Evidence map›Paper›PMID 38603673›Full record

ArticlePloS one2024

Mathematical modeling of transdermal delivery of topical drug formulations in a dynamic microfluidic diffusion chamber in health and disease.

Gábor Szederkényi, Dorottya Kocsis, Mihály A Vághy, Domonkos Czárán, Péter Sasvári, Miléna Lengyel, Márton Bese Naszlady, Fabiola Kreis, István Antal, Roland Csépányi-Kömi and 1 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.4field-weighted citation impact, top 45% 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

3 citing papers in PubMed, 2 citations in OpenAlex.

  1. Review
  2. Article
  3. 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

11 authors at 2 institutions in 1 country.

Gábor SzederkényiFaculty of Information Technology and Bionics, Pázmány Péter Catholic University, Budapest, Hungary.
Dorottya KocsisFaculty of Information Technology and Bionics, Pázmány Péter Catholic University, Budapest, Hungary.ORCID 0000-0001-7908-3248
Mihály A VághyFaculty of Information Technology and Bionics, Pázmány Péter Catholic University, Budapest, Hungary.ORCID 0000-0002-6280-2514
Domonkos CzáránDepartment of Physiology, Semmelweis University, Budapest, Hungary.ORCID 0000-0003-3438-1094
Péter SasváriDepartment of Physiology, Semmelweis University, Budapest, Hungary.ORCID 0000-0002-6026-9226
Miléna LengyelDepartment of Pharmaceutics, Semmelweis University, Budapest, Hungary.
Márton Bese NaszladyFaculty of Information Technology and Bionics, Pázmány Péter Catholic University, Budapest, Hungary.ORCID 0000-0001-8114-1750
Fabiola KreisDepartment of Physiology, Semmelweis University, Budapest, Hungary.
István AntalDepartment of Pharmaceutics, Semmelweis University, Budapest, Hungary.
Roland Csépányi-KömiDepartment of Physiology, Semmelweis University, Budapest, Hungary.
Franciska ErdőFaculty of Information Technology and Bionics, Pázmány Péter Catholic University, Budapest, Hungary.ORCID 0000-0001-6265-3777
Semmelweis University · HUPázmány Péter Catholic University · HU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mathematical models of epidermal and dermal transport are essential for optimization and development of products for percutaneous delivery both for local and systemic indication and for evaluation of dermal exposure to chemicals for assessing their toxicity. These models often help directly by providing information on the rate of drug penetration through the skin and thus on the dermal or systemic concentration of drugs which is the base of their pharmacological effect. The simulations are also helpful in analyzing experimental data, reducing the number of experiments and translating the in vitro investigations to an in-vivo setting. In this study skin penetration of topically administered caffeine cream was investigated in a skin-on-a-chip microfluidic diffusion chamber at room temperature and at 32°C. Also the transdermal penetration of caffeine in healthy and diseased conditions was compared in mouse skins from intact, psoriatic and allergic animals. In the last experimental setup dexamethasone, indomethacin, piroxicam and diclofenac were examined as a cream formulation for absorption across the dermal barrier. All the measured data were used for making mathematical simulation in a three-compartmental model. The calculated and measured results showed a good match, which findings indicate that our mathematical model might be applied for prediction of drug delivery through the skin under different circumstances and for various drugs in the novel, miniaturized diffusion chamber.

Indexed as

CaffeineSkin AbsorptionAdministration, CutaneousAnimalsDrug CompoundingMiceMicrofluidicsModels, TheoreticalSkinCaffeine

Identifiers

PMID38603673
PMCPMC11008853
OpenAlexW4394713390

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.