Stability of Mangiferin in Lotion and its Antioxidant Activity

Article Preview

Abstract:

The antioxidant lotion containing 1% mangiferin, which was previously isolated from leaves of mango variety Nam Doc Mai (purity 93.15%, HPTLC analysis), was prepared. The lotion was an o/w type of emulsion with slightly yellow and coconut scent. The viscosity and pH of the lotion were 19,809 centipoise and 5.94, respectively. Stability studies were performed at room temperature (25±5 °C) with 70±10%RH and at high temperature (45±2 °C) with 75%RH. The amount of mangiferin in the lotion was investigated at various time intervals by HPTLC. The results showed that mangiferin in the lotion remained 80.30±1.87%LA after storage for 3 months at room temperature. While it remained less than 80%LA after storage for 2 weeks at high temperature and only 38.51±0.35%LA remained after 3 months of storage. An unknown degradant was detected at the Rf value of 0.24. It was produced increasingly when storage peroid taken longer, especially at the high temperature. UV spectra of the degradant and mangiferin suggested the similarity of their chemical structures. Antioxidant activity of the lotion was evaluated by DPPH radical scavenging method. Interestingly, the activity has not decreased at both temperatures during storage times even if mangiferin degraded. It was possible that the degradant could scavenge DPPH redical and chemical structure of the degradant might be xanthone.

You might also be interested in these eBooks

Info:

Periodical:

Pages:

79-84

Citation:

Online since:

August 2019

Export:

Price:

Permissions CCC:

Permissions PLS:

Сopyright:

© 2019 Trans Tech Publications Ltd. All Rights Reserved

Share:

Citation:

* - Corresponding Author

[1] H. Masaki, Role of antioxidants in the skin: anti-aging effects, J. Dermatol. Sci. 58 (2010) 85-90.

Google Scholar

[2] A. Ryu, K. Arakane, C. Koide, H. Arai, T. Nagano, Squalene as a target molecule in skin hyperpigmentation caused by singlet oxygen, Biol. Pharm. Bull. 32 (2009), 1504-1509.

DOI: 10.1248/bpb.32.1504

Google Scholar

[3] Y. Shindo, E. Witt, D. Han, W. Epstein, L. Packer, Enzymic and non-enzymic antioxidants in epidermis and dermis of human skin, J. Invest. Dermatol. 102 (1994), 122-124.

DOI: 10.1111/1523-1747.ep12371744

Google Scholar

[4] M. Yamada, M.U. Udono, M. Hori, R. Hirose, S. Sato, T. Mori, O. Nikaido, Aged human skin removes UVB-induced pyrimidine dimers from the epidermis more slowly than younger adult skin in vivo, Arch. Dermatol. Res. 297 (2006), 294-302.

DOI: 10.1007/s00403-005-0618-0

Google Scholar

[5] J.C. Barreto, M.T.S. Trevisan, W.E. Hull, G. Erben, E.S. De Brito, B. Pfundstein, G. Würtele, B. Spiegelhalder, R.W. Owen, Characterization and quantitation of polyphenolic compounds in bark kernel, leaves, and peel of mango (Mangifera indica L.), J. Agric. Food Chem. 56 (2008) 5599-5610.

DOI: 10.1021/jf800738r

Google Scholar

[6] A. Jutiviboonsuk, C. Sardsaengjun, Mangiferin in leaves of three Thai mango (Mangifera indica L.), IJPS. 6 (2010) 122-129.

Google Scholar

[7] A. Dar, S. Faizi, S. Naqvi, T. Roome, S. Zikr-ur-Rehman, M. Ali, S. Firdous, S.T. Moin, Analgesic and antioxidant activity of mangiferin and its derivatives: the structure activity relationship, Biol. Pharm. Bull. 28 (2005), 596-600.

DOI: 10.1248/bpb.28.596

Google Scholar

[8] J. Rodrίguez, D.D. Pierro, M. Gioia, S. Monaco, R. Delgado, M. Coletta, S. Marini, Effects of a natural extract from Mangifera indica L, and its active compound, mangiferin, on energy state and lipid peroxidation of red blood cells, Biochim. Biophys. Acta. 1760 (2006), 1333-1342.

DOI: 10.1016/j.bbagen.2006.04.005

Google Scholar

[9] S. Muruganandan, J. Lal, P.K. Gupta, Immunotherapeutic effects of mangiferin mediated by the inhibition of oxidative stress to activated lymphocytes, neutrophils and macrophages, Toxicology. 215 (2005), 57-68.

DOI: 10.1016/j.tox.2005.06.008

Google Scholar

[10] J.J. Jeong, S.E. Jang, S.R. Hyam, M.J. Han, D.H. Kim, Mangiferin ameliorates colitis by inhibiting IRAK1 phosphorylation in NF-kB and MAPK pathways, Eur. J. Pharmacol. 740 (2014), 652-661.

DOI: 10.1016/j.ejphar.2014.06.013

Google Scholar

[11] C.W. Pan, Z.Z. Pan, J.J. Hu, W.L. Chen, G.Y. Zhou, W. Lin, L.X. Jin, C.L. Xu, Mangiferin alleviates lipopolysaccharide and D-galactosamine-induced acute liver injury by activating the Nrf2 pathway and inhibiting NLRP3 inflammasome activation, Eur. J. Pharmacol. 770 (2016), 85-91.

DOI: 10.1016/j.ejphar.2015.12.006

Google Scholar

[12] X. Gong, L. Zhang, R. Jiang, M. Ye, X. Yin, J. Wan, Anti-inflammatory effects of mangiferin on sepsis-induced lung injury in mice via up-regulation of heme oxygenase-1, J. Nutr. Biochem. 24 (2013), 1173-1181.

DOI: 10.1016/j.jnutbio.2012.09.003

Google Scholar

[13] F. Gold-Smith, A. Fernandez, K. Bishop, Mangiferin and cancer: mechanisms of action, Nutrients. 8, 396 (2016).

DOI: 10.3390/nu8070396

Google Scholar

[14] S. Chae, M.J. Piao, K.A. Kang, R. Zhang, K.C. Kim, U.J. Youn, K.W. Nam, J.H. Lee, J.W. Hyun, Inhibition of matrix metalloproteinase-1 induced by oxidative stress in human keratinocytes by mangiferin isolated from Anemarrhena asphodeloides, Biosci. Biotechnol. Biochem. 75 (2011), 2321-2325.

DOI: 10.1271/bbb.110465

Google Scholar

[15] R. Ochocka, A. Hering, J. Stefanowicz-Hajduk, K. Cal, H. Barańska, The effect of mangiferin on skin: penetration, permeation and inhibition of ECM enzymes, PLoS ONE. 12, e0181542 (2017).

DOI: 10.1371/journal.pone.0181542

Google Scholar

[16] Y. Prado, N. Merino, J. Acosta, JA. Herrera, Y. Luque, I. Hernández, E. Prado, G. Garrido, R. Delgado, I. Rodeiro, Acute and 28-day subchronic toxicity studies of mangiferin, a glucosyl xanthone isolated from Mangifera indica L. stem bark, J. Pharm. Pharmacogn. Res. 3 (2015), 13-23.

DOI: 10.1002/ptr.5177

Google Scholar

[17] W. Leeprechanon, A. Jutiviboonsuk, Quantitative determination of mangiferin isolated from leaves of Mangifera indica L. variety Nam Doc Mai using HPTLC and its DPPH scavenging activity, Proceedings of the 6th international conference of Suan Sunandha Rajabhat University. 2015 Apr 28-29; Bangkok, Thailand (2015).

DOI: 10.7763/ijiet.2015.v5.587

Google Scholar

[18] E. Chielie, N. Romiti, G. Garrido, In vitro effects of Mangifera indica and polyphenols derived on ABCB1/P-glycoprotein activity, Food Chem. Toxicol. 47 (2009), 2703-2710.

DOI: 10.1016/j.fct.2009.07.017

Google Scholar

[19] MF. Hsu, CN Lin, MC Lu, JP Wang, Inhibition of the arachinodic acid cascade by norathyriol via blockade of cyclooxygenase and lipoxygenase activity in neutrophils, Naunyn Schmiedebergs Arch Pharmacol. 369 (2004), 507-515.

DOI: 10.1007/s00210-004-0922-9

Google Scholar

[20] J. Li, M. Malakhova, M. Mottamal, K. Reddy, I. Kurinov, A. Carper, A. Langfald, N. Oi, MO. Kim, F. Zhu, CP. Sosa, K. Zhou, A.M. Bode, Z. Dong, Norathyriol suppresses solar UV-induced skin cáncer by targeting ERKs, Cancer Res. 72 (2012), 260-270.

DOI: 10.1158/0008-5472.can-11-2596

Google Scholar

[21] C. Jo, KY. Yoon, EJ. Jang, TH. Kim, Degradation products of mangiferin by gamma irradiation with inhibitory effects on NO production, Biosci. Biotechnol. Biochem. 80 (2016), 2022-2024.

DOI: 10.1080/09168451.2016.1191335

Google Scholar