Microtechnology-based organ systems and whole-body models for drug screening

Seung Hwan Lee, Sang Keun Ha, Inwook Choi, Nakwon Choi, Tai Hyun Park, Jong Hwan Sung

Research output: Contribution to journalReview articlepeer-review

21 Scopus citations

Abstract

After drug administration, the drugs are absorbed, distributed, metabolized, and excreted (ADME). Because ADME processes affect drug efficacy, various in vitro models have been developed based on the ADME processes. Although these models have been widely accepted as a tool for predicting the effects of drugs, the differences between in vivo and in vitro systems result in high attrition rates of drugs during the development process and remain a major limitation. Recent advances in microtechnology enable more accurate mimicking of the in vivo environment, where cellular behavior and physiological responses to drugs are more realistic; this has led to the development of novel in vitro systems, known as ”organ-on-a-chip“ systems. The development of organ-on-a-chip systems has progressed to include the reproduction of multiple organ interactions, which is an important step towards ”body-on-a-chip“ systems that will ultimately predict whole-body responses to drugs. In this review, we summarize the application of microtechnology for the development of in vitro systems that accurately mimic in vivo environments and reconstruct multiple organ models.

Original languageEnglish
Pages (from-to)746-756
Number of pages11
JournalBiotechnology Journal
Volume11
Issue number6
DOIs
StatePublished - 1 Jun 2016

Bibliographical note

Publisher Copyright:
Copyright © 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim

Keywords

  • In vitro systems
  • Microfluidics
  • Microtechnology
  • Multiple organ interaction
  • Organ-on-a-chip

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