Abstract

Due to the restrictions in accessing research laboratories and the challenges in providing proper storage and transportation of cells during the COVID‐19 pandemic, having an effective and feasible mean to solve these challenges would be of immense help. Therefore, we developed a 3D culture setting of cancer cells using alginate beads and tested its effectiveness in different storage and transportation conditions. The viability and proliferation of cancer cells were assessed using trypan blue staining and quantitative CCK‐8 kit, respectively. The developed beads allowed cancer cells survival up to 4 weeks with less frequent maintenance measures such as change of the culture media or subculture of cells. In addition, the recovery of cancer cells and proliferation pattern were significantly faster with better outcomes in the developed 3D alginate beads compared to the standard cryopreservation of cells or the 2D culture conditions. The 3D alginate beads also supported the viability of cells while the shipment at room temperature for a duration of up to 5 days with no humidity or CO2 support. Therefore, 3D culture in alginate beads can be used to store or ship biological cells with ease at room temperature with minimal preparations.

Highlights

  • With continuously changing situations because of COVID-­19, lockdowns are suddenly enforced

  • With the short notice given before enforcing the complete lockdown, the cell culture laboratories become congested with insufficient time to cryopreserve the cells or prepare them for shipping, which usually needs special reagents for cryopreservation and shipping in dry ice.[1]

  • The results above proved the practicability of 3D cell culture in alginate beads as a tool to maintain the cells and recover them with minimal laboratory work and equipment use

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Summary

Introduction

With continuously changing situations because of COVID-­19, lockdowns are suddenly enforced. We tested 3D cell culture as a method for maintaining cells for up to 4 weeks with minimal laboratory work needed. During the first 8 days, the cells were tested for cell viability using semi-­quantitative trypan blue assay method and for proliferation potential using the quantitative colourimetric Cell Counting Kit 8 (CCK-­8)[3] (Supplementary Information S1) and compared the results with a control group of 2D culture.

Results
Conclusion
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