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Advanced in vitro and in silico models to predict and prevent deep venous thrombosis

Project Description

Deep vein thrombosis (DVT) is a life-threatening and debilitating condition where blood clots form within the deep veins (e.g. the femoral vein in the leg). These clots can become unstable and cause fatal conditions such as pulmonary embolism (PE) [1,2]. DVT and PE combined cause 25,000 deaths annually in the UK [3]. At the moment, it is impossible to perform early prediction of DVT and the pathology is only diagnosed once the symptoms present themselves. Typically, this happens during the triage stage and relies mostly on the ability of the operator to identify a thrombus with a Doppler machine. If a thrombus is unstable, the only solution is an emergency surgery to remove it. As a result, many patients with DVT symptoms are treated with anti-coagulants as a preventive approach although the actual number of confirmed DVT cases is just a small fraction of the total suspected. The need for a prediction tool is widely recognised. Such a tool will not only help identify and potentially help save the lives of those at risk from thrombosis but could also reduce the use of dangerous anti-coagulants for the majority of the treated patients that do not need them.
With this project, we aim to investigate and understand the predictors of DVT based on a novel closer-to-reality in-vitro and in silico model developed by reproducing the anatomy of animal models, in particular mouse deep veins, available in literature, in order to reduce their unnecessary use.
In addition to generally accepted biochemical mechanisms of clotting, we propose the importance of altered blood flow in its development. We have already developed computational simulations [4,5] and experimental microfluidic models [6] of flow disturbances around valves of the veins. Here, we will develop advanced microfluidic in-vitro models, in which endothelial cells will be grown to mimic blood vessels and flexible valves without the need of sacrificing animals. We will then study the influence of blood flow characteristics on thrombus development based on clinical evidence including high definition imaging of healthy and thrombotic veins and valves. Additionally, we will develop computational simulations validated by the results obtained from the advanced in vitro approach. In the in-silico model we will be able to finely tune the three-dimensional geometry of the vein and valves, and to independently quantify the relative influence of each parameter (blood rheology, flexibility of vein and valve leaflets, bio-chemical and coagulation factors, etc.) on the insurgence of DVT. This novel approach will clarify the role of pathological blood flow in thrombosis initiation and propagation, and identify new factors predisposing to DVT. Based on these results we will then be able to establish anatomical and flow characteristics linked to the development of DVT. This will allow a personalized approach to identification and prophylaxis of people at major risk, for instance those with cancer, the aged and pregnant women. Moreover, we will be able to follow the thrombus formation process and analyse the anatomical characteristics increasing thrombosis incidence. This is particular important as current protocols based on in-vivo studies failed to identify this. Currently one of the preferred methods of studying thrombosis consist in fact of inducing thrombus formation by surgically restrict a major vein in a mouse and then sacrificing it to recover the clot after its detection is confirmed [7–9]. This limits the analyses to the clot composition preventing the understanding of its formation dynamics. Moreover, this approach requires the use of thousands of animals worldwide that can be saved by implementing our advanced approach. Our model will in fact provide a more reliable and standardise platform in which to study DVT and other blood flow related diseases, rendering the use of at least 40-50% of animals unnecessary.
The project is intrinsically multi-disciplinary and thus will require the PhD candidate to be highly motivated and interested in learning a wide range of scientifically challenging topics including microfluidics, cell biology, computational fluid dynamics, soft matter and biotechnology. Previous experience with optical microscope, cell culture and computational methods will be highly appreciated but are not strictly required to apply.
Applicants should have a Bioengineering, Chemical Engineering, Biophysics or Chemistry degree. International applicants should hold an IELTS English Score of 6 with no less than 5.5 in any band.

Funding Notes

This project is fully funded by the NC3Rs (joint award with the BHF).
The award pays tuition fees at UK Research Councils fee level (approx £5,000 per year) plus an annual tax-free stipend at UK Research Councils UK/EU rates (£15,009 for 2019/20).
Due to funding restrictions, the position is fully funded for UK/EU applicants only. Non-EU applicants may still apply for the position but in case of acceptance of the position they will be required to pay the additional fee for international students (approx £15,000 per year).
Please send your CV to


[1] C. T. Esmon, Blood Rev. 23, 225 (2009).
[2] E. G. Bovill and A. van der Vliet, Annu. Rev. Physiol. 73, 527 (2011).
[3] B. J. Hunt, Br. J. Haematol. 144, 642 (2009).
[4] M. Ariane, W. Wen, D. Vigolo, A. Brill, F. G. B. Nash, M. Barigou, and A. Alexiadis, Comput. Biol. Med. 89, 96 (2017).
[5] M. Ariane, D. Vigolo, A. Brill, F. G. . Nash, M. Barigou, and A. Alexiadis, Comput. Fluids 166, 57 (2018).
[6] Z. Schofield, A. Brill, A. Alexiadis, G. Nash, and D. Vigolo, Submitted (2019).
[7] J. A. Diaz, A. T. Obi, D. D. Myers, S. K. Wrobleski, P. K. Henke, N. MacKman, and T. W. Wakefield, Arterioscler. Thromb. Vasc. Biol. 32, 556 (2012).
[8] A. Brill, T. A. Fuchs, A. K. Chauhan, J. J. Yang, S. F. De Meyer, M. Kollnberger, T. W. Wakefield, B. Lammle, S. Massberg, and D. D. Wagner, Blood 117, 1400 (2011).
[9] P. D. Weinberg and C. Ross Ethier, J. Biomech. 40, 1594 (2007).

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