3D-Printed conductive polymeric scaffolds with direct current electrical stimulation for enhanced bone regeneration

被引:15
作者
Dixon, Damion T. [1 ]
Gomillion, Cheryl T. [2 ,3 ]
机构
[1] Univ Georgia, Coll Engn, Sch Environm Civil Agr & Mech Engn, Athens, GA USA
[2] Univ Georgia, Coll Engn, Sch Chem Mat & Biomed Engn, Athens, GA USA
[3] Univ Georgia, Coll Engn, Sch Chem Mat & Biomed Engn, Athens, GA 30602 USA
关键词
3D printing; bone regeneration; bone tissue engineering; conductive bone scaffold; electrical cell response; electrical stimulation; OSTEOGENIC DIFFERENTIATION; COMPOSITE SCAFFOLDS; POROUS SCAFFOLDS; TISSUE; BIOMATERIALS; POLYLACTIDE; MARROW; FABRICATION; BEHAVIOR; CALCIUM;
D O I
10.1002/jbm.b.35239
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Various methods have been used to treat bone defects caused by genetic disorders, injury, or disease. Yet, there is still great need to develop alternative approaches to repair damaged bone tissue. Bones naturally exhibit piezoelectric potential, or the ability to convert mechanical stresses into electrical impulses. This phenomenon has been utilized clinically to enhance bone regeneration in conjunction with electrical stimulation (ES) therapies; however, oftentimes with critical-sized bone defects, the bioelectric potential at the site of injury is compromised, resulting in less desirable outcomes. In the present study, the potential of a 3D-printed conductive polymer blend to enhance bone formation through restoration of the bioelectrical microenvironment was evaluated. A commercially available 3D printer was used to create circular, thin-film scaffolds consisting of either polylactide (PLA) or a conductive PLA (CPLA) composite. Preosteoblast cells were seeded onto the scaffolds and subjected to direct current ES via a purpose-built cell culture chamber. It was found that CPLA scaffolds had no adverse effects on cell viability, proliferation or differentiation when compared with control scaffolds. The addition of ES, however, resulted in a significant increase in the expression of osteocalcin, a protein indicative of osteoblast maturation, after 14 days of culture. Furthermore, xylenol orange staining also showed the presence of increased mineralized calcium nodules in cultures undergoing stimulation. This study demonstrates the potential for low-cost, conductive scaffolding materials to support cell viability and enhance in vitro mineralization in conjunction with ES.
引用
收藏
页码:1351 / 1364
页数:14
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