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Automated fabrication of a scalable heart-on-a-chip device by 3D printing of thermoplastic elastomer nanocomposite and hot embossing

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摘要 The successful translation of organ-on-a-chip devices requires the development of an automated workflow for device fabrication, which is challenged by the need for precise deposition of multiple classes of materials in micro-meter scaled configurations. Many current heart-on-a-chip devices are produced manually, requiring the expertise and dexterity of skilled operators. Here, we devised an automated and scalable fabrication method to engineer a Biowire II multiwell platform to generate human iPSC-derived cardiac tissues. This high-throughput heart-on-a-chip platform incorporated fluorescent nanocomposite microwires as force sensors, produced from quantum dots and thermoplastic elastomer, and 3D printed on top of a polystyrene tissue culture base patterned by hot embossing. An array of built-in carbon electrodes was embedded in a single step into the base, flanking the microwells on both sides. The facile and rapid 3D printing approach efficiently and seamlessly scaled up the Biowire II system from an 8-well chip to a 24-well and a 96-well format, resulting in an increase of platform fabrication efficiency by 17,5000-69,000% per well. The device’s compatibility with long-term electrical stimulation in each well facilitated the targeted generation of mature human iPSC-derived cardiac tissues, evident through a positive force-frequency relationship, post-rest potentiation, and well-aligned sarcomeric apparatus. This system’s ease of use and its capacity to gauge drug responses in matured cardiac tissue make it a powerful and reliable platform for rapid preclinical drug screening and development.
出处 《Bioactive Materials》 SCIE CSCD 2024年第3期46-60,共15页 生物活性材料(英文)
基金 funded by the Natural Sciences and Engineering Research Council of Canada(NSERC)Discovery Grant(RGPIN 326982-10) NSERC Strategic Grant(STPGP 506689-17) Canadian Institutes of Health Research(CIHR)Foundation Grant FDN-167274 National Institutes of Health Grant 2R01 HL076485 and Canada Foundation for Innovation Project 36442 along with the associated Ontario Research Fund Grant.M R is supported by Canada Research Chairs and Killam Fellowship.Q W is supported by CIHR,the Centre for Research and Applications in Fluidic Technologies(CRAFT) NSERC CREATE Training Program in Organ-on-a-Chip Engineering and Entrepreneurship(TOeP)Fellowships。
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