Ee Xien Ng
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Ee Xien Ng has a total of 8 co-authors. Here are the top co-authors by number of shared publications:
- Chia-Hung Chen
Department of Biomedical Engineering, City University of Hong Kong, 83 Tat Chee Avenue, Kowloon Tong, Hong Kong, China
1 shared publication Chia‐Hung Chen
Department of Biomedical Engineering National University of Singapore Singapore 117574 Singapore
1 shared publicationChing Ann Tee
Critical Analytics for Manufacturing Personalized‐Medicine CREATE Singapore‐MIT Alliance for Research and Technology Singapore 138602 Singapore
1 shared publicationGuoyun Sun
Department of Biomedical Engineering, National University of Singapore, Singapore
1 shared publication- Krystyn J. Van Vliet
Departments of Materials Science & Engineering and Biomedical Engineering, Cornell University
1 shared publication Ming Wang
NUS Graduate School for Integrative Sciences and Engineering National University of Singapore Singapore 117456 Singapore
1 shared publication
Latest Publications
- 13 October 2020
- Published by Wiley in Biotechnology Journal
- Vol. 16 (3) , e2000048
Dissolvable Gelatin‐Based Microcarriers Generated through Droplet Microfluidics for Expansion and Culture of Mesenchymal Stromal Cells
Microcarriers are synthetic particles used in bioreactor‐based cell manufacturing of anchorage‐dependent cells to promote proliferation at efficient physical volumes, mainly by increasing the surface area‐to‐volume ratio. Mesenchymal stromal cells (MSCs) are adherent cells that are used for numerous clinical trials of autologous and allogeneic cell therapy, thus requiring avenues for large‐scale cell production at efficiently low volumes and cost. Here, a dissolvable gelatin‐based microcarrier is developed for MSC expansion. This novel microcarrier shows comparable cell attachment efficiency and proliferation rate when compared to several commercial microcarriers, but with higher harvesting yield due to the direct dissolution of microcarrier particles and thus reduced cell loss at the cell harvesting step. Furthermore, gene expression and in vitro differentiation suggest that MSCs cultured on gelatin microcarriers maintain trilineage differentiation with similar adipogenic differentiation efficiency and higher chondrogenic and osteogenic differentiation efficiency when compared to MSCs cultured on 2D planar polystyrene tissue culture flask; on the contrary, MSCs cultured on conventional microcarriers appear to be bipotent along osteochondral lineages whereby adipogenic differentiation potential is impeded. These results suggest that these gelatin microcarriers are suitable for MSC culture and expansion, and can also potentially be extended for other types of anchorage‐dependent cells.
- 13 October 2020
- Published by Wiley in Biotechnology Journal
- Vol. 16 (3) , e2000048
Dissolvable Gelatin‐Based Microcarriers Generated through Droplet Microfluidics for Expansion and Culture of Mesenchymal Stromal Cells
Microcarriers are synthetic particles used in bioreactor‐based cell manufacturing of anchorage‐dependent cells to promote proliferation at efficient physical volumes, mainly by increasing the surface area‐to‐volume ratio. Mesenchymal stromal cells (MSCs) are adherent cells that are used for numerous clinical trials of autologous and allogeneic cell therapy, thus requiring avenues for large‐scale cell production at efficiently low volumes and cost. Here, a dissolvable gelatin‐based microcarrier is developed for MSC expansion. This novel microcarrier shows comparable cell attachment efficiency and proliferation rate when compared to several commercial microcarriers, but with higher harvesting yield due to the direct dissolution of microcarrier particles and thus reduced cell loss at the cell harvesting step. Furthermore, gene expression and in vitro differentiation suggest that MSCs cultured on gelatin microcarriers maintain trilineage differentiation with similar adipogenic differentiation efficiency and higher chondrogenic and osteogenic differentiation efficiency when compared to MSCs cultured on 2D planar polystyrene tissue culture flask; on the contrary, MSCs cultured on conventional microcarriers appear to be bipotent along osteochondral lineages whereby adipogenic differentiation potential is impeded. These results suggest that these gelatin microcarriers are suitable for MSC culture and expansion, and can also potentially be extended for other types of anchorage‐dependent cells.
- 1 January 2019
- Published by Elsevier
- Vol. 628, 59-94
Single-cell assays using integrated continuous-flow microfluidics
- 1 January 2019
- Published by Elsevier
- Vol. 628, 59-94
Single-cell assays using integrated continuous-flow microfluidics