Background And Aims: Neuropathic pain is a significant medical problem needing more effective treatments with fewer side effects. Overactive glutamatergic transmission via N-methyl-d-aspartate receptors (NMDARs) are known to play a role in central sensitization and neuropathic pain. Although ketamine, a NMDAR channel-blocking antagonist, is often used for neuropathic pain, its side-effect profile and abusive potential has prompted the search for a safer effective oral analgesic.
View Article and Find Full Text PDFJ Biomater Sci Polym Ed
February 2010
A family of biodegradable poly(ester amide) (PEA) co-polymers based on naturally occurring alpha-amino acids has been developed for applications ranging from biomedical device coatings to delivery of therapeutic biologics. An important feature of PEA co-polymer coatings may be their ability to promote a natural healing response. To gain insight into this process, representative elastomeric PEAs designed for a cardiovascular stent coating were compared to non-degradable and biodegradable polymers in a series of in vitro assays to examine blood and cellular responses.
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