Title :
Microbubble-Size Dependence of Focused Ultrasound-Induced Blood–Brain Barrier Opening in Mice In Vivo
Author :
Choi, James J. ; Feshitan, Jameel A. ; Baseri, Babak ; Wang, Shougang ; Tung, Yao-Sheng ; Borden, Mark A. ; Konofagou, Elisa E.
Author_Institution :
Dept. of Biomed. Eng., Columbia Univ., New York, NY, USA
Abstract :
The therapeutic efficacy of neurological agents is severely limited, because large compounds do not cross the blood-brain barrier (BBB). Focused ultrasound (FUS) sonication in the presence of microbubbles has been shown to temporarily open the BBB, allowing systemically administered agents into the brain. Until now, polydispersed microbubbles (1-10 ??m in diameter) were used, and, therefore, the bubble sizes better suited for inducing the opening remain unknown. Here, the FUS-induced BBB opening dependence on microbubble size is investigated. Bubbles at 1-2 and 4-5 ??m in diameter were separately size-isolated using differential centrifugation before being systemically administered in mice (n = 28). The BBB opening pressure threshold was identified by varying the peak-rarefactional pressure amplitude. BBB opening was determined by fluorescence enhancement due to systemically administered, fluorescent-tagged, 3-kDa dextran. The identified threshold fell between 0.30 and 0.46 MPa in the case of 1-2 ??m bubbles and between 0.15 and 0.30 MPa in the 4-5 ??m case. At every pressure studied, the fluorescence was greater with the 4-5 ??m than with the 1-2 ??m bubbles. At 0.61 MPa, in the 1-2 ??m bubble case, the fluorescence amount and area were greater in the thalamus than in the hippocampus. In conclusion, it was determined that the FUS-induced BBB opening was dependent on both the size distribution in the injected microbubble volume and the brain region targeted.
Keywords :
biological effects of acoustic radiation; biomedical ultrasonics; blood; brain; drug delivery systems; fluorescence; FUS sonication; blood brain barrier opening; centrifugation; fluorescence enhancement; focused ultrasound; hippocampus; mice in vivo; microbubble size dependence; neurological agents; size 1 mum to 10 mum; thalamus; therapeutic efficacy; Acoustic pulses; Biomedical engineering; Chemicals; Drug delivery; Fluorescence; Frequency; Helium; Hemorrhaging; Hippocampus; In vivo; Mice; Permeability; Ultrasonic imaging; Blood–brain barrier; brain drug delivery; focused ultrasound (FUS); microbubbles; opening; permeability; Animals; Blood-Brain Barrier; Brain Chemistry; Drug Delivery Systems; Echoencephalography; Histocytochemistry; Male; Mice; Mice, Inbred C57BL; Microbubbles; Microscopy, Fluorescence; Permeability; Ultrasonography;
Journal_Title :
Biomedical Engineering, IEEE Transactions on
DOI :
10.1109/TBME.2009.2034533