Delivery of Brain-Derived Neurotrophic Factor by 3D Biocompatible Polymeric Scaffolds for Neural Tissue Engineering and Neuronal Regeneration
Perrone Donnorso, M.
Di Fabrizio, Enzo M.
KAUST DepartmentAnalytical Chemistry Core Lab
Biological and Environmental Sciences and Engineering (BESE) Division
Material Science and Engineering Program
Physical Science and Engineering (PSE) Division
Online Publication Date2018-03-29
Print Publication Date2018-12
Permanent link to this recordhttp://hdl.handle.net/10754/627626
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AbstractBiopolymers are increasingly employed for neuroscience applications as scaffolds to drive and promote neural regrowth, thanks to their ability to mediate the upload and subsequent release of active molecules and drugs. Synthetic degradable polymers are characterized by different responses ranging from tunable distension or shrinkage to total dissolution, depending on the function they are designed for. In this paper we present a biocompatible microfabricated poly-ε-caprolactone (PCL) scaffold for primary neuron growth and maturation that has been optimized for the in vitro controlled release of brain-derived neurotrophic factor (BDNF). We demonstrate that the designed morphology confers to these devices an enhanced drug delivery capability with respect to monolithic unstructured supports. After incubation with BDNF, micropillared PCL devices progressively release the neurotrophin over 21 days in vitro. Moreover, the bioactivity of released BDNF is confirmed using primary neuronal cultures, where it mediates a consistent activation of BDNF signaling cascades, increased synaptic density, and neuronal survival. These results provide the proof-of-principle on the fabrication process of micropatterned PCL devices, which represent a promising therapeutic option to enhance neuronal regeneration after lesion and for neural tissue engineering and prosthetics.
CitationLimongi T, Rocchi A, Cesca F, Tan H, Miele E, et al. (2018) Delivery of Brain-Derived Neurotrophic Factor by 3D Biocompatible Polymeric Scaffolds for Neural Tissue Engineering and Neuronal Regeneration. Molecular Neurobiology. Available: http://dx.doi.org/10.1007/s12035-018-1022-z.
SponsorsThe work was supported by the King Abdullah University of Science and Technology start-up funding and by research grants from the European Union FP7 BNeuroscaffolds^ (grant number 604263 to FB), Compagnia di San Paolo-Italy (to FC).
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