ORCID Profile
0000-0003-4729-0108
Current Organisation
University of South Australia
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Publisher: Springer Science and Business Media LLC
Date: 26-05-2023
DOI: 10.1007/S43939-023-00046-6
Abstract: The conducting polymer poly(3,4-ethylenedioxythiophene) (known as PEDOT) is routinely fabricated into doped thin films for investigation of its inherent properties as well as for a range of applications. Fabrication of PEDOT is often achieved via oxidative polymerisation, where the conducting polymer is polymerised and doped (oxidised) to yield a conductive polymer thin film. The oxidiser and the polymerisation temperature are two parameters that may influence the properties and performance of the resultant PEDOT thin film. In this study, the role of temperature for the chemical polymerisation of PEDOT using the oxidiser iron tosylate is investigated from a computational and experimental viewpoint. While computations of the doping energetics suggest increasing doping with increasing temperature, x-ray photoelectron spectroscopy of fabricated PEDOT thin films indicate doping is much more complicated. With the aid of computations of the spatial distribution functions for tosylate in PEDOT, experiments indicate that two different populations of tosylate anions exist in the PEDOT matrix. Their relative populations change as a function of the polymerisation temperature. Therefore, polymerisation temperature plays a critical role in tailoring the properties of PEDOT in pursuit of being fit-for-purpose for the desired application.
Publisher: American Chemical Society (ACS)
Date: 15-03-2017
Publisher: Elsevier BV
Date: 03-2017
Publisher: Royal Society of Chemistry (RSC)
Date: 2016
DOI: 10.1039/C6CP03438A
Abstract: Plasma synthesised Si QDs are deposited in liquids to decouple confinement and passivation effects on their optical properties.
Publisher: Elsevier BV
Date: 04-2019
Publisher: Hindawi Limited
Date: 2015
DOI: 10.1155/2015/216375
Abstract: Poor aqueous solubility of some drug molecules is a major problem in drug formulation. Drug nanosuspensions emerged as one solution to delivering such hydrophobic drugs. Scaling down to nanoparticles enhances drug aqueous solubility and bioavailability by increasing drug surface area that comes into contact with biological media. Nanosuspensions that have attracted particular attention are those sterically stabilised by steric polymers such as polyethylene glycol (PEG) with a typical size range of 10–100 nm. These nanoparticles are capable of accumulating in targeted areas such as cancer tissues and infarct zones with minimal damage to healthy tissues. Nanosuspensions are often prepared by commercially available methods such as high pressure homogenization, media milling, emulsification, and melt emulsification. Solidification and surface modification methods are post-processing techniques used to add particular properties for advanced therapies. In this review, we firstly describe preparation methods for nanosuspensions. Secondly, we highlight typical characterization techniques. Finally, we describe several practical application of applications for drug delivery design and different administration routes such as parenteral, pulmonary, oral, and ocular.
Publisher: Hindawi Limited
Date: 2017
DOI: 10.1155/2013/170201
Abstract: The aim of the present research is to formulate and evaluate polymeric nanosuspensions containing three model water insoluble drugs, nifedipine (NIF), carbamazepine (CBZ), and ibuprofen (IBU) with various physicochemical properties. The nanosuspensions were prepared from hydroxypropyl methylcellulose (HPMC) and polyvinylpyrrolidone (PVP) by a cosolvent technique with polyethylene glycol (PEG-300) and water as the cosolvents. Physicochemical and morphological characteristics of the nanosuspensions (particle size, polydispersity index, and crystallinity) have been correlated with the drug release behaviour. The effects of polymer, drug ratio on the physical, morphological, and dissolution characteristics of the drugs are reported. Drug release is significantly enhanced from the nanosuspensions for ex le, the maximum NIF, IBU, and CBZ concentrations after 8-hour dissolution are increased approximately 37, 2, and 1.2 times, respectively, in comparison with the pure powdered drugs. Based on this solubilization enhancement performance, the nanosuspensions have potential for increasing the orally dosed bioavailability of NIF, IBU, and CBZ.
No related grants have been discovered for Roya Rudd.