In situ preparation of TiO2/f-MWCNT catalyst using Pluronic F127 assisted sol-gel process for sonocatalytic degradation of methylene blue.

In this study, titanium dioxide- Pluronics @F127/functionalized -multi walled carbon nanotubes (TiO2-F127f-/MWCNT) nanocatalysts were prepared, characterized, and used in methylene blue (MB) degradation under ultrasonic conditions. The characterization studies were performed using TEM, SEM, and XRD analyses to reveal the morphological and chemical properties of TiO2-F127/MWCNT nanocatalysts. To detect the optimum parameters for MB degradation using TiO2-F127/f-MWCNT nanocatalysts, several experimental parameters were conducted at various conditions such as different temperatures, pH, catalyst amount, hydrogen peroxide (H2O2) concentration, and various reaction contents. Transmission electron microscopy (TEM) analyses showed that TiO2-F127/f-MWCNT nanocatalysts consisted of a homogenous structure and have a 12.23 nm particle size. The crystalline particle size of TiO2-F127/MWCNT nanocatalysts was found to be 13.31 nm. Scanning electron microscope (SEM) analyses revealed the surface structure of TiO2-F127/f-MWCNT nanocatalysts turned to be modified after TiO2 loaded on MWCNT. Under the optimum conditions; pH: 4, MB concentration: 25 mg/L, H2O2 concentration: 30 mol/L, reaction time: and catalyst dose: 24 mg/L, chemical oxygen demand (COD) removal efficiency reached a maximum of 92%. To detect the radical effectiveness, three scavenger solvents were tested. Reuse experiments revealed that TiO2-F127/f-MWCNT nanocatalysts retained 84.2% catalytical activity after 5 cycles. Gas chromatography-mass spectrometry (GC-MS) was successfully used to identify the generated intermediates. Based on the experimental results, it has been suggested that •OH radicals are the main active species responsible for the degradation reaction in the presence of the TiO2-F127/f-MWCNT nanocatalysts.

Nitric Oxide Detection Using a Corona Phase Molecular Recognition Site on Chiral Single-Walled Carbon Nanotubes.

Semiconducting single-walled carbon nanotubes (s-SWCNT) are structures that fluoresce in the near-infrared region. By coating SWCNT surfaces with polymeric materials such as single-chain DNA, changes in fluorescence emission occur in the presence of reagents. In this way, polymer-coated SWCNT structures allow them to be used as optical sensors for single molecule detection. Especially today, the inadequacy of the methods used in the detection of cellular molecules makes the early diagnosis of diseases such as cancer difficult at the single-molecule level. In this study, the detection of nitric oxide (NO) signals, which are a marker of cancer, was carried out at the single-molecule level. In this context, a sensor structure was formed by coating the 7,6-chiral s-SWCNT surface with ssDNA with different oligonucleotide lengths (AT). The sensor structure was characterized by using UV-vis spectroscopy and Raman spectroscopy microscopy. After formation of the sensor structure, a selectivity library was created using various molecules. As a result of the coating of the SWCNT (7,6) surface with DNA corona phase formation, Raman peaks at 195 and 276 cm-1 were observed to shift to the right. Additionally, the selectivity library results showed that the (AT)30 sequence can be used in NO detection. As a result of the studies using SWCNT (7.6)- (AT)30, the limit of detection (LOD) and limit of determination (LOQ) values of the sensor against NO were found to be 1.24 and 4.13 µM, respectively.

A sensitive, fast, selective, and reusable enzyme-free glucose sensor based on monodisperse AuNi alloy nanoparticles on activated carbon support.

In this study, a glucose sensor modified with activated carbon supported gold-nickel (AuNi@AC) metal nanoparticles was prepared for the early diagnosis of diabetes. Electrochemical tests were carried out by determining the optimum working conditions of the prepared glucose sensor. The characterization analyses of the designed glucose sensor were performed by Transmission Electron Microscopy (TEM), X-Ray Diffraction (XRD), X-Ray Photoelectron Spectroscopy (XPS) and Raman Spectroscopy. It was determined that the average particle size of the nanoparticles in the AuNi alloy structure was 2.03 ± 0.37 nm. The determined detection limit of the AuNi@AC nanosensor was calculated as 0.41 µM as a result of the high linear range provided up to 1.7 mM. In addition, the sensitivity of AuNi@AC nanosensor to glucose, which has a high sensitivity value of 1955 µA mM-1 cm-2, was determined.

Synthesis and application of AuNi@AC nano adsorbents for the removal of Maxilon Blue 5G azo dye from aquatic mediums.

In this research, gold-nicel supported on activated carbon (AC) nanoadsorbent (AuNi@AC) synthesized by following a series of physicochemical procedures was prepared for the removal of Maxilon Blue 5G (MB) which is a cationic textile dye. Experimental studies based on parameters specifically pH, contact time, nano catalytic adsorbent particle, initial MB dye concentration and temperature effect were conducted in aqueous solutions in a batch system. AuNi@AC nanoadsorbents (NAs) reached the equilibrium in 30 min under optimum conditions in adsorption of the dye. The pseudo-first, second-order, and intra-particle diffusion models were tested to evaluate a the experimental results. Adsorption kinetics were found to be represented by the pseudo-second-order model, and the maximum adsorption capacity (qmax.) was calculated to be 542.90 mg/g (or 2.041 mmol/g). The synthesized magnetic AuNi@AC nanoadsorbent showed a high-efficiency reusability effect of about 64% after five reuse runs. Also, thermodynamic function parameters such as activation energy (Ea), Gibbs free energy (ΔG *), and entropy (ΔS *) were investigated in the sorption study. After all evaluation of data, it was concluded that the novel AuNi@AC nanoadsorbent could be considered as an effective support material for the removal of various organic pollutants in aquation solution especially for the removal of MB.

Comparison of functional and maximal exercise capacity, respiratory and peripheral muscle strength, dyspnea, and fatigue in patients with heart failure with pacemakers and healthy controls: a cross-sectional study.

Background: Despite major breakthroughs that have recently been made in pacemakers implanted in patients with heart failure (HF), it is clear that functional impairments and symptoms often remain. However, only limited studies have investigated exercise capacity, muscle strength, pulmonary function, dyspnea, and fatigue in these patients. Therefore, we aimed to compare aforementioned outcomes in patients and healthy controls. Methods: A cross-sectional study. Fifty patients with HF with pacemakers (58.90 ± 10.69 years, NYHA II-III, LVEF: 30.79 ± 8.78%) and 40 controls (56.33 ± 5.82 years) were compared. Functional (6-Minute Walking test (6-MWT)) and maximal exercise capacity (Incremental Shuttle Walk test (ISWT)), respiratory (Mouth pressure device) and peripheral muscle strength (Dynamometer), pulmonary function (Spirometry), dyspnea (Modified Medical Research Council Dyspnea scale), and fatigue (Fatigue Severity scale) were evaluated. ClinicalTrial number: NCT03701854. Results: 6-MWT (412.62 ± 96.51 m versus 610.16 ± 59.48 m) and ISWT (279.97 m versus 655 m) distances (p ˂ 0.001), pulmonary function (p˂0.001), respiratory and peripheral muscle strength (p ˂ 0.001) were significantly lower; dyspnea (p ˂ 0.001) and fatigue (p = .030) scores were higher in patients compared with controls. Conclusion: Maximal and functional exercise capacity is impaired in the majority of patients with HF with pacemakers, respiratory and peripheral muscles are weakened, dyspnea and fatigue perceptions are increased. Patients with pacemakers have to be included in cardiac rehabilitation programs to improve impairments.

Tramadol sensing in non-invasive biological fluids using a voltammetric electronic tongue and an electrochemical sensor based on biomimetic recognition.

Tramadol (TRA) is a weak opioid analgesic, prescribed to relieve mild to moderately severe pain. However, side effects of TRA overdoses, including vomiting, depression, tachycardia, convulsions, morbidity and mortality are often reported. In this study, an electrochemical sensor based on molecularly imprinted conductive polymer was firstly developed for the quantitative and non-invasive detection of TRA. Secondly, a voltammetric electronic tongue (VE-Tongue) combined with chemometric methods was used for the qualitative analysis. The MIP sensor was constructed by self-assembling a poly-aniline layer coated with silver nanoparticles (PANI-AgNPs) on a screen-printed gold electrode (Au-SPE). Then, 2-amino-thiophenol was polymerised in the presence of TRA. The electronic device exhibits, under optimal conditions, responses proportional to TRA concentrations (0.01-100 µg/mL) with detection and quantification limits of 9.42 µg/mL and 28.55 µg/mL, respectively. Moreover, its selectivity was proven by insignificant interferences of substances (paracetamol and citric acid). Spiked saliva and urine samples were used for the sensor practical application with a significant recovery above 90% and standard deviations below 4.5%. Besides, urine samples' analyses using VE-Tongue and pattern recognition methods show good discrimination, classification, and prediction results with scores above 95%. Correspondingly, both electro-analytical devices could be viable for monitoring drugs in biological matrices.

A critical review on the use of potentiometric based biosensors for biomarkers detection.

Potentiometric-based biosensors have the potential to advance the detection of several biological compounds and help in early diagnosis of various diseases. They belong to the portable analytical class of biosensors for monitoring biomarkers in the human body. They contain ion-sensitive membranes sensors can be used to determine potassium, sodium, and chloride ions activity while being used as a biomarker to gauge human health. The potentiometric based ion-sensitive membrane systems can be coupled with various techniques to create a sensitive tool for the fast and early detection of cancer biomarkers and other critical biological compounds. This paper discusses the application of potentiometric-based biosensors and classifies them into four major categories: photoelectrochemical potentiometric biomarkers, potentiometric biosensors amplified with molecular imprinted polymer systems, wearable potentiometric biomarkers and light-addressable potentiometric biosensors. This review demonstrated the development of several innovative biosensor-based techniques that could potentially provide reliable tools to test biomarkers. Some challenges however remain, but these can be removed by coupling techniques to maximize the testing sensitivity.

Comparison of functional exercise capacity, quality of life and respiratory and peripheral muscle strength between patients with stable angina and healthy controls.

OBJECTIVE: We aimed to compare functional exercise capacity, respiratory and peripheral muscle strength, pulmonary function and quality of life between patients with stable angina and healthy controls. METHODS: We compared 33 patients with stable angina (55.21 ± 6.12 years old, Canada Class II-III, left ventricular ejection fraction: 61.92 ± 7.55) and 30 healthy controls (52.70 ± 4.22 years old). Functional capacity (6-minute walk test (6-MWT)), respiratory muscle strength (mouth pressure device), peripheral muscle strength (dynamometer), pulmonary function (spirometer) and quality of life (Short Form 36 (SF-36)) were evaluated. RESULTS: 6-MWT distance (499.20 ± 51.91 m versus 633.05 ± 57.62 m), maximal inspiratory pressure (85.42 ± 20.52 cmH2O versus 110.44 ± 32.95 cmH2O), maximal expiratory pressure (83.33 ± 19.05 cmH2O versus 147.96 ± 54.80 cmH2O) and peripheral muscle strength, pulmonary function and SF-36 sub-scores were lower in the angina group versus the healthy controls, respectively. CONCLUSION: Impaired peripheral and respiratory muscle strength, reduction in exercise capacity and quality of life are obvious in patients with stable angina. Therefore, these parameters should be considered in stable angina physiotherapy programmes to improve impairments.

Magnetic nanocomposites decorated on multiwalled carbon nanotube for removal of Maxilon Blue 5G using the sono-Fenton method.

Herein, multiwalled carbon nanotube-based Fe3O4 nano-adsorbents (Fe3O4@MWCNT) were synthesized by ultrasonic reduction method. The synthesized nano-adsorbent (Fe3O4@MWCNT) exhibited efficient sonocatalytic activity to remove Maxilon Blue 5G, a textile dye, and present in a cationic form, in aqueous solution under ultrasonic irradiation. The magnetic nano-adsorbent particles were characterized by high-resolution transmission electron microscopy (HR-TEM), transmission electron microscopy (TEM), Raman spectroscopy and X-ray diffraction (XRD). Some important parameters such as nano-adsorbent dosage, solution pH, initial dye and H2O2 concentration, reaction time, ultrasonic power and temperature were tested to determine the optimum conditions for the elimination of Maxilon Blue 5G dye. The reusability results showed that Fe3O4@MWCNT nano-adsorbent has a decrease of about 32.15% in the removal efficiency of Maxilon Blue 5G under ultrasonic irradiation after six times reuse. Additionally, in order to reveal the sufficient kinetic explanation, various experiments were performed at different temperatures and testing three kinetic models like the pseudo-first-order, pseudo-second-order and intraparticle diffusion for removal adsorption process of Maxilon Blue 5G using Fe3O4@MWCNT nano-adsorbent. The experimental kinetic results revealed that the adsorption process of Maxilon Blue 5G in the aquatic mediums using sono-Fenton method was found to be compatible with the intraparticle diffusion. Using kinetic models and studies, some activation parameters like enthalpy, entropy and Gibbs free energy for the adsorption process were calculated. The activation parameters indicated that Fe3O4@MWCNT nano-adsorbent could be used as an effective adsorbent for the removal of Maxilon Blue 5G as a textile dye and the adsorption process of Maxilon Blue 5G with Fe3O4@MWCNT nano-adsorbent is spontaneous.

Multiwalled carbon nanotube-based nanosensor for ultrasensitive detection of uric acid, dopamine, and ascorbic acid.

A novel multiwalled carbon nanotube (MWCNT) based sensor was fabricated as a highly precise and stable electrochemical sensor. The synthesized sensor which consists of ZnNi bimetallic nanoalloy called the ZnNi NPs@f-MWCNT sensor, have been used for the simultaneous detection of uric acid (UA), dopamine (DA) and ascorbic acid (AA). The ZnNi NPs@f-MWCNT sensor obtained based on the microwave irradiation process, and its characterization was performed by using several physical techniques such as XRD, XPS, TEM, Raman, etc. The characterization showed that this sensor has excellent properties such as rich pore channels, excellent structural durability, and large surface area. These properties facilitated mass transfer and electron conductions. It was observed that the obtained sensor gave high electrochemical activity and wide linear responses (0.3-1.1 mM AA, 0.2-1.2 mM DA, 0.2-1.1 mM UA) in the detection of uric acid (UA), dopamine (DA) and ascorbic acid (AA). In addition to these properties, it has been found that the sensor has excellent anti-interferents properties towards AlCl3, KCl3, glucose, etc. and ZnNi NPs@f-MWCNT sensor was further applied to determine uric acid (UA), dopamine (DA) and ascorbic acid (AA) in real samples.

Composites of Bimetallic Platinum-Cobalt Alloy Nanoparticles and Reduced Graphene Oxide for Electrochemical Determination of Ascorbic Acid, Dopamine, and Uric Acid.

The ultimate aim of this study is to produce a composite of bimetallic platinum-cobalt nanoparticles and reduced graphene oxide (Pt-Co@rGO) based biosensor for the detection of ascorbic acid (AA), dopamine (DA) and uric acid (UA). Those are biologically important molecules with the key functions for the human body. Pt-Co@rGO was synthesized using a microwave-assisted technique and utilized for the production of a highly sensitive and stable electrochemical biosensor. Detailed spectral XPS and Raman analysis, XRD, and TEM/HR-TEM characterization were also studied. Due to the superior activity and excellent conductivity of rGO, well-separated oxidation peaks of these biomolecules is proven by DPV (differential pulse voltammetry) and CV (cyclic voltammetry) measurements. The prepared Pt-Co@rGO-based biosensor showed high electrochemical activity, a broad linear response, high sensitivity, and acceptable limit of detection values for individual and simultaneous determination of AA, DA, and UA, under optimized conditions. The linear range of Pt-Co@rGO was found to be 170-200; 35-1500 and 5-800 µM for AA, DA, and UA, respectively. Moreover, the detection limit of the prepared composite was calculated as 0.345; 0.051; 0.172 µM for AA, DA, and UA, respectively. In the field of electrochemical biosensors, Pt-Co@rGO based sensor is highly promising due to its superior sensitivity and good selectivity properties.

In vivo biosensing via tissue-localizable near-infrared-fluorescent single-walled carbon nanotubes.

Single-walled carbon nanotubes are particularly attractive for biomedical applications, because they exhibit a fluorescent signal in a spectral region where there is minimal interference from biological media. Although single-walled carbon nanotubes have been used as highly sensitive detectors for various compounds, their use as in vivo biomarkers requires the simultaneous optimization of various parameters, including biocompatibility, molecular recognition, high fluorescence quantum efficiency and signal transduction. Here we show that a polyethylene glycol ligated copolymer stabilizes near-infrared-fluorescent single-walled carbon nanotubes sensors in solution, enabling intravenous injection into mice and the selective detection of local nitric oxide concentration with a detection limit of 1 µM. The half-life for liver retention is 4 h, with sensors clearing the lungs within 2 h after injection, thus avoiding a dominant route of in vivo nanotoxicology. After localization within the liver, it is possible to follow the transient inflammation using nitric oxide as a marker and signalling molecule. To this end, we also report a spatial-spectral imaging algorithm to deconvolute fluorescence intensity and spatial information from measurements. Finally, we demonstrate that alginate-encapsulated single-walled carbon nanotubes can function as implantable inflammation sensors for nitric oxide detection, with no intrinsic immune reactivity or other adverse response for more than 400 days.

Molecular recognition using corona phase complexes made of synthetic polymers adsorbed on carbon nanotubes.

Understanding molecular recognition is of fundamental importance in applications such as therapeutics, chemical catalysis and sensor design. The most common recognition motifs involve biological macromolecules such as antibodies and aptamers. The key to biorecognition consists of a unique three-dimensional structure formed by a folded and constrained bioheteropolymer that creates a binding pocket, or an interface, able to recognize a specific molecule. Here, we show that synthetic heteropolymers, once constrained onto a single-walled carbon nanotube by chemical adsorption, also form a new corona phase that exhibits highly selective recognition for specific molecules. To prove the generality of this phenomenon, we report three examples of heteropolymer-nanotube recognition complexes for riboflavin, L-thyroxine and oestradiol. In each case, the recognition was predicted using a two-dimensional thermodynamic model of surface interactions in which the dissociation constants can be tuned by perturbing the chemical structure of the heteropolymer. Moreover, these complexes can be used as new types of spatiotemporal sensors based on modulation of the carbon nanotube photoemission in the near-infrared, as we show by tracking riboflavin diffusion in murine macrophages.

Effects of sodium hypochlorite on gutta-percha and Resilon cones: an atomic force microscopy and scanning electron microscopy study.

The aim of this study was to evaluate the effects of 6% sodium hypochlorite (NaOCl) on gutta-percha (GP) and Resilon cones. Six standardized GP and Resilon cones were selected and cut 3mm from their tip. One GP and 1 Resilon cone were used as control samples. Cones were immersed in 6% NaOCl for 1, 5, 10, 20, and 30 minutes, thoroughly rinsed with nanopure water, and dried with filter paper. Then, surface topography was analyzed by atomic force microscopy and scanning electron microscopy coupled to an energy-dispersive x-ray (EDX) spectrometer. According to the root mean square and depth analysis values obtained from atomic force microscopic evalution, there were no significant differences found among the GP groups. However significant differences were found among Resilon cones (P ≤ .05). SEM images and EDX graphics showed that there were no prominent differences between GP and Resilon groups. These results showed that 6% NaOCl solution can be used in the disinfection of GP and Resilon cones. No alterations were observed on the GP cones, but it can change the surface of Resilon cones.