Abstract
Bergenia species (Saxifragaceae) are important sources of herbal medicines in Asia, mainly in Russia. Various plant parts are valued for their antibacterial, anti-inflammatory, antioxidant sand adaptogenic effect, and used for the dissolution of kidney and bladder stones. In this study a rapid reversed phase liquid chromatography (RP-HPLC) method has been developed for rapid screening and identifying of the main active components in leaf samples of Bergenia accessions. The main goal of this study was to develop an efficient method for the simultaneous identification and detection of arbutin, bergenin and gallic acid from Bergenia leaf samples, which were extracted with a methanolic solvent mixture [methanol:water = 1:1 (v/v)]. Chromatographic separations were performed on a reversed phase Luna C18(2)-HST HPLC column. This chromatographic system provided increased speed and efficiency for separations, without the need for ultra-high pressures. Reversed phase HPLC coupled with diode array detector method was used for the analysis. The method was validated using ICH guidelines. The level of gallic acid was significantly higher in Bergenia crassifolia samples compared to Bergenia cordifolia. However, the samples of the two Bergenia species did not differ substantially regarding the concentrations of arbutin and bergenin. The novel method proved to be fast and allowed sufficient separation and quantification of arbutin, bergenin and gallic acid, the most important bioactive compounds of Bergenia leaves; thus facilitating rapid screening and quality assessment of Bergenia samples of various botanical and geographical origins.
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References
Harborne JB (1993) Phytochemistry 33:1279. doi:10.1016/0031-9422(93)85072-Y
Shilova I, Pisareva S, Krasnov E, Bruzhes M, Pyak A (2006) Pharm Chem J 40:620–623
Pozharitskaya ON, Ivanova SA, Shikov AN, Makarov VG, Galambosi B (2007) J Sep Sci 30:2447–2451. doi:10.1002/jssc.200700178
Panossian A, Wikman G (2005) Arquivos Brasileiros de Fitomedicina Científica 2:109–131
Shikov AN, Pozharitskaya ON, Makarova MN, Dorman HJD, Makarov VG, Hiltunen R, Galambosi B (2010) J Funct Foods 2:71–76. doi:10.1016/j/jff.2009.11.003
Shikov AN, Pozharitskaya ON, Dorman HJD, Makarov VG, Tikhonov VP, Hiltunen R (2007) Planta Med 73:897–897
Reddy UDC, Chawla AS, Deepak M, Singh D, Handa SS (1999) Phytochem Anal 10:44–47. doi:10.1002/(sici)1099-1565(199901/02)10:1<44:aid-pca424>3.0.co;2-4
Singh DP, Srivastava SK, Govindarajan R, Rawat AKS (2007) Acta Chromatogr 19:246–252
Galambosi B, Galambosi Z, Siivari J (2009) Acta Hortic 860:129
Dharmender R, Madhavi T, Reena A, Sheetal A (2010) Pharmceutica Anal Acta 1:104
Swarnalakshmi T, Sethuraman MG, Sulochana N, Arivudainambi R (1984) Curr Sci 53:917–917
Lim HK, Kim HS, Choi HS, Oh S, Choi J (2000) J Ethnopharmacol 72:469–474. doi:10.1016/s0378-8741(00)00260-9
Takahashi H, Kosaka M, Watanabe Y, Nakade K, Fukuyama Y (2003) Bioorg Med Chem 11:1781–1788. doi:10.1016/s0968-0896(02)00666-1
Romm A, Yarnell E, Winston D (2010) Botanical medicine for women’s health. Elsevier, Amsterdam
Novak J (2010) Z Fur Arznei Gewurzpflanzen 15:170–173
Gallarate M, Carlotti ME, Trotta M, Grande AE, Talarico C (2004) J Cosmet Sci 55:139–148
Lin C-H, Wu H-L, Huang Y-L (2005) J Chromatogr B 829:149–152. doi:10.1016/j.jchromb.2005.10.008
Kittipongpatana N, Tangjai T, Srimanee A, Kittipongpatana O (2007) Chiang Mai Univ J 6:219
Pyka A, Bober K, Stolarczyk A (2007) Acta Pol Pharm 63:395–400
Lamien-Meda A, Lukas B, Schmiderer C, Franz C, Novak J (2009) Phytochem Anal 20:416–420. doi:10.1002/pca.1142
Lukas B, Schmiderer C, Mitteregger U, Novak J (2010) Food Chem 121:185–190. doi:10.1016/j.foodchem.2009.12.028
Pop C, Vlase L, Tamas M (2009) Not Bot Hortic Agrobot Cluj Napoca 37:129–132
Chauhan SK, Singh B, Agrawal S (2000) J AOAC Int 83:1480–1483
Srivastava S, Rawat AKS (2007) Jpc J Planar Chromatogr Modern Tlc 20:275–277. doi:10.1556/jpc.2007.6002
Dhalwal K, Shinde VM, Biradar YS, Mahadik KR (2008) J Food Compos Anal 21:496–500. doi:10.1016/j.jfca.2008.02.008
Acknowledgments
This research was realized in the frames of TÁMOP 4.2.4. A/2-11-1-2012-0001 “National Excellence Program—Elaborating and operating an inland student and researcher personal support system.” The project was subsidized by the European Union and co-financed by the European Social Fund. The work was supported by the grants OTKA K75717, SROP-4.2.2/08/1/2008-0011, and SROP-4.2.1.B-10/2/KONV-2010-0002. Dr. Tivadar Farkas (Phenomenex, Torrance, CA, USA) is acknowledged for the donation of the Luna 2.5 C18(2)-HST column used in this work.
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Published in the special paper collection 9th Balaton Symposium on High-Performance Separations Methods with guest editor Attila Felinger.
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Boros, B., Jakabová, S., Madarász, T. et al. Validated HPLC Method for Simultaneous Quantitation of Bergenin, Arbutin, and Gallic Acid in Leaves of Different Bergenia Species. Chromatographia 77, 1129–1135 (2014). https://doi.org/10.1007/s10337-014-2624-x
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DOI: https://doi.org/10.1007/s10337-014-2624-x