Evaluation of accuracy of FAD-GDH- and mutant Q-GDH-based blood glucose monitors in multi-patient populations.

BACKGROUND: Glucose dehydrogenases have been highly promoted to high-accuracy blood glucose (BG) monitors. The flavin adenine dinucleotide glucose dehydrogenase (FAD-GDH) and mutant variant of quinoprotein glucose dehydrogenase (Mut. Q-GDH) are widely used in high-performance BG monitors for multi-patient use. Therefore we conducted accuracy evaluation of the GDH monitors, FAD-GDH-based GM700 and Mut. Q-GDH-based Performa. METHODS: Different patients were enrolled: patients with and without diabetes, patients receiving respiratory therapies, hemodialysis (HD) and peritoneal dialysis (PD) patients, and neonates. The accuracy evaluation of FAD-GDH- and Mut. Q-GDH-based monitors referred to ISO 15197:2013 which applies new criteria for the minion accuracy requirements: more than 95% of the blood glucose readings shall fall within ±15mg/dL of the reference method at glucose concentration <100mg/dL and within ±15% of the reference method at glucose concentration ≥100mg/dL. Bland-Altman plots were used to evaluate the 2 GDH monitors as well. RESULTS: Bland-Altman plots visualized excellent precision of the BG monitors. The 95% limit agreement of overall results for the FAD-GDH-based monitors was within ±12% and that for the Mut. Q-GDH-based monitors was from -10 to +17%. Both BG monitors met the accuracy requirements of ISO 15197:2013. The FAD-GDH-based monitor performed better with neonates and patients with and without diabetes, and the Mut. Q-GDH-based monitor performed better with HD and PD patients. CONCLUSIONS: Analytical results prove that the GDH-based monitors tolerate a broad BG concentration range, are oxygen independent, have BG specificity, and have minimal interference from hematocrit. The GDH-based monitors are reliable for multi-patient use.

Activated nickel platform for electrochemical sensing of phosphate.

We report here a highly selective enzymeless approach for the determination of phosphate (PO(4)(3-)) by flow injection analysis (FIA). In this system, the activation of barrel plated nickel electrode (Ni-BPE) in alkaline media to form a Ni(OH)(2)/NiO(OH) film was found to trigger the adsorption of phosphate at the electrode surface. Based on the suppressed current of the electrocatalytic oxidation of glucose at the activated Ni-BPE in 0.1 M NaOH solution caused by adsorption of phosphate, we develop an FIA detection scheme for the determination of phosphate. Under the optimized conditions of flow rate = 300 microL/min and detection potential = 0.55 V vs Ag/AgCl with 25 microM glucose in 0.1 M NaOH as carrier solution, the calibration curve showed a linear range up to 1 mM. Possible interferences from the coexisting ions were also investigated. The results demonstrated that sensor could be used for the determination of phosphate in the presence of nitrate, chloride, sulfate, acetate, oxalate, carbonate, and some anionic species of toxicological and environmental interest, such as chlorate, chromate, and arsenate ions. The electrode can be effectively regenerated without extra treatment under the hydrodynamic condition. For eight continuous injections of 40 microM PO(4)(3-), a relative standard deviation of 0.28% was obtained, indicating good reproducibility of the proposed method. The detection limit (S/N = 3) was calculated as 0.3 microM.

Determination of tranexamic acid in cosmetic products by high-performance liquid chromatography coupled with barrel plating nickel electrode.

Tranexamic acid (TA) is an important reagent in cosmetic skin-whitening formulation and a drug for the inhibition of plasminogen to plasmin in blood. Since there is no chromophore in tranexamic acid molecule to enable direct analysis by UV-visible absorption spectrophotometry, derivatization is thus required by excluding use of UV or fluorescence detection. We report here a relatively simple electrochemical TA detection method by using a barrel plating nickel electrode. Chromatographic separation was performed on a Hamilton PRP-X100 anion-exchange column (150 mm x 4.1 mm i.d., 10 microm particle size) with a (85:15, v/v) mixture of 0.1 mol l(-1) NaOH and acetonitrile as mobile phase and pumped at a flow rate of 0.9 ml min(-1). By detecting at +0.55 V vs. Ag/AgCl, the calibration plot was linear in the concentration window of 3-1000 ppm with regression coefficient and detection limit (S/N=3) of 0.9993 and 0.13 ppm (0.84 micromol l(-1)), respectively. Successive injections (n=10) of 50 ppm tranexamic acid showed a R.S.D. value of only 0.3% indicating good reproducibility of the proposed system. The method was successfully applied to the analysis of the content of tranexamic acid in cosmetic products and proved to be suitable for rapid and reliable quality control.

Voltammetric peak separation of dopamine from uric acid in the presence of ascorbic acid at greater than ambient solution temperatures.

Peak overlap in voltammetry poses challenges for the quantitative analysis of electroactive species. Dopamine and uric acid are typically challenging to determine voltammetrically because of their very similar oxidation peak potentials. We report preliminary results of the use of a screen-printed carbon electrode for the determination of dopamine and uric acid in an electrolyte solution maintained above ambient temperatures. Higher temperatures resulted in dramatic shifting of the dopamine oxidation peak toward lower potentials, while the uric acid peak was essentially stationary. Ascorbic acid, an interference in voltammetric uric acid determinations, is effectively suppressed at higher temperatures. This resulted in a greater peak separation of dopamine from uric acid at higher temperatures, which is desirable for better peak integration. In addition, greater current responses for both species were recorded at higher temperatures. The cause for such an increase in peak current is unraveled using ac impedance measurements. Presented are preliminary results for determining dopamine and uric acid at temperatures higher than ambient. Much improved voltammetric peak separation and sensitivity is obtained at these higher temperatures compared to ambient.

Photoelectrocatalytic oxidation of o-phenols on copper-plated screen-printed electrodes.

A novel and sensitive detection method based on photoelectrocatalytic oxidation of o-diphenols was demonstrated on a copper-plated screen-printed carbon electrode (designated CuSPE) in pH 8 phosphate buffer solution. The o-diphenols can be detected amperometrically through electrochemical oxidation at a low applied potential of -0.1 V versus Ag/AgCl, where the CuSPE is much less subject to interfering reactions. The mechanism that induces good selectivity of the CuSPE is explained in terms of the formation of a cyclic five-member complex intermediate (Cu(II)-o-quinolate). A prototype homemade flow through cell design is described for incorporating the photoelectrode and light source. Electrode irradiation results in a large increase in anodic current. The oxidative photocurrents produced by irradiation increase with light intensity presumably because of the formation of semiconductor Cu(2)O. The principle used in this study has an opportunity to extend into various research applications.