College of Engineering, Nanjing Agricultural University, Nanjing 210031, China.
Biosensors (Basel). 2022 May 10;12(5):319. doi: 10.3390/bios12050319.
Although phosphate (Pi) is a necessary nutrient for the growth of aquatic organisms, the presence of excess Pi leads to water eutrophication; thus, it is necessary to accurately determine the content of Pi in water. A method for the determination of trace Pi in aquaculture water was developed based on surface-enhanced Raman spectroscopy (SERS) combined with rhodamine 6G (R6G)-modified silver nanoparticles (AgNPs) as the active substrate. The adsorption of R6G on the AgNP surfaces led to a strong SERS signal. However, in the presence of Pi and ammonium molybdate, phosphomolybdic acid formed, which further associated with R6G to form a stable R6G-PMoO association complex, thereby hindering the adsorption of R6G on the AgNPs, and reducing the SERS intensity; this sequence formed the basis of Pi detection. The decrease in the SERS intensity was linear with respect to the Pi concentration (0.2-20 μM), and the limit of detection was 29.3 nM. Upon the application of this method to the determination of Pi in aquaculture water, a recovery of 94.4-107.2% was obtained (RSD 1.77-6.18%). This study provides an accurate, rapid, and sensitive method for the trace determination of Pi in aquaculture water, which is suitable for on-site detection.
尽管磷酸盐(Pi)是水生生物生长所必需的营养物质,但过量的 Pi 会导致水体富营养化;因此,有必要准确测定水中的 Pi 含量。本研究基于表面增强拉曼光谱(SERS),结合罗丹明 6G(R6G)修饰的银纳米颗粒(AgNPs)作为活性基底,开发了一种用于水产养殖水中痕量 Pi 测定的方法。R6G 在 AgNP 表面的吸附会产生强的 SERS 信号。然而,在 Pi 和钼酸铵存在下,会形成磷钼酸,其进一步与 R6G 形成稳定的 R6G-PMoO 缔合配合物,从而阻碍 R6G 在 AgNPs 上的吸附,降低 SERS 强度;这一系列反应构成了 Pi 检测的基础。SERS 强度的降低与 Pi 浓度(0.2-20 μM)呈线性关系,检测限为 29.3 nM。将该方法应用于水产养殖水中 Pi 的测定,得到了 94.4-107.2%的回收率(RSD 为 1.77-6.18%)。本研究为水产养殖水中 Pi 的痕量测定提供了一种准确、快速、灵敏的方法,适用于现场检测。