On-site extraction and purification of bacterial nucleic acids from blood samples using an unpowered microfluidic device
[Display omitted] •Unpowered sample pretreatment method was devised based on the membrane filter and the finger-actuated microfluidic unit.•Using unpowered plasma separation chip, the plasma was separated and collected successfully from blood sample without electrical device.•The entire nucleic acid...
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Veröffentlicht in: | Sensors and actuators. B, Chemical Chemical, 2020-10, Vol.320, p.128346, Article 128346 |
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Sprache: | eng |
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•Unpowered sample pretreatment method was devised based on the membrane filter and the finger-actuated microfluidic unit.•Using unpowered plasma separation chip, the plasma was separated and collected successfully from blood sample without electrical device.•The entire nucleic acid extractionwas conducted simply by pressing the buttons on unpowered nucleic acid extraction chip.•A manual sample preparation method was efficient even at low concentrations of 103 CFU/mL of E. coli in the blood samples.
Molecular diagnostics is a powerful technique for detecting pathogens with high sensitivity, but it has complicated sample preparation procedures that rely not only on a manual operation by experts but also on bulky equipment. Here, we report the use of an unpowered, microfluidic sample preparation device in on-site molecular diagnosis without the necessity of expertise and electrical devices. The device is assembled with two units, a plasma separation chip, and a nucleic acid extraction and purification chip. As a model pathogen, Escherichia coli (E. coli) O157:H7 was first separated from the blood sample using the unpowered plasma separation chip, and then the DNA was extracted and purified from the separated bacteria by using the finter-actuated nucleic acid extraction and purification chip. 103 to 108 CFU/mL of E. coli O157:H7 was infiltered from the blood sample with ∼1% of permeation efficiency. The extracted DNA was successfully purified and confirmed by gel electrophoresis after the polymerase chain reaction. This unpowered sample pretreatment method is precise and reliable, even at low concentrations of down to 103 CFU/mL of E. coli in the blood sample. |
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ISSN: | 0925-4005 1873-3077 |
DOI: | 10.1016/j.snb.2020.128346 |