converted/reduced to Li x TiO 2 nanoparticles (NPs) and metallic Co NPs, respectively, which suggested the electrochemical in situ formation of bimetallic transition-metal oxides (see figure). Bimetallic transition-metal oxides, which exhibit superior electrochemical properties compared with pristine single-metal oxides, have recently become a topic of significant research interest for applications in lithium-ion batteries (LIBs). Herein, we report a simple and scalable electrospinning method to synthesize porous CoTiO 3 nanofibers as the precursor for nanostructured bimetallic transition-metal oxides formed electrochemically in situ. This strategy ensures uniform mixing and perfect contact between two constituent transition-metal oxides during the lithiation/delithiation process. Furthermore, CoTiO 3 nanofibers based on ultrafine CoTiO 3 nanocrystals are interconnected to form a nano/microstructured 3D network, which ensures the high stability of the in situ formed structure composed of bimetallic transition-metal oxides, and also fast ion/electron transfer and electrolyte penetration into the electrode. Electrochemical measurements revealed the excellent lithium storage (647 mAh g −1 at 0.1 Ag −1 ) and retention properties (600 mAh g −1 at 1 Ag −1 after 1200 cycles) of the CoO/TiO 2 electrode. Moreover, the electrochemical reaction mechanism was explored by using ex situ X-ray photoelectric spectroscopy and cyclic voltammetry tests, which confirmed the two-phase reaction processes in the electrodes. These results clearly validate the potential of CoTiO 3 with a unique nano/microstructured morphology as the precursor for a bimetallic transition-metal oxide for use as the anode material for long-life LIBs.
研究领域:
材料科学
·
电化学
✓ 已验证
产品关联
DOI
PubMed
高影响因子
ACS Applied Materials & Interfaces
·
2022
·
IF 10.383
Chengyu Shi,Chunyu Zhao,Yinghao Chen,Youshen Wu,Junjie Zhang,Gang Chang,Ling He,Aizhao Pan
Conservation of sandstone-based cultural heritage has attracted a great deal of interest. We propose herein a novel protecting strategy, via in situ fabrication of bentonite-based hydrogels (B-H) inside sandstones, where the bentonite-based hydrogels serve as the underlying cement. To create bentonite-based hydrogels with controllable structure, possessing good mechanical and anti-swelling properties, we have optimized forming time, appearance, and viscosity. The hydrogel precursor penetrated into the pores of the sandstone; the hydrogel would then form within 3–5 h. As found by employing a fluorescent tracer, the precursor remained controllably in place without any apparent change in the sandstone morphology. The bentonite-based hydrogels that formed inside the sandstones presented strong hydrogen bonding, coordination, and ionic bonding, as well as strong mechanical interlocking to the sandstone matrix. As a result, the sandstones possessed enhanced mechanical compressive strength and excellent resistance to acid, salt, and freeze–thaw cycles. Our approach provides for a non-destructive, eco-friendly, easy-to-use, and long-term strategy for cultural preservation, one with excellent protection effects.
研究领域:
文化遗产保护
·
材料科学
·
地质学
✓ 已验证
DOI
高影响因子
CHEMICAL ENGINEERING JOURNAL
·
2024
·
IF 13.3
Zixuan Zhou,Zheng Chen,Chao Ji,Chenghao Wu,Jingzhu Li,Yicheng Ma,Shunxin Jin,Xiaowan Fang,Yixin Wu,Jingnan Xun,Shichu Xiao,Shige Wang,Yongjun Zheng
Burn wounds are characterized by complex physiological and pathophysiological response and the management of burn wounds is challenging. In situ-forming hydrogels and photothermal therapy (PTT) are promising treatments for wound healing. However, current research on biomaterials for burn treatment mainly focuses on either promoting healing or inhibiting scar formation, few studies have combined the two functions of one material. In this study, we prepared a multifunctional, in-situ cross-linked hydrogel termed CPOD hydrogel, which integrates carboxymethyl chitosan (CMCS), polyvinyl alcohol (PVA), oxidized hyaluronic acid (OHA), and dopamine (DA), coupled with photothermal therapy (PTT). In vitro experiments showed that the CPOD hydrogel had outstanding biocompatibility, suitable tissue adhesion and mechanical properties, excellent antimicrobial and antioxidant properties. This hydrogel showed PTT properties, which could produce mild heat in the early stage and higher temperatures in the later stage under NIR radiation. In the treatment of burn wounds of mice, application of CPOD hydrogel with PTT significantly promoted wound healing in the early stage and inhibited scar formation in the later stage, showing great potential for future innovation and application.
研究领域:
材料科学
·
生物医学工程
·
伤口愈合
✓ 已验证
产品关联
DOI
高影响因子
INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES
·
2020
·
IF 5.162
Linlin Hou,Yaliang Huang,Weilin Hou,Yurou Yan,Jinlin Liu,Ning Xia
Sensitive and accurate quantification of wild-type p53 protein is of great importance for biological research and clinical diagnosis. Herein, a modification-free amperometric biosensor was proposed for sensitive detection of wild-type p53 protein by the signal amplification of silver nanoparticles (AgNPs) networks formed in situ on electrode surface. Double-stranded DNA (dsDNA) probe containing two consensus sites was immobilized on gold electrode surface to capture wild-type p53 protein. The cysteine thiol and amine groups on the exterior of the protein allowed for the attachment of bare AgNPs through the Ag S or Ag N interactions. Meanwhile, benzene-1,4-dithiol (BDT) molecules in solution triggered the assembly of more AgNPs on electrode surface through the Ag S interactions, thus leading to the in situ formation of AgNPs networks for signal amplification. The target at the concentration as low as 0.1 pM can be readily determined. This method was further applied to determine wild-type p53 protein in spiked human serum and cell lysates with satisfactory results. Moreover, the biosensor is regenerative and does not require the modification of AgNPs with recognition element for signal readout. The modification-free strategy can potentially be applied to develop novel biosensors for detection of other biological macromolecules.
研究领域:
生物传感器
·
癌症诊断
·
分析化学
·
分子生物学
✓ 已验证
产品关联
DOI
PubMed
高影响因子
危险品化学品经营许可证（带存储）