Progress in Biomedical Polymers 1990
DOI: 10.1007/978-1-4899-0768-4_26
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Biodegradable Polyamides Based on 4,4′-Spirobibutyrolactone

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Cited by 10 publications
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“…The appearance of the carbonyl stretching found at a high wavenumber and hydroxyl group absorptions were attributed to the esterification of the epoxide with γ-carboxylic acids as most of amino acids exist as inactive species at 180 °C [ 22 ]. The C=O stretch at 1692 cm −1 likely corresponds to amide I of the 5-membered lactam bonds produced by the internal cyclization of Glu with a few γ-carboxylic acids that did not react with epoxy groups, which is a well-known transformation of Glu under high temperature [ 20 , 34 ]. The epoxy conversion of EGS-1 at 180 °C was slightly higher than that of EG.…”
Section: Resultsmentioning
confidence: 99%
“…The appearance of the carbonyl stretching found at a high wavenumber and hydroxyl group absorptions were attributed to the esterification of the epoxide with γ-carboxylic acids as most of amino acids exist as inactive species at 180 °C [ 22 ]. The C=O stretch at 1692 cm −1 likely corresponds to amide I of the 5-membered lactam bonds produced by the internal cyclization of Glu with a few γ-carboxylic acids that did not react with epoxy groups, which is a well-known transformation of Glu under high temperature [ 20 , 34 ]. The epoxy conversion of EGS-1 at 180 °C was slightly higher than that of EG.…”
Section: Resultsmentioning
confidence: 99%
“…It is also the area where the kinetics of the degradation processes have been most widely studied. Though several classes of biodegradable synthetic polymers have been developed, including polyamides based on 4, 4 -spirobibutyrolactone [13] and poly(hydroxylalkanoates), it is the poly(α-esters) that have been most widely utilized for biomedical applications. Let us look at a specific example of synthetic polymers for resorbable suture material.…”
Section: Biological Degradationmentioning
confidence: 99%