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        <identifier>oai:www.ideals.illinois.edu:2142/100421</identifier>
        <datestamp>2023-07-11</datestamp>
        <setSpec>col_2142_5131</setSpec>
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        <thesis xmlns="http://www.ndltd.org/standards/metadata/etdms/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:dc="http://purl.org/dc/elements/1.1/" xsi:schemaLocation="http://www.ndltd.org/standards/metadata/etdms/1.1/ http://www.ndltd.org/standards/metadata/etdms/1.1/etdms11.xsd http://purl.org/dc/elements/1.1/ http://www.ndltd.org/standards/metadata/etdms/1.1/etdmsdc.xsd">
          <dc:contributor>Kong, Hyunjoon</dc:contributor>
          <dc:contributor>Kong, Hyunjoon</dc:contributor>
          <dc:creator>Smith, Cartney</dc:creator>
          <dc:date>2018-08-14T21:37:14Z</dc:date>
          <dc:date>2018-08-14T21:37:14Z</dc:date>
          <dc:date>2020-08-15T09:15:30Z</dc:date>
          <dc:date>2013-07-15</dc:date>
          <dc:date>2013-08</dc:date>
          <dc:description>Micro- and nanoparticles are designed to deliver drugs and contrast agents to their target site in a controlled manner. One of the greatest obstacles in the performance of such delivery vehicles is their stability in the presence of serum. Here we investigate a method to stabilize a class of liposomes in which lipid vesicles are modified post- fabrication through surface adsorption and anchoring. We hypothesized that the sequential adsorption of functional units followed by covalent cross-linking of the liposome would provide enhanced stability in the presence of human serum. To investigate this hypothesis, liposomes composed of diyne-containing lipids were assembled and functionalized via chitosan conjugated with a hydrophobic anchor and the magnetic resonance (MR) contrast agent, gadolinium, as a model functionality. This strategy served to stabilize the thermodynamically favorable association between liposome and modified functional chitosan. Furthermore, the chitosan-coated, cross-linked liposomes proved more effective as delivery vehicles of MR contrast agents than uncross-linked liposomes due to the reduced liposome degradation and chitosan desorption. Overall, this study demonstrates a useful method to stabilize a broad class of particles used for systemic delivery of various molecular cargos.</dc:description>
          <dc:description>Submission published under a 24 month embargo labeled 'Closed Access', the embargo will last until 2015-08-01</dc:description>
          <dc:description>The student, Cartney Smith, accepted the attached license on 2013-07-10 at 00:06.</dc:description>
          <dc:description>The student, Cartney Smith, submitted this Thesis for approval on 2013-07-11 at 12:15.</dc:description>
          <dc:description>This Thesis was approved for publication on 2013-07-15 at 09:33.</dc:description>
          <dc:format>application/pdf</dc:format>
          <dc:identifier>http://hdl.handle.net/2142/100421</dc:identifier>
          <dc:rights>Copyright 2013 Cartney E. Smith</dc:rights>
          <dc:subject>Cross-Linkable Lipids</dc:subject>
          <dc:subject>Magnetic Resonance Imaging</dc:subject>
          <dc:subject>Chitosan</dc:subject>
          <dc:subject>Liposome</dc:subject>
          <dc:title>Stabilization of liposomal functional anchors by cross-linkable lipids</dc:title>
          <dc:type>text</dc:type>
          <dc:type>text</dc:type>
          <degree>
            <department>Chemical &amp; Biomolecular Engr</department>
            <discipline>Chemical Engineering</discipline>
            <grantor>University of Illinois at Urbana-Champaign</grantor>
            <level>Thesis</level>
            <name>M.S.</name>
          </degree>
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