| Literature DB >> 33530643 |
Barbara Vigani1, Caterina Valentino1, Valeria Cavalloro1, Laura Catenacci1, Milena Sorrenti1, Giuseppina Sandri1, Maria Cristina Bonferoni1, Chiara Bozzi1, Simona Collina1, Silvia Rossi1, Franca Ferrari1.
Abstract
Injuries to the nervous system affect more than one billion people worldwide, and dramatically impact on the patient's quality of life. The present work aimed to design and develop a gellan gum (GG)-based composite system for the local delivery of the neuroprotective sigma-1 receptor agonist, 1-[3-(1,1'-biphen)-4-yl] butylpiperidine (RC-33), as a potential tool for the treatment of tissue nervous injuries. The system, consisting of cross-linked electrospun nanofibers embedded in a RC-33-loaded freeze-dried matrix, was designed to bridge the lesion gap, control drug delivery and enhance axonal regrowth. The gradual matrix degradation should ensure the progressive interaction between the inner fibrous mat and the surrounding cellular environment. Nanofibers, prepared by electrospinning polymeric solutions containing GG, two different grades of poly (ethylene oxide) and poloxamer, were cross-linked with calcium ions. GG-based matrices, loaded with different amounts of RC-33, were prepared by freeze-drying. Dialysis studies and solid-state characterization pointed out the formation of an interaction product between GG and RC-33. RC-33-loaded freeze-dried matrices were characterized by the capability to absorb a high buffer content, forming a gel with marked viscoelastic properties, and by RC-33 controlled release properties. The presence of cross-linked nanofibers increased matrix mechanical resistance.Entities:
Keywords: RC-33/GG interaction product; S1R agonist; cross-linking; electrospinning; freeze-drying; gellan gum; nanofibers; nervous tissue injuries; porous matrices
Year: 2021 PMID: 33530643 DOI: 10.3390/pharmaceutics13020164
Source DB: PubMed Journal: Pharmaceutics ISSN: 1999-4923 Impact factor: 6.321