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基于生物支架纳米结构和 SERS 标签的集成阵列微腔的 SERS 芯片原位检测抑菌过程中的内毒素

In Situ Detection of Endotoxin in Bacteriostatic Process by SERS Chip Integrated Array Microchambers within Bioscaffold Nanostructures and SERS Tags.

机构信息

Key Disciplines Lab of Novel Micro-Nano Devices and System Technology, Key Laboratory of Optoelectronic Technology and Systems, Ministry of Education, Chongqing University, Shapingba, Chongqing 400044, China.

School of Chemistry and Chemical Engineering, Chongqing University, Shapingba, Chongqing 400044, China.

出版信息

ACS Appl Mater Interfaces. 2020 Jul 1;12(26):28985-28992. doi: 10.1021/acsami.0c04897. Epub 2020 Jun 17.

Abstract

In order to achieve real-time and in situ detection of endotoxin, which is an important and significant clinical test index, surface-enhanced Raman spectroscopy (SERS) chip integrated array microchambers within bioscaffold nanostructures and a SERS monitoring strategy were proposed in this paper. After sputtering of nanogold on the cicada wing, which was selected as a natural template, and polydimethylsiloxane bonding, array-type chambers within bioscaffold nanostructures were prepared for in situ bacterial culture and monitoring of endotoxin in the bacteriostasis process by SERS. Meanwhile, the SERS tag modified with the DNA aptamer was prepared and added into this complex biochemical reaction to further improve the sensitivity and selectivity. A new method for in situ detection of endotoxin was thus established. The detection time was shortened to 100 s, and the detection limit was as low as 6.25 ng/mL. was cultured in situ in the chamber of the SERS chip with antimicrobial agents in 0-72 h. The endotoxin released in the antibacterial process was monitored by the designed SERS detection strategy. The results obtained by SERS analysis were consistent with those of the ELISA kit.

摘要

为了实现内毒素的实时和原位检测,这是一个重要且有意义的临床检测指标,本文提出了一种基于生物支架纳米结构的表面增强拉曼光谱(SERS)芯片集成阵列微室和 SERS 监测策略。在选择作为天然模板的蝉翼上溅射纳米金,并进行聚二甲基硅氧烷键合后,制备了用于原位细菌培养和通过 SERS 监测抑菌过程中内毒素的阵列型生物支架纳米结构内室。同时,制备了带有 DNA 适体的 SERS 标记物并添加到这个复杂的生化反应中,以进一步提高灵敏度和选择性。因此,建立了一种用于内毒素原位检测的新方法。检测时间缩短至 100 s,检测限低至 6.25 ng/mL。在有抗菌剂的 SERS 芯片室内原位培养,通过设计的 SERS 检测策略监测抗菌过程中释放的内毒素。SERS 分析得到的结果与 ELISA 试剂盒的结果一致。

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