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Generation of microgrooved silica nanotube membranes with sustained drug delivery and cell contact guidance ability by using a Teflon microfluidic chip.
Chen, Song; Shi, Xuetao; Chinnathambi, Shanmugavel; Wu, Hongkai; Hanagata, Nobutaka.
Affiliation
  • Chen S; JSPS Research Fellow, 8 Ichibancho, Chiyoda-ku, Tokyo 102-8472, Japan; Biomaterials Unit, National Institute for Materials Science, Sengen, Tsukuba, 305-0047, Japan.
  • Shi X; WPI Advanced Institute for Materials Research, Tohoku University, Katahira 2-1-1, Aobaku, Sendai 980-8577, Japan.
  • Chinnathambi S; Biomaterials Unit, National Institute for Materials Science, Sengen, Tsukuba, 305-0047, Japan; Department of Medical Physics, Anna University, Chennai 600-025, India.
  • Wu H; WPI Advanced Institute for Materials Research, Tohoku University, Katahira 2-1-1, Aobaku, Sendai 980-8577, Japan; Department of Chemistry, Hong Kong University of Science and Technology, Clear Water Bay, Kowloon, Hong Kong, People's Republic of China.
  • Hanagata N; Biomaterials Unit, National Institute for Materials Science, Sengen, Tsukuba, 305-0047, Japan; Nanotechnology Innovation Station, National Institute for Materials Science, 1-2-1 Sengen, Tsukuba, Ibaraki 305-0047, Japan; Graduate School of Life Science, Hokkaido University, N10W8, Kita-ku, Sapporo 06
Sci Technol Adv Mater ; 14(1): 015005, 2013 Feb.
Article in En | MEDLINE | ID: mdl-27877563
Silica nanotubes have been extensively applied in the biomedical field. However, very little attention has been paid to the fabrication and application of micropatterned silica nanotubes. In the present study, microgrooved silica nanotube membranes were fabricated in situ by microgrooving silica-coated collagen hybrid fibril hydrogels in a Teflon microfluidic chip followed by calcination for removal of collagen fibrils. Scanning electron microscopy images showed that the resulting silica nanotube membranes displayed a typical microgroove/ridge surface topography with ∼50 µm microgroove width and ∼120 µm ridge width. They supported adsorption of bone morphogenetic protein 2 (BMP-2) and exhibited a sustained release behavior for BMP-2. After culturing with osteoblast MC3T3-E1 cells, they induced an enhanced osteoblast differentiation due to the release of biologically active BMP-2 and a strong contact guidance ability to directly align and elongate osteoblasts due to the presence of microgrooved surface topography, indicating their potential application as a multi-functional cell-supporting matrix for tissue generation.
Key words

Full text: 1 Database: MEDLINE Type of study: Guideline Language: En Year: 2013 Type: Article

Full text: 1 Database: MEDLINE Type of study: Guideline Language: En Year: 2013 Type: Article