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Multi-timescale Microscopy Methods for the Characterization of Fluorescently-labeled Microbubbles for Ultrasound-Triggered Drug Release
Published on: June 12, 2021
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Ultrasound triggered drug delivery with liposomal nested microbubbles
1Department of Chemical Engineering, Drexel University, 3141 Chestnut St, Philadelphia, PA 19104, United States.
Ultrasonics
|July 9, 2015
Summary
Ultrasound contrast microbubbles within liposomes enable triggered drug release. Microbubble cavitation damages liposomes, releasing their contents, with release rates dependent on ultrasound pressure.
Area of Science:
- Biomaterials Science
- Acoustic Engineering
- Drug Delivery Systems
Background:
- Liposomes are widely used for drug delivery due to their biocompatibility.
- Controlled release of encapsulated drugs from liposomes remains a challenge.
- Ultrasound contrast agents offer potential for triggered therapeutic applications.
Purpose of the Study:
- To investigate the triggered release of liposomal contents using ultrasound contrast agent microbubbles.
- To characterize the mechanisms of liposome membrane disruption by microbubble cavitation.
- To determine the influence of ultrasound parameters on drug release kinetics.
Main Methods:
- Encapsulation of ultrasound contrast agent microbubbles within liposomes.
- Exposure of liposomes to focused ultrasound (1 MHz) at varying pressures.
- Quantification of aqueous core release using fluorescence assays.
- Qualitative assessment of membrane integrity via optical microscopy.
Main Results:
- Triggered release of liposomal contents was dependent on the presence of microbubbles.
- Two distinct release regimes were observed based on ultrasound pressure.
- High pressures (2.1-3.7 MPa) induced rapid release and permanent membrane damage.
- Low pressures (0.54-1.7 MPa) resulted in slower release, dilation, and temporary poration.
Conclusions:
- Microbubble-mediated ultrasound cavitation provides a viable method for triggered liposomal drug release.
- Ultrasound pressure is a critical parameter controlling the rate and extent of liposome membrane disruption.
- This approach holds promise for targeted and controlled drug delivery applications.
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