Journal
ACS SENSORS
Volume 6, Issue 7, Pages 2584-2592Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acssensors.1c00117
Keywords
microfluidics; in situ patterning; silver nanoparticles; SERS; sensing; biomolecules
Funding
- NIH Director's Transformative Research Award [R01HL137157]
- NSF [ECCS 1128677, 1309686, 1509369]
- Div Of Electrical, Commun & Cyber Sys
- Directorate For Engineering [1509369, 1309686] Funding Source: National Science Foundation
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This work integrates microfluidic devices, nanoparticle synthesis, and on-chip sensing for high-resolution biomolecular detection. Researchers explore how microfluidic geometry affects nanoparticle patterning for enhanced SERS-based sensing, providing insights into the rational design of continuous microfluidic systems for SERS applications. The integrated system demonstrates potential applications in label-free on-chip detection of biomolecules, promoting system integration, miniaturization, and on-site biological applications.
This work integrates the advantages of microfluidic devices, nanoparticle synthesis, and on-chip sensing of biomolecules. The concept of microreactors brings new opportunities in chemical synthesis, especially for metallic nanoparticles favorable in surface-enhanced Raman spectroscopy (SERS) for high-resolution and low-limit detection of biomolecules. However, still missing is our understanding of reactions at the microscale and how microsystems can be exploited in biosensing applications via precise control of nanomaterial synthesis. We investigate how microfluidic geometry affects nanoparticle patterning for highresolution SERS-based sensing and propose a spiral-shaped microchannel that can achieve enhanced mixing, rapid reaction at room temperature, and uniform in situ patterning. The roles of channel geometry as the key parameter on patterning have been studied systematically to provide insight into the rational design of continuous microfluidic systems for SERS applications. We also demonstrate potential applications of this integrated system in label-free on-chip detection of 1 pM rhodamine B (enhancement factor, similar to 4.3 x 10(11)) and a 1 nM 41-base single-stranded deoxyribonucleic acid (DNA) sequence (enhancement factor, similar to 1.5 x 10(8)). Our ready-to-use multifunctional system provides an alternative strategy for the facile fabrication of SERS-active substrates and promotes system integration, miniaturization, and on-site biological applications.
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