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SEPARATION AND PURIFICATION TECHNOLOGY · 2022 · IF 9.136

HKUST-1-Derived Cu@Cu(I)@Cu(II)/Carbon adsorbents for ciprofloxacin removal with high adsorption performance

Fei Yu,Xueting Bai,Mingxing Liang,Jie Ma

Considering the increasingly serious levels of antibiotic pollution, it is necessary to find new and efficient adsorbents. In this study, the adsorptive removal of a model quinolone antibiotic, ciprofloxacin (CIP), from wastewater is presented using a metal–organic framework (MOF)-derived carbon. HKUST-1-derived carbon (HDC-1100) was obtained by high-temperature carbonization of the HKUST-1 precursor at 1100 °C. HDC-1100 has a regular octahedron shape decorated with Cu/Cu 2 O particles and has a microporous and mesoporous structure with abundant oxygen-containing functional groups on the surface. Within 48 h, HDC-1100 could reach adsorption equilibrium for 30 mg·L -1 CIP, and the kinetic data were fitted with a pseudo-first-order model and a pseudo-second-order model. In this study, the maximum adsorption capacity of HDC-1100 for CIP was as high as 592 mg·g −1 . The high adsorption capacity is attributed mainly to metal–organic complexation, electrostatic interactions, and hydrogen bonding. Also, the effects of environmental factors, such as pH, ionic strength, and humic acid, on the adsorption capacity were considered. This study is significant for the treatment of high-concentration antibiotic-polluted wastewater.

CAS / MDL: 64-17-5
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Advanced Optical Materials · 2022 ·Vol. 10 ·期 13 ·2200278 · IF 10.05

Highly Luminescent Copper(I) Halide Phosphors Encapsulated in Fumed Silica for Anti-Counterfeiting and Color-Converting Applications

Maosheng Chen,Chenyu Ye,Chengqin Dai,Ruijuan Qi,Hanmei Fu,Chunhua Luo,Hui Peng,Hechun Lin

Luminescent Cu(I) hybrid materials are currently receiving increasing attention due to their rich photophysical properties with promising phosphors applications. However, the complex synthesis processes usually involving chemotoxic organic solutions largely hinder their practical applications. Herein, the authors introduce the highly luminescent copper(I) halide phosphors encapsulated in fumed silica synthesized via aqueous mechanochemical process. By using different precursors, they obtain blue, green, and orange emission copper(I) halide phosphors with high photoluminescence quantum yields. The green emission is owing to the formation of the well-known 0D (18-crown-6) 2 Na 2 (H 2 O) 3 Cu 4 I 6 (CNCI), while the blue and orange emissions are ascribed to the formation of the novel 1D (18-crown-6) 2 Na 2 (H 2 O) 3 Cu 2 Cl 4 (CNCCl) and 0D (18-crown-6) 2 Na 2 (H 2 O) 3 Cu 4 Br 6 (CNCBr) crystal structures, respectively. It is demonstrated that waterborne luminescent inks can be directly prepared from those phosphors via blending them with various waterborne polymers. The combination of three primary colors can lead to various spectra with multiple anti-counterfeiting functions. Further, such phosphors can also be embedded into polystyrene resin to form homogeneous luminescent composites, which can be used to prepare free-standing luminescent films and fabricate light-emitting diode (LED) with tunable emissions. This strategy opens a new avenue for the development of low-cost, highly luminescent phosphors.

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Analytical Methods · 2022 ·Vol. 14 ·期 20 ·1963-1972 · IF 3.532

The recognition of aristolochic acid I based on fluorescence quenching of bovine serum albumin-stabilized gold nanoclusters

Yating Lu,Yue Guo,Xiao Liang,Huimin Huang,Xue Ling,Zhiheng Su,Yonghong Liang

Aristolochic acid I (AAI) is one of the nephrotoxic derivatives present in genera Aristolochia and Asarum. Although some detection strategies for monitoring AAI have been reported, the application of these methods is limited because they involve tedious preparation and require professional operation. In this work, bovine serum albumin (BSA) has been introduced as a reducing agent and stabilizing agent to synthesize gold nanoclusters with strong red fluorescence for the rapid and effective detection of AAI. Under excitation at 328 nm, the fluorescence intensity at the maximum emission wavelength of the bovine serum albumin-stabilized gold nanoclusters (BSA-AuNCs) decreased with the addition of AAI, and the degree of quenching showed a linear relationship with the concentration of AAI from 0.1–12.8 μg mL−1. The obtained BSA-AuNCs were stable, and quenching in the presence of AAI could be achieved within 10 seconds. Here, we have focused on the application of these gold nanoclusters as an optical sensing material for AAI in rat urine samples, including a discussion on the detection mechanism. The detection result of the fluorescent probe was consistent with that of the HPLC method. In view of this reality, the reported protein-AuNCs sensing platform can serve as a convenient detection strategy in toxicological analyses.

CAS / MDL: 16961-25-4 1310-73-2
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COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS · 2022 · IF 5.518

Evaluation of copper(I)-doped zinc oxide composite nanoparticles on both gram-negative and gram-positive bacteria

Jing Kong,Sufen Zhang,Ming Shen,Jingui Zhang,Sabesan Yoganathan

Antibiotic resistance is a serious problem all over the world. Inorganic metal oxide nanoparticles are suitable substitutional treatments for organic antibiotic-resistant bacterial infections. Various copper dopped ZnO nanocomposites were prepared with chemical deposition method in aqueous solution. X-ray diffraction (XRD) coupled with energy dispersive spectroscopy results reveals that cuprous oxide is uniformly doped on the surface of ZnO nanoparticles , forming Cu 2 O/ZnO nanocomposites. In addition, from Transmission electron microscopy (TEM) and scanning electron microscopy analysis , the average size of prepared Cu 2 O/ZnO composite is about 30 nm. The antibacterial activity of the Cu 2 O/ZnO composite was examined on two bacteria strains: Gram-positive Staphylococcus aureus ( S. aureus ) and Gram-negative Escherichia coli ( E. coli ). When the doping amount of Cu 2 O reaches more than 5%, a 3.58 log-reduction of S. aureus growth under visible light within 30 mins treatment was observed. The antibacterial activity of Cu 2 O/ZnO is 2.7-fold higher than pure ZnO and killing bacteria on E. coli with a 1.0 log-reduction in viability. Meanwhile, the bacteriological properties of Cu doped ZnO composites with different valence states (Cu 2+ , CuO, Cu 2 O, and Cu 0 ) were compared. Furthermore, the antibacterial mechanism was further discussed in this paper.

CAS / MDL: 3317-61-1
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Journal of Physical Chemistry C · 2022 · IF 4.177

Immunoaffinity-Induced Signal Depression of Cu-MOF-74 for Label-Free Electrochemical Detection of Cardiac Troponin I

Yun Ling,Ya-ru Chu,Feng Gao,Qing-yun Feng,Hui-qi Xie,Yong Shao,Qing-xiang Wang

The unique chemical and physical properties of metal–organic frameworks (MOFs) endow them with promising applications in the electrochemical sensing field. Herein, a novel label-free electrochemical sensing strategy for cardiac troponin I (cTnI) has been constructed on the basis of immunoaffinity-induced depression of the electrochemical signal of Cu-MOF-74. The electrochemical assay shows that the immunoaffinity reaction between cTnI and anti-cTnI on the electrode surface can effectively inhibit the electrochemical signal of electrode-confined Cu-MOF-74, suggesting that the Cu-MOF-74-based interface may find application in the label-free analysis of cTnI. Thus, Cu-MOF-74 acts as a bifunctional material in this strategy, namely, the immobilization matrix of probe molecules and the signal source of the sensing analysis. In addition, the reason for the electrochemical signal depression of Cu-MOF-74 induced by immunoaffinity reaction is attributed to the increase in the insulation layer and the blocking of the electrolyte diffusion from the bulk solution to the electrode surface. In this strategy, the analytical range of cTnI is from 0.01 pg mL–1 to 1.0 ng mL–1 and the detection limit is 4.5 fg mL–1. The Cu-MOF-74-based sensing interface is also reliable for cTnI analysis in real serum samples, showing that the biosensor has promising application in point-of-care testing (POCT) of myocardial injury-related diseases.

CAS / MDL: 610-92-4
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ANALYTICA CHIMICA ACTA · 2022 · IF 6.911

2H–MoS2/Co3O4 nanohybrid with type I nitroreductase-mimicking activity for the electrochemical assays of nitroaromatic compounds

Yujie Ma,Mingshi Deng,Xuefeng Wang,Xinghua Gao,Haixiang Song,Yongheng Zhu,Lingyan Feng,Yuan Zhang

A type I nitroreductase-mimicking nanocatalyst based on 2H–MoS 2 /Co 3 O 4 nanohybrids for trace nitroaromatic compounds detection is reported in this work. For the preparation of nanocatalyst, ultrathin Co 3 O 4 nanoflakes array was in-situ grown onto 2H–MoS 2 nanosheets forming three-dimensional (3D) nanohybrid with large specific surface area as well as abundant active sites. The as-prepared nanocatalyst shows a specific affinity as well as high catalytic activity towards nitroaromatic compounds. Given the favorable nitroreductase-mimicking catalytic activity of 2H–MoS 2 /Co 3 O 4 nanohybrid, a sensitive and efficient electrochemical microsensor has been constructed for the detection of 2, 4, 6-trinitrotoluene (TNT). Under optimized conditions, the microsensor displayed sensitive response from μM to pM levels with a limit of detection (LOD) of 1 pM. We further employed photoelectron spectroscopy (XPS) analysis and high-performance liquid chromatography tandem mass spectrometry (HPLC-MS/MS) method to identify the nitroreductase-mimicking mechanism of 2H–MoS 2 /Co 3 O 4 nanohybrids towards 2, 4, 6- TNT. It was found that the abundant oxygen vacancies in ultrathin Co 3 O 4 nanoflakes played an essential role in determining its catalytic performance. Moreover, the developed MoS 2 /Co 3 O 4 nanozyme has a lower Michaelis-Menten constant (k m ) than that of nature nitroreductase demonstrating a good enzymatic affinity towards its substrates, and further generating a high catalytic activity. This research not only proposed a new type of nanozyme, but also developed a portable electrochemical microsensor for the detection of 2, 4, 6-TNT.

CAS / MDL: 10026-22-9
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Experimental and Therapeutic Medicine · 2021 ·Vol. 22 ·期 5 ·1-12 · IF 2.447

Autophagy is involved in neurofibromatosis type I gene‑modulated osteogenic differentiation in human bone mesenchymal stem cells

Yiqiang Li,Mingwei Zhu,Xuemei Lin,Jingchun Li,Zhe Yuan,Yanhan Liu,Hongwen Xu

Neurofibromatosis type I (NF1) is an autosomal dominant genetic disease that is caused by mutations in the NF1 gene. Various studies have previously demonstrated that the mTOR complex 1 signaling pathway is essential for the NF1‑modulated osteogenic differentiation of bone mesenchymal stem cells (BMSCs). Additionally, the mTOR signaling pathway plays a notable role in autophagy. The present study hypothesized that NF1 could modulate the osteogenic differentiation of BMSCs by regulating the autophagic activities of BMSCs. In the present study, human BMSCs were cultured in an osteogenic induction medium. The expression of the NF1 gene was either knocked down or overexpressed by transfection with a specific small interfering RNA (siRNA) targeting NF1 or the pcDNA3.0 NF1‑overexpression plasmid, respectively. Autophagic activities of BMSCs (Beclin‑1, P62, LC3B I, and LC3B II) were determined using western blotting, electron microscopy, acridine orange (AO) staining and autophagic flux/lysosomal detection by fluorescence microscopy. In addition, the autophagy activator rapamycin (RAPA) and inhibitor 3‑methyladenine (3‑MA) were used to investigate the effects of autophagy on NF1‑modulated osteogenic differentiation in BMSCs. Inhibiting NF1 with siRNA significantly decreased the expression levels of autophagy markers Beclin‑1 and LC3B‑II, in addition to osteogenic differentiation markers osterix, runt‑related transcription factor 2 and alkaline phosphatase. By contrast, overexpressing NF1 with pcDNA3.0 significantly increased their levels. Transmission electron microscopy, AO staining and autophagic flux/lysosomal detection assays revealed that the extent of autophagosome formation was significantly decreased in the NF1‑siRNA group but significantly increased in the NF1‑pcDNA3.0 group when compared with the NC‑siRNA and pcDNA3.0 groups, respectively. In addition, the activity of the PI3K/AKT/mTOR pathway [phosphorylated (p)‑PI3K, p‑AKT, p‑mTOR and p‑p70S6 kinase] was significantly upregulated in the NF1‑siRNA group compared with the NC‑siRNA group, and significantly inhibited in the NF1‑pcDNA3.0 group, compared with the pcDNA3.0 group. The knockdown effects of NF1‑siRNA on the autophagy and osteogenic differentiation of BMSCs were reversed by the autophagy activator RAPA, while the overexpression effects of NF1‑pcDNA3.0 on the autophagy and osteogenic differentiation of BMSCs were reversed by the autophagy inhibitor 3‑MA. In conclusion, results from the present study suggest at the involvement of autophagy in the NF1‑modulated osteogenic differentiation of BMSCs. Furthermore, NF1 may partially regulate the autophagic activity of BMSCs through the PI3K/AKT/mTOR signaling pathway.

CAS / MDL: 50-81-7 50-02-2
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JOURNAL OF BIOLOGICAL CHEMISTRY · 2021 ·Vol. 297 ·期 4 · IF 5.157

Marine bacterial exopolysaccharide EPS11 inhibits migration and invasion of liver cancer cells by directly targeting collagen I

Ge Liu,Rui Liu,Yeqi Shan,Chaomin Sun

Many natural polysaccharides have significant anticancer activity with low toxicity, but the complex chemical structures make in-depth studies of the involved mechanisms extremely difficult. The purpose of this study was to investigate the effect of the marine bacterial exopolysaccharide (exopolysaccharide 11 [EPS11]) on liver cancer metastasis to explore the underlying target protein and molecular mechanism. We found that EPS11 significantly suppressed cell adhesion, migration, and invasion in liver cancer cells. Proteomic analysis showed that EPS11 induced downregulation of proteins related to the extracellular matrix–receptor interaction signaling pathway. In addition, the direct pharmacological target of EPS11 was identified as collagen I using cellular thermal shift assays. Surface plasmon resonance and pull-down assays further confirmed the specific binding of EPS11 to collagen I. Moreover, EPS11 was shown to inhibit tumor metastasis by directly modulating collagen I activity via the β1-integrin–mediated signaling pathway. Collectively, our study demonstrated for the first time that collagen I could be a direct pharmacological target of polysaccharide drugs. Moreover, directly targeting collagen I may be a promising strategy for finding novel carbohydrate-based drugs.

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FOOD CHEMISTRY · 2021 · IF 7.514

Amplified electrochemical sensor employing Ag NPs functionalized graphene paper electrode for high sensitive analysis of Sudan I

Fanxing Meng,Yanan Qin,Wenrui Zhang,Fei Chen,Li Zheng,Jun Xing,Aihemaitijiang Aihaiti,Minwei Zhang

In this study, a high-performance flexible reduced graphene oxide (rGO) paper electrode composed of silver nanoparticles (Ag NPs) for the detection of Sudan I was fabricated. Ag NPs were doped with rGO nanoheets by self-assemble and assembled into a paper electrode with layer-by-layer structure via vacuum filtration. Thanks to the highly efficient electrocatalysis of Ag NPs towards reduction of azo bond, the as-prepared hybrid paper can be used alone as a flexible sensor for the detection of Sudan I in chili powder, with the high sensitivity (22.93 μA μmol/L) and the low detection limit (41.3 nmol/L). The sensor also expressed good selectivity, repeatability, reproducibility, stability and recovery between 96.1% and 101.8% (RSD < 6%). With the advantages of low-cost and scalable production capacity, such Ag NPs/rGO functional papers can be used as flexible disposable sensors for electrochemical detection of Sudan I.

CAS / MDL: 7761-88-8
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JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY · 2021 · IF 4.291

Monoacylphosphine oxides with substituents in the phosphonyl moiety as Norrish I photoinitiators: Synthesis, photoinitiattion properties and mechanism

Haodong Duan,Kangwei Leng,Xiaolei Xu,Qianmin Li,Dayong Liu,Yuxi Han,Jun Gao,Qing Yu,Zhongwei Wang

In order to study the effect of the substituents in the phosphonyl moiety of monoacylphosphine oxide (MAPO) on its stability and initiation performance, (2,4,6-trimethylphenyl)(phenyl)(benzoyl)phosphine oxide (TMBPO), (4-tolyl)(phenyl)(2,4,6-trimethylbenzoyl)phosphine oxide (4-MTPO) and (2,4-xylyl)(phenyl)(2,4,6-trimethylbenzoyl)phosphine oxide (2,4-DMTPO) were designed and prepared. Studies on TMBPO showed that the introduction of methyl groups into the phosphonyl moiety of MAPO significantly enhanced its stability and light absorption abilities. The photopolymerization of trimethylolpropane triacrylate (TMPTA) showed that the initiation efficiency of 4-MTPO and 2,4-DMTPO were higher than that of TPO, regardless of whether it was initiated upon LED at 385 nm or 420 nm. In addition, the migration rates of 4-MTPO and 2,4-DMTPO in cured TMPTA were approximately 1/2 and 1/4 that of TPO, respectively.

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JOURNAL OF FOOD SCIENCE · 2021 ·Vol. 86 ·期 6 ·2457-2467 · IF 3.167

Purification and characterization of a novel angiotensin I-converting enzyme-inhibitory peptide derived from Alaska pollack skins

Guilan Yang,Song Qin,Wenjun Li

Hydrolysates containing angiotensin I-converting enzyme (ACE)-inhibitory peptide were prepared from protein of Alaska pollack skins using alcalase and trypsin. The protein hydrolysate was separated by ultrafiltration, Sephadex G-25 gel filtration chromatography and reversed phase high-performance liquid chromatography (HPLC), from which a novel purified peptide was obtained. Both random coil structure and β-sheet in the purified peptide were revealed in Fourier transform infrared spectrum. The amino sequence of the purified peptide was identified as GPLGVP, VLYPVK, VFLENVLR, and FEEF by HPLC-Q-TOF-MS (HPLC-quadrupole time-of-flight mass spectrometry). The peptide GPLGVP whose molecular weight was 538.31 Da showed the highest ACE inhibitory activity (IC 50 = 105.8 µM). The purified peptide featured a noncompetitive inhibition kinetic mechanism was shown in the Lineweaver–Burk plots and was susceptible to enzymes as indicated in the studies on stability of gastrointestinal proteases. Moreover, the peptide GPLGVP can combine ACE catalytic pocket through hydrogen bonds and other forces with high binding power as disclosed in molecular docking simulation, which provides the inhibitory effect of GPLGVP on ACE.

CAS / MDL: 76-05-1
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TALANTA · 2021 · IF 6.057

Dual dye-labeled G-quadruplex aptasensor for detection of thallium(I) using ratiometric fluorescence resonance energy transfer

Tongtong Li,Yan Zhang,Xiaohong Sun,Yanjin Zhang,Yongan Wang,Zhiyong Nie

A fluorescent probe was developed for ratiometric detection of thallium ions in mineral water samples by modifying a G-rich aptamer (PS2.M − 7) with a fluorescence donor (Cyanine-3, Cy 3 ) and a quencher (Cyanine-5, Cy 5 ). The probe had a random coil structure that changed into a G-quadruplex structure upon binding with Tl + . This change in structure decreased the distance between the donor and acceptor moieties, which resulted in fluorescence resonance energy transfer between Cy 3 and Cy 5 . Under optimized conditions, the limit of detection and linear concentration range for Tl + were 30.1 μM (3σ) and 10 μM–10 mM ( R 2  = 0.9981), respectively. This simple and cost-effective fluorescence sensor provided satisfactory results for detection of thallium ions in spiked mineral water samples.

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