Development of cryogenic prototyping for tissue engineering

被引:20
作者
Lim, T. C. [1 ]
Bang, C. P. [1 ]
Chian, K. S. [1 ]
Leong, K. F. [1 ]
机构
[1] Nanyang Technol Univ, Sch Mech & Aerosp Engn, 50 Nanyang Ave, Singapore 639798, Singapore
关键词
tissue engineering; rapid prototyping; scaffold; freezing;
D O I
10.1080/17452750701799303
中图分类号
T [工业技术];
学科分类号
08 [工学];
摘要
A major challenge in tissue engineering has been the creation of scaffolds with controlled complex geometries. Rapid prototyping (RP) has the ability to produce complex three-dimensional structures with precise control of pore size, geometry and connectivity. In this paper, a novel technique utilising RP technology for the fabrication of tissue engineering scaffolds is presented. The main advantage of this cryogenic prototyping (CP) technique is the low operating temperatures which will allow the processing of temperature sensitive and bioactive components. Microstructure of CP Chitosan scaffolds fabricated can be controlled by processing parameters, such as the processing temperature. The macrostructure of the scaffolds is controlled by 3D computer aided design (CAD). In addition, in vitro studies with Chitosan CP scaffolds have shown that the scaffold designs are useful in promoting cell infiltration and alignment. Preliminary in vivo studies show encouraging results of cellular infiltration as well as vascularisation.
引用
收藏
页码:25 / 31
页数:7
相关论文
共 13 条
[1]
Rapid prototyping: from product development to medicine and beyond [J].
Gibson, Ian .
VIRTUAL AND PHYSICAL PROTOTYPING, 2006, 1 (01) :31-42
[2]
Emerging design principles in Biomaterials and scaffolds for tissue engineering [J].
Griffith, LG .
REPARATIVE MEDICINE: GROWING TISSUES AND ORGANS, 2002, 961 :83-95
[3]
Fabrication of soft tissue engineering scaffolds by means of rapid prototyping techniques [J].
Landers, R ;
Pfister, A ;
Hübner, U ;
John, H ;
Schmelzeisen, R ;
Mülhaupt, R .
JOURNAL OF MATERIALS SCIENCE, 2002, 37 (15) :3107-3116
[4]
TISSUE ENGINEERING [J].
LANGER, R ;
VACANTI, JP .
SCIENCE, 1993, 260 (5110) :920-926
[5]
Langer R, 2007, TISSUE ENG, V13, P1, DOI 10.1089/ten.2006.0219
[6]
Scaffolds for tissue fabrication [J].
Ma, Peter X. .
MATERIALS TODAY, 2004, 7 (05) :30-40
[7]
In vitro and in vivo characteristics of PCL scaffolds with pore size gradient fabricated by a centrifugation method [J].
Oh, Se Heang ;
Park, Il Kyu ;
Kim, Jin Man ;
Lee, Jin Ho .
BIOMATERIALS, 2007, 28 (09) :1664-1671
[8]
Scaffold development using selective laser sintering of polyetheretherketone-hydroxyapatite biocomposite blends [J].
Tan, KH ;
Chua, CK ;
Leong, KF ;
Cheah, CM ;
Cheang, P ;
Abu Bakar, MS ;
Cha, SW .
BIOMATERIALS, 2003, 24 (18) :3115-3123
[9]
The design of scaffolds for use in tissue engineering. Part 1. Traditional factors [J].
Yang, SF ;
Leong, KF ;
Du, ZH ;
Chua, CK .
TISSUE ENGINEERING, 2001, 7 (06) :679-689
[10]
The design of scaffolds for use in tissue engineering. Part II. Rapid prototyping techniques [J].
Yang, SF ;
Leong, KF ;
Du, ZH ;
Chua, CK .
TISSUE ENGINEERING, 2002, 8 (01) :1-11