Examples of general-purpose, scalable actuators based on engineered skeletal muscle. Examples of general-purpose, scalable actuators based on engineered.

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Date of download: 10/13/2017 Copyright © ASME. All rights reserved.
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Examples of general-purpose, scalable actuators based on engineered skeletal muscle. Examples of general-purpose, scalable actuators based on engineered skeletal muscle. Different categories are represented: In vitro grown myooids (A), cantilevers/bridges (B), hydrogels and thin films (C), optogenetically modified cells and bioprinted structures (D), and insect embryonic stem cells (E). (A) Myooid engineered in vitro (top), its cross-sectional area (bottom left), and the peak twitch force recorded (bottom right) (50). Reprinted from (50) with permission from Springer. (B) Systems based on cantilevers/bridges. (B1) Contractile myotube assembled on a microfabricated cantilever (53). Reprinted from (53) with permission from Springer. (B2) Si-MEMS device seeded with skeletal muscle cells are able to contract after their differentiation in myotubes (54). Reprinted from (54) with permission from Springer. (B3) One-dimensional PDMS structure populated by myoblasts (55). Reprinted from (55) with permission from the Royal Society of Chemistry. (C) Systems based on engineered hydrogels and thin polymetric substrates. (C1) Ultrathin polylactic acid films cultured with skeletal muscle cells (57). Reprinted from (57) with permission from Springer. (C2) Fibrin gel provided with myotube line patterns and contracted through microelectrode arrays (58). Reprinted from (58) with permission from the Royal Society of Chemistry. (C3) Linear bioactuator based on a 3D rolled PDMS structure cultured with myoblasts (63). (C4) PEDOT/MWCNT sheet cultured with skeletal muscle cells and subjected to crawling-based locomotion (64). (D) Systems based on optogenetically modified cells and bioprinting. (D1) Optogenetically modified skeletal muscle microtissue tethered to elastic force sensors, recording its static and dynamic tension generated after optical stimulation (66). (D2) Top: Modular “ring” design enables ready transfer of skeletal muscle bioactuators to a range of flexible 3D-printed skeletons. Bottom: Light stimulation (left) of an optogenetic muscle-powered biobot drives muscle contraction (middle) and directional locomotion across a substrate (right) (68). (D3) Damaged muscle can self-heal completely within 2 days, restoring bioactuator force production (69). Reprinted from (69) with permission from Wiley. (E) Contractile tissue construct based on larval M. sexta muscle fibers provided with silk sutures and measurement of stress production (73). All images are reproduced or adapted with permission. Leonardo Ricotti et al. Sci. Robotics 2017;2:eaaq0495 Copyright © 2017 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works