Evidence map›Paper›PMID 32349460›Full record

ArticlePharmaceutics2020

Nanocrystals for Improved Drug Delivery of Dexamethasone in Skin Investigated by EPR Spectroscopy.

Silke B Lohan, Siavash Saeidpour, Miriam Colombo, Sven Staufenbiel, Michael Unbehauen, Amanuel Wolde-Kidan, Roland R Netz, Roland Bodmeier, Rainer Haag, Christian Teutloff and 2 more

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 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.7field-weighted citation impact, top 9% 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, 31 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

12 authors at 2 institutions in 1 country.

Silke B LohanDepartment of Dermatology, Venerology and Allergology, Center of Experimental and Applied Cutaneous Physiology, Charité-Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, 10117 Berlin, Germany.
Siavash SaeidpourFachbereich Physik, Freie Universität Berlin, 14195 Berlin, Germany.
Miriam ColomboPharmazeutische Technologie, Institut für Pharmazie, Freie Universität Berlin, 14195 Berlin, Germany.
Sven StaufenbielPharmazeutische Technologie, Institut für Pharmazie, Freie Universität Berlin, 14195 Berlin, Germany.
Michael UnbehauenInstitut für Chemie und Biochemie, Freie Universität Berlin, 14195 Berlin, Germany.
Amanuel Wolde-KidanFachbereich Physik, Freie Universität Berlin, 14195 Berlin, Germany.
Roland R NetzFachbereich Physik, Freie Universität Berlin, 14195 Berlin, Germany.
Roland BodmeierPharmazeutische Technologie, Institut für Pharmazie, Freie Universität Berlin, 14195 Berlin, Germany.
Rainer HaagInstitut für Chemie und Biochemie, Freie Universität Berlin, 14195 Berlin, Germany.ORCID 0000-0003-3840-162X
Christian TeutloffFachbereich Physik, Freie Universität Berlin, 14195 Berlin, Germany.
Robert BittlFachbereich Physik, Freie Universität Berlin, 14195 Berlin, Germany.
Martina C MeinkeDepartment of Dermatology, Venerology and Allergology, Center of Experimental and Applied Cutaneous Physiology, Charité-Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, 10117 Berlin, Germany.
Freie Universität Berlin · DEHumboldt-Universität zu Berlin · DE

Funding

Deutsche Forschungsgemeinschaft SFB1112
6 · The paper itself

Abstract

Nanocrystals represent an improvement over the traditional nanocarriers for dermal application, providing the advantages of 100% drug loading, a large surface area, increased adhesion, and the potential for hair follicle targeting. To investigate their advantage for drug delivery, compared to a base cream formulation, dexamethasone (Dx), a synthetic glucocorticoid frequently used for the treatment of inflammatory skin diseases, was covalently linked with the paramagnetic probe 3-(carboxy)-2,2,5,5-tetramethyl-1-pyrrolidinyloxy (PCA) to DxPCA. To investigate the penetration efficiency between these two vehicles, electron paramagnetic resonance (EPR) spectroscopy was used, which allows the quantification of a spin-labeled drug in different skin layers and the monitoring of the drug release. The penetration behavior in excised healthy and barrier-disrupted porcine skin was monitored by EPR, and subsequently analyzed using a numerical diffusion model. As a result, diffusion constants and free energy values in the different layers of the skin were identified for both formulations. Dx-nanocrystals showed a significantly increased drug amount that penetrated into viable epidermis and dermis of intact (factor 3) and barrier-disrupted skin (factor 2.1) compared to the base cream formulation. Furthermore, the observed fast delivery of the spin-labeled drug into the skin (80% DxPCA within 30 min) and a successive release from the aggregate unit into the viable tissue makes these nanocrystals very attractive for clinical applications.

Indexed as

1D general diffusion equationelectron paramagnetic resonance (EPR) spectroscopynanocarriersnanocrystalspenetration kineticsskin penetration

Identifiers

PMID32349460
PMCPMC7284345
OpenAlexW3017446353

What OpenQuestion holds

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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.