Design and synthesis of proteoglycan analogues for tissue repair and regeneration

This thesis is concerned with the design and synthesis of a novel, injectable proteoglycan analogue for tissue repair. This is of particular relevance to the restoration of disc height to a degraded nucleus pulposus of the intervertebral disc. The focus is on the use of sulfonate monomers as proteog...

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Main Author: Bramhill, Jane
Published: Aston University 2012
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Online Access:http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.550610
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spelling ndltd-bl.uk-oai-ethos.bl.uk-5506102017-04-20T03:25:34ZDesign and synthesis of proteoglycan analogues for tissue repair and regenerationBramhill, Jane2012This thesis is concerned with the design and synthesis of a novel, injectable proteoglycan analogue for tissue repair. This is of particular relevance to the restoration of disc height to a degraded nucleus pulposus of the intervertebral disc. The focus is on the use of sulfonate monomers as proteoglycan analogues, in particular sodium 2-acrylamido-2-methylpropane sulfonic acid and the potassium salt of 3-sulfopropyl acrylate. For most biomedical applications, synthetic hydrogels need to show dimensional stability to changes in pH, osmolarity, and temperature. This is readily achieved by neutral structures however ionic sulfonate containing hydrogels are responsive to environmental change which renders them difficult to manage in most tissue replacement applications. In this case osmotic responsiveness rather than stability is desirable. Therefore sulfonate based materials possess advantageous properties. This is a result of the sulfonate becoming an ideal surrogate for the sulfate group present within the structure of natural proteoglycans. This thesis reports polymerisation studies based on the production of a redox initiated copolymer system capable of polymerising in situ within a timescale of circa. 5-7 minutes. The rheological properties, osmotic drive, and residual monomer content of successful compositions is analysed. Properties are adapted to mimic those of the target natural tissue. The adaptation of the material for use as an injectable intra-ocular lens, with hyaluronic acid as an interpenetrate is reported. The synthesis of a radiopaque macromer to allow visibility of the repair system once in situ is investigated and discussed. The results presented in this thesis describe a suitable proteoglycan tissue analogue which is injectable, biomimetic, osmotically responsive and mechanically stable in its desired application.610.28Aston Universityhttp://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.550610http://publications.aston.ac.uk/16436/Electronic Thesis or Dissertation
collection NDLTD
sources NDLTD
topic 610.28
spellingShingle 610.28
Bramhill, Jane
Design and synthesis of proteoglycan analogues for tissue repair and regeneration
description This thesis is concerned with the design and synthesis of a novel, injectable proteoglycan analogue for tissue repair. This is of particular relevance to the restoration of disc height to a degraded nucleus pulposus of the intervertebral disc. The focus is on the use of sulfonate monomers as proteoglycan analogues, in particular sodium 2-acrylamido-2-methylpropane sulfonic acid and the potassium salt of 3-sulfopropyl acrylate. For most biomedical applications, synthetic hydrogels need to show dimensional stability to changes in pH, osmolarity, and temperature. This is readily achieved by neutral structures however ionic sulfonate containing hydrogels are responsive to environmental change which renders them difficult to manage in most tissue replacement applications. In this case osmotic responsiveness rather than stability is desirable. Therefore sulfonate based materials possess advantageous properties. This is a result of the sulfonate becoming an ideal surrogate for the sulfate group present within the structure of natural proteoglycans. This thesis reports polymerisation studies based on the production of a redox initiated copolymer system capable of polymerising in situ within a timescale of circa. 5-7 minutes. The rheological properties, osmotic drive, and residual monomer content of successful compositions is analysed. Properties are adapted to mimic those of the target natural tissue. The adaptation of the material for use as an injectable intra-ocular lens, with hyaluronic acid as an interpenetrate is reported. The synthesis of a radiopaque macromer to allow visibility of the repair system once in situ is investigated and discussed. The results presented in this thesis describe a suitable proteoglycan tissue analogue which is injectable, biomimetic, osmotically responsive and mechanically stable in its desired application.
author Bramhill, Jane
author_facet Bramhill, Jane
author_sort Bramhill, Jane
title Design and synthesis of proteoglycan analogues for tissue repair and regeneration
title_short Design and synthesis of proteoglycan analogues for tissue repair and regeneration
title_full Design and synthesis of proteoglycan analogues for tissue repair and regeneration
title_fullStr Design and synthesis of proteoglycan analogues for tissue repair and regeneration
title_full_unstemmed Design and synthesis of proteoglycan analogues for tissue repair and regeneration
title_sort design and synthesis of proteoglycan analogues for tissue repair and regeneration
publisher Aston University
publishDate 2012
url http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.550610
work_keys_str_mv AT bramhilljane designandsynthesisofproteoglycananaloguesfortissuerepairandregeneration
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