Effect of biomimetic conditions on mechanical and structural integrity of PGA/P4HB and electrospun PCL scaffolds

被引:36
作者
Klouda, Leda [1 ,2 ]
Vaz, Claudia M. [2 ]
Mol, Anita [2 ]
Baaijens, Frank P. T. [2 ]
Bouten, Carlijn V. C. [2 ]
机构
[1] Rice Univ, Dept Bioengn, Houston, TX 77251 USA
[2] Eindhoven Univ Technol, Dept Biomed Engn, Div Biomech & Tissue Engn, NL-5600 MB Eindhoven, Netherlands
关键词
D O I
10.1007/s10856-007-0171-9
中图分类号
R318 [生物医学工程];
学科分类号
0831 [生物医学工程];
摘要
The selection of an appropriate scaffold represents one major key to success in tissue engineering. In cardiovascular applications, where a load-bearing structure is required, scaffolds need to demonstrate sufficient mechanical properties and importantly, reliable retention of these properties during the developmental phase of the tissue engineered construct. The effect of in vitro culture conditions, time and mechanical loading on the retention of mechanical properties of two scaffold types was investigated. First candidate tested was a poly-glycolic acid non-woven fiber mesh, coated with poly-4-hydroxybutyrate (PGA/P4HB), the standard scaffold used successfully in cardiovascular tissue engineering applications. As an alternative, an electrospun poly-epsilon-caprolactone (PCL) scaffold was used. A 15-day dynamic loading protocol was applied to the scaffolds. Additionally, control scaffolds were incubated statically. All studies were performed in a simulated physiological environment (phosphate-buffered saline solution, T = 37C). PGA/P4HB scaffolds showed a dramatic decrease in mechanical properties as a function of incubation time and straining. Mechanical loading had a significant effect on PCL scaffold properties. Degradation as well as fiber fatigue caused by loading promote loss of mechanical properties in PGA/P4HB scaffolds. For PCL, fiber reorganization due to straining seems to be the main reason behind the brittle behavior that was pronounced in these scaffolds. It is suggested that those changes in scaffolds' mechanical properties must be considered at the application of in vitro tissue engineering protocols and should ideally be taken over by tissue formation to maintain mechanically stable tissue constructs.
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页码:1137 / 1144
页数:8
相关论文
共 28 条
[1]
Precipitation casting of polycaprolactone for applications in tissue engineering and drug delivery [J].
Coombes, AGA ;
Rizzi, SC ;
Williamson, M ;
Barralet, JE ;
Downes, S ;
Wallace, WA .
BIOMATERIALS, 2004, 25 (02) :315-325
[2]
THERMODYNAMICS OF FUSION OF POLY-BETA-PROPIOLACTONE AND POLY-EPSILON-CAPROLACTONE - COMPARATIVE ANALYSIS OF MELTING OF ALIPHATIC POLYLACTONE AND POLYESTER CHAINS [J].
CRESCENZI, V ;
MANZINI, G ;
CALZOLARI, G ;
BORRI, C .
EUROPEAN POLYMER JOURNAL, 1972, 8 (03) :449-+
[3]
A novel bioreactor for the dynamic flexural stimulation of tissue engineered heart valve biomaterials [J].
Engelmayr, GC ;
Hildebrand, DK ;
Sutherland, FWH ;
Mayer, JE ;
Sacks, MS .
BIOMATERIALS, 2003, 24 (14) :2523-2532
[4]
Hoerstrup SP, 2000, CIRCULATION, V102, P44
[5]
Tissue engineering of small caliber vascular grafts [J].
Hoerstrup, SP ;
Zünd, G ;
Sodian, R ;
Schnell, AM ;
Grünenfelder, J ;
Turina, MI .
EUROPEAN JOURNAL OF CARDIO-THORACIC SURGERY, 2001, 20 (01) :164-169
[6]
New pulsatile bioreactor for in vitro formation of tissue engineered heart valves [J].
Hoerstrup, SP ;
Sodian, R ;
Sperling, JS ;
Vacanti, JP ;
Mayer, JE .
TISSUE ENGINEERING, 2000, 6 (01) :75-79
[7]
Hutmacher DW, 2001, J BIOMED MATER RES, V55, P203, DOI 10.1002/1097-4636(200105)55:2<203::AID-JBM1007>3.3.CO
[8]
2-Z
[9]
Scaffolds in tissue engineering bone and cartilage [J].
Hutmacher, DW .
BIOMATERIALS, 2000, 21 (24) :2529-2543
[10]
Scaffolds for engineering smooth muscle under cyclic mechanical strain conditions [J].
Kim, BS ;
Mooney, DJ .
JOURNAL OF BIOMECHANICAL ENGINEERING-TRANSACTIONS OF THE ASME, 2000, 122 (03) :210-215