Evidence map›Paper›PMID 30893796›Full record

ArticlePharmaceutics2019

Evaluation of a Methylcellulose and Hyaluronic Acid Hydrogel as a Vehicle for Rectal Delivery of Biologics.

Andreea Aprodu, Julia Mantaj, Bahijja Raimi-Abraham, Driton Vllasaliu

Abstract read
In one paragraph

Article in Pharmaceutics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
–field-weighted citation impact
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

15 citing papers in PubMed.

  1. Review
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  14. Development of a MucoadhesivePharmaceutics · 2019
    Article
  15. Antioxidant and Anti-Inflammatory Properties of aAntioxidants (Basel, Switzerland) · 2019
    Article
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.

Andreea AproduFaculty of Life Sciences & Medicine, School of Cancer and Pharmaceutical Sciences, King's College London, London SE1 9NH, UK. andreea.aprodu@kcl.ac.uk.
Julia MantajFaculty of Life Sciences & Medicine, School of Cancer and Pharmaceutical Sciences, King's College London, London SE1 9NH, UK. julia.mantaj@kcl.ac.uk.
Bahijja Raimi-AbrahamFaculty of Life Sciences & Medicine, School of Cancer and Pharmaceutical Sciences, King's College London, London SE1 9NH, UK. bahijja.raimi-abraham@kcl.ac.uk.ORCID 0000-0002-5330-3967
Driton VllasaliuFaculty of Life Sciences & Medicine, School of Cancer and Pharmaceutical Sciences, King's College London, London SE1 9NH, UK. driton.vllasaliu@kcl.ac.uk.ORCID 0000-0002-4379-6171

Funding

Engineering and Physical Sciences Research Council EP/P002544/2
6 · The paper itself

Abstract

Biologics have changed the management of Inflammatory Bowel Disease (IBD), but there are concerns regarding unexpected systemic toxicity and loss of therapeutic response following administration by injection. Local delivery of biologics directly to the inflamed mucosa via rectal enema administration addresses the problems associated with systemic administration. Hydrogels are potentially useful delivery vehicles enabling rectal administration of biologics. Here, we prepared a hydrogel system based on methylcellulose (MC) and hyaluronic acid (HA), which possesses mucosal healing properties, incorporating a model macromolecular drug, namely (fluorescently-labeled) bovine serum albumin (BSA). The BSA-loaded MCHA hydrogel showed temperature-dependent gelation (liquid-like at 20 °C and gel-like at 37 °C) and shear thinning behavior, with these being important and desirable characteristics for rectal application (enabling easy application and retention). BSA release from the MCHA system at 37 °C was linear, with 50% of the loaded drug released within 2 h. The system demonstrated acceptable toxicity towards intestinal (colon) Caco-2 epithelial cells, even at high concentrations. Importantly, application of the BSA-loaded MCHA hydrogel to polarized Caco-2 monolayers, with or without an exemplar absorption enhancer, resulted in transintestinal permeability of BSA. The study therefore indicates that the MCHA hydrogel shows potential for topical (rectal) delivery of biologics in IBD.

Indexed as

biologicsbiologics deliveryhyaluronic acidhydrogelsinflammatory bowel diseaseintestinal deliverymethylcellulose (MC)

Identifiers

PMID30893796
PMCPMC6471061

What OpenQuestion holds

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Registered trials

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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.