Evidence map›Paper›PMID 35439573›Full record

ArticleInternational journal of pharmaceutics2022

Ex vivo transtympanic permeation of the liposome encapsulated S. pneumoniae endolysin MSlys.

Maria Daniela Silva, Kaelin Ray, Miguel Gama, Aaron K Remenschneider, Sanna Sillankorva

Open access · bronzeAbstract read
In one paragraph

Article in International journal of pharmaceutics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.4field-weighted citation impact, top 43% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Endolysins: targetingFrontiers in microbiology · 2025
    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

5 authors at 3 institutions in 2 countries.

Maria Daniela SilvaCEB-Centre of Biological Engineering, University of Minho, 4710-057 Braga, Portugal; INL-International Iberian Nanotechnology Laboratory, 4715-330 Braga, Portugal; Department of Otolaryngology, Massachusetts Eye and Ear, 02114 Boston, MA, United States; Wyss Institute for Biologically Inspired Engineering, 02115 Boston, MA, United States.
Kaelin RayDepartment of Otolaryngology, Massachusetts Eye and Ear, 02114 Boston, MA, United States; Wyss Institute for Biologically Inspired Engineering, 02115 Boston, MA, United States.
Miguel GamaCEB-Centre of Biological Engineering, University of Minho, 4710-057 Braga, Portugal.
Aaron K RemenschneiderDepartment of Otolaryngology, Massachusetts Eye and Ear, 02114 Boston, MA, United States; Department of Otolaryngology, UMass Memorial Medical Center, UMass Chan Medical School, 01655 Worcester, Massachussets, United States. Electronic address: aaron_remenschneider@meei.harvard.edu.
Sanna SillankorvaINL-International Iberian Nanotechnology Laboratory, 4715-330 Braga, Portugal. Electronic address: sanna.sillankorva@inl.int.
Massachusetts Eye and Ear Infirmary · USUniversity of Minho · PTInternational Iberian Nanotechnology Laboratory · PT

Funding

Mechanisms of Conductive Presbycusis in HumansK08DC018575 · NIDCD · MASSACHUSETTS EYE AND EAR INFIRMARY · PI REMENSCHNEIDER, AARON KYLE · 2020 to 2024
$950k
NIDCD NIH HHS K08 DC018575
6 · The paper itself

Abstract

An increase in bacterial resistance to systemic antibiotics has sparked interest into alternative antimicrobial compounds as well as methods for effective local, non-invasive drug delivery. Topical treatments, however, may be hindered by the presence of biological barriers, such as the tympanic membrane in the case of otitis media. Herein, the transtympanic permeation ability of liposomes loaded with the pneumococcal endolysin MSlys and of free MSlys was evaluated ex vivo. MSlys loaded in PEGylated liposomes showed an increased permeation across human tympanic membranes, as compared to its free form, being able to reduce the pneumococcal cell load after 2 h of permeation. However, antipneumococcal activity was no longer detected after 4 h of permeation and hydrolysis of the endolysin was observed after an extended incubation time (≥48 h). This work provides a first assessment of a successful, non-invasive delivery method for endolysins across an intact tympanic membrane. Findings have implications for non-systemic, local treatment of otitis media.

Indexed as

LiposomesOtitis MediaAnti-Bacterial AgentsEndopeptidasesHumansStreptococcus pneumoniaeAnti-Bacterial AgentsendolysinEndopeptidasesLiposomesDrug deliveryEndolysinLiposomeMSlysStreptococcus pneumoniaeTranstympanic

Identifiers

PMID35439573
PMCPMC10789506
OpenAlexW4223962474

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.