Pitt Shield

Polymeric perfluorocarbon nanoemulsions are ultrasound-activated wireless drug infusion catheters.

Authors: Zhong Q, Yoon BC, Aryal M, Wang JB, Ilovitsh T, Baikoghli MA, Hosseini-Nassab N, Karthik A, Cheng RH, Ferrara KW, Airan RD

Catheter-based intra-arterial drug therapies have proven effective for a range of oncologic, neurologic, and cardiovascular applications. However, these procedures are limited by their invasiveness and relatively broad drug spatial distribution. The ideal technique for local pharmacotherapy would be noninvasive and would flexibly deliver a given drug to any region of the body with high spatial and temporal precision. Combining polymeric perfluorocarbon nanoemulsions with existent clinical focused ultrasound systems could in principle meet these needs, but it has not been clear whether these nanoparticles could provide the necessary drug loading, stability, and generalizability across a range of drugs, beyond a few niche applications. Here, we develop polymeric perfluorocarbon nanoemulsions into a generalized platform for ultrasound-targeted delivery of hydrophobic drugs with high potential for clinical translation. We demonstrate that a wide variety of drugs may be effectively uncaged with ultrasound using these nanoparticles, with drug loading increasing with hydrophobicity. We also set the stage for clinical translation by delineating production protocols that are scalable and yield sterile, stable, and optimized ultrasound-activated drug-loaded nanoemulsions. Finally, we exhibit a new potential application of these nanoemulsions for local control of vascular tone. This work establishes the power of polymeric perfluorocarbon nanoemulsions as a clinically-translatable platform for efficacious, noninvasive, and localized ultrasonic drug uncaging for myriad targets in the brain and body.

Introduction

Purpose Drug delivery WITHOUT BBB opening
Study Objective To develop polymeric perfluorocarbon nanoemulsions as a scalable, sterile, and generalizable platform for ultrasound-targeted noninvasive uncaging of hydrophobic drugs for localized therapy.
Animal model / Human subject Long Evans rats
Targeted brain region(s) Lower Abdominal Aorta, Frontal Cortex
Target coordinates 7 mm anterior to interaural line; 2mm lateral of midline
Cargo name and characteristics Propofol; nicardipine; doxorubicin
Route of administration Intravenous

Outcomes and Safety

Summary of Outcomes Polymeric perfluorocarbon nanoemulsions enable ultrasound-triggered uncaging of a wide variety of hydrophobic drugs (with drug loading increasing with hydrophobicity), provide noninvasive, localized control of vascular tone, and can be produced in scalable, sterile, and stable formulations suitable for clinical translation.
Safety-related matter No adverse effects or safety concerns are reported in the provided text; the authors state the production protocols yield sterile, stable nanoemulsions and indicate potential for clinical translation.

Brain Region

Ultrasound Parameters

Ultrasound instrument Focused ultrasound transducer (Image Guided Therapy, Pessac, France)
FUS Frequency 650 kHz
FUS Pressure 1.5 Mpa
FUS Mode pulsed
Pulse duration 50 ms
Duration of a single FUS session 4 min
Focal Characteristics Focal depth: None; Focal length: None; Aperture size: None
Treatment frequency Single

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