Volume 106, Issue 2 pp. 780-786
Original Research Report

A self-deploying drug release device using polymeric films

Taro Kondo

Taro Kondo

Department of Finemechanics, Graduate School of Engineering, Tohoku University, Sendai, 980-8579 Japan

Both authors contributed equally to this work.

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Zhaleh Kashkouli Nezhad

Zhaleh Kashkouli Nezhad

Division of Clinical Cell Therapy, United Centers for Advanced Research and Translational Medicine (ART), Tohoku University Graduate School of Medicine, Sendai, 980-8575 Japan

Both authors contributed equally to this work.

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Jin Suzuki

Jin Suzuki

Department of Finemechanics, Graduate School of Engineering, Tohoku University, Sendai, 980-8579 Japan

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Nobuhiro Nagai

Nobuhiro Nagai

Division of Clinical Cell Therapy, United Centers for Advanced Research and Translational Medicine (ART), Tohoku University Graduate School of Medicine, Sendai, 980-8575 Japan

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Matsuhiko Nishizawa

Matsuhiko Nishizawa

Department of Finemechanics, Graduate School of Engineering, Tohoku University, Sendai, 980-8579 Japan

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Toshiaki Abe

Toshiaki Abe

Division of Clinical Cell Therapy, United Centers for Advanced Research and Translational Medicine (ART), Tohoku University Graduate School of Medicine, Sendai, 980-8575 Japan

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Hirokazu Kaji

Corresponding Author

Hirokazu Kaji

Department of Finemechanics, Graduate School of Engineering, Tohoku University, Sendai, 980-8579 Japan

Correspondence to: H. Kaji; e-mail: [email protected]Search for more papers by this author
First published: 29 March 2017
Citations: 4

Abstract

Herein, we report a sheet-type device capable of self-deployment and sustained release of protein type drugs. The device consisted of a thin photopolymerized polyethylene glycol dimethacrylate (PEGDM) sheet and collagen microparticles (COLs), which were embedded in the sheet as drug carriers and for increased drug permeation. When the density of the COLs in the sheet was increased to be sufficiently interconnected, the drug permeability was increased. In addition, since protein type drugs electrostatically interacted with the COLs, a prolonged sustained release was possible. The PEGDM/COLs device was flexible enough to be rolled up, and the device maintained its structure due to van der Waals attractive forces between the sheet surfaces. When the device was immersed in water, the attractive forces acting between the sheet surfaces were relieved by water. Subsequently, the device unfolded by bending-stress relaxation. Moreover, the rolled-up device could be injected through a conventional syringe needle into water to recover its original shape. The developed sheet-type device provides the possibility of minimally invasive transplantation into diseased tissues and organs, and could provide better therapeutic outcomes and reduce possible side effects. © 2017 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater, 106B: 780–786, 2018.

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