Cell-interactive alginate-chitosan biopolymer systems with tunable mechanics and antibody release rates

被引:12
|
作者
Fletcher, Nathan A. [1 ]
Von Nieda, Evelyn L. [1 ]
Krebs, Melissa D. [1 ]
机构
[1] Colorado Sch Mines, Dept Chem & Biol Engn, 431 Alderson Hall,1613 Illinois St, Golden, CO 80401 USA
关键词
Alginate; Chitosan; Polyelectrolyte complex; Mechanical properties; Hydrogel; Sustained protein release; STEM-CELLS; MATRIX; HYDROGELS; STIFFNESS; FATE; 3D;
D O I
10.1016/j.carbpol.2017.08.035
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
This work investigates techniques to produce biocompatible hydrogels with tunable stiffness without the addition of crosslinking agents or altering cell binding sites. Alginate and water-soluble chitosan salts were used to form polyelectrolyte complexes (PECs), where the storage and loss moduli could be increased by raising gelation temperatures. The largest change, a 6.5-fold increase in storage modulus, occurred when the crosslinking temperature was increased from 37 to 50 degrees C while using chitosan with chlorine counterions. Osteogenic MC3T3 cells were shown to have significantly higher proliferation on the stiffer PECs prepared at 50 degrees C compared to 37 degrees C. Gelation temperature showed minimal effect on antibody release, but the inclusion of CaSO4 provided a longer overall release where the rate was nearly linear for several weeks. However, CaSO4 inhibited the strengthening effect of increased gelation temperature. PECs containing glutamate counterions demonstrated an increase in stiffness with decreased chitosan content. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:765 / 772
页数:8
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