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Direct Ink Write (DIW) 3D Printed Cellulose Nanocrystal Aerogel Structures.
Li, Vincent Chi-Fung; Dunn, Conner K; Zhang, Zhe; Deng, Yulin; Qi, H Jerry.
Afiliação
  • Li VC; Renewable Bioproducts Institute at Georgia Institute of Technology, School of Chemical & Biomolecular Engineering, Atlanta, GA, 30318, USA.
  • Dunn CK; Renewable Bioproducts Institute at Georgia Institute of Technology, George W. Woodruff School of Mechanical Engineering, Atlanta, GA, 30332, USA.
  • Zhang Z; Renewable Bioproducts Institute at Georgia Institute of Technology, School of Chemical & Biomolecular Engineering, Atlanta, GA, 30318, USA.
  • Deng Y; Renewable Bioproducts Institute at Georgia Institute of Technology, School of Chemical & Biomolecular Engineering, Atlanta, GA, 30318, USA. yulin.deng@rbi.gatech.edu.
  • Qi HJ; Renewable Bioproducts Institute at Georgia Institute of Technology, George W. Woodruff School of Mechanical Engineering, Atlanta, GA, 30332, USA. qih@me.gatech.edu.
Sci Rep ; 7(1): 8018, 2017 08 14.
Article em En | MEDLINE | ID: mdl-28808235
Pure cellulose nanocrystal (CNC) aerogels with controlled 3D structures and inner pore architecture are printed using the direct ink write (DIW) technique. While traditional cellulosic aerogel processing approaches lack the ability to easily fabricate complete aerogel structures, DIW 3D printing followed by freeze drying can overcome this shortcoming and can produce CNC aerogels with minimal structural shrinkage or damage. The resultant products have great potential in applications such as tissue scaffold templates, drug delivery, packaging, etc., due to their inherent sustainability, biocompatibility, and biodegradability. Various 3D structures are successfully printed without support material, and the print quality can be improved with increasing CNC concentration and printing resolution. Dual pore CNC aerogel scaffolds are also successfully printed, where the customizable 3D structure and inner pore architecture can potentially enable advance CNC scaffold designs suited for specific cell integration requirements.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2017 Tipo de documento: Article