Ultrasound-Responsive Microdroplets for Multi-Drug Delivery Applications

This work explores the controlled release of multiple drugs through ultrasound(US)-responsive perfluorocarbon (PFC) droplets, using acoustic droplet vaporization. Two types of PFC droplets were studied, both with a perfluoropentane core containing fluorescein sodium salt, but with different shell compositions: lipid-based and surfactant-based. Microfluidics was used for synthesis, and low-intensity pulsed US (38 kHz, 20%, 100 Hz, 5 min) was applied at 25–125 kPa. Morphological changes were analyzed by Hirox microscopy; drug release was quantified with the Victor Nivo system. At 50 kPa, lipid-shelled droplets ruptured and released 28% of their content, while surfactant-shelled droplets remained intact. Efficient release from surfactant droplets (33%) required 100 kPa. These results show that different activation thresholds enable sequential, pressure-controlled release of two drugs. This approach may support the future development of US-responsive patches or scaffolds for multi-drug delivery.

Publication Details

Journal
Electronic Theses and Dissertations Repository (University of Pisa)
Published
2025-05-31
Primary Topic
Ultrasound and Hyperthermia Applications
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Ultrasound-Responsive Microdroplets for Multi-Drug Delivery Applications

Electronic Theses and Dissertations Repository (University of Pisa)
Ultrasound and Hyperthermia Applications
article

Ultrasound-Responsive Microdroplets for Multi-Drug Delivery Applications

article en

Abstract

This work explores the controlled release of multiple drugs through ultrasound(US)-responsive perfluorocarbon (PFC) droplets, using acoustic droplet vaporization. Two types of PFC droplets were studied, both with a perfluoropentane core containing fluorescein sodium salt, but with different shell compositions: lipid-based and surfactant-based. Microfluidics was used for synthesis, and low-intensity pulsed US (38 kHz, 20%, 100 Hz, 5 min) was applied at 25–125 kPa. Morphological changes were analyzed by Hirox microscopy; drug release was quantified with the Victor Nivo system. At 50 kPa, lipid-shelled droplets ruptured and released 28% of their content, while surfactant-shelled droplets remained intact. Efficient release from surfactant droplets (33%) required 100 kPa. These results show that different activation thresholds enable sequential, pressure-controlled release of two drugs. This approach may support the future development of US-responsive patches or scaffolds for multi-drug delivery.

Electronic Theses and Dissertations Repository (University of Pisa)
Good health and well-being
Openalex Percentile: Top 52%
Ultrasound and Hyperthermia Applications
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.