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62 MARINE INGREDIENTS


120 100 80 60 40 20 0


Control * * **


300 250 200 150 100 50 0


0.6 1.8 % of xPL


Figure 1: Release (%) of ATP in fibroblasts treated for 48 hours (*p<0.05; **p<0.01 versus control)


more efficiently, and maintain a healthier, more radiant appearance as well as healthy longevity.


Material and methods Source and composition An extract of the red alga Polysiphonia lanosa (L.) T.A.Chr, referred to here as xPL, was produced, standardized for digeneaside content and tested for its beneficial effects on skin.


In vitro studies The application of xPL on normal human keratinocytes (NHK) and fibroblasts (NHF) in several biological models showed that it protects the lysosomal and mitochondrial networks in NHK and NHF and stimulates mitophagy and autophagy activities in skin cells, thus preserving cell and tissue longevity.


6 Control ** * **


0.6


1.8 % of xPL


Figure 2: Autophagic activity (%) in fibroblasts treated with xPL 48 hours (MDC probe, *p<0.05; **p<0.01 versus control)


Boosting cell energy and regeneration Fibroblasts were treated with xPL for 48 hours after which the ATP (the cellular energy molecule) content was measured and the cells were labelled with the monodansyl cadaverine (MDC) probe to assess autophagic activity. The increase in the synthesis of ATP (Figure 1) is dose-dependent, showing a direct effect of the extract on the cell energy production. At a concentration of 1.8%, xPL boosts the synthesis of ATP by 46%. 1.8% of xPL stimulates up to 20% increases in autophagic activity (Figure 2).


Protecting cell integrity To demonstrate the protective effects of xPL on cell integrity, we preventively applied xPL for 24 hours, then submitted the mitochondrial and lysosomal networks of keratinocytes and


fibroblasts to UVA irradiation. xPL was reapplied for 24 hours, after which the mitochondrial and lysosomal networks were stained with MitoTracker or LysoTracker to visually reveal the effects. UVA irradiation disrupted both mitochondrial


and lysosomal networks, reflecting oxidative damage and impaired cellular function. Treatment with xPL at 1.8% preserved the organization and integrity of these cellular structures, confirming its protective effect against oxidative stress (Figure 3).


Building a stronger skin matrix To evaluate its effect on skin structure, human dermal fibroblasts isolated from a 55-year-old donor were treated with 2% xPL for 48 hours. The production of three key extracellular matrix biomarkers: collagen 1, elastin and hyaluronic acid was then quantified using ELISA assays.


6


Figure 3: Effect of xPL on Mitochondrial & Lysosomal networks in NHK and NHF cells exposed to UVA irradiation Mitochondrial NHF


Mitochondrial NHK Lysosomal NHF PERSONAL CARE MAGAZINE October 2026


Lysosomal NHK www.personalcaremagazine.com


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