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SERS Barcode Libraries: A Microfluidic Approach.
Sevim, Semih; Franco, Carlos; Chen, Xiang-Zhong; Sorrenti, Alessandro; Rodríguez-San-Miguel, David; Pané, Salvador; deMello, Andrew J; Puigmartí-Luis, Josep.
Afiliação
  • Sevim S; Institute of Chemical and Bioengineering ETH Zurich Vladimir Prelog Weg 1 Zurich 8093 Switzerland.
  • Franco C; Institute of Chemical and Bioengineering ETH Zurich Vladimir Prelog Weg 1 Zurich 8093 Switzerland.
  • Chen XZ; Multi-Scale Robotics Lab (MSRL) Institute of Robotics and Intelligent Systems ETH Zurich Tannenstrasse 3 Zurich 8092 Switzerland.
  • Sorrenti A; Institute of Chemical and Bioengineering ETH Zurich Vladimir Prelog Weg 1 Zurich 8093 Switzerland.
  • Rodríguez-San-Miguel D; Institute of Chemical and Bioengineering ETH Zurich Vladimir Prelog Weg 1 Zurich 8093 Switzerland.
  • Pané S; Multi-Scale Robotics Lab (MSRL) Institute of Robotics and Intelligent Systems ETH Zurich Tannenstrasse 3 Zurich 8092 Switzerland.
  • deMello AJ; Institute of Chemical and Bioengineering ETH Zurich Vladimir Prelog Weg 1 Zurich 8093 Switzerland.
  • Puigmartí-Luis J; Institute of Chemical and Bioengineering ETH Zurich Vladimir Prelog Weg 1 Zurich 8093 Switzerland.
Adv Sci (Weinh) ; 7(12): 1903172, 2020 Jun.
Article em En | MEDLINE | ID: mdl-32596108
ABSTRACT
Microfluidic technologies have emerged as advanced tools for surface-enhanced Raman spectroscopy (SERS). They have proved to be particularly appealing for in situ and real-time detection of analytes at extremely low concentrations and down to the 10 × 10-15 m level. However, the ability to prepare reconfigurable and reusable devices endowing multiple detection capabilities is an unresolved challenge. Herein, a microfluidic-based method that allows an extraordinary spatial control over the localization of multiple active SERS substrates in a single microfluidic channel is presented. It is shown that this technology provides for exquisite control over analyte transport to specific detection points, while avoiding cross-contamination; a feature that enables the simultaneous detection of multiple analytes within the same microfluidic channel. Additionally, it is demonstrated that the SERS substrates can be rationally designed in a straightforward manner and that they allow for the detection of single molecules (at concentrations as low as 10-14 m). Finally, it is shown that rapid etching and reconstruction of SERS substrates provides for reconfigurable and reusable operation.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2020 Tipo de documento: Article