Microsphere-based scaffolds for cartilage tissue engineering: Using subcritical CO2 as a sintering agent☆
Received 13 May 2009; received in revised form 15 July 2009; accepted 30 July 2009. published online 05 August 2009.
Abstract
Shape-specific, macroporous tissue engineering scaffolds were fabricated and homogeneously seeded with cells in a single step. This method brings together CO2 polymer processing and microparticle-based scaffolds in a manner that allows each to solve the key limitation of the other. Specifically, microparticle-based scaffolds have suffered from the limitation that conventional microsphere sintering methods (e.g., heat, solvents) are not cytocompatible, yet we have shown that cell viability was sustained with subcritical (i.e., gaseous) CO2 sintering of microspheres in the presence of cells at near-ambient temperatures. On the other hand, the fused microspheres provided the pore interconnectivity that has eluded supercritical CO2 foaming approaches. Here, fused poly(lactide-co-glycolide) microsphere scaffolds were seeded with human umbilical cord mesenchymal stromal cells to demonstrate the feasibility of utilizing these matrices for cartilage regeneration. We also demonstrated that the approach may be modified to produce thin cell-loaded patches as a promising alternative for skin tissue engineering applications.
aDepartment of Bioengineering, Rice University, Houston, TX, USA
bDepartment of Biomedical Engineering, University of Michigan, Ann Arbor, MI, USA
cDepartment of Chemical and Petroleum Engineering, University of Kansas, Lawrence, KS, USA
dDepartment of Pharmaceutical Chemistry, University of Kansas, Lawrence, KS, USA
Corresponding author. Address: University of Kansas, Department of Chemical and Petroleum Engineering, Learned Hall, Room 4132, 1530 W. 15th St., Lawrence, KS 66045, USA. Tel.: +1 785 864 4943; fax: +1 785 864 4967.
☆ Published abstract: “Subcritical CO2-melded Microsphere-based Scaffolds for Cartilage Tissue Engineering”, BMES Annual Fall Meeting, Chicago, IL, 2008.