Russell Kirk Pirlo

Dr. Russell Kirk Pirlo

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Research Focus & Metrics

Academic Career Length

21Years (2006-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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9 August 2011 in Biotechnology and Bioengineering
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Journal Article
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RPRussell Kirk Pirlo
Russell Kirk Pirlo
PWPeter Wu
Peter Wu
JLJinny Liu
Jinny Liu
BRBradley Ringeisen
Bradley Ringeisen

14 October 2013 in MRS Bulletin
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BRBradley R. Ringeisen
Bradley R. Ringeisen
RPRussell Kirk Pirlo
Russell Kirk Pirlo
PWPeter K. Wu
Peter K. Wu
Thomas BolandThomas Boland
Thomas Boland
YHYong Huang
Yong Huang
Douglas B. ChriseyDouglas B. Chrisey
Douglas B. Chrisey

19 September 2006 in Biotechnology Journal
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Journal Article
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RPRussell Kirk Pirlo
Russell Kirk Pirlo
DDDelphine M. D. Dean
Delphine M. D. Dean
DKDaniel R. Knapp
Daniel R. Knapp
BGBruce Zhi Gao
Bruce Zhi Gao

9 December 2015 in Journal of Biomedical Materials Research Part A
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LBLauren L. Bischel
Lauren L. Bischel
PCPeter N. Coneski
Peter N. Coneski
JLJeffrey G. Lundin
Jeffrey G. Lundin
PWPeter K. Wu
Peter K. Wu
CGCarl B. Giller
Carl B. Giller
RPRussell Kirk Pirlo
Russell Kirk Pirlo

1 January 2011 in Review of Scientific Instruments
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Journal Article
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RPRussell Kirk Pirlo
Russell Kirk Pirlo
ZMZhen Ma
Zhen Ma
ASAndrew Sweeney
Andrew Sweeney
HLHonghai Liu
Honghai Liu
JYJulie X. Yun
Julie X. Yun
BGBruce Zhi Gao
Bruce Zhi Gao
Employing optical force, our laser-guided cell micropatterning system, is capable of patterning different cell types onto and within standard cell research devices, including commercially available multielectrode arrays (MEAs) with glass culture rings, 35 mm Petri dishes, and microdevices microfabricated with polydimethylsiloxane on 22 mm × 22 mm cover glasses. We discuss the theory of optical forces for generating laser guidance and the calculation of optimal beam characteristics for cell guidance. We describe the hardware design and software program for the cell patterning system. Finally, we demonstrate the capabilities of the system by (1) patterning neurons to form an arbitrary pattern, (2) patterning neurons onto the electrodes of a standard MEA, and (3) patterning and aligning adult cardiomyocytes in a polystyrene Petri dish.

1 March 2011 in Biomicrofluidics
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Journal Article
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RPRussell Kirk Pirlo
Russell Kirk Pirlo
ASA. J. Sweeney
A. J. Sweeney
BRB. R. Ringeisen
B. R. Ringeisen
MKM. Kindy
M. Kindy
BGB. Z. Gao
B. Z. Gao
Axon path-finding plays an important role in normal and pathogenic brain development as well as in neurological regenerative medicine. In both scenarios, axonal growth is influenced by the microenvironment including the soluble molecules and contact-mediated signaling from guiding cells and cellular matrix. Microfluidic devices are a powerful tool for creating a microenvironment at the single cell level. In this paper, an asymmetrical-channel-based biochip, which can be later incorporated into microfluidic devices for neuronal network study, was developed to investigate geometric as well as supporting cell control of polarized axonal growth in forming a defined neuronal circuitry. A laser cell deposition system was used to place single cells, including neuron-glia pairs, into specific microwells of the device, enabling axonal growth without the influence of cytophilic/phobic surface patterns. Phase microscopy showed that a novel “snag” channel structure influenced axonal growth in the intended direction 4:1 over the opposite direction. In heterotypic experiments, glial cell influence over the axonal growth path was observed with time-lapse microscopy. Thus, it is shown that single cell and heterotypic neuronal path-finding models can be developed in laser patterned biochips.