Sandovalkeith4112

The probe itself is weakly emissive. In the presence of H2O2, the boronate bond is cleaved, and the chromophore BHC-OH and the drug luteolin are released, which produces evident NIR-II fluorescent/optoacoustic signals for imaging and wields therapeutic effect respectively. The probe BHC-Lut has been used in DEN-induced hepatic injury model in mice, and the results evince BHC-Lut's capability for in-situ biomarker-activatable detection and imaging of the acute liver injury site as well as in-situ biomarker-triggered drug release for therapy.In sample preparation, simultaneous extraction of analytes of very different polarity from biological matrixes represents a challenge. In this work, verapamil hydrochloride (VRP), amitriptyline (AMP), tyramine (TYR), atenolol (ATN), metopropol (MTP) and nortriptyline (NRP) were used as basic model analytes and simultaneously extracted from urine samples by liquid-phase microextraction (LPME) in a microfluidic device. The model analytes (target compounds) were pharmaceuticals with 0.4 less then log P less then 5. Different organic solvents and mixtures of them were investigated as supported liquid membrane (SLM), and a mixture of 21 (v/v) tributyl phosphate (TBP) and dihexyl ether (DHE) was found to be highly efficient for the simultaneous extraction of the non-polar and polar model analytes. TBP reduced the intrinsic hydrophobicity of the SLM and facilitated extraction of polar analytes, while DHE served to minimize trapping of non-polar analytes. Sample and acceptor phase composition were adjusted to pH 12 and pH 1.5, respectively. Urine samples were pumped into the microfluidic system at 1 μL min-1 and the extraction was completed in 7 min. Recoveries exceeded 78% for the target analytes, and the relative standard deviation (n = 4) was below 7% in all cases. Using five microliters of SLM, the microfluidic extraction system showed good long-term stability, and the same SLM was used for more than 18 consecutive extractions.Atherosclerosis (AS) is the main cause of coronary heart disease, cerebral infarction and peripheral vascular disease, which is an important disease threatening human health. Abnormal levels of protein phosphorylation are closely related to the occurrence and development of diseases. Herein, the ratiometric fluorescence nanosensor (PCN/W- B@BSA) was prepared by using metal-organic frameworks (PCN-224) and fluorescent nanocluster wool-balls, which was applied for ratiometric fluorescence imaging of protein phosphorylation level in the AS mice model. Specific recognition of phosphorylation sites was achieved via specific interaction between active center Zr(IV) and phosphate. Using the two-photon property of porphyrin, the background is significantly reduced, and the sensitivity of imaging analysis is improved by combining with ratio imaging. Bovine serum albumin (BSA) was used to modify the surface of the nanosensor to reduce the non-specific adsorption and improve the biocompatibility of the nanosensor. Finally, the fluorescence nanosensor was successfully apply to fluorescence imaging of protein phosphorylation level in AS mice model, and the results showed that the protein phosphorylation level in the AS mice model was lower than that of the normal mice. The present study provides suitable fluorescence tool for further revealing phosphorylation related signaling pathways and disease mechanisms.Luminescent organic molecules are of important realistic significance to the human health and ecological environment due to their fascinating applications. Here we report the design and synthesis of luminescent organic-molecules by introducing two or four NH-pyrazolate groups as mercury-binding moieties to aromatic cores. Interestingly, the new aromatic tetraphenylene-bridged multi-NH-pyrazoles exhibit strong fluorescence in both aggregate and solid state and constitutes highly selective proof-of-concept luminescent sensor for Hg(II) ion among various competitive transition-metal ions in both organic and mixed solutions via metal-nitrogen binding. Especially, the present sensor including two NH-pyrazolyl groups showed an extremely high sensitivity with low limit of detection of 7.26 and 3.67 nM. The proposed design strategy provides a wide scope for the construction of unique turn-on sensors with substantial potential in the sense of heavy metal pollution in enviromental water samples.Metabolism studies are one of the important steps in pharmaceutical research. LC-MS combined with metabolomics data-processing approaches have been developed for rapid screening of drug metabolites. Mass defect filter (MDF) is one of the LC/MS-based metabolomics data processing approaches and has been applied to screen drug metabolites. Although MDF can remove most interference ions from an incubation sample, the true positive rate of the retaining ions is relatively low (approximately 10%). To improve the efficacy of MDF, we developed a two-stage data-processing approach by combining MDF and stable isotope tracing (SIT) for metabolite identification. Pioglitazone (PIO), which is an antidiabetic drug used to treat type 2 diabetes mellitus, was taken as an example drug. Our results demonstrated that this new approach could substantially increase the validated rate from about 10% to 74%. Most of these validated metabolite signals (13/14) could be verified as PIO structure-related metabolites. In addition, we applied this approach to identify uncommon metabolite signals (a mass change beyond the window of 50 Da around its parent drug, MDF1). SIT could remove most interference ions (approximately 98%) identified by MDF1, and four out of five validated metabolite signals could be verified as PIO structure-related metabolites. Interestingly, a lot of the verified metabolites (10/17) were novel PIO metabolites. Among these novel metabolites, nine were thiazolidinedione ring-opening signals that might be related to the toxicity of PIO. Our developed approach could significantly improve the efficacy in drug metabolite identification compared with that of MDF.A novel flower-like phosphorous-doped titanium oxide nanocomposite coating was in situ grown on nickel-titanium alloy (NiTi) fiber by hydrothermal treatment in phosphoric acid solution. The experimental results demonstrated that phosphorous-doped titanium oxide nanoflakes (P-TiONFs) with an average thickness of 80 nm were formed on the NiTi fiber substrate in 0.1 mol L-1 H3PO4 at 150 °C for 6 h. Thereafter, the resulting P-TiONFs were used as SPME fiber coatings for the adsorption of typical aromatic analytes from environmental water samples, which were determined by HPLC-UV. These P-TiONFs exhibited good adsorption selectivity for hydrophobic PAHs. After optimizing microextraction conditions, linear responses were achieved in the ranges of 0.05-200 μg L-1 for the determination of PAHs with determination coefficients higher than 0.999. LODs (S/N = 3) ranged from 0.009 to 0.132 μg L-1, while LOQs (S/N = 10) ranged from 0.030 to 0.441 μg L-1. RSDs for intra-day and inter-day analyses with a single fiber varied from 4.46% to 5.56% and 5.14%-6.75%, respectively. The relative recoveries of 83.60%-119.0% were achieved for the determination of PAHs in real water samples spiked at the concentration levels of 5.0 μg L-1 and 10.0 μg L-1 with RSDs below 7.38%. In addition, the fibers exhibited no significant decrease in adsorption efficiency after being used 240 adsorption and desorption cycles. The proposed method was successfully applied to the selective enrichment and determination of target PAHs in different water samples.Oxidative stress of aquatic microorganisms under heavy metal stress is closely reflected by metabolite changes in cells but it is very difficult to study due to the fast metabolism process and severe in-situ measurements hurdle. Herein, the oxidative stress of cadmium on Euglena gracilis was systematically studied through multi-combined techniques. In particular, for the first time electrochemical approach was associated with Raman spectroscopy imaging to vividly to investigate temporal-spatially varied oxidative stress and its effects on cells metabolism, in which former real-time measured a volcanic relation of extracellular hydrogen peroxide versus the increase of cadmium stress, while the latter shows the corresponding metabolic changes by Raman imaging of single cells. This work builds a bridge to unravel the mechanism of cellular oxidative stress under harsh conditions in a more systematic and holistic approach, while holding a great promise to construct heavy metal biosensors precisely monitoring high heavy metal tolerance strains for environmental modification.Here we have studied the effect of the thickness and printing orientation using PolyJet 3D printing to fabricate single-material cartridges with built-in porous frits enabling solid-phase extraction (SPE) by packing commercial sorbents. This is achieved by tuning the degree of interpenetration of the building material and the water-soluble support material used in PolyJet 3D printing by modifying the orientation of the print head respective to the frit. Selleck AZD1480 SPE cartridges printed at an orientation of 30° with a 150 μm thick integrated frit were selected for the SPE experiments in a compromise between frit permeability to flow and stability to retain commercial sorbents for SPE. The performance of the 3D printed cartridges was evaluated for the SPE of the endocrine-disrupting phenols 4-tert-octylphenol (4-tOP) and 4-nonylphenol (4-NP), comparing three commercial SPE sorbents (Evolute Express ABN, Bond Elut PPL, and Silica-C18). The best overall extraction performance was obtained using Silica-C18, and the main extraction parameters were optimized. Detection limits of 0.3 μg L-1 for 4-tOP and 1.1 μg L-1 for 4-NP were achieved using HPLC-DAD for analyte separation and quantification. Enrichment factors of 30.1 (4-tOP) and 16.2 (4-NP) were obtained under the selected conditions. The developed method was applied to water and milk powder samples obtaining satisfactory recoveries ranging from 97% to 103%. These results demonstrate the suitability of PolyJet 3D printing for the fabrication of miniaturized cartridges with integrated frits for SPE applications.In this paper, simultaneous enrichment and separation of ions and amphoteric components were successfully demonstrated by using electric field (E) and pH gradient (double gradient) in the ion depletion zone of anion concentration polarization interface established on a paper fluid channel. Experimental results were visualized with colored ions (bright blue and amaranth) and protein probes (phycocyanin and cytochrome C). With optimization, colored phycocyanin and bovine hemoglobin with similar pI as that of albumin and immunoglobulin respectively were well separated in 900 s with 10-fold enrichment effect. Based on the separation and enrichment function of this paper-based analytical device (PAD) and rapid selective staining of human serum albumin (HSA) with bromophenol blue, a rapid colorimetric detection of HSA was implemented with smartphone camera. A limit of detection (LOD) of 5.2 mg·L-1 was achieved in the clinically significant range of 10-300 mg·L-1 (R2 = 0.99). This method was applied to real human urine samples with good agreement (ɑ = 0.