| Literature DB >> 24468582 |
Kelsey A Potter1, Mehdi Jorfi2, Kyle T Householder1, E Johan Foster2, Christoph Weder2, Jeffrey R Capadona3.
Abstract
The cellular and molecular mechanisms by which neuroinflammatory pathways respond to and propagate the reactive tissue response to intracortical microelectrodes remain active areas of research. We previously demonstrated that both the mechanical mismatch between rigid implants and the much softer brain tissue, as well as oxidative stress, contribute to the neurodegenerative reactive tissue response to intracortical implants. In this study, we utilize physiologically responsive, mechanically adaptive polymer implants based on poly(vinyl alcohol) (PVA), with the capability to also locally administer the antioxidant curcumin. The goal of this study is to investigate if the combination of two independently effective mechanisms - softening of the implant and antioxidant release - leads to synergistic effects in vivo. Over the first 4weeks of the implantation, curcumin-releasing, mechanically adaptive implants were associated with higher neuron survival and a more stable blood-brain barrier at the implant-tissue interface than the neat PVA controls. 12weeks post-implantation, the benefits of the curcumin release were lost, and both sets of compliant materials (with and without curcumin) had no statistically significant differences in neuronal density distribution profiles. Overall, however, the curcumin-releasing softening polymer implants cause minimal implant-mediated neuroinflammation, and embody the new concept of localized drug delivery from mechanically adaptive intracortical implants. Published by Elsevier Ltd.Entities:
Keywords: Blood–brain barrier; Curcumin; Intracortical microelectrodes; Mechanically adaptive; Neuroinflammation
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Year: 2014 PMID: 24468582 DOI: 10.1016/j.actbio.2014.01.018
Source DB: PubMed Journal: Acta Biomater ISSN: 1742-7061 Impact factor: 8.947