Microfluidic purification and preconcentration of mRNA by flow-through polymeric monolith

Brent C. Satterfield, Seth Stern, Michael Caplan, Kyle W. Hukari, Jay A A West

Research output: Contribution to journalArticlepeer-review

43 Scopus citations

Abstract

Efficient and rapid isolation of mRNA is important in the field of genomics as well as in the clinical and pharmaceutical arena. We have developed UV-initiated methacrylate-based porous polymer monoliths (PPM) for microfluidic trapping and concentration of eukaryotic mRNA. PPM are cast-to-shape and are tunable for functionalization using a variety of amine-terminated molecules. Efficient isolation of eukaryotic mRNA from total RNA was first mathematically modeled and then achieved using PPM in capillaries. Purification protocols using oligo dT's, locked nucleic acid substituted dT's, and tetramethylammonium chloride salts were characterized. mRNA yield and purity were compared with mRNA isolated by commercial kits with statistically equivalent yields and purities (determined by qPCR ratio of 18s rRNA and Gusb mRNA markers). Even after extracting 16 μg of mRNA from 315 μg of total RNA, the 0.4-μL volume monolith showed no signs of saturation. Elution volumes were below 20 μL with concentrations up to 1 μg/μL. In addition, the polymeric material exhibited exceptional stability in a range of conditions (pH, temperature, dryness) and was stable for a period of months. All of these characteristics make porous polymer monoliths good candidates for potential microfluidic sample preconcentrators and purifiers.

Original languageEnglish (US)
Pages (from-to)6230-6235
Number of pages6
JournalAnalytical chemistry
Volume79
Issue number16
DOIs
StatePublished - Aug 15 2007

ASJC Scopus subject areas

  • Analytical Chemistry

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