A proposed implantable voltammetric carbon fiber-based microsensor for corticosteroid monitoring by cochlear implants.

A novel carbon fiber microsensor (CFMS) with the capability of being inserted in the cochlear implant structure is introduced for in situ measurement of corticosteroid concentration. The microsensor structure is composed of a carbon microfiber, an Ag wire, and a Pt wire acting respectively as a working electrode, a reference electrode, and a counter electrode. In addition, a silicone septum is used for isolation purposes in place of the epoxy resin. The septum-insulated microsensor is capable of monitoring the concentration of the corticosteroids in the perilymph fluid without a need for sampling from the inner ear fluid and the consequent ex vivo analysis. The electrochemical determination of the corticosteroids was investigated on the carbon fiber electrode surface by differential pulse voltammetry. During the reduction of dexamethasone (DEX), a cathodic peak with a peak potential of -1.3 V appeared at the CFMS. Using the CFMS under optimized conditions, a calibration plot of the dexamethasone (DEX) in the artificial perilymph solution exhibited two linear ranges from 10 nM to 2 µM and 2 to 40 µM (sensitivity equal to 16.55 µA µM-1 cm-2; LOD = 4 nM) conforming with the DEX concentration range inside the inner ear after the insertion of a drug-eluting cochlear implant electrode (CIE). Furthermore, the interferences occurring in the hearing functions of the CIE after the presence and function of the CFMS were simulated numerically using the finite element method. According to our results, decreasing the size of the microsensor introduces lower interferences with the auditory function of the cochlear implant electrode.

Preparation and in vivo evaluation of in situ gel system as dual thermo-/pH-responsive nanocarriers for sustained ocular drug delivery.

OBJECTIVE: Ciprofloxacin (CIP) was effective in treating bacterial keratitis. The purpose of this study was to prepare an effective prolonged-release of CIP by both temperature and pH-triggered in situ nanogels for the treatment of keratitis. MATERIALS AND METHODS: Poly(N-isopropylacrylamide-methacrylicacide-vinylpyrrolidone) [P (NIPAAm-MAA-VP)] nanoparticles was synthesised and used for preparation of CIP-loaded nanogels. Antimicrobial and in vivo animal studies of the CIP-loaded nanoformulation were performed. RESULTS: Nanoformulation with a mean particle size between 10 and 50 nm and higher than 95% encapsulation efficiency was obtained. Ciprofloxacin released from the nanoparticles showed an enhanced antibacterial effect as determined by minimal inhibitory concentrations. In vivo studies demonstrated reasonable efficacy in severe keratitis using the developed nanoformulation. CONCLUSIONS: Nanoformulation had acceptable efficacy in treating bacterial keratitis in an animal model. Therefore, the developed system has the potential to be used in localised application for the treatment of keratitis.

Nonenzymatic glucose sensor design based on carbon fiber ultra-microelectrode: Controlled with a manual micro adjuster.

Interest in designing and manufacturing glucose sensors based on metal oxide-modified microelectrodes is growing and leading to the increased research efforts to develop continuous glucose measurements. A non-enzymatic glucose sensor based on an ultra-microelectrode is presented. A carbon fiber microelectrode electrodeposited by nickel nanoparticles (NiCFME) and activated as a nonenzymatic glucose sensor. The modified carbon microfiber was attached to a micro adjuster to adjust the height of the electrode inside the solution, which improved the accuracy of the microelectrode performance. The microstructure and morphology of the electrodes and nanoparticles investigated using SEM, EDX and XRD. The electrocatalytic glucose oxidation behavior of the sensing NiCFME got analyzed by cyclic voltammetry and amperometric measurements in alkaline medium. Achieved results demonstrated that the fabricated sensor displays the sensitivity up to 8.5 µA µM-1 cm-2 with a low detection limit of 3.0 µM, LOQ of 10.0 µM, with a linearity range of 10.0 µM-150.0 µM and response time about 0.4 s for glucose detection. Designed sensor had an appropriate good stability and significant selectivity towards glucose. Finally, the proposed sensor was successfully applied in determination of glucose in human blood plasma samples. The results illustrated; the proposed design is a promising candidate for the development of nonenzymatic glucose sensors.

Electrochemical Determination of Dexamethasone by Graphene Modified Electrode: Experimental and Theoretical Investigations.

We report on a combined experimental and theoretical study concerning the electrochemical behavior of the dexamethasone (DEX) on a graphene modified glassy carbon electrode (GCE). A good agreement between experiments and density functional theory (DFT)-based calculations is observed for the DEX reduction. The electrochemical behavior of the DEX was investigated on the surface of a glassy carbon electrode (GCE) modified with different type of graphenes, including graphene quantum dot (GQD), graphene oxide (GO), electrochemically synthesized graphene (EG), graphene synthesized by the Hummer method (HG) and graphene nanoplate (GNP) using voltammetric techniques (CV, DPV and SWV). The results exhibited a significant increase in the reduction of the peak current of the DEX in  the GNP modified GCE (GNP/GCE) in comparison to other modified electrodes and bare GCE. The unique morphology, size and electro catalytic properties of the GNP cause a sensitive response of the DEX in a novel sensor. Under the optimized experimental condition, the GNP/ GCE showed two linear dynamic ranges of 0.1-50 µM and 50-5000 µM with a low detection limit of 15 nM for determination of the DEX. The novel sensor is successfully applied to the sensitive determination of the DEX in human plasma samples with satisfactory recoveries. Energy of the LUMO and HUMO orbitals and energy calculations for the DEX molecule interacting with graphene were performed using the density functional B3LYP/6-31G. The theoretical results allied to significant charge transfer took place due to the interaction of the DEX with the applied graphene.

Physicochemical characteristics of Fe3O4 magnetic nanocomposites based on Poly(N-isopropylacrylamide) for anti-cancer drug delivery.

BACKGROUND: Hydrogels are a class of polymers that can absorb water or biological fluids and swell to several times their dry volume, dependent on changes in the external environment. In recent years, hydrogels and hydrogel nanocomposites have found a variety of biomedical applications, including drug delivery and cancer treatment. The incorporation of nanoparticulates into a hydrogel matrix can result in unique material characteristics such as enhanced mechanical properties, swelling response, and capability of remote controlled actuation. MATERIALS AND METHODS: In this work, synthesis of hydrogel nanocomposites containing magnetic nanoparticles are studied. At first, magnetic nanoparticles (Fe3O4) with an average size 10 nm were prepared. At second approach, thermo and pH-sensitive poly (N-isopropylacrylamide -co-methacrylic acid-co-vinyl pyrrolidone) (NIPAAm-MAA- VP) were prepared. Swelling behavior of co-polymer was studied in buffer solutions with different pH values (pH=5.8, pH=7.4) at 37 °C. Magnetic iron oxide nanoparticles (Fe3O4) and doxorubicin were incorporated into copolymer and drug loading was studied. The release of drug, carried out at different pH and temperatures. Finally, chemical composition, magnetic properties and morphology of doxorubicin-loaded magnetic hydrogel nanocomposites were analyzed by FT- IR, vibrating sample magnetometry (VSM), scanning electron microscopy (SEM). RESULTS: The results indicated that drug loading efficiency was increased by increasing the drug ratio to polymer. Doxorubicin was released more at 40 °C and in acidic pH compared to that 37 °C and basic pH. CONCLUSIONS: This study suggested that the poly (NIPAAm-MAA-VP) magnetic hydrogel nanocomposite could be an effective carrier for targeting drug delivery systems of anti-cancer drugs due to its temperature sensitive properties.

PLGA-based nanoparticles as cancer drug delivery systems.

Poly (lactic-co-glycolic acid) (PLGA) is one of the most effective biodegradable polymeric nanoparticles (NPs). It has been approved by the US FDA to use in drug delivery systems due to controlled and sustained- release properties, low toxicity, and biocompatibility with tissue and cells. In the present review, the structure and properties of PLGA copolymers synthesized by ring-opening polymerization of DL-lactide and glicolide were characterized using 1H nuclear magnetic resonance spectroscopy, gel permeation chromatography, Fourier transform infrared spectroscopy and differential scanning calorimetry. Methods of preparation and characterization, various surface modifications, encapsulation of diverse anticancer drugs, active or passive tumor targeting and different release mechanisms of PLGA nanoparticles are discussed. Increasing experience in the application of PLGA nanoparticles has provided a promising future for use of these nanoparticles in cancer treatment, with high efficacy and few side effects.