Casey G. Lim
University of Maryland, College Park
4 Papers
Casey G. Lim is an academic researcher from University of Maryland, College Park. The author has contributed to research in topics: Mesenchymal stem cell & Chondrogenesis. The author has an hindex of 4, co-authored 4 publications.
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Papers
3D printing PLGA: a quantitative examination of the effects of polymer composition and printing parameters on print resolution.
Ting Guo,Timothy R Holzberg,Casey G. Lim,Feng Gao,Ankit Gargava,Jordan E. Trachtenberg,Antonios G. Mikos,John P. Fisher +7 more
TL;DR: A statistical model is built to reveal the correlation and predominant factors that determine printing precision and showed a strong linear relationship between the actual and predicted precision under different combinations of printing conditions and material compositions.
Three dimensional extrusion printing induces polymer molecule alignment and cell organization within engineered cartilage.
Ting Guo,Julia P. Ringel,Casey G. Lim,Laura G. Bracaglia,Maeesha Noshin,Hannah B. Baker,Douglas A. Powell,John P. Fisher +7 more
TL;DR: In this paper, a 3D extrusion based printing at high temperature and pressure will result an aligned effect on the polymer molecules, and this molecular arrangement will further induce the cell alignment and different differentiation capacities.
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3D Printing Bioactive PLGA Scaffolds Using DMSO as a Removable Solvent.
TL;DR: The use of DMSO for 3D printed scaffold fabrication with bioactive items is a revolutionary methodology in advancing regenerative medicine and opens pathways to more therapeutic uses for3D printing in treating damaged or deteriorating native tissue.
Effect of Dynamic Culture and Periodic Compression on Human Mesenchymal Stem Cell Proliferation and Chondrogenesis
Ting Guo,Li Yu,Casey G. Lim,Addison S. Goodley,Xuan Xiao,Jesse K. Placone,Kimberly M. Ferlin,Bao-Ngoc B. Nguyen,Adam H. Hsieh,John P. Fisher +9 more
TL;DR: Results suggest that a combination of dynamic culture with proper mechanical stimulation may promote efficient progenitor cell expansion in vitro, thereby allowing the culture of clinically relevant articular chondrocytes for the treatment of articular cartilage defects.