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http://dx.doi.org/10.20307/nps.2016.22.1.20

Biological Activities and Stability of a Standardized Pentacyclic Triterpene Enriched Centella asiatica Extract  

Puttarak, Panupong (Department of Pharmacognosy and Pharmaceutical Botany, Faculty of Pharmaceutical Sciences, Prince of Songkla University)
Brantner, Adelheid (Institute of Pharmaceutical Sciences, Department of Pharmacognosy, University of Graz)
Panichayupakaranant, Pharkphoom (Department of Pharmacognosy and Pharmaceutical Botany, Faculty of Pharmaceutical Sciences, Prince of Songkla University)
Publication Information
Natural Product Sciences / v.22, no.1, 2016 , pp. 20-24 More about this Journal
Abstract
Pentacyclic triterpenes, mainly, asiatic acid, madecassic acid, asiaticoside, and madecassoside are the active constituents of Centella asiatica. A pentacyclic triterpene enriched C. asiatica extract (PRE) was prepared and standardized to contain a total pentacyclic triterpenes not less than 65% w/w. This work was focused on determination of antiinflammatory, antioxidant, and tyrosinase inhibitory activities of PRE and its stability. The PRE exhibited a satisfactory nitric oxide inhibitory effect, with an $IC_{50}$ value of $64.6{\mu}g/mL$. In addition, the PRE inhibited tyrosinase enzyme activity with an $IC_{50}$ value of $104.8{\mu}g/mL$. In contrast, the PRE possessed only weak antioxidant activity. The PRE was stable over a period of four months when stored as a dried powder but only in a well-closed container protected from light at $4^{\circ}C$. An aqueous alcoholic solution of the PRE was stable at pH values of 5.8 and 7.0, but was not stable at a pH of 8.2. Preparations of the PRE in an aqueous solution should be performed in acidic or neutral conditions.
Keywords
Centella asiatica; Pentacyclic triterpenes; Antiinflammatory; Antioxidant; Tyrosinase inhibition; Stability;
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1 Bonte, F.; Dumas, M.; Chaudagne, C.; Meybeck A. Planta Med. 1994, 60, 133-135.   DOI
2 Maquart, F. X.; Bellon, G.; Gillery, P.; Wegrowski, Y.; Borel, J. P. Connect. Tissue Res. 1990, 24, 107-120.   DOI
3 Yun, K. J.; Kim, J. Y.; Kim, J. B.; Lee, K. W.; Jeong, S. Y.; Park, H. J.; Jung, H. J.; Cho, Y. W.; Yun, K.; Lee, K. T. Int. Immunopharmacol. 2008, 8, 431-441.   DOI
4 Won, J. H.; Shin, J. S.; Park, H. J.; Jung, H. J.; Koh, D. J.; Jo, B. G.; Lee, J. Y.; Yun, K.; Lee, K. T. Planta Med. 2010, 76, 251-257.   DOI
5 Cheng, C. L.; Guo, J. S.; Luk, J.; Koo, M. W. L. Life Sci. 2004, 74, 2237-2249.   DOI
6 Puttarak P.; Panichayupakaranant, P. Nat. Prod. Res. 2013, 27, 684-686.   DOI
7 Park, B. C.; Bosire, K. O.; Lee, E. S.; Lee, Y. S.; Kim, J. A. Cancer Lett. 2005, 218, 81-90.   DOI
8 Kaewchoothong, A.; Tewtrakul, S.; Panichayupakaranant, P. Phytother. Res. 2012, 26, 1789-1792.   DOI
9 Panichayupakaranant, P.; Itsuriya, A.; Sirikatitham, A. Pharm. Biol. 2010, 48, 201-205.   DOI
10 Burits M.; Bucar, F. Phytother. Res. 2000, 14, 323-328.   DOI
11 Rangkadilok, N.; Sitthimonchai, S.; Worasuttayangkurn, L.; Mahidol, C.; Ruchirawat, M.; Satayavivad, J. Food Chem. Toxicol. 2007, 45, 328-336.   DOI
12 Puttarak, P.; Charoonratana, T.; Panichayupakaranant, P. Phytomedicine 2010, 17, 323-327.   DOI
13 Pittella, F.; Dutra, R. C.; Junior, D. D.; Lopes, M. T.; Barbosa, N. R. Int. J. Mol. Sci. 2009, 10, 3713-3721.   DOI
14 Ariffin, F.; Chew, S. H.; Bhupinder, K.; Karim, A. A.; Huda, N. J. Sci. Food Agric. 2011, 91, 2731-2739.   DOI
15 Subban, R.; Veerakumar, A.; Manimaran, R.; Hashim, K. M.; Balachandran, I. J. Nat. Med. 2008, 62, 369-373.   DOI
16 Kubo, I.; Kinst-Hori, I; Chaudhuri, S.K.; Kubo, Y; Sanchez, Y; Ogura, T. Bioorg. Med. Chem. 2000, 8, 1749-1755.   DOI