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Beneficial effect of hydrophilized porous polymer scaffolds in tissue‐engineered cartilage formation
Author(s) -
Ju Young Min,
Park Kwideok,
Son Jun Sik,
Kim JaeJin,
Rhie JongWon,
Han Dong Keun
Publication year - 2008
Publication title -
journal of biomedical materials research part b: applied biomaterials
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.665
H-Index - 108
eISSN - 1552-4981
pISSN - 1552-4973
DOI - 10.1002/jbm.b.30943
Subject(s) - chemical engineering , polymer , adhesion , porosity , materials science , tissue engineering , chemistry , chondrocyte , polymerization , polymer chemistry , tropoelastin , acrylic acid , hydrophilization , extracellular matrix , biomedical engineering , composite material , biochemistry , medicine , engineering , monomer , in vitro
Three dimensional (3D) porous poly( L ‐lactic acid) (PLLA) scaffolds were fabricated using a modified gas foaming method whose effervescent porogens were a mixture of sodium bicarbonate and citric acid. To improve chondrocyte adhesion, the scaffolds were then hydrophilized through oxygen plasma treatment and in situ graft polymerization of acrylic acid (AA). When the physical properties of AA‐grafted scaffolds were examined, the porosity and pore size were 87 ∼ 93% and 100 ∼ 300 μm, respectively. The pore sizes were highly dependent on the varying ratios (w/w) between porogen and polymer solution. Influenced by their pore sizes, the compressive moduli of scaffolds significantly decreased with increasing pore size. The altered surface characteristics were clearly reflected in the reduced water contact angles that meant a significant hydrophilization with the modified polymer surface. Electron spectroscopy for chemical analysis (ESCA) and time‐of‐flight secondary ion mass spectrometer (ToF‐SIMS) also confirmed the altered surface chemistry. When chondrocytes were seeded onto the AA‐grafted PLLA scaffolds, cell adhesion and proliferation were substantially improved as compared to the unmodified scaffolds. The benefit of the modified scaffolds was clear in the gene expressions of collagen type II that was significantly upregulated after 4‐week culture. Safranin‐O staining also identified greater glycosaminoglycan (GAG) deposition in the modified scaffold. The AA‐grafted porous polymer scaffolds were effective for cell adhesion and differentiation, making them a suitable platform for tissue‐engineered cartilage. © 2007 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater, 2008