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
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

119706

Informations 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.

Auteurs

Adrienn Kazsoki (A)

University Pharmacy Department of Pharmacy Administration, Semmelweis University, Hőgyes Endre utca 7-9, H-1092 Budapest, Hungary.

Attila Farkas (A)

Department of Organic Chemistry and Technology, Budapest University of Technology and Economics, Műegyetem rakpart 3, H-1111 Budapest, Hungary.

Diána Balogh-Weiser (D)

Department of Organic Chemistry and Technology, Budapest University of Technology and Economics, Műegyetem rakpart 3, H-1111 Budapest, Hungary; Department of Physical Chemistry and Materials Science, Budapest University of Technology and Economics, Műegyetem rakpart 3, H-1111 Budapest, Hungary.

Elena Mancuso (E)

Nanotechnology and Integrated Bio-Engineering Centre (NIBEC), Ulster University, Jordanstown campus, UK.

Preetam K Sharma (PK)

Nanotechnology and Integrated Bio-Engineering Centre (NIBEC), Ulster University, Jordanstown campus, UK.

Dimitrios A Lamprou (DA)

School of Pharmacy, Queen's University Belfast, 97 Lisburn Road, Belfast BT9 7BL, UK.

Romána Zelkó (R)

University Pharmacy Department of Pharmacy Administration, Semmelweis University, Hőgyes Endre utca 7-9, H-1092 Budapest, Hungary. Electronic address: zelko.romana@pharma.semmelweis-univ.hu.

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