A Novel Method to Precisely Assemble Loose Nanofiber Structures for Regenerative Medicine Applications

被引:30
作者
Beachley, Vince [1 ,2 ,3 ]
Katsanevakis, Eleni [1 ]
Zhang, Ning [1 ,4 ]
Wen, Xuejun [1 ,4 ]
机构
[1] Clemson Univ, Clemson MUSC Bioengn Program, Dept Bioengn, Charleston, SC 29425 USA
[2] Johns Hopkins Univ, Translat Tissue Engn Ctr, Wilmer Eye Inst, Baltimore, MD 21231 USA
[3] Johns Hopkins Univ, Dept Biomed Engn, Baltimore, MD 21231 USA
[4] Med Univ S Carolina, Dept Regenerat Med & Cell Biol, Charleston, SC 29425 USA
基金
美国国家科学基金会;
关键词
POLYMER NANOFIBERS; LIVING ORGANISMS; ELECTROSPUN; MICROFIBER; SCAFFOLDS; ADHESION; RELEASE; DESIGN; FIBERS;
D O I
10.1002/adhm.201200125
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Polymer nanofibers are favorable for tissue engineering scaffolds because of their high surface-to-volume ratio and biomimicry of the extracellular matrix. Random and uniaxially oriented polymer nanofibers are easily fabricated by conventional electrospinning techniques; however, control over fiber organization within nanofiber structures is limited when they are collected directly from an electrospinning jet. The regenerative medicine applications of electrospun scaffolds could be expanded by developing assembly methods that allow better control of fiber organization. Here, a novel technique is presented that utilizes parallel automated tracks to orient and collect nanofibers from an electrospinning jet. The stabilized fibers are then subsequently assembled into desirable structures. It is difficult to assemble complex structures directly from an electrospinning jet because of high electrical charge and velocities, so this technology adds an intermediate step where nanofibers are immobilized on automated tracks. The result is a continuous steady-state delivery of static stabilized nanofibers that provides a unique and promising platform for automated post processing into useful nanofiber structures. This technique also allows for an indefinite amount of time, as determined by design parameters, for fibers to dry or cool before they contact other nanofibers in the collection site, thus eliminating potential for fiber-to-fiber adhesions even with slow evaporating solvents or high-temperature melts. To demonstrate potential in regenerative medicine applications, several nanofiber structures were fabricated, including: 2D structures with well-controlled fiber density; 3D loosely assembled aligned nanofiber structures with good cell penetration properties; and, complex layer-by-layer 3D aligned fiber structures assembled by integration with post-processing techniques.
引用
收藏
页码:343 / 351
页数:9
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