Evidence map›Paper›PMID 30078983›Full record

ArticleMolecular vision2018

Anti-inflammatory activity of CKC-containing cationic emulsion eye drop vehicles.

Philippe Daull, Samuel Guenin, Valérie Hamon de Almeida, Jean-Sébastien Garrigue

Open access · greenAbstract read
In one paragraph

Article in Molecular vision, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

5 citing papers in PubMed, 13 citations in OpenAlex.

  1. Use of a Cationic Emulsion of Latanoprost to Treat Glaucoma Patients with Ocular Surface Disease: A Preclinical Review.Journal of ocular pharmacology and therapeutics : the official journal of the Association for Ocular Pharmacology and Therapeutics · 2023
    Review
  2. Review
  3. Article
  4. Article
  5. Cationic Emulsion-Based Artificial Tears as a Mimic of Functional Healthy Tear Film for Restoration of Ocular Surface Homeostasis in Dry Eye Disease.Journal of ocular pharmacology and therapeutics : the official journal of the Association for Ocular Pharmacology and Therapeutics
    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.

Philippe DaullSANTEN SAS, Novagali Innovation center, 1, rue Pierre Fontaine, Bâtiment Genavenir IV, F-91058 Evry Cedex, France.
Samuel GueninBIOalternatives, 1 bis rue des plantes, F-86160 Gençay, France.
Valérie Hamon de AlmeidaBIOalternatives, 1 bis rue des plantes, F-86160 Gençay, France.
Jean-Sébastien GarrigueSANTEN SAS, Novagali Innovation center, 1, rue Pierre Fontaine, Bâtiment Genavenir IV, F-91058 Evry Cedex, France.
Biologie des Plantes et Innovation · FRSanten (France) · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: Preservative-free cationic emulsion-based artificial tears (ATs) or drug vehicles are innovative eye drop formulations with tear film stabilization and drug delivery properties, and valuable in vivo anti-inflammatory and wound healing properties. These ATs have recently reached the market as ATs for the management of dry eye disease (DED) symptoms (i.e., Cationorm) or as a drug vehicle for cyclosporine (Ikervis). The aim of the present study was to explore the mechanism of action underlying the intrinsic anti-inflammatory and wound-healing efficacies harbored by the cationic emulsions of cetalkonium chloride (CE-CKC). Methods: The anti-inflammatory activity of two CE-CKC (0.002% and 0.005% CKC) emulsions was evaluated by assessing the expression of proinflammatory genes and the secretion of various markers in the following human cell types stressed by different agents: peripheral blood mononuclear cells (PBMCs; stimulation with anti-CD3/anti-CD28 or lipopolysaccharide (LPS)), CD4 Results: The CE-CKC emulsions decreased inflammatory gene expression in LPS-stimulated PBMCs ( Conclusions: This study indicates that the CE-CKC emulsions are able to directly modulate the secretion and expression of proinflammatory cytokines and chemokines. The results also suggest that CKC and tyloxapol are pharmacologically active excipients with potentially beneficial effects in vivo. These data shed new light on the efficacy observed on the DED signs of these CE-CKC emulsions in clinical trials.

Indexed as

Anti-Inflammatory AgentsCD4-Positive T-LymphocytesCell LineChemokine CCL2Chemokine CXCL9CorneaEmulsionsEpithelial CellsFatty AlcoholsGene Expression RegulationHumansInterferon-gammaInterleukin-17Interleukin-6Interleukin-6 InhibitorsInterleukin-8Anti-Inflammatory AgentsCCL2 protein, humancetalkonium chlorideChemokine CCL2Chemokine CXCL9CXCL9 protein, humanEmulsionsFatty AlcoholsIL6 protein, humanInterferon-gammaInterleukin-17Interleukin-6Interleukin-6 InhibitorsInterleukin-8LipopolysaccharidesLubricant Eye DropsQuaternary Ammonium CompoundsThrombospondin 1thrombospondin-1, humanTumor Necrosis Factor-alpha

Identifiers

PMID30078983
PMCPMC6054836
OpenAlexW2947775545

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.