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Cited 9 time in webofscience Cited 11 time in scopus
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A simple and reliable analytical method based on HPLC-UV to determine oleanonic acid content in Chios gum mastic for quality control

Authors
Jin, Y.[Jin, Y.]Zhao, J.[Zhao, J.]Jeong, K.M.[Jeong, K.M.]Yoo, D.E.[Yoo, D.E.]Han, S.Y.[Han, S.Y.]Choi, S.-Y.[ Choi, S.-Y.]Ko, D.-H.[ Ko, D.-H.]Kim, H.-J.[ Kim, H.-J.]Sung, N.-H.[ Sung, N.-H.]Lee, J.[Lee, J.]
Issue Date
Jan-2017
Publisher
PHARMACEUTICAL SOC KOREA
Keywords
Chios gum mastic; Oleanonic acid; Method validation; Quality control
Citation
ARCHIVES OF PHARMACAL RESEARCH, v.40, no.1, pp.49 - 56
Indexed
SCIE
SCOPUS
KCI
Journal Title
ARCHIVES OF PHARMACAL RESEARCH
Volume
40
Number
1
Start Page
49
End Page
56
URI
https://scholarworks.bwise.kr/skku/handle/2021.sw.skku/30659
DOI
10.1007/s12272-016-0853-2
ISSN
0253-6269
Abstract
A reliable analytical method based on high-performance liquid chromatography-ultraviolet detection was established for the determination of oleanonic acid (OA) content in Chios gum mastic (CGM). A simple method involving methanol extraction of CGM powder followed by basification and ether extraction was developed to isolate the triterpenic fraction including OA. The triterpenic fraction was chromatographed on a Phenomenex Gemini C-18 column (150 x 4.6 mm, 5 A mu m) under a simple gradient elution of a mobile phase containing acetonitrile and water at a flow rate of 1.0 mL min(-1). The detection wavelength was set at 210 nm. Good linearity was achieved in the range of 100.0-1000.0 mu g mL(-1) with r(2) > 0.9993, and the limit of quantification was 32.22 mu g mL(-1). Accuracy measured at three concentration levels was in the range of 93.72-99.56%, while intra-day and inter-day precisions estimated using both OA standard and CGM samples were no more than 2.83 and 4.57% RSD, respectively. Finally, this method was applied to real CGM samples from various batches, revealing that the OA contents were between 88.13 and 100.83 mu g mg(-1). These results suggest that the current method can be applied as an efficient analytical method for quality control of CGM.
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