Masters Theses
Keywords and Phrases
BCA; HUVEC; Microparticles; NHS; PLGA; PLL
Abstract
"Tissue engineering is a process of developing new tissues in a host. Tissue engineering draws upon revitalizing damaged tissues that otherwise would not heal completely from the body's natural response. To augment the body's natural response to impairment, cells can be transplanted to the afflicted area to boost the healing response. Implementing these cells onto scaffolds and transplanting them into the body improves the healing response dramatically. Tissue regeneration improves when a biodegradable scaffold is used in conjunction with cells to augment the body's healing response. Microparticles provide a surface that can mimic the environment cells perceive in vivo, allowing cells to proliferate and grow on the microparticle surface optimally. When these microparticles are transplanted into the body, the accompanying cells transition into the host tissue as the microparticles degrade. Proteins comprising the extracellular matrix (ECM), like collagen, fibronectin, and laminin, are used to facilitate cell binding to substrates, whether a biomaterial material ex vivo or an enzyme in vivo. Functionalizing the surface of microparticles with ECM proteins improves the adherence of cells which increases the area of tissue regenerated. When cells bind to ECM proteins on a biomaterial, a cascade of signals is initiated which communicates to the cell to spread on the surface of the biomaterial and begin the process of mitosis, leading to proliferation. Cationic polymers have also been shown to improve cell-surface interactions. Functionalizing particles with cationic polymers and extracellular matrix proteins provides a surface optimized for cell attachment and spreading"--Abstract, page iv.
Advisor(s)
Barua, Sutapa
Committee Member(s)
Barua, Dipak
Wang, Jee C.
Department(s)
Chemical and Biochemical Engineering
Degree Name
M.S. in Chemical Engineering
Publisher
Missouri University of Science and Technology
Publication Date
Spring 2018
Journal article titles appearing in thesis/dissertation
- PLGA microparticles as vehicles for cell transport
- Correction in bicinchoninic acid (BCA) absorbance assay to analyze protein concentration
Pagination
xi, 71 pages
Note about bibliography
Includes bibliographical references.
Rights
© 2018 Daniel Smith, All rights reserved.
Document Type
Thesis - Open Access
File Type
text
Language
English
Thesis Number
T 11319
Electronic OCLC #
1041858877
Recommended Citation
Smith, Daniel, "Cellular hitchhiking via injectable microparticles" (2018). Masters Theses. 7784.
https://scholarsmine.mst.edu/masters_theses/7784