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Covalent organic frameworks (COFs), as one of the most significant members of the porous organic frameworks, have been well used in the photocatalysis owing to their outspread π-conjugated framework, high crystallinity and regular pore structure. Herein, after reducing the labile imine-linked COF-300 to the more stable amine-linked COF-300-AR, we for the first time demonstrated that COF-300-AR was the light-responsive oxidase mimic. COF-300-AR exhibited excellent oxidase-mimicking activity under purple light stimulation (λ = 400 nm), which can catalyze the oxidation of classical substrates such as 3,3',5,5'-tetramethylbenzydine (TMB) and 2,2'-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS) by the formation of •OH and O2•- free radicals in the presence of dissolved oxygen. The COF-300-AR oxidase mimic has outstanding advantages of easy light control, high stability, good reusability, and highly catalytic oxidation capacity and has been applied to detect glutathione (GSH) levels in HL60 cells with good selectivity and high sensitivity. This study will broaden the sensing applications of COFs and offer a promising build block for the construction of artificial enzymes.

The purpose of present study is to investigate the inhibitory effects of epicatechin (EC) on the formation of ALEs. A chemical model containing bovine serum albumin (BSA, 1 mg/mL) and fish oil (0.5 mg/mL) under accelerated metal-catalyzed oxidation (37 °C, 72 h) was established to mimic the generation of ALEs. The incorporation of EC (0.25, 0.5, 1, and 2 mmol/L) significantly reduced TBARS content in a dose-dependent manner (P

Levodopa (L-DOPA) is promising as chiral stationary phase for open tubular capillary electrochromatography (OT-CEC) enantioseparation owing to its self-polymerization adhesive property and chiral recognition potential. In this work, CuSO4/H2O2 was used as a trigger agent to accelerate the polymerization process of L-DOPA and the poly-levodopa (poly-(L-DOPA)) coated column was successfully prepared for the first time by depositing it on the inner wall of fused silica capillary via the rapid and in-situ approach at room temperature. The performance of the poly-(L-DOPA) coated capillary was validated by the separation of different chiral analytes, including chiral amine drugs, neurotransmitters and amino acids, and the good enantioseparation efficiencies were achieved. For five consecutive runs, the relative standard deviations (RSDs) for the migration time of the analytes for intra-day, inter-day and column-to-column were in the range of 0.19-1.33%, 0.96-4.47%, and 2.21-7.79%, respectively. Additionally, the poly-(L-DOPA) coated capillary column could be successively used over 250 runs without observable change in the separation efficiency.

An ingenious and viable method for preparing heterogeneous Co3O4 dodecahedrons that contain carbon and encapsulated Au nanoparticles (Au@C-Co3O4) was proposed via pyrolysis of Au nanoparticle-encapsulated zeolitic imidazolate framework-67 (Au@ZIF-67). The obtained Au@C-Co3O4 possessed hierarchically porous structure, abundant active sites, excellent conductivity, and durability, all of which can significantly improve the analysis performance of the biosensor. Meanwhile, the fabricated electrode based on the porous Au@C-Co3O4 showed remarkable electrocatalytic performance towards H2O2 with a limit of detection of 19 nM and ultra-high sensitivity of 7553 μA mM−1 cm−2, even when the Au content in the composite was as low as 0.85 wt%. This novel biosensor was successfully used to monitor H2O2 concentration released from living cells, and the results can be used to identify cancer cells, thus advancing the use of transition metal oxides in the field of biosensing.

Silicon nanoparticles (SiNPs) have attracted increasing attentions due to their unique properties and related applications. However, previously reported SiNPs generally showed emission band only in the blue- or green-light regions, which limited their applications in biochemical samples. So far, synthesis of longer wavelength emissive SiNPs remains a challenge. In this paper, the yellow-emitting fluorescent SiNPs were prepared via a facile room temperature procedure, which avoided heating and pressurizing operation, multistep and time-consuming post-modified procedures. The obtained SiNPs displayed excellent water-solubility, pH-stability, salt-tolerance, and photo-stability. Significantly, the fluorescence of SiNPs could be remarkably quenched by crystal violet (CV) via synergistic effect of inner filter effect (IFE) and fluorescence resonance energy transfer (FRET). Based on this phenomenon, a method for the determination of CV was established. Under the optimum conditions, the method showed a wide linearity range from 0.075 to 15.0 μg/mL with a limit of detection of 25 ng/mL. Furthermore, the method was successfully applied to the analysis of CV in fish tissues samples.

In this work, CoFe2O4 nanoparticles coated with polyethylene glycol (PEG) were successfully synthesized via a hydrothermal technique. Morphological studies of the samples confirmed the formation of polycrystalline pure-phase PEG-CoFe2O4 nanoparticles with sizes of about 24 nm. Toxicity induced by CoFe2O4 nanoparticles was investigated, and biological assays were performed to check the toxicity effects of CoFe2O4 nanoparticles. Moreover, the healing effect of toxicity induced in living organisms was studied using curcumin and it was found that biochemical indexes detoxified and improved to reach its normal level after curcumin administration. Thus, PEG-coated CoFe2O4 synthesized through a hydrothermal method can be utilized in biomedical applications and curcumin, which is a natural chemical with no side effects, can be used for the treatment of toxicity induced by the nanoparticles in living organisms.

A novel ternary transition metal oxide (TTMO) FeMnO3 microcube with an average diameter of about 1.0 μm was successfully fabricated via the pyrolysis of Mn-Fe Prussian blue analogue (PBA) at 650 °C. As an anode material for lithium ion batteries (LIBs), it showed a steady reversible capacity of 710 mAh g−1 at a high current density of 1 A g−1 after 200 cycles with 80% retention. The remarkable electrochemical storage properties are attributed to the microcubic structure inherited from the precursor and structure stability, which can effectively buffer the volume expansion during the discharge-charge process. Its excellent features, such as low cost, environmentally friendliness, simple preparation and outstanding electrochemical properties, make the obtained FeMnO3 a promising electrode material for electrochemical storage devices.

In this work, we report a durable and sensitive H2O2 biosensor based on boronic acid functionalized metal-organic frameworks (denoted as MIL-100(Cr)-B) as an efficient immobilization matrix of horseradish peroxidase (HRP). MIL-100(Cr)-B features a hierarchical porous structure, extremely high surface area, and sufficient recognition sites, which can significantly increase HRP loading and prevent them from leakage and deactivation. The H2O2 biosensor can be easily achieved without any complex processing. Meanwhile, the immobilized HRP exhibited enhanced stability and remarkable catalytic activity towards H2O2 reduction. Under optimal conditions, the biosensor showed a fast response time (less than 4s) to H2O2 in a wide linear range of 0.5-3000μM with a low detection limit of 0.1μM, as well as good anti-interference ability and long-term storage stability. These excellent performances substantially enable the proposed biosensor to be used for the real-time detection of H2O2 released from living cells with satisfactory results, thus showing the potential application in the study of H2O2-involved dynamic pathological and physiological process.

Heteroatom-doped carbon nanoparticles (CNPs) have attracted considerable attention due to an effective improvement in their intrinsic properties. Here, a facile and simple synthesis of nitrogen, boron co-doped carbon nanoparticles (NB-CNPs) from a sole precursor, 3-aminophenylboronic acid, was performed via a one-step solid-phase approach. Because of the presence of boronic acid, NB-CNPs can be used directly as a fluorescent probe for glucose. Based on a boronic acid-triggered specific reaction, we developed a simple NB-CNP probe without surface modification for the detection of glucose. When glucose was introduced, the fluorescence of NB-CNPs was suppressed through a surface-quenching states mechanism. Obvious fluorescence quenching allowed the highly sensitive determination of glucose with a limit of detection of 1.8 μM. Moreover, the proposed method has been successfully used to detect glucose in urine from people with diabetes, suggesting potential application in sensing glucose.

In this work, molybdenum disulfide quantum dots (MOS2 QDs) were firstly prepared by hydrothermal method using sodium molybdate and glutathione as precursors, and applied in ascorbic acid detection. When joining MnO2 nanosheets into MOS2 QDs solution, they produced an obvious fluorescence quenching, which should be due to inner filter effect (IFE). Meanwhile, the fluorescent probe was formed. Interestingly, we found that this quenching phenomenon disappeared with the addition of ascorbic acid. In other words, the fluorescence gradually restored. This recovery phenomenon is mainly due to the reduction effect of ascorbic acid for MnO2 nanosheets. Under the optimum conditions, the limit of detection (LOD) of 39 nmol/L for ascorbic acid was achieved with a linear range of 0.33-5.00 mu mol/L. The repeatability was better than 5.0% for ascorbic acid in both standard and fruit samples (n=3). Moreover, the as-fabricated fluorescent sensing system was successfully employed to detect the ascorbic acid levels in hawthorn and jujube with satisfactory results. (C) 2016 Chinese Chemical Society and Institute of Materia Medica, Chinese Academy of Medical Sciences. Published by Elsevier B.V. All rights reserved.

Developing simple methods for separation of analytes that belong to different classes is of great importance. Herein, we developed a simple one-dimensional (1-D) capillary electrochromatography method to demonstrate the simultaneous separation of target fractions that belong to two different classes (i.e., cationic and neutral analytes) without switching buffer solution by a zeolitic imidazolate framework ZIF-8 coated capillary column. Owing to the difference of charge-to-mass ratio of the cationic analytes, the interaction of the cationic analytes and coating material ZIF-8 and the hydrophobic interactions between the neutral analytes and the microporous framework of ZIF-8, six cationic analytes and four neutral analytes were simultaneously separated in a single run by 1-D capillary electrochromatography. The relative standard deviations (RSDs) of the analytes migration time for intra-day, inter-day and column-to-column were in the range of 0.11-0.87%, 0.54-2.04% and 2.00-6.89% and the RSDs of the analytes peak area for intra-day, inter-day and column-to-column were in the range of 0.70-4.45%, 1.33-6.20% and 2.27-11.88%. Additionally, the developed method was employed in the analysis of urine samples with satisfactory recoveries.

Two-dimensional (2D) COFs have been successfully applied for various applications, such as capillary electrochromatography (CEC). Compared with 2D COFs, three-dimensional (3D) COFs have higher surface area and lower density, which should have superior potential as the separation medium in CEC. However, the 3D COFs on the inner wall of capillary is hard to fabricate in situ. Up to date, the application of 3D COFs in open-tubular capillary electrochromatography (OT-CEC) is still considered a challenge. For the first time the COF-300-coated capillary was prepared by in situ growth (COF-300 was made from terephthalaldehyde and tetra-(4-anilyl)-methane) on OT-CEC. Benzene, methylbenzene, styrene, ethylbenzene, naphthalene, 1-methylnaphthalene, and propylbenzene were used to evaluate the performance of the COF-300-coated capillary by OT-CEC. For three consecutive runs, the intraday relative standard deviations (RSDs) of migration time and peak areas were 0.1-0.4% and 2.5-8.3%, respectively. The interday RSDs of migration time and peak areas were 0.2-0.5% and 1.0-10.8%, respectively. Five groups of aromatic co mpounds were used to further study the separation mechanism, which indicated that hydrophobic interaction and size selection interaction are the main factors. It should be noted that the COF-300-coated capillary can be used for more than 140 runs with no observable changes of the separation efficiency. Graphical abstract The 3D COF-300-coated capillary was prepared by in situ growth for OT-CEC. Six groups of aromatic compounds were separated by 3D COF-300-coated capillary. Size selection and hydrophobic interaction affect the migration time of analytes.

With the rapid development of portable and wearable electronics, fiber-based supercapacitors as one type of flexible and lightweight energy storage devices have attracted intensive attention. However, most of the reported fiber-based supercapacitors are based on a symmetric device configuration, whose narrow operating voltage window and low energy densities as well as the poor electrochemical performance hinder the practical applications of fiber-based supercapacitors. In this report, we developed a fiber-based flexible all-solid-state asymmetric supercapacitor, using nickel wire/Co3O4@MnO2 nanowire arrays and carbon fibers/graphene as the two electrodes. The fiber-based all-solid-state asymmetric supercapacitor exhibited remarkable electrochemical performance with high capacitance (13.9 mF cm−2 at 0.1 mA cm−2) and high cycling stability (82% retention, even after 1000 cycles at 0.6 mA cm−2). The obtained fiber-based supercapacitor is a promising power source candidate for flexible, portable and wearable electronics.

Here we demonstrate the seed-mediated growth approach, one of the most reliable and versatile methods to control the size and shape of nanocrystals (NCs), for rapid synthesis of high performance red-emitting core/shell CdTe quantum dots (QDs) in aqueous phase. Critical parameters (including the pH value, Cd:Te molar ratio, MPA:Cd molar ratio, and the amount of CdTe seeds) affecting the growth of core/shell CdTe QDs are systematically introduced and analyzed. Under optimal conditions, the growth behaviors can be well controlled, and the high performance typically offered by the seed-mediated growth method was obtained as expected. The emission peak position quickly shifted from 540 to 680 nm in 30 min, and the red-emitting CdTe QDs thus obtained performed well, giving good size distribution, narrow full width at half maximum and high quantum yield. The growth mechanism and the resulting high structural and optical properties were also elucidated. Finally, the obtained CdTe QDs were successfully applied to highly reactive oxygen species (hROS) sensing, suggesting that this method may be useful in bioimaging and biolabeling.

In recent years, covalent organic frameworks (COFs) play an important role in the field of chromatographic separation. However, COFs are used rarely in open-tubular capillary electrochromatography (OT-CEC) so far, and the reported methods have not been applied to actual sample analysis. Herein, a novel azine-linked COF (N0-COF) coated capillary was prepared as OT-CEC separation channel and a new method for separation and detection of environmental endocrine disruptors, i.e., bisphenol A (BPA) and its analogues was established. Under optimal separation conditions, the analytes were baseline separated by the N0-COF coated capillary with 20 min. The intra-day, inter-day and column-to-column relative standard deviations were 0.07–2.99%, 1.05–3.20% and 1.31–5.83% for the migration time; 1.68–5.50%, 1.52–9.24% and 4.04–9.14% for the peak area. The method was further applied to separate and determine BPA and its analogues in beverage samples, and the recovery ranged from 91.0–112.0%.

Exploration of the simple and stable coating methods is of great significance in capillary electrochromatography (CEC). In this work, a lysozyme assemble supramolecular membrane coated capillary column was developed for CEC chiral separation. Taking advantage of phase transformation of lysozyme, the coating process was achieved within 1.0 h thus to a large extent reduced the capillary preparation time and simplified the coating procedure. The successful fabrication of the supramolecular membrane coated capillary was verified by scanning electron microscopy (SEM), Fourier transform-infrared spectroscopy (FT-IR), fluorescence imaging, and electroosmotic flow (EOF). The separation capacity of the coated capillary was evaluated by analysis of different chiral analytes, including chiral amine drug and neurotransmitters, and good enantioseparation efficiency was achieved for the three pairs of enantiomers. For three consecutive runs, the relative standard deviations (RSD) for the migration time of the analytes for intra-day (n = 3), inter-day (n = 3) and column-to-column (n = 3) were in the range of 0.7–1.5%, 2.7–3.6%, and 4.5–5.8%, respectively. Additionally, the supramolecular membrane coated capillary column could run consecutively 100 times without observable change in the separation efficiency, proving the feasibility of the coating method based on the adhesion of the protein-based supramolecular membrane.

In recent years, artificial materials with double helix structure have attracted widespread attention due to their unique properties such as the DNA like double-helicity, intrinsic chirality and diverse functional groups. Developing novel chiral stationary phases (CSPs) for capillary electrochromatography enantioseparation is of intriguing interest. Herein, a novel homochiral zeolite-like metal-organic framework (ZMOF) JLU-Liu23 with unique DNA like double-helicity structure was firstly utilized as the CSP in open tubular capillary electrochromatography (OT-CEC) for enantioseparation of chiral monoamine neurotransmitters and analogues. Owing to the unique DNA like double-helicity structure of the homochiral ZMOF JLU-Liu23, the good enantioseparation of four monoamine neurotransmitters and analogues was achieved on the prepared homochiral ZMOF JLU-Liu23 coated capillary column. The relative standard deviations (RSDs) of the analytes migration time for intra-day, inter-day and column-to-column were in the range of 0.3-0.6%, 0.8-2.2% and 3.5-6.5%, respectively.

The popularity of novel nanoparticles coated capillary column has aroused widespread attention of researchers. Metal organic frameworks (MOFs) with special structure and chemical properties have received great interest in separation sciences. This work presents the investigation of HKUST-1 (Hong Kong University of Science and Technology-1, called Cu3(BTC)2 or MOF-199) nanoparticles as a new type of coating material for capillary electrochromatography. For the first time, three layers coating (3-LC), five layers coating (5-LC), ten layers coating (10-LC), fifteen layers coating (15-LC), twenty layers coating(20-LC) and twenty-five layers coating (25-LC) capillary columns coated with HKUST-1 nanoparticles were synthesized by covalent bond with in situ, layer-by-layer self-assembly approach. The results of scanning electron microscopy (SEM), X-ray diffraction (XRD) and plasma atomic emission spectrometry (ICP-AES) indicated that HKUST-1 was successfully grafted on the inner wall of the capillary. The separating performances of 3-LC, 5-LC, 10-LC, 15-LC, 20-LC and 25-LC open tubular (OT) capillary columns were studied with some neutral small organic molecules. The results indicated that the neutral small organic molecules were separated successfully with 10-LC, 15-LC and 20-LC OT capillary columns because of the size selectivity of lattice aperture and hydrophobicity of organic ligands. In addition, 10-LC and 15-LC OT capillary columns showed better performance for the separation of certain phenolic compounds. Furthermore, 10-LC, 15-LC and 20-LC OT capillary columns exhibited good intra-day repeatability with the relative standard deviations (RSDs; %) of migration time and peak areas lying in the range of 0.3-1.2% and 0.5-4.2%, respectively. For inter-day reproducibility, the RSDs of the three OT capillary columns were found to be lying in the range of 0.3-5.5% and 0.3-4.5% for migration time and peak area, respectively. The RSDs of retention times for column-to-column for three batches of 10-LC, 15-LC and 20-LC OT capillary columns were in the range from 2.3% to 7.2%. Moreover, the fabricated 10-LC, 15-LC and 20-LC OT capillary columns exhibited good repeatability and stability for separation, which could be used successively for more than 120 runs with no observable changes on the separation efficiency.

Inspired by the chiral recognition ability of β-cyclodextrin and the natural adhesive properties of polydopamine under alkaline conditions, in this study, a rapid and in situ modification strategy was developed to fabricate β-cyclodextrin/polydopamine composite material coated-capillary columns for open tubular capillary electrochromatography. The results of scanning electron microscopy, FTIR spectroscopy, streaming potential and electro-osmotic flow studies indicated that β-cyclodextrin/polydopamine was successfully fixed on the inner wall of the capillary column. This coating can be achieved within 1 h affording a greatly reduced capillary preparation time. The performance of the β-cyclodextrin/polydopamine-coated capillary was validated by the analysis of seven pairs of chiral analytes, namely epinephrine, norepinephrine, isoprenaline, terbutaline, verapamil, tryptophane, carvedilol. Good enantioseparation efficiencies were achieved for all. For three consecutive runs, the relative standard deviations for the migration times of the analytes for intra-day, inter-day and column-to-column repeatability were in the range of 0.41–1.74%, 1.03–4.18%, and 1.66–8.24%, respectively. Moreover, the separation efficiency of the β-cyclodextrin/polydopamine-coated capillary column did not decrease obviously over 90 runs. The strategy should also be feasible to introduce and immobilize other chiral selectors on the inner walls surface of capillary columns. This article is protected by copyright. All rights reserved

Covalent organic frameworks (COFs) have attracted much attention because of their permanent nanoscale porosity and higher surface area compared to zeolites as well as robustness. COFs have great potential in several fields such as hydrogen storage, gas separation, and catalysis. However, COFs have not yet been applied in capillary electrochromatography. Herein, covalent organic frameworks-LZU1 (COF-LZU1) was used as the stationary phase in open-tubular capillary electrochromatography for the first time. Compared to the monoliths used in electrochromatography, the preparation technique of a COF-LZU1-coated capillary was simple and practical. The baseline separation of model analytes including alkylbenzenes, polyaromatic hydrocarbons, and anilines by the COF-LZU1-coated capillary was achieved based on the size selectivity of COF-LZU1 porous structure and hydrophobic interactions between the model analytes and organic ligands of COF-LZU1. The load capacity of the COF-LZU1-coated capillary for naphthalene was 0.6mg/mL. For three consecutive runs, the intraday relative standard deviations (RSDs) were 1.4-2.6% for the migration time and 2.7-8.7% for the peak area. The interday RSDs were 1.3-3.9% for the migration time and 3.7-9.7% for the peak area. The column-to-column reproducibility of migration time was in the range 1.0-3.9%. Moreover, the coated capillary was used for >300 runs with no changes in the separation efficiency. Thus, COFs have great potential in capillary electrochromatography and may provide a new method for chromatographic separation.