| Literature DB >> 28734608 |
Radim Knob1, Daniel B Nelson2, Richard A Robison2, Adam T Woolley3.
Abstract
Antibiotic resistance of bacteria is a growing problem and presents a challenge for prompt treatment in patients with sepsis. Currently used methods rely on culturing or amplification; however, these steps are either time consuming or suffer from interference issues. A microfluidic device was made from black polypropylene, with a monolithic column modified with a capture oligonucleotide for sequence selective solid-phase extraction of a complementary target from a lysate sample. Porous properties of the monolith allow flow and hybridization of a target complementary to the probe immobilized on the column surface. Good flow-through properties enable extraction of a 100μL sample and elution of target DNA in 12min total time. Using a fluorescently labeled target oligonucleotide related to Verona Integron-Mediated Metallo-β-lactamase it was possible to extract and detect a 1pM sample with 83% recovery. Temperature-mediated elution by heating above the duplex melting point provides a clean extract without any agents that interfere with base pairing, allowing various labeling methods or further downstream processing of the eluent. Further integration of this extraction module with a system for isolation and lysis of bacteria from blood, as well as combining with single-molecule detection should allow rapid determination of antibiotic resistance.Entities:
Keywords: Hybridization; Microfluidics; Monolith; Sepsis
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Year: 2017 PMID: 28734608 PMCID: PMC5675797 DOI: 10.1016/j.chroma.2017.07.028
Source DB: PubMed Journal: J Chromatogr A ISSN: 0021-9673 Impact factor: 4.759