Biomedical Engineering Reference
In-Depth Information
The change of mechanical properties associated with degradation has been
studied for various biodegradable polymers. Raghunath et al. [
25
] characterised
solid sheets of biodegradable polyhedral oligomeric silsesquioxane modified
poly(caprolactone/carbonate) urethane/urea during accelerated
in vitro
degradation
of up to eight weeks. Kang et al. [
26
] studied the
in vitro
degradation of a porous
poly(l-lactic acid)/
β
-tricalcium phosphate scaffold, fabricated by particulate leach-
ing, of up to six weeks and reported the effect on the compressive strength.
While the mechanics of electro-spun degradable scaffolds has been investigated
prior to degradation, the information on the effects of the degradation process on
the mechanical properties is limited. Lee et al. [
23
] studied the maintenance of ten-
sile properties of electro-spun poly(
ε
-caprolactone)/collagen scaffolds subjected to
a perfusion bioreactor environment for up to four weeks. Henry et al. [
27
] mechani-
cally characterised electro-spun meshes of a slow degrading polyester-urethane dur-
ing hydrolytic
in vitro
degradation of up to 346 days.
We investigated a highly porous, electro-spun structure made from a fast-
degrading polyester-urethane. The change of structural and mechanical properties
of the scaffold was studied during hydrolytic
in vitro
degradation of up to 34 days.
Based on these data, a constitutive model for the scaffold was developed that specif-
ically aims at representing the changes in scaffold mechanical properties due to
degradation. This is important as the tissue ingrowth and scaffold degradation oc-
curs simultaneously and scaffold contribution during healing must be tailored to
compliment that of the new tissue [
28
].
2 Effects of Degradation on Mechanical Scaffold Properties
2.1 Scaffold Material
DegraPol
®
(ab medica S.p.A, Lainate, Italy) is a biodegradable polyester-urethane
that consists of poly(3-(R-hydroxybutyrate)-co-(
ε
-caprolactone))-diol (hard seg-
ment) and poly(
ε
-caprolactone-co-glycolide)-diol (soft segment). Both polymer
segments are biodegradable and their degradation products are non-toxic [
29
]. By
using different ratios of hard and soft segment the mechanical properties of the final
product can be modulated, whereas by changing the ratio of
ε
caprolactone to gly-
colide the degradation characteristics can be modulated. This versatility, combined
with the non-toxicity and haemocompatibility makes DegraPol
®
a promising choice
for tissue engineering scaffolds. DegraPol
®
DP30 has a
ε
-caprolactone-to-glycolide
ratio of 70:30 and a hard-to-soft segment ratio of 40:60 (unpublished data). The
electro-spinning solution was prepared by dissolving DegraPol
®
DP30 in chloro-
form with a 20 % by weight concentration at room temperature and subsequently
sonicating in distilled water at 37 °C for 90 min.
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