A Review of Three-Dimensional In Vitro Tissue Models for Drug Discovery and Transport Studies
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 ne...
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Published in | Journal of pharmaceutical sciences Vol. 100; no. 1; pp. 59 - 74 |
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Main Authors | , |
Format | Journal Article |
Language | English |
Published |
Hoboken
Elsevier Inc
01.01.2011
Wiley Subscription Services, Inc., A Wiley Company Wiley American Pharmaceutical Association Elsevier Limited |
Subjects | |
Online Access | Get full text |
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Summary: | 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. |
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Bibliography: | istex:0D325C45474A594219069F0B982A8149B44E1FB2 ark:/67375/WNG-330F277W-N ArticleID:JPS22257 ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-3 content type line 23 ObjectType-Review-2 |
ISSN: | 0022-3549 1520-6017 |
DOI: | 10.1002/jps.22257 |