Joseph M. DeSimone

Prof. Dr. Joseph M. DeSimone


Research Focus & Metrics

Academic Career Length

37Years (1990-Present)

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

Representative Publications

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19 August 2008 in Proceedings of the National Academy of Sciences
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Journal Article
Closed access
SGStephanie E. A. Gratton
Stephanie E. A. Gratton
PRPatricia A. Ropp
Patricia A. Ropp
PPPatrick D. Pohlhaus
Patrick D. Pohlhaus
JLJ. Christopher Luft
J. Christopher Luft
VMVictoria J. Madden
Victoria J. Madden
JDJoseph M. DeSimone
Joseph M. DeSimone
The interaction of particles with cells is known to be strongly influenced by particle size, but little is known about the interdependent role that size, shape, and surface chemistry have on cellular internalization and intracellular trafficking. We report on the internalization of specially designed, monodisperse hydrogel particles into HeLa cells as a function of size, shape, and surface charge. We employ a top-down particle fabrication technique called PRINT that is able to generate uniform populations of organic micro- and nanoparticles with complete control of size, shape, and surface chemistry. Evidence of particle internalization was obtained by using conventional biological techniques and transmission electron microscopy. These findings suggest that HeLa cells readily internalize nonspherical particles with dimensions as large as 3 μm by using several different mechanisms of endocytosis. Moreover, it was found that rod-like particles enjoy an appreciable advantage when it comes to internalization rates, reminiscent of the advantage that many rod-like bacteria have for internalization in nonphagocytic cells.

20 March 2015 in Science
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Journal Article
Closed access
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JTJohn R. Tumbleston
John R. Tumbleston
DSDavid Shirvanyants
David Shirvanyants
NENikita Ermoshkin
Nikita Ermoshkin
RJRima Janusziewicz
Rima Janusziewicz
AJAshley R. Johnson
Ashley R. Johnson
JDJoseph M. DeSimone
Joseph M. DeSimone
Fast, continuous, 3D printing: Although three-dimensional (3D) printing is now possible using relatively small and low-cost machines, it is still a fairly slow process. This is because 3D printers require a series of steps to cure, replenish, and reposition themselves for each additive cycle. Tumbleston et al. devised a process to effectively grow solid structures out of a liquid bath. The key to the process is the creation of an oxygen-containing “dead zone” between the solid part and the liquid precursor where solidification cannot occur. The precursor liquid is then renewed by the upward movement of the growing solid part. This approach made structures tens of centimeters in size that could contain features with a resolution below 100 µm. Science , this issue p. 1349

2 August 2002 in Science
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Journal Article
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JDJoseph M. DeSimone
Joseph M. DeSimone
Solvents are widely used in commercial manufacturing and service industries. Despite abundant precaution, they inevitably contaminate our air, land, and water because they are difficult to contain and recycle. Researchers have therefore focused on reducing solvent use through the development of solvent-free processes and more efficient recycling protocols. However, these approaches have their limitations, necessitating a pollution prevention approach and the search for environmentally benign solvent alternatives. This report highlights opportunities for the practical implementation of such green solvents.

27 August 2012 in Nano Letters
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Journal Article
Closed access
JPJillian L. Perry
Jillian L. Perry
KRKevin G. Reuter
Kevin G. Reuter
MKMarc P. Kai
Marc P. Kai
KHKevin P. Herlihy
Kevin P. Herlihy
SJStephen W. Jones
Stephen W. Jones
JDJoseph M. DeSimone
Joseph M. DeSimone

4 January 2011 in Proceedings of the National Academy of Sciences
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Journal Article
Closed access
PDF file
TMTimothy J. Merkel
Timothy J. Merkel
SJStephen W. Jones
Stephen W. Jones
KHKevin P. Herlihy
Kevin P. Herlihy
FKFarrell R. Kersey
Farrell R. Kersey
ASAdam R. Shields
Adam R. Shields
JDJoseph M. DeSimone
Joseph M. DeSimone
It has long been hypothesized that elastic modulus governs the biodistribution and circulation times of particles and cells in blood; however, this notion has never been rigorously tested. We synthesized hydrogel microparticles with tunable elasticity in the physiological range, which resemble red blood cells in size and shape, and tested their behavior in vivo. Decreasing the modulus of these particles altered their biodistribution properties, allowing them to bypass several organs, such as the lung, that entrapped their more rigid counterparts, resulting in increasingly longer circulation times well past those of conventional microparticles. An 8-fold decrease in hydrogel modulus correlated to a greater than 30-fold increase in the elimination phase half-life for these particles. These results demonstrate a critical design parameter for hydrogel microparticles.

22 June 2011 in Small
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Journal Article
Closed access
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JWJin Wang
Jin Wang
JBJames D. Byrne
James D. Byrne
MNMary E. Napier
Mary E. Napier
JDJoseph M. DeSimone
Joseph M. DeSimone