Formation of miniaturized 3D tumour spheroids for drug screening

Cancer is one of the most life-threatening diseases and has affected many in the world. Currently, anti-cancer drugs are being tested by in vitro cell- based study and animal testing before drugs can move on to clinical trials. Traditional 2D cell culture is widely used for in vitro study due to the...

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Bibliographic Details
Main Author: Cheah, Cheryl Jia Le
Other Authors: Tan Lay Poh
Format: Final Year Project
Language:English
Published: 2019
Subjects:
Online Access:http://hdl.handle.net/10356/77993
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Institution: Nanyang Technological University
Language: English
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Summary:Cancer is one of the most life-threatening diseases and has affected many in the world. Currently, anti-cancer drugs are being tested by in vitro cell- based study and animal testing before drugs can move on to clinical trials. Traditional 2D cell culture is widely used for in vitro study due to the lower cost and simplicity. However, in recent years, 2D cell culture is increasingly reported to have inaccurate and misleading data. This led to an increase interest in developing 3D culture platform for the screening of anti-cancer drugs. Among the 3D cell culture models, multi-cellular spheroids are commonly used as they accurately mimic tumour architecture. There are many existing methods to fabricate multi-cellular spheroids but lacked high throughput and consistency. In this study, co-axial electrospray will be used to fabricate hydrogel spheroids with core-shell structure and its parameters will be optimised in order to obtain the desired size and consistent shape. Effect of voltage, hardening bath, needle size, total flow rate and flow rate ratio will be studied based on the morphology of spheroids and its consistency. With the optimised parameters, MCF-7 and L929 cells will be encapsulated in core and shell compartment respectively to form multi-cellular spheroids as proof of concepts. Cell viability and cellular spheroids formation will be characterized with fluorescence staining.