TY - JOUR
T1 - Biostability of polyether-urethane scaffolds: A comparison of two novel processing methods and the effect of higher gamma-irradiation dose
AU - Haugen, H.J.
AU - Gerhardt, L.C.
AU - Will, J.
AU - Wintermantel, E.
PY - 2005
Y1 - 2005
N2 - This article deals with enzyme-induced biodegradation behavior of thermoplastic polyether–urethane (TPU). Porous scaffolds were processed by a new foaming method applied in hot pressing and injection molding. The scaffolds were subsequently ¿ sterilized. The samples were incubated with cholesterol esterase (CE) for 28 days to simulate an enzymatic degradation order to assess polymer biostability. The main focus of degradation products was the most toxic one: methylene dianiline (MDA). LC/MS was used to separate the breakdown products and to identify possible MDA amounts. The results showed that (a) the hot-pressed sample released an MDA amount almost twice as large (0.26 ng ± 0.008) as that of the injection-molded samples (0.15 ng ± 0.003) after incubation with enzyme activity in the physiological range, and (b) a tenfold increase in CE activity revealed considerably higher MDA amounts (7540.0 ng ± 0.004). This enzyme concentration is physiologically unlikely, however, but may occur for extreme high inflammation behavior. Even for extremely high levels of CE enzyme, the scaffold will not discharge MDA above toxic levels. The injection-molded samples sterilized at 25 kGy seem to represent the most promising processing method. Therefore, the new injection-molding foaming process of polyether–urethane can be considered appropriate for use as a biomaterial.
AB - This article deals with enzyme-induced biodegradation behavior of thermoplastic polyether–urethane (TPU). Porous scaffolds were processed by a new foaming method applied in hot pressing and injection molding. The scaffolds were subsequently ¿ sterilized. The samples were incubated with cholesterol esterase (CE) for 28 days to simulate an enzymatic degradation order to assess polymer biostability. The main focus of degradation products was the most toxic one: methylene dianiline (MDA). LC/MS was used to separate the breakdown products and to identify possible MDA amounts. The results showed that (a) the hot-pressed sample released an MDA amount almost twice as large (0.26 ng ± 0.008) as that of the injection-molded samples (0.15 ng ± 0.003) after incubation with enzyme activity in the physiological range, and (b) a tenfold increase in CE activity revealed considerably higher MDA amounts (7540.0 ng ± 0.004). This enzyme concentration is physiologically unlikely, however, but may occur for extreme high inflammation behavior. Even for extremely high levels of CE enzyme, the scaffold will not discharge MDA above toxic levels. The injection-molded samples sterilized at 25 kGy seem to represent the most promising processing method. Therefore, the new injection-molding foaming process of polyether–urethane can be considered appropriate for use as a biomaterial.
U2 - 10.1002/jbm.b.30237
DO - 10.1002/jbm.b.30237
M3 - Article
C2 - 15756657
SN - 1552-4973
VL - 73B
SP - 229
EP - 237
JO - Journal of Biomedical Materials Research, Part B: Applied Biomaterials
JF - Journal of Biomedical Materials Research, Part B: Applied Biomaterials
IS - 2
ER -