Cacodylate sensor and its application for the determination of amino acid levels in biological samples
Abstract Background The importance of recognizing and quantifying chemical anions/cations found in various types of samples, including environmental and biological samples, is extensively studied. Recent findings suggest the possibility of health risk caused by organic dimethylarsininc acid (DMAs) compound itself, not its arsenic inorganic metabolite. Objective This article aims to fabricate polymeric-membrane electrochemical sensors with high sensitivity and selectivity for dimethylarsinate (cacodylic acid sodium salt, DMAs) based on silver diethyldithiocarbamate (AgDDTC) and CuIIphthalocyanine (CuPC) as novel neutral carriers and their applications. Methods DMAs calibration relations and titrations were carried out using a potentiometric workstation equipped with a double-junction reference electrode, in conjunction with the fabricated working electrodes. Results Sensors revealed fast and stable anionic response with near-Nernstian slopes (-38.6 ± 0.9 and -31.5 ± 0.6 mV/decade), within concentration ranges (1.7x10−5 - 1.0x10−2 and 3.0x10−5 - 1.0x10−2 M) and detection limits (1.0x10−5 and 1.6x10−5 M) for AgDDTC- and CuPC-based sensors, respectively. Sensors are characterized with their extended life-time, signal stability, high precision and short response times. Selectivity for cacodylate anion over most common anions is tested for proposed electrodes. Sensors were satisfactorily applied for DMAs quantification in biological matrices with recoveries ranging between 96.2 and 99.0%. Membrane sensors were interfaced with a flow-through system for continuous monitoring of DMAs. The sensors were tested for the assay of different amino acids based on their reaction with cacodylate, where reaction end-points were monitored with the proposed electrodes using direct potentiometric determination and flow injection analysis (FIA).