Use this URL to cite or link to this record in EThOS: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.765813
Title: Methacrylate based nanogels as drug delivery system and Pickering-Ramsden emulsion stabiliser
Author: Chianello, Giorgio
ISNI:       0000 0004 7652 2673
Awarding Body: Queen Mary University of London
Current Institution: Queen Mary, University of London
Date of Award: 2016
Availability of Full Text:
Access from EThOS:
Access from Institution:
Abstract:
A novel methacrylate based nanogel system has been designed and developed for drug delivery applications. Methacrylates are optimal tuneable materials in terms of polarity, with combination of hydrophobic and hydrophilic moieties. Synthesis of these nanogels (NGs) was achieved via high dilution radical polymerisation using 2-(tert-butylamino)ethyl methacrylate (tBAEMA) as functional monomer, methacrylic acid (MAA) or ethylene glycol methyl ether methacrylate (EGMMA) as co-monomer and N,N'-methylenebis(acrylamide) (MBA) as cross-linker. Fabricated nanoparticles (NPs) were shown to possess water solubility higher than 2 mg/mL and diameter ranging from 5 to 20 nm (depending on nanogels' composition) as confirmed by either dynamic light scattering (DLS) and transmission electron microscopy (TEM). Moreover, nanogels produced have shown the ability to be employed as Pickering-Ramsden emulsion stabiliser. Their reduced size together with their emulsion capabilities make these nanoparticles a promising system for drug delivery, in particular taking into account skin as administration route. The size is in fact small enough to favour their penetration through the stratum corneum. Furthermore, in the view of their ability to form emulsions, nanogels could be used both as drug carrier and emulsifier in a final pharmaceutical formulation. NGs proved to be able to incorporate both small molecule such as fenoprofen (an anti-inflammatory non-steroidal drug) and big macromolecule such as siRNA. Cytotoxicity and cell metabolism were also evaluated by transfecting normal human dermal fibroblasts (NHDF), keratinocytes (HaCaT) and HeLa cells with nanogels. Data showed that nanoparticles did not affect viability, cells' morphology and adenosine triphosphate (ATP) levels up to high concentration of 100 μg/mL. In addition, preliminary studies indicated the ability of the nanogels to internalise and release their payload inside cells. In conclusion, the results confirmed that this novel system possesses all the desired characteristics to be used as a promising platform for drug delivery.
Supervisor: Not available Sponsor: European Commission
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.765813  DOI: Not available
Keywords: Biological and Chemical Sciences ; Nanogels ; Drug delivery
Share: