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微流控多器官芯片系统在重现药物药代动力学方面的最新进展:当前的技术水平。

An update on microfluidic multi-organ-on-a-chip systems for reproducing drug pharmacokinetics: the current state-of-the-art.

机构信息

CellChipGroup, Institute of Applied Synthetic Chemistry, Technische Universitaet Wien, Vienna, Austria.

Karl Chiari Lab for Orthopaedic Biology, Department of Orthopedics and Trauma Surgery, Medical University of Vienna, Vienna, Austria.

出版信息

Expert Opin Drug Metab Toxicol. 2024 Jun;20(6):459-471. doi: 10.1080/17425255.2024.2362183. Epub 2024 Jun 4.

Abstract

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.

摘要

简介

制造技术和基于 iPSC 的建模的可及性的进步加速了器官芯片的整体进展。值得注意的是,多器官系统的进展并没有以相同的速度进行,这表明仍然存在需要克服的重大技术障碍,其中可能包括生物学相关性、技术可用性以及整体可及性。

涵盖领域

我们在此回顾了 SARS-CoV-2 大流行前后多组织和整体器官芯片领域的进展,并回顾了五项具有越来越复杂的多器官芯片的选定研究,这些研究旨在进行药理学研究。

专家意见

我们讨论了多器官芯片领域的未来和必要进展,包括如何克服细胞多样性、改善培养条件、模型可转化性以及传感器集成方面的挑战,以实现微系统不仅在毒代动力学方面,而且更重要的是在药效动力学和动力学研究中涵盖器官间相互作用。

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