Evidence map›Paper›PMID 35088236›Full record

ArticlePharmaceutical research2022

Transdermal Delivery of a Hydrogen Sulphide Donor, ADT-OH Using Aqueous Gel Formulations for the Treatment of Impaired Vascular Function: an Ex Vivo Study.

Mandeep Kaur Marwah, Hala Shokr, Lissette Sanchez-Aranguren, Raj Kumar Singh Badhan, Keqing Wang, Shakil Ahmad

Open access · hybridAbstract read
In one paragraph

Article in Pharmaceutical research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.8field-weighted citation impact, top 11% 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

12 citing papers in PubMed, 25 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

6 authors at 1 institution in 1 country.

Mandeep Kaur MarwahAston Medical School, College of Health and Life Sciences, Aston University, Birmingham, UK.
Hala ShokrAston Medical School, College of Health and Life Sciences, Aston University, Birmingham, UK.
Lissette Sanchez-ArangurenAston Medical School, College of Health and Life Sciences, Aston University, Birmingham, UK.
Raj Kumar Singh BadhanSchool of Pharmacy, College of Health and Life Sciences, Aston University, Birmingham, UK.
Keqing WangAston Medical School, College of Health and Life Sciences, Aston University, Birmingham, UK.
Shakil AhmadAston Medical School, College of Health and Life Sciences, Aston University, Birmingham, UK. s.ahmad@aston.ac.uk.ORCID http://orcid.org/0000-0002-9294-0475
Aston University · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeHydrogen sulphide (H

methodsAqueous hypromellose gels (5% w/v) were prepared with up to 10% v/v propylene glycol (PG) or deformable liposomes with 0.025% w/w ADT-OH. ADT-OH permeation from formulations across excised murine skin into PBS was quantified over 24 h using HPLC-UV detection. Media was collected and applied to HUVEC cells to evidence ADT-OH functionality following permeation. Tube formation assays were performed as indicative of angiogenesis and mitochondrial oxygen consumption was evaluated using a Seahorse XF24.

resultsIncreasing the loading of PG caused an increase in ADT-OH permeation rate across skin and a decrease in dermal drug retention whereas liposomal gels produced a slow-release profile. Treatment of HUVEC's using conditioned media collected from the ADT-OH loaded permeation studies enhanced tube formation and the basal oxygen consumption rates after 30 min of treatment.

conclusionsThese findings demonstrate that transdermal delivery of ADT-OH may provide a promising approach in the treatment of impaired vascular function. Gels prepared with 10% v/v PG have the potential for use in conditions requiring rapid H

Indexed as

Skin AbsorptionAdministration, CutaneousAnimalsCell MovementCells, CulturedDrug CompoundingEnergy MetabolismFemaleGelsHumansHuman Umbilical Vein Endothelial CellsHydrogen SulfideMiceMitochondriaNeovascularization, PhysiologicOxygen Consumption5-(4-hydroxyphenyl)-3H-1,2-dithiole-3-thioneGelsHydrogen SulfideThionescontrolled releasehydrogen sulphide donorsrelease kineticsskin penetration enhancertransdermal drug delivery

Identifiers

PMID35088236
PMCPMC8881439
OpenAlexW4210681706

What OpenQuestion holds

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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.