A combined compression molding, heating, and leaching process for fabrication of micro-porous poly(ε-caprolactone) scaffolds. Issue 16 (2nd November 2018)

• Record Type: Journal Article
• Authors: Sempertegui, Nicole D.; Narkhede, Akshay A.; Thomas, Vinoy; Rao, Shreyas S.
• Is Part Of: Journal of biomaterials science. Volume 29:Issue 16(2018)
• Page Start: 1978
• Page End: 1993
• Publication Date: 2018-11-02
• Subjects: poly(ε-caprolactone) -- micro-porous -- scaffolds -- compression molding -- heating -- leaching; Polymers -- Biocompatibility -- Periodicals; Biomedical materials -- Periodicals; 572.33
• DOI: 10.1080/09205063.2018.1498719
• Languages: English
• ISSNs: 0920-5063

Abstract

Abstract: Biomaterial scaffolds have been increasingly used for tissue engineering applications as well as three dimensional (3D) cell culture models. Herein, we report a simple procedure combining compression molding, heating, and leaching methods for the fabrication of 3D micro-porous poly(ε-caprolactone) (PCL) biomaterial scaffolds. In this procedure, PCL micro particles are mixed with NaCl of defined sizes and compression molded, followed by heating and subsequent leaching of NaCl particles. This technique eliminates the gas foaming method, which is commonly used in the fabrication of PCL scaffolds. Process and scaffold parameters (i.e., heating time, NaCl concentration, and NaCl particle size) were varied and analyzed to determine their impact on the overall scaffold structural and mechanical properties. An increase in NaCl particle size led to an increase in pore area but did not significantly impact the mechanical properties of the scaffolds. Additionally, NaCl concentration did not show a significant effect on pore area, but considerably impacted the mechanical properties, water absorption capacity and porosity of the scaffolds. Variations in the heating time did not have an effect in the pore area, porosity, water absorption capacity or mechanical properties of the scaffolds. We also demonstrated the ability of these scaffolds to support the proliferation of breast cancer cells. Overall, these results elucidated structure-property relationships in the fabricated micro-porous PCL scaffolds. Further, this procedure could be potentially scaled up for the fabrication of micro-porous PCL scaffolds.