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Functional NIRS study of blood brain barrier disruption when induced by focused ultrasound and intra-arterial mannitol infusion

Myllylä, Teemu; Kaakinen, Mika; Vihriälä, Erkki; Jukkola, Jari; Zhao, Zuomin; Ferdinando, Hany; Korhonen, Vesa; Kiviniemi, Vesa; Eklund, Lauri (2020-05-05)

 
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URL:
https://doi.org/10.1117/12.2555843

Myllylä, Teemu
Kaakinen, Mika
Vihriälä, Erkki
Jukkola, Jari
Zhao, Zuomin
Ferdinando, Hany
Korhonen, Vesa
Kiviniemi, Vesa
Eklund, Lauri
SPIE
05.05.2020

Teemu Myllylä, Mika Kaakinen, Erkki Vihriälä, Jari Jukkola, Zuomin Zhao, Hany Ferdinando, Vesa Korhonen, Vesa Kiviniemi, Lauri Eklund, "Functional NIRS study of blood brain barrier disruption when induced by focused ultrasound and intra-arterial mannitol infusion," Proc. SPIE 11363, Tissue Optics and Photonics, 113630T (5 May 2020); doi: 10.1117/12.2555843

https://rightsstatements.org/vocab/InC/1.0/
© 2020 SPIE. The Definitive Version of Record can be found online at: https://doi.org/10.1117/12.2555843.
https://rightsstatements.org/vocab/InC/1.0/
doi:https://doi.org/10.1117/12.2555843
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https://urn.fi/URN:NBN:fi-fe2020112593010
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Abstract

Enhancing brain fluid movement across blood brain barrier (BBB) has been recognized as a potential treatment ofneurodegenerative diseases. Moreover, BBB opening is of high interest also in brain drug delivery in the treatment ofbrain tumors/cancers. However, efficient therapies which are based on BBB opening are still limited because ofinsufficient understanding of mechanisms and safety issues. Currently, there are few promising methodologically diverseBBB opening approaches.

In this paper, we use functional near-infrared spectroscopy (fNIRS) for the first time for monitoring cerebral hemoglobinand water concentration changes during BBB opening in mouse brain by using two different techniques: intra-arterialmannitol infusion (IAM) and focused ultrasound (FUS). Both of these BBB opening techniques are already in clinicaluse but their hemo- and hydrodynamic implications have not been investigated from comparative aspect. Two fibredetectors were attached on both sides of the mouse brain and the source fibre was attached on middle of forehead.Further, by using a combination of three wavelengths 690nm, 830nm and 980nm, that have sufficient light penetration inthe mouse brain, we can show average dynamics of hemoglobin and water in the whole brain, synchronized with BBBopening. To validate the level of BBB opening we used Evans blue dye and show its accumulation in the brainparenchyma tissue with the corresponding fNIRS responses.

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