| EPSRC Reference: |
EP/R013624/1 |
| Title: |
Bubbles to Bond Broken Bones: targeted drug delivery for fracture repair |
| Principal Investigator: |
Stride, Professor E |
| Other Investigators: |
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| Researcher Co-Investigators: |
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| Project Partners: |
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| Department: |
Engineering Science |
| Organisation: |
University of Oxford |
| Scheme: |
Standard Research |
| Starts: |
01 August 2018 |
Ends: |
31 January 2022 |
Value (£): |
390,969
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| EPSRC Research Topic Classifications: |
| Drug Formulation & Delivery |
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| EPSRC Industrial Sector Classifications: |
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| Related Grants: |
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| Panel History: |
| Panel Date | Panel Name | Outcome |
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11 Sep 2017
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HT Investigator-led Panel Meeting - September 2017
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Announced
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Summary on Grant Application Form |
Bone fractures are a major societal problem costing the UK economy more than £2 billion/year. This figure is predicted to increase markedly in the future as the average age of the population increases. A significant portion of this cost can be attributed to the 5-10% of bone fractures that fail to heal appropriately with current clinical interventions, leading to patients requiring major surgery and extensive rehabilitation. Hence there is an urgent need for new, minimally invasive and cost-effective treatments to be developed.
The aim of the proposed research is to address this need by investigating the potential for targeted delivery of drugs that promote bone healing. This will be achieved using a combination of focused ultrasound applied externally to the body and drug-loaded nanodroplets (NDs) delivered by intravenous injection. NDs consist of particles (~200nm in diameter) of a volatile liquid that can be used to encapsulate a range of different types of drug. In preliminary work in a mouse model we have shown that upon exposure to ultrasound they undergo rapid expansion to form gas microbubbles, simultaneously releasing their drug payload and stimulating cell uptake. We have also demonstrated that NDs can be engineered to accumulate at bone fracture sites. These observations now provides the exciting possibility of controlling remotely the delivery of ND-loaded drugs at fracture sites. Our approach has the advantage of delivering molecules selectively to the injury site at the correct phase of healing and - importantly - also preserves the granulation and hematoma tissue, which are strong positive regulators of good fracture healing outcomes. Many molecules can have both positive and negative effects on fracture healing depending on the time and site of action, and so correct timing is fundamental to treatment efficacy.
In this project, we plan firstly to build on our established ND chemistries to enable the delivery of proteins and small molecules known to be positive regulators of fracture healing in different temporal context, for example bone morphogenetic protein (BMP) and WNT protein. Building on our preliminary data, we will concurrently test what ultrasound parameters result in the optimal release, payload uptake and intracellular pathway activation, before assessing their osteogenic effects in cell culture, bioreactor culture and ex vivo systems of cell culture. In parallel, we will determine which ultrasound parameters are optimal to ensure molecule release and activation in vivo. Finally we will test whether optimised ND preparations can promote fracture healing in vivo using a combination of high resolution computed tomography, molecular and histological techniques.
We have assembled a world-leading interdisciplinary team to conduct this research, comprising experts in ultrasound and drug release, bone repair, stem cell biology and nanoparticle chemistry. In addition, our research proposal has been developed in close collaboration with clinicians specialising in bone fracture treatment. We will also work closely with non-RCUK public sector stakeholders, Dstl, who have a strong interest in our technology as a means of better treatment of injured service personnel, and with commercial partners who will provide us with clinically approved materials and equipment. It is our aim that through these interactions, the outcomes of the work will have direct impact upon clinical practice and commercial uptake. Finally our results will also be of wide academic and applied relevance to other medical conditions for which control over timing and location of treatment delivery is important, for example, stroke and cardiovascular disease.
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Key Findings |
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This information can now be found on Gateway to Research (GtR) http://gtr.rcuk.ac.uk
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Potential use in non-academic contexts |
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This information can now be found on Gateway to Research (GtR) http://gtr.rcuk.ac.uk
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Impacts |
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| Description |
This information can now be found on Gateway to Research (GtR) http://gtr.rcuk.ac.uk |
| Summary |
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| Date Materialised |
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Sectors submitted by the Researcher |
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This information can now be found on Gateway to Research (GtR) http://gtr.rcuk.ac.uk
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| Project URL: |
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| Further Information: |
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| Organisation Website: |
http://www.ox.ac.uk |