Zhang Runzi, Xie Shunbi, Zhang Qianyan, Gao Ying, He Xiang, Jin Shanshan, Leng Junhao, Zhang Lian, He Yi
School of Science, Xihua University, Chengdu, 610039, PR China.
Key Laboratory for Resource Utilization of Heavy Metal Wastewater, Chongqing University of Arts and Sciences, Chongqing, 402160, PR China.
Anal Chim Acta. 2024 Dec 1;1331:343308. doi: 10.1016/j.aca.2024.343308. Epub 2024 Oct 10.
Chloramphenicol (CAP) is a broad-spectrum antibiotic, and its continuous use in human medicine, livestock has resulted disturbances in ecosystem stability. The complex background and low concentration of CAP in aquatic environments present significant scientific challenges for its sensitive detection. Currently detection techniques such as high-performance liquid chromatography (HPLC) and gas chromatography-mass spectrometry (GC-MS) are hindered by their complex procedures and high costs. Surface-enhanced Raman spectroscopy (SERS), due to its unique ability for fingerprint recognition, has emerged as a powerful tool for analysis and detection. However, it is often limited by the low kurtosis expression of the target.
The water-soluble explosive polyethylenimide grafted calcium carbonate (PEI@CaCO3) microcapsule was utilized to encapsulate the signal probe Ag@4-NTP and combine it with a semiconductor SERS substrate ZnCeO, enabling ultra-sensitive detection of CAP through a signal attenuation strategy. Moreover, magnetic molecularly imprinted polymers (MMIP) and nucleic acid aptamers were employed as capture probes for achieving rapid and direct magnetic separation, followed by layer-by-layer assembly to construct the sensor probe. In the presence of CAP, the aptamers and rMMIPs selectively recognized the target, forming a PEI@CaCO@Ag@4-NTP@Apt@CAP@rMMIPs "sandwich" structure (Microcapsule@Apt@rMMIPs). After multiple magnetic separations, the "igniter" EDTA solution was added, causing the CaCO capsules to rapidly "explode" and release a significant amount of Ag@4-NTP. This was then applied to the "signal booster" semiconductor SERS substrate. Under optimal conditions, this method exhibited a detection range of 1.0 × 10 M to 1.0 × 10 M, with a detection limit of 6.84 × 10 M.
The unite of magnetic MIP and nucleic acid aptamer to form a "sandwich" structure, in combination with a semiconductor SERS substrate, not only enhances the sensor's sensitivity but also offers significant economic advantages. Moreover, this innovative technology holds great promise for accurate and highly sensitive detection of pollutants in complex environments.
氯霉素(CAP)是一种广谱抗生素,其在人类医学和畜牧业中的持续使用导致了生态系统稳定性的干扰。CAP 在水生环境中的复杂背景和低浓度给其敏感检测带来了重大的科学挑战。目前,高效液相色谱(HPLC)和气相色谱-质谱联用(GC-MS)等检测技术由于其复杂的程序和高昂的成本而受到限制。表面增强拉曼光谱(SERS)由于其独特的指纹识别能力,已成为一种强大的分析和检测工具。然而,它通常受到目标低峰度表达的限制。
利用水溶性炸药聚乙烯亚胺接枝碳酸钙(PEI@CaCO3)微胶囊包裹信号探针 Ag@4-NTP,并与半导体 SERS 基底 ZnCeO 结合,通过信号衰减策略实现对 CAP 的超灵敏检测。此外,磁性分子印迹聚合物(MMIP)和核酸适体被用作捕获探针,以实现快速和直接的磁分离,然后通过层层组装构建传感器探针。在 CAP 的存在下,适体和 rMMIP 选择性地识别靶标,形成 PEI@CaCO@Ag@4-NTP@Apt@CAP@rMMIPs“三明治”结构(微胶囊@Apt@rMMIPs)。经过多次磁分离后,加入“点火剂”EDTA 溶液,导致 CaCO3 胶囊迅速“爆炸”并释放大量 Ag@4-NTP。然后将其应用于“信号增强剂”半导体 SERS 基底。在最佳条件下,该方法的检测范围为 1.0×10-7 M 至 1.0×10-5 M,检测限为 6.84×10-7 M。
将磁性 MIP 和核酸适体结合形成“三明治”结构,与半导体 SERS 基底相结合,不仅提高了传感器的灵敏度,而且具有显著的经济优势。此外,这项创新技术有望为复杂环境中污染物的准确、高灵敏度检测提供新的思路。