Robert Peyton Wilkes
University of Texas at San Antonio
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Surgical Innovation | 2012
Robert Peyton Wilkes; Deepak V. Kilpad; Yabin Zhao; Richard Marvin Kazala; Amy Mcnulty
A novel closed incision management with negative pressure wound therapy (CIM) has been developed for convenient use with closed incisions that has the potential to be beneficial for patients at risk for postoperative complications. Incisions are typically under lateral tension. This study explored the biomechanical mechanisms by which integrity of the incisional closure is enhanced by CIM. CIM was hypothesized to affect local stresses around closed incisions in a beneficial manner. Finite element analyses (FEA) indicated that application of CIM decreased the lateral stresses ~50% around the incision and changed the direction of the stresses to a distribution that is typical of intact tissue. Bench evaluations corroborated findings that CIM significantly increased the force required to disrupt the closed incision by ~50% as compared with closure alone. In conclusion, using 2 FEAs and bench modeling, CIM was shown to reduce and normalize tissue stresses and bolster appositional forces at the incision.
Tissue Engineering | 1996
Robert Peyton Wilkes; Kyriacos A. Athanasiou
This paper presents a new methodology, apparatus design, and the experimental results of ongoing research into the measurement of the mechanical properties of musculoskeletal tissue at the cellular level. A microchamber was constructed that provides a controlled hydrostatic pressure environment for these cells where optical sectioning, via epifluorescence microscopy, was used to acquire volume information about the individual cell. The microchamber was integrated into a hydraulic system that, via computer control, provided a regulated adjustable hydrostatic pressure environment for living cells suspended in culture media. The techniques applied in this study include fluorescent labeling of the cell volume, hydrostatic pressure application, optical sectioning, and digital volume reconstruction. To determine the mechanical response (compressibility) of cultured MG-63 osteoblast-like cells under physiologically high hydrostatic pressures two experiments were devised: In the first experiment changes in volume of 10 cells were measured as the applied hydrostatic pressure was increased from 0 to 7 MPa. Volume changes in response to pressure magnitudes were not significant (p > 0.49). In the second experiment, the mechanical role of the plasma membrane to act as a supportive component in cell compressibility was studied by permeabilizing the membrane of six cells and again applying hydrostatic pressure. Again, no significant volume differences between pressurized and unpressurized cells were found (p > 0.46). A retrospective power analysis of the results of the first and second experiments indicates that the sample size was sufficient. The results of this study show that MG-63 osteoblast-like cells are intrinsically incompressible in the 0-7 MPa hydrostatic pressure range. They also support the hypothesis that the plasma membrane plays an insignificant mechanical role in terms of cell compressibility.
Volume 1A: Abdominal Aortic Aneurysms; Active and Reactive Soft Matter; Atherosclerosis; BioFluid Mechanics; Education; Biotransport Phenomena; Bone, Joint and Spine Mechanics; Brain Injury; Cardiac Mechanics; Cardiovascular Devices, Fluids and Imaging; Cartilage and Disc Mechanics; Cell and Tissue Engineering; Cerebral Aneurysms; Computational Biofluid Dynamics; Device Design, Human Dynamics, and Rehabilitation; Drug Delivery and Disease Treatment; Engineered Cellular Environments | 2013
Matthew A. Reilly; Robert Peyton Wilkes
Recent work has shown that cyclic stresses from accommodation may induce changes in resistance to aqueous outflow through the trabecular meshwork. We developed a finite element model of the whole globe to examine changes in stress due to radial forces produced by the ciliary muscle. The mean equivalent stresses in the trabecular meshwork decreased significantly during accommodation.Copyright
Archive | 2009
Robert Peyton Wilkes; Justin Alexander Long; Richard Marvin Kazala; Li Yao; Erick Woodson Barta; Christopher Brian Locke
Archive | 2009
Richard Marvin Kazala; Justin Alexander Long; Eric Woodson Barta; Li Yao; Robert Peyton Wilkes
Archive | 2009
Robert Peyton Wilkes; Justin Alexander Long; Richard Marvin Kazala
Archive | 2009
Justin Alexander Long; Richard Marvin Kazala; Robert Peyton Wilkes; Eric Woodson Barta; Francis Cavanaugh Ii Matthew; Larry Tab Randolph; Li Yao
Archive | 2009
Robert Peyton Wilkes; Justin Alexander Long; Richard Marvin Kazala
Archive | 2009
Richard Marvin Kazala; Justin Alexander Long; Robert Peyton Wilkes; Carrie Ann Kauffman
Archive | 2009
Richard Marvin Kazala; Justin Alexander Long; Robert Peyton Wilkes; Royce W. Johnson