Evidence map›Paper›PMID 29329746›Full record

ArticleEuropean journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences2019

Evaluation of a transtympanic delivery system in Mus musculus for extended release steroids.

Nathan H Dormer, Jennifer Nelson-Brantley, Hinrich Staecker, Cory J Berkland

Abstract read
In one paragraph

Article in European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

9 citing papers in PubMed, 16 citations in OpenAlex.

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  7. [Development of novel drug carrier via round window membrane].Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology head and neck surgery · 2021
    Review
  8. Local Drug Delivery for Prevention of Hearing Loss.Frontiers in cellular neuroscience · 2019
    Review
  9. Review
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

4 authors at 2 institutions in 1 country.

Nathan H DormerOrbis Biosciences, 8006 Reeder Street, Lenexa, KS, USA. Electronic address: nate@orbisbio.com.
Jennifer Nelson-BrantleyThe University of Kansas Medical Center, Department of Otolaryngology-Head and Neck Surgery, 3901 Rainbow Boulevard, Kansas City, KS, USA.
Hinrich StaeckerThe University of Kansas Medical Center, Department of Otolaryngology-Head and Neck Surgery, 3901 Rainbow Boulevard, Kansas City, KS, USA.
Cory J BerklandOrbis Biosciences, 8006 Reeder Street, Lenexa, KS, USA; The University of Kansas Department of Pharmaceutical Chemistry, 2030 Becker Drive, Lawrence, KS, USA.
Orbis Biosciences (United States) · USUniversity of Kansas Medical Center · US

Funding

Precision Betamethasone Microspheres for Transtympanic Delivery & SSNHL TreatmentR44DC012749 · NIDCD · ORBIS BIOSCIENCES, INC. · PI DORMER, NATHAN H · 2015 to 2016
$1.5M
Precision Particle Fabrication-enabled Betamethasone-loaded Microspheres for TranR43DC012749 · NIDCD · ORBIS BIOSCIENCES, INC. · PI BERKLAND, CORY, DORMER, NATHAN H · 2012 to 2012
$287k
NIDCD NIH HHS R43 DC012749NIDCD NIH HHS R44 DC012749
6 · The paper itself

Abstract

objectiveThe current investigation evaluated a novel extended release delivery system for treating inner ear diseases. The platform technology consists of a film forming agent (FFA) and microsphere component to localize and extend drug delivery within the ear. STUDY

designStudies evaluated dissolution kinetics of microspheres with multiple encapsulates, testing of a variety of FFAs, and ability to localize to the round window membrane in mice in vivo.

settingStudies were completed at Orbis Biosciences and The University of Kansas Medical Center. SUBJECTS: In conjunction with in vitro characterization, an infrared dye-containing microsphere formulation was evaluated for round window membrane (RWM) localization and general tolerability in C57/BL6 Mus musculus for 35 days.

methodsIn vitro characterization was performed using upright diffusion cells on cellulose acetate membranes, with drug content quantified by high performance liquid chromatography. Mus musculus dosing of infrared dye-containing microspheres was performed under anesthesia with a 27 GA needle and 2.0 μL injection volume

resultsIn vitro dissolution demonstrates the ability of the FFA with microsphere platform to release steroids, proteins, peptides, and nucleic acids for at least one month, while necroscopy shows the ability of the FFA with dye-loaded microspheres to remain localized to Mus musculus RWM for the same period of time, with favorable tolerability.

conclusionsCombining FFA and microsphere for localized drug delivery may enable cost-effective, extended release local delivery to the inner ear of new and existing small molecules, proteins, peptides, and nucleic acids.

Indexed as

AnimalsCelluloseDelayed-Action PreparationsDrug CarriersDrug LiberationFluorescent DyesHumansInjection, IntratympanicLabyrinth DiseasesMembranes, ArtificialMice, Inbred C57BLMicrospheresPolylactic Acid-Polyglycolic Acid CopolymerRound Window, EarSteroidsacetylcelluloseCelluloseDelayed-Action PreparationsDrug CarriersFluorescent DyesMembranes, ArtificialPolylactic Acid-Polyglycolic Acid CopolymerSteroidsMicrospheresRound window membraneSteroidSudden hearing lossTranstympanic

Identifiers

PMID29329746
PMCPMC6039288
OpenAlexW2782865288

What OpenQuestion holds

Textmetadata
LicenceTDM
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.