Openable artificial intestinal tract device integrated with a permeable filter for evaluating drug permeation through cells

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作者
Satoshi Konishi
Shingo Ishibashi
Shiho Shimizu
Keita Watanabe
Rodi Abdalkader
Takuya Fujita
机构
[1] Ritsumeikan University,Department of Mechanical Engineering, College of Science and Engineering
[2] Ritsumeikan University,Graduate Course of Science and Engineering
[3] Ritsumeikan Advanced Research Academy,Ritsumeikan Global Innovation Research Organization
[4] Ritsumeikan University,Graduate School of Pharmaceutical Sciences
[5] Ritsumeikan University,Department of Pharmaceutical Sciences
[6] Ritsumeikan University,undefined
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Scientific Reports | / 13卷
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摘要
Organs-on-chips using cultured cells have been developed and applied for evaluating in vitro biological phenomena. We previously reported an openable artificial intestinal tract system, as an in vitro model of the small intestine, for in vitro drug screening. The intestinal tract device could be transformed using an integrated artificial muscle actuator. An initial flat state was suitable for cell culture, and the transformed tubular structure was used as a fluidic channel for perfusion tests. The previously developed intestinal tract system could be used to evaluate drug absorption by cells through perfusion testing. This study presents an improved artificial intestinal tract system for analysis of drug permeation, in addition to absorption. Permeable filters were integrated into the intestinal tract device. Integration of additional filters into the design of the existing artificial muscle actuator was accomplished by considering device performance and available filter locations. Filter permeability was evaluated by perfusion testing. MDCK-II cells were cultured on the device and visually and electrically evaluated. The openable device, equipped with new functions for further pharmacokinetic analysis, could perform and evaluate drug disposition using cultured cells. We anticipate that the improved, openable organ-on-a-chip device system will contribute to advances in in vitro drug screening technology.
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