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Magnetic resonance imaging enhanced by superparamagnetic iron oxide particles: Usefulness for distinguishing between focused ultrasound-induced blood–brain barrier disruption and brain hemorrhage

✍ Scribed by Hao-Li Liu; Po-Hong Hsu; Po-Chun Chu; Yau-Yau Wai; Jin-Chung Chen; Chia-Rui Shen; Tzu-Chen Yen; Jiun-Jie Wang


Publisher
John Wiley and Sons
Year
2009
Tongue
English
Weight
612 KB
Volume
29
Category
Article
ISSN
1053-1807

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✦ Synopsis


Abstract

Purpose

To investigate the usefulness of a fully flow‐compensated heavy T2*‐weighted imaging enhanced by superparamagnetic iron oxide (SPIO) particles for distinguishing between focused ultrasound‐induced disruption of blood–brain barrier (BBB) and brain hemorrhage.

Materials and Methods

Focused ultrasound (frequency: 1.5 MHz) was used to induce disruption of the BBB in 39 rats. Two T2*‐weighted images were obtained before and after SPIO administration. Preenhanced T2*‐weighted images were used to detect hemorrhage. Detection of BBB disruption was performed on SPIO‐enhanced images. Thirty‐four rats were sacrificed after magnetic resonance (MR) scanning for histological confirmation of brain lesions. Theremaining five animals were followed up for 35 days. Prussian blue staining was performed on histological sections to detect SPIO particles in the brain.

Results

After SPIO injection the areas of BBB disruption in rat brain were significantly enlarged. The area of mismatch between the T2*‐weighted images indicated a safe region where BBB opening occurred without hemorrhagic complications. In the longitudinal study, removal of SPIO occurred at a faster rate in hemorrhagic areas, albeit being closer to that occurring in the liver. The presence of SPIO was confirmed by Prussian blue staining in brain parenchyma and capillary endothelial cells in areas of BBB disruption.

Conclusion

T2*‐weighted images—either with and without SPIO enhancement—may differentiate focused ultrasound‐induced BBB disruption from brain hemorrhage. J. Magn. Reson. Imaging 2009;29:31–38. © 2008 Wiley‐Liss, Inc.