Michael Stacey

Dr. Michael Stacey

orcid

Research Focus & Metrics

Academic Career Length

40Years (1987-Present)

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

Representative Publications

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16 June 2008 in Applied Physics Letters
Verified
Journal Article
Closed access
JKJuergen Kolb
Juergen Kolb
AMAbdel-Aleam Mohamed
Abdel-Aleam Mohamed
RPR. O. Price
R. O. Price
RSR. J. Swanson
R. J. Swanson
ABA. Bowman
A. Bowman
KSK. H. Schoenbach
K. H. Schoenbach
By flowing atmospheric pressure air through a direct current powered microhollow cathode discharge, we were able to generate a 2cm long plasma jet. With increasing flow rate, the flow becomes turbulent and temperatures of the jet are reduced to values close to room temperature. Utilizing the jet, yeast grown on agar can be eradicated with a treatment of only a few seconds. Conversely, animal studies show no skin damage even with exposures ten times longer than needed for pathogen extermination. This cold plasma jet provides an effective mode of treatment for yeast infections of the skin.

21 June 2004 in Proceedings of the IEEE
Verified
Journal Article
Closed access
KSK.H. Schoenbach
K.H. Schoenbach
RJR.P. Joshi
R.P. Joshi
JKJuergen Kolb
Juergen Kolb
NCNianyong Chen
Nianyong Chen
MSMichael Stacey
Michael Stacey
SBStephen J. Beebe
Stephen J. Beebe
An electrical model for biological cells predicts that for pulses with durations shorter than the charging time of the outer membrane, there is an increasing probability of electric field interactions with intracellular structures. Experimental studies in which human cells were exposed to pulsed electric fields of up to 300-kV/cm amplitude, with durations as short as 10 ns, have confirmed this hypothesis. The observed effects include the breaching of intracellular granule membranes without permanent damage to the cell membrane, abrupt rises in intracellular free calcium levels, and enhanced expression of genes. At increased electric fields, the application of submicrosecond pulses induces apoptosis (programmed cell death) in biological cells, an effect that has been shown to reduce the growth of tumors. Possible applications of the intracellular electroeffect are enhancing gene delivery to the nucleus, controlling cell functions that depend on calcium release (causing cell immobilization), and treating tumors.

8 October 2007 in IEEE Transactions on Dielectrics and Electrical Insulation
Verified
Journal Article
Closed access
KSKarl H. Schoenbach
Karl H. Schoenbach
BHBarbara Hargrave
Barbara Hargrave
RJRavindra P. Joshi
Ravindra P. Joshi
JKJuergen Kolb
Juergen Kolb
RNRichard Nuccitelli
Richard Nuccitelli
EBE. Stephen Buescher
E. Stephen Buescher
Electrical models for biological cells predict that reducing the duration of applied electrical pulses to values below the charging time of the outer cell membrane (which is on the order of 100 ns for mammalian cells) causes a strong increase in the probability of electric field interactions with intracellular structures due to displacement currents. For electric field amplitudes exceeding MV/m, such pulses are also expected to allow access to the cell interior through conduction currents flowing through the permeabilized plasma membrane. In both cases, limiting the duration of the electrical pulses to nanoseconds ensures only nonthermal interactions of the electric field with subcellular structures. This intracellular access allows the manipulation of cell functions. Experimental studies, in which human cells were exposed to pulsed electric fields of up to 300 kV/cm amplitude with durations as short as 3 ns, have confirmed this hypothesis and have shown that it is possible to selectively alter the behavior and/or survival of cells. Observed nanosecond pulsed effects at moderate electric fields include intracellular release of calcium and enhanced gene expression, which could have long term implications on cell behavior and function. At increased electric fields, the application of nanosecond pulses induces a type of programmed cell death, apoptosis, in biological cells. Cell survival studies with 10 ns pulses have shown that the viability of the cells scales inversely with the electrical energy density, which is similar to the "dose" effect caused by ionizing radiation. On the other hand, there is experimental evidence that, for pulses of varying durations, the onset of a range of observed biological effects is determined by the electrical charge that is transferred to the cell membrane during pulsing. This leads to an empirical similarity law for nanosecond pulse effects, with the product of electric field intensity, pulse duration, and the square root of the number of pulses as the similarity parameter. The similarity law allows one not only to predict cell viability based on pulse parameters, but has also been shown to be applicable for inducing platelet aggregation, an effect which is triggered by internal calcium release. Applications for nanosecond pulse effects cover a wide range: from a rather simple use as preventing biofouling in cooling water systems, to advanced medical applications, such as gene therapy and tumor treatment. Results of this continuing research are leading to the development of wound healing and skin cancer treatments, which are discussed in some detail.

1 July 1996 in Nature Genetics
Verified
Journal Article
Closed access
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JMJudith A. Metcalfe
Judith A. Metcalfe
JPJulian Parkhill
Julian Parkhill
LCLouise Campbell
Louise Campbell
MSMichael Stacey
Michael Stacey
PBPaul Biggs
Paul Biggs
ATA. Malcolm R. Taylor
A. Malcolm R. Taylor

1 December 2003 in Mutation Research - Genetic Toxicology and Environmental Mutagenesis
Verified
Journal Article
Closed access
MSMichael Stacey
Michael Stacey
JSJ Stickley
J Stickley
PFP Fox
P Fox
VSV Statler
V Statler
KSK Schoenbach
K Schoenbach
SBS Buescher
S Buescher

1 October 2006 in Journal of Pediatric Surgery
Verified
Journal Article
Closed access
HCHeather A. Creswick
Heather A. Creswick
MSMichael Stacey
Michael Stacey
RKRobert E. Kelly
Robert E. Kelly
TGTina Gustin
Tina Gustin
DNDonald Nuss
Donald Nuss
VPVirginia K. Proud
Virginia K. Proud