Evidence map›Paper›PMID 31480533›Full record

ArticlePharmaceutics2019

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

Moira Loepfe, Anja Duss, Katerina-Alexandra Zafeiropoulou, Oddny Björgvinsdóttir, Matteo D'Este, David Eglin, Giuseppino Fortunato, Juergen Klasen, Stephen J Ferguson, Karin Wuertz-Kozak and 1 more

Open access · goldAbstract read
In one paragraph

Article in Pharmaceutics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.5field-weighted citation impact, top 17% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed, 22 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 4 institutions in 2 countries.

Moira LoepfeInstitute for Biomechanics, ETH Zurich, Hönggerbergring 64, 8093 Zurich, Switzerland.
Anja DussInstitute for Biomechanics, ETH Zurich, Hönggerbergring 64, 8093 Zurich, Switzerland.
Katerina-Alexandra ZafeiropoulouInstitute for Biomechanics, ETH Zurich, Hönggerbergring 64, 8093 Zurich, Switzerland.
Oddny BjörgvinsdóttirInstitute for Biomechanics, ETH Zurich, Hönggerbergring 64, 8093 Zurich, Switzerland.
Matteo D'EsteAO Research Institute Davos, Clavadelerstrasse 8, 7270 Davos, Switzerland.
David EglinAO Research Institute Davos, Clavadelerstrasse 8, 7270 Davos, Switzerland.ORCID 0000-0002-8500-6887
Giuseppino FortunatoEmpa, Swiss Federal Laboratories for Materials Science and Technology, Laboratory for Biomimetic Membranes and Textiles, Lerchenfeldstr. 5, 9014 St. Gallen, Switzerland.
Juergen KlasenClinic Prodorso, Walchestrasse 15, 8006 Zurich, Switzerland.
Stephen J FergusonInstitute for Biomechanics, ETH Zurich, Hönggerbergring 64, 8093 Zurich, Switzerland.
Karin Wuertz-KozakInstitute for Biomechanics, ETH Zurich, Hönggerbergring 64, 8093 Zurich, Switzerland.ORCID 0000-0002-3281-4629
Olga KrupkovaInstitute for Biomechanics, ETH Zurich, Hönggerbergring 64, 8093 Zurich, Switzerland. okrupkova@ethz.ch.ORCID 0000-0002-2041-8557
ETH Zurich · CHAO Foundation · CHSwiss Federal Laboratories for Materials Science and Technology · CHUniversity of Potsdam · DE

Funding

CABMM Start-up grant (2015)IBSA foundation (2017)
6 · The paper itself

Abstract

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.

Indexed as

degenerative disc diseasedrug deliveryEGCGelectrosprayinginflammationinjectable biomaterialmicroparticles

Identifiers

PMID31480533
PMCPMC6781552
OpenAlexW2970259813

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.