Title Information
Title
Microcavitation as a neural cell damage mechanism in an in vitro model of blast traumatic brain injury
Name: Personal
Name Part
Estrada, Jonathan Bartholomew
Role
Role Term: Text
creator
Name: Personal
Name Part
Franck, Christian
Role
Role Term: Text
Advisor
Name: Personal
Name Part
Hoffman-Kim, Diane
Role
Role Term: Text
Reader
Name: Personal
Name Part
Henann, David
Role
Role Term: Text
Reader
Name: Corporate
Name Part
Brown University. Engineering: Mechanics of Solids
Role
Role Term: Text
sponsor
Origin Information
Copyright Date
2017
Physical Description
Extent
20, 151 p.
digitalOrigin
born digital
Note: thesis
Thesis (Ph. D.)--Brown University, 2017
Genre (aat)
theses
Abstract
Blast traumatic brain injury is a serious type of injury in the armed forces and considered the signature injury of the wars in Iraq and Afghanistan. While compressive hydrostatic pressures resulting from blast waves have been investigated, negative pressures resulting from the blast wave and wave-brain tissue interaction have the potential to nucleate bubbles in the nearly-incompressible tissue, leading to a separate damage mechanism of inertial cavitation. The specific relation between the mechanics of inertial cavitation and primary cell injury, to date, has not been investigated in detail. While inertial cavitation damage to free surfaces has been well-studied in the field of fluid dynamics, bubble interactions within 3D neural cultures and hydrogels are in their infancy, particularly experimentally. With the goal of quantifying the specific effects of inertial microcavitation as the proposed cellular injury mechanism in blast traumatic brain injury, presented here is an experimental approach of initiating inertial microcavitation in primary dissociated 3D neural cultures coupled with a new analysis technique for computing the critical local strains and stresses around cells that are found to induce cellular injury and mechanical disruption. Bubble dynamics during injury are quantified using high-speed imaging and custom image processing algorithms, while laser scanning confocal microscope image stacks of neurons before and after cavitation injury correlate bubble kinematics to fragmentation and disruption of cytoskeletal proteins. To get the high-rate constitutive behavior of the surrounding matrix, and subsequently spatiotemporal strains, strain rates, and stresses on the cells during cavitation, an approach called inertial microcavitation-based ultra-high-strain rate rheometry (IMUR) is presented as a new theoretical-numerical technique to assess local rheological properties of soft materials.
Subject
Topic
traumatic brain injury
Subject (fast) (authorityURI="http://id.worldcat.org/fast", valueURI="http://id.worldcat.org/fast/01036436")
Topic
Neurons
Subject (fast) (authorityURI="http://id.worldcat.org/fast", valueURI="http://id.worldcat.org/fast/00849936")
Topic
Cavitation
Subject
Topic
rheometry
Subject (fast) (authorityURI="http://id.worldcat.org/fast", valueURI="http://id.worldcat.org/fast/01167814")
Topic
Viscoelasticity
Subject (fast) (authorityURI="http://id.worldcat.org/fast", valueURI="http://id.worldcat.org/fast/00875028")
Topic
Confocal microscopy
Subject
Topic
primary injury
Language
Language Term (ISO639-2B)
English
Record Information
Record Content Source (marcorg)
RPB
Record Creation Date (encoding="iso8601")
20170616
Identifier: DOI
10.7301/Z0028PZM
Access Condition: rights statement (href="http://rightsstatements.org/vocab/InC/1.0/")
In Copyright
Access Condition: restriction on access
Collection is open for research.
Type of Resource (primo)
dissertations