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High-performance liquid chromatographic determination of bergenin ...

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elution were not observed (match factors ≥95%). Linearity and limits <strong>of</strong>detection (LOD) and quantification (LOQ) were evaluated for quantitativepurposes (Table II). LOD for <strong>bergenin</strong> and gallic acid were 1.16 and 0.66µg mL −1 and LOQ were 3.9 and 4.2 µg mL −1 , respectively, implying themethod was suitable for quantification <strong>of</strong> these compound. R 2 values forthe compounds were >0.98, confirming the linearity <strong>of</strong> the method. Themethod can therefore be regarded as suitable for quality control and standardization<strong>of</strong> Bergenia species.Table IIRetention times, correlation coefficients and linear range from regression analysis, andlimits <strong>of</strong> quantification (LOQ) and detection (LOD)Compound t R (min) a R 2 Linear range LOD LOQ(µg mL −1 ) (µg mL −1 ) (µg mL −1 )Gallic acid 5.91 ± 0.12 0.990 10–200 0.66 4.2Bergenin 11.06 ± 0.23 0.957 5–50 1.16 3.9a Means from ten replicates ± SDThese results suggest B. ciliata and B. stracheyi are better sources<strong>of</strong> <strong>bergenin</strong> than B. ligulata and that their biological activity will be greater.ACKNOWLEDGEMENTThe authors are grateful to Dr Rakesh Tuli, Director, NBRI forproviding the facilities to conduct this research work.REFERENCES[1] L.V. Asolkar, K.K. Kakkar, and O.J. Chakre, Glossary <strong>of</strong> IndianMedicinal Plants with Active Principles. PID, CSIR, New Delhi,1992, p. 122[2] K.K. Singh, Indian Int. J. Pharmacol., 35, 105 (1997)[3] S.K. Kapur, J. Econ. Tax. Bot., 17, 395 (1993)[4] P.B. Singh and B.S. Aswal, Bull. Med. Ethnobot. Res.,13, 172 (1992)- 251 -

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