Kyle A. Mancuso
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Research Interests
Kyle A. Mancuso has a total of 6 co-authors. Here are the top co-authors by number of shared publications:
- Anyang Wang
University of Massachusetts Amherst
1 shared publication - Kwang W. Oh
Sensors and MicroActuators Learning Lab (SMALL), Department of Electrical Engineering, The State University of New York at Buffalo, Buffalo, NY 14260, USA
1 shared publication - Liam B. Christie
SMALL (Sensors and Micro Actuators Learning Lab), Department of Electrical Engineering, University at Buffalo, The State University of New York (SUNY at Buffalo), Buffalo, NY 14260, USA
1 shared publication - Philip J. Schneider
SMALL (Sensors and Micro Actuators Learning Lab), Department of Electrical Engineering, University at Buffalo, The State University of New York (SUNY at Buffalo), Buffalo, NY 14260, USA
1 shared publication - Samaneh Moghadasi Boroujeni
Department of Chemical and Biological Engineering, University at Buffalo, State University of New York (SUNY-Buffalo), Buffalo, NY 14260, USA
1 shared publication - Stelios T. Andreadis
Department of Chemical and Biological Engineering University at Buffalo Buffalo New York USA
1 shared publication
Latest Publications
- Open Access
- 23 April 2021
- Published by MDPI AG in Micromachines
- Vol. 12 (5) , 482
An Integrated Centrifugal Degassed PDMS-Based Microfluidic Device for Serial Dilution
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 to with about 8 μL 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.- 23 April 2021
- Published by MDPI AG in Micromachines
- Vol. 12 (5) , 482
Open AccessAn Integrated Centrifugal Degassed PDMS-Based Microfluidic Device for Serial Dilution
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 to with about 8 μL 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.