Journal
ANTIBIOTICS-BASEL
Volume 11, Issue 4, Pages -Publisher
MDPI
DOI: 10.3390/antibiotics11040481
Keywords
marine natural products; seaweeds; skin microbiota; dermatological applications; antimicrobial activity; Rhodophyta; acne vulgaris; skincare; Staphylococcus epidermidis; red algae
Categories
Funding
- Portuguese Foundation for Science and Technology (FCT) through the POCI project [01-0247-FEDER-070155]
- FEDER-European Regional Development Fund of the European Union, under the Portugal 2020 Programme, through COMPETE 2020-Competitiveness and Internationalization Operational Program
- FCT [UIDP/04292/2020, UIDB/04292/2020, UIDP/Multi/04046/2020, UIDB/04046/2020]
- COMPETE [POCI-01-0145-FEDER-029250, PTDC/BIA-OUT/29250/2017]
- Molecules for Health [PTDC/BIA-BQM/28355/2017]
- FEDER through COMPETE 2020 [022161]
- FEDER through POCI [022161]
- FEDER through PORL [022161]
- FCT through PIDDAC [022161]
- Project Operational Programme MAR2020 [MAR-04.03.01-FEAMP-0101]
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In recent decades, seaweeds have been recognized as an excellent source of bioactive molecules. Gelidium corneum, a type of seaweed harvested in a specific area of the Portuguese coast, has the potential to be a sustainable source of antimicrobial ingredients. The chemical characterization and antimicrobial evaluation of sequential extractions revealed that fractions F2 and F3 showed the strongest inhibitory effects against Cutibacterium acnes, suggesting their potential therapeutic advantages for skin dysbiosis-related diseases.
In recent decades, seaweeds have proven to be an excellent source of bioactive molecules. Presently, the seaweed Gelidium corneum is harvested in a small area of the Portuguese coast exclusively for agar extraction. The aim of this work was to fully disclosure Gelidium corneum as a sustainable source of antimicrobial ingredients for new dermatological formulations, highlighting its potential to be explored in a circular economy context. For this purpose, after a green sequential extraction, these seaweed fractions (F1-F5) were chemically characterized (H-1 NMR) and evaluated for their antimicrobial potential against Staphylococcus aureus, Staphylococcus epidermidis and Cutibacterium acnes. The most active fractions were also evaluated for their effects on membrane potential, membrane integrity and DNA damage. Fractions F2 and F3 displayed the best results, with IC50 values of 16.1 (7.27-23.02) mu g/mL and 51.04 (43.36-59.74) mu g/mL against C. acnes, respectively, and 53.29 (48.75-57.91) mu g/mL and 102.80 (87.15-122.30) mu g/mL against S. epidermidis, respectively. The antimicrobial effects of both fractions seem to be related to membrane hyperpolarization and DNA damage. This dual mechanism of action may provide therapeutic advantages for the treatment of skin dysbiosis-related diseases.
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