Massachusetts Institute of Technology
Nanoscale influences on bioactivity : ultrastructure and nanomechanics of model bioactive hydroxyapatite based biomaterials
Abstract
dc:description.abstractThere 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.
Degree
thesis:*- Department dc:contributor.department
- Massachusetts Institute of Technology. Dept. of Materials Science and Engineering.
- Grantor dc:publisher
- Massachusetts Institute of Technology
- Year dc:date.issued
- 2006
Author and committee
dc:creator, dc:contributor.*- Author dc:creator
-
- Vandiver, Jennifer M. (Jennifer McKeehan)
- Advisor dc:contributor.advisor
-
- Christine Ortiz.
Subjects
dc:subject × 1Rights
dc:rights- Statement dc:rights
-
- 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.
- Licence dc:rights.uri
- Language dc:language.iso
- eng
Identifiers
dc:identifier.*- Handle dc:identifier.uri
- http://hdl.handle.net/1721.1/37569
- OAI identifier oai:identifier
- oai:dspace.mit.edu:1721.1/37569