Frontiers in Pharmacology
·
2021
·
IF 5.811
Li Pengfei,Peng Jun,Li Yuexin,Gong Lili,Lv Yali,Liu He,Zhang Tianhong,Yang Song,Liu Hongchuan,Li Jinglai,Liu Lihong
Background: Akebia saponin D (ASD) has a variety of biological activities and great medicinal potential, but its oral bioavailability is so low as to limit its development. Its pharmacokinetic profiles and excretion and metabolism in vivo have not been fully elucidated. This study was an attempt in this area.Methods: A simple LC-MS/MS method to simultaneously quantify ASD and its metabolites M1∼M5 in rat plasma, feces, urine and bile was established with a negative ESI model using dexketoprofen as the internal standard. Meanwhile, the UPLC-HR/MS system was used to screen all possible metabolites in the urine, feces and bile of rats, as compared with blank samples collected before administration. Absolute quantitative analysis was for M0, M3, M4, and M5, while semi-quantitative analysis was for M1, M2, and Orbitrap data.Results: The AUC0-t values after intravenous administration of 10 mg/kg and intragastrical administration of 100 mg/kg ASD were 19.05 ± 8.64 and 0.047 ± 0.030 h*μg/ml respectively. The oral bioavailability was determined to be extremely low (0.025%) in rats. The exposure of M4 and M5 in the oral group was higher than that of M0 in the terminal phase of the plasma concentration time profile, and ASD was stable in the liver microsome incubation system of rats, but metabolism was relatively rapid during anaerobic incubation of intestinal contents of rats, suggesting that the low bioavailability of ASD might have been attributed to the poor gastrointestinal permeability and extensive pre-absorption degradation rather than to the potent first pass metabolism. This assertion was further verified by a series of intervention studies, where improvement of lipid solubility and intestinal permeability as well as inhibition of intestinal flora increased the relative bioavailability to different extents without being changed by P-gp inhibition. After intravenous administration, the cumulative excretion rates of ASD in the urine and bile were 14.79 ± 1.87%, and 21.76 ± 17.61% respectively, but only 0.011% in feces, suggesting that the urine and bile were the main excretion pathways and that there was a large amount of biotransformation in the gastrointestinal tract. Fifteen possible metabolites were observed in the urine, feces and bile. The main metabolites were ASD deglycosylation, demethylation, dehydroxylation, decarbonylation, decarboxylation, hydroxylation, hydroxymethylation, hydroxyethylation and hydrolysis.Conclusion: The pharmacokinetics, bioavailability, metabolism and excretion of ASD in rats were systematically evaluated for the first time in this study. It has been confirmed that the ultra-low oral bioavailability is due to poor gastrointestinal permeability, extensive pre-absorption degradation and biotransformation. ASD after iv administration is not only excreted by the urine and bile, but possibly undergoes complex metabolic elimination.
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JOURNAL OF MOLECULAR LIQUIDS
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2021
·
IF 6.165
Hongjun Zang,Jing Lou,Shuolei Jiao,Huanxin Li,Yannan Du,Jiao Wang
Chitin and its derivatives contain biologically fixed nitrogen elements, which can provide nitrogen sources for N-containing chemicals. Herein, a series of pyridinium-based ionic liquids were synthesized to directly catalyze the conversion of N -acetyl-D-glucosamine (NAG, the monomer of chitin) to 3-acetamido-5-acetylfuran (3A5AF). The yield of 3A5AF in 1-carboxymethyl pyridinium chloride ionic liquid reached 37.49%, without any additives. Using B 2 O 3 and CaCl 2 as additives, the optimum yield increased to 67.37% at 180 °C in 20 min. In addition, HPLC-MS analysis has been utilized to elucidate the reaction mechanism. This research on turning “waste” into “wealth” opens up new ways for the utilization of biomass waste, which not only reduces environmental pollution but also has potential economic value.
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JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY
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2020
·
IF 4.192
Xutian Zheng,Chaolun Liu,Jiye Hu
Since 2,4-dichlorophenoxy acetic acid (2,4-D) was discovered in the 1940s, 2,4-D and its derivatives remain among most commonly used herbicides in the world. There have been recent increases in using 2,4-D products in a combination with other herbicides such as metribuzin and acetochlor to control noxious weeds. However, accurate analysis of 2,4-D isooctyl ester remains to be improved due to long analysis time and rapid conversion of the ester to acid (i.e., under-reporting residues). In this work, a simple hydrolysis procedure was introduced to provide a quantitative hydrolytic rate of the ester (>95%) and did not affect the other pH-sensitive compounds. Analysis parameters and sample pretreatments were optimized for improved selectivity and accuracy. The hydrolysis-QuEChERS (quick, easy, cheap, effective, rugged, and safe) technique for multidetermination of 2,4-D isooctyl ester, metribuzin, acetochlor, and 2-ethyl-6-methylaniline in corn and soybeans via high performance liquid chromatography–tandem mass spectrometry was established. The method had average recoveries of 74–109% with relative standard deviations ≤13.5% and limits of quantifications (LOQs) of 0.05 mg/kg. The terminal residues of these compounds found in real edible matrixes were less than the corresponding LOQs at harvest time. The risk quotients were far below 100%, indicating a low health risk to consumers.
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ChemSusChem
·
2019
·Vol. 13
·期 4
·803-810
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IF 7.804
Chengyi Zhu,Yannan Zhang,Xiaohua Yu,Peng Dong,Jianguo Duan,Jiaming Liu,Jianxiong Liu,Yingjie Zhang
Graphical Progress towards the positive : A facile strategy through manipulating KMnO 4 concentration is introduced to precisely fabricate 1 D LiMn 2 O 4 nanorods with four distinct diameter gradients. The LiMn 2 O 4 nanorod with a critical diameter of approximately 70–80 nm displays the highest discharge capacity and promising cycling performance. The role of 1 D crystal size in effecting interface chemical species and electrochemical performance is elucidated by comparative characterization methods. The morphology and size of nanoelectrode materials determine their properties. Compared to the bulk structure electrodes, 1 D electrode materials for Li-ion batteries have been intensively studied owing to their excellent Li + diffusion kinetics. It is generally accepted that smaller-sized electrode materials lead to better Li storage kinetics. In this study, this is found to not be the case in 1 D LiMn 2 O 4 positive materials. A facile strategy of manipulating the KMnO 4 concentration is introduced to precisely fabricate 1 D LiMn 2 O 4 nanorods with four distinct diameter gradients from 30 to 170 nm. The role of 1 D crystal size in effecting interface chemical species and electrochemical performance is elucidated by comparative characterization methods. X-ray photoelectron spectroscopy (XPS) Ar-ion etching technology shows that the Mn 2+ is electrochemically inactive on the surface of the sample, which explains the adverse effects observed on LiMn 2 O 4 nanorods with the minimum diameter of 30–40 nm, such as decreased discharge capacity. The LiMn 2 O 4 nanorod with a critical diameter of approximately 70–80 nm displays the highest discharge capacity and promising cycling performance. This work clarifies an important property that has previously been neglected and deepens the understanding for design of Mn-based positive materials.
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Journal of Oleo Science
·
2023
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IF 1.5
Ting Wu,Yueqing Xie,Zhikai Wu,Yifei Li,Mingzhen Jiang,Hongsen Yu,Xuhai Li,Jingjing Wang,Ershun Zhou,Zhengtao Yang
Acute liver injury (ALI), posing a serious threaten to our life, has emerged as a public health issue around the world. β-carotene has plenty of pharmacologic effects, such as anti-inflammatory, antioxidant, and antitumor activities. In this study, we focused on studying the protective role and potential molecular mechanisms of β-carotene against D-galactosamine (D-GalN) and lipopolysaccharide (LPS) induced ALI. Our results indicated that β-carotene pretreatment effectively hindered abnormal changes induced by LPS/D-GalN in liver histopathology. Meanwhile, serum levels of alanine aminotransferase (ALT) and aspartate aminotransferase (AST) were downgraded with β-carotene pretreatment. β-carotene pretreatment also decreased malondialdehyde content and myeloperoxidase activity, increased glutathione peroxidase and superoxide dismutase levels, and reduced the levels of tumor necrosis factor-a (TNF-α) and interleukin 6 (IL-6) in liver tissues. Further investigations found that β-carotene mediated multiple signaling pathways in LPS/D-GalN-induced ALI, inhibiting NF-κB and MAPK signaling and upregulating the expression of Nrf2 and HO-1 proteins. All findings indicate that β-carotene appears to protect mice against LPS/D-GalN induced ALI by reducing oxidative stress and inflammation, possibly via regulating NF-κB, MAPK, and Nrf2 signaling.
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Advanced Healthcare Materials
·
2023
·
IF 10
Hanru Zhang,Zhiyu Wu,Jingjing Zhou,Zhaopeng Wang,Changyan Yang,Panpan Wang,Muhammad Subaan Fareed,Yuhang He,Jie Su,Ruitao Cha,Kairong Wang
Peptide hydrogels were believed to be potential biomaterials with wide application in the biomedical field because of their good biocompatibility, injectability, and three-dimensional (3D) printability. Most of the previously reported polypeptide hydrogels are composed of L-peptides, while the hydrogels formed by self-assembly of D-peptides are rarely reported. Herein, we reported a peptide hydrogel constructed by D-J-1, which was the all-D-enantiomer of antimicrobial peptide Jelleine-1. Field emission scanning electron microscope (FE-SEM) and rheologic study were performed to characterize the hydrogel. Antimicrobial, hemostatic, and anti-adhesion studies were carried out to evaluate its biofunction. Our results showed that D-J-1 hydrogel was formed by self-assembly and cross-linking driven by hydrogen bonding, hydrophobic interaction, and π-π stacking force of aromatic ring in the structure of D-J-1. It exhibited promising antimicrobial activity, hemostatic activity, and anti-adhesion efficiency in a rat sidewall defect-cecum abrasion model. In addition, it also exhibited good biocompatibility. Notably, D-J-1 hydrogel showed improved in vitro and in vivo stability when compared with its L-enantiomer J-1 hydrogel. Therefore, the present study would provide new insight into the application of D-peptide hydrogel, and provide a new peptide hydrogel with antibacterial, hemostatic, and anti-adhesion efficacy for clinical use. This article is protected by copyright. All rights reserved
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OPTICS AND LASER TECHNOLOGY
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2023
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IF 5
Ke Yang,Zhengkun Wang,Jie Zhang
To address the non-uniformity of hotspots and large background noise signals in the Raman spectrum of traditional surface-enhanced Raman scattering (SERS) probes, this paper presents a high-sensitivity and high-uniformity D-shaped fiber (DSF) SERS probe. The probe is prepared by transferring monolayer silver nanoparticles (AgNPs) with different particle sizes onto the DSF using a liquid-liquid interface method. The electromagnetic distribution on the DSF SERS probe is analyzed with FDTD (finite difference time domain) Solutions simulation software, and the corresponding theoretical enhancement factors are calculated. The DSF SERS probe decorated by AgNPs with a diameter of 100 nm exhibits the largest electric field value among our prepared samples. The experiments are conducted to compare two collection methods with backward and vertical directions The results show that vertical collection offers better Raman enhancement due to the suppression of background noise of the fiber, with a limit of detection (LOD) of 10 −11 mol/L for Rhodamine 6G (R6G). The experimental analytical enhancement factor (AEF) at 611 cm −1 is 1.7 × 10 9 . Furthermore, the multi-molecular detection performance of the DSF SERS probe is experimentally studied and realized successfully.
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AFRICAN JOURNAL OF BIOTECHNOLOGY
·
2017
·Vol. 16
·期 50
·2307-2316
·
IF 0
Haiyuan Liu,Shu Han,Liping Xie,Jie Pan,Wei Zhang,Guihua Gong,Youjia Hu
2-C-Methyl-D-erythritol-4-phosphate (MEP) pathway has been extensively employed for terpenoids biosynthesis in Escherichia coli. In this study, to obtain key-enzymes of MEP pathway for squalene production, overexpression of different combination of MEP pathway genes were compared. Squalene production in strain YSS12 with overexpressed dxs, idi and ispA of MEP pathway from E. coli was improved by 71-fold when compared with strain YSS3 which only contained double copy SQS. Analysis of transcriptional levels of MEP pathway genes in engineering strains showed that different squalene production can be attributed to changed transcriptional levels of co-overexpressed genes dxs, idi, ispG and ispA in engineering strains. Furthermore, different E. coli expression hosts were compared for squalene production, among which BL21(DE3) was the best squalene producer. These results illustrate that dxs, idi and ispA of the MEP pathway from E. coli were key-enzymes for squalene production in E. coli. These key-enzymes of MEP pathway could also be applied to other terpenoids production in E. coli.
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APPLIED CATALYSIS B-ENVIRONMENTAL
·
2025
·
IF 21.1
Su Li,Jinkai Qiu,Zijun Bian,Bin Shao,Zhicheng Liu,Cheng Lian,Honglai Liu,Jun Hu
The dry reforming of carbonate with methane (CaDRM) can be one of the breakthrough technologies to address the challenge of mitigating inevitable CO 2 emissions into value-added chemicals but remains great challenges for efficient catalysts design. In this study, we break the trade-off between the catalytic activity and the carbon deposit by tailoring the d-band center of Ni through Fe doping, which matches the energy level of CH 4 * dehydrogenation but is far away from that of the over cleavage of CH* . In this light, the porous spherical Fe x Ni/Al 2 O 3 catalysts with Ni 3 Fe alloy nanoaggregates are obtained through a one-step spray drying method. The optimized Fe 0.6 Ni/Al 2 O 3 catalyst shows an excellent catalytic activity with a superior CO selectivity of 91.75 % at a complete CaCO 3 conversion at 700°C, and successfully prevents the carbon deposit to maintain its excellent stability. Moreover, the extremely low activation energy of 45.2 kJ/mol and the good porosity of Fe x Ni/Al 2 O 3 ensure its fast dynamics. Therefore, this tailoring d-band center approach through the formation of alloy catalysts supplied a novel strategy for effectively cracking hydrogen species while avoiding over cleavage of CH x * in the thermal catalysis, which promoted the CaDRM technology to be a promising solution for carbon neutrality in industrial sectors in near future.
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RSC Advances
·
2013
·Vol. 3
·期 30
·12313-12319
·
IF 2.562
Bing Liu,Zehui Zhang
In this study, prepared silica supported sulfonic acid was used as a heterogeneous catalyst for the production of 5-ethoxymethylfurfural (EMF) from fructose based carbohydrates and the synthesis of ethyl D-glucopyranoside from glucose based carbohydrates in ethanol. EMF was obtained in a high yield of 83.8% from 5-hydroxymethylfurfural (HMF) after 10 h, and a 63.1% yield was obtained from fructose at 100 °C for 24 h. Temperature experiments demonstrated that a higher reaction temperature (in the case of 120 °C) resulted in side reactions such as polymerization of HMF and alcoholysis of HMF into ethyl levulinates. When di- and poly-saccharides (sucrose and inulin) were used, the fructose moieties in sucrose and inulin were also successfully converted into EMF. However, the silica supported sulfonic acid catalyst was inert for the production of EMF from aldose based carbohydrates such as glucose and cellobiose. Ethyl D-glucopyranoside was formed in a high yield of 91.7% from glucose. More importantly, the catalyst could be reused several times without losing its catalytic activity with an average EMF yield of around 60% from a one-pot reaction of fructose. This work provides a good outlook for the conversion of carbohydrates into fine chemicals and biofuel additive.
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APPLIED CATALYSIS B-ENVIRONMENTAL
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2024
·
IF 20.2
Yuan Qin,Zihao Ou,Chaozhong Guo,Yao Liu,Rong Jin,Chuanlan Xu,Haifeng Chen,Yujun Si,Honglin Li
Regulating the electronic structure by phosphor-doping is a preferred strategy to boost the performance of carbon-based catalysts for oxygen reduction reaction (ORR). Here, a porous Fe, P, N-codoped carbon catalyst (PCF-FeTz-900) is designed by a phytic acid-assisted thermal etching strategy, in which P atoms are first doped into the carbon matrix to form a stable P C bond, and then FeN 4 sites are produced from Fe-2,4,6-Tris(2-pyridyl)-s-triazine complex (Fe-TPTz). Theoretical calculations suggest that the electrons are transferred from the doped P atom to the neighboring FeN 4 sites, which facilitates the ORR at the Fe sites by reducing the energy barrier and the adsorption energy of intermediates. Additionally, the P-doped FeN 4 (FeN 4 P) structure manifests a lower free energy difference than that of FeN 4 and the d -band center of Fe is also lowered, which further ensures its higher ORR catalytic ability. As a result, the PCF-FeTz-900 catalyst exhibits superior ORR activity and stability in alkaline electrolyte, and the assembled primary zinc-air battery shows greater performances compared to the commercial Pt/C catalyst. This work can provide an effective pathway for modulating the performance of doped-carbon materials in energy conversion devices.
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ADVANCED MATERIALS
·
2025
·
IF 26.8
Rubing Bai,Peihao Huo,Nanlong Zheng,Yujia Li,Wenchao Yan,Peiyu Fang,Xiaoyu Zhou,Zuqiang Bian,Zhiwei Liu
Light-emitting electrochemical cells (LECs) have good prospects in the solid-state lighting field due to their simple single-layer structure and low manufacturing cost. However, the lack of high-efficiency blue LECs limits their development and further application. To solve this problem, many luminescent materials with various mechanisms such as fluorescence, phosphorescence, and thermally-activated delayed fluorescence are studied as emitters in LECs. Besides these materials, herein lanthanide europium(II) (Eu(II)) complex with d-f transition is demonstrated as a new type of emitter for LECs. In detail, a blue emitting Eu(II) complex bis[hydrotris(3-tert-butylpyrazolyl)borate]europium(II) is dispersed into 9-(3-(triphenylsilyl)phenyl)-9H-3,9′-bicarbazole host and tetrahexylammonium tetrafluoroborate electrolyte to make a blend film, which attains a high photoluminescence quantum yield of ≈100%. The LEC using the blend film as an active layer achieves a blue emission with Commission Internationale de L'Eclairage coordinates of (0.12, 0.18) and a record-breaking external quantum efficiency of 19.8%, corresponding to an exciton utilization efficiency of ≈100%. This work reveals that Eu(II) complex with d-f transition is a promising emitter toward high-performance blue LECs, which can inspire further research on Eu(II) complex based LECs.
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