Pitt Shield

Fabricating and Labeling Microbubbles with Fluorescent and Radioactive Tracers.

Authors: Rajora MA, Leung C, Chen J, Zheng G

Microbubbles are lipid-shelled, gas-filled particles that have evolved from vascular ultrasound contrast agents into revolutionary cancer therapy platforms. When combined with therapeutic focused ultrasound (FUS), they can safely and locally overcome physiological barriers (e.g., blood-brain barrier), deliver drugs to otherwise inaccessible cancers (e.g., glioblastoma and pancreatic cancer), and treat neurodegenerative diseases. The therapeutic arsenal of microbubble-FUS is advancing in new directions, including synergistic combination radiotherapy, multimodal imaging, and all-in-one drug loading and delivery from microbubble shells. Labeling microbubbles with radiotracers is key to establishing these expanded theranostic capabilities. However, existing microbubble radiolabeling strategies rely on purification methodologies known to perturb microbubble physicochemical properties, use short-lived radioisotopes, and do not always yield stable chelation. Collectively, this creates ambiguity surrounding the accuracy of microbubble radioimaging and the efficiency of tumor radioisotope delivery. This protocol describes a new one-pot, purification-free microbubble labeling methodology that preserves microbubble physicochemical properties while achieving >95% radioisotope chelation efficiency. It is versatile and can be applied successfully across custom and commercial microbubble formulations with differing acyl lipid chain length, charge, and chelator/probe (porphyrin, DTPA, DiI) composition. It can be adaptively applied during ground-up microbubble fabrication and to pre-made microbubble formulations with modular customizability of fluorescence and multimodal fluorescence/radioactive properties. Accordingly, this flexible method enables the production of tailored, traceable (radio, fluorescent, or radio/fluorescent active) multimodal microbubbles that are useful for advancing mechanistic, imaging, and therapeutic microbubble-FUS applications.

Introduction

Purpose Other
Study Objective To develop and describe methods for fabricating microbubbles and labeling them with fluorescent and radioactive tracers.
Animal model / Human subject not specified
Disease model cancers
MRI or image guidance method Not specified
Targeted brain region(s) Not Specified
Target coordinates Not provided
Cargo name and characteristics neurodegenerative disease drugs
Route of administration not specified

Outcomes and Safety

Summary of Outcomes The study established methods to fabricate and label microbubbles with fluorescent and radioactive tracers for imaging/tracking applications.
Duration of biological effect not specofied
Safety-related matter No safety issues or adverse effects are mentioned in the provided text.

Brain Region

Ultrasound Parameters

Ultrasound instrument Not provided
FUS Frequency Not provided
FUS Intensity Not provided
FUS Pressure Not provided
FUS Mode Not provided
Pulse duration Not provided
Duration of a single FUS session Not provided
Focal Characteristics Not provided
Treatment frequency Not specified

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