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使用基于金-二硫化钨纳米杂化物的表面增强拉曼散射(SERS)基底进行高灵敏度无标记生物分子检测。

Highly sensitive label-free biomolecular detection using Au-WS nanohybrid based SERS substrates.

作者信息

Prakash Om, T Abhijith, Nagpal Priya, Perumal Vivekanandan, Karak Supravat, Singh Udai B, Ghosh Santanu

机构信息

Nanostech Laboratory, Department of Physics, Indian Institute of Technology Delhi New Delhi 110016 India

Organic and Hybrid Electronic Device Laboratory, Department of Energy Science and Engineering, Indian Institute of Technology Delhi New Delhi 110016 India.

出版信息

Nanoscale Adv. 2024 Sep 30;6(23):5978-87. doi: 10.1039/d4na00464g.

Abstract

Recent advancements in nanotechnology have led to the development of surface-enhanced Raman spectroscopy (SERS) based rapid and low-cost technologies for ultra-sensitive label-free detection and identification of molecular analytes. Herein, we utilized the synergistic plasmonic and chemical enhancement effects of Au-WS nanohybrids to attain the high-intensity Raman signals of targeted analytes. To develop these nanohybrids, a series of monodispersed Au nanoparticles (NPs) of varying diameters from 20 to 80 nm was chemically synthesized and successively blended with liquid-phase exfoliated WS nano-flakes of average lateral size 90 nm. They provided a maximum enhancement factor (EF) of ∼1.80 × 10 corresponding to the characteristic peaks at 1364 cm and 1512 cm for R6G analyte molecules. Theoretical studies based on the finite-difference time-domain simulations on Au-WS nanohybrid systems revealed a huge field-intensity enhancement with an EF of more than 1000 at the plasmonic hotspots, which was induced by the strong coupling of individual plasmon oscillations of the adjacent Au NPs upon light interactions. These electromagnetic effects along with the chemical enhancement effects of WS nanoflakes were found to be mainly responsible for such huge enhancement in Raman signals. Furthermore, these hybrids were successfully employed for achieving highly sensitive detection of the ATCC 35218 bacterial strain with a concentration of 10 CFU mL in phosphate-buffered saline media, indicating their real capabilities for practical scenarios. The findings of the present study will indeed provide vital information in the development of innovative nanomaterial-based biosensors, that will offer new possibilities for addressing critical public health concerns.

摘要

纳米技术的最新进展推动了基于表面增强拉曼光谱(SERS)的快速低成本技术的发展,用于超灵敏的无标记分子分析物检测和识别。在此,我们利用金-二硫化钨(Au-WS)纳米杂化物的协同等离子体和化学增强效应来获得目标分析物的高强度拉曼信号。为了制备这些纳米杂化物,化学合成了一系列直径从20到80纳米不等的单分散金纳米颗粒(NPs),并将其与平均横向尺寸为90纳米的液相剥离WS纳米片依次混合。对于罗丹明6G(R6G)分析物分子,它们在1364厘米和1512厘米处的特征峰对应的最大增强因子(EF)约为1.80×10。基于对Au-WS纳米杂化系统的时域有限差分模拟的理论研究表明,在等离子体热点处,由于相邻金纳米颗粒在光相互作用时单个等离子体振荡的强耦合,场强增强巨大,增强因子超过1000。发现这些电磁效应以及WS纳米片的化学增强效应是拉曼信号如此巨大增强的主要原因。此外,这些杂化物成功用于在磷酸盐缓冲盐水介质中对浓度为10 CFU/mL的美国典型培养物保藏中心(ATCC)35218菌株进行高灵敏度检测,表明它们在实际场景中的实际能力。本研究的结果确实将为创新的基于纳米材料的生物传感器的开发提供重要信息,这将为解决关键的公共卫生问题提供新的可能性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5f48/11575664/b4bf8e7340aa/d4na00464g-f1.jpg

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