Assay of Famotidine in Pure Solutions and Pharmaceutical Preparatives using the Coated- graphite Electrode as a Detector in the FlA System

A simple electrochemical method was developed to estimate famotidine (FMT) in pure solutions and pharmaceutical preparatives by a flow-injection analysis system (FlA). This method includes preparation of a coated graphite electrode using FMT with the Phosphotungstic acid precipitant (PTA), di-butyl phthalate (DBP) and poly vinyl chloride (PVC). The electrode characteristics were examined by studying the optimum conditions, the carrier current, the injected model size, flow rate, the reaction coil length, pH, the range of concentrations, the minimum Nernst response, the response time, the detection limits, and the study also included identifying the electrode selectivity of the toward other interfering ions. The electrode showed that the best Nernst slope for the calibration curve was at 33.82 mv/decade within linear range of (1.0 × 10-6- 1.0 × 10-1M), correlation coefficient (R2) 0.9999, response time 10 seconds, the estimating speed is 90 sample/hour, while the rate of dilution degree (D) is 2.6452. The obtained results confirmed that it is of high accuracy and precision (Err 0.119%), (Rec 100.11%), (RSD 0.1233%). The proposed method was successfully applied to assay of FMT in commercial tablet forms.

Arrays of Copper Microelectrodes from Disposable Chips: Fabrication and Characterization

A simple, fast, and low-cost process to fabricate arrays of copper microelectrodes (CuMEs) based on disposable electronic microchips is described. Arrays with 8 to 20 CuMEs were characterized by energy-dispersive X-ray spectroscopy and cyclic voltammetry techniques. The closest interelectrode distance in the arrays is 358 ± 22 μm, and the minor radius ranged from 10.6 to 13.5 μm. The microchips with CuMEs were sealed in epoxy resin to fabricate the rod and flat-shaped platforms, allowing the CuMEs to be addressed separately. Glucose, hydrazine, and nitrate were used as analyte models for voltammetric and amperometric detection at CuMEs arrays, showing excellent performance in batch and flow-through cells. Glucose measurements carried out with flow injection analysis system with amperometric detection at an array of 20 CuMEs showed a wide linear range (0.020-4.0 mmol L-1), high sensitivity (734.1 μA L mmol-1 cm-2), and a limit of detection of 1.7 μmol L-1.

Studying the Reaction of Peroxynitrite with Myoglobin for Meat Extract Samples Using Cobalt Phthalocyanine-Modified Screen-Printed Carbon Electrodes and a Flow Injection Analysis System

Reactive oxygen/nitrogen species (ROS/RNS) have a great impact on cellular response to stress, cell proliferation, cell death, cancer, aging, or male infertility. Additionally, in the food industry and for consumers as well, it is very important to monitor quality and freshness of raw meat. Different factors are a sign of meat alteration (e.g., discoloration, rancidity, alteration of flavor). One pathway of alteration is the scavenging activity of myoglobin towards RNS (such as peroxynitrite, PON). This paper presents the development of an electrochemical PON sensor using cobalt phthalocyanine (CoPc) as a simple, cost effective, highly thermally stable, biomimetic catalyst, and the application of this electrochemical screen-printed carbon electrode (SPCE)-based sensor to meat extract samples, using flow injection analysis (FIA). The reduction of peroxynitrite, mediated by CoPc, occurs at a very low potential (around 0.1 V vs. Ag/AgCl pseudoreference); as for higher potentials, the mechanism of mediation changes, and the electro-oxidation of PON is observed. The surface of the modified electrode was characterized using SEM, FTIR and Cyclic Voltametry. The interaction of PON with myoglobin was studied using both UV-Vis and chronoamperometry (at 0.1 V, using the FIA system). The calibration of the electrode was performed: Ired (nA) = 6.313·CPON (µM) + 17.469; (R² = 0.9938). The calculated LOD was equal to 2.37 µM and the linear range was 3–180 µM. The performance of the electrode can be further improved using a pre-treatment (electro-reduction of the CoPc deposited film, at −0.3 V, during 60s). This could help us monitor and quantify how much PON was decomposed and when meat extracts are spiked with different PON concentrations, in a highly selective, sensitive, and reproducible way.

A Multi-Pump Magnetohydrodynamics Lab-On-A-Chip Device for Automated Flow Control and Analyte Delivery

This article shows the development of a computer-controlled lab-on-a-chip device with three magnetohydrodynamic (MHD) pumps and a pneumatic valve. The chip was made of a stack of layers of polymethylmethacrylate (PMMA), cut using a laser engraver and thermally bonded. The MHD pumps were built using permanent magnets (neodymium) and platinum electrodes, all of them controlled by an Arduino board and a set of relays. The implemented pumps were able to drive solutions in the open channels with a flow rate that increased proportionally with the channel width and applied voltage. To address the characteristic low pressures generated by this kind of pump, all channels were interconnected. Because the electrodes were immersed in the electrolyte, causing electrolysis and pH variations, the composition and ionic strength of the electrolyte solution were controlled. Additionally, side structures for releasing bubbles were integrated. With this multi-pump and valve solution, the device was used to demonstrate the possibility of performing an injection sequence in a system that resembles a traditional flow injection analysis system. Ultimately, the results demonstrate the possibility of performing injection sequences using an array of MHD pumps that can perform fluid handling in the 0–5 µL s−1 range.