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Dive into the research topics where Tom O. McDonald is active.

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Featured researches published by Tom O. McDonald.


Biomaterials Science | 2013

Enzyme responsive materials: design strategies and future developments

Mischa Zelzer; Simon J. Todd; Andrew R. Hirst; Tom O. McDonald; Rein V. Ulijn

Enzyme responsive materials (ERMs) are a class of stimuli responsive materials with broad application potential in biological settings. This review highlights current and potential future design strategies for ERMs and provides an overview of the present state of the art in the area.


Nature Chemistry | 2015

Spatially resolved multicomponent gels

Emily R. Draper; Edward G. B. Eden; Tom O. McDonald; Dave J. Adams

Multicomponent supramolecular systems could be used to prepare exciting new functional materials, but it is often challenging to control the assembly across multiple length scales. Here we report a simple approach to forming patterned, spatially resolved multicomponent supramolecular hydrogels. A multicomponent gel is first formed from two low-molecular-weight gelators and consists of two types of fibre, each formed by only one gelator. One type of fibre in this ‘self-sorted network’ is then removed selectively by a light-triggered gel-to-sol transition. We show that the remaining network has the same mechanical properties as it would have done if it initially formed alone. The selective irradiation of sections of the gel through a mask leads to the formation of patterned multicomponent networks, in which either one or two networks can be present at a particular position with a high degree of spatial control. Multicomponent supramolecular hydrogels have been prepared using a self-sorting mixture of two different gelators—one of which is photosensitive. Irradiation of the gels through a mask leads to the photosensitive network being selectively removed by a light-triggered gel-to-sol transition in a process that can be used to produce patterned gels with spatially controlled properties.


Journal of the American Chemical Society | 2013

Dynamic Nuclear Polarization NMR Spectroscopy Allows High-Throughput Characterization of Microporous Organic Polymers

Frédéric Blanc; Samantha Y. Chong; Tom O. McDonald; Dave J. Adams; Shane Pawsey; Marc A. Caporini; Andrew I. Cooper

Dynamic nuclear polarization (DNP) solid-state NMR was used to obtain natural abundance (13)C and (15)N CP MAS NMR spectra of microporous organic polymers with excellent signal-to-noise ratio, allowing for unprecedented details in the molecular structure to be determined for these complex polymer networks. Sensitivity enhancements larger than 10 were obtained with bis-nitroxide radical at 14.1 T and low temperature (∼105 K). This DNP MAS NMR approach allows efficient, high-throughput characterization of libraries of porous polymers prepared by combinatorial chemistry methods.


Journal of Materials Chemistry C | 2014

Air-stable photoconductive films formed from perylene bisimide gelators

Emily R. Draper; James J. Walsh; Tom O. McDonald; Martijn A. Zwijnenburg; Petra J. Cameron; Alexander J. Cowan; Dave J. Adams

We show that amino acid-PBIs can form one-dimensional structures at high pH and then gels at low pH. Both the dried solutions and dried gels are photoconductive. Interestingly, photoconductivity of these materials requires that the incident light has a wavelength shorter than 400 nm, in stark contrast with the absorption maxima of the PBIs. The photoconductivity correlates with the formation of the perylene radical anion, which is unusually highly stable in air for many hours.


Advanced Healthcare Materials | 2014

Antiretroviral solid drug nanoparticles with enhanced oral bioavailability: production, characterization, and in vitro-in vivo correlation.

Tom O. McDonald; Marco Giardiello; Philip Martin; Marco Siccardi; Neill J. Liptrott; Darren Smith; Phill Roberts; Paul Curley; Alessandro Schipani; Saye Khoo; James Long; Alison Jayne Foster; Steven Paul Rannard; Andrew Owen

Nanomedicine strategies have produced many commercial products. However, no orally dosed HIV nanomedicines are available clinically to patients. Although nanosuspensions of drug particles have demonstrated many benefits, experimentally achieving >25 wt% of drug relative to stabilizers is highly challenging. In this study, the emulsion-templated freeze-drying technique for nanoparticles formation is applied for the first time to optimize a nanodispersion of the leading non-nucleoside reverse transcriptase inhibitor efavirenz, using clinically acceptable polymers and surfactants. Dry monoliths containing solid drug nanoparticles with extremely high drug loading (70 wt% relative to polymer and surfactant stabilizers) are stable for several months and reconstitute in aqueous media to provide nanodispersions with z-average diameters of 300 nm. The solid drug nanoparticles exhibit reduced cytoxicity and increased in vitro transport through model gut epithelium. In vivo studies confirm bioavailability benefits with an approximately four-fold higher pharmacokinetic exposure after oral administration to rodents, and predictive modeling suggests dose reduction with the new formulation may be possible.


RSC Advances | 2013

Salt-induced hydrogels from functionalised-dipeptides

Lin Chen; Tom O. McDonald; Dave J. Adams

A range of functionalised-dipeptides are shown here to form gels on addition of Ca2+ to solutions at high pH. We show that the ability to form gels correlates with the hydrophobicity of the dipeptides, which determines whether worm-like micelles are formed at high pH. The dipeptides can be functionalised with a number of different groups including naphthalene rings as well as alkyl chains. The effect of aging on stock solutions and gels is discussed. We show that gels can also be formed when trivalent or polyvalent salts are added.


Chemical Science | 2014

Hyperbranched polydendrons: a new controlled macromolecular architecture with self-assembly in water and organic solvents

Fiona L. Hatton; Pierre Chambon; Tom O. McDonald; Andrew Owen; Steven Paul Rannard

A new macromolecular architecture (hyperbranched polydendrons) is presented. Combining aspects of linear-dendritic hybrids, controlled radical polymerisation and branched vinyl polymerisation, the materials have very high molecular weight (Mw > 1 MDa) and surface functionality. Although dispersities are broad (Đ up to 25) the structures behave with remarkable uniformity upon manipulation of solvent environment. Comparisons of conventional linear-dendritic hybrids and hyperbranched polydendrons are presented, including aspects of their synthesis. Under solvent exchange in organic media, a reversible self-assembly to form monodispersed nanoparticles (PDI as low as 0.013) is observed. Self-assembly and encapsulation is also observed during aqueous nanoprecipitation of the hyperbranched materials, with nanoparticle size (diameters from 60–140 nm) controlled through modification of precipitation conditions and the generation of the ideally branched dendrons at one end of each primary chain. The aqueous nanoparticles are highly stable and offer considerable opportunities for tailored functionality and future advanced applications.


Materials horizons | 2014

Electrochemically-triggered spatially and temporally resolved multi-component gels

Jaclyn Raeburn; Ben Alston; Jeanne Kroeger; Tom O. McDonald; Jonathan R. Howse; Petra J. Cameron; Dave J. Adams

Spatial control over gelation with low molecular weight gelators is possible using an electrochemically-driven pH triggering method. Gelation occurs at the electrode surface. We show here that composition control in multi-component low molecular weight hydrogels can also be achieved, allowing simultaneous spatial, temporal and compositional control.


Macromolecules | 2013

Shedding Light on Structure-Property Relationships for Conjugated Microporous Polymers: The Importance of Rings and Strain.

Martijn A. Zwijnenburg; Ge Cheng; Tom O. McDonald; Kim E. Jelfs; Jia-Xing Jiang; Shijie Ren; Tom Hasell; Frédéric Blanc; Andrew I. Cooper; Dave J. Adams

The photophysical properties of insoluble porous pyrene networks, which are central to their function, differ strongly from those of analogous soluble linear and branched polymers and dendrimers. This can be rationalized by the presence of strained closed rings in the networks. A combined experimental and computational approach was used to obtain atomic scale insight into the structure of amorphous conjugated microporous polymers. The optical absorption and fluorescence spectra of a series of pyrene-based materials were compared with theoretical time-dependent density functional theory predictions for model clusters. Comparison of computation and experiment sheds light on the probable structural chromophores in the various materials.


Biomacromolecules | 2015

Lipase-catalyzed dissipative self-assembly of a thixotropic Peptide bolaamphiphile hydrogel for human umbilical cord stem-cell proliferation.

Apurba K. Das; Indrajit Maity; Hamendra S. Parmar; Tom O. McDonald; Maruthi Konda

We report lipase-catalyzed inclusion of p-hydroxy benzylalcohol to peptide bolaamphiphiles. The lipase-catalyzed reactions of peptide bolaamphiphiles with p-hydroxy benzylalcohol generate dynamic combinatorial libraries (DCL) in aqueous medium that mimic the natural dissipative system. The peptide bolaamphiphile 1 (HO-WY-Suc-YW-OH) reacts with p-hydroxy benzylalcohol in the presence of lipase forming an activated diester building block. The activated diester building block self-assembles to produce nanofibrillar thixotropic hydrogel. The subsequent hydrolysis results in the dissipation of energy to form nonassembling bolaamphiphile 1 with collapsed nanofibers. The thixotropic DCL hydrogel matrix is used for 3D cell culture experiments for different periods of time, significantly supporting the cell survival and proliferation of human umbilical cord mesenchymal stem cells.

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Andrew Owen

University of Liverpool

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