Solid supports for extraction and preconcentration of proteins and peptides in microfluidic devices: A review

Determination of proteins and peptides is among the main challenges of today's bioanalytical chemistry. The application of microchip technology in this field is an exhaustively developed concept that aims to create integrated and fully automated analytical devices able to quantify or detect one...

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Veröffentlicht in:Analytica chimica acta 2017-02, Vol.955, p.1-26
Hauptverfasser: Dziomba, Szymon, Araya-Farias, Monica, Smadja, Claire, Taverna, Myriam, Carbonnier, Benjamin, Tran, N. Thuy
Format: Artikel
Sprache:eng
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Zusammenfassung:Determination of proteins and peptides is among the main challenges of today's bioanalytical chemistry. The application of microchip technology in this field is an exhaustively developed concept that aims to create integrated and fully automated analytical devices able to quantify or detect one or several proteins from a complex matrix. Selective extraction and preconcentration of targeted proteins and peptides especially from biological fluids is of the highest importance for a successful realization of these microsystems. Incorporation of solid structures or supports is a convenient solution employed to face these demands. This review presents a critical view on the latest achievements in sample processing techniques for protein determination using solid supports in microfluidics. The study covers the period from 2006 to 2015 and focuses mainly on the strategies based on microbeads, monolithic materials and membranes. Less common approaches are also briefly discussed. The reviewed literature suggests future trends which are discussed in the concluding remarks. [Display omitted] •Miniaturization offers unique opportunities for extraction and preconcentration.•Solid supports include microbeads, monoliths and membranes.•High performances are achieved via the synergy of microfluidics and solid supports.•Integrated microsystems enable analysis of complex samples.
ISSN:0003-2670
1873-4324
DOI:10.1016/j.aca.2016.12.017