Effect of Different Solvent on Phytochemical Content, Tyrosinase Inhibition and Antioxidant Activities of Campolay (Pouteria campechiana kunth. [Baehni.])
DOI:
https://doi.org/10.3889/oamjms.2022.8204Keywords:
Pouteria campechiana, Tyrosinase, Antioxidant, QuercitrinAbstract
BACKGROUND: Pouteria campechiana leaves are reported to have phenol and flavonoid compounds. Phenolic and flavonoid compounds can act as tyrosinase inhibitor and antioxidant.
AIM: The purpose of this study was to compare phytochemical content, tyrosinase inhibition, antioxidant activities, and determine of marker compound from P. campechiana leaves extract with different polarities solvent.
METHODS: In addition, the content of marker compound from P. campechaina leaves extract was determined by HPLC.
RESULTS: The highest total phenolic content (TPC) 7.83 GAE/100 g extract, IC50 of tyrosinase 171.512 ± 1.352 and IC50 of DPPH 0.968 ± 0.008 was given by ethanolic extract (DE). Meanwhile ethyl acetate extract (DEA) had the highest of total flavonoid content 2.544 ± 0.554 QEA/100 g extract. The TPC correlated with tyrosinase inhibitory activity and antioxidant activity.
CONCLUSION: Quercitrin was as marker compound from P. campechiana leaves extract, and quercitrin content in the DEA of P. campechiana leaves was 3.539%, while in the DE was 0.153%.Downloads
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Chunhakant S, Chaicharoenpong C. Antityrosinase, antioxidant, and cytotoxic activities of phytochemical constituents from Manilkara zapota L. Bark. Molecule. 2019;2798(24):1-19. https://doi.org/10.3390/molecules24152798 PMid:31370334 DOI: https://doi.org/10.3390/molecules24152798
Muddathir AM, Yamuchi K, Batubara I, Mohieldin EA, Mitsunaga T. Anti-tyrosinase, total phenolic content and antioxidant activity of selected Sundanese medicinal plant. South Afr J Bot. 2017;l09:9-15. http://dx.doi.org/10.1016/j.sajb.2016.12.013 DOI: https://doi.org/10.1016/j.sajb.2016.12.013
Prota G. An introduction to melanin research. In: Prota, G. editor. Melanins and Melanogenesis. San Diego, CA, USA: Academic Press; 1992. p. 1-9. DOI: https://doi.org/10.1016/B978-0-12-565970-3.50007-8
Ferrer S, Lopez AR, Carmon JG. Tyrosinase: A comprehensive review of its mechanism. Biochim Biophys Acta. 1995;1247(1):1-11. https://doi.org/10.1016/0167-4838(94)00204-t PMid:7873577 DOI: https://doi.org/10.1016/0167-4838(94)00204-T
Kumar S, Pandey AK. Chemistry and biological activities of flavonoids: An overview. Sci World J. 2013;2013:162750. https://doi.org/10.1155/2013/162750 PMid:24470791 DOI: https://doi.org/10.1155/2013/162750
Batubara I, Darusman LK, Mitsunaga T, Rahminiwati M, Djauhari E. Potency of Indonesian medicinal plants as tyrosinase inhibitor and antioxidant agent. J Biol Sci. 2010;10(2):138-44. https://doi.org/10.3923/jbs.2010.138.144 DOI: https://doi.org/10.3923/jbs.2010.138.144
Saraswaty V, Suparta NW, Setiyanto H, Rachmawati H, Adnyana IK. Transformation of melinjo seed micropowders into nanopowder enhances extractability of phenolic compounds and tyrosinase inhibitory activity. Sains Malaysiana. 2019;48(5):983-90. https://doi.org/10.17576/jsm-2019-4805-06 DOI: https://doi.org/10.17576/jsm-2019-4805-06
Ma J, Yang H, Basile MJ, Kennelly EJ. Analysis of polyphenolic antioxidants from the fruit of three Pouteria species by selected ion monitoring liquid chromatography-mass spectrometry. J Agric Food Chem. 2004;52(19):5873-8. https://doi.org/10.1021/jf049950k PMid:15366835 DOI: https://doi.org/10.1021/jf049950k
Hernandez CL, Villasenor IM, Joseph E, Tolliday N. Isolation and evaluation of antimitotic activity of phenolic compounds from Pouteria campechiana Baehni. Philippine J Sci. 2008;137(1):1-10.
Pourmurad F, Hosseinimehr SJ, Shahabimajd N. Antioxidant activity, phenol and flavonoid contents of some selected Iranian medicinal plants. Afr J Biotechnol. 2006;5(11):1142-5.
Chang CC, Yang MH, Wen HM, Chem JC. Estimation of total flavonoid content in propolis by two complementary colorimetric methods. J Food Drug Anal. 2002;10(3):178-82. https://doi.org/10.38212/2224-6614.2748 DOI: https://doi.org/10.38212/2224-6614.2748
Masuda T, Yamashita D, Takeda Y, Yonemori S. Screening for tyrosinase inhibitors among extract of seashore plants and identification of potent inihibitors from Garcinia subelliptica. Biosci Biotechnol Biochem. 2005;69(1):197-201. https://doi.org/10.1271/bbb.69.197 PMid:15665485 DOI: https://doi.org/10.1271/bbb.69.197
Blois MS. Antioxidant determinations by the use of a stable free radical. Nature 1958;181:1199-200. DOI: https://doi.org/10.1038/1811199a0
Scherer R, Godoy HT. Antioxidant activity index (AAI) by the 2,2-diphenil-1-picrylhydrazyl method. Food Chem. 2009;112:654-8. https://doi.org/10.1016/j.foodchem.2008.06.026 DOI: https://doi.org/10.1016/j.foodchem.2008.06.026
Tanase C, Cosarca S, Muntean DL. A critical review of phenolic compounds extracted from the bark of woody vascular plants and their potential biology activity. Molecules. 2019;24(1182):1182. https://doi.org/10.3390/molecules24061182 PMid:30917556 DOI: https://doi.org/10.3390/molecules24061182
Treml J, and Smejkal K. Flavonoids as potent scavengers of hydroxyl radicals. Compr Rev Food Sci Food Saf. 2016;15(1):720-38. https://doi.org/10.1111/1541-4337.12204 DOI: https://doi.org/10.1111/1541-4337.12204
Chen CY, Lin LC, Yang WF, Bordon J, Wang HMD. An update organic classification of tyrosinase. Curr Org Chem. 2015;19(1):4-18. https://doi.org/10.2174/1385272819666141107224800036 DOI: https://doi.org/10.2174/1385272819666141107224806
Kim YJ, Uyama H. Review: Tyrosinase inhibitors from natural and synthetic sources: Structure, inhibition mechanism and perspective. Cell Mol Life Sci. 2005;62(15):1707-23. https://doi.org/10.1007/s00018-005-5054-y PMid:15968468 DOI: https://doi.org/10.1007/s00018-005-5054-y
Rao GV, Sahoo MR, Madhavi MS, Mukhopadhay T. Phytoconstituents from the leaves and seeds of Manilkara zapota Linn. Pharm Lett. 2014;6(2):69-73.
Baky MH, Kamal AK, Elgindi MR, Haggag EG. A review on phenolic compounds from family sapotaceae. J Pharmacogn Phytochem. 2016;5(2):280-7.
Hardiyanti R, Marpaung L, Andyana IK, Simanjuntak P. Isolation of quercitrin from Dendrophthoe pentandra (L.) and it’s antioxidant and antibacterial activities. Rasayan J Chem. 2019;12(4):1822-7. https://doi.org/10.31788/RJC.2019.1235353 DOI: https://doi.org/10.31788/RJC.2019.1235353
Yin Y, Li W, Son Y, Sun L, Lu J, Kim D, et al. Quercitrin protects skin from UVB-induced oxidative damage. Toxicol Appl Pharmacol. 2013;269(2):88-99. https://doi.org/10.1016/j.taap.2013.03.015 PMid:23545178 DOI: https://doi.org/10.1016/j.taap.2013.03.015
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Copyright (c) 2022 Sani Nurlaela Fitriansyah, Rika Hartati, Irda Fidrianny (Author)
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