Development of surface functionalization strategies for 3D-printed polystyrene constructs

被引:6
作者
Lerman, Max J. [1 ,2 ,3 ]
Muramoto, Shin [2 ]
Arumugasaamy, Navein [3 ,4 ,5 ]
Van Order, Michael [1 ]
Lembong, Josephine [3 ,4 ]
Gerald, Anushka G. [3 ,4 ]
Gillen, Greg [2 ]
Fisher, John P. [3 ,4 ]
机构
[1] Univ Maryland, Dept Mat Sci & Engn, College Pk, MD 20742 USA
[2] NIST, Surface & Trace Chem Anal Grp, Mat Measurement Lab, Gaithersburg, MD 20899 USA
[3] Univ Maryland, Ctr Engn Complex Tissues, College Pk, MD 20742 USA
[4] Univ Maryland, Fischell Dept Bioengn, College Pk, MD 20742 USA
[5] Childrens Natl Hlth Syst, Sheikh Zayed Inst Pediat Surg Innovat, Washington, DC USA
基金
美国国家卫生研究院;
关键词
polystyrene; surface chemical modification; plasma treatment; protein adhesion; 3D printing; MESENCHYMAL STEM-CELLS; IN-VITRO; PROTEIN ADSORPTION; PLASMA TREATMENT; ACTIN POLYMERIZATION; CONTACT-ANGLE; ADHESION; FIBRONECTIN; CULTURE; DIFFERENTIATION;
D O I
10.1002/jbm.b.34347
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
There is a growing interest in 3D printing to fabricate culture substrates; however, the surface properties of the scaffold remain pertinent to elicit targeted and expected cell responses. Traditional 2D polystyrene (PS) culture systems typically require surface functionalization (oxidation) to facilitate and encourage cell adhesion. Determining the surface properties which enhance protein adhesion from media and cellular extracellular matrix (ECM) production remains the first step to translating 2D PS systems to a 3D culture surface. Here we show that the presence of carbonyl groups to PS surfaces correlated well with successful adhesion of ECM proteins and sustaining ECM production of deposited human mesenchymal stem cells, if the surface has a water contact angle between 50 degrees and 55 degrees. Translation of these findings to custom-fabricated 3D PS scaffolds reveals carbonyl groups continued to enhance spreading and growth in 3D culture. Cumulatively, these data present a method for 3D printing PS and the design considerations required for understanding cell-material interactions. (c) 2019 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater 107B:2566-2578, 2019.
引用
收藏
页码:2566 / 2578
页数:13
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