Tack energy and switchable adhesion of liquid crystal elastomers

The mechanical properties of liquid crystal elastomers (LCEs) make them suitable candidates for pressure-sensitive adhesives (PSAs). Using the nematic dumbbell constitutive model, and the block model of PSAs, we study their tack energy and the debonding process as could be measured experimentally in the probe-tack test. To investigate their performance as switchable PSAs we compare the tack energy for the director aligned parallel, and perpendicular to the substrate normal, and for the isotropic state. We find that the tack energy is larger in the parallel alignment than the isotropic case by over a factor of two. The tack energy for the perpendicular alignment can be 50% less than the isotropic case. We propose a mechanism for reversibly switchable adhesion based on the reversibility of the isotropic to nematic transition. Finally we consider the influence of several material parameters that could be used to tune the stress-strain response

Manipulating the monolayer : responsive and reversible control of colloidal inorganic nanoparticle properties

Funding: EPSRC EP/K016342/1; Leverhulme Trust: RPG-2015-042For a wide range of nanomaterials, surface-bound molecules play a central role in defining properties, and are key to integration with other components – be they molecules, surfaces, or other nanoparticles. Predictable and general methods for manipulating the surface monolayer are therefore crucial to exploiting this new region of chemical space. This review highlights limitations of the few established methods for controlling nanoparticle-bound molecular functionality, then focuses on emerging new strategies. In particular, approaches that can achieve stimuli-responsive and reversible modification of surface-bound molecules in colloidal solution are examined, with an emphasis on using these methods to control nanoparticle properties such as solvent compatibility, catalytic activity and cytotoxicity. Finally, the outstanding challenges and future potential for precisely controlled nanoparticle bound monolayers are discussed.Publisher PDFPeer reviewe

A Racist Attack Managing Complex Relationships with Traumatised Service Users – a Psychodynamic Approach

Notions of whiteness, white supremacy and racial hatred such as the recent multiple racist murders by a white supremacist in New Zealand are at the forefront of public consciousness. How does whiteness and racism play out in a clinical and social welfare context? This article illustrates the impact of trauma on a vulnerable young white woman who although was not the direct target of a racist assault was left traumatized by witnessing it. It discusses how initially she sought refuge in a racist solution synonymous with a psychic retreat to her own detriment. Working with such complex, unconscious and bewildering dynamics are extremely challenging for clinicians. It describes the impact of these dynamics on a clinician of colour who attempted to work with this young woman in a child and adolescent mental health service after the family were referred as a consequence of her assaulting her child shortly after witnessing the racist attack. The unconscious responses to trauma and challenges for clinicians and clinician of colour in particular when working with racism in the consulting room are also discussed

Mixed accents: Scottish children with English parents

We discuss accent mixture and the creation of idiosyncratic phonological systems in acquisition, with a focus on Scottish English. Such mixing is in addition to the relatively stable sociolinguistic systems of variation expected within a speech community, and arises when parents have radically different accents from each other or from the child's peers or other adult models. In terms of traditional geographic dialectology, there are a number of isoglosses around the Scotland/England border, but modern social mobility means that in some Scottish cities there are large numbers of families with at least one non-Scottish adult accent acting as a model for acquisition, which may feed into phonological change. Of particular interest is the influence of Southern British English accents. We exemplify the issues with two short case studies. The first concerns a child with mixed Scottish/English input in the home. His speech patterns do indeed indicate the acquisition of a mixed system. The second focuses on inter-sibling variation, looking at two sibling pairs who exemplify a different mix of accent features from each other. We examine two main diagnostics: monophthongal vs. diphthongal productions of the vowels in FACE and GOAT; and rhoticity. We also describe a parental demographic and accent attitude questionnaire as part of Case Study 2. The results support the need for speaker-by-speaker study of how incompatibility between two target systems is handled. We conclude that descriptions of mixed accents should be more common in the literature and approached on a feature-by-feature basis to help develop models of accent interference.caslpub3959pu

Identification of the Rheumatoid Arthritis Shared Epitope Binding Site on Calreticulin

Background: The rheumatoid arthritis (RA) shared epitope (SE), a major risk factor for severe disease, is a five amino acid motif in the third allelic hypervariable region of the HLA-DRb chain. The molecular mechanisms by which the SE affects susceptibility to – and severity of- RA are unknown. We have recently demonstrated that the SE acts as a ligand that interacts with cell surface calreticulin (CRT) and activates innate immune signaling. In order to better understand the molecular basis of SE-RA association, here we have undertaken to map the SE binding site on CRT. Principal Findings: Surface plasmon resonance (SPR) experiments with domain deletion mutants suggested that the SE binding site is located in the P-domain of CRT. The role of this domain as a SE-binding region was further confirmed by a sulfosuccinimidyl-2-[6-(biotinamido)-2-(p-azido-benzamido) hexanoamido] ethyl-1,3-dithiopropionate (sulfo-SBED) photoactive cross-linking method. In silico analysis of docking interactions between a conformationally intact SE ligand and the CRT P-domain predicted the region within amino acid residues 217–224 as a potential SE binding site. Site-directed mutagenesis demonstrated involvement of residues Glu 217 and Glu 223- and to a lesser extent residue Asp 220- in cell-free SPR-based binding and signal transduction assays. Significance: We have characterized here the molecular basis of a novel ligand-receptor interaction between the SE and CRT. The interaction represents a structurally and functionally well-defined example of cross talk between the adaptive an

A randomised controlled trial of a digital intervention (Renewed) to support symptom management, wellbeing and quality of life in cancer survivors

Background: Many cancer survivors following primary treatment have prolonged poor quality of life.Aim: To determine the effectiveness of a bespoke digital intervention to support cancer survivors.Design: Pragmatic parallel open randomised trial.Setting: UK general practices.Methods: People having finished primary treatment (&lt;= 10 years previously) for colo-rectal, breast or prostate cancers, with European-Organization-for-Research-and-Treatment-of-Cancer QLQ-C30 score &lt;85, were randomised by online software to: 1) detailed ‘generic’ digital NHS support (‘LiveWell’;n=906), 2) a bespoke complex digital intervention (‘Renewed’;n=903) addressing symptom management, physical activity, diet, weight loss, distress, or 3) ‘Renewed-with-support’ (n=903): ‘Renewed’ with additional brief email and telephone support. Results: Mixed linear regression provided estimates of the differences between each intervention group and generic advice: at 6 months (primary time point: n’s respectively 806;749;705) all groups improved, with no significant between-group differences for EORTC QLQ-C30, but global health improved more in both intervention groups. By 12 months there were: small improvements in EORTC QLQ-C30 for Renewed-with-support (versus generic advice: 1.42, 95% CIs 0.33-2.51); both groups improved global health (12 months: renewed: 3.06, 1.39-4.74; renewed-with-support: 2.78, 1.08-4.48), dyspnoea, constipation, and enablement, and lower NHS costs (generic advice £265: in comparison respectively £141 (153-128) and £77 (90-65) lower); and for Renewed-with-support improvement in several other symptom subscales. No harms were identified.Conclusion: Cancer survivors quality of life improved with detailed generic online support. Robustly developed bespoke digital support provides limited additional short term benefit, but additional longer term improvement in global healthenablement and symptom management, with substantially lower NHS costs.<br/