Biomimetic 3D Tissue Models for Advanced High-Throughput Drug Screening
- PMID: 25385716
- PMCID: PMC4459652
- DOI: 10.1177/2211068214557813
Biomimetic 3D Tissue Models for Advanced High-Throughput Drug Screening
Abstract
Most current drug screening assays used to identify new drug candidates are 2D cell-based systems, even though such in vitro assays do not adequately re-create the in vivo complexity of 3D tissues. Inadequate representation of the human tissue environment during a preclinical test can result in inaccurate predictions of compound effects on overall tissue functionality. Screening for compound efficacy by focusing on a single pathway or protein target, coupled with difficulties in maintaining long-term 2D monolayers, can serve to exacerbate these issues when using such simplistic model systems for physiological drug screening applications. Numerous studies have shown that cell responses to drugs in 3D culture are improved from those in 2D, with respect to modeling in vivo tissue functionality, which highlights the advantages of using 3D-based models for preclinical drug screens. In this review, we discuss the development of microengineered 3D tissue models that accurately mimic the physiological properties of native tissue samples and highlight the advantages of using such 3D microtissue models over conventional cell-based assays for future drug screening applications. We also discuss biomimetic 3D environments, based on engineered tissues as potential preclinical models for the development of more predictive drug screening assays for specific disease models.
Keywords: bio-nanotechnology; biomimetic microenvironment; high-throughput drug screening; microengineered 3D tissue models; organ-on-chip.
© 2014 Society for Laboratory Automation and Screening.
Figures
Similar articles
-
Biomimetic cardiac microsystems for pathophysiological studies and drug screens.J Lab Autom. 2015 Apr;20(2):96-106. doi: 10.1177/2211068214560903. Epub 2014 Dec 18. J Lab Autom. 2015. PMID: 25524490 Review.
-
Tissue-Engineered 3D In Vitro Disease Models for High-Throughput Drug Screening.Tissue Eng Regen Med. 2023 Jul;20(4):523-538. doi: 10.1007/s13770-023-00522-3. Epub 2023 Mar 9. Tissue Eng Regen Med. 2023. PMID: 36892736 Free PMC article. Review.
-
3D Engineering of Ocular Tissues for Disease Modeling and Drug Testing.Adv Exp Med Biol. 2019;1186:171-193. doi: 10.1007/978-3-030-28471-8_7. Adv Exp Med Biol. 2019. PMID: 31654390
-
A biomimetic Schlemm's canal inner wall: A model to study outflow physiology, glaucoma pathology and high-throughput drug screening.Biomaterials. 2015 Oct;65:86-92. doi: 10.1016/j.biomaterials.2015.06.034. Epub 2015 Jun 20. Biomaterials. 2015. PMID: 26142779 Free PMC article.
-
An integrated biomimetic array chip for high-throughput co-culture of liver and tumor microtissues for advanced anticancer bioactivity screening.Lab Chip. 2020 Jul 14;20(14):2482-2494. doi: 10.1039/d0lc00288g. Lab Chip. 2020. PMID: 32542294
Cited by
-
3D Bioprinting in Tissue Engineering for Medical Applications: The Classic and the Hybrid.Polymers (Basel). 2020 Jul 31;12(8):1717. doi: 10.3390/polym12081717. Polymers (Basel). 2020. PMID: 32751797 Free PMC article. Review.
-
Myocardial slices come to age: an intermediate complexity in vitro cardiac model for translational research.Cardiovasc Res. 2020 Jun 1;116(7):1275-1287. doi: 10.1093/cvr/cvz341. Cardiovasc Res. 2020. PMID: 31868875 Free PMC article. Review.
-
Engineering in vitro immune-competent tissue models for testing and evaluation of therapeutics.Adv Drug Deliv Rev. 2022 Mar;182:114111. doi: 10.1016/j.addr.2022.114111. Epub 2022 Jan 11. Adv Drug Deliv Rev. 2022. PMID: 35031388 Free PMC article. Review.
-
Design of synthetic extracellular matrices for probing breast cancer cell growth using robust cyctocompatible nucleophilic thiol-yne addition chemistry.Biomaterials. 2018 Sep;178:435-447. doi: 10.1016/j.biomaterials.2018.04.046. Epub 2018 May 7. Biomaterials. 2018. PMID: 29773227 Free PMC article.
-
3D engineered tissue models for studying human-specific infectious viral diseases.Bioact Mater. 2022 Sep 22;21:576-594. doi: 10.1016/j.bioactmat.2022.09.010. eCollection 2023 Mar. Bioact Mater. 2022. PMID: 36204281 Free PMC article. Review.
References
-
- May MS, Wardell WM, Lasagna L. New drug development during after a period of regulatory change: Clinical research activity of major United States pharmaceutical firms, 1958 to 1979. Clinical Pharmacology Therapeutics. 1983;33:691–700. - PubMed
-
- Eschenhagen T, Zimmermann WH. Engineering myocardial tissue. Circ Res. 2005;97:1220–1231. - PubMed
-
- Mathers CD, Bernard C, Iburg KM, Inoue M, Ma Fat D, Shibuya K, Stein C, Tomijima N, Xu H. Global burden of disease: Data sources, methods and results. World Health Organization; Geneva, Switzerland: 2008.
Publication types
MeSH terms
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources