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Antioxidant and anti-aging potential of a peptide formulation (Gal 2 -Pep) conjugated with gallic acid.
- Source :
-
RSC advances [RSC Adv] 2021 Sep 16; Vol. 11 (47), pp. 29407-29415. Date of Electronic Publication: 2021 Sep 16 (Print Publication: 2021). - Publication Year :
- 2021
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Abstract
- Skin is highly vulnerable to premature aging due to external stress, therefore, in this study, a peptide formulation, (galloyl) <subscript>2</subscript> -KTPPTTP (Gal <subscript>2</subscript> -Pep) was synthesized by combining TPPTTP peptide, and gallic acid (GA). All peptides were synthesized on 2-chlorotrityl chloride resin using solid-phase peptide synthesis (SPPS), and analyzed on an electrospray ionization (ESI)/quadrupole-time-of-flight (Q-TOF) tandem mass spectroscopy (MS) system. Initially, Gal <subscript>2</subscript> -Pep showed no toxicity below the concentration 100 μM with cell survival rate of 88% for keratinocytes and fibroblasts. The reactive oxygen species (ROS) scavenging activity of Gal <subscript>2</subscript> -Pep was more stable compared to GA alone; and after four weeks at room temperature, its ROS scavenging activity remained higher than 50%. Moreover, the peptide formulation, Gal <subscript>2</subscript> -Pep also exhibited elastase inhibitory effect in CCD-1064Sk fibroblast cells. Based on the results of RT-qPCR, it was proved in this study that Gal <subscript>2</subscript> -Pep increased the expression of PGC-1α to prevent oxidative stress, and validated its potential as an anti-aging agent through increasing the expression of type I collagen and by decreasing the expression of matrix metalloproteinase-1 (MMP1). The findings obtained reinforce the suggestion that the peptide formulation synthesized in this study could be used as a natural antioxidant and anti-aging agent for its cosmetic applications.<br />Competing Interests: There are no conflicts to declare.<br /> (This journal is © The Royal Society of Chemistry.)
Details
- Language :
- English
- ISSN :
- 2046-2069
- Volume :
- 11
- Issue :
- 47
- Database :
- MEDLINE
- Journal :
- RSC advances
- Publication Type :
- Academic Journal
- Accession number :
- 35479554
- Full Text :
- https://doi.org/10.1039/d1ra03421a