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Role of three-dimensional cell culture in therapeutics and diagnostics: an updated review

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DRUG DELIVERY AND TRANSLATIONAL RESEARCH
卷 13, 期 9, 页码 2239-2253

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SPRINGER HEIDELBERG
DOI: 10.1007/s13346-023-01327-6

关键词

Three-dimensional cell culture models; Drug testing; Preclinical validation; Drug toxicity screening; High-throughput screening; 2D cell culture

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Drug development and testing are time-consuming and expensive, with uncertainties in clinical success and preclinical validation. Currently, most therapeutic drug manufacturers use 2D cell culture models, but they have limitations in mimicking cellular mechanisms and environmental interactions. To overcome these limitations, newer in vivo drug testing models, such as 3D cell culture models, are required. This review article outlines the advancements, types, significance, limitations, and applications of cell culture models in drug toxicity screening and preclinical testing.
Drug development and testing are a tedious and expensive process with a high degree of uncertainty in the clinical success and preclinical validation of manufactured therapeutic agents. Currently, to understand the drug action, disease mechanism, and drug testing, most therapeutic drug manufacturers use 2D cell culture models to validate the drug action. However, there are many uncertainties and limitations with the conventional use of 2D (monolayer) cell culture models for drug testing that are primarily attributed due to poor mimicking of cellular mechanisms, disturbance in environmental interaction, and changes in structural morphology. To overcome such odds and difficulties in the preclinical validation of therapeutic medications, newer in vivo drug testing cell culture models with higher screening efficiencies are required. One such promising and advanced cell culture model reported recently is the three-dimensional cell culture model. The 3D cell culture models are reported to show evident benefits over conventional 2D cell models. This review article outlines and describes the current advancement in cell culture models, their types, significance in high-throughput screening, limitations, applications in drug toxicity screening, and preclinical testing methodologies to predict in vivo efficacy.

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