Plant and Microalgae Derived Peptides Are Advantageously Employed as Bioactive Compounds in Cosmetics
- PMID: 31244874
- PMCID: PMC6581726
- DOI: 10.3389/fpls.2019.00756
Plant and Microalgae Derived Peptides Are Advantageously Employed as Bioactive Compounds in Cosmetics
Abstract
Bioactive peptides (BP) are specific protein fragments that are physiologically important for most living organisms. It is proven that in humans they are involved in a wide range of therapeutic activities as antihypertensive, antioxidant, anti-tumoral, anti-proliferative, hypocholesterolemic, and anti-inflammatory. In plants, BP are involved in the defense response, as well as in the cellular signaling and the development regulation. Most of the peptides used as ingredients in health-promoting foods, dietary supplements, pharmaceutical, and cosmeceutical preparations are obtained by chemical synthesis or by partial digestion of animal proteins. This makes them not fully accepted by the consumers because of the risks associated with solvent contamination or the use of animal derived substances. On the other hand, plant and microalgae derived peptides are known to be selective, effective, safe, and well tolerated once consumed, thus they have got a great potential for use in functional foods, drugs, and cosmetic products. In fact, the interest in the plant and microalgae derived BP is rapidly increasing and in this review, we highlight and discuss the current knowledge about their studies and applications in the cosmetic field.
Keywords: bioactive; cosmetics; microalgae; peptide; plant.
References
-
- Apone F., Barbulova A., Zappelli C., Colucci G. (2017). Green Biotechnology in Cosmetics: Using Plant Cell Cultures as Sources of Active Ingredients. Milano MI: Teknoscienze publisher & event organiser.
-
- Apone F., Tito A., Carola A., Arciello S., Tortora A., Filippini L., et al. (2010). A mixture of peptides and sugars derived from plant cell walls increases plant defense responses to stress and attenuates ageing-associated molecular changes in cultured skin cells. J. Biotechnol. 145 367–376. 10.1016/j.jbiotec.2009.11.021 - DOI - PubMed
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