Facile and rapid generation of 3D chemical gradients within hydrogels for high-throughput drug screening applications

被引:32
作者
Ahadian, Samad [1 ]
Ramon-Azcon, Javier [1 ]
Estili, Mehdi [2 ]
Obregon, Raquel [3 ]
Shiku, Hitoshi [3 ]
Matsue, Tomokazu [1 ,3 ]
机构
[1] Tohoku Univ, WPI Adv Inst Mat Res, Sendai, Miyagi 980, Japan
[2] NIMS, Int Ctr Young Scientists ICYS, Tsukuba, Ibaraki 3050047, Japan
[3] Tohoku Univ, Grad Sch Environm Studies, Sendai, Miyagi 980, Japan
基金
日本学术振兴会;
关键词
Chemical gradients; Dielectrophoresis; Drug release; High-throughput; Hydrogels; ELECTRICAL-STIMULATION; GOLD NANOPARTICLES; CARBON NANOTUBES; CELL; DELIVERY; ORGANIZATION; BIOLOGY; ARRAY; CHIP;
D O I
10.1016/j.bios.2014.03.031
中图分类号
Q6 [生物物理学];
学科分类号
071011 [生物物理学];
摘要
We propose a novel application of dielectrophoresis (DEP) to make three-dimensional (3D) methacrylated gelatin (GelMA) hydrogels with gradients of micro- and nanoparticles. DEP forces were able to manipulate micro- and nanoparticles of different sizes and materials (i.e., C2C12 myoblasts, polystyrene beads, gold microparticles, and carbon nanotubes) within GelMA hydrogels in a rapid and facile way and create 3D gradients of these particles in a microchamber. Immobilization of drugs, such as fluorescein isothiocyanate-dextran (FITC-dextran) and 6-hydroxydopamine (6-OHDA), on gold microparticles allowed us to investigate the high-throughput release of these drugs from GelMA-gold microparticle gradient systems. The latter gradient constructs were incubated with C2C12 myoblasts for 24 h to examine the cell viability through the release of 6-OHDA. The drug was released from the microparticles in a gradient manner, inducing a cell viability gradient. This novel approach to create 3D chemical gradients within hydrogels is scalable to any arbitrary length scale. It is useful for making anisotropic biomimetic materials and high-throughput platforms to investigate cell-microenvironment interactions in a rapid, simple, cost-effective, and reproducible manner. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:166 / 173
页数:8
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