30 research outputs found

    Turn-On and Near-Infrared Fluorescent Sensing for 2,4,6-Trinitrotoluene Based on Hybrid (Gold Nanorod)−(Quantum Dots) Assembly

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    In this study, we design a FRET system consisting of gold nanorod (AuNR) and quantum dots (QDs) for turn-on fluorescent sensing of 2,4,6-trinitrotoluene (TNT) in near-infrared region. The amine-terminated AuNR and carboxyl-terminated QDs first form a compact hybrid assembly through amine−carboxyl attractive interaction, which leads to a high-efficiency (>92%) FRET from QDs to AuNRs and an almost complete emission quenching. Next, added TNT molecules break the preformed assembly because they can replace the QDs around AuNRs, based on the specific reaction of forming Meisenheimer complexes between TNT and primary amines. Thus, the FRET is switched off, and a more than 10 times fluorescent enhancement is obtained. The fluorescence turn-on is immediate, and the limit of detection for TNT is as low as 0.1 nM. Importantly, TNT can be well distinguished from its analogues due to their electron deficiency difference. The developed method is successfully applied to TNT sensing in real environmental samples

    Gold Nanocluster-Based Fluorescent Probes for Near-Infrared and Turn-On Sensing of Glutathione in Living Cells

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    In this study, a novel Au nanocluster (NC)-based fluorescent sensor has been designed for near-infrared (NIR) and turn-on sensing of glutathione (GSH) in both living cells and human blood samples. The large Stokes-shifted (140 nm) fluorescent Au NCs with NIR emission and long-wavelength excitation have been rapidly synthesized for 2 h by means of a microwave-assisted method in aqueous solution. The addition of Hg<sup>II</sup> leads to an almost complete emission quenching (98%) of Au NCs because of the interaction of Hg<sup>II</sup> and Au<sup>I</sup> on the surface of Au NCs. After introducing GSH to the Au NC–Hg<sup>II</sup> system, a more than 20 times fluorescent enhancement is obtained because of the preferable affinity of GSH with Hg<sup>II</sup>. Under optimum conditions, the fluorescence recovery is linearly proportional to the concentration of GSH between 0.04 and 16.0 μM and the detection limit is as low as 7.0 nM. This Au NC-based sensor with high sensitivity and low spectral interference has been proven to facilitate biosensing applications

    Plasma-Induced Oxygen Vacancies in Ultrathin Hematite Nanoflakes Promoting Photoelectrochemical Water Oxidation

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    The incorporation of oxygen vacancies in hematite has been investigated as a promising route to improve oxygen evolution reaction activity of hematite photoanodes used in photoelectrochemical water oxidation. However, introducing oxygen vacancies intentionally in α-Fe<sub>2</sub>O<sub>3</sub> for active solar water splitting through facile and effective methods remains a challenge. Herein, air plasma treatment is shown to produce oxygen vacancies in α-Fe<sub>2</sub>O<sub>3</sub>, and ultrathin α-Fe<sub>2</sub>O<sub>3</sub> nanoflakes are used to investigate the effect of oxygen vacancies on the performance of photoelectrochemical oxygen oxidation. Increasing the plasma treatment duration and power is found to increase the density of oxygen vacancies and leads to a significant enhancement of the photocurrent response. The nanoflake photoanode with the optimized plasma treatment yields an incident photo-to-current conversion efficiency of 35.4% at 350 nm under 1.6 V vs RHE without resorting to any other cocatalysts, an efficiency far exceeding that of the pristine α-Fe<sub>2</sub>O<sub>3</sub> nanoflakes (∼2.2%). Evidence for the presence of high density of oxygen vacancies confined in nanoflakes is clarified by X-ray photoelectron spectroscopy. The increased number of oxygen vacancies after plasma treatment resulting in an increased carrier density is interpreted as the main cause for the enhanced oxygen evolution reaction activity

    <i>PLOS ONE</i> clinical studies checklist.

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    This prospective observational study explored the predictive value of CD86 in the early diagnosis of sepsis in the emergency department. The primary endpoint was the factors associated with a diagnosis of sepsis. The secondary endpoint was the factors associated with mortality among patients with sepsis. It enrolled inpatients with infection or high clinical suspicion of infection in the emergency department of a tertiary Hospital between September 2019 and June 2021. The patients were divided into the sepsis and non-sepsis groups according to the Sepsis-3 standard. The non-sepsis group included 56 patients, and the sepsis group included 65 patients (19 of whom ultimately died). The multivariable analysis showed that CD86% (odds ratio [OR] = 1.22, 95% confidence interval [CI]: 1.04–1.44, P = 0.015), platelet count (OR = 0.99, 95%CI: 0.986–0.997, P = 0.001), interleukin-10 (OR = 1.01, 95%CI: 1.004–1.025, P = 0.009), and procalcitonin (OR = 1.17, 95%CI: 1.01–1.37, P = 0.043) were independent risk factors for sepsis, while human leukocyte antigen (HLA%) (OR = 0.96, 05%CI: 0.935–0.995, P = 0.022), respiratory rate (OR = 1.16, 95%CI: 1.03–1.30, P = 0.014), and platelet count (OR = 1.01, 95%CI: 1.002–1.016, P = 0.016) were independent risk factors for death in patients with sepsis. The model for sepsis (CD86%, platelets, interleukin-10, and procalcitonin) and the model for death (HLA%, respiratory rate, and platelets) had an area under the curve (AUC) of 0.870 and 0.843, respectively. CD86% in the first 24 h after admission for acute infection was independently associated with the occurrence of sepsis in the emergency department.</div

    Fig 2 -

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    (A) CD86%, human leukocyte antigen (HLA%), and CD86 mRNA in the sepsis and non-sepsis groups. CD86% expression was lower in the non-sepsis group and higher in the sepsis-death group. In contrast, HLA% was lower in the sepsis-death group and higher in the non-sepsis group. There were no significant differences in CD86 mRNA among the three groups. (B) Flow cytometry outputs of CD86 among the three groups.</p

    Table_1_Mapping the research trends and hot topics of ventricular arrhythmia: A bibliometric analysis from 2001 to 2020.docx

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    BackgroundStudies of ventricular arrhythmia (VA) have drawn much scholarly attention over the past two decades. Our study aimed to assess the current situation and detect the changing research trends of VA quantitatively and qualitatively.Materials and methodsAll the information used in our statistical and bibliometric analysis were collected and summarized from papers retrieved from the Web of Science Core Collection (WoSCC) database on December 22, 2021 using certain criteria. Visual analytics were realized using CiteSpace, VOSviewer, the bibliometrix R package, and the bibliometric online analysis platform.ResultsA total of 6,897 papers (6,711 original articles, 182 proceedings papers, three book chapters, and one data paper) were published in 796 journals that concentrated on the research areas of cardiovascular and critical care medicine. The most productive country and influential institution was the USA and the Mayo Clinic, respectively. Heart Rhythm (551 articles and 8,342 local citations) published the most manuscripts. The keyword co-occurrence and co-citation network of references analyses revealed that the most popular terms were ventricular tachycardia, ventricular fibrillation, catheter ablation, implantable cardioverter defibrillator (ICD), and sudden cardiac death (SCD). Further, the burst detection analysis demonstrated that topics strongly associated with clinical prognosis, such as meta-analysis, long-term outcomes, and impact, were new concerns.ConclusionOur study offers a comprehensive picture of VA research and provides profound insights into the current research status. Moreover, we show that new topics within the VA research field have focused more on prognosis and evidence-based clinical guidelines.</p

    Brighter, More Stable, and Less Toxic: A Host–Guest Interaction-Aided Strategy for Fabricating Fluorescent Silica Nanoparticles and Applying Them in Bioimaging and Biosensing at the Cellular Level

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    The exploration of fluorescent tools with distinguished optical properties and favorable biocompatibility is significant for biosensing and bioimaging. We herein present a host–guest interactions aided strategy for fabricating fluorescent silica nanoparticles (FSNPs), which is enabled by cyclodextrin (CD) supermolecules. Compared with conventional FSNPs, the modified products (are named as fluorophore@CD@SNPs) possess several advantages. First, the incorporated fluorophores can thoroughly get rid of their intrinsic aggregation due to CD’s inclusion effect, and the fluorescence intensity of the obtained fluorophore@CD@SNPs can enhance 48–67%. The fluorophores can then be well-fixed by the host CD molecules. As a result, the leak rates of the incorporated fluorophores are only 15–17%, which is about 3 times lower than that of conventional ones (42–48%). Notably, the as-prepared fluorophore@CD@SNPs show observable less cytotoxicity as compared with their conventional counterparts, probably due to the substantially decreased leakage of the incorporated fluorophores. Because of prominent properties and versatile fabrication, the proposed fluorophore@CD@SNPs not only possess better performances for cell-imaging but are competent for ratiometric sensing of pH value at living cell using (indicator-reference) integrative silica NPs

    STROBE statement—checklist of items that should be included in reports of observational studies.

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    STROBE statement—checklist of items that should be included in reports of observational studies.</p

    Study flowchart.

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    This prospective observational study explored the predictive value of CD86 in the early diagnosis of sepsis in the emergency department. The primary endpoint was the factors associated with a diagnosis of sepsis. The secondary endpoint was the factors associated with mortality among patients with sepsis. It enrolled inpatients with infection or high clinical suspicion of infection in the emergency department of a tertiary Hospital between September 2019 and June 2021. The patients were divided into the sepsis and non-sepsis groups according to the Sepsis-3 standard. The non-sepsis group included 56 patients, and the sepsis group included 65 patients (19 of whom ultimately died). The multivariable analysis showed that CD86% (odds ratio [OR] = 1.22, 95% confidence interval [CI]: 1.04–1.44, P = 0.015), platelet count (OR = 0.99, 95%CI: 0.986–0.997, P = 0.001), interleukin-10 (OR = 1.01, 95%CI: 1.004–1.025, P = 0.009), and procalcitonin (OR = 1.17, 95%CI: 1.01–1.37, P = 0.043) were independent risk factors for sepsis, while human leukocyte antigen (HLA%) (OR = 0.96, 05%CI: 0.935–0.995, P = 0.022), respiratory rate (OR = 1.16, 95%CI: 1.03–1.30, P = 0.014), and platelet count (OR = 1.01, 95%CI: 1.002–1.016, P = 0.016) were independent risk factors for death in patients with sepsis. The model for sepsis (CD86%, platelets, interleukin-10, and procalcitonin) and the model for death (HLA%, respiratory rate, and platelets) had an area under the curve (AUC) of 0.870 and 0.843, respectively. CD86% in the first 24 h after admission for acute infection was independently associated with the occurrence of sepsis in the emergency department.</div
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