Lakeporterfield5498

Small extracellular vesicles (SEVs), are cell-derived, membrane-enclosed nanometer-sized vesicles that play vital roles in many biological processes. Recent years, more and more evidences proved that small EVs have close relationship with many diseases such as cancers and Alzheimer's disease. The use of phosphoproteins in SEVs as potential biomarkers is a promising new choice for early diagnosis and prognosis of cancer. However, current techniques for SEVs isolation still facing many challenges, such as highly instrument dependent, time consuming and insufficient purity. Furthermore, complex enrichment procedures and low microgram amounts of proteins available from clinical sources largely limit the throughput and the coveage depth of SEVs phosphoproteome mapping. Here, we synthesized Ti4+-modified magnetic graphene-oxide composites (GFST) and developed a "one-material" strategy for facile and efficient phosphoproteome enrichment and identification in SEVs from human serum. By taking advantage of chelation and electrostatic interactions between metal ions and phosphate groups, GFST shows excellent performance in both SEVs isolation and phosphopeptide enrichment. Close to 85% recovery is achieved within a few minutes by simple incubation with GFST and magnetic separation. Proteome profiling of the isolated serum SEVs without phosphopeptide enrichment results in 515 proteins, which is approximately one-fold more than those otained by ultracentrifugation or coprecipitation kits. Further application of GFST in one-material-based enrichment led to identification of 859 phosphosites in 530 phosphoproteins. Kinase-substrate correlation analysis reveals enriched substrates of CAMK in serum SEVs phosphoproteome. Therefore, we expect that the low instrument dependency and the limited sample requirement of this new strategy may facilitate clinical investigations in SEV-based transportation of abnormal kinases and substrates for drug target discovery and cancer monitoring.No analytical assay is currently available for the simultaneous determination of CBD major metabolites in serum or urine samples of individuals treated with medical cannabis or CBD-based pharmaceuticals. We developed and validated a method using ultra-high-performance liquid chromatography coupled with tandem mass spectrometry (UHPLC-MS/MS) for quantifying cannabidiol (CBD) and its metabolites, cannabidiol-7-oic acid (7-COOH-CBD), 7- hydroxycannabidiol (7-OH-CBD), 6-alpha-hydroxycannabidiol (6-α-OH-CBD) and 6-beta-hydroxycannabidiol (6-β-OH-CBD) in serum and urine samples of an individual treated with medical cannabis. The ionization was performed by electrospray in negative mode to reach the sensitivity required to detect trace amounts, with limits of quantification ranging from 0.05 to 0.1 ng/mL. The method is accurate (average inter/intra-day error, less then 15%), precise (inter/intra-day imprecision, less then 15%) and fast (8 min run time) and it is an essential tool to investigate CBD pharmacokinetics and pharmacodynamics in individuals treated with medical cannabis or with CBD-based medical preparations.The analysis of platinum (Pt), palladium (Pd) and rhodium (Rh) in aquatic samples by the diffusive gradients in thin films (DGT) technique using chelating resins, specific designed for the accumulation of PGEs, namely Purolite S914, S920 and Italmatch Chemicals IONQUEST® MPX-317. may however, still be influenced by the accumulation of other elements such (Cu, Zn, Pb, etc.) which will be extracted simultaneously by the hot aqua regia extraction and interfere with the Inductively Coupled Plasma Mass Spectrometry (ICPMS) analysis of the Platinum Group Elements (PGEs). Selective extractions were investigated to release the interfering elements without loss of the Platinum Group Elements (PGEs) from the resin gels. . A rinse with deionized water removes over 95% of Sr and Rb and a second rinse with 0.05 mol L-1 H2SO4 can be used to as a common eluent to remove an important fraction of the interfering elements from S920 and S914 without loss of PGEs but this results in loss of around 15% of the PGEs from MPX-317. It was shown that selective extractions can be used to remove specific interferences from each resin gel.Selenosulfate (SeSO32-) has been shown to occur in certain industrial process waters, and selenopolythionates (SenSxO62-) can be suspected to form from SeSO32- via oxidative or addition reactions. We report here the first observation of selenopolythionates in waters by mass spectrometry. compound 3k The high mass accuracy and ultra-high resolution of Fourier transform-ion cyclotron resonance-mass Spectrometry with electrospray ionization (ESI-FT-ICR-MS) were used to analyze the isotope patterns of selenium (Se), sulfur (S), and oxygen (O) satellites, in order to provide unequivocal determination of the molecular sum formula of three different selenopolythionates. An aged aqueous solution of SeSO32- was shown to contain the sodium adducts of selenotrithionate (NaSeS2O6-), diselenotetrathionate (NaSe2S2O6-), and triselenopentathionate (NaSe3S2O6-). The identity of these ions was confirmed by accurate mass determination (Δ m/z less then 3 ppm error) and by isotopic intensity ratio analysis of the [MIS+2] satellites. Furthermore, Collision Induced Dissociation (CID) was applied to selenotrithionate to distinguish between isomers, and the fragmentation mass spectrum reveals that the Se atom in NaSeS2O6- is located in the middle of the chalcogen chain. Ion chromatographic analysis of the analyzed selenosulfate solutions indicates that selenopolythionates are not suitable for determination by common separations employed for Se speciation analysis, which emphasizes the value of ESI-FT-ICR-MS for complete qualitative characterization of trace element speciation in solution.With a hybrid coumarin-dicyanoisophorone as report unit and dimethylthiocarbamate as response site, a novel reaction-based fluorescence probe (CDCI-HClO) was synthesized herein for rapid detection of hypochlorous acid (HOCl). CDCI-HClO can respond to HOCl quickly (almost in seconds), selectively, and sensitively, and give an obviously enhanced signal of near-infrared fluorescence at 700 nm. link2 The detection limit of CDCI-HClO for HOCl is about 4 nM. Moreover, with the merit of a large Stokes shift (190 nm), CDCI-HClO was successfully applied to the imaging of HOCl in live cell, zebrafish, and living mice. All results demonstrated that CDCI-HClO is a valuable new NIR fluorescence imaging tool to detect hypochlorous acid in living systems.Trace concentrations of antimony in aquatic samples were determined by high resolution continuum-source atomic absorption spectrometry (HR-CS AAS) after electrochemical pre-concentration and electrochemical hydride generation. Antimony was electrochemically deposited in a microporous glassy carbon electrode as elemental antimony then was electrochemically converted at the same electrode surface to antimony hydride which was transported by argon gas to the quartz cuvette of the spectrometer. The detection limit and precision of the method are below 0.1 μg L-1 and 3-5%, respectively. The method was employed for the determination of antimony in a CRM and water samples including surface, underground and waste water.Room-temperature plasma treated graphene based FET was firstly proposed for the DNA hybridization detection. Affinity and electrical properties of the graphene based DNA-FET sensor were studied and improved benefits from the surface modification. The facile room-temperature Ar plasma easily removes residues from the graphene surface and changes the hydrophilic properties of graphene, which is important for our solution gated DNA-FET sensor. Limit of the detection of below 10 aM is obtained in our experiment. Especially, DNA concentration (CDNA)/the amount of net drain current (ΔI) and the negative shift in the VCNP value of the GFET sensor with the plasma treated 30 s are all improved compared with that without treatment. link3 It shows that the easily plasma treatment of the graphene surface can be used for the solution gated FET sensor.In this work, a novel and high-throughput parallel-dispersive droplet extraction (Pa-DDE) based on in situ formation of the hydrophobic MILs ([Co(C4IM)4+2]2[NTf2-], [Ni(C4IM)4+2]2[NTf2-] and [Ni(BeIM)4+2]2[NTf2-]) is demonstrated, for the first time, for the determination of benzophenone, metolachlor, triclocarban, pendimethalin, 4-methylbenzylidene camphor, and 2-ethylhexyl-4-methoxycinnamate from aqueous environmental samples. This experimental setup is comprised of a 96-well plate system containing a set of magnetic pins which were used to collect the MIL droplet after in situ formation. This consolidated system enabled simultaneous extraction of up to 96 samples and MIL production in one step. Using this apparatus, sample preparation times of 0.78 min per sample was achieved. The experimental conditions were carefully optimized using uni and multivariate approaches. The optimal conditions were comprised of sample volume of 1.25 mL, 4 mg of [Co(C4IM)4+2]2[Cl-] and 40 μL of LiNTf2 for the in situ formation, and dilution in 20 μL of acetonitrile. The analytical parameters of merit were successfully determined with LODs ranging from 7.5 to 25 μg L-1 and coefficients of determination higher than 0.989. Intraday and interday precision ranged from 6.4 to 20.6% (n = 3) and 11.6-22.9% (n = 9), respectively, with analyte relative recovery ranging between 53.9 and 129.1%.Cysteine (Cys) as a vital antioxidant molecule and an effective biomarker for illness, plays an essential role in physiological functions and pathological processes. Extensive work has been done to explore the physiological functions of Cys and develop probes for detection of biothiols. However, the challenge to differentiate Cys from glutathione and homocystine remains. In this work, we constructed a novel near-infrared (NIR) probe, termed TMN-Cys, using TMN-NH2 and thionoesters. The probe could selectively detect Cys over homocysteine and glutathione in solution. It displayed a large Stokes shift (210 nm) upon treatment with Cys, and its detection limit was as low as 79 nM. Moreover, this probe showed low toxicity and was successfully employed in monitoring endogenous Cys in living cells and mice.A new way of electrochemical DNA sensor using as a screening tool for the determination of phytochemicals with high genoprotective functionality is proposed. The biosensor's detection layer was prepared with double stranded deoxyribonucleic acid (ds DNA) that were subjected to oxidative stress induced by •OH radicals generated by Fenton reaction. The oxidized guanine derivative, 8-oxo-7,8-dihydro-2'-deoxyguanosine, was treated as an indicator of DNA oxidative damage. This derivative may cause mutation through its ability to pair with adenine. The abnormalities of DNA structure and DNA repair system are known to be directly related to progressive neurodegeneration. The present study showed that during oxidative stress, the 2.5% oregano extract protected guanine from undergoing oxidation to 8-oxoguanine. The results revealed that this genoprotective effectiveness can make oregano a very efficient protective barrier against oxidative stress. Due to these unique properties of oregano we propose the recipe of a functional bread with its addition.