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Polyanhydride blends as drug delivery matrices to control biofilms, bone and nerve regeneration
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Johnson, Michelle Linette. Polyanhydride blends as drug delivery matrices to control biofilms, bone and nerve regeneration. Retrieved from https://doi.org/doi:10.7282/T3NV9JK8

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Uniform TitlePolyanhydride blends as drug delivery matrices to control biofilms, bone and nerve regeneration
NameJohnson, Michelle Linette (author); Uhrich, Kathryn (chair); Li, Jing (internal member); Taylor, John (internal member); Patwardhan, Dinesh (outside member); Rutgers University; Graduate School - New Brunswick
Date Created2008
Other Date2008-05 (degree)
SubjectChemistry and Chemical Biology, Drug delivery systems
Extentxix, 151 pages
DescriptionBiodegradable polyanhydrides were fabricated into disks, coatings, microspheres, and tubes for controlled drug delivery as well as enhanced thermal and mechanical properties. The polymer systems were evaluated as potential treatments for periodontal disease, orthopedic injuries, nerve regeneration, and biofilm formation. The polymers contained the non-steroidal anti-inflammatory drug (NSAID), salicylic acid and the antibiotic, ampicillin, in the polymer backbone, which are subsequently released as the polymers degrade. Significantly, the polymers can be fabricated into these different geometries that would not be possible with the drug molecules alone.
This dissertation characterizes the in vitro degradation of the polyanhydrides specifically for the multiple applications. Polymer degradation was monitored by high pressure liquid chromatography (HPLC) for final degradation products. The effect of physically admixing additional drugs into the polymer matrix was studied as well, where the admixed drugs were delineated from the chemically incorporated drugs by HPLC. Accelerated in vitro degradation rates were developed using highly basic media.
Mechanical and thermal properties were examined for potential orthopedic and nerve applications. The compliance and modulus of polymer blends and composites were measured to characterize the flexibility and strength of each system. Additionally, properties, such as glass transition temperature (Tg) and decomposition temperature (Td) were measured to monitor polymer changes as a result of processing and degradation.
Overall, the fundamental chemical, thermal and mechanical properties of each polyanhydride system were monitored. This dissertation describes the optimization of controlled drug release rates for specific applications through composites and blends of ceramics (hydroxyapatite), drugs (antimicrobials and NSAIDs), and polymers (polyanhydrides).
NotePh.D.
NoteIncludes bibliographical references.
Genretheses, ETD doctoral
Persistent URLhttps://doi.org/doi:10.7282/T3NV9JK8
LanguageEnglish
CollectionGraduate School - New Brunswick Electronic Theses and Dissertations
Organization NameRutgers, The State University of New Jersey
RightsThe author owns the copyright to this work.
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