Department of Chemistry, Yazd University, Safaieh, 89195-741 Yazd, Iran.
Department of Chemistry, Yazd University, Safaieh, 89195-741 Yazd, Iran.
Food Chem. 2017 Apr 15;221:783-789. doi: 10.1016/j.foodchem.2016.11.103. Epub 2016 Nov 22.
This study presents a novel, simple and efficient pseudo-stir bar solid phase microextraction method for separation and preconcentration of sulfadiazine. To develop the method, a graphene oxide-silica composite reinforced hollow fiber was prepared via sol-gel technology and used as a novel device to extract sulfadiazine. The retained sulfadiazine was eluted using 180μL of methanol/acetic acid (6:4) and quantified by fiber optic linear array spectrophotometry based on the formation of its azo dye with thenoyltrifluoroacetone. Under optimized conditions, the method exhibited a linear dynamic range of 5-150μgL with a detection limit of 1.5μgL and an enrichment factor of 100. The relative standard deviations of 2.9% and 5.8% (n=6) were obtained at 60μgL level of sulfadiazine for intra- and inter-day analysis respectively. The method was successfully applied to determine sulfadiazine in honey, milk, human urine and environmental water samples.
本研究提出了一种新颖、简单、高效的伪搅拌棒固相微萃取方法,用于磺胺嘧啶的分离和预浓缩。为了开发该方法,通过溶胶-凝胶技术制备了氧化石墨烯-二氧化硅复合增强中空纤维,并将其用作提取磺胺嘧啶的新型装置。保留的磺胺嘧啶用 180μL 甲醇/乙酸(6:4)洗脱,并通过光纤线阵分光光度法定量,基于其与三氟乙酰丙酮形成偶氮染料。在优化条件下,该方法在 5-150μgL 的线性动态范围内具有检测限为 1.5μgL 和富集因子为 100 的线性动态范围。在磺胺嘧啶 60μgL 水平下,日内和日间分析的相对标准偏差分别为 2.9%和 5.8%(n=6)。该方法成功应用于蜂蜜、牛奶、人尿和环境水样中磺胺嘧啶的测定。