4.7 Article

3D-printed microfluidics integrated with optical nanostructured porous aptasensors for protein detection

期刊

MICROCHIMICA ACTA
卷 188, 期 3, 页码 -

出版社

SPRINGER WIEN
DOI: 10.1007/s00604-021-04725-0

关键词

Porous silicon; 3D-printing; Polyacrylate; PDMS; Microfluidics; Biosensor

资金

  1. German Research Foundation (DFG) [SCHE 279/32-1]
  2. Emmy Noether Programme [346772917]
  3. German Technion Society
  4. Projekt DEAL

向作者/读者索取更多资源

Microfluidic integration of a 3D-printed polyacrylate-based platform with a label-free PSi-based optical aptasensor has been achieved for the first time, showing improved selectivity and detection limit for a model target protein. Superior performance of the 3D-printed microfluidic aptasensor was demonstrated compared to a conventional PDMS-based microfluidic platform with similar dimensions.
Microfluidic integration of biosensors enables improved biosensing performance and sophisticated lab-on-a-chip platform design for numerous applications. While soft lithography and polydimethylsiloxane (PDMS)-based microfluidics are still considered the gold standard, 3D-printing has emerged as a promising fabrication alternative for microfluidic systems. Herein, a 3D-printed polyacrylate-based microfluidic platform is integrated for the first time with a label-free porous silicon (PSi)-based optical aptasensor via a facile bonding method. The latter utilizes a UV-curable adhesive as an intermediate layer, while preserving the delicate nanostructure of the porous regions within the microchannels. As a proof-of-concept, a generic model aptasensor for label-free detection of his-tagged proteins is constructed, characterized, and compared to non-microfluidic and PDMS-based microfluidic setups. Detection of the target protein is carried out by real-time monitoring reflectivity changes of the PSi, induced by the target binding to the immobilized aptamers within the porous nanostructure. The microfluidic integrated aptasensor has been successfully used for detection of a model target protein, in the range 0.25 to 18 mu M, with a good selectivity and an improved limit of detection, when compared to a non-microfluidic biosensing platform (0.04 mu M vs. 2.7 mu M, respectively). Furthermore, a superior performance of the 3D-printed microfluidic aptasensor is obtained, compared to a conventional PDMS-based microfluidic platform with similar dimensions.

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