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Minimization of residual tin in the controlled Sn(II)octoate‐catalyzed polymerization of ε‐caprolactone
Author(s) -
Stjerndahl A.,
FinneWistrand A.,
Albertsson A.C.,
Bäckesjö C. M.,
Lindgren U.
Publication year - 2008
Publication title -
journal of biomedical materials research part a
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.849
H-Index - 150
eISSN - 1552-4965
pISSN - 1549-3296
DOI - 10.1002/jbm.a.31733
Subject(s) - materials science , tin , monomer , polymerization , polymer , chemical engineering , catalysis , dispersity , leaching (pedology) , caprolactone , porosity , polymer chemistry , nuclear chemistry , composite material , organic chemistry , metallurgy , chemistry , environmental science , soil science , engineering , soil water
Abstract By using less catalyst in the ring‐opening polymerization of ε‐caprolactone, a residual tin content of 5 ppm was reached without the need for additional purification. The initial amount of tin (II) 2‐ethylhexanoate [Sn(Oct) 2 ] was varied using catalyst:monomer ratios of 1:1000, 1:10,000, and 1:20,000. The impact on the final conversion, reaction control, average molecular weight, and polydispersity was studied. The amount of Sn(Oct) 2 could be significantly reduced without influencing the reaction results. The residual amount of tin was reduced from 176ppm with a catalyst:monomer ratio of 1:1000 in the polymer, to 5 ppm with the ratio 1:10,000. It was thus concluded that a catalyst:monomer ratio of 1:10,000 or lower is required to achieve a polymer with tin content suitable for biomedical applications. The materials were also tested in a proliferation study with mesenchymal stem cells from mouse. Porous scaffolds were fabricated from the polymers, using a salt leaching technique, and the cell growth on the porous scaffolds as well as on homogeneous films was determined by light absorbance measurements. In this study, the cell proliferation results showed that cells could grow on all polymers with an efficiency equal to or better than that on normal tissue culture plastic. © 2008 Wiley Periodicals, Inc. J Biomed Mater Res 2008