Mechanically reinforced cell-laden scaffolds formed using alginate-based bioink printed onto the surface of a PCL/alginate mesh structure for regeneration of hard tissue

被引:40
作者
Kim, Yong Bok [1 ]
Lee, Hyeongjin [1 ]
Yang, Gi-Hoon [1 ]
Choi, Chang Hyun [1 ]
Lee, DaeWeon [1 ]
Hwang, Heon [1 ]
Jung, Won-Kyo [2 ]
Yoon, Hyeon [3 ]
Kim, Geun Hyung [1 ]
机构
[1] Sungkyunkwan Univ, Dept Biomechatron Engn, Suwon, South Korea
[2] Pukyong Natl Univ, Dept Biomed Engn, Busan 608737, South Korea
[3] Hallym Univ, Hangang Sacred Heart Hosp, Burn Inst, Seoul, South Korea
关键词
Bioink; Cell-laden process; Scaffold; Tissue engineering; ENGINEERED CARTILAGE; IN-VIVO; FABRICATION; BIOMATERIALS; MODEL; BONE;
D O I
10.1016/j.jcis.2015.09.044
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Cell-printing technology has provided a new paradigm for biofabrication, with potential to overcome several shortcomings of conventional scaffold-based tissue regeneration strategies via controlled delivery of various cell types in well-defined target regions. Here we describe a cell-printing method to obtain mechanically reinforced multi-layered cell-embedded scaffolds, formed of micron-scale poly(E-caprolactone) (PCL)/alginate struts coated with alginate-based bioink. To compare the physical and cellular activities, we used a scaffold composed of pure alginate (without cells) coated PCL/alginate struts as a control. We systematically varied the ratio of alginate cross-linking agent, and determined the optimal cell-coating conditions to form the PCL/alginate struts. Following fabrication of the cell (MG63)-laden PCL/alginate scaffold, the bioactivity was evaluated in vitro. The laden cells exhibited a substantially more developed cytoskeleton compared with those on a control scaffold consisting of the same material composition. Based on these results, the printed cells exhibited a significantly more homogenous distribution within the scaffold compared with the control. Cell proliferation was determined via MIT assays at 1, 3, 7, and 14 days of culture, and the proliferation of the cell-printed scaffold was substantially in excess (similar to 2.4-fold) of that on the control. Furthermore, the osteogenic activity such as ALP was measured, and the cell-laden scaffold exhibited significantly greater activity (similar to 3.2-fold) compared with the control scaffold. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:359 / 368
页数:10
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