Development of the HPLC-ELSD method for the determination of phytochelatins and glutathione in Perilla frutescens under cadmium stress conditions.

A rapid, accurate and simple method was developed for the simultaneous determination of glutathione (GSH) and phytochelatins (PCs) by high-performance liquid chromatography (HPLC) with an evaporative light-scattering detector. GSH, phytochelatin 2 (PC2), PC3, PC4, PC5 and PC6 can be separated with baseline separation within 9 min using a Venusil AA column (250 mm × 4.6 mm i.d., 5 µm particle sizes). Acetonitrile and water containing 0.1% trifluoroacetic acid (0.1%) were employed as the mobile phase for the gradient elution. The drift tube temperature and flow rate of the carrier gas (N2) were 50°C and 1.5 l min-1, respectively. Under optimum conditions, good linear regression equations of six analytes were obtained with the detection limits ranging from 0.2 to 0.5 µg ml-1. The proposed method has been applied successfully for the quantification of GSH and PCs in Perilla frutescens (a cadmium hyperaccumulator) under cadmium stress. The recoveries were between 82.9% and 115.3%.

Highly sensitive determination of lead(ii) and cadmium(ii) by a large surface area mesoporous alumina modified carbon paste electrode.

Nanosized mesoporous γ-alumina (M-γ-Al2O3) was first prepared and then modified into a carbon paste to fabricate a novel modified carbon paste electrode. The prepared alumina has pores with an amorphous wall and large surface area. The electrochemical behavior of the modified carbon paste electrode was investigated using cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS) methods. The modified carbon paste electrode was employed to determine Pb2+ and Cd2+ simultaneously by a differential pulse voltammetry (DPV) method. Amperometric determination was carried out in 0.1 mol L-1 NaAc-HAc buffer solution (pH 6.0) after enriching for 360 s at -1.0 V. The oxidation peak currents of Pb2+ and Cd2+ were proportional to their concentration in the range of 0.001-10 µmol L-1 and 0.01-10 µmol L-1, respectively. The detection limits of Pb2+ and Cd2+ were 0.20 nmol L-1 and 2.0 nmol L-1 (S/N = 3), respectively. The modified carbon paste electrode shows good stability, repeatability and sensitivity. The proposed method was applied to the determination of Pb2+ and Cd2+ in water samples with satisfactory results.

Electrochemical investigation and determination of procaterol hydrochloride on poly(glutamic acid)/carboxyl functionalized multiwalled carbon nanotubes/polyvinyl alcohol modified glassy carbon electrode.

Poly(glutamic acid) (P-GLU)/carboxyl functionalized multiwalled carbon nanotubes (MWCNTs-COOH)/polyvinyl alcohol (PVA) modified glassy carbon electrode (GCE) has been successfully prepared and the electrochemical behavior of procaterol hydrochloride (ProH) was studied. The results show that the as-prepared modified electrode exhibits a good electrocatalytic property towards the oxidation of ProH in 0.2M phosphate buffer solution (PBS) (pH 6.0) due to the enhanced oxidation peak current at ~+0.59V. Under optimal reaction conditions, the oxidation peak current of ProH is proportional to its concentration in the linear dynamic ranges of 0.060 - 8.0µM (R = 0.9974), with a detection limit of 8.0 × 10-9M. Finally, this method was efficiently used for the determination of ProH in tablets and human urine with recoveries of 88.5~98.7% and 89.2 ~ 108.0%, respectively.