Transdermal permeation is often restricted by the stratum corneum, necessitating either chemical enhancers or wired sonophoresis hardware. A compact, flexible, laser-activated cavitation patch that converts nanosecond optical pulses into mid-frequency (≈100 kHz) ultrasound, generating inertial cavitation in a 1 mm-deep micro-reservoir directly above the skin, is demonstrated. A 50 nm gold (Au) film on a quartz disc serves as an opto-acoustic transducer and is encapsulated in an elastomer scaffold that conforms to curved surfaces, sealing the drug reservoir. Multiphysics modeling predicts peak pressures of ≈3 MPa at the laser focus and greater than 0.2 MPa at a 3 millimeter tissue depth; hydrophone and high-speed videography corroborate these values. Ex vivo porcine-skin assays show that a 3-minute exposure at 290 mW increases the cumulative flux of niacinamide eight- to tenfold and extends its penetration depth to ≈450 microns. At the same time, vitamin C reaches ≈650 microns with a temperature increase limited to below 3 °C. The battery-free architecture, sub-cm2 drug induction sites, and raster-scan free wide area scalable delivery system fabrication position the device as a promising platform for on-demand dermatological therapy and precision cosmeceutical delivery.

Plasmon‐Mediated Transdermal Ultrasonic Photo‐Elastic Patch for Efficient Drug Delivery

Roberto Caputo;
2025-01-01

Abstract

Transdermal permeation is often restricted by the stratum corneum, necessitating either chemical enhancers or wired sonophoresis hardware. A compact, flexible, laser-activated cavitation patch that converts nanosecond optical pulses into mid-frequency (≈100 kHz) ultrasound, generating inertial cavitation in a 1 mm-deep micro-reservoir directly above the skin, is demonstrated. A 50 nm gold (Au) film on a quartz disc serves as an opto-acoustic transducer and is encapsulated in an elastomer scaffold that conforms to curved surfaces, sealing the drug reservoir. Multiphysics modeling predicts peak pressures of ≈3 MPa at the laser focus and greater than 0.2 MPa at a 3 millimeter tissue depth; hydrophone and high-speed videography corroborate these values. Ex vivo porcine-skin assays show that a 3-minute exposure at 290 mW increases the cumulative flux of niacinamide eight- to tenfold and extends its penetration depth to ≈450 microns. At the same time, vitamin C reaches ≈650 microns with a temperature increase limited to below 3 °C. The battery-free architecture, sub-cm2 drug induction sites, and raster-scan free wide area scalable delivery system fabrication position the device as a promising platform for on-demand dermatological therapy and precision cosmeceutical delivery.
2025
Ultrasonic, Biosensor, Drug delivery
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.11770/399368
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