
Building biomaterial-based three-dimensional in-vitro models for understanding tissue and disease pathophysiology is a key challenge in tissue engineering. The conventional tissue culture models do not replicate the complexities of human tissue, whereas animal models are costly, time-consuming, and raise severe ethical concerns. However, biomaterial-based 3D models can bridge both techniques as well as overcome their limitations. The development of platforms for drug screening is one area where in-vitro models are underrepresented yet can have an immediate impact. In-vitro models like this have the potential to address growing concerns about drug failures in clinical trials due to inefficacy or unforeseen side effects. This methods collection aims to highlight technologies for developing such in-vitro biomaterial-based drug screening platforms with a focus on tumor spheroid and organoid models. Methods to fabricate such platforms might include static cultures, microfluidic technologies, additive manufacturing, droplet-based technologies, and others. Of further interest are methods focused on the assessment of cell responses to drug screening, such as imaging modalities, staining protocols, mechanical testing, and others.
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Cited by 5
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2022
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Glioblastoma spheroid formation and encapsulation in tunable polyethylene glycol hydrogels.
Joseph Bruns1,
Silviya Zustiak*1
1Saint Louis University