Solsona, IA, Smith, RB, Livingstone, C and Davis, J (2006) Metabolic mimics: Thiol responsive drug release. JOURNAL OF COLLOID AND INTERFACE SCIENCE, 302 (2). pp. 698-701. [Journal article]
Full text not available from this repository.
A new approach to the design of selective release interfaces is assessed in which a hydrophobic component is functionalised with a receptor reactive toward reduced thiol peptides-principally glutathione. The assembly has been characterised using electrochemical techniques and its ability to form a coherent, water insoluble coating is demonstrated. The subsequent reaction with glutathione creates a supramolecular conjugate that exploits the hydrophilic nature of the amino acid chain as a route through which the protective coating can be eroded and hence the underlying substrate exposed. The efficacy of the release process has been critically assessed with a view to establishing the action and selectivity of the trigger mechanism. (c) 2006 Elsevier Inc. All rights reserved.
|Item Type:||Journal article|
|Faculties and Schools:||Faculty of Computing & Engineering|
Faculty of Computing & Engineering > School of Engineering
|Research Institutes and Groups:||Engineering Research Institute|
Engineering Research Institute > Nanotechnology & Integrated BioEngineering Centre (NIBEC)
|Deposited By:||Professor James Davis|
|Deposited On:||01 Jul 2010 09:14|
|Last Modified:||18 Aug 2011 11:19|
Repository Staff Only: item control page