School of Environmental Sciences, Jawaharlal Nehru University, New Delhi, 110067, India.
Department of Chemistry, School of Chemical and Life Sciences, Jamia Hamdard, New Delhi, 110062, India.
Mikrochim Acta. 2019 Oct 9;186(11):687. doi: 10.1007/s00604-019-3802-1.
A dual-mode assay is described for immunological determination of the anemia biomarker ferritin. It is based on the use of a gold@carbon dot (Au@CD) nanoconjugate as a colorimetric and fluorescent probe. Au@CD is hydrophilic, easily surface modified and stable in aqueous solution. The Au@CD have a red color with blue-green fluorescence and were modified with antibody against ferritin. This allows bi-modal detection of ferritin. Assays can be performed in phosphate buffer and were also analyzed in (Bovine Serum Albumin) BSA and (Fetal Bovine Serum) FBS. Detection is based on antigen-antibody interaction underlying the classical sandwich model. Response to ferritin can be detected by spectrophotometry (at 570 nm) or fluorescence (at excitation/emission maxima of 354/454 nm). Under optimal conditions, the assay has a linear response in the 1 to 120 ngmL ferritin concentration range and detection limits of 20 ng (colorimetrically) and 64 ng (fluorometrically). Graphical abstract Schematic representation of the function of the designed nanoprobe. The Au@CD nanoconjugates are functionalized with ferritin antibody in the initial step which specifically interacts with ferritin molecules leading to aggregation and subsequent changes in the optical and fluorescence signals.
一种用于免疫测定贫血生物标志物铁蛋白的双模测定法。它基于使用金@碳点(Au@CD)纳米复合物作为比色和荧光探针。Au@CD 具有亲水性,易于表面修饰,在水溶液中稳定。Au@CD 具有红色的颜色和蓝绿色的荧光,并被针对铁蛋白的抗体修饰。这允许铁蛋白的双模检测。测定可以在磷酸盐缓冲液中进行,并且也在(牛血清白蛋白)BSA 和(胎牛血清)FBS 中进行分析。检测基于经典三明治模型下的抗原 - 抗体相互作用。通过分光光度法(在 570nm 处)或荧光法(在 354/454nm 的激发/发射最大值处)可以检测到对铁蛋白的响应。在最佳条件下,该测定法在 1 至 120ngmL 铁蛋白浓度范围内具有线性响应,检测限为 20ng(比色法)和 64ng(荧光法)。