The impact of evidence lineups on fingerprint expert decisions

Forensic examiners routinely compare a crime‐relevant mark of unknown origin against a single suspect's sample, which may create an expectation that the two will match. We tested how embedding the suspect's sample among known‐innocent fillers (i.e., an evidence lineup ) affects expert decision‐making. Experienced fingerprint examiners (N = 43) compared crime‐relevant marks against either individual suspect fingerprints (i.e., the standard procedure) or arrays of fingerprints (i.e., evidence lineups), with a matching fingerprint either present or absent. Evidence lineups promoted conservative decision‐making, as evidenced by fewer correct IDs and a higher rate of inconclusive judgments. Though errors were rare, evidence lineups also occasionally revealed errors that would have otherwise gone undetected. Our findings thus support arguments that evidence lineups can expose fraud, identify flawed methodologies, and curb overconfidence. The potential benefits and challenges of implementing evidence lineups in forensic laboratories are discussed

Dual-responsive supramolecular colloidal microcapsules from cucurbit[8]uril molecular recognition in microfluidic droplets

The macrocyclic host, cucurbit[8]uril, is used to facilitate cross-linking of colloidal particles and polymers in microdroplets resulting in thermo- and photo-responsive supramolecular colloidal microcapsules. Methyl viologen-bearing colloidal particles were prepared using template polymerisation and combined with cucurbit[8]uril and an azobenzene-functionalised polymer within microfluidic droplets. The colloidal particles self-assembled at the droplet interface, whereupon polymeric cross-links formed $\textit{via}$ ternary host-guest complexation with cucurbit[8]uril. The resultant supramolecular colloidal microcapsules were uniform in size and were able to retain a macromolecular cargo. It is shown that the capsule skin porosity, and consequently the rate of release of encapsulated cargo, can be remotely controlled $\textit{via}$ either temperature or light triggers. This simple and versatile method could be extended to other polymer or colloidal derivatives for the fabrication of nano- and microcapsules with dual stimuli response for controlled release.Engineering and Physical Sciences Research Council (Grant IDs: EP/K503496/1, EP/H046593/1), CSC Cambridge Scholarshi

Prospects for terahertz imaging the human skin cancer with the help of gold-nanoparticles-based terahertz-to-infrared converter

The design is suggested, and possible operation parameters are discussed, of an instrument to inspect a skin cancer tumour in the terahertz (THz) range, transferring the image into the infrared (IR) and making it visible with the help of standard IR camera. The central element of the device is the THz-to-IR converter, a Teflon or silicon film matrix with embedded 8.5 nm diameter gold nanoparticles. The use of external THz source for irradiating the biological tissue sample is presumed. The converter's temporal characteristics enable its performance in a real-time scale. The details of design suited for the operation in transmission mode (in vitro) or on the human skin in reflection mode {in vivo) are specified.Comment: To be published in the proceedings of the FANEM2018 workshop - Minsk, 3-5 June 201

Phase evolution and electrical behaviour of samarium-substituted bismuth ferrite ceramics

Bi1-xSmxFeO3 (x = 0.15–0.18) ceramics with high density were produced using spark plasma sintering. The effects of composition, synthesis conditions and temperature on the phase evolution were studied, using XRD, TEM and dielectric spectroscopy. The coexistence of the ferroelectric R3c, antiferroelectric Pnam and paraelectric Pnma phases was revealed, with relative phase fractions affected by both calcination conditions and Sm concentration. Experiments on powdered samples calcined at different temperatures up to 950 °C suggest higher calcination temperatures promote Sm diffusion, allowing samples to reach compositional homogeneity. The structural transitions from the Pnam and R3c phases to the Pnma phase were comprehensively investigated, with phase transition temperatures clearly identified. The dielectric permittivity, electrical resistivity and breakdown strength were increased upon Sm-substitution, while ferroelectric switching was suppressed. The polarization-electric field loop became increasingly narrow with increasing Sm-content, but double hysteresis loops, which may reflect a reversible antiferroelectric to ferroelectric transformation, were not observed

Phase evolution and electrical behaviour of samarium-substituted bismuth ferrite ceramics

Bi1-xSmxFeO3 (x = 0.15–0.18) ceramics with high density were produced using spark plasma sintering. The effects of composition, synthesis conditions and temperature on the phase evolution were studied, using XRD, TEM and dielectric spectroscopy. The coexistence of the ferroelectric R3c, antiferroelectric Pnam and paraelectric Pnma phases was revealed, with relative phase fractions affected by both calcination conditions and Sm concentration. Experiments on powdered samples calcined at different temperatures up to 950 °C suggest higher calcination temperatures promote Sm diffusion, allowing samples to reach compositional homogeneity. The structural transitions from the Pnam and R3c phases to the Pnma phase were comprehensively investigated, with phase transition temperatures clearly identified. The dielectric permittivity, electrical resistivity and breakdown strength were increased upon Sm-substitution, while ferroelectric switching was suppressed. The polarization-electric field loop became increasingly narrow with increasing Sm-content, but double hysteresis loops, which may reflect a reversible antiferroelectric to ferroelectric transformation, were not observed

Comparative immunological evaluation of recombinant Salmonella Typhimurium strains expressing model antigens as live oral vaccines

BACKGROUND: Despite the development of various systems to generate live recombinant Salmonella Typhimurium vaccine strains, little work has been performed to systematically evaluate and compare their relative immunogenicity. Such information would provide invaluable guidance for the future rational design of live recombinant Salmonella oral vaccines. RESULT: To compare vaccine strains encoded with different antigen delivery and expression strategies, a series of recombinant Salmonella Typhimurium strains were constructed that expressed either the enhanced green fluorescent protein (EGFP) or a fragment of the hemagglutinin (HA) protein from the H5N1 influenza virus, as model antigens. The antigens were expressed from the chromosome, from high or low-copy plasmids, or encoded on a eukaryotic expression plasmid. Antigens were targeted for expression in either the cytoplasm or the outer membrane. Combinations of strategies were employed to evaluate the efficacy of combined delivery/expression approaches. After investigating in vitro and in vivo antigen expression, growth and infection abilities; the immunogenicity of the constructed recombinant Salmonella strains was evaluated in mice. Using the soluble model antigen EGFP, our results indicated that vaccine strains with high and stable antigen expression exhibited high B cell responses, whilst eukaryotic expression or colonization with good construct stability was critical for T cell responses. For the insoluble model antigen HA, an outer membrane expression strategy induced better B cell and T cell responses than a cytoplasmic strategy. Most notably, the combination of two different expression strategies did not increase the immune response elicited. CONCLUSION: Through systematically evaluating and comparing the immunogenicity of the constructed recombinant Salmonella strains in mice, we identified their respective advantages and deleterious or synergistic effects. Different construction strategies were optimally-required for soluble versus insoluble forms of the protein antigens. If an antigen, such as EGFP, is soluble and expressed at high levels, a low-copy plasmid-cytoplasmic expression strategy is recommended; since it provokes the highest B cell responses and also induces good T cell responses. If a T cell response is preferred, a eukaryotic expression plasmid or a chromosome-based, cytoplasmic-expression strategy is more effective. For insoluble antigens such as HA, an outer membrane expression strategy is recommended

Emergent Properties of Tumor Microenvironment in a Real-life Model of Multicell Tumor Spheroids

Multicellular tumor spheroids are an important {\it in vitro} model of the pre-vascular phase of solid tumors, for sizes well below the diagnostic limit: therefore a biophysical model of spheroids has the ability to shed light on the internal workings and organization of tumors at a critical phase of their development. To this end, we have developed a computer program that integrates the behavior of individual cells and their interactions with other cells and the surrounding environment. It is based on a quantitative description of metabolism, growth, proliferation and death of single tumor cells, and on equations that model biochemical and mechanical cell-cell and cell-environment interactions. The program reproduces existing experimental data on spheroids, and yields unique views of their microenvironment. Simulations show complex internal flows and motions of nutrients, metabolites and cells, that are otherwise unobservable with current experimental techniques, and give novel clues on tumor development and strong hints for future therapies.Comment: 20 pages, 10 figures. Accepted for publication in PLOS One. The published version contains links to a supplementary text and three video file

Distinct RNA profiles in subpopulations of extracellular vesicles: apoptotic bodies, microvesicles and exosomes

Introduction: In recent years, there has been an exponential increase in the number of studies aiming to understand the biology of exosomes, as well as other extracellular vesicles. However, classification of membrane vesicles and the appropriate protocols for their isolation are still under intense discussion and investigation. When isolating vesicles, it is crucial to use systems that are able to separate them, to avoid cross-contamination. Method: EVs released from three different kinds of cell lines: HMC-1, TF-1 and BV-2 were isolated using two centrifugation-based protocols. In protocol 1, apoptotic bodies were collected at 2,000×g, followed by filtering the supernatant through 0.8 µm pores and pelleting of microvesicles at 12,200×g. In protocol 2, apoptotic bodies and microvesicles were collected together at 16,500×g, followed by filtering of the supernatant through 0.2 µm pores and pelleting of exosomes at 120,000×g. Extracellular vesicles were analyzed by transmission electron microscopy, flow cytometry and the RNA profiles were investigated using a Bioanalyzer®. Results: RNA profiles showed that ribosomal RNA was primary detectable in apoptotic bodies and smaller RNAs without prominent ribosomal RNA peaks in exosomes. In contrast, microvesicles contained little or no RNA except for microvesicles collected from TF-1 cell cultures. The different vesicle pellets showed highly different distribution of size, shape and electron density with typical apoptotic body, microvesicle and exosome characteristics when analyzed by transmission electron microscopy. Flow cytometry revealed the presence of CD63 and CD81 in all vesicles investigated, as well as CD9 except in the TF-1-derived vesicles, as these cells do not express CD9. Conclusions: Our results demonstrate that centrifugation-based protocols are simple and fast systems to distinguish subpopulations of extracellular vesicles. Different vesicles show different RNA profiles and morphological characteristics, but they are indistinguishable using CD63-coated beads for flow cytometry analysis