| Literature DB >> 32241442 |
Mathie Najberg1, Muhammad Haji Mansor2, Théodore Taillé2, Céline Bouré2, Rodolfo Molina-Peña2, Frank Boury2, José Luis Cenis3, Emmanuel Garcion4, Carmen Alvarez-Lorenzo5.
Abstract
This work aims to design biocompatible aerogel sponges that can host and control the release of stromal cell-derived factor-1α (SDF-1α or CXCL12), a key protein for applications ranging from regenerative medicine to cancer therapy (notably for neural tissues). Miscibility of silk fibroin (SF) and hyaluronic acid (HA) was investigated by means of fluorescence and scanning electron microscopy to identify processing conditions. Series of freeze-dried sponges were prepared by associating and cross-linking within the same 3D structure, HA, SF, poly-l-lysine (PLL) and heparin (hep). Aerogel sponges presented high swelling degree and porosity (∼90 %), adequate mean pore diameter (ca. 60 μm) and connectivity for welcoming cells, and a soft texture close to that of the brain (6-13 kPa Young's Modulus). Addition of SF yielded sponges with slower biodegradation. SF-HA and SF-HA-hep sponges retained 75 % and 93 % of the SDF-1α respectively after 7 days and were found to be cytocompatible in vitro.Entities:
Keywords: Aerogel sponges; Brain biomimicry; Porous scaffold; SDF-1α controlled release; Silk fibroin
Year: 2020 PMID: 32241442 DOI: 10.1016/j.carbpol.2020.116107
Source DB: PubMed Journal: Carbohydr Polym ISSN: 0144-8617 Impact factor: 9.381