Norfloxacin-Loaded Electrospun Scaffolds: Montmorillonite Nanocomposite vs. Free Drug.

antimicrobial properties chitosan electrospinning fibroblasts proliferation glycosaminoglycans scaffolds

Journal

Pharmaceutics
ISSN: 1999-4923
Titre abrégé: Pharmaceutics
Pays: Switzerland
ID NLM: 101534003

Informations de publication

Date de publication:
04 Apr 2020
Historique:
received: 24 02 2020
revised: 26 03 2020
accepted: 27 03 2020
entrez: 9 4 2020
pubmed: 9 4 2020
medline: 9 4 2020
Statut: epublish

Résumé

Infections in nonhealing wounds remain one of the major challenges. Recently, nanomedicine approach seems a valid option to overcome the antibiotic resistance mechanisms. The aim of this study was the development of three types of polysaccharide-based scaffolds (chitosan-based (CH), chitosan/chondroitin sulfate-based (CH/CS), chitosan/hyaluronic acid-based (CH/HA)), as dermal substitutes, to be loaded with norfloxacin, intended for the treatment of infected wounds. The scaffolds have been loaded with norfloxacin as a free drug (N scaffolds) or in montmorillonite nanocomposite (H-hybrid-scaffolds). Chitosan/glycosaminoglycan (chondroitin sulfate or hyaluronic acid) scaffolds were prepared by means of electrospinning with a simple, one-step process. The scaffolds were characterized by 500 nm diameter fibers with homogeneous structures when norfloxacin was loaded as a free drug. On the contrary, the presence of nanocomposite caused a certain degree of surface roughness, with fibers having 1000 nm diameters. The presence of norfloxacin-montmorillonite nanocomposite (1%) caused higher deformability (90%-120%) and lower elasticity (5-10 mN/cm

Identifiants

pubmed: 32260441
pii: pharmaceutics12040325
doi: 10.3390/pharmaceutics12040325
pmc: PMC7238150
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : Horizon 2020 Research and Innovation Programme
ID : 814607

Déclaration de conflit d'intérêts

The authors declare no conflict of interest.

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Auteurs

Angela Faccendini (A)

Department of Drug Sciences, University of Pavia, Viale Taramelli 12, 27100 Pavia, Italy.

Marco Ruggeri (M)

Department of Drug Sciences, University of Pavia, Viale Taramelli 12, 27100 Pavia, Italy.

Dalila Miele (D)

Department of Drug Sciences, University of Pavia, Viale Taramelli 12, 27100 Pavia, Italy.

Silvia Rossi (S)

Department of Drug Sciences, University of Pavia, Viale Taramelli 12, 27100 Pavia, Italy.

Maria Cristina Bonferoni (MC)

Department of Drug Sciences, University of Pavia, Viale Taramelli 12, 27100 Pavia, Italy.

Carola Aguzzi (C)

Department of Pharmacy and Pharmaceutical Technology, Faculty of Pharmacy. University of Granada, Campus of Cartuja, 18071 s/n Granada, Spain.

Pietro Grisoli (P)

Department of Drug Sciences, University of Pavia, Viale Taramelli 12, 27100 Pavia, Italy.

Cesar Viseras (C)

Department of Pharmacy and Pharmaceutical Technology, Faculty of Pharmacy. University of Granada, Campus of Cartuja, 18071 s/n Granada, Spain.

Barbara Vigani (B)

Department of Drug Sciences, University of Pavia, Viale Taramelli 12, 27100 Pavia, Italy.

Giuseppina Sandri (G)

Department of Drug Sciences, University of Pavia, Viale Taramelli 12, 27100 Pavia, Italy.

Fraanca Ferrari (F)

Department of Drug Sciences, University of Pavia, Viale Taramelli 12, 27100 Pavia, Italy.

Classifications MeSH