| Spinal cord injuries (SCI) still remain a major challenge in current biomedicalresearch. In spite of several advances in the understanding of
 its mechanisms there has not been an equal significant translation into
 the clinics. As a result, there is no effective treatment that can overcome
 the biochemical and cellular adverse reactions that lead to a chronic
 severely impaired condition. One of the first opportunities to minimize
 these drastic consequences is to control the secondary events that follow
 the trauma. We are proposing the local delivery of an anti-inflammatory
 corticosteroid - methylprednisolone (MP) - in an attempt to
 modulate the noxious effects of the inflammation in the acute SCI. A
 sustained delivery as the one provided by these nanoparticles (NP) can
 be highly advantageous, maximizing the drug’s potency in the target
 site. Therefore, we synthesized MP-loaded NPs composed of an inner
 poly/(amido)amine (PAMAM) dendrimeric core and grafted with carboxymethylchitosan
 (CMCht). Chemical and biological characterization
 studies were carried out showing that the NPs are stable in acidic
 and neutral buffer solutions. Also, the viability of primary glial cultures
 was not compromised by the presence of 200 lg/mL of NP. In turn, an
 MP action in microglial cultures was observed in dosages above 1 mg/
 mL showing that MP is being released from the NPs inside the cells.
 The uptake profile of these NPs is time dependent and reaches itsmaximum
 24 h after incubation with astrocytes, oligodendrocytes and
 microglia. In a preview of a possible therapeutic effect, the NPs were
 administered in hemisected spinal cord injured rats. To assess the efficacy
 of local injections around the lesion site the animals were sacrificed
 3 h after surgery and frozen sections were observed. The
 fluorescently labeled-NPs were detected in the injury and in the surrounding
 spinal tissue indicating a successful delivery of the NP to the
 spinal tissue. The local injections were repeated in hemisected rats that
 were kept for 1 month, performing the BBB locomotory test weekly.
 Significant differences in the BBB test were found between the MPloaded
 NPs injected rats and the sham group as well as the ones
 injected with MP, demonstrating a favorable action of the MP-NPs in
 the acute phase of the injury. This work revealed that sustained delivery
 of MP via a NP system can be highly beneficial in the management
 of the secondary injury that follows SCI improving the overall functional
 outcome of the injured animals.
 
 
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