Development of an in Vitro 3D Tumor Model to Study Therapeutic Efficiency of an Anticancer Drug

被引:105
作者
Shin, Crystal S. [1 ]
Kwak, Bongseop [2 ]
Han, Bumsoo [2 ,3 ]
Park, Kinam [1 ,3 ]
机构
[1] Purdue Univ, Dept Ind & Phys Pharm, W Lafayette, IN 47907 USA
[2] Purdue Univ, Sch Mech Engn, W Lafayette, IN 47907 USA
[3] Purdue Univ, Weldon Sch Biomed Engn, W Lafayette, IN 47907 USA
关键词
3D tumor model; multicellular tumor spheroids; hydrogel; microfluidic channel; drug delivery systems; BREAST-CANCER; MULTICELLULAR SPHEROIDS; CELL-CULTURE; GLUTARALDEHYDE; FABRICATION; GELATIN;
D O I
10.1021/mp300595a
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The importance and advantages of three-dimensional (3D) cell cultures have been well-recognized. Tumor cells cultured in a 3D culture system as multicellular tumor spheroids (MTS) can bridge the gap between in vitro and in vivo anticancer drug evaluations. An in vitro 3D tumor model capable of providing close predictions of in vivo drug efficacy will enhance our understanding, design, and development of better drug delivery systems Here, we developed an in vitro 3D tumor model by adapting the hydrogel template strategy to culture uniformly sized spheroids in a hydrogel scaffold containing microwells. The in vitro 3D tumor model was to closely simulate an in vivo solid tumor and its microenvironment for evaluation of anticancer drug delivery systems. MTS cultured in the hydrogel scaffold are used to examine the effect of culture conditions on the drug responses Free NITS released from the scaffold are transferred to a microfluidic channel to simulate a dynamic in vivo rnicroenvironment. The in vitro 3D tumor model that mimics biologically relevant parameters of in vivo microenvironments such as cell-cell and cell-ECM interactions, and a dynamic environment would be a valuable device to examine efficiency of anticancer drug and targeting specificity. These models have potential to provide in vivo correlated information to improve and optimize drug delivery systems for an effective chemotherapy.
引用
收藏
页码:2167 / 2175
页数:9
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