University of Surrey

Test tubes in the lab Research in the ATI Dance Research

Synthesis and characterisation of peptide-polymer conjugate hydrogels for biomedical applications.

Mai, Cuc (2018) Synthesis and characterisation of peptide-polymer conjugate hydrogels for biomedical applications. Doctoral thesis, University of Surrey.

[img]
Preview
Text
__surrey.ac.uk_personal_HS228_tm00125_downloads_Cuc Thu Mai_Final Thesis.pdf - Version of Record
Available under License Creative Commons Attribution Non-commercial Share Alike.

Download (10MB) | Preview

Abstract

This study involved two separate projects, both of which explored the application of RAFT polymerisation for the synthesis of well-defined star polymer-peptide conjugates and developed hydrogels from synthesised star polymer conjugates. The first project aimed to develop an in situ forming hydrogel from star poly(N-(2hydroxypropyl)methacrylamide) (PHPMA) via covalent cross-linking, catalysed by Sortase A enzyme (SrtA). The use of SrtA as a cross-linking enzyme for hydrogel-based tissue engineering has been only reported previously by Broguiere et al., Arkenberg and Lin. 1,2 Both groups employed mutant enzymes with enhanced kinetics to achieve fast gelation whereas a wild type SrtA was employed in this work. Well defined star PHPMA (Ð<1.30) were successfully functionalised with SrtA-peptide substrates via a two-step synthesis consisting of an aminolysis and followed by a radical thiol-ene addition reaction. Unfortunately, cross-linking of 4-arm star PHPMA conjugations mediated by SrtA did not yield gelation which could be due to the slow kinetics of wild type SrtA. The second project focused on developing thermo-responsive hydrogels of the selfassembling peptide CFEFEFKFKK by doping the hydrogels with star (2-, 3-, and 4- arm) poly(N-isopropylacrylamide) (PNIPAM)/CFEFEFKFKK conjugates (C, cysteine; F, phenylalanine; E, glutamic acid; K, lysine). The work was based on a study by Maslovskis et al. who created the novel composite hydrogels containing FEFEFKFK peptide and linear PNIPAM-FEFEFKFK conjugates.3 Well-defined star PNIPAM (Ð<1.25) were modified via a three step synthesis consisting of an aminolysis, a vinylsulfone functionalisation, and finally Michael thiol-ene addition with CFEFEFKFK. The doping was found to introduce thermoresponsiveness to the peptide hydrogels with a lower critical solution temperature (LCST) around 36 °C. This suggested that the hydrogels a potential application in human body. The hydrogels doped with 3-arm conjugate 46 kDa, 4-arm conjugate 17 kDa, or 2-arm conjugate 4 kDa exhibited higher elasticity. This indicated that the peptides on the conjugates took part in the self-assembly with the free peptides and that the polymer chains anchored and interacted with the peptide fibres through hydrogen bonding.

Item Type: Thesis (Doctoral)
Divisions : Theses
Authors :
NameEmailORCID
Mai, Cuc
Date : 21 December 2018
Funders : University of Surrey
DOI : 10.15126/thesis.00850019
Contributors :
ContributionNameEmailORCID
http://www.loc.gov/loc.terms/relators/THSWhelligan, DanielD.Whelligan@surrey.ac.uk
Depositing User : Cuc Mai
Date Deposited : 25 Jan 2019 09:45
Last Modified : 25 Jan 2019 09:45
URI: http://epubs.surrey.ac.uk/id/eprint/850019

Actions (login required)

View Item View Item

Downloads

Downloads per month over past year


Information about this web site

© The University of Surrey, Guildford, Surrey, GU2 7XH, United Kingdom.
+44 (0)1483 300800