Novel combination of non-invasive morphological and solid-state characterisation of drug-loaded core-shell electrospun fibres.
Chloroform (PubChem CID: 6212)
Coaxial electrospinning
Core-shell electrospun fibres
Drug delivery
Ethanol (PubChem CID: 702)
Hydroxypropyl-beta-cyclodextrin (PubChem CID:14049689)
Levofloxacin (PubChem CID: 149096)
N,N-dimethylformamide (PubChem CID: 6228)
Naproxen-sodium (PubChem CID: 23681059)
Polylactic acid (PubChem CID: 612)
Polysorbate 80 (PubChem CID: 5284448)
Polyvinyl pyrrolidone (PubChem CID: 131751496)
Raman spectroscopy
Transmission electron microscopy
Journal
International journal of pharmaceutics
ISSN: 1873-3476
Titre abrégé: Int J Pharm
Pays: Netherlands
ID NLM: 7804127
Informations de publication
Date de publication:
25 Sep 2020
25 Sep 2020
Historique:
received:
20
04
2020
revised:
24
07
2020
accepted:
25
07
2020
pubmed:
3
8
2020
medline:
22
6
2021
entrez:
3
8
2020
Statut:
ppublish
Résumé
In recent years, core-shell nanofibrous drug delivery systems have received increasing attention due to their ability to incorporate two or more active pharmaceutical ingredients (APIs) individually into the desired layer (either core or sheath) and thereby finely tune the release profiles of even incompatible drugs in one system. This study aims to perform formulation and solid-state characterisation of levofloxacin-loaded polylactic acid (PLA) - naproxen-sodium-loaded polyvinyl pyrrolidone (PVP) bicomponent core-shell fibrous sheets and examine the electro spinnability of the precursor combinations. The selected drugs have potential therapeutic relevance in similar systems intended for wound healing; however, in this study, they are used as model drugs to understand the physicochemical properties of a drug loaded system. In order to determine the best core- and shell-solution combination, a full factorial experimental design is used. A combination of various morphological (scanning electron microscopy and transmission electron microscopy) and microstructural characterisation techniques (X-ray photoelectron spectroscopy and Raman spectroscopy) was applied to non-invasively obtain information about the structure of the fibres and the embedded drugs. The results indicate that core-shell fibres of different compositions could be successfully prepared with various structural homogeneities. The best core-shell structure was obtained using a combination of 15% (w/w) shell concentration and 8% (w/w) PLA solution concentration. In addition to the conventional core-shell structural verification methods, the Raman spectroscopy method was implemented to reveal not only the core-shell structure of the PLA/PVP nanofibers but also the form of the embedded drugs. The Raman mapping of the fibres confirm the above results, and it is shown that an amorphous solid dispersion is formed as a result of the coaxial electrospinning process.
Identifiants
pubmed: 32739390
pii: S0378-5173(20)30690-6
doi: 10.1016/j.ijpharm.2020.119706
pii:
doi:
Substances chimiques
Drug Carriers
0
Povidone
FZ989GH94E
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
119706Informations de copyright
Copyright © 2020 Elsevier B.V. All rights reserved.
Déclaration de conflit d'intérêts
Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.