4.6 Article

An Integrated Centrifugal Degassed PDMS-Based Microfluidic Device for Serial Dilution

期刊

MICROMACHINES
卷 12, 期 5, 页码 -

出版社

MDPI
DOI: 10.3390/mi12050482

关键词

microfluidic; vacuum pumping; centrifugal pumping; serial dilution; qPCR; PDMS

资金

  1. Mark Diamond Research Fund of the Graduate Student Association at the University at Buffalo
  2. State University of New York
  3. Qualcomm Faculty Award

向作者/读者索取更多资源

An integrated serial dilution generator utilizing centrifugal force and vacuum-driven force was proposed, allowing for easy adjustment of dilution ratio and chamber volume by changing the geometrical designs of the device. The device was used for sample metering and transferring, as well as sample loading and mixing, with successful preparation of ten-fold serial dilutions and good agreement with manually prepared samples in subsequent analysis.
We propose an integrated serial dilution generator utilizing centrifugal force with a degassed polydimethylsiloxane (PDMS) microfluidic device. Using gas-soluble PDMS as a centrifugal microfluidic device material, the sample can be dragged in any arbitrary direction using vacuum-driven force, as opposed to in a single direction, without adding further actuation components. The vacuum-driven force allows the device to avoid the formation of air bubbles and exhibit high tolerance in the surface condition. The device was then used for sample metering and sample transferring. In addition, centrifugal force was used for sample loading and sample mixing. In this study, a series of ten-fold serial dilutions ranging from 100 to 10-4 with about 8 mu L in each chamber was achieved, while the serial dilution ratio and chamber volume could easily be altered by changing the geometrical designs of the device. As a proof of concept of our hybrid approach with the centrifugal and vacuum-driven forces, ten-fold serial dilutions of a cDNA (complementary DNA) sample were prepared using the device. Then, the diluted samples were collected by fine needles and subject to a quantitative polymerase chain reaction (qPCR), and the results were found to be in good agreement with those for samples prepared by manual pipetting.

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