Rivera Rolen Brian P, Unabia Romnick B, Reazo Renzo Luis D, Lapening Melbagrace A, Lumod Ryan M, Ruda Archie G, Omping Jahor L, Magdadaro Miceh Rose D, Sayson Noel Lito B, Latayada Felmer S, Capangpangan Rey Y, Dumancas Gerard G, Malaluan Roberto M, Lubguban Arnold A, Petalcorin Gaudencio C, Alguno Arnold C
Research Center for Energy Efficient Materials (RCEEM), Premier Research Institute of Science and Mathematics (PRISM), Mindanao State University-Iligan Institute of Technology, 9200 Iligan City, Philippines.
Department of Physics, Mindanao State University-Iligan Institute of Technology, 9200 Iligan City, Philippines.
ACS Omega. 2024 Jul 22;9(31):33652-33661. doi: 10.1021/acsomega.4c02023. eCollection 2024 Aug 6.
Histamine is a well-known biogenic amine (BA) that is often associated with allergic reactions and is a significant cause of foodborne illnesses resulting from the consumption of spoiled food. Detecting histamine is essential for maintaining food safety standards and preserving the quality. In this work, we developed a simple, low-cost, and rapid colorimetric method for detecting histamine. Gold nanoparticles (AuNPs) of different sizes (16, 25, and 40 nm) were synthesized by using the citrate reduction method. The particle size was controlled by adjusting the precursor molar ratio (MR), with smaller ratios leading to larger particles and a red-shift in the surface plasmon resonance (SPR) peak (520, 524, and 528 nm). The nanoparticles were allowed to interact with increasing concentrations of histamine (ranging from 1 to 100 ppm), and the changes in the absorbance spectra and color of the solution were monitored. AuNP aggregation was induced by interaction with histamine through amino and imidazole groups that will coordinate with the AuNP's surface via electrostatic and hydrogen-bonding interactions, causing the solution to turn blue from red. The size variations of AuNPs significantly affected the colorimetric response to histamine. Among the varied sizes, 25 nm AuNPs exhibited the lowest detection limit of 0.72 μM and a linear detection range of 1-10 ppm. Notably, this sensor offered rapid detection (under 1 min) and a remarkable selectivity toward histamine analyte, highlighting its potential for practical applications.
组胺是一种众所周知的生物胺(BA),通常与过敏反应相关,也是食用变质食物导致食源性疾病的一个重要原因。检测组胺对于维持食品安全标准和保持食品质量至关重要。在这项工作中,我们开发了一种简单、低成本且快速的比色法来检测组胺。采用柠檬酸盐还原法合成了不同尺寸(16、25和40纳米)的金纳米颗粒(AuNPs)。通过调节前驱体摩尔比(MR)来控制粒径,较小的比例会导致颗粒更大,表面等离子体共振(SPR)峰出现红移(520、524和528纳米)。使纳米颗粒与浓度不断增加的组胺(范围为1至100 ppm)相互作用,并监测溶液吸光度光谱和颜色的变化。组胺通过氨基和咪唑基团与AuNP相互作用,这些基团将通过静电和氢键相互作用与AuNP表面配位,从而诱导AuNP聚集,导致溶液从红色变为蓝色。AuNPs的尺寸变化显著影响了对组胺的比色响应。在不同尺寸中,25纳米的AuNPs表现出最低检测限为0.72 μM,线性检测范围为1至10 ppm。值得注意的是,该传感器提供快速检测(1分钟内),并且对组胺分析物具有显著的选择性,突出了其在实际应用中的潜力。