Evidence map›Paper›PMID 36986587›Full record

ArticlePharmaceutics2023

Dual Drug Delivery in Cochlear Implants: In Vivo Study of Dexamethasone Combined with Diclofenac or Immunophilin Inhibitor MM284 in Guinea Pigs.

Wiebke Behrends, Katharina Wulf, Stefan Raggl, Max Fröhlich, Thomas Eickner, Dana Dohr, Karl-Heinz Esser, Thomas Lenarz, Verena Scheper, Gerrit Paasche

Abstract read
In one paragraph

Article in Pharmaceutics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
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

7 citing papers in PubMed.

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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

10 authors.

Wiebke BehrendsDepartment of Otolaryngology, Hannover Medical School, 30625 Hannover, Germany.
Katharina WulfInstitute for Biomedical Engineering, Rostock University Medical Center, 18119 Rostock, Germany.ORCID 0000-0002-9891-5174
Stefan RagglMED-EL Medical Electronics, 6020 Innsbruck, Austria.
Max FröhlichDepartment of Otolaryngology, Hannover Medical School, 30625 Hannover, Germany.
Thomas EicknerInstitute for Biomedical Engineering, Rostock University Medical Center, 18119 Rostock, Germany.
Dana DohrDepartment of Otorhinolaryngology, Head and Neck Surgery "Otto Körner", Rostock University Medical Center, 18057 Rostock, Germany.
Karl-Heinz EsserAuditory Neuroethology and Neurobiology, Institute of Zoology, University of Veterinary Medicine Hannover Foundation, 30559 Hannover, Germany.
Thomas LenarzDepartment of Otolaryngology, Hannover Medical School, 30625 Hannover, Germany.ORCID 0000-0002-9307-5989
Verena ScheperDepartment of Otolaryngology, Hannover Medical School, 30625 Hannover, Germany.ORCID 0000-0001-8618-8793
Gerrit PaascheDepartment of Otolaryngology, Hannover Medical School, 30625 Hannover, Germany.

Funding

Federal Ministry of Education and Research 03ZZ0933AFederal Ministry of Education and Research 03ZZ0933GFederal Ministry of Education and Research 03ZZ0933H
6 · The paper itself

Abstract

Cochlear implants are well established to treat severe hearing impairments. Despite many different approaches to reduce the formation of connective tissue after electrode insertion and to keep electrical impedances low, results are not yet satisfying. Therefore, the aim of the current study was to combine the incorporation of 5% dexamethasone in the silicone body of the electrode array with an additional polymeric coating releasing diclofenac or the immunophilin inhibitor MM284, some anti-inflammatory substances not yet tested in the inner ear. Guinea pigs were implanted for four weeks and hearing thresholds were determined before implantation and after the observation time. Impedances were monitored over time and, finally, connective tissue and the survival of spiral ganglion neurons (SGNs) were quantified. Impedances increased in all groups to a similar extent but this increase was delayed in the groups with an additional release of diclofenac or MM284. Using Poly-L-lactide (PLLA)-coated electrodes, the damage caused during insertion was much higher than without the coating. Only in these groups, connective tissue could extend to the apex of the cochlea. Despite this, numbers of SGNs were only reduced in PLLA and PLLA plus diclofenac groups. Even though the polymeric coating was not flexible enough, MM284 seems to especially have potential for further evaluation in connection with cochlear implantation.

Indexed as

cochlear implantsdiclofenacdual drug deliveryimmunophilin inhibitor MM284polymeric coating

Identifiers

PMID36986587
PMCPMC10058822

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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.