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Direct brain infusion can be enhanced with focused ultrasound and microbubbles.

Authors: Wang S, Karakatsani ME, Fung C, Sun T, Acosta C, Konofagou E

The delivery of most therapeutic agents is rendered ineffective for the treatment of brain diseases due to the presence of the blood-brain barrier (BBB). The goal of this study was to investigate the effect of pre-infusion focused ultrasound (FUS) and microbubbles on the distribution of direct brain infusion in vivo. A single-element FUS transducer was used in all sonications, which were carried out immediately prior to direct infusion procedures. Mice received direct infusion of either Gadolinium-labeled albumin (Gd-albumin, 74 kDa) or adeno-associated virus (AAV, ∼4 MDa). The volumes of Gd-albumin at 30 min were deemed comparable ( P = 0.334) between the direct infusion (DI)-only group and the FUS + DI group. At 120 min, the FUS + DI group showed significantly higher contrast-enhanced volume (9.76 ± 0.74 mm<sup>3</sup>) than the DI-only group (7.14 ± 0.34 mm<sup>3</sup>). For mice infused with AAV, the total volume of transduction was estimated as GFP-positive regions and FUS + DI group demonstrated significantly higher ( P = 0.017) transduction efficiency in vivo. In conclusion, enhanced bio-distribution of directly infused agents was observed when the targeted region was pre-conditioned with FUS and microbubbles. Focused ultrasound has the potential, as an adjuvant technique, to significantly enhance direct brain infusion and achieve the desired therapeutic outcomes.

Introduction

Purpose Drug delivery WITHOUT BBB opening
Study Objective To determine whether pre-infusion focused ultrasound with microbubbles enhances the in vivo distribution of directly infused agents in the brain.
Animal model / Human subject Mouse (mice); strain: not specified; age: not specified; sex: not specified
Disease model Healthy
Cargo name and characteristics Gadolinium-labeled albumin (Gd-albumin), ~74 kDa protein tracer; Adeno-associated virus (AAV), ~4 MDa viral vector (AAV delivering GFP transgene for transduction)
Route of administration direct brain infusion (intracerebral/intraparenchymal)

Outcomes and Safety

Summary of Outcomes Pre‑conditioning the targeted brain region with focused ultrasound (single‑element transducer) and microbubbles immediately before direct infusion increased distribution of Gd‑albumin at 120 min and significantly enhanced AAV transduction volume in vivo. The successful parameter was pre‑infusion FUS with microbubbles (single‑element transducer; sonication performed immediately prior to direct infusion).
Duration of biological effect 120 min
Safety-related matter The paper does not report any safety data or mention adverse effects; no adverse events were noted.

Brain Region

Visualization unavailable

Ultrasound Parameters

Focal Characteristics Focal depth: None; Focal length: None; Aperture size: None
Treatment frequency single session

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