P. Vermette et al., Commercial polyurethanes: The potential influence of auxiliary chemicals on the biodegradation process, J BIOM SC P, 10(7), 1999, pp. 729-749
This investigation elucidates some aspects of auxiliary chemicals on the bi
odegradation of two commercial polyurethanes (Pellethane(R) and Corethane(R
)). The materials were incubated for 28 days with cholesterol esterase and/
or with phosphatidylcholine. Extraction studies were carried out on the two
materials, using different solvents, chosen on the basis of solvent polari
ty, FT-IR spectra for the extracted materials indicated the presence of pol
y(methylene)(n) oxide moities, silicone oil, bis-ethylene-stearamide, aroma
tic moities, and alkyd-urea compounds in Pellethane(R). Corethane(R) materi
als were shown to contain some fatty acids, hydrocarbon waxes, ester-based
species, and chlorinated compounds. Analysis of incubation solutions by hig
h performance liquid chromatography failed to isolate methylene dianiline (
MDA) or any of its derivatives from the various polymer incubation solution
s. However, a methanol extract of Corethane(R) samples that were incubated
for 28 days in cholesterol esterase did show the presence of MDA, The absen
ce of MDA in the Pellethane methanol extracted samples may reflect the diff
erences in surface additives found for this material versus the Corethane.
FT-IR/ATR analysis of polymer surfaces exposed to cholesterol esterase/phos
pholipids mixture showed that there was an increase in the uptake of phosph
olipids over samples that were incubated in phospholipid dispersion alone.
The results of this study show that some of the auxiliary chemicals found i
n commercial polyurethanes may hinder the specific release of hydrolytic de
gradation products and delay polymer degradation. However, it should be rec
ognized that the surface layer containing these compounds is susceptible to
change following the interaction between the polyurethane-based devices an
d elements of the host environment (i.e. lipids, enzymes, etc.). Hence, rec
ognition and identification of these changes will ultimately be important i
n assessing a commercial polymer's blood compatibility characteristics.