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Título

Silk-elastin-like polymers for acute intraparenchymal treatment of the traumatically injured spinal cord: a first systematic experimental approach

AutorGonzález, Pau; González-Fernández, Carlos; Maqueda, Alfredo CSIC; Pérez, Virginia; Escalera-Anzola, Sara; Rodríguez de Lope, Ángel; Arias, Francisco Javier; Girotti, Alessandra; Rodríguez, Francisco Javier
Palabras claveSpinal cord injury
Silk-elastin-like polymers
(EIS)2-RGD6
Fecha de publicación2022
EditorMultidisciplinary Digital Publishing Institute
CitaciónPharmaceutics 14(12): 2713 (2022)
ResumenDespite the promising potential of hydrogel-based therapeutic approaches for spinal cord injury (SCI), the need for new biomaterials to design effective strategies for SCI treatment and the outstanding properties of silk-elastin-like polymers (SELP), the potential use of SELPs in SCI is currently unknown. In this context, we assessed the effects elicited by the in vivo acute intraparenchymal injection of an SELP named (EIS)2-RGD6 in a clinically relevant model of SCI. After optimization of the injection system, the distribution, structure, biodegradability, and cell infiltration capacity of (EIS)2-RGD6 were assessed. Finally, the effects exerted by the (EIS)2-RGD6 injection—in terms of motor function, myelin preservation, astroglial and microglia/macrophage reactivity, and fibrosis—were evaluated. We found that (EIS)2-RGD6 can be acutely injected in the lesioned spinal cord without inducing further damage, showing a widespread distribution covering all lesioned areas with a single injection and facilitating the formation of a slow-degrading porous scaffold at the lesion site that allows for the infiltration and/or proliferation of endogenous cells with no signs of collapse and without inducing further microglial and astroglial reactivity, as well as even reducing SCI-associated fibrosis. Altogether, these observations suggest that (EIS)2-RGD6—and, by extension, SELPs—could be promising polymers for the design of therapeutic strategies for SCI treatment.
Versión del editorhttp://dx.doi.org/10.3390/pharmaceutics14122713
URIhttp://hdl.handle.net/10261/296316
DOI10.3390/pharmaceutics14122713
Identificadoresdoi: 10.3390/pharmaceutics14122713
e-issn: 1999-4923
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