Çağlar Yasemin, Saka Ece Tuğba, Alp Hakan, Kantekin Halit, Ocak Ümmühan, Ocak Miraç
Department of Chemistry, Faculty of Sciences, Karadeniz Technical University, 61080, Trabzon, Turkey.
J Fluoresc. 2016 Jul;26(4):1381-9. doi: 10.1007/s10895-016-1829-9. Epub 2016 Jun 2.
A new nickel(II)-phthalocyanine complex (NiPc) was synthesized and used as a fluorescent ligand in determination of iron in real samples. The NiPc compound, when excited at 350 nm, decreases of emission with increases of the iron(III) concentration at 425 nm were used analytical response in a modified standard addition method. The method was validated by analyzing two certified reference materials (CRM-SA-C Sandy Soil C and Mixed Polish Herbs (INCT-MPH-2). Food and drug samples were digested in a closed microwave system using nitric acid and hydrogen peroxide. Therefore, all iron in the samples converted to iron(III) ion. These solutions were used directly in determination of iron(III) ion. No cleanup or enrichment of the solutions was required. The calibration graph was linear until 14.00 μg mL(-1). Detection limit and quantification limit were 1.29 μg mL(-1) and 3.88 μg mL(-1), respectively. The method provided accurate results for the majority of the food samples tested, including spanich, dill, mint, purslane, rocket, red lentils, dry beans and two iron medicinal tablets. Also, the high recovery (95.6 %) was obtained for a fortified stream water sample. The simple and cost-effective method is suitable for monitoring total iron concentration in foods and drug samples.
合成了一种新型镍(II)-酞菁配合物(NiPc),并将其用作荧光配体用于测定实际样品中的铁。当在350nm处激发时,NiPc化合物在425nm处的发射强度随铁(III)浓度的增加而降低,利用这种变化采用改进的标准加入法进行分析测定。通过分析两种有证标准物质(CRM-SA-C沙质土壤C和波兰混合草药(INCT-MPH-2))对该方法进行了验证。食品和药品样品在密闭微波系统中用硝酸和过氧化氢进行消解。因此,样品中的所有铁都转化为铁(III)离子。这些溶液直接用于铁(III)离子的测定,无需对溶液进行净化或富集。校准曲线在14.00μg mL⁻¹范围内呈线性。检测限和定量限分别为1.29μg mL⁻¹和3.88μg mL⁻¹。该方法为大多数测试的食品样品提供了准确的结果,包括菠菜、莳萝、薄荷、马齿苋、芝麻菜、红扁豆、干豆和两种铁剂药片。此外,对加标溪水样品的回收率高达95.6%。这种简单且经济高效的方法适用于监测食品和药品样品中的总铁浓度。