Protein preconcentration using nanofractures generated by nanoparticle-assisted electric breakdown at junction gaps

• Published in: PloS one Vol. 9; no. 7; p. e102050
• Main Authors: Jen, Chun-Ping, Amstislavskaya, Tamara G, Kuo, Chen-Chi, Chen, Yu-Hung
• Format: Journal Article
• Language: English
• Published: United States Public Library of Science 15.07.2014; Public Library of Science (PLoS)
• Subjects: Analytical chemistry; Breakdown; Electrokinetics; Engineering and Technology; Enrichment; Fluidics; Immunoassay; Low concentrations; Mechanical engineering; Membranes; Microchannels; Microfluidic Analytical Techniques - instrumentation; Microfluidic Analytical Techniques - methods; Nanofluids; Nanoparticles; Nanoparticles - chemistry; Nanostructures; Polydimethylsiloxane; Proteins; Proteins - chemistry; Semiconductors; Taiwan
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0102050

Sample preconcentration is an important step that increases the accuracy of subsequent detection, especially for samples with extremely low concentrations. Due to the overlapping of electrical double layers in the nanofluidic channel, the concentration polarization effect can be generated by applying an electric field. Therefore, a nonlinear electrokinetic flow is induced, which results in the fast accumulation of proteins in front of the induced ionic depletion zone, the so-called exclusion-enrichment effect. Nanofractures were created in this work to preconcentrate proteins via the exclusion-enrichment effect. The protein sample was driven by electroosmotic flow and accumulated at a specific location. The preconcentration chip for proteins was fabricated using simple standard soft lithography with a polydimethylsiloxane replica. Nanofractures were formed by utilizing nanoparticle-assisted electric breakdown. The proposed method for nanofracture formation that utilizes nanoparticle deposition at the junction gap between microchannels greatly decreases the required electric breakdown voltage. The experimental results indicate that a protein sample with an extremely low concentration of 1 nM was concentrated to 1.5×10(4)-fold in 60 min using the proposed chip.