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Merck

A chitosan coated monolith for nucleic acid capture in a thermoplastic microfluidic chip.

Biomicrofluidics (2014-11-08)
Eric L Kendall, Erik Wienhold, Don L DeVoe
ZUSAMMENFASSUNG

A technique for microfluidic, pH modulated DNA capture and purification using chitosan functionalized glycidyl methacrylate monoliths is presented. Highly porous polymer monoliths are formed and subsequently functionalized off-chip in a batch process before insertion into thermoplastic microchannels prior to solvent bonding, simplifying the overall fabrication process by eliminating the need for on-chip surface modifications. The monolith anchoring method allows for the use of large cross-section monoliths enabling high flowrates and high DNA capture capacity with a minimum of added design complexity. Using monolith capture elements requiring less than 1 mm(2) of chip surface area, loading levels above 100 ng are demonstrated, with DNA capture and elution efficiency of 54.2% ± 14.2% achieved.

MATERIALIEN
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Marke
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Sigma-Aldrich
Methanol, suitable for HPLC, ≥99.9%
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Natriumphosphat, ACS reagent, ≥99.0%
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Ethyl alcohol, Pure, 200 proof, meets USP testing specifications
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Ethyl alcohol, Pure, 190 proof, for molecular biology
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Methanol, anhydrous, 99.8%
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Natriumphosphat, puriss. p.a., ACS reagent, anhydrous, ≥99.0% (T)
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Methanol, Laboratory Reagent, ≥99.6%
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Methanol, Absolute - Acetone free
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Methanol, ACS spectrophotometric grade, ≥99.9%
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USP
Methylalkohol, United States Pharmacopeia (USP) Reference Standard
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