Magnolol against enterovirus 71 by targeting Nrf2-SLC7A11-GSH pathway.

Enterovirus 71 (EV71), a prominent pathogen associated with hand, foot, and mouth disease (HFMD), has been reported worldwide. To date, the advancement of effective drugs targeting EV71 remains in the preliminary experimental stage. In this study, magnolol demonstrated a significant dose-dependent inhibition of EV71 replication in vitro.

Fabricating and regulating peroxidase-like activity of eggshell membrane-templated gold nanoclusters for colorimetric detection of staphylococcal enterotoxin B.

Fluorescent eggshell membrane-templated gold nanoclusters (Au-ESM) can be obtained in a facile and low-cost manner in this study. The fluorescence of the Au-ESM may be significantly quenched by mercapto-compounds and peroxidase-like activity of Au-ESM could be regulated by the reaction process with glutathione. Moreover, the catalytic activity of the mimetic enzyme membrane could be modulated by immunoreactions.

Absorbable polymeric surgical clips for appendicular stump closure: A randomized control trial of laparoscopic appendectomy with lapro-clips.

A randomized control trial was performed to evaluate the effectiveness and safety of absorbable polymeric clips for appendicular stump closure in laparoscopic appendectomy (LA). Patients were randomly enrolled into an experimental group (ligation of the appendicular base with Lapro-Clips, L-C group) or control group (ligation of the appendicular base with Hem-o-lok Clips, H-C group). We identified 1,100 patients who underwent LA between April 1, 2012 and February 3, 2015.

Strategy To Fabricate Naked-Eye Readout Ultrasensitive Plasmonic Nanosensor Based on Enzyme Mimetic Gold Nanoclusters.

It is broadly interesting but remains a big challenge to explore nanomaterials-based methods to enable naked-eye observation and determination of ultratrace biomarkers and drugs. In this study, we developed a straightforward and extendable plasmonic nanosensor to enable visually quantitative determination of ultratrace target molecules through combining the use of enzyme-mimetic gold nanoclusters (AuNCs). Starting from sandwiched antibody-antigen (i.

Multiplex sensor for detection of different metal ions based on on-off of fluorescent gold nanoclusters.

In this study, a multiplex fluorescence sensor for successive detection of Fe(3+), Cu(2+) and Hg(2+) ions based on "on-off" of fluorescence of a single type of gold nanoclusters (Au NCs) is described. Any of the Fe(3+), Cu(2+) and Hg(2+) ions can cause quenching fluorescence of Au NCs, which established a sensitive sensor for detection of these ions respectively. With the introduction of ethylene diamine tetraacetic acid (EDTA) to the system of Au NCs and metal ions, a restoration of fluorescence may be found with the exception of Hg(2+).

Colorimetric and ultra-sensitive fluorescence resonance energy transfer determination of H2O2 and glucose by multi-functional Au nanoclusters.

Ultra-sensitive colorimetric determination of H2O2 is accomplished based on the intrinsic peroxidase-like activity of Au nanoclusters (AuNCs) stabilized by glutathione (GSH). The color change of 3,3,5,5-tetramethylbenzidine (TMB) catalyzed by AuNCs offers an indirect method to measure glucose. This sensing platform makes use of a dual optical signal change, including the color change in an aqueous solution under visible light illumination and an ultra-sensitive fluorescent assay arising from efficient fluorescence resonance energy transfer (FRET) between the AuNCs and oxidized TMB.

A novel method for aqueous synthesis of CdTe duantum dots.

We have developed a simple and an economical one-pot method to synthesize water-soluble CdTe quantum dots (QDs) using hydroxylamine hydrochloride (HAH) as reduction and l-cysteine (CYS) as the ligand. The size of the CdTe QDs could easily be controlled by the duration of reflux and monitored by absorption and photoluminescence spectra. The factors influencing the photoluminescence quantum yields (PL QYs) on the QYs of CdTe NCs were investigated and the optimum conditions were determined.

An ultrasensitive method for the determination of melamine using cadmium telluride quantum dots as fluorescence probes.

An ultrasensitive and simple method for the determination of melamine was developed based on the fluorescence quenching of thioglycolic acid (TGA) capped CdTe quantum dots (QDs) at pH 11.0. In strong alkaline aqueous solution, the selectivity of the method has been greatly improved due to most heavy metal ions show no interference as they are in the precipitation form or in their anion form.

Ultrasensitive determination of copper in complex biological media based on modulation of plasmonic properties of gold nanorods.

Accurate determination of copper in complex biological media such as cells is quite difficult, and an analytical strategy based on copper-modulated formation of core-shell gold nanorods is described. Selective and label-free sensing can be achieved by measuring the change in the localized surface plasmon resonance absorption. The technique can determine trace amounts of copper in human serum, urine, and red blood cells without or with minimal sample pretreatment.

Multiplex plasmonic sensor for detection of different metal ions based on a single type of gold nanorod.

In this paper, a label-free multiplex plasmonic sensor has been developed to selectively determine different metal ions including Fe(3+), Hg(2+), Cu(2+), and Ag(+) ions based on a single type of gold nanorod (GNR). Under proper conditions, these metal ions can react with GNRs, resulting in changes of nanostructure and composition. The determination of Fe(3+), Hg(2+), Cu(2+), and Ag(+) ions is therefore readily implemented due to changes of longitudinal plasmon wavelength (LPW) of nanorods.

Enhanced fluorescence of chitosan based on size change of micelles and application to directly selective detecting Fe³⁺ in human serum.

In this paper, we have developed an approach to significantly enhance fluorescence of chitosan by simply heated the inherently low fluorescent chitosan aqueous solution. Enhanced blue fluorescence of chitosan solution was observed as originated from the formation of small size of chitosan micelle after long time heated. The fluorescence of chitosan micelles was quenched and recovered when Fe³⁺ ions were combined and released from chitosan micelles.

Sensitive and simultaneous detection of different disease markers using multiplexed gold nanorods.

A multiplexed bioanalytical assay is produced by incorporating two types of gold nanorods (GNRs). Besides retaining the desirable features of common GNRs LSPR sensors, this sensor is easy to fabricate and requires only a visible-NIR spectrometer for detection. This assay can simultaneously detect different acceptor-ligand pairs by choosing the proper GNRs possessing various LPWs in a wide detection wavelength range and can be developed into a high-throughput detection method.

High-sensitivity biosensors fabricated by tailoring the localized surface plasmon resonance property of core-shell gold nanorods.

An enhanced sensitive biosensor has been developed to detect biological targets by tailoring the localized surface plasmon resonance property of core-shell gold nanorods. In this new concept, a shell layer is produced on gold nanorods by generating a layer of chalcogenide on the gold nanorod surface after attachment of the recognition reagent, namely, goat IgG and antigen of schistosomiasis japonica. The bioactivity of these attached biomolecules is retained and the sensitivity of this biosensor is thus enhanced significantly.

A novel method for iodate determination using cadmium sulfide quantum dots as fluorescence probes.

We have developed a novel method for the determination of iodate based on the carboxymethyl cellulose-capped CdS quantum dots (QDs). Factors affecting the iodate detection were investigated, and the optimum conditions were determined. Under the optimum conditions, the relative fluorescence intensity of CdS quantum dots was linearly proportional to IO(3)(-) over a concentration range from 1.

Optical and biological sensing capabilities of Au2S/AuAgS coated gold nanorods.

Gold nanorods coated with a multiplex component, namely Au(2)S/AuAgS coated gold nanorods, are produced without precipitation and aggregation among the nanorods. Both the thickness of the shell and size of the core can be readily controlled by this technique allowing one to tune the plasmon resonance of the nanocomposites over a range of several hundred nanometers. These Au(2)S/AuAgS coated gold nanorods exhibit interesting optical properties and are suitable for many biological sensing applications.

Label-free optical biosensors based on Au2S-coated gold nanorods.

In this research, two new types of optical biosensors were explored from Au(2)S-coated gold nanorods (Au(2)S-coated GNRs) chemically attached with human IgG as recognizing probes. The first type of biosensors were suspended GNRs and exhibited sensitive shift of longitudinal plasmon wavelength in response to anti-human IgG, with the limit of detection down to 67 pM. The second type of sensors were on-chip-immobilized GNRs, able to be used repeatedly through measuring the change of plasmon absorption intensity at a fixed wavelength, with the limit of detection down to 33 pM.

Label-free optical biosensor based on localized surface plasmon resonance of immobilized gold nanorods.

We describe the fabrication and characterization of a localized surface plasmon resonance (LSPR) biosensor that utilizes gold nanorods immobilized as the optical transducer which requires the intensity change at a single wavelength to be monitored as a function of receptor-analyte binding at the nanorod surface. In contrary to free gold nanorods suspended in an aqueous solution with high sensitivity to the longitudinal plasmon wavelength to the surrounding environment, the intensity of the longitudinal plasmon band based on immobilized gold nanorods is more sensitive to changes in the surrounding dielectric properties than the change in the longitudinal plasmon wavelength. Quantitative calculation gives a linear equation between the concentration (X) of the test sample and intensity of LPB (Y) as Y=0.

A novel label-free multi-throughput optical biosensor based on localized surface plasmon resonance.

A novel and sensitive multi-throughput localized surface plasmon resonance (MLSPR) biosensor was developed for the first time. Various gold nanorods with different aspect ratios were used to fabricate the optical sensor. Five kinds of gold nanorods with different aspect ratios were chosen to construct five throughputs of MLSPR.

Preparation and optical properties of worm-like gold nanorods.

A type of worm-like nanorods was successfully synthesized through conventional gold nanorods reacting with Na2S2O3 or Na2S. The generated worm-like gold nanorods comprise shrunk nanorod cores and enwrapped shells. Therefore, a gold-gold sulfide core-shell structure is formed in the process, distinguishing from their original counterparts.

A novel density-tunable nanocomposites of CdTe quantum dots linked to dendrimer-tethered multi-wall carbon nanotubes.

A novel nanocomposite of CdTe-PAMAM-MWNT was synthesized by covalently linking CdTe quantum dots (QDs) onto highly water-soluble multi-wall carbon nanotubes (MWNTs) functionalized with dendritic poly(amidoamine) (PAMAM). The IR, UV-vis and TEM methods has been used for the characterization of the composites. A facile method for controlling the density of QDs in the composite by simply changing the ratio of CdTe QDs/PAMAM-MWNT, as was verified by the TEM images.

Novel looped enzyme-polyamidoamine dendrimer nanohybrids used as biosensor matrix.

We report the synthesis of a novel looped enzyme-polyamidoamine nanocomposite with high enzyme loading density and long-term retention of bioactivity. The horseradish peroxidase (HRP) is first immobilized on fourth-grade (G4) poly(amidoamine) (PAMAM) dendrimer to form relatively a small enzyme-PAMAM composite, which is allowed to grow up into a larger one. The looped horseradish peroxidase-polyamidoamine (HRP-PAMAM) nanohybrid was characterized by TEM.

Simultaneous electrochemical determination of uric acid and ascorbic acid on a glassy carbon electrode modified with cobalt(II) tetrakisphenylporphyrin.

A cobalt(II) tetrakisphenylporphyrin (Co(II)TPP) film modified glassy carbon electrode (Co(II)TPP-GCE) was prepared by just coating Co(II)TPP solution on the surface of the electrode. It can be used for the simultaneous determination of ascorbic acid and uric acid. The anodic peaks of AA and UA can be separated well.