Rapid prototyping of chitosan-coated alginate scaffolds through the use of a 3D fiber deposition technique

被引:70
作者
Colosi, Cristina [1 ]
Costantini, Marco [1 ]
Latini, Roberta [1 ]
Ciccarelli, Serena [1 ]
Stampella, Alessandra [3 ]
Barbetta, Andrea [1 ]
Massimi, Mara [2 ]
Devirgiliis, Laura Conti [3 ]
Dentini, Mariella [1 ]
机构
[1] Univ Roma La Sapienza, Dept Chem, I-00185 Rome, Italy
[2] Univ Aquila, Dept Life Hlth & Environm Sci, I-67100 Laquila, Italy
[3] Univ Roma La Sapienza, Dept Biol & Biotechnol C Darwin, I-00185 Rome, Italy
关键词
HEPARG CELLS; TISSUE; FABRICATION; MODEL; HYDROGELS; DESIGN; METABOLISM; MANNURONAN; TOXICITY; GELATIN;
D O I
10.1039/c4tb00732h
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
082905 [生物质能源与材料]; 100103 [病原生物学];
摘要
Three dimensional, periodic scaffolds of chitosan-coated alginate are fabricated in a layer-by-layer fashion by rapid prototyping. A novel dispensing system based on two coaxial needles delivers simultaneously alginate and calcium chloride solutions permitting the direct deposition of alginate fibers according to any designed pattern. Coating of the alginate fiber with chitosan and subsequent cross-linking with EDC and genipin assured the endurance of the scaffold in the culture environment for a prolonged period of time. The cross-linking protocol adopted imparted to the scaffold a hierarchical chemical structure as evidenced by Confocal Laser Microscopy and FTIR spectroscopy. The core of the fibers making up the scaffold is represented by alginate chains cross-linked by ester bonds only, the periphery of the fiber is constituted by an inter-polyelectrolyte complex of alginate and chitosan cross-linked in all pair combinations. Fibers belonging to adjacent layers are glued together by the chitosan coating. Mechanical behavior of the scaffolds characterized by different layouts of deposition was determined revealing anisotropic properties. The biocompatibility and capability of the scaffolds to sustain hepatocyte (HepaRG) cultures were demonstrated. Typical hepatic functions such as albumin and urea secretion and induction of CYP3A4 enzyme activity following drug administration were excellent, thus proving the potential of these constructs in monitoring the liver specific function.
引用
收藏
页码:6779 / 6791
页数:13
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