Electrospray-Based Microencapsulation of Epigallocatechin 3-Gallate for Local Delivery into the Intervertebral Disc.

EGCG degenerative disc disease drug delivery electrospraying inflammation injectable biomaterial microparticles

Journal

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

Informations de publication

Date de publication:
01 Sep 2019
Historique:
received: 13 07 2019
revised: 16 08 2019
accepted: 20 08 2019
entrez: 5 9 2019
pubmed: 5 9 2019
medline: 5 9 2019
Statut: epublish

Résumé

Locally delivered anti-inflammatory compounds can restore the homeostasis of the degenerated intervertebral disc (IVD). With beneficial effects on IVD cells, epigallocatechin 3-gallate (EGCG) is a promising therapeutic candidate. However, EGCG is prone to rapid degradation and/or depletion. Therefore, the purpose of this study was to develop a method for controlled EGCG delivery in the degenerated IVD. Primary IVD cells were isolated from human donors undergoing IVD surgeries. EGCG was encapsulated into microparticles by electrospraying of glutaraldehyde-crosslinked gelatin. The resulting particles were characterized in terms of cytocompatibility and anti-inflammatory activity, and combined with a thermoresponsive carrier to produce an injectable EGCG delivery system. Subsequently, electrospraying was scaled up using the industrial NANOSPIDER™ technology. The produced EGCG microparticles reduced the expression of inflammatory (IL-6, IL-8, COX-2) and catabolic (MMP1, MMP3, MMP13) mediators in pro-inflammatory 3D cell cultures. Combining the EGCG microparticles with the carrier showed a trend towards modulating EGCG activity/release. Electrospray upscaling was achieved, leading to particles with homogenous spherical morphologies. In conclusion, electrospray-based encapsulation of EGCG resulted in cytocompatible microparticles that preserved the activity of EGCG and showed the potential to control EGCG release, thus favoring IVD health by downregulating local inflammation. Future studies will focus on further exploring the biological activity of the developed delivery system for potential clinical use.

Identifiants

pubmed: 31480533
pii: pharmaceutics11090435
doi: 10.3390/pharmaceutics11090435
pmc: PMC6781552
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : IBSA foundation
ID : (2017)
Organisme : CABMM Start-up grant
ID : (2015)

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Auteurs

Moira Loepfe (M)

Institute for Biomechanics, ETH Zurich, Hönggerbergring 64, 8093 Zurich, Switzerland.

Anja Duss (A)

Institute for Biomechanics, ETH Zurich, Hönggerbergring 64, 8093 Zurich, Switzerland.

Katerina-Alexandra Zafeiropoulou (KA)

Institute for Biomechanics, ETH Zurich, Hönggerbergring 64, 8093 Zurich, Switzerland.

Oddny Björgvinsdóttir (O)

Institute for Biomechanics, ETH Zurich, Hönggerbergring 64, 8093 Zurich, Switzerland.

Matteo D'Este (M)

AO Research Institute Davos, Clavadelerstrasse 8, 7270 Davos, Switzerland.

David Eglin (D)

AO Research Institute Davos, Clavadelerstrasse 8, 7270 Davos, Switzerland.

Giuseppino Fortunato (G)

Empa, Swiss Federal Laboratories for Materials Science and Technology, Laboratory for Biomimetic Membranes and Textiles, Lerchenfeldstr. 5, 9014 St. Gallen, Switzerland.

Juergen Klasen (J)

Clinic Prodorso, Walchestrasse 15, 8006 Zurich, Switzerland.

Stephen J Ferguson (SJ)

Institute for Biomechanics, ETH Zurich, Hönggerbergring 64, 8093 Zurich, Switzerland.

Karin Wuertz-Kozak (K)

Institute for Biomechanics, ETH Zurich, Hönggerbergring 64, 8093 Zurich, Switzerland.
Schön Clinic Munich Harlaching, Spine Center, Academic Teaching Hospital and Spine Research Institute of the Paracelsus Medical University Salzburg (AU), Harlachinger Str. 51, 81547 Munich, Germany.
Department of Health Sciences, University of Potsdam, Am Neuen Palais 10, 14469 Potsdam, Germany.

Olga Krupkova (O)

Institute for Biomechanics, ETH Zurich, Hönggerbergring 64, 8093 Zurich, Switzerland. okrupkova@ethz.ch.

Classifications MeSH