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Three laryngeal models were used to investigate the aerodynamic and elastic properties of vocal fold vibration: cadaveric human, excised canine, and synthetic silicone vocal folds. The aim was to compare the characteristics of these models to enhance our understanding of phonatory mechanisms. Flow and medial glottal wall geometry were acquired via particle image velocimetry. Elastic properties were assessed from force–displacement tests. Relatively, the human larynges had higher fundamental frequency values, while canine and synthetic models exhibited greater flow rates. Canine models demonstrated the highest divergence angles and vertical stiffness gradients followed by the human model, both displaying flow separation vortices during closing. Synthetic models, whose advantage is their accessibility and repeatability, displayed the lowest glottal divergence angles and total circulation values compared to tissue models with no flow separation vortices. The elasticity tests revealed that tissue models showed significant hysteresis and vertical stiffness gradients, unlike the synthetic models. These results underscore the importance of model selection based on specific research needs and highlight the potential of canine and synthetic models for controlled experimental studies in phonation.

The vocal folds (VFs) are constantly exposed to mechanical stimulation leading to changes in biomechanical properties, structure, and composition. The development of long-term strategies for VF treatment depends on the characterization of related cells, biomaterials, or engineered tissues in a controlled mechanical environment. Our aim was to design, develop, and characterize a scalable and high-throughput platform that mimics the mechanical microenvironment of the VFs in vitro. The platform consists of a 24-well plate fitted with a flexible membrane atop a waveguide equipped with piezoelectric speakers which allows for cells to be exposed to various phonatory stimuli. The displacements of the flexible membrane were characterized via Laser Doppler Vibrometry (LDV). Human VF fibroblasts and mesenchymal stem cells were seeded, exposed to various vibratory regimes, and the expression of pro-fibrotic and pro-inflammatory genes was analyzed. Compared to current bioreactor designs, the platform developed in this study can incorporate commercial assay formats ranging from 6- to 96-well plates which represents a significant improvement in scalability. This platform is modular and allows for tunable frequency regimes.