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Tzung K. Hsiai

Publications and source records attributed to Tzung K. Hsiai.

2 recordsLinked to original sources

Electrically functionalized body surface for deep-tissue bioelectrical recording

Directly probing deep tissue activities from body surfaces offers a noninvasive approach to monitoring essential physiological processes1-3. However, this method is technically challenged by rapid signal attenuation toward the body surface and confounding motion artifacts4-6 primarily due to excessive contact impedance and mechanical mismatch with conventional electrodes. Herein, by formulating and directly spray coating biocompatible two-dimensional nanosheet ink onto the human body under ambient conditions, we create microscopically conformal and adaptive van der Waals thin films (VDWTFs) that seamlessly merge with non-Euclidean, hairy, and dynamically evolving body surfaces. Unlike traditional deposition methods, which often struggle with conformality and adaptability while retaining high electronic performance, this gentle process enables the formation of high-performance VDWTFs directly on the body surface under bio-friendly conditions, making it ideal for biological applications. This results in low-impedance electrically functionalized body surfaces (EFBS), enabling highly robust monitoring of biopotential and bioimpedance modulations associated with deep-tissue activities, such as blood circulation, muscle movements, and brain activities. Compared to commercial solutions, our VDWTF-EFBS exhibits nearly two-orders of magnitude lower contact impedance and substantially reduces the extrinsic motion artifacts, enabling reliable extraction of bioelectrical signals from irregular surfaces, such as unshaved human scalps. This advancement defines a technology for continuous, noninvasive monitoring of deep-tissue activities during routine body movements.

physics.med-ph↗

Optimal occlusion uniformly partitions red blood cells fluxes within a microvascular network

In animals, gas exchange between blood and tissues occurs in narrow vessels, whose diameter is comparable to that of a red blood cell. Red blood cells must deform to squeeze through these narrow vessels, transiently blocking or occluding the vessels they pass through. Although the dynamics of vessel occlusion have been studied extensively, it remains an open question why microvessels need to be so narrow. We study occlusive dynamics within a model microvascular network: the embryonic zebrafish trunk. We show that pressure feedbacks created when red blood cells enter the finest vessels of the trunk act together to uniformly partition red blood cells through the microvasculature. Using mathematical models as well as direct observation, we show that these occlusive feedbacks are tuned throughout the trunk network to prevent the vessels closest to the heart from short-circuiting the network. Thus occlusion is linked with another open question of microvascular function: how are red blood cells delivered at the same rate to each micro-vessel? Our analysis shows that tuning of occlusive feedbacks increase the total dissipation within the network by a factor of 11, showing that uniformity of flows rather than minimization of transport costs may be prioritized by the microvascular network.

q-bio.TO↗