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Sturdy under the sea graphic development approach determined by sun light and reflectivity.
In particular, the GLUT1 inhibitor probe offers the potential use for glycolysis-based diagnostic imaging in triple-negative breast cancer which is claimed to have unsatisfactory results with FDG/PET diagnosis, thus remaining a highly metastatic and lethal disease with a need for sensitive and precise identification.In this study, a dual mixed-mode polymer sorbent was prepared via one-step thermally initiated polymerization of 4-vinylpyridine (VP), methacrylic acid (MAA) and ethylene glycol dimethacrylate (EGDMA) for the solid-phase extraction (SPE) of basic and acidic drugs. The use of VP and MAA as ionizable functional monomers allowed the tailoring of ion-exchange and hydrophobic features of the polymer. The obtained polymer was characterized by Fourier-transform infrared spectroscopy and scanning electron microscopy. Next, the retention behavior of dual mixed-mode polymer towards basic and acidic drugs was investigated. Moreover, the practical capability of this novel material was tested for the extraction of relevant drugs such as cocaine, 3-methylmethcathinone, and diazepam in oral fluid samples. Recovery values (at different spiked levels in blank oral fluid samples), ranging from 69 to 99%, and limits of detection (LODs), between 0.10 and 0.25 μg L-1, were obtained.Noble metal nanoparticles are known to electrocatalyze various redox reactions by improving the electron transfer kinetics. In the present study, we have introduced a facile bioinspired synthesis of PtNPs and their integration for the formation of PtNPs/graphene nanocomposite using Psidium guajava (guava) leaves extract. Graphene used in nanocomposite formulation was synthesized by exfoliation of graphite in water/acetone (2575 v/v) mixture followed by mechanical shearing using ultrasonication and microwave irradiation. PtNPs/graphene nanocomposite was drop-cast onto a glassy carbon electrode (GCE, 3 mm dia). The electrocatalytic activity of PtNPs/graphene nanocomposite was tested in a three-electrode system for sensing of metabolic products of dipyrone (DIP) formed through 1 e- and 2 e- transfer reactions. The modified electrode exhibited almost 50% reduction in electrode resistance. The limit of detection was found to be 0.142 μM with sensitivities of 0.820 and 0.445 μA․μM-1cm-2 for DIP concentration below and above 100 μM, respectively, using square wave voltammetry. The signal of sensing of metabolites of DIP was almost invariant in the presence of glucose, dopamine, uric acid, and ciprofloxacin; however, the response current was decayed by 20% within the 10th cycle. The sensing of DIP spiked in treated sewage-water and running tap-water samples was ∼100% recoverable and comparable with HPLC.Here, a novel electrically conductive thermoplastic material composed of graphite/acrylonitrile butadiene styrene (G/ABS) is reported for the first time. This material was explored on the production of 3D printing-based electrochemical sensors with enhanced sensitivity using a novel fabrication approach. The developed G/ABS electrodes showed lower charge transfer resistance (157 vs. 3279 Ω), higher electroactive area (0.61 vs. 0.19 cm2) and peak currents ca. 69% higher when compared with electrodes fabricated using carbon black/polylactic acid (CB/PLA) commercial filament, which has been widely explored in recent literature. Moreover, the G/ABS sensor provided satisfactory repeatability, reproducibility and stability (relative standard deviations (RSDs) were 1.14%, 6.81% and 10.62%, respectively). This improved performance can be attributed to the fabrication protocol developed here, which allows the incorporation of greater amounts of conductive material in the polymeric matrix. The G/ABS electrode also required a simpler and quicker protocol for activation when compared to CB/PLA. As proof of concept, the G/ABS sensor was employed for electroanalytical quantification of paracetamol (PAR) in pharmaceutical products. The linear concentration range was observed from 0.20 to 30 μmol L-1 and the limit of detection achieved was 54 nmol L-1, much lower than several recent studies dealing with the same analyte. The sensitivity of the G/ABS electrode regarding PAR was also far better when compared to CB/PLA sensor (0.50 μA/μmol L-1 vs. D34-919 solubility dmso 0.12 μA/μmol L-1). Analyses in commercial pill samples showed good accuracy (recoveries ca. 108%) and precision (RSDs less then 5%), suggesting great potential for use of this novel conductive thermoplastic in electroanalytical applications based on 3D printing.A rapid and reliable oxygen elimination system was evaluated here for the electroanalytical study of metals. Dissolved oxygen was removed locally in the vicinity of a sensor by the means of electrochemical oxygen filter constructed from platinum grids. Three metals (Cd, Pb, and Zn) were determined by stripping chronopotentiometry (SCP) at a mercury film screen-printed electrode. Limits of detection of metals were in the nanomolar range under optimized experimental conditions. The electrochemical device was also tested for metal quantification in simple electrolyte solutions and in a natural water matrix. The proposed combination of oxygen elimination system with the metal sensor completely removes the need to purge the sample before SCP measurement. This makes the determination of metals by SCP faster, portable and more suited for on-field applications.Efficient identification of pathogenic bacteria is greatly concerned with microbial food safety and foodborne diseases diagnosis. Surface-enhanced Raman scattering (SERS) tags are among the cutting-edge tools for bioanalysis, but facing troubles in either SERS sensitivity, durability, interfering signals, or universal recognition agents for target bacteria. This work proposed a multivariate scheme enabled by polyphenolic chemistry for the green synthesis, facile stabilization (functionalization), protective encapsulation, and bio-affinitive design of metal-phenolic networks (MPNs)-encapsulated silver SERS nanotags (AgNPs@4-mercaptobenzonitrile@MPNs). With remarkable SERS properties, shelf stability, and bacterial affinity, AgNPs@4-mercaptobenzonitrile@MPNs tags enabled rapid, reproducible, and interference-free SERS detection of two representative foodborne pathogens (i.e., E. coli O157 H7 and S. aureus) in the assistance of an aptamer-labelled magnetic probe, reaching good sensitivity and selectivity. Moreover, this SERS biosensor worked well in real food samples, manifesting the potential of polyphenolic chemistry in the customization of bio-affinitive SERS nanotags for food safety detection.
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