Research Center of Analytical Instrumentation, Key Laboratory of Bio-Resource and Eco-Environment, Ministry of Education, College of Life Science, Sichuan University, Chengdu, 610064, China.
Department of Laboratory Science in Public Health, West China School of Public Health, Sichuan University, Chengdu, 610041, China.
Anal Chim Acta. 2017 Sep 1;984:177-184. doi: 10.1016/j.aca.2017.06.037. Epub 2017 Jun 30.
Antibiotic abuse has been bringing serious pollution in water, which is closely related to human health. It is desirable to develop a new strategy for antibiotic detection. To address this problem, a sensitive fluorescent aptasensor for antibiotic detection was developed by utilizing gold nanoparticles modified magnetic bead composites (AuNPs/MBs) and nicking enzyme. AuNPs/MBs were synthesized with the help of polyethylenimine (PEI). The prepared AuNPs/MBs acted as dual-functional scaffolds that owned excellent magnetic separation capacity and strong covalent bio-conjugation. The non-specifically absorbed aptamers in AuNPs/MBs were less than that in MBs. Hence, the fluorescent aptasensor based on AuNPs/MBs show a better signal to background ratio than that based on carboxyl modified magnetic beads (MBs). In this work, ampicillin was employed as a model analyte. In the presence of ampicillin, the specific binding between ampicillin and aptamer induced structure-switching that led to the release of partial complementary DNA (cDNA) of aptamer. Then, the released cDNA initiated the cycle of nicking enzyme assisted signal amplification (NEASA). Therefore, a large amount of taqman probes were cleaved and fluorescence signal was amplified. The prepared fluorescent aptasensor bring sensitive detection in range of 0.1-100 ng mL with the limit of detection of 0.07 ng mL. Furthermore, this aptasensor was also successfully applied in real sample detection with acceptable accuracy. The fluorescent aptasensor provides a promising method for efficient, rapid and sensitive antibiotic detection.
抗生素滥用给水体带来了严重的污染,而水体污染与人类健康息息相关。因此,开发新的抗生素检测策略势在必行。针对这一问题,本研究利用金纳米粒子修饰的磁性纳米微球(AuNPs/MBs)和核酸内切酶构建了一种用于抗生素检测的高灵敏荧光适体传感器。PEI 辅助合成了 AuNPs/MBs,该纳米复合材料不仅具有优异的磁分离能力,而且能够实现共价生物偶联。此外,AuNPs/MBs 还具有较少的非特异性吸附适体,因此,基于 AuNPs/MBs 的荧光适体传感器具有比基于羧基化磁性纳米微球(MBs)更高的信号背景比。在本研究中,氨苄西林被用作模型分析物。在氨苄西林存在的情况下,氨苄西林与适体的特异性结合诱导了结构转变,导致适体的部分互补 DNA(cDNA)被释放。然后,释放的 cDNA 引发了核酸内切酶辅助信号放大(NEASA)循环。因此,大量的 Taqman 探针被切割,荧光信号被放大。所制备的荧光适体传感器在 0.1-100ng/mL 的范围内实现了灵敏的检测,检测限为 0.07ng/mL。此外,该传感器还成功地应用于实际样品的检测,具有可接受的准确性。该荧光适体传感器为高效、快速、灵敏的抗生素检测提供了一种有前景的方法。