A Review of Three-Dimensional In Vitro Tissue Models for Drug Discovery and Transport Studies

被引:345
作者
Elliott, Nelita T. [1 ]
Yuan, Fan [1 ]
机构
[1] Duke Univ, Dept Biomed Engn, Durham, NC 27708 USA
基金
美国国家科学基金会;
关键词
in vitro models; tissue engineering; transport; cancer; cell culture; MAMMARY EPITHELIAL-CELLS; HUMAN CORNEAL EQUIVALENT; HEPATIC STELLATE CELLS; MESENCHYMAL STEM-CELLS; HUMAN LIVER-CELLS; MULTICELLULAR TUMOR SPHEROIDS; SKELETAL-MUSCLE CONSTRUCTS; FIBER BIOARTIFICIAL LIVER; LONG-TERM CULTURE; NORMAL RAT-LIVER;
D O I
10.1002/jps.22257
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The use of animal models in drug discovery studies presents issues with feasibility and ethical concerns. To address these limitations, in vitro tissue models have been developed to provide a means for systematic, repetitive, and quantitative investigation of drugs. By eliminating or reducing the need for animal subjects, these models can serve as platforms for more tightly controlled, high-throughput screening of drugs and for pharmacokinetic and pharmacodynamic analyses of drugs. The focus of this review is three-dimensional (3D) tissue models that can capture cell-cell and cell-matrix interactions. Compared to the 2D culture of cell monolayers, 3D models more closely mimic native tissues since the cellular microenvironment established in the 3D models often plays a significant role in disease progression and cellular responses to drugs. A growing body of research has been published in the literature, which highlights the benefits of the 3D in vitro models of various tissues. This review provides an overview of some successful 3D in vitro models that have been developed to mimic liver, breast, cardiac, muscle, bone, and corneal tissues as well as malignant tissues in solid tumors. (C) 2010 Wiley-Liss, Inc. and the American Pharmacists Association J Pharm Sci 100:59-74, 2011
引用
收藏
页码:59 / 74
页数:16
相关论文
共 204 条
[1]   Construction of a complete rabbit cornea substitute using a fibrin-agarose scaffold [J].
Alaminos, Miguel ;
Del Carmen Sanchez-Quevdo, Maria ;
Munoz-Avila, Jose Ignacio ;
Serrano, Daniel ;
Medialdea, Santiago ;
Carreras, Ignacio ;
Campos, Antonio .
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2006, 47 (08) :3311-3317
[2]   Design of tissue engineering scaffolds as delivery devices for mechanical and mechanically modulated signals [J].
Anderson, Eric J. ;
Knothe, Melissa L. .
TISSUE ENGINEERING, 2007, 13 (10) :2525-2538
[3]   FORMATION OF EXTRACELLULAR-MATRIX IN NORMAL RAT-LIVER - LIPOCYTES AS A MAJOR SOURCE OF PROTEOGLYCAN [J].
ARENSON, DM ;
FRIEDMAN, SL ;
BISSELL, DM .
GASTROENTEROLOGY, 1988, 95 (02) :441-447
[4]   A three-dimensional in vitro model system to study the adaptation of craniofacial skeletal muscle following mechanostimulation [J].
Auluck, A ;
Mudera, V ;
Hunt, NP ;
Lewis, MP .
EUROPEAN JOURNAL OF ORAL SCIENCES, 2005, 113 (03) :218-224
[5]  
Auth M K, 1998, Transpl Int, V11 Suppl 1, pS439, DOI 10.1007/s001470050516
[6]   3-D coculture of hepatic sinusoidal cells with primary hepatocytes - Design of an organotypical model [J].
Bader, A ;
Knop, E ;
Kern, A ;
Boker, K ;
Fruhauf, N ;
Crome, O ;
Esselmann, H ;
Pape, C ;
Kempka, G ;
Sewing, KF .
EXPERIMENTAL CELL RESEARCH, 1996, 226 (01) :223-233
[7]   RECONSTRUCTION OF LIVER-TISSUE IN-VITRO - GEOMETRY OF CHARACTERISTIC FLAT BED, HOLLOW-FIBER, AND SPOUTED BED BIOREACTORS WITH REFERENCE TO THE IN-VIVO LIVER [J].
BADER, A ;
KNOP, E ;
FRUHAUF, N ;
CROME, O ;
BOKER, K ;
CHRISTIANS, U ;
OLDHAFER, K ;
RINGE, B ;
PICHLMAYR, R ;
SEWING, KF .
ARTIFICIAL ORGANS, 1995, 19 (09) :941-950
[8]   Differentiation of human embryonic stem cells into hepatocytes in 2D and 3D culture systems in vitro [J].
Baharvand, Hossein ;
Hashemi, Seyed M. ;
Kazemi Ashtian, Saeid ;
Farrokhi, Ali .
INTERNATIONAL JOURNAL OF DEVELOPMENTAL BIOLOGY, 2006, 50 (07) :645-652
[9]   Design of a flow perfusion bioreactor system for bone tissue-engineering applications [J].
Bancroft, GN ;
Sikavitsas, VI ;
Mikos, AG .
TISSUE ENGINEERING, 2003, 9 (03) :549-554
[10]   Three-dimensional in vitro reaggregates of embryonic cardiomyocytes:: A potential model system for monitoring effects of bioactive agents [J].
Bartholomä, P ;
Gorjup, E ;
Monz, D ;
Reininger-Mack, A ;
Thielecke, H ;
Robitzki, A .
JOURNAL OF BIOMOLECULAR SCREENING, 2005, 10 (08) :814-822