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Costas Arvanitis

Publications and source records attributed to Costas Arvanitis.

3 recordsLinked to original sources

A CMUT-Based Transcranial Focused Ultrasound Platform for Blood-Brain Barrier Opening in Small Animal Models

Drug delivery to the brain is limited by the blood-brain barrier (BBB). We developed a capacitive micromachined ultrasonic transducer (CMUT)-based transcranial focused ultrasound system capable of both delivering therapy via BBB opening and monitoring microbubble activity across a broad frequency range. The performance of the geometrically focused half-ring array consisting of five transmitters and one receiving element was first assessed through simulations and in-vitro acoustic measurements with microbubbles. Use of phase-inversion (PI) during transmission effectively suppressed CMUT-generated harmonics and enhanced broadband detection of microbubble emissions. In rats, the same system achieved spatially localized BBB opening, confirmed by T1-weighted magnetic resonance imaging. BBB permeability mapping using dynamic contrast-enhanced magnetic resonance imaging (Ktrans) scaled with pressure. Time-resolved acoustic spectra captured microbubble arrival and decay kinetics, and 7-20dB enhancement in the effective dynamic range is observed with PI processing of acoustic emission signals. Together, these findings establish an integrated CMUT platform for combined therapeutic and sensing applications for BBB opening in small animal models, providing a foundation for future real-time, frequency-agile, closed-loop control of ultrasound-mediated drug delivery to the brain.

physics.med-ph

Quantitative acoustic monitoring of ensembles of weakly nonlinear microbubble oscillations in optically inaccessible environments

A growing class of ultrasound-mediated diagnostic and therapeutic technologies, including sonoporation and blood-brain barrier modulation, relies on microbubble contrast agents, where precise control of microbubble dynamics governs biological responses, efficiency, and safety. However, quantitative monitoring of microbubble oscillations in the stable, weakly nonlinear regime remains challenging, particularly in optically opaque and deep-tissue environments. Here, we introduce a linear acoustic wave propagation and superposition (LAWPS) framework that reconstructs microbubble radius-time dynamics directly from passively recorded acoustic emissions. By coupling Fourier-series representations of weakly nonlinear oscillations with linear monopole radiation theory, LAWPS extends classical monopole models to establish a reversible relationship between multi-frequency acoustic emissions and underlying radial bubble dynamics. Extending this framework to monodisperse microbubble ensembles, we derive optimal excitation and receive configurations and population-level correction factors that enable quantitative reconstruction of the ensemble-averaged microbubble dynamics. Using simultaneous optical and acoustic measurements, we demonstrate recovery of microbubble oscillations with ~5% relative error for oscillation amplitudes up to ~15% of equilibrium radius. Finally, we show that oscillations within the framework's operating regime (20% oscillation) generate sonoporation-relevant mechanical stress in vesicles as small as 10 micrometers (capillary number > 0.01), under physiologically relevant conditions. Together, this work establishes a quantitative framework for acoustic emission-based monitoring of weakly nonlinear microbubble oscillations in clinically relevant, optically inaccessible environments to enable improved control of emerging ultrasound diagnostic and therapeutic technologies.

physics.ins-det

Morphological Reconstruction Improves Microvessel Mapping in Super-Resolution Ultrasound

Generation of super-resolution (SR) ultrasound (US) images, created from the successive local-ization of individual microbubbles in the circulation, has enabled the visualization of microvascular structure and flow at a level of detail that was not possible previously. Despite rapid progress, tradeoffs between spatial and temporal resolution may challenge the translation of this promising technology to the clinic. To temper these trade-offs, we propose a method based on morphological image reconstriction. This method can extract from ultrafast contrast-enhanced ultrasound (CEUS) images hundreds of microbubble peaks per image (312-by-180 pixels) with intensity values varying by an order of magnitude. Specifically, it offers a fourfold increase in the number of peaks detected per frame, requires on the order of 100 ms for processing, and is robust to additive electronic noise (down to 3.6 dB CNR in CEUS images). By integrating this method to a SR framework we demonstrate a 6-fold improvement in spatial resolution, as compared to CEUS, in imaging chicken embryo microvessels. This method that is computationally efficient and, thus, scalable to large data sets, may augment the abilities of SR-US in imaging microvascular structure and function.

eess.IV