用于再现药物药代动力学的微流控芯片多器官系统的最新进展:当前最新技术。

Mateo Gabriel Vasconez Martinez, Martin Frauenlob, Mario Rothbauer
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引用次数: 0

摘要

导言:制造技术和基于 iPSC 的建模技术的进步加快了芯片上器官的整体进展。值得注意的是,多器官系统的进展速度不尽相同,这表明仍有重大技术障碍需要克服,其中可能包括生物学相关性、技术可用性以及整体可及性:我们在此回顾了 SARS-CoV-2 大流行前后在多组织芯片和体细胞芯片领域取得的进展,并回顾了以药理学研究为目的、使用日益复杂的多器官芯片进行的五项精选研究:我们讨论了多器官芯片领域未来和必要的进展,包括如何克服细胞多样性、改进培养条件、模型可移植性以及传感器集成等方面的挑战,以使微系统不仅能在毒物动力学研究中,更重要的是在药效学和动力学研究中涵盖器官间的相互作用。
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An update on microfluidic multi-organ-on-a-chip systems for reproducing drug pharmacokinetics: the current state-of-the-art.

Introduction: Advances in the accessibility of manufacturing technologies and iPSC-based modeling have accelerated the overall progress of organs-on-a-chip. Notably, the progress in multi-organ systems is not progressing with equal speed, indicating that there are still major technological barriers to overcome that may include biological relevance, technological usability as well as overall accessibility.

Areas covered: We here review the progress in the field of multi-tissue- and body-on-a-chip pre and post- SARS-CoV-2 pandemic and review five selected studies with increasingly complex multi-organ chips aiming at pharmacological studies.

Expert opinion: We discuss future and necessary advances in the field of multi-organ chips including how to overcome challenges regarding cell diversity, improved culture conditions, model translatability as well as sensor integrations to enable microsystems to cover organ-organ interactions in not only toxicokinetic but more importantly pharmacodynamic and -kinetic studies.

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