College of Ecology and Environment, Chengdu University of Technology, Chengdu 610059, China.
Chengdu Ecological and Environmental Monitoring Center of Sichuan Province, Chengdu, Sichuan 610066, China.
J Colloid Interface Sci. 2024 Oct 15;672:236-243. doi: 10.1016/j.jcis.2024.05.109. Epub 2024 May 16.
This study reports the development of a photocatalytic electrochemical aptasensor for the purpose of detecting chloramphenicol (CAP) antibiotic residues in water by utilizing SYBR Green I (SG) and chemically exfoliated MoS (ce-MoS) as synergistically signal-amplification platforms. The Au nanoparticles (AuNPs) were electrodeposited onto the surface of an indium tin oxide (ITO) electrode. After that, the thiolate-modified cDNA, also known as capture DNA, was combined with the aptamer. Subsequently, photosensitized SG molecules and ce-MoS nanomaterial were inserted into the groove of the resultant double-stranded DNA (dsDNA). The activation of the photocatalytic process upon exposure to light resulted in the generation of singlet oxygen. The singlet oxygen effectively split the dsDNA, resulting in significant enhancement in the current of [Fe(CN)]. When the CAP was present, both SG molecules and ce-MoS broke away from the dsDNA, which turned off the photosensitization response, leading to significant reduction in the current of [Fe(CN)]. Under the optimal conditions, the aptasensor exhibited a linear relationship between the current of [Fe(CN)] with logarithmic concentrations of CAP from 20 to 1000 nM, with a detection of limit (3σ) of 3.391 nM. The aptasensor also demonstrated good selectivity towards CAP in the presence of interfering antibiotics, such as tetracycline, streptomycin, levofloxacin, ciprofloxacin, and sulfadimethoxine. Additionally, the results obtained from the analysis of natural water samples using the proposed aptasensor were consistent with the findings acquired through the use of a liquid chromatograph-mass spectrometer. Therefore, with its simplicity and high selectivity, this aptasensor can potentially detect alternative antibiotics in environmental water samples by replacing the aptamers based on photosensitization.
本研究报告了一种光催化电化学生物传感器的开发,旨在利用 SYBR Green I(SG)和化学剥离的 MoS(ce-MoS)作为协同信号放大平台,检测水中的氯霉素(CAP)抗生素残留。将金纳米粒子(AuNPs)电沉积在氧化铟锡(ITO)电极表面。之后,巯基修饰的 cDNA,也称为捕获 DNA,与适体结合。随后,光敏化的 SG 分子和 ce-MoS 纳米材料被插入到所得双链 DNA(dsDNA)的沟槽中。暴露于光下时,光催化过程的激活导致单线态氧的产生。单线态氧有效地分裂 dsDNA,导致 [Fe(CN)]电流显著增强。当存在 CAP 时,SG 分子和 ce-MoS 都从 dsDNA 中脱离,从而关闭了光致敏化反应,导致 [Fe(CN)]电流显著降低。在最佳条件下,该适体传感器的 [Fe(CN)]电流与 CAP 的对数浓度在 20 至 1000 nM 之间呈线性关系,检测限(3σ)为 3.391 nM。该适体传感器在存在干扰抗生素(如四环素、链霉素、左氧氟沙星、环丙沙星和磺胺二甲氧嘧啶)时对 CAP 也表现出良好的选择性。此外,使用所提出的适体传感器对天然水样进行分析的结果与使用液相色谱-质谱联用仪获得的结果一致。因此,该适体传感器具有简单、高选择性的特点,通过替换基于光致敏化的适体,有可能检测环境水样中的替代抗生素。