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Development of Self-assembled Muscle-powered Microdevices

机译:自组装肌肉动力微型设备的开发

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As microcomponents in engineered systems, biological muscles have unique advantages such as large force transduction, utilization of biochemical fuel, and self-assembly from single cells, over other inorganic actuators for biomedical engineering applications. Successful integration of muscles with inorganic fabricated structures and electronics promises the capability of precisely characterizing muscles' mechanical properties and fabricating self-assembled controllable autonomous structures powered by ubiquitous glucose. However, the use of extracted muscle tissue from animals on these devices is impractical and inefficient, as the tissues must be dissected and incorporated into each device by hand with crude interfaces between the biological tissue and inorganic materials. Integration of muscle with fabricated structures would be optimally achieved through self-assembling muscle cells on MEMS. The construction of self-assembled muscle-powered MEMS structures is complicated by the stringent requirements to spatially direct the cell growth, control the tight connection of these differentiated structures with MEMS structures, and enable the cells and the integrated hybrid freedom to move. Conventional and soft photolithography techniques have been extensively employed to pattern the growth of a variety of cell types and investigate their interaction with substrate in the micrometer level. However, all studies are only suitable for patterning static cells on an immobile surface, so a novel system of spatially patterning the contractible cells must be developed to enable the cells and the integrated hybrid devices to be free to move. We present a novel system of self-assembling myocytes on MEMS devices. This system has shown its capability of spatially and selectively directed growth and differentiation of myocytes into single muscle bundles, attachment of these functional bundles to MEMS structures, and the controlled partial release of the resultant hybrid devices. Two groups of self-assembled muscle-MEMS devices, force-measuring cantilevers and muscle-powered microrobots have been created. Here the further detailed studies of this system are discussed, especially the concept of the self-assembly and the material interfacial problems in this system.
机译:作为工程系统中的微组件,与其他用于生物医学工程应用的无机致动器相比,生物肌肉具有独特的优势,例如大的力传导,生物化学燃料的利用以及单细胞的自组装。肌肉与无机制造的结构和电子设备的成功集成有望精确表征肌肉的机械性能,并制造由普遍存在的葡萄糖驱动的自组装可控自主结构。然而,在这些装置上使用从动物中提取的肌肉组织是不切实际且效率低下的,因为必须通过生物组织和无机材料之间的粗糙界面来手工解剖组织并将其结合到每个装置中。通过在MEMS上自组装肌肉细胞,可以最佳地实现肌肉与结构的整合。自组装的肌肉动力MEMS结构的构造由于在空间上指导细胞生长,控制这些差异化结构与MEMS结构的紧密连接以及使细胞和集成的混合自由移动的严格要求而变得复杂。常规和软光刻技术已被广泛采用,以图案化各种细胞类型的生长,并研究它们在微米水平上与底物的相互作用。但是,所有研究仅适用于在固定表面上对静态细胞进行构图,因此必须开发一种在空间上对可收缩细胞进行构图的新颖系统,以使细胞和集成的混合设备能够自由移动。我们提出了一种在MEMS设备上自我组装的心肌细胞的新型系统。该系统显示了其在空间上和选择性地指导心肌细胞生长和分化为单个肌肉束,将这些功能束附着于MEMS结构以及控制所得混合设备部分释放的能力。已经创建了两组自组装的肌肉MEMS设备,测力悬臂和肌肉动力微型机器人。这里讨论了对该系统的进一步详细研究,特别是该系统中的自组装概念和材料界面问题。

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