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Effect of solid freeform fabrication-based polycaprolactone/poly(lactic-co-glycolic acid)/collagen scaffolds on cellular activities of human adipose-derived stem cells and rat primary hepatocytes SCIE SCOPUS

Title
Effect of solid freeform fabrication-based polycaprolactone/poly(lactic-co-glycolic acid)/collagen scaffolds on cellular activities of human adipose-derived stem cells and rat primary hepatocytes
Authors
Shim, JHKim, AJPark, JYYi, NKang, IPark, JRhie, JWCho, DW
Date Issued
2013-04
Publisher
JOURNAL OF MATERIALS SCIENCE-MATERIALS IN MEDICINE
Abstract
Highly biocompatible polycaprolactone (PCL)/poly(lactic-co-glycolic acid) (PLGA)/collagen scaffolds in which the PCL/PLGA collagen solution was selectively dispensed into every other space between the struts were fabricated using solid freeform fabrication (SFF) technology, as we described previously. The objective of this study was to evaluate and compare the PCL/PLGA/collagen scaffolds (group 3) with PCL/PLGA-only scaffolds (group 1) and PCL/PLGA scaffolds with collagen by the dip-coating method (group 2) using human adipose-derived stem cells (hASCs) and rat primary hepatocytes. The selectively dispensed collagen formed a three-dimensional (3D) network of nanofibers in group 3, as observed by scanning electron microscopy. The compressive strength and modulus of group 3 were approximately 140 and 510 times higher, respectively, than those of a sponge-type collagen scaffold whose weak mechanical properties were regarded as a critical drawback. Proliferation and osteogenic differentiation of hASCs were promoted significantly in group 3 compared to groups 1 and 2. In addition, we found that the viability and albumin secretion ability of rat primary hepatocytes were highly retained for 10 days in group 3 but not group 1. Interestingly, hepatocyte aggregation, which enhances hepatic function through cell-cell interactions, was observed particularly in group 3. In conclusion, group 3, in which the collagen was selectively dispensed in the 3D space of the porous PCL/PLGA framework, will be a promising 3D scaffold for culturing various cell types.
Keywords
SURFACE MODIFICATION; TISSUE REGENERATION; DIFFERENTIATION; DEPOSITION; MICROSTEREOLITHOGRAPHY; PROLIFERATION; BIOMATERIALS; ATTACHMENT; GENERATION; HYDROGELS
URI
https://oasis.postech.ac.kr/handle/2014.oak/14770
DOI
10.1007/S10856-013-4867-8
ISSN
0957-4530
Article Type
Article
Citation
JOURNAL OF MATERIALS SCIENCE-MATERIALS IN MEDICINE, vol. 24, no. 4, page. 1053 - 1065, 2013-04
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조동우CHO, DONG WOO
Dept of Mechanical Enginrg
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