3D fiber-deposited electrospun integrated scaffolds enhance cartilage tissue formation

被引:170
作者
Moroni, Lorenzo [1 ]
Schotel, Roka [2 ]
Hamann, Doreen [1 ]
de Wijn, Joost R. [1 ]
van Blitterswijk, Clemens A. [1 ]
机构
[1] Univ Twente, BMTI, NL-7500 AE Enschede, Netherlands
[2] CellCoTec, NL-3723 MB Bilthoven, Netherlands
关键词
D O I
10.1002/adfm.200601158
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Despite the periodical and completely interconnected pore network that characterizes rapid prototyped scaffolds, cell seeding efficiency remains still a critical factor for optimal tissue regeneration. This can be mainly attributed to the current resolution limits in pore size. We present here novel three-dimensional (3D) scaffolds fabricated by combining 3D fiber deposition (3DF) and electrospinning (ESP). Scaffolds consisted of integrated 3DF periodical macrofiber and random ESP microfiber networks (3DFESP). The 3DF scaffold provides structural integrity and mechanical properties, while the ESP network works as a "sieving" and cell entrapment system and offers-at the same time-cues at the extracellular matrix (ECM) scale. Primary bovine articular chondrocytes were isolated, seeded, and cultured for four weeks on 3DF and 3DFESP scaffolds to evaluate the influence of the integrated ESP network on cell entrapment and on cartilage tissue formation. 3DFESP scaffolds enhanced cell entrapment as compared to 3DF scaffolds. This was accompanied by a higher amount of ECM (expressed in terms of sulphated glycosaminoglycans or GAG) and a significantly higher GAG/DNA ratio after 28 days. SEM analysis revealed rounded cell morphology on 3DFESP scaffolds. Spread morphology was observed on 3DF scaffolds, suggesting a direct influence of fiber dimensions on cell differentiation. Furthermore, the ESP surface topology also influenced cell morphology. Thus, the integration of 3DF and ESP techniques provide a new set of "smart" scaffolds for tissue engineering applications.
引用
收藏
页码:53 / 60
页数:8
相关论文
共 61 条
[1]   Three-dimensional bioactive and biodegradable scaffolds fabricated by surface-selective laser sintering [J].
Antonov, EN ;
Bagratashvili, VN ;
Whitaker, MJ ;
Barry, JJA ;
Shakesheff, KM ;
Konovalov, AN ;
Popov, VK ;
Howdle, SM .
ADVANCED MATERIALS, 2005, 17 (03) :327-+
[2]   Effect of fiber diameter on spreading, proliferation, and differentiation of osteoblastic cells on electrospun poly(lactic acid) substrates [J].
Badami, AS ;
Kreke, MR ;
Thompson, MS ;
Riffle, JS ;
Goldstein, AS .
BIOMATERIALS, 2006, 27 (04) :596-606
[3]   EFFECT OF IMPLANTATION SITE ON PHAGOCYTE POLYMER INTERACTION AND FIBROUS CAPSULE FORMATION [J].
BAKKER, D ;
VANBLITTERSWIJK, CA ;
HESSELING, SC ;
GROTE, JJ ;
DAEMS, WT .
BIOMATERIALS, 1988, 9 (01) :14-23
[4]   Porous methacrylate scaffolds: supercritical fluid fabrication and in vitro chondrocyte responses [J].
Barry, JJA ;
Gidda, HS ;
Scotchford, CA ;
Howdle, SM .
BIOMATERIALS, 2004, 25 (17) :3559-3568
[5]   DEGRADATIVE BEHAVIOR OF POLYMERIC MATRICES IN (SUB)DERMAL AND MUSCLE-TISSUE OF THE RAT - A QUANTITATIVE STUDY [J].
BEUMER, GJ ;
VANBLITTERSWIJK, CA ;
PONEC, M .
BIOMATERIALS, 1994, 15 (07) :551-559
[6]   BIOCOMPATIBILITY OF A BIODEGRADABLE MATRIX USED AS A SKIN SUBSTITUTE - AN IN-VIVO EVALUATION [J].
BEUMER, GJ ;
VANBLITTERSWIJK, CA ;
PONEC, M .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH, 1994, 28 (05) :545-552
[7]   A controlled release system for proteins based on poly(ether ester) block-copolymers: polymer network characterization [J].
Bezemer, JM ;
Grijpma, DW ;
Dijkstra, PJ ;
van Blitterswijk, CA ;
Feijen, J .
JOURNAL OF CONTROLLED RELEASE, 1999, 62 (03) :393-405
[8]  
Bognitzki M, 2001, ADV MATER, V13, P70, DOI 10.1002/1521-4095(200101)13:1<70::AID-ADMA70>3.0.CO
[9]  
2-H
[10]  
BOLAND E, 2005, ACTA BIOMATER, P115