Evidence map›Paper›PMID 30482196›Full record

ArticleJournal of nanobiotechnology2018

In vitro and in vivo delivery of a sustained release nanocarrier-based formulation of an MRTF/SRF inhibitor in conjunctival fibrosis.

Aristides D Tagalakis, Shivam Madaan, Scott D Larsen, Richard R Neubig, Peng T Khaw, Ian Rodrigues, Saurabh Goyal, Kin Sheng Lim, Cynthia Yu-Wai-Man

Open access · goldAbstract read
In one paragraph

Article in Journal of nanobiotechnology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
5.6field-weighted citation impact, top 3% 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

16 citing papers in PubMed, 40 citations in OpenAlex.

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  9. O-GlcNAcylation inhibits hepatic stellate cell activation.Journal of gastroenterology and hepatology · 2021
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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

9 authors at 6 institutions in 3 countries.

Aristides D TagalakisDepartment of Biology, Edge Hill University, Ormskirk, L39 4QP, UK.
Shivam MadaanUCL School of Pharmacy, London, WC1N 1AX, UK.
Scott D LarsenVahlteich Medicinal Chemistry Core, College of Pharmacy, University of Michigan, Ann Arbor, MI, USA.
Richard R NeubigDepartment of Pharmacology and Toxicology, Michigan State University, East Lansing, MI, USA.
Peng T KhawUCL Institute of Ophthalmology, 11-43 Bath Street, London, EC1V 9EL, UK.
Ian RodriguesDepartment of Ophthalmology, King's College London, Westminster Bridge Road, London, SE1 7EH, UK.
Saurabh GoyalDepartment of Ophthalmology, King's College London, Westminster Bridge Road, London, SE1 7EH, UK.
Kin Sheng LimDepartment of Ophthalmology, King's College London, Westminster Bridge Road, London, SE1 7EH, UK.
Cynthia Yu-Wai-ManDepartment of Ophthalmology, King's College London, Westminster Bridge Road, London, SE1 7EH, UK. cynthia.yu-wai-man@kcl.ac.uk.ORCID http://orcid.org/0000-0003-4868-5187
King's College London · GBEdge Hill University · GBMichigan State University · USThe London College · GBUniversity College London · GBUniversity of Michigan · US

Funding

Medical Research Council 535333Medical Research Council MC_PC_15037
6 · The paper itself

Abstract

backgroundSustained drug delivery is a large unmet clinical need in glaucoma. Here, we incorporated a Myocardin-Related Transcription Factor/Serum Response Factor inhibitor, CCG-222740, into slow release large unilamellar vesicles derived from the liposomes DOTMA (1,2-di-O-octadecenyl-3-trimethylammonium propane) and DOPC (1,2-dioleoyl-sn-glycero-3-phosphocholine), and tested their effects in vitro and in vivo.

resultsThe vesicles were spherical particles of around 130 nm and were strongly cationic. A large amount of inhibitor could be incorporated into the vesicles. We showed that the nanocarrier CCG-222740 formulation gradually released the inhibitor over 14 days using high performance liquid chromatography. Nanocarrier CCG-222740 significantly decreased ACTA2 gene expression and was not cytotoxic in human conjunctival fibroblasts. In vivo, nanocarrier CCG-222740 doubled the bleb survival from 11.0 ± 0.6 days to 22.0 ± 1.3 days (p = 0.001), decreased conjunctival scarring and did not have any local or systemic adverse effects in a rabbit model of glaucoma filtration surgery.

conclusionsOur study demonstrates proof-of-concept that a nanocarrier-based formulation efficiently achieves a sustained release of a Myocardin-Related Transcription Factor/Serum Response Factor inhibitor and prevents conjunctival fibrosis in an established rabbit model of glaucoma filtration surgery.

Indexed as

Drug Delivery SystemsAnimalsConjunctival DiseasesDelayed-Action PreparationsFemaleFibroblastsFibrosisHumansLiposomesMyocardinNuclear ProteinsRabbitsSerum Response FactorTissue DistributionTrans-ActivatorsTranscription FactorsDelayed-Action PreparationsLiposomesMyocardinNuclear ProteinsSerum Response FactorTrans-ActivatorsTranscription FactorsFibrosisGlaucomaInhibitorNanocarrierSustained release

Identifiers

PMID30482196
PMCPMC6258153
OpenAlexW2902469892

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.