4.5 Article

Rapid automatic nucleic acid purification system based on gas-liquid immiscible phase

Journal

JOURNAL OF SEPARATION SCIENCE
Volume 46, Issue 6, Pages -

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/jssc.202200801

Keywords

automatic nucleic acid extraction; gas-liquid immiscible phase; magnetic beads; microfluidic chip; rapid nucleic acid extraction

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This study proposes a fast, highly automated, and low-consumption nucleic acid extraction method. By analyzing the process of magnetic beads crossing the gas-liquid interface, large magnetic bead packages were driven to cross the interface using a low magnetic field strength. This method provides a solution for high magnetic bead recovery rate in solid-phase extraction with a low-surfactant system based on a gas-liquid immiscible phase valve. The recovery rate of magnetic beads was improved to 90%-95%, and the carryover of reagents was below 1%.
The continuous expansion of nucleic acid detection applications has resulted in constant developments in rapid, low-consumption, and highly automated nucleic acid extraction methods. Nucleic acid extraction using magnetic beads across an immiscible phase interface offers significant simplification and parallelization potential. The gas-liquid immiscible phase valve eliminates the requirement for complicated cassettes and is suitable for automation applications. By analyzing the process of magnetic beads crossing the gas-liquid interface, we utilized a low magnetic field strength to drive large magnetic bead packages to cross the gas-liquid interface, providing a solution of high magnetic bead recovery rate for solid-phase extraction with a low-surfactant system based on gas-liquid immiscible phase valve. The recovery rate of magnetic beads was further improved to 90%-95% and the carryover of the reagents was below 1%. Consequently, a chip and an automatic system were developed to verify the applicability of this method for nucleic acid extraction. The Hepatitis B virus serum standard was used for the extraction test. The extraction of four samples was performed within 7 minutes, with nucleic acid recovery maintained above 80% and good purity. Thus, through analysis and experiments, a fast, highly automated, and low-consumption nucleic acid recovery method was proposed in this study.

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