Matches in SemOpenAlex for { <https://semopenalex.org/work/W2514474430> ?p ?o ?g. }
- W2514474430 abstract "The continuous sun exposure is a major factor causing oxidative stress, stains and aging skin. The growth of the cosmetics market in the world, the growing interest of people for youthful skin, free of wrinkles and spots, has stimulated researchers to search for new assets for this purpose. Kojic acid is a well known and widely used depigmenting, mainly produced by fungi of the genus Aspergillus which has also been reported as an antioxidant and rejuvenating. However, kojic acid has disadvantages such as low stability and poor inhibition at low concentrations which encourages researchers to search for more active compounds or changes in the molecule in order to seek more active derivatives, stable and secure. Thus, this work aimed at studying the potential of nine Kojic acid derivatives synthesized by researchers at the Federal University of Para UFPA in order to obtain compounds with depigmenting activity, antioxidants and rejuvenating superior to those reported kojic acid. In this study we performed cytotoxicity assays, evaluation of antioxidant activity in vitro and enzyme in vitro inhibition of elastase, tyrosinase, collagenase and hyaluronidase. We evaluated the inhibition of tyrosinase activity and melanin production in B16F10 and alterations on tyrosinase gene expression. Of the nine derivatives studied, only three of them, kojato zinc, kojato copper (Cu-AK) and oleikojato copper (Cu-Ok), showed in vitro inhibitory activity on mushroom tyrosinase and were selected for the present study. The inhibition of tyrosinase in vitro kojato zinc (IC50 30.4 ± 0.89μM) was higher than that presented by the kojic acid (IC50 60.2 ± 1.83μM) and its other derivatives Cu-AK (IC50 – 133.3 ± 6.59μM) and Cu-Ok (IC50 77.6 ± 4.31μM). These compounds were not cytotoxic to B16F10 cells and human dermal fibroblasts at 100 μM and showed no hemolytic potential at the concentration of 250 μM. The Kojic acid and derivatives, Cu-AK and Cu-Ok, were selected to evaluate the action on melanogenesis and enzymes that act on skin aging, as well as antioxidant activity. AK, AK-Cu and Cu-OK, apresenaram low antioxidant activity in the DPPH assay at 50 μg/mL, however, proved to be powerful metal chelating agents. In the studied concentration, 50 μg/mL, OK-Cu (76.0 ± 5.7%) showed chelating activity slightly higher than the AK (58.9 ± 5.63%) and AK-Cu (57.4 ± 5 24). The tyrosinase activity in B16F10 was strongly inhibited by Cu-AK (86.7%) and CuOK (92.5%), melanin production decreased by approximately 60.2% and 61.6% respectively. There were no changes in levels of gene expression of tyrosinase and there was no significant inhibition of other enzymes studied. Our results suggest that the action on melanogenesis observed for Cu-OK and Cu-AK occurs through inhibition of tyrosinase associated with an antioxidant mechanism. The compounds studied have great potential for use as cosmetic depigmenting agents." @default.
- W2514474430 created "2016-09-16" @default.
- W2514474430 creator A5031989783 @default.
- W2514474430 date "2013-01-01" @default.
- W2514474430 modified "2023-09-27" @default.
- W2514474430 title "UNIVERSIDADE FEDERAL DO AMAZONAS FACULDADE DE CIÊNCIAS FARMACÊUTICAS PROGRAMA DE PÓS-GRADUAÇÃO EM CIÊNCIAS FARMACÊUTICAS - PPGCF AVALIAÇÃO DO POTENCIAL DE DERIVADOS DO ÁCIDO KÓJICO SOBRE A MELANOGÊNESE E O ENVELHECIMENTO CUTÂNEO" @default.
- W2514474430 cites W1499715395 @default.
- W2514474430 cites W1535002104 @default.
- W2514474430 cites W1536649387 @default.
- W2514474430 cites W1572216769 @default.
- W2514474430 cites W1580572448 @default.
- W2514474430 cites W1581160743 @default.
- W2514474430 cites W1728722352 @default.
- W2514474430 cites W1775749144 @default.
- W2514474430 cites W1784455061 @default.
- W2514474430 cites W1920149506 @default.
- W2514474430 cites W1966326996 @default.
- W2514474430 cites W1967025428 @default.
- W2514474430 cites W1968470648 @default.
- W2514474430 cites W1974180929 @default.
- W2514474430 cites W1975629953 @default.
- W2514474430 cites W1976384532 @default.
- W2514474430 cites W1977109311 @default.
- W2514474430 cites W1977889890 @default.
- W2514474430 cites W1978169313 @default.
- W2514474430 cites W1978340010 @default.
- W2514474430 cites W1978634070 @default.
- W2514474430 cites W1980605405 @default.
- W2514474430 cites W1983125814 @default.
- W2514474430 cites W1983905718 @default.
- W2514474430 cites W1986112503 @default.
- W2514474430 cites W1990210839 @default.
- W2514474430 cites W1993624173 @default.
- W2514474430 cites W1994462831 @default.
- W2514474430 cites W1995537344 @default.
- W2514474430 cites W1995852654 @default.
- W2514474430 cites W1997214401 @default.
- W2514474430 cites W1997490650 @default.
- W2514474430 cites W1997508994 @default.
- W2514474430 cites W2002049533 @default.
- W2514474430 cites W2002160314 @default.
- W2514474430 cites W2002463152 @default.
- W2514474430 cites W2006597186 @default.
- W2514474430 cites W2007628396 @default.
- W2514474430 cites W2007779376 @default.
- W2514474430 cites W2008185529 @default.
- W2514474430 cites W2010365463 @default.
- W2514474430 cites W2010608377 @default.
- W2514474430 cites W2013634364 @default.
- W2514474430 cites W2014859921 @default.
- W2514474430 cites W2014973713 @default.
- W2514474430 cites W2016070926 @default.
- W2514474430 cites W2019068169 @default.
- W2514474430 cites W2019894619 @default.
- W2514474430 cites W2021324722 @default.
- W2514474430 cites W2022864983 @default.
- W2514474430 cites W2023303284 @default.
- W2514474430 cites W2024877560 @default.
- W2514474430 cites W2029366701 @default.
- W2514474430 cites W2033636202 @default.
- W2514474430 cites W2033803337 @default.
- W2514474430 cites W2035825200 @default.
- W2514474430 cites W2038843436 @default.
- W2514474430 cites W2040914101 @default.
- W2514474430 cites W2042022331 @default.
- W2514474430 cites W2044175778 @default.
- W2514474430 cites W2048457862 @default.
- W2514474430 cites W2050102197 @default.
- W2514474430 cites W2050275563 @default.
- W2514474430 cites W2051232917 @default.
- W2514474430 cites W2053188169 @default.
- W2514474430 cites W2054083814 @default.
- W2514474430 cites W2054272824 @default.
- W2514474430 cites W2060185403 @default.
- W2514474430 cites W2060552070 @default.
- W2514474430 cites W2061661556 @default.
- W2514474430 cites W2062502442 @default.
- W2514474430 cites W2065020294 @default.
- W2514474430 cites W2067172444 @default.
- W2514474430 cites W2068388923 @default.
- W2514474430 cites W2070884866 @default.
- W2514474430 cites W2071952696 @default.
- W2514474430 cites W2075427028 @default.
- W2514474430 cites W2076568600 @default.
- W2514474430 cites W2077481746 @default.
- W2514474430 cites W2077667641 @default.
- W2514474430 cites W2078063810 @default.
- W2514474430 cites W2078090806 @default.
- W2514474430 cites W2081311369 @default.
- W2514474430 cites W2081500438 @default.
- W2514474430 cites W2083326631 @default.
- W2514474430 cites W2086676786 @default.
- W2514474430 cites W2087631391 @default.
- W2514474430 cites W2087861898 @default.
- W2514474430 cites W2088337539 @default.
- W2514474430 cites W2089115016 @default.
- W2514474430 cites W2089267505 @default.
- W2514474430 cites W2096070694 @default.
- W2514474430 cites W2097985608 @default.
- W2514474430 cites W2100409705 @default.