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Magnetic targeting to enhance microbubble delivery in an occluded microarterial bifurcation

Magnetic targeting to enhance microbubble delivery in an occluded microarterial bifurcation
Magnetic targeting to enhance microbubble delivery in an occluded microarterial bifurcation
Ultrasound and microbubbles have been shown to accelerate the breakdown of blood clots both in vitro and in vivo. Clinical translation of this technology is still limited, however, in part by inefficient microbubble delivery to the thrombus. This study examines the obstacles to delivery posed by fluid dynamic conditions in occluded vasculature and investigates whether magnetic targeting can improve microbubble delivery. A two-dimensional computational fluid dynamic (CFD) model of a fully occluded Y-shaped microarterial bifurcation was developed to determine: (i) the fluid dynamic field in the vessel with inlet velocities from 1-100 mm/s (corresponding to Reynolds numbers 0.25-25); (ii) the transport dynamics of fibrinolytic drugs; and (iii) the flow behavior of microbubbles with diameters in the clinically-relevant range (0.6-5µm). In vitro experiments were carried out in a custom built microfluidic device. The flow field was characterized using tracer particles, and fibrinolytic drug transport was assessed using fluorescence microscopy. Lipid-shelled magnetic microbubbles were fluorescently labelled to determine their spatial distribution within the microvascular model. In both the simulations and experiments, the formation of laminar vortices and an abrupt reduction of fluid velocity were observed in the occluded branch of the bifurcation, severely limiting drug transport towards the occlusion. In the absence of a magnetic field, no microbubbles reached the occlusion, remaining trapped in the first vortex, within 350µm from the bifurcation center. The number of microbubbles trapped within the vortex decreased as the inlet velocity increased, but was independent of microbubble size. Application of a magnetic field (magnetic flux density of 76 mT, magnetic flux density gradient of 10.90T/m at the centre of the bifurcation) enabled delivery of microbubbles to the occlusion and the number of microbubbles delivered increased with bubble size and with decreasing inlet velocity.
0031-9155
7451-7470
de Saint Victor, Marie
b558a637-b7b6-4b5f-ad84-1a93f74a425e
Carugo, Dario
0a4be6cd-e309-4ed8-a620-20256ce01179
Barnsley, Lester C.
da7b9324-6305-4b35-8e4e-0f4a6410aa25
Owen, Joshua
4e7fc6bc-f2c5-4622-894f-9e811eca84cd
Coussios, Constantin
55b78f4c-f241-4676-87d5-9ea5fb295f4f
Stride, Eleanor
c0143e95-81fa-47c8-b9bc-5b4fc319bba6
de Saint Victor, Marie
b558a637-b7b6-4b5f-ad84-1a93f74a425e
Carugo, Dario
0a4be6cd-e309-4ed8-a620-20256ce01179
Barnsley, Lester C.
da7b9324-6305-4b35-8e4e-0f4a6410aa25
Owen, Joshua
4e7fc6bc-f2c5-4622-894f-9e811eca84cd
Coussios, Constantin
55b78f4c-f241-4676-87d5-9ea5fb295f4f
Stride, Eleanor
c0143e95-81fa-47c8-b9bc-5b4fc319bba6

de Saint Victor, Marie, Carugo, Dario, Barnsley, Lester C., Owen, Joshua, Coussios, Constantin and Stride, Eleanor (2017) Magnetic targeting to enhance microbubble delivery in an occluded microarterial bifurcation. Physics in Medicine and Biology, 62 (18), 7451-7470. (doi:10.1088/1361-6560/aa858f).

Record type: Article

Abstract

Ultrasound and microbubbles have been shown to accelerate the breakdown of blood clots both in vitro and in vivo. Clinical translation of this technology is still limited, however, in part by inefficient microbubble delivery to the thrombus. This study examines the obstacles to delivery posed by fluid dynamic conditions in occluded vasculature and investigates whether magnetic targeting can improve microbubble delivery. A two-dimensional computational fluid dynamic (CFD) model of a fully occluded Y-shaped microarterial bifurcation was developed to determine: (i) the fluid dynamic field in the vessel with inlet velocities from 1-100 mm/s (corresponding to Reynolds numbers 0.25-25); (ii) the transport dynamics of fibrinolytic drugs; and (iii) the flow behavior of microbubbles with diameters in the clinically-relevant range (0.6-5µm). In vitro experiments were carried out in a custom built microfluidic device. The flow field was characterized using tracer particles, and fibrinolytic drug transport was assessed using fluorescence microscopy. Lipid-shelled magnetic microbubbles were fluorescently labelled to determine their spatial distribution within the microvascular model. In both the simulations and experiments, the formation of laminar vortices and an abrupt reduction of fluid velocity were observed in the occluded branch of the bifurcation, severely limiting drug transport towards the occlusion. In the absence of a magnetic field, no microbubbles reached the occlusion, remaining trapped in the first vortex, within 350µm from the bifurcation center. The number of microbubbles trapped within the vortex decreased as the inlet velocity increased, but was independent of microbubble size. Application of a magnetic field (magnetic flux density of 76 mT, magnetic flux density gradient of 10.90T/m at the centre of the bifurcation) enabled delivery of microbubbles to the occlusion and the number of microbubbles delivered increased with bubble size and with decreasing inlet velocity.

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Accepted/In Press date: 8 August 2017
e-pub ahead of print date: 10 August 2017
Published date: 5 September 2017

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Local EPrints ID: 412977
URI: http://eprints.soton.ac.uk/id/eprint/412977
ISSN: 0031-9155
PURE UUID: 7f4e98cc-cbaf-4a7d-8b5f-b5becb7f7676

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Date deposited: 10 Aug 2017 16:30
Last modified: 16 Mar 2024 05:37

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Contributors

Author: Marie de Saint Victor
Author: Dario Carugo
Author: Lester C. Barnsley
Author: Joshua Owen
Author: Constantin Coussios
Author: Eleanor Stride

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