Natale Anna, Nardiello Donatella, Palermo Carmen, Muscarella Marilena, Quinto Maurizio, Centonze Diego
Dipartimento di Scienze Agrarie, degli Alimenti e dell'Ambiente and CSRA - Centro Servizi di Ricerca Applicata, Università degli Studi di Foggia, Via Napoli, 25, 71100 Foggia, Italy.
Dipartimento di Scienze Agrarie, degli Alimenti e dell'Ambiente and CSRA - Centro Servizi di Ricerca Applicata, Università degli Studi di Foggia, Via Napoli, 25, 71100 Foggia, Italy.
J Chromatogr A. 2015 Nov 13;1420:66-73. doi: 10.1016/j.chroma.2015.09.082. Epub 2015 Oct 1.
A sensitive and accurate method for the determination of polyphenolic compounds in artichoke bract extracts and olive mill wastewaters by liquid chromatography coupled with pulsed amperometric detection at a glassy carbon working electrode was developed. Preliminary experiments were carried out by cyclic voltammetry to investigate the electrochemical behavior of polyphenols under different mobile phase compositions, and to test the detection and cleaning electrode potentials. Chromatographic separations were performed by using a core-shell C18 column, eluted with acetic acid and acetonitrile, by combined concave-linear binary gradients. Under the optimized experimental conditions, a good column efficiency and peak symmetry were observed, also for stereo and positional isomeric compounds. The developed three-step potential waveform for pulsed amperometric detection was successfully applied for the sensitive chromatographic determination of polyphenols in artichoke extracts and olive mill wastewaters. Linearity, precision and sensitivity of the proposed method have been evaluated. A wide linear range of response (up to 20 mg/L) has been obtained for all the investigated compounds. Detection and quantification limits in the vegetable origin sample extracts were in the range 0.004-0.6 mg/L and 0.01-2mg/L, respectively, while the injection-to-injection repeatability (n=6) ranged from 5 to 13%. The obtained results confirmed the excellent sensitivity of the electrochemical detection, and its suitability for the determination of electroactive polyphenolic compounds at low concentration levels.
建立了一种灵敏且准确的方法,用于通过液相色谱结合在玻碳工作电极上的脉冲安培检测来测定洋蓟苞片提取物和橄榄油厂废水中的多酚类化合物。通过循环伏安法进行初步实验,以研究不同流动相组成下多酚的电化学行为,并测试检测和清洁电极电位。使用核壳C18柱进行色谱分离,通过组合凹线性二元梯度用乙酸和乙腈洗脱。在优化的实验条件下,对于立体和位置异构体化合物,也观察到了良好的柱效和峰对称性。所开发的用于脉冲安培检测的三步电位波形成功应用于洋蓟提取物和橄榄油厂废水中多酚的灵敏色谱测定。评估了该方法的线性、精密度和灵敏度。对于所有研究的化合物,都获得了宽响应线性范围(高达20mg/L)。植物源样品提取物中的检测限和定量限分别在0.004-0.6mg/L和0.01-2mg/L范围内,而进样间重复性(n=6)范围为5至13%。所得结果证实了电化学检测的优异灵敏度及其适用于低浓度水平电活性多酚类化合物的测定。