Multiplexed 'Touch and Tell' Optical Molecular Sensing and Imaging
Lead Research Organisation:
University of Edinburgh
Department Name: Sch of Chemistry
Abstract
This project is all about multi-disciplinary collaboration - and capitalisation in a clinical setting of the many new vistas and opportunities that will arise. As such this research programme brings together a group of world class scientists (physicists, chemists, engineers and computer experts) and clinicians to design, make and test a cutting-edge bedside technology platform which will help doctors in the intensive care unit (ICU) make rapid and accurate diagnoses that would inform therapy and ensure patients get the right treatment, quickly. While we are developing our technology platform with a focus on ICU, it will also be applicable to a wide range of other healthcare situations.
ICU patients suffer high death and disability rates and are responsible for a disproportionate financial burden on the health service. Potentially fatal lung complications are a common problem in ventilated ICU patients and doctors caring for these patients in the ICU face many challenges, often needing to make snap decisions without the information necessary to properly inform those decisions. The technology platform developed in this programme will provide doctors with important information on the state of ICU patients and whether they have infections, inflammation or scarring in their lungs. Currently there are no methods to do this accurately. This information will aid them in making decisions about treatment. A new approach to rapidly diagnose lung complications in ICU would enable doctors to target the correct drugs to the appropriate patients and to withdraw drugs with confidence, with resultant improvement in patient outcomes and major cost efficiencies - thus revolutionising ICU care.
Using advanced fibre optic technology and micro-electronics and new sensor arrays our ground-breaking solution is to create a novel fibre-based probe that can readily be passed into the gas exchanging areas of the lung and blood vessels of ICU patients. The probe will house a variety of special optical fibres, some of which allow clinicians to "view" inside the lung while others will be modified with sensors that can measure important parameters such as oxygen concentration and acidity in both blood and lung. In addition the fibre will deliver tiny amounts (microdoses) of 'smart reagents' that fluorescently detect specific bacteria and other agents that can damage the lung. When integrated together these signals will provide highly specific information about the degree or type of lung damage and the potential causative 'bug' if an infection is suspected. Because of the large amount of information generated and in order to make it easily interpreted by doctors, computing experts will convert these signals into easy-to-understand disease readouts for our clinicians.
Work on the different elements needed to create this technology platform will be undertaken by groups of chemists, physicists, engineers, computer scientists and biologists working at Bath, Heriot Watt and Edinburgh universities. Crucially, this programme will bring these scientific disciplines together in a "hub" where they will work side-by-side, promoting integration of purpose and to ensure that advances are rapidly translated into the clinical setting. This interdisciplinary hub will also provide a fertile training base for new PhD students who will learn the cross-disciplinary skills that will equip them to meet the challenges of translating the current 'revolution' in physical sciences into benefit for UK healthcare.
In summary this project will generate; 1) a new cohort of scientists trained in physical and biological science that have a full appreciation of clinical translational and commercialisation pathways and who are equipped to meet the challenges of converting advances in basic science into healthcare benefit and; 2) a cutting-edge bedside technology platform which will help doctors in the ICU make rapid and accurate diagnoses.
ICU patients suffer high death and disability rates and are responsible for a disproportionate financial burden on the health service. Potentially fatal lung complications are a common problem in ventilated ICU patients and doctors caring for these patients in the ICU face many challenges, often needing to make snap decisions without the information necessary to properly inform those decisions. The technology platform developed in this programme will provide doctors with important information on the state of ICU patients and whether they have infections, inflammation or scarring in their lungs. Currently there are no methods to do this accurately. This information will aid them in making decisions about treatment. A new approach to rapidly diagnose lung complications in ICU would enable doctors to target the correct drugs to the appropriate patients and to withdraw drugs with confidence, with resultant improvement in patient outcomes and major cost efficiencies - thus revolutionising ICU care.
Using advanced fibre optic technology and micro-electronics and new sensor arrays our ground-breaking solution is to create a novel fibre-based probe that can readily be passed into the gas exchanging areas of the lung and blood vessels of ICU patients. The probe will house a variety of special optical fibres, some of which allow clinicians to "view" inside the lung while others will be modified with sensors that can measure important parameters such as oxygen concentration and acidity in both blood and lung. In addition the fibre will deliver tiny amounts (microdoses) of 'smart reagents' that fluorescently detect specific bacteria and other agents that can damage the lung. When integrated together these signals will provide highly specific information about the degree or type of lung damage and the potential causative 'bug' if an infection is suspected. Because of the large amount of information generated and in order to make it easily interpreted by doctors, computing experts will convert these signals into easy-to-understand disease readouts for our clinicians.
Work on the different elements needed to create this technology platform will be undertaken by groups of chemists, physicists, engineers, computer scientists and biologists working at Bath, Heriot Watt and Edinburgh universities. Crucially, this programme will bring these scientific disciplines together in a "hub" where they will work side-by-side, promoting integration of purpose and to ensure that advances are rapidly translated into the clinical setting. This interdisciplinary hub will also provide a fertile training base for new PhD students who will learn the cross-disciplinary skills that will equip them to meet the challenges of translating the current 'revolution' in physical sciences into benefit for UK healthcare.
In summary this project will generate; 1) a new cohort of scientists trained in physical and biological science that have a full appreciation of clinical translational and commercialisation pathways and who are equipped to meet the challenges of converting advances in basic science into healthcare benefit and; 2) a cutting-edge bedside technology platform which will help doctors in the ICU make rapid and accurate diagnoses.
Planned Impact
Our proposed research programme will generate numerous avenues for the realisation of impact:
Patients: FOSIP will provide a unique opportunity for clinicians to rapidly monitor key physiological and pathological events simultaneously in the lungs and blood of critically ill patients in 'real time' at the bedside without the need for cumbersome equipment or ionizing radiation. This will permit rapid 'point-of-care diagnosis and informed decision-making in intensive care units. It will also enable patient stratification for 'personalised' new/expensive drug therapy thereby significantly reducing morbidity and mortality. FOSIP would also be readily applicable to other diseased organs accessible to fibrescopes, particularly the genitourinary tract and the upper and lower gastrointestinal tract.
NHS: Although patient numbers in ICUs are comparatively small, the economic burden is disproportionately huge. Rapid and incisive bedside diagnosis, particularly of specific infections or inflammation/scarring processes would lead to stratification of patient care and tailored prescribing patterns, including the use/non-use of expensive and potentially toxic anti-bacterials. Ultimately this would translate into reduced ventilator dependency and reduced mortality and morbidity with a proportionate economic benefit.
UK PLC: UK Healthcare must reap the dividend of the current 'revolution' in physical sciences. This research programme will deliver new leading-edge multi and cross-disciplinary research in exciting and highly translatable areas of optics, imaging, data analysis and chemistry. Our proposed programme is driven by a clear "healthcare pull" from ICU (with application to diseases in other organs); it fits squarely with EPSRC goals in the Healthcare and Life Sciences sector. Enabling activities through our IRC will create a new generation of scientists, engineers and technologists with a translational agenda and mind-set for the benefit of the UK economy.
Training: A central part of our agenda is to break down traditional 'barriers' between physical and biomedical sciences. The PDRA's will benefit immensely from the interdisciplinary, translational thrust of the programme and the cross-fertilisation that will derive from the 'hub' in work package 6. Moreover, through our PhD students specifically engaged in cross-disciplinary projects we will create a new cadre of scientist who are multi-skilled and equipped to meet the challenges of applying new technologies to healthcare provision in the new era. They will gain a wide variety of both "hard and soft" skills that will be readily applied in a variety of employment sectors.
Industry: All the applicants have major interactions with industry, and most have direct personal experience of spin-off/spin-out companies. As the programme progresses new commercial opportunities will undoubtedly arise in fibre technology, engineering, novel chemical probes, image analysis and computing. When the integrative capacity of the programme is realised and FOSIP is applied to human disease and its models, commercialization prospects in the global healthcare arena will be significant.
General: Our multidisciplinary programme will provide many opportunities for involvement in public engagement and dissemination. Research fellows will participate at the International Science Festivals and become involved in a variety of out-reach activities such as the 'Researchers-in-Residence Programme' which places postgraduate students in local secondary schools allowing the public to benefit, as well as engaging the next generation of scientists.
Patients: FOSIP will provide a unique opportunity for clinicians to rapidly monitor key physiological and pathological events simultaneously in the lungs and blood of critically ill patients in 'real time' at the bedside without the need for cumbersome equipment or ionizing radiation. This will permit rapid 'point-of-care diagnosis and informed decision-making in intensive care units. It will also enable patient stratification for 'personalised' new/expensive drug therapy thereby significantly reducing morbidity and mortality. FOSIP would also be readily applicable to other diseased organs accessible to fibrescopes, particularly the genitourinary tract and the upper and lower gastrointestinal tract.
NHS: Although patient numbers in ICUs are comparatively small, the economic burden is disproportionately huge. Rapid and incisive bedside diagnosis, particularly of specific infections or inflammation/scarring processes would lead to stratification of patient care and tailored prescribing patterns, including the use/non-use of expensive and potentially toxic anti-bacterials. Ultimately this would translate into reduced ventilator dependency and reduced mortality and morbidity with a proportionate economic benefit.
UK PLC: UK Healthcare must reap the dividend of the current 'revolution' in physical sciences. This research programme will deliver new leading-edge multi and cross-disciplinary research in exciting and highly translatable areas of optics, imaging, data analysis and chemistry. Our proposed programme is driven by a clear "healthcare pull" from ICU (with application to diseases in other organs); it fits squarely with EPSRC goals in the Healthcare and Life Sciences sector. Enabling activities through our IRC will create a new generation of scientists, engineers and technologists with a translational agenda and mind-set for the benefit of the UK economy.
Training: A central part of our agenda is to break down traditional 'barriers' between physical and biomedical sciences. The PDRA's will benefit immensely from the interdisciplinary, translational thrust of the programme and the cross-fertilisation that will derive from the 'hub' in work package 6. Moreover, through our PhD students specifically engaged in cross-disciplinary projects we will create a new cadre of scientist who are multi-skilled and equipped to meet the challenges of applying new technologies to healthcare provision in the new era. They will gain a wide variety of both "hard and soft" skills that will be readily applied in a variety of employment sectors.
Industry: All the applicants have major interactions with industry, and most have direct personal experience of spin-off/spin-out companies. As the programme progresses new commercial opportunities will undoubtedly arise in fibre technology, engineering, novel chemical probes, image analysis and computing. When the integrative capacity of the programme is realised and FOSIP is applied to human disease and its models, commercialization prospects in the global healthcare arena will be significant.
General: Our multidisciplinary programme will provide many opportunities for involvement in public engagement and dissemination. Research fellows will participate at the International Science Festivals and become involved in a variety of out-reach activities such as the 'Researchers-in-Residence Programme' which places postgraduate students in local secondary schools allowing the public to benefit, as well as engaging the next generation of scientists.
Organisations
- University of Edinburgh, United Kingdom (Lead Research Organisation)
- University of Bath, Bath (Collaboration)
- Heriot-Watt University, United Kingdom (Collaboration)
- Carestream Health Inc, United States (Project Partner)
- Edinburgh Biosciences Limited, United Kingdom (Project Partner)
- ST Microelectronics Limited (UK), United Kingdom (Project Partner)
- UK Astronomy Technology Centre, United Kingdom (Project Partner)
Publications

Wood HAC
(2017)
Quantitative characterization of endoscopic imaging fibers.
in Optics express

Wood HAC
(2018)
High-resolution air-clad imaging fibers.
in Optics letters

Yerolatsitis S
(2019)
Ultra-low background Raman sensing using a negative-curvature fibre and no distal optics.
in Journal of biophotonics

Yerolatsitis S
(2020)
Birefringent Anti-Resonant Hollow-Core Fiber
in Journal of Lightwave Technology

Zhang S
(2021)
Solid-Phase Synthesis of Fluorescent Probes for Plasma Membrane Labelling.
in Molecules (Basel, Switzerland)

Zhao C
(2016)
Searching for the Optimal Fluorophore to Label Antimicrobial Peptides.
in ACS combinatorial science
Title | PROTEUS ART EXHIBITION |
Description | Ron O'Donnell - Photographs |
Type Of Art | Artwork |
Year Produced | 2015 |
Impact | • Proteus Art Exhibition - Introducing Proteus science through contemporary art. (Edinburgh/China) March 2015/ June 2015 Audience: Wider members of the public, academics, patients Engagement methods: Working with a contemporary artist to create portraits of our researchers which allowed dialogue about the specifics of their science research. Impact: High level of interest - changed hearts and minds in terms of who our scientists are and what the science can achieve- reflected in a questionnaire- high levels of satisfaction and desire to learn more. Event in China as sparked interest in examining how science communication can grow and become established in the Chinese culture - work still on going. |
Title | • Proteus Science Ceilidh: Smart Probes Light Up Science Ceilidh |
Description | • Proteus Science Ceilidh: Smart Probes Light Up Science Ceilidh (Edinburgh) December 2015 Audience: Wider members of the public (adult audience) Engagement methods: Dance and Music (using the arts to explain Smart Probe science) Impact: Increased public's appetite for more creative science engagement - learning through fun and accessible methods. More hits on Proteus website/Social Media post event. Feedback suggested participants would attend a similar event. |
Type Of Art | Performance (Music, Dance, Drama, etc) |
Year Produced | 2015 |
Impact | • Proteus Science Ceilidh: Smart Probes Light Up Science Ceilidh (Edinburgh) December 2015 Audience: Wider members of the public (adult audience) Engagement methods: Dance and Music (using the arts to explain Smart Probe science) Impact: Increased public's appetite for more creative science engagement - learning through fun and accessible methods. More hits on Proteus website/Social Media post event. Feedback suggested participants would attend a similar event. |
Description | New world-leading fibres for imaging and sensing - including disposable imaging fibre, Raman fibre (background free), flexible imaging fibres. New world-leading CMSO SPAD detectors and their integration into systems that are entering clinic to allow a whole new dimension in optical medical imaging. New world-leading chemical probes and their in-human use - for cancer margins and fibrosis and bacteria. Major collaborations with industry to develop and push the technology in the area of cancer imaging/detection. Highly trained staff - that are much in demand. Two PDRA's have won fellowships/gained fully independent academic positions. |
Exploitation Route | Many elements have gone into clinic. Many elements are being used together and combined for clinical studies - with Phase-II studies on going. 12 Patents filed and we are looking to explore these in spinout ventures and in collaboration with various companies. |
Sectors | Healthcare |
URL | http://www.proteus.ac.uk |
Description | We have been hugely active in the area of public engagement and advocacy. Please see the listed details for more depth - but in brief we have put in place a permeant exhibit ion the Glasgow Science centre, we worked with a local photography to put exhibits in local shopping centres, we have worked with the London Science Museum, we have (twice) been on the UK stand at AAAS and we have worked with a patient choir to help improve our standing of their needs and wants (rather than imposition). Teaching aids we have helped develop are being used in High Schools in Scotland. Clinical Translation: We have developed a regulatory pathway that has allowed us to carry out first in-human studies (both device and probes). Proteus has, to date, delivered into the clinic a device (VersiColour) and three imaging reagents (Bac- One, Bac-Two and Fib-One) Patients: Proteus is providing unique opportunities for clinicians to rapidly monitor events deep in the lungs of critically ill patients in 'real time' at the bedside. This will permit rapid point-of-care diagnosis and informed decision-making in intensive care units and patient stratification. We are actively involving patients in our programme to increase impact and involve patients in our research ideas and plans. NHS: The economic burden of ICU patients is huge. Rapid and incisive bedside diagnosis, particularly of specific infections would lead to stratification of patient care and tailored prescribing patterns, including the use/non-use of expensive and potentially toxic anti-bacterials. Ultimately this would translate into reduced antibiotic use, reduced ventilator dependency and reduced mortality and morbidity with a proportionate economic benefit. The aim of the Proteus platform is to provide in vivo in situ molecular pathological characterisation of diseased tissues, with an initial focus on the injured and inflamed lung of mechanically ventilated critically ill patients. Critical care is the highest cost area of the modern hospitals with costs of >£3000 per day. In the USA, a staggering 1% of GDP is spent annually in the Intensive Care Unit (ICU) environment. Key goals include delineating infection from sterile inflammation in the lung. Currently no bedside methods exist that are able to delineate pathological processes deep in the human lung in vivo in situ. Hence, the platform offers a disruptive paradigm changing technology. |
First Year Of Impact | 2015 |
Sector | Education,Healthcare,Government, Democracy and Justice,Pharmaceuticals and Medical Biotechnology |
Impact Types | Cultural,Societal,Policy & public services |
Description | American Association for the Advancement of Science Meeting 2018 - Invited to the meeting as a Flagship EPSRC project representing UK science on the main exhibition stage as well as the International Reception. Engagement Methods -Proteus Digital Lung Game - Designed by Proteus team in collaboration with Glasgow Science Centre. Impact: Raised awareness of EPSRC Proteus with UKRI CEO and wider RIUK team. Networked with senior academics, policy makers and US industries. Received media coverage for the project from the BBC. |
Geographic Reach | Local/Municipal/Regional |
Policy Influence Type | Influenced training of practitioners or researchers |
Impact | Impact: Raised awareness of EPSRC Proteus with UKRI CEO and wider RIUK team. Engaged with senior academics, policy makers and US industries and wider public. Received media coverage for the project from the BBC. |
URL | http://www.bbc.co.uk/news/science-environment-43076783 |
Description | Awarded The Royal Academy of Engineering Ingenious Grant - (Audience: Scottish Schools (students and teachers) and Research Centre for Teachers continuous Development. Engagement methods: Education tools that describe Proteus biomedical research. Impact: Embed Proteus Circuits! tools into Scottish curriculum to teach 12/13 year old students about bioengineering and its applications around health and wellbeing. |
Geographic Reach | Local/Municipal/Regional |
Policy Influence Type | Influenced training of practitioners or researchers |
Impact | Inspire Students to consider STEM subjects and careers. Teach students about biomedical engineering in new engaging ways. bridge gaps between high school teachers and university research. Empower teachers to teach students about cutting edge research. Provide training and skills for researchers to engage widely and with confidence and expertise. |
URL | https://proteus.ac.uk/public-engagement/ingenious/our-project-circuits/ |
Description | House of Lords Science and Technology Committee |
Geographic Reach | National |
Policy Influence Type | Gave evidence to a government review |
URL | http://www.parliamentlive.tv/Event/Index/3a9d05fd-a47f-411f-8173-5d99a1d53327 |
Description | Proteus Showcase Event (Edinburgh) October 2014 - Note none of the options allowed below fit ! An open text box would be more useful ! |
Geographic Reach | National |
Policy Influence Type | Influenced training of practitioners or researchers |
Description | The Royal Society of Edinburgh AMR (Antimicrobial Resistance) October 2014 |
Geographic Reach | National |
Policy Influence Type | Participation in a national consultation |
Impact | -- |
Description | • ICU Engagement Event February 2016 Audience: NHS ICU staff Engagement methods: Hands on demonstrations, posters, written materials Impact: Raise awareness of Proteus Science to end users - strengthened engagement, created possibilities for ongoing dialogue. • ICU Research Nurses Event February 2018 Audience: NHS ICU Research nurses Engagement methods: Hands on demonstrations, posters, written materials Impact: Raise awareness of Proteus Science to research nurses who may use Proteus technology. Introduced nurses to members of the Proteus team, strengthen engagement and interdisciplinary work. |
Geographic Reach | Local/Municipal/Regional |
Policy Influence Type | Influenced training of practitioners or researchers |
Impact | -- |
Description | • Public and Patient Involvement - Funding Award Received from ACCORD February 2018 Audience: Respiratory Patients (Breathtakers and Breatheasy) Engagement methods: Dialogue sessions with patients, creative story telling workshops Impact: Creation of Proteus research pod at Glasgow science. Work ongoing to develop pilot studies for patient engagement using the Proteus interdisciplinarity model as an engagement framework. |
Geographic Reach | Local/Municipal/Regional |
Policy Influence Type | Influenced training of practitioners or researchers |
Impact | -- |
Description | • Science and the Parliament (Edinburgh) November 2016 Audience: MPs, Senior Academics, Industry, Healthcare Professionals Engagement methods: Hands on demonstrations, videos, written materials Impact: Raise awareness of Proteus Science, forged a link with Scottish Chief Medical Officer - arranged meeting to visit Proteus labs post event. |
Geographic Reach | National |
Policy Influence Type | Participation in a national consultation |
Description | Accurate, Rapid, Robust and Economical diagnostic technoliogieS for Tuberculosis |
Amount | € 4,400,000 (EUR) |
Funding ID | 825931 |
Organisation | European Commission |
Sector | Public |
Country | European Union (EU) |
Start | 01/2020 |
End | 12/2022 |
Description | EPSRC IRC Proteus - Multiplexed 'Touch and Tell' Optical Molecular Sensing and Imaging - Lifetime and Beyond |
Amount | £3,852,991 (GBP) |
Funding ID | EP/R005257/1 |
Organisation | Engineering and Physical Sciences Research Council (EPSRC) |
Sector | Public |
Country | United Kingdom |
Start | 01/2019 |
End | 12/2022 |
Description | IRC Next Steps Plus: Photonic Pathogen Theranostics - Point-of-care image guided photonic therapy of bacterial and fungal infection |
Amount | £1,100,000 (GBP) |
Funding ID | EP/R018669/1 |
Organisation | Engineering and Physical Sciences Research Council (EPSRC) |
Sector | Public |
Country | United Kingdom |
Start | 04/2019 |
End | 03/2022 |
Description | IRC Next steps funding |
Amount | £3,900,000 (GBP) |
Funding ID | EP/R005257/1 |
Organisation | Engineering and Physical Sciences Research Council (EPSRC) |
Sector | Public |
Country | United Kingdom |
Start | 03/2019 |
End | 02/2023 |
Description | Multi-modal Manufacturing of Medical Devices (4MD) |
Amount | £1,302,969 (GBP) |
Funding ID | EP/P027415/1 |
Organisation | Engineering and Physical Sciences Research Council (EPSRC) |
Sector | Public |
Country | United Kingdom |
Start | 07/2017 |
End | 07/2022 |
Description | Next generation endoscopes |
Amount | £665,103 (GBP) |
Funding ID | EP/S001123/1 |
Organisation | Engineering and Physical Sciences Research Council (EPSRC) |
Sector | Public |
Country | United Kingdom |
Start | 06/2018 |
End | 06/2021 |
Description | Next-Generation Sensing For Human In Vivo Pharmacology- Accelerating Drug Development In Inflammatory Diseases |
Amount | £1,071,136 (GBP) |
Funding ID | EP/S025987/1 |
Organisation | Engineering and Physical Sciences Research Council (EPSRC) |
Sector | Public |
Country | United Kingdom |
Start | 04/2019 |
End | 04/2022 |
Description | Single Photons - Expanding the Spectrum (SPEXS) |
Amount | £5,265,567 (GBP) |
Funding ID | EP/S026428/1 |
Organisation | Engineering and Physical Sciences Research Council (EPSRC) |
Sector | Public |
Country | United Kingdom |
Start | 09/2019 |
End | 09/2024 |
Description | Through-body TCSPC based real-time tracking to guide interventional medical procedures |
Amount | £315,108 (GBP) |
Funding ID | ST/S000763/1 |
Organisation | Science and Technologies Facilities Council (STFC) |
Sector | Public |
Country | United Kingdom |
Start | 09/2018 |
End | 03/2021 |
Description | WT/CARB-X (none of the "type of funding" given below are really suitable) |
Amount | £2,500,000 (GBP) |
Funding ID | 208608/Z/17/Z |
Organisation | Wellcome Trust |
Sector | Charity/Non Profit |
Country | United Kingdom |
Start | 05/2017 |
End | 12/2022 |
Title | Data for "High resolution air-clad imaging fibers" |
Description | The data supporting the results presented in the paper "High resolution air-clad imaging fibers". This body of work is designed to provide an indication of the imaging performance of a novel, high resolution imaging coherent fibre bundle fabricated in the University of Bath's Centre for Photonics and Photonic Materials' facilities. Traditionally, the imaging fibres such as those used in medical endoscopes consist of solid doped and undoped silica glass. The novelty of our design is in having the cladding that is comprised of air-filled silica capillaries, achieving a cladding index close to that of air. This increase in index contrast with the cores (still solid doped silica) provides a higher numerical aperture waveguide. As a result, the light is better confined to the cores, and higher resolution, or a wider operational bandwidth, can be achieved. |
Type Of Material | Database/Collection of data |
Year Produced | 2018 |
Provided To Others? | Yes |
Title | Data for Quantitative characterisation of imaging fibres |
Description | Images, code and data used to produce the figures in the paper Quantitative characterisation of imaging fibres. |
Type Of Material | Database/Collection of data |
Year Produced | 2017 |
Provided To Others? | Yes |
Title | Data for the publication: Low index contrast imaging fibers |
Description | This contains the images and raw data presented in the paper Low index contrast imaging fibres published in Optics Letters. The data includes the individual images used to demonstrate how the new fibres are made and the raw data used to determine the performance of the imaging fibres presented in the publication. |
Type Of Material | Database/Collection of data |
Year Produced | 2017 |
Provided To Others? | Yes |
Title | Dataset for Ultra-low background Raman sensing using a negative-curvature fibre and no distal optics |
Description | Collected data for the results presented in "Ultra-low background Raman sensing using a negative-curvature fibre and no distal optics" demonstrating the use of a single hollow core negative curvature fibre for Raman and surface enhanced Raman spectroscopy sensing. This new optical fibre shows a 1000x background reduction compared to conventional fibres while maintaining the same collection efficiency. The dataset includes Raman and SERS spectra from different samples and attenuation data for a range of wavelengths for the negative curvature fibre. |
Type Of Material | Database/Collection of data |
Year Produced | 2018 |
Provided To Others? | Yes |
Description | This is an IRC - it is by definition a collaboration |
Organisation | Heriot-Watt University |
Country | United Kingdom |
Sector | Academic/University |
PI Contribution | The IRC team comprises the Universities of Edinburgh, Heriot Watt and Bath. |
Collaborator Contribution | Massive collaborations (please see the web site www.proteus.ac.uk) |
Impact | Please see list of publications/patents/engagement activities on the Proteus web site. |
Start Year | 2013 |
Description | This is an IRC - it is by definition a collaboration |
Organisation | University of Bath |
Country | United Kingdom |
Sector | Academic/University |
PI Contribution | The IRC team comprises the Universities of Edinburgh, Heriot Watt and Bath. |
Collaborator Contribution | Massive collaborations (please see the web site www.proteus.ac.uk) |
Impact | Please see list of publications/patents/engagement activities on the Proteus web site. |
Start Year | 2013 |
Title | - OPTICAL PROBE FOR THROMBIN |
Description | OPTICAL PROBE FOR THROMBIN |
IP Reference | WO2016151297 |
Protection | Patent application published |
Year Protection Granted | |
Licensed | Commercial In Confidence |
Impact | Confidential |
Title | A SENSING STRUCTURE AND METHOD OF FORMING A SENSING STRUCTURE |
Description | A SENSING STRUCTURE AND METHOD OF FORMING A SENSING STRUCTURE |
IP Reference | WO2017203272 |
Protection | Patent application published |
Year Protection Granted | |
Licensed | Commercial In Confidence |
Impact | Confidential |
Title | ENDOSCOPIC IMAGING APPARATUS AND METHOD |
Description | ENDOSCOPIC IMAGING APPARATUS AND METHOD |
IP Reference | WO2017174998 |
Protection | Patent application published |
Year Protection Granted | |
Licensed | Commercial In Confidence |
Impact | Confidentail |
Title | FLUORESCENT POLYBRANCHED PROBES FOR DETECTING BACTERIA AND/OR FUNGI IN VITRO AND IN VIVO |
Description | FLUORESCENT POLYBRANCHED PROBES FOR DETECTING BACTERIA AND/OR FUNGI IN VITRO AND IN VIVO |
IP Reference | WO2016075484 |
Protection | Patent application published |
Year Protection Granted | |
Licensed | Commercial In Confidence |
Impact | Confidential |
Title | FRAME SELECTION IN MEDICAL IMAGE DATA |
Description | FRAME SELECTION IN MEDICAL IMAGE DATA |
IP Reference | WO2017149310 |
Protection | Patent application published |
Year Protection Granted | |
Licensed | Commercial In Confidence |
Impact | Confidential |
Title | FRET MOLECULAR PROBES WITH CLEAVABLE LINKERS FOR DETECTING BACTERIA AND/OR FUNGI IN VITRO AND IN VIVO |
Description | FRET MOLECULAR PROBES WITH CLEAVABLE LINKERS FOR DETECTING BACTERIA AND/OR FUNGI IN VITRO AND IN VIVO |
IP Reference | WO2016075481 |
Protection | Patent application published |
Year Protection Granted | |
Licensed | Commercial In Confidence |
Impact | Confidential |
Title | Molecular probes for detecting gram-negative bacteria in vitro and in vivo |
Description | Molecular probes for detecting gram-negative bacteria in vitro and in vivo |
IP Reference | WO2016075483 |
Protection | Patent application published |
Year Protection Granted | |
Licensed | Commercial In Confidence |
Impact | Confidential |
Title | OPTICAL IMAGING PROBES |
Description | OPTICAL IMAGING PROBES |
IP Reference | WO2012136958 |
Protection | Patent granted |
Year Protection Granted | 2017 |
Licensed | Commercial In Confidence |
Impact | Confidential |
Title | OPTICAL PROBES FOR MATRIX METALLOPROTEINASES (the question below is wrong - protection is not received from a filing or if the PCT is published it has to go through national phases - and I cannot add this unless I put a date). |
Description | OPTICAL PROBES FOR MATRIX METALLOPROTEINASES |
IP Reference | WO2016151299 |
Protection | Patent application published |
Year Protection Granted | 2016 |
Licensed | Commercial In Confidence |
Impact | confidential |
Title | OPTICAL SYSTEM AND METHOD |
Description | A system comprises a waveguide apparatus comprising a plurality of input waveguides, a multimode waveguide, and a guided-wave transition coupling the plurality of input waveguides to the multimode waveguide. The system further comprises at least one light source configured to excite in turn each of a plurality of the input waveguides, or each of a plurality of combinations of the input waveguides, thereby generating a plurality of different light patterns in turn at an output of the waveguide apparatus. The waveguide apparatus is configured to direct each of the plurality of different light patterns to a target region. The system further comprises at least one detector configured to detect light transmitted, reflected or emitted from the target region in response to each of the different light patterns, and to output signals representing the detected light. |
IP Reference | WO2018203088 |
Protection | Patent application published |
Year Protection Granted | 2018 |
Licensed | Commercial In Confidence |
Impact | Confidential |
Title | SERS PROBE COMPRISING A DUAL-CORE OPTICAL FIBER AND A SPACER ONTO WHICH SERS-ACTIVE NANOPARTICLES ARE ATTACHED |
Description | SERS PROBE COMPRISING A DUAL-CORE OPTICAL FIBER AND A SPACER ONTO WHICH SERS-ACTIVE NANOPARTICLES ARE ATTACHED |
IP Reference | WO2017158331 |
Protection | Patent application published |
Year Protection Granted | |
Licensed | Commercial In Confidence |
Impact | Confidential |
Title | Bac-II |
Description | Critically ill patients are often ventilated in dedicated critical care units to provide respiratory support. Despite best practice patients can often develop a condition called adult respiratory distress syndrome (ARDS), which is characterised by deterioration in their respiratory function, and changes on chest x-ray. The correct management for ARDS is identifying the underlying condition causing the deterioration and identifying appropriate targeted therapy. One such cause is pneumonia, caused by a bacterial infection in the lungs of a ventilated patient. The patients may have been ventilated due to pneumonia but they may also develop pneumonia whilst ventilated. Ventilator associated pneumonia (VAP) has significant mortality. Despite all the clinical and laboratory data at the investigators' disposal there remains great difficulty in the accurate diagnosis of pneumonia and therefore treatment is often given empirically. Therefore, there is an urgent clinical need for accurate methods to diagnose the presence of bacteria deep in the lung in ventilated critically ill patients. As such, the investigating team have developed and synthesised an imaging agent called BAC TWO. BAC TWO will be instilled directly into the lungs of 12 patients to assess whether it can label gram-negative bacteria in the human lung. |
Type | Diagnostic Tool - Imaging |
Current Stage Of Development | Early clinical assessment |
Year Development Stage Completed | 2016 |
Development Status | Under active development/distribution |
Clinical Trial? | Yes |
Impact | Critically ill patients are often ventilated in dedicated critical care units to provide respiratory support. Despite best practice patients can often develop a condition called adult respiratory distress syndrome (ARDS), which is characterised by deterioration in their respiratory function, and changes on chest x-ray. The correct management for ARDS is identifying the underlying condition causing the deterioration and identifying appropriate targeted therapy. One such cause is pneumonia, caused by a bacterial infection in the lungs of a ventilated patient. The patients may have been ventilated due to pneumonia but they may also develop pneumonia whilst ventilated. Ventilator associated pneumonia (VAP) has significant mortality. Despite all the clinical and laboratory data at the investigators' disposal there remains great difficulty in the accurate diagnosis of pneumonia and therefore treatment is often given empirically. Therefore, there is an urgent clinical need for accurate methods to diagnose the presence of bacteria deep in the lung in ventilated critically ill patients. As such, the investigating team have developed and synthesised an imaging agent called BAC TWO. BAC TWO will be instilled directly into the lungs of 12 patients to assess whether it can label gram-negative bacteria in the human lung. |
URL | https://clinicaltrials.gov/ct2/show/NCT02491164?term=NCT02491164&rank=1 |
Title | Exploratory clinical study of intrapulmonary microdosing of the BACterial detection probe (BAC ONE) |
Description | Critically ill patients are often ventilated in dedicated critical care units to provide respiratory support. Despite best practice patients can often develop a condition called adult respiratory distress syndrome (ARDS), which is characterised by deterioration in their respiratory function, and changes on chest x-ray. The correct management for ARDS is identifying the underlying condition causing the deterioration and identifying appropriate targeted therapy. One such cause is pneumonia, caused by a bacterial infection in the lungs of a ventilated patient. The patients may have been ventilated due to pneumonia but they may also develop pneumonia whilst ventilated. Ventilator associated pneumonia (VAP) has significant mortality. Despite all the clinical and laboratory data at the investigators' disposal there remains great difficulty in the accurate diagnosis of pneumonia and therefore treatment is often given empirically. Therefore, there is an urgent clinical need for accurate methods to diagnose the presence of bacteria deep in the lung in ventilated critically ill patients. As such, the investigating team have developed and synthesised an imaging agent called BAC ONE. BAC ONE will be instilled directly into the lungs of 12 patients (with and without lung infection) to assess whether it can label bacteria in the human lung. |
Type | Diagnostic Tool - Imaging |
Current Stage Of Development | Early clinical assessment |
Year Development Stage Completed | 2018 |
Development Status | Under active development/distribution |
Clinical Trial? | Yes |
Impact | Critically ill patients are often ventilated in dedicated critical care units to provide respiratory support. Despite best practice patients can often develop a condition called adult respiratory distress syndrome (ARDS), which is characterised by deterioration in their respiratory function, and changes on chest x-ray. The correct management for ARDS is identifying the underlying condition causing the deterioration and identifying appropriate targeted therapy. One such cause is pneumonia, caused by a bacterial infection in the lungs of a ventilated patient. The patients may have been ventilated due to pneumonia but they may also develop pneumonia whilst ventilated. Ventilator associated pneumonia (VAP) has significant mortality. Despite all the clinical and laboratory data at the investigators' disposal there remains great difficulty in the accurate diagnosis of pneumonia and therefore treatment is often given empirically. Therefore, there is an urgent clinical need for accurate methods to diagnose the presence of bacteria deep in the lung in ventilated critically ill patients. As such, the investigating team have developed and synthesised an imaging agent called BAC ONE. BAC ONE will be instilled directly into the lungs of 12 patients (with and without lung infection) to assess whether it can label bacteria in the human lung. |
URL | https://clinicaltrials.gov/ct2/show/NCT02558062?term=NCT02558062&rank=1 |
Title | Exploratory study to optically visualise activated neutrophils and the proto-oncogene, c-MET, in lung masses using DUAL colour fibre-based endomicroscopy (DUAL) |
Description | Lung cancer is currently a major health problem in the UK. Despite being one of the most common cancers, lung cancer has a poor prognosis compared to other types of cancer and is the leading cause of cancer death in the world. As opposed to other organs, the lung is highly susceptible to inflammatory insults, for example from bacterial infection-induced and tobacco-induced inflammation. It has long been known that the cellular microenvironment that nurtures tumour growth and development is linked to sites of chronic inflammation but molecular insights into how external inflammation boosts or inhibits cancer in the lungs remains unclear. This study aims to directly visualise the expression of a well known marker of cancerous tissue, c-MET, and the activity of neutrophils in human lung cancer in vivo in situ using fibre-based endomicroscopy. |
Type | Diagnostic Tool - Imaging |
Current Stage Of Development | Early clinical assessment |
Year Development Stage Completed | 2018 |
Development Status | Under active development/distribution |
Clinical Trial? | Yes |
Impact | Lung cancer is currently a major health problem in the UK. Despite being one of the most common cancers, lung cancer has a poor prognosis compared to other types of cancer and is the leading cause of cancer death in the world. As opposed to other organs, the lung is highly susceptible to inflammatory insults, for example from bacterial infection-induced and tobacco-induced inflammation. It has long been known that the cellular microenvironment that nurtures tumour growth and development is linked to sites of chronic inflammation but molecular insights into how external inflammation boosts or inhibits cancer in the lungs remains unclear. This study aims to directly visualise the expression of a well known marker of cancerous tissue, c-MET, and the activity of neutrophils in human lung cancer in vivo in situ using fibre-based endomicroscopy. |
URL | https://clinicaltrials.gov/ct2/show/NCT02676050?term=NCT02676050&rank=1 |
Title | FIB-ONE |
Description | Brief Summary: While the process of fibrosis is essential for normal wound healing, an excessive and uncontrolled 'fibrotic' response can result in impaired tissue structure and function. In other words, affected 'fibrotic' tissues are unable to heal back to normal and therefore don't work as effectively as they normally would. In the case of the lung, fibrosis can occur across large parts of the lung such as in conditions like Idiopathic Pulmonary Fibrosis (IPF) and sarcoidosis or it can occur in much smaller patches such as around the borders of some lung tumours. At the moment the investigators don't fully understand the mechanisms of fibrosis and so therefore cannot monitor or treat these conditions as effectively as the investigators could. Despite the significant global financial burden of these diseases, treatment options are very limited and monitoring of disease progression remains a real challenge. In an effort to address this problem, the research team have designed and synthesised an imaging agent (FIB ONE) that can detect fibrosis in the lung. FIB ONE will be used at very low concentrations in patients with a lung condition characterised by excessive activity of the fibroproliferative pathway either scheduled for a routine bronchoscopy or elective surgery. FIB ONE will be administered directly into the lungs during a bronchoscopy procedure and images of the lungs will be analysed. As part of this study, the research team's novel endomicroscopy detection system will be compared to equipment that is routinely used in the NHS when imaging the FIB ONE probe. |
Type | Diagnostic Tool - Imaging |
Current Stage Of Development | Early clinical assessment |
Year Development Stage Completed | 2017 |
Development Status | Under active development/distribution |
Clinical Trial? | Yes |
Impact | Brief Summary: While the process of fibrosis is essential for normal wound healing, an excessive and uncontrolled 'fibrotic' response can result in impaired tissue structure and function. In other words, affected 'fibrotic' tissues are unable to heal back to normal and therefore don't work as effectively as they normally would. In the case of the lung, fibrosis can occur across large parts of the lung such as in conditions like Idiopathic Pulmonary Fibrosis (IPF) and sarcoidosis or it can occur in much smaller patches such as around the borders of some lung tumours. At the moment the investigators don't fully understand the mechanisms of fibrosis and so therefore cannot monitor or treat these conditions as effectively as the investigators could. Despite the significant global financial burden of these diseases, treatment options are very limited and monitoring of disease progression remains a real challenge. In an effort to address this problem, the research team have designed and synthesised an imaging agent (FIB ONE) that can detect fibrosis in the lung. FIB ONE will be used at very low concentrations in patients with a lung condition characterised by excessive activity of the fibroproliferative pathway either scheduled for a routine bronchoscopy or elective surgery. FIB ONE will be administered directly into the lungs during a bronchoscopy procedure and images of the lungs will be analysed. As part of this study, the research team's novel endomicroscopy detection system will be compared to equipment that is routinely used in the NHS when imaging the FIB ONE probe. |
URL | https://clinicaltrials.gov/ct2/show/NCT02604862?term=NCT02604862&rank=1 |
Title | SNAP-IT (NAP IN ICU) |
Description | Critically ill patients often succumb to acute respiratory disease (rapidly developing disease affecting the lungs). The lungs are the commonest organ to fail and require support in the intensive care environment. However, no accurate methods exist that can be used at the bedside to tell what is causing deterioration in a person's lungs. There are various examples of acute respiratory diseases that can occur as a result of numerous different causes, have a high risk of death and cannot be treated easily with drugs. When trying to accurately diagnose and classify these lung diseases there is a risk that the type of respiratory disease is misdiagnosed, missed or the level of severity is not captured. By using the field of optical molecular imaging and employing novel techniques and technologies, the investigators hope to demonstrate here that a bespoke chemical probe administered in micro doses (tiny doses) directly into the distal lung can rapidly and accurately detect activated neutrophils (cells of the immune system that are implicated in the development of these severe conditions), and so work towards a bedside test which could be used to diagnose, monitor and classify the disease in patients who are critically ill in the future. The population for this study are in intensive care where patients are normally intubated (have a breathing tube) due to the severity of their illness, this may be because of respiratory problems or respiratory problems can rapidly develop. Participants will have the chemical probe administered into their lungs and pictures taken through the tube already in place. As this probe lights up when it comes into contact with neutrophils the investigators will be able to tell if neutrophils are present. This will inform a larger study in which it's hoped that the method can be used to inform clinical decisions. The first procedure will take place within two days of initiation of mechanical ventilation and the direct contact with the study team will be completed within nine days. |
Type | Diagnostic Tool - Imaging |
Current Stage Of Development | Early clinical assessment |
Year Development Stage Completed | 2017 |
Development Status | Under active development/distribution |
Clinical Trial? | Yes |
Impact | Critically ill patients often succumb to acute respiratory disease (rapidly developing disease affecting the lungs). The lungs are the commonest organ to fail and require support in the intensive care environment. However, no accurate methods exist that can be used at the bedside to tell what is causing deterioration in a person's lungs. There are various examples of acute respiratory diseases that can occur as a result of numerous different causes, have a high risk of death and cannot be treated easily with drugs. When trying to accurately diagnose and classify these lung diseases there is a risk that the type of respiratory disease is misdiagnosed, missed or the level of severity is not captured. By using the field of optical molecular imaging and employing novel techniques and technologies, the investigators hope to demonstrate here that a bespoke chemical probe administered in micro doses (tiny doses) directly into the distal lung can rapidly and accurately detect activated neutrophils (cells of the immune system that are implicated in the development of these severe conditions), and so work towards a bedside test which could be used to diagnose, monitor and classify the disease in patients who are critically ill in the future. The population for this study are in intensive care where patients are normally intubated (have a breathing tube) due to the severity of their illness, this may be because of respiratory problems or respiratory problems can rapidly develop. Participants will have the chemical probe administered into their lungs and pictures taken through the tube already in place. As this probe lights up when it comes into contact with neutrophils the investigators will be able to tell if neutrophils are present. This will inform a larger study in which it's hoped that the method can be used to inform clinical decisions. The first procedure will take place within two days of initiation of mechanical ventilation and the direct contact with the study team will be completed within nine days. |
URL | https://clinicaltrials.gov/ct2/show/NCT02804854?term=NCT02804854&rank=1 |
Description | AAAS Meeting 2019 |
Form Of Engagement Activity | A talk or presentation |
Part Of Official Scheme? | No |
Geographic Reach | International |
Primary Audience | Policymakers/politicians |
Results and Impact | AAAS Meeting 2019 - Invited to the meeting as a Flagship EPSRC project representing UK science on the main exhibition stage as well as the International Reception. Feb 2019 Audience: American Academics, Members of Congress, American Industries, RIUK team lead by Sir Mark Walport (CEO) World Media Teams, Global stakeholders (academics, policy makers) students and wider publics Engagement methods: Proteus Technology Versicolour Impact: Raised awareness of EPSRC Proteus with UKRI CEO and wider RIUK team. Networked with senior academics, policy makers and US industries. Created new collaborations with industrial partners |
Year(s) Of Engagement Activity | 2019 |
URL | https://www.ukri.org/aaas/ |
Description | Development of an ICU Patient and Public Involvement Group |
Form Of Engagement Activity | Participation in an activity, workshop or similar |
Part Of Official Scheme? | No |
Geographic Reach | National |
Primary Audience | Patients, carers and/or patient groups |
Results and Impact | Public and Patient Involvement -I CU PPI GROUP March 2018 Audience: ICU Patients and families Engagement methods: Dialogue sessions with patients, partnership building activities, developing PPI projects Impact: Creation of Edinburgh's first ICU PPI group, working with the Critical Care Team in Edinburgh and nationally with ICU Steps - has allowed ICU patients to take part in Proteus engagement activities and has strengthen Proteus' PPI portfolio |
Year(s) Of Engagement Activity | 2018 |
URL | https://www.ed.ac.uk/clinical-sciences/divisionpgdi/anaesthesia/news-views/icusteps-patient-and-fami... |
Description | EPSRC Our Health - Dr Henk Mulder Visit (Science Shop Expert, The University of Groningen) |
Form Of Engagement Activity | A talk or presentation |
Part Of Official Scheme? | No |
Geographic Reach | Local |
Primary Audience | Professional Practitioners |
Results and Impact | EPSRC Our Health - Dr Henk Mulder Visit (Science Shop Expert, The University of Groningen) April 2018 Audience: Local community, patient groups, undergraduates/postgraduates, academics and Public Engagement Professionals Engagement methods: Presentation and workshop Impact: Dr Henk Mulder's visit for part of a University wide consultation around the Science Shop model for community/patient engagement and resulted in the funding and launch of Our Health |
Year(s) Of Engagement Activity | 2018 |
Description | EPSRC Our Health - The First UK Interdisciplinary Science Shop |
Form Of Engagement Activity | A formal working group, expert panel or dialogue |
Part Of Official Scheme? | No |
Geographic Reach | International |
Primary Audience | Public/other audiences |
Results and Impact | EPSRC Our Health - The First UK Interdisciplinary Science Shop June 2018 Audience: Local community, patient groups, undergraduates/postgraduates, academics and Public Engagement professionals Engagement methods: Community based research projects around Health and well being Impact: EPSRC Our Health (within first 6 months of launch) has created national and international impact. Our Health was selected to host the Experienced Practice Learning Exchange for international delegates as part of The National Co ordinating Centre's National ENGAGE 2018 Conference. EPSRC Our Health has also been asked to work in partnership with UKRI International PE team to develop global projects for Our Health. Our Health has impacted the local community by creating new knowledge around health and well being with community partners. |
Year(s) Of Engagement Activity | 2018 |
URL | https://proteus.ac.uk/public-engagement/developing-community-partnerships/our-health/about-our-healt... |
Description | Living Knowledge 2018 |
Form Of Engagement Activity | A talk or presentation |
Part Of Official Scheme? | No |
Geographic Reach | International |
Primary Audience | Professional Practitioners |
Results and Impact | Living Knowledge 2018 - Invited as a speaker to the Living Knowledge Confrenec (Budapest) to present EPSRC Our Health and share best practice around this new Interdisciplinary model of a science shop July 2018 Audience: International Public Engagement Delegates and Community partners Engagement methods: Workshops, presentations and visits to local communities to talk with people about their involvement in PE. Impact: EPSRC Our Health is now established with in the European community and is part of a wider network and a leader in the field of interdisciplinary community research |
Year(s) Of Engagement Activity | 2018 |
URL | https://www.livingknowledge.org/lk8/ |
Description | Proteus Partnership with Msc Science Communication Programme |
Form Of Engagement Activity | Participation in an activity, workshop or similar |
Part Of Official Scheme? | No |
Geographic Reach | Local |
Primary Audience | Public/other audiences |
Results and Impact | Proteus Partnership with Msc Science Communication Programme 2018 Audience: Eight Science Communication Master Students work with Proteus each year engaging wider publics and community partners. Engagement methods: science writing, activity based presentations, dialogic workshops and creative co inquiry. Impact: developed a community of public engagement practice throughout the university and with local universities. Sharing of best practice, improving quality and impact of public engagement work. Work created by students have promoted and raised the profile of Proteus across a wide range of project stakeholders. |
Year(s) Of Engagement Activity | 2018 |
Description | Proteus Public Engagement (PE) Strategic Influence |
Form Of Engagement Activity | A formal working group, expert panel or dialogue |
Part Of Official Scheme? | No |
Geographic Reach | National |
Primary Audience | Professional Practitioners |
Results and Impact | Proteus Public Engagement (PE) Strategic Influence - Proteus represented at the Strategic PE Group, The University of Edinburgh March 2018 Audience: Senior colleagues working within PE and members of the wider public, The University of Edinburgh (UoE) Engagement methods: Committee discussions, development of UoE PE strategy Impact: Proteus PE influences the strategic direction of PE for The University of Edinburgh |
Year(s) Of Engagement Activity | 2018 |
URL | https://www.ed.ac.uk/institute-academic-development/research-roles/public-engagement/pe-strategy |
Description | Science at Heriot Watt 2018 |
Form Of Engagement Activity | Participation in an activity, workshop or similar |
Part Of Official Scheme? | No |
Geographic Reach | Local |
Primary Audience | Public/other audiences |
Results and Impact | Science at Heriot Watt 2018 (Heriot Watt University) April 2018 Audience: Wider Public Engagement methods: Hands on demonstrations, activities and storytelling Impact: Raise awareness of Proteus Science with family audience. Strengthened links with Heriot Watt University. |
Year(s) Of Engagement Activity | 2018 |
Description | The Edinburgh International Science Festival (Edinburgh) |
Form Of Engagement Activity | Participation in an activity, workshop or similar |
Part Of Official Scheme? | No |
Geographic Reach | Local |
Primary Audience | Public/other audiences |
Results and Impact | The Edinburgh International Science Festival (Edinburgh) April 2018 Audience: Wider Public Engagement methods: Hands on demonstrations, activities and storytelling Impact: Raised awareness of Proteus Science with family audiences. Created interest amongst researcher working in infectious diseases in Roslin centre - formed new collaboration with Dr Kenneth Ballie around PE activities |
Year(s) Of Engagement Activity | 2018 |
Description | The International Edinburgh Book Festival - EPSRC Proteus/ EPSRC Our Health |
Form Of Engagement Activity | Participation in an activity, workshop or similar |
Part Of Official Scheme? | No |
Geographic Reach | Local |
Primary Audience | Public/other audiences |
Results and Impact | The International Edinburgh Book Festival August 2018 Audience: Wider Public Engagement methods: Hands on demonstrations and research art exhibition. Our Health students and community partners formed a choir and sang. Impact: Principal of The University of Edinburgh attended and gave strong support for Proteus/Our Health. As a consequence of this event the The University of Edinburgh, Proteus/Our Health and The International Edinburgh Book Festival have agreed to work together on further PE activities |
Year(s) Of Engagement Activity | 2018 |