dc.contributor.author
Fluhr, Joachim W.
dc.contributor.author
Tfayli, Ali
dc.contributor.author
Darlenski, Razvigor
dc.contributor.author
Darvin, Maxim E.
dc.contributor.author
Joly‐Tonetti, Nicolas
dc.contributor.author
Lachmann, Nadège
dc.date.accessioned
2025-03-24T14:36:11Z
dc.date.available
2025-03-24T14:36:11Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/47016
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-46731
dc.description.abstract
The epidermal protective functions are closely associated with skin hydration homeostasis. The understanding of different states of water binding is a rising concept in assessing topically applied formulations and their interaction within the stratum corneum (SC). In addition to global water content, primary bound water, partially bound water, and unbound water and barrier-related lipid lateral packing and protein secondary structure can be measured by Raman spectroscopy. This study aimed to establish an in vitro SC model to evaluate differences in the efficacy of a natural sugar-derived complex in combination with glycerol and a botanical extract in modulating SC water binding and structural proteins and barrier lipids. These compounds were selected due to their water-binding and soothing properties. The SC water profiles were assessed at the surface and in 8 mu m SC depth. After a 12-hour hyperhydration and subsequent product incubation the measurements were performed during a 6 hours desiccation phase. The maximal water caption and the time until reaching a steady state are measured as well as water retention and resistance against water loss. Global water content, partially bound, and unbound water, as well as lipid and protein structures were assessed with confocal Raman microspectroscopy. Both the natural sugar-derived mixture and more pronounced, the same mixture with additional glycerol increased all three water-binding parameters at the surface and in 8 mu m SC depth at the beginning and during the desiccation phase. Further addition of botanical extract did not result in an additional increase of the water-binding. All three formulations showed an increase in the lipid lateral packing values prevented the protein alteration as measured by beta-sheets signal compared to blank. The present model is suited for screening studies comparing the specific effects of different compounds on hydration states. The natural sugar-derived mixture Aquaxyl showed evidence for an improvement of all SC hydration states, lipid and protein structure which was further enhanced by the addition of glycerol 5%. This improvement was evidenced at the surface and within the SC for all hydration-related parameters, and the lipid as well the protein structures. The addition of botanical extract phytoessence blue daisy did not show further improvement.
en
dc.rights.uri
https://creativecommons.org/licenses/by/4.0/
dc.subject
in vitro model
en
dc.subject
lipid lateral packing
en
dc.subject
partially bound water
en
dc.subject
Raman spectroscopy
en
dc.subject
beta-sheet signal
en
dc.subject
stratum corneum hydration
en
dc.subject
unbound water
en
dc.subject
water binding capacity
en
dc.subject.ddc
600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit::610 Medizin und Gesundheit
dc.title
Glycerol and natural sugar‐derived complex modulate differentially stratum corneum water‐binding properties and structural parameters in an in vitro Raman‐desorption model
dc.type
Wissenschaftlicher Artikel
dcterms.bibliographicCitation.articlenumber
e202200201
dcterms.bibliographicCitation.doi
10.1002/jbio.202200201
dcterms.bibliographicCitation.journaltitle
Journal of Biophotonics
dcterms.bibliographicCitation.number
1
dcterms.bibliographicCitation.originalpublishername
Wiley
dcterms.bibliographicCitation.volume
16
refubium.affiliation
Charité - Universitätsmedizin Berlin
refubium.funding
DEAL Wiley
refubium.resourceType.isindependentpub
no
dcterms.accessRights.openaire
open access
dcterms.bibliographicCitation.pmid
36153668
dcterms.isPartOf.issn
1864-063X
dcterms.isPartOf.eissn
1864-0648