<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-09-20T18:10:33Z</responseDate><request verb="GetRecord" identifier="oai:dspace.mit.edu:1721.1/37569" metadataPrefix="dim">https://dspace.mit.edu/server/oai/request</request><GetRecord><record><header><identifier>oai:dspace.mit.edu:1721.1/37569</identifier><datestamp>2022-01-13T07:54:33Z</datestamp><setSpec>com_1721.1_7582</setSpec><setSpec>com_1721.1_7581</setSpec><setSpec>col_1721.1_131022</setSpec></header><metadata><dim:dim xmlns:dim="http://www.dspace.org/xmlns/dspace/dim" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://www.dspace.org/xmlns/dspace/dim http://www.dspace.org/schema/dim.xsd">
   <dim:field mdschema="dc" element="contributor" qualifier="advisor" lang="en_US">Christine Ortiz.</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="author" lang="en_US">Vandiver, Jennifer M. (Jennifer McKeehan)</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="other" lang="en_US">Massachusetts Institute of Technology. Dept. of Materials Science and Engineering.</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="department">Massachusetts Institute of Technology. Department of Materials Science and Engineering</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="accessioned">2007-05-16T19:00:27Z</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="available">2007-05-16T19:00:27Z</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="copyright" lang="en_US">2006</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="issued" lang="en_US">2006</dim:field>
   <dim:field mdschema="dc" element="identifier" qualifier="uri">http://hdl.handle.net/1721.1/37569</dim:field>
   <dim:field mdschema="dc" element="identifier" qualifier="oclc" lang="en_US">76904806</dim:field>
   <dim:field mdschema="dc" element="description" lang="en_US">Thesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Materials Science and Engineering, 2006.</dim:field>
   <dim:field mdschema="dc" element="description" lang="en_US">Includes bibliographical references.</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="abstract" lang="en_US">There is a significant need for improved synthetic materials as orthopedic implants to replace human bone lost and damaged due to disease or injury. Certain ceramics, such as hydroxyapatite (HA), have the special property of being bioactive, meaning that an interfacial bond between the implant and the surrounding tissue forms, leading to good fixation. Bioactive ceramics are being investigated in a wide variety of forms for use in different bone implant applications. Three model synthetic HA based bioceramic systems were examined; phase pure, dense, polycrystalline HA; phase pure, dense, polycrystalline HA with 0.8 wt% silicon substituted into the lattice (SiHA); and phase pure, dense, nanostructured HA (nanoHA) with grain sizes less than 100 nm. SiHA has shown markedly enhanced bioactivity over non-substituted HA yet they have similar micro- and meso-scale properties and nanoHA has shown increased bioactivity over traditionally structured HA although they are chemically identical. The form of a biomaterial, the nanoscale surface chemical properties (e.g. surface functional groups, charge distribution, Hamaker constant), and morphological structure (e.g. grain size, shape, distribution, roughness) will govern its interaction with the biological environment.</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="abstract" lang="en_US">(cont.) The three main processes thought to occur upon implantation of a bioactive material are the adsorption of ions and biomolecules, formation of calcium phosphate layers, and interactions with various cells [5]. These physiochemical processes are expected to be highly dependent on nanoscale properties since this is the length scale of proteins and cell membrane adhesion molecules. The direct measurement of ultrastructure and nanoscale surface forces of model HA based biomaterials through atomic force microscopy and positionally- and chemically-specific high resolution force spectroscopy compared with in vitro and in vivo data will lead to better understanding of the impact these properties have on the physiochemical processes occurring at the biomaterial-biological interfaces influencing bioactivity. Although numerous studies of HA based biomaterials have been reported, there has been little clarification of the molecular mechanisms influencing bioactivity, partly due to lack of rigorous analytical tools for characterizing nanoscale physical and chemical surface properties. Quantifying all possible contributions to bioactivity is critical to the optimization, development, and design of new HA based biomaterials.</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="statementofresponsibility" lang="en_US">by Jennifer M. Vandiver.</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="degree" lang="en_US">Ph.D.</dim:field>
   <dim:field mdschema="dc" element="format" qualifier="extent" lang="en_US">150 leaves</dim:field>
   <dim:field mdschema="dc" element="language" qualifier="iso" lang="en_US">eng</dim:field>
   <dim:field mdschema="dc" element="publisher" lang="en_US">Massachusetts Institute of Technology</dim:field>
   <dim:field mdschema="dc" element="rights" lang="en_US">M.I.T. theses are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission. See provided URL for inquiries about permission.</dim:field>
   <dim:field mdschema="dc" element="rights" qualifier="uri">http://dspace.mit.edu/handle/1721.1/7582</dim:field>
   <dim:field mdschema="dc" element="subject" lang="en_US">Materials Science and Engineering.</dim:field>
   <dim:field mdschema="dc" element="title" lang="en_US">Nanoscale influences on bioactivity : ultrastructure and nanomechanics of model bioactive hydroxyapatite based biomaterials</dim:field>
   <dim:field mdschema="dc" element="type" lang="en_US">Thesis</dim:field>
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   	&lt;Title>Nanoscale influences on bioactivity : ultrastructure and nanomechanics of model bioactive hydroxyapatite based biomaterials&lt;/Title>
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   	&lt;PublicationDate>2006&lt;/PublicationDate>
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        	&lt;DisplayName>Vandiver, Jennifer M. (Jennifer McKeehan)&lt;/DisplayName>
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            &lt;DisplayName>Massachusetts Institute of Technology&lt;/DisplayName>
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    &lt;Keyword>Materials Science and Engineering.&lt;/Keyword>
   	&lt;Abstract>There is a significant need for improved synthetic materials as orthopedic implants to replace human bone lost and damaged due to disease or injury. Certain ceramics, such as hydroxyapatite (HA), have the special property of being bioactive, meaning that an interfacial bond between the implant and the surrounding tissue forms, leading to good fixation. Bioactive ceramics are being investigated in a wide variety of forms for use in different bone implant applications. Three model synthetic HA based bioceramic systems were examined; phase pure, dense, polycrystalline HA; phase pure, dense, polycrystalline HA with 0.8 wt% silicon substituted into the lattice (SiHA); and phase pure, dense, nanostructured HA (nanoHA) with grain sizes less than 100 nm. SiHA has shown markedly enhanced bioactivity over non-substituted HA yet they have similar micro- and meso-scale properties and nanoHA has shown increased bioactivity over traditionally structured HA although they are chemically identical. The form of a biomaterial, the nanoscale surface chemical properties (e.g. surface functional groups, charge distribution, Hamaker constant), and morphological structure (e.g. grain size, shape, distribution, roughness) will govern its interaction with the biological environment.&lt;/Abstract>
   	&lt;Abstract>(cont.) The three main processes thought to occur upon implantation of a bioactive material are the adsorption of ions and biomolecules, formation of calcium phosphate layers, and interactions with various cells [5]. These physiochemical processes are expected to be highly dependent on nanoscale properties since this is the length scale of proteins and cell membrane adhesion molecules. The direct measurement of ultrastructure and nanoscale surface forces of model HA based biomaterials through atomic force microscopy and positionally- and chemically-specific high resolution force spectroscopy compared with in vitro and in vivo data will lead to better understanding of the impact these properties have on the physiochemical processes occurring at the biomaterial-biological interfaces influencing bioactivity. Although numerous studies of HA based biomaterials have been reported, there has been little clarification of the molecular mechanisms influencing bioactivity, partly due to lack of rigorous analytical tools for characterizing nanoscale physical and chemical surface properties. Quantifying all possible contributions to bioactivity is critical to the optimization, development, and design of new HA based biomaterials.&lt;/Abstract>
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