A novel fluorescent probe based imprinted polymer-coated magnetite for the detection of imatinib leukemia anti-cancer drug traces in human plasma samples.

Myeloid leukemia is a chronic cancer, which associated with abnormal BCR-ABL tyrosine kinase activity. Imatinib (IMB) acts as a tyrosine kinase inhibitor and averts tumor growth in cancer cells by controlling cell division, so it is urgent to develop an effective assay to detect and monitor its IMB concentration. Therefore, an innovative fluorescent biomimetic sensor is a promising sensing material that constructed for the efficient recognition of IMB and displays excellent selectivity and sensitivity stemming from molecularly imprinted polymer@Fe3O4 (MIP@Fe3O4). The detection strategy depends on the recognition of IMB molecules at the imprinted sites in the presence of coexisting molecules, which are then transferred to the fluorescence signal. The synthesized MIP@Fe3O4 was characterized using Fourier-transform infrared spectroscopy (FT-IR), scanning electron microscopy (SEM), and atomic force microscopy (AFM). Furthermore, computational studies of the band gap (EHOMO-ELUMO) of the monomers, IMB, and their complexes were performed. These results confirmed that the copolymer is the most appropriate and has high stability (Binding energy; 0.004 x 10-19 KJ) and low reactivity. A comprehensive linear response over IMB concentrations from 5 × 10-6 mol/L to 8 × 10-4 mol/L with a low detection limit of 9.3 × 10-7 mol/L was achieved. Furthermore, the proposed technique displayed long-term stability (over 2 months), high intermediate precision (RSD<2.1 %), good reproducibility (RSD <1.9 %), and outstanding selectivity toward IMB over analogous molecules with similar chemical and spatial structure (no interference by 100 to 150-fold of the competitors). Owing to these merits, the proposed fluorescence sensor was utilized to detect IMB in drug tablets and human plasma, and satisfactory results (99.3-100.4 %) were obtained. Thus, the synthesized fluorescence sensor is a promising platform for IMB sensing in various applications.

A rational study of transduction mechanisms of different materials for all solid contact-ISEs.

The new era of solid contact ion selective electrodes (SC-ISEs) miniaturized design has received an extensive amount of concern. Because it eliminated the requirement for ongoing internal solution composition optimization and created a two-phase system with stronger detection limitations. Herein, the determination of venlafaxine HCl is based on a comparison study between different ion- to electron transduction materials (such as; multiwalled carbon nanotubes (MWCNTs), polyaniline (PANi), and ferrocene) and illustrating their mechanisms in their applied sensors. Their different electrochemical features (such as bulk resistance (Rb**), double-layer capacitance (Cdl), geometric capacitance (Cg), and specific capacitance (Cp)) were evaluated and discussed by using the Electrochemical Impedance Spectroscopy (EIS), Chronopotentiometry (CP), and Cyclic Voltammetry (CV) experiments. The results indicated that each transducer's influence on the proposed sensor's electrochemical characteristics is determined by their unique chemical and physical properties. The electrochemical features vary for different solid contact materials used in transduction mechanisms. The results confirm that the MWCNT sensor revealed the best electrochemical behavior with the potentiometric response of a near-Nernestian slope of 56.1 ± 0.8 mV/decade with detection limits of 3.8 × 10-6 mol/L (r2 = 0.999) and a low potential drift (∆E/∆t) of 34.6 µV/s. Also, the selectivity study was performed in the presence of different interfering species either in single or complex matrices. This demonstrates excellent selectivity, stability, conductivity, and reliability as a VEN-TPB ion pair sensor for accurately measuring VEN in its various formulations. The proposed method was compared to HPLC reported technique and confirmed no significant difference between them. So, the proposed sensors fulfill their solutions' demand features for VEN appraisal.

Electrochemical sensor based on amine- and thiol-modified multi-walled carbon nanotubes for sensitive and selective determination of uranyl ions in real water samples.

Novel selective and sensitive electrochemical sensors based on the modification of a carbon paste electrode (CPE) with novel amine- and thiol-functionalized multi-walled carbon nanotubes (MWCNT) have been developed for the detection and monitoring of uranyl ions in different real water samples. Multiwalled carbon nanotubes were grafted with 2-aminothiazole (AT/MWCNT) and melamine thiourea (MT/MWCNT) via an amidation reaction in the presence of dicyclohexyl carbodiimide (DCC) as a coupling agent. This modification for multiwalled carbon nanotubes has never been reported before. The amine and thiol groups were considered to be promising functional groups due to their high affinity toward coordination with uranyl ions. The modified multi-walled carbon nanotubes were characterized using different analytical techniques including FTIR, SEM, XPS, and elemental analysis. Subsequently, 10 wt% MT/MWCNT was mixed with 60 wt% graphite powder in the presence of 30 wt% paraffin oil to obtain a modified carbon paste electrode (MT/MWCNT/CPE). The electrochemical behavior and applications of the prepared sensors were examined using cyclic voltammetry, differential pulse anodic stripping voltammetry, and electrochemical impedance spectroscopy. The MT/MWCNT/CPE sensor exhibited a good linearity for UO22+ in the concentration range of 5.0 × 10-3 to 1.0 × 10-10 mol L-1 with low limits of detection (LOD = 2.1 × 10-11 mol L-1) and quantification (LOQ = 7 × 10-11 mol L-1). In addition, high precision (RSD = 2.7%), good reproducibility (RSD = 2.1%), and high stability (six weeks) were displayed. Finally, MT-MWCNT@CPE was successfully utilized to measure the uranyl ions in an actual water sample with excellent recoveries (97.8-99.3%). These results demonstrate that MT-MWCNT@CPE possesses appropriate accuracy and is appropriate for environmental applications.

Electrochemical sensing of sodium dehydroacetate in preserved strawberries based onin situ pyrrole electropolymerization at modified carbon paste electrodes.

Sodium dehydroacetate (SDA) is one of the most common additives and preservatives in food, especially for strawberries, due to its fungicidal and antibacterial effects. Therefore, an innovative electrochemical sensor, depending on carbon paste electrode (CPE) modulated with multi-walled carbon nanotubes and molecularly imprinted polymers, was constructed for in situ detection of SDA. Based on density functional theory calculations, the polymer film was imprinted on the modified CPE surface via electrochemical polymerization of pyrrole in the presence of SDA. The morphology and electrochemical behavior of the synthesized sensors were characterized using different techniques. Under optimal conditions,a wide linear range (4.1 × 10-6 -1.2 mM)with a detection limit of 0.13 nM was obtained using differential pulse voltammetry and electrochemical impedance spectroscopy. The proposed sensor displayed superb selectivity for SDA, good precision (RSD = 2.7%), and high stability (˃4 weeks). Thus, it was successfully applied to determine SDA in strawberry samples with excellent recoveries (96.7%-100%).

Applications of electrochemical techniques for determination of anticoagulant drug (Rivaroxaban) in real samples.

The electrochemical behavior of rivaroxaban (RIV), a direct Factor Xa inhibitor, was investigated using a glassy carbon electrode (GCE) based on molecularly imprinted polymer (MIP). The MIP was developed by co-polymerization of different monomers (acrylamide and methacrylic acid) with the cross-linker (ethylene glycol dimethacrylate (EGDMA)) in the presence of initiator (potassium persulphate) and RIV as a template. Fourier transform infrared spectroscopy (FT-IR), atomic force microscopy (AFM), energy dispersive X-ray (EDX), and scanning electron microscope (SEM) were used for the characterization of the fabricated polymers. To prepare the potentiometric sensor, the MIP was incorporated in polyvinyl chloride (PVC) in the presence of a plasticizer and coated on the GCE as one layer. While the voltammetric sensor was prepared by drop coating technique, in which the graphene oxide and MIP were deposited on the bare GCE, respectively. Linear response over RIV concentrations in the range of 1.2 × 10-9 - 1 × 10-3 mol L-1 and 5.4 × 10-11 - 3.1 × 10-3 mol L-1 with detection limits of 2.4 × 10-10 mol L-1 and 2.3 × 10-12 mol L-1 were achieved for potentiometric and voltammetric sensors, respectively. Both sensors have high precision, selectivity, and good stability. Due to the abovementioned merits, both sensors were successfully applied for the detection of RIV in different blood samples and in pharmaceutical tablets, and acceptable mean recoveries (99.3-100.3%) were obtained.

Selective preconcentration separation of Hg(ii) and Cd(ii) from water, fish muscles, and cucumber samples using recycled aluminum adsorbents.

Modified aluminum scrap waste was used in the selective extraction of Hg(ii), and Cd(ii) ions. The aluminum scraps were modified with dibenzoylmethane, or isatoic anhydride, or 5-(2-chloroacetamide)-2-hydroxybenzoic acid. The modified aluminum sorbents were characterized by FT-IR, SEM, XRD, XPS, TGA, and elemental analysis. Modes of chelation between adsorbents and target metal ions were deduced via DFT. The highest adsorption capacity was observed for benzo-amino aluminum (BAA) toward Hg(ii), which reached 234.56 mg g-1, while other modified sorbents ranged from 135.28 mg g-1 to 229.3 mg g-1. Under the optimized conditions, the BAA adsorbent showed a lower limit of detection (1.1 mg L-1) and limit of quantification (3.66 mg L-1) for mercury ions than other sorbents. The prepared aluminum adsorbents also exhibited significant selectivities for Hg(ii) and Cd(ii) ions in the presence of competing metal ions.

Selective separation of uranyl ions from some lanthanide elements using a promising ß-enaminoester ligand by cloud point extraction.

For uranyl extraction, a distinctive chelating ligand, namely ethyl 2-amino-6-hydroxy-5-(4-methoxyphenyldiazenyl)-4-phenyl-4H-benzo[f]chromene-3-carboxylate, has been synthesized and characterized using FT-IR, NMR, and ESI-MS. Subsequently, a cloud point extraction (CPE) protocol has been developed for the selective separation of the trace amounts of uranyl ions from some lanthanide ions after being captured by the ligand in the presence of non-ionic surfactant (Triton X-114). The extraction procedure has been optimized based on the concentration of the complexing agent and the non-ionic surfactant, phase separation temperatures, pH, and ionic strength. The developed CPE procedure exhibited a relatively low detection limit of 0.5 ng mL-1 in the linear range from 3 ng mL-1 to 250 ng mL-1. Furthermore, interference studies have been carried out to study the selectivity of our protocol. These studies revealed that the recoveries of uranyl ions were in the range from 96.1% to 99.9% in the presence of some lanthanide ions such as Th4+, Gd3+, and Sm3+. It is worth mentioning that the geometry optimization, reactivity, and molecular electrostatic potential maps of the ligand and the proposed UO2 2+ complex were acquired via DFT calculations to study their stabilities based on the geometry and binding affinity. The theoretical data confirmed the octahedral geometry of the UO2 2+ complex with the lowest energy and excellent stability. The robustness of the proposed methodology was evaluated by the detection of uranyl ions in different environmental samples and synthetic mixtures.

Selective and sensitive electrochemical sensors based on an ion imprinting polymer and graphene oxide for the detection of ultra-trace Cd(ii) in biological samples.

New selective and sensitive electrochemical sensors were designed based on the deposition of a promising ion imprinted polymer (IIP) on the surface of glassy carbon electrode (GCE) for the detection and monitoring of Cd(ii) in different real samples. Herein, a highly selective Cd-imprinted polymer was successfully synthesized using a novel heterocyclic compound based on the benzo[f]chromene scaffold that acted as a complexing agent and a functional monomer in the presence of azobisisobutyronitrile (initiator) and ethylene glycol dimethacrylate (cross-linker). The characterization of the synthesized chelating agent and IIP was performed using FT-IR, SEM, 1H-NMR, EIMS, and EDX analyses. After that, the voltammetric sensor was manufactured by introducing graphene oxide (GO) on the surface of GCE; then, the IIP was grown by a drop coating technique. The electrochemical characterization of the voltammetric sensor (IIP/GO@GCE) was performed by CV and EIS. For comparison, the potentiometric sensor was also prepared by embedding IIP in plasticized polyvinyl chloride and depositing it as one layer on the GCE surface. Anodic stripping voltammetry was used to construct the calibration graph; the IIP/GO@GCE exhibited a wider detection range (4.2 × 10-12-5.6 × 10-3 mol L-1) and extremely low detection limit (7 × 10-14 mol L-1) for Cd(ii). Meanwhile, the potentiometric sensor showed a linear calibration curve for Cd(ii) over a concentration range from 7.3 × 10-8 mol L-1 to 2.4 × 10-3 mol L-1 with a detection limit of 6.3 × 10-10 mol L-1. Furthermore, both sensors offered outstanding selectivity for Cd(ii) over a wide assortment of other common ions, high reproducibility, and excellent stability.

Molecularly Imprinted Polymer Based GCE for Ultra-sensitive Voltammetric and Potentiometric Bio Sensing of Topiramate.

Topiramate (TOP) drug is classified as one of the most commonly used human drugs for anticonvulsants and antiepileptic, so its rapid detection and monitoring is of great importance. In this work, new potentiometric (MIP/PVC/GCE) and voltammetric (MIP/GO/GCE) sensors for the selective and sensitive determination of TOP were fabricated based on the molecularly imprinted polymer (MIP) approach. The MIP was synthesized by the polymerization of acrylamide and methacrylic acid as monomers, in the presence of TOP as a template and ethylene glycol dimethacrylate as a cross-linker. The obtained products were characterized by FT-IR, SEM, BET, and EDX. The MIP was embedded in a plasticized polyvinyl chloride membrane and used as a potentiometric sensor for sensing TOP. Alternatively, the synthesized MIP and graphene oxide (GO) were deposited layer-by-layer on the surface of GCE to construct a voltammetric sensor for studying the electrochemical behavior of the drug. Under optimized conditions, both electrochemical sensors showed excellent linear relationships between the concentration of TOP and the response signals of MIP/GO/GCE or MIP/PVC/GCE sensors in the 2.7 × 10-10 to 4.9 × 10-3 M and 1 × 10-9 to 3.4 × 10-3 M ranges, respectively. Also, both sensors have good reproducibility and high stability for up to 15 days for a voltammetric sensor and 28 days for a potentiometric sensor. The utility of these sensors was checked for TOP analysis in different real samples with good recovery (92.8 - 99%).

Psychopathology and HIV risk behaviors among injection drug users in and out of treatment.

To replicate prior descriptions of injection drug users (IDUs), 158 IDUs recruited via a street-outreach program were compared to 320 non-IDUs on measures of substance use, lifetime psychopathology, and HIV risk behavior. IDUs were more likely to receive a diagnosis of antisocial personality disorder, but not other psychiatric diagnoses, and to report dependence on multiple substances. IDUs reported more HIV risk behaviors, but perceived HIV risk did not differ from non-IDUs. Compared to IDUs who declined treatment, IDUs willing to accept treatment did not differ on drug-related problems, lifetime psychopathology, or perceived HIV risk.