Institute of Graduate Studies, Istanbul University-Cerrahpaşa, 34320 Avcilar, Istanbul, Turkey.
Department of Chemistry, Faculty of Engineering, Istanbul University-Cerrahpaşa, 34320 Avcilar, Istanbul, Turkey.
Mikrochim Acta. 2020 Sep 30;187(10):586. doi: 10.1007/s00604-020-04478-2.
As a first of its kind, we developed a highly sensitive colorimetric nanoprobe for phytic acid (PA) and Fe(III) ion detection based on 4-mercaptophenol (4MP) and thioglycolic acid (TGA)-functionalized gold nanoparticles {AuNPs@(4MP-TGA)}. AuNPs were easily derivatized by 4MP and TGA through -SH binding to gold. Fe(III) ions possibly are bound first to the phenolate groups of 4MP-AuNPs, and further coordinated several nanoparticles via the carboxylate groups of TGA-AuNPs to cause aggregation, resulting in a red-to-purple color change and a bathochromic shift in the SPR absorption band of the nanoprobe. With the addition of PA to the AuNPs@(4MP-TGA)-Fe(III) system, the aggregated particles were released due to strong complex formation between Fe(III) and PA, resulting in a restoration of the color (purple-to-red) and of the SPR band to the original 520 nm wavelength maximum. Thus, the 650-nm absorption is attenuated and the 520-nm band is enhanced upon PA-Fe(III) chelation. This means that the absorption ratio A/A is an indication of Fe(III) whereas the reverse ratio A/A of the PA content of complex samples. The limits of detection (LOD) of the AuNPs@(4MP-TGA) were 1.0 μM for Fe(III) ions and 0.15 μM for PA. Phytic acid extracted from bean grains was determined with the proposed probe, yielding good recoveries. In addition, common metal ions, anions, and several biomolecules did not show an adverse effect on the nanoprobe performance for ferric ions and phytate. The developed method was statistically validated against a LC-MS/MS literature method. Graphical abstract Mercaptophenolate (4MP)- and thioglycolic acid (TGA)-functionalized gold nanoparticles were prepared as nanoprobes to detect Fe(III) ions through nanoparticle aggregation accompanied by red-to-purple color shift. The same nanoprobe determined phytic acid in food through disaggregation of Fe(III)-aggregated nanoparticles by strong Fe(III)-phytate chelation and restoration of solution color from purple to red.
作为首例,我们基于 4-巯基苯酚(4MP)和巯基乙酸(TGA)功能化的金纳米粒子 {AuNPs@(4MP-TGA)},开发了一种用于检测植酸(PA)和 Fe(III)离子的高灵敏比色纳米探针。金纳米粒子很容易通过 -SH 键与金结合被 4MP 和 TGA 衍生化。Fe(III) 离子可能首先与 4MP-AuNPs 的酚盐基团结合,然后通过 TGA-AuNPs 的羧酸盐基团进一步与几个纳米粒子配位,导致聚集,从而导致纳米探针的 SPR 吸收带发生红移到紫移。当向 AuNPs@(4MP-TGA)-Fe(III) 体系中添加 PA 时,由于 Fe(III)和 PA 之间形成强络合物,聚集的颗粒被释放,导致颜色(紫变红)和 SPR 带恢复到原始的 520nm 波长最大值。因此,PA-Fe(III)螯合时,650nm 吸收被衰减,520nm 带被增强。这意味着吸收比 A/A 是 Fe(III)的指示,而复杂样品的 PA 含量的相反比 A/A 是指示。AuNPs@(4MP-TGA)的检测限(LOD)分别为 1.0μM 的 Fe(III)离子和 0.15μM 的 PA。从豆粒中提取的植酸用所提出的探针进行测定,回收率良好。此外,常见的金属离子、阴离子和几种生物分子对铁离子和植酸盐的纳米探针性能没有不利影响。该方法与文献中的 LC-MS/MS 方法进行了统计学验证。摘要 制备巯基苯并噻唑(4MP)和巯基乙酸(TGA)功能化的金纳米粒子作为纳米探针,通过纳米粒子聚集伴随红移到紫移来检测 Fe(III)离子。通过 Fe(III)-植酸盐的强螯合作用使 Fe(III)聚集的纳米粒子解聚集,并使溶液颜色从紫色恢复到红色,从而利用相同的纳米探针测定食品中的植酸。