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Labib, S.

Publications and source records attributed to Labib, S..

2 recordsLinked to original sources

Machine learning-based optimization of a single-element transcranial focused ultrasound transducer for deep brain neuromodulation in mice

Transcranial focused ultrasound is an emerging noninvasive neuromodulation technique that offers high spatial precision and the potential for deep brain penetration. However, due to skull-induced attenuation and acoustic aberrations, precisely stimulating deep brain regions in mice remains challenging. To address this challenge, this study introduces a machine-learning-based computational framework to optimize single-element transducer designs for accurate deep-brain targeting in a mouse model. This framework includes a surrogate model consisting of a Random Forest regressor and classifier, trained on acoustic simulation results to predict performance from design parameters. A total of 72 transducer designs were simulated across coronal and sagittal planes, systematically varying frequency (1-6 MHz), radius of curvature (5-7 mm), and f-number (0.58-1.0). Each design was evaluated using five performance metrics: focal length, focal shape, maximum pressure at the focal region, pressure maximum location, and sidelobe suppression. The surrogate models were then combined with the Non-Dominated Sorting Genetic Algorithm II (NSGA-II) to perform multi-objective optimization and identify high-performing transducer designs. The optimized design produced a compact, symmetric focal region and accurate energy delivery to deep targets, with minimal off-target exposure, even in complex skull anatomy. Results show that lower f-numbers, moderate radius of curvature, and higher frequencies facilitate precise deep brain targeting. Overall, this data-driven approach enables practical design of single-element transducers for deep-brain neuromodulation in mice and provides a framework for designing transcranial transducers for other brain targets, potentially accelerating the clinical translation of focused ultrasound technologies.

bioengineering↗

Cartilage-penetrating hyaluronic acid hydrogel preserves tissue content and reduces chondrocyte catabolism

Articular cartilage injuries have a limited healing capacity and, due to inflammatory and catabolic activities, often experience progressive degeneration towards osteoarthritis. Current repair techniques generally provide short-term symptomatic relief; however, the regeneration of hyaline cartilage remains elusive, leaving both the repair tissue and surrounding healthy tissue susceptible to long-term wear. Therefore, methods to preserve cartilage following injury, especially from matrix loss and catabolism, are needed to delay, or even prevent, the deteriorative process. The goal of this study was to develop and evaluate a cartiage-penetrating hyaluronic-acid (HA) hydrogel to improve damaged cartilage biomechanics and prevent tissue degeneration. At time zero, the HA-based hydrogel provided a 46.5% increase in compressive modulus and a decrease in permeability after simulated degeneration of explants (collagenase application). Next, in a degenerative culture model (interleukin-1 {beta} [IL-1{beta}] for 2 weeks), hydrogel application prior to or midway through the culture mitigated detrimental changes to compressive modulus and permeability observed in non-treated explants. Furthermore, localized loss of proteoglycan was observed in degenerative culture conditions alone (non-treated), but hydrogel administration significantly improved the retention of matrix elements. Finally, NITEGE staining and gene expression analysis showed the ability of the HA gel to decrease chondrocyte catabolic activity. These results highlight the importance of reinforcing damaged cartilage with a biomaterial system to both preserve tissue content and reduce catabolism associated with injury and inflammation.

bioengineering↗