Research Center for Bioengineering and Sensing Technology, University of Science and Technology-Beijing, Beijing 100083, People's Republic of China.
School of Biomedical Engineering, Shenzhen University, Shenzhen, Guangdong 518060, People's Republic of China.
Anal Chem. 2020 Jun 2;92(11):7816-7821. doi: 10.1021/acs.analchem.0c01011. Epub 2020 May 15.
Enrichment and enhancement are two important aspects of ultratrace biomolecule recognition in complex biological samples. Here we integrate acoustic aggregation of modified Au nanorods with Raman enhancement for all-in-one ultratrace rapid biomolecule detection in one microliter solution. Arising from the interaction between individual nanoparticles and the acoustic field, the aggregation of Au nanorods results in rapid migration of specifically modified Au nanorods toward pressure node in a few seconds and accompanies the enrichment of specific biomolecular. As a proof concept, rapid and sensitive surface-enhanced Raman scattering (SERS) detection of nucleic acids (10 M) in microliter-scale (10 L) sample is achieved. Such an approach integrates ultrasonic aggregation-induced enrichment (uAIE) with Raman enhancement, holding considerable promise for efficient, sensitive, and rapid on-chip detection of ultratrace biomarkers in a clinical sample solution.
在复杂生物样本中进行超痕量生物分子识别时,富集和增强是两个重要方面。在这里,我们将修饰后的金纳米棒的声聚集与 Raman 增强相结合,实现在一微升溶液中进行一体化的超痕量快速生物分子检测。由于单个纳米粒子与声场之间的相互作用,金纳米棒的聚集导致经特殊修饰的金纳米棒在几秒钟内迅速向压力节点迁移,并伴随着特定生物分子的富集。作为一个概念验证,我们实现了在微升规模(10 μL)样品中对核酸(10 μM)进行快速灵敏的表面增强 Raman 散射(SERS)检测。这种方法将超声聚集诱导富集(uAIE)与 Raman 增强相结合,有望在临床样品溶液中实现超痕量生物标志物的高效、灵敏和快速的片上检测。