## Abstract A technique for producing controlled interconnected porous structures for application as a tissue engineering scaffold is presented in this article. The technique is based on the fabrication of a template of interconnected poly(ethyl methacrylate) (PEMA) microspheres, the introduction o
Polyester Scaffolds with Bimodal Pore Size Distribution for Tissue Engineering
✍ Scribed by Stanislaw Sosnowski; Piotr Woźniak; Małgorzata Lewandowska-Szumieł
- Publisher
- John Wiley and Sons
- Year
- 2006
- Tongue
- English
- Weight
- 414 KB
- Volume
- 6
- Category
- Article
- ISSN
- 1616-5187
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Summary: This paper presents a method for the preparation of porous poly(L‐lactide)/poly[(L‐lactide)‐co‐glycolide] scaffolds for tissue engineering. Scaffolds were prepared by a mold pressing‐salt leaching technique from structured microparticles. The total porosity was in the range 70–85%. The pore size distribution was bimodal. Large pores, susceptible for osteoblasts growth and proliferation had the dimensions 50–400 µm. Small pores, dedicated to the diffusion of nutrients or/and metabolites of bone forming cells, as well as the products of hydrolysis of polyesters from the walls of the scaffold, had sizes in the range 2 nm–5 µm. The scaffolds had good mechanical strength (compressive modulus equal to 41 MPa and a strength of 1.64 MPa for 74% porosity). Scaffolds were tested in vitro with human osteoblast‐like cells (MG‐63). It was found that the viability of cells seeded within the scaffolds obtained using the mold pressing‐salt leaching technique from structured microparticles was better when compared to cells cultured in scaffolds obtained by traditional methods. After 34 d of culture, cells within the tested scaffolds were organized in a tissue‐like structure.
Photos of section of macro‐ and mesoporous PLLA/PLGA scaffold containing 50 wt.‐% of PLGA microspheres after 34 d of culture. Dark spots mark MG‐63 cells, white areas belong to the scaffold. The specimen was stained with haematoxylin/eosin. Bar = 100 µm.
magnified imagePhotos of section of macro‐ and mesoporous PLLA/PLGA scaffold containing 50 wt.‐% of PLGA microspheres after 34 d of culture. Dark spots mark MG‐63 cells, white areas belong to the scaffold. The specimen was stained with haematoxylin/eosin. Bar = 100 µm.
📜 SIMILAR VOLUMES
## Abstract In this study, the alginate/calcium phosphate cement (CPC) scaffolds with oriented pore structure were fabricated by unidirectional freeze casting and poly (lactic‐__co__‐glycolic acid) (PLGA) was used to infiltrate into the macropores to strengthen the scaffolds. By modifying the liqui
## Abstract A method is proposed in which the geometric properties of 3D scaffolds with application in tissue engineering can be tailored: porosity, pore size, and interconnection throat size. The architecture of the fabricated scaffolds is analyzed by scanning electron microscopy. The mechanical p
## Abstract __In vitro__ degradation of seven three‐dimensional porous scaffolds composed of PLGA85/15, a very useful poly(D,L‐lactide‐__co__‐glycolide), was performed in phosphate‐buffered saline solution at 37°C up to 26 weeks, and effects of porosity (80–95%) and pore size (50–450 μm) on the deg