Evidence map›Paper›PMID 33374233›Full record

ArticlePharmaceutics2020

Development and In Vitro Evaluation of 5-Fluorouracil-Eluting Stents for the Treatment of Colorectal Cancer and Cancer-Related Obstruction.

Mohammad Arafat, Paris Fouladian, Anthony Wignall, Yunmei Song, Ankit Parikh, Hugo Albrecht, Clive A Prestidge, Sanjay Garg, Anton Blencowe

Open access · goldAbstract read
In one paragraph

Article in Pharmaceutics, 2020. 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
1.3field-weighted citation impact, top 16% 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

7 citing papers in PubMed, 28 citations in OpenAlex.

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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 1 institution in 1 country.

Mohammad ArafatPharmaceutical Innovation and Development (PIDG) Group, Clinical and Health Sciences, University of South Australia (UniSA), Adelaide, SA 5000, Australia.ORCID 0000-0003-0882-5149
Paris FouladianPharmaceutical Innovation and Development (PIDG) Group, Clinical and Health Sciences, University of South Australia (UniSA), Adelaide, SA 5000, Australia.
Anthony WignallARC Centre of Excellence in Convergent Bio-Nano Science and Technology, Clinical and Health Sciences, University of South Australia (UniSA), Adelaide, SA 5000, Australia.
Yunmei SongPharmaceutical Innovation and Development (PIDG) Group, Clinical and Health Sciences, University of South Australia (UniSA), Adelaide, SA 5000, Australia.
Ankit ParikhPharmaceutical Innovation and Development (PIDG) Group, Clinical and Health Sciences, University of South Australia (UniSA), Adelaide, SA 5000, Australia.
Hugo AlbrechtDrug Discovery and Development Group, Clinical and Health Sciences, University of South Australia (UniSA), Adelaide, SA 5000, Australia.ORCID 0000-0002-3951-1866
Clive A PrestidgeARC Centre of Excellence in Convergent Bio-Nano Science and Technology, Clinical and Health Sciences, University of South Australia (UniSA), Adelaide, SA 5000, Australia.ORCID 0000-0001-5401-7535
Sanjay GargPharmaceutical Innovation and Development (PIDG) Group, Clinical and Health Sciences, University of South Australia (UniSA), Adelaide, SA 5000, Australia.ORCID 0000-0001-7253-2629
Anton BlencoweApplied Chemistry and Translational Biomaterials (ACTB) Group, Clinical and Health Sciences, University of South Australia (UniSA), Adelaide, SA 5000, Australia.ORCID 0000-0002-7630-4874
University of South Australia · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Self-expanding metal stents (SEMSs) are currently the gold standard for the localised management of malignant gastrointestinal (GI) stenosis and/or obstructions. Despite encouraging clinical success, in-stent restenosis caused by tumour growth is a significant challenge. Incorporating chemotherapeutic drugs into GI stents is an emerging strategy to provide localised and sustained release of drugs to intestinal malignant tissues to prevent tumour growth. Therefore, the aim of this work was to develop and evaluate a local GI stent-based delivery system that provides a controlled release of 5-fluorouracil (5FU) over a course of several weeks to months, for the treatment of colorectal cancer and cancer-related stenosis/obstructions. The 5FU-loaded GI stents were fabricated via sequential dip-coating of commercial GI stents with a drug-loaded polyurethane (PU) basecoat and a drug-free poly(ethylene-

Indexed as

5-fluorouracildip-coatingdrug-eluting stentgastrointestinal cancerlocalised drug delivery

Identifiers

PMID33374233
PMCPMC7823773
OpenAlexW3117726923

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.