싸리나무 추출물의 Xanthoangelol 분리 및 HPLC-DAD 밸리데이션

This study was undertaken to determine the characteristics of xanthoangelol, the major chalcone constituent derived from the extracts of different parts of Lespedeza bicolor. Xanthoangelol was isolated from the root extract using column chromatography and used as a standard for quantitative analysis...

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Published inHan'guk Sikp'um Kwahakhoe Chi = Korean Journal of Food Science and Technology Vol. 52; no. 1; pp. 26 - 30
Main Authors 우현심(Hyun Sim Woo), 김영수(Yeong-Su Kim), 오유진(Yu Jin Oh), 조해진(Hae Jin Cho), 송세규(Se-Kyu Song), 김대욱(Dae Wook Kim)
Format Journal Article
LanguageKorean
Published Seoul 한국식품과학회 01.02.2020
Korean Society of Food Science & Technology
Subjects
Online AccessGet full text
ISSN0367-6293
2383-9635
DOI10.9721/KJFST.2020.52.1.26

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Abstract This study was undertaken to determine the characteristics of xanthoangelol, the major chalcone constituent derived from the extracts of different parts of Lespedeza bicolor. Xanthoangelol was isolated from the root extract using column chromatography and used as a standard for quantitative analysis. The structure of the isolated compound was established based on spectroscopic evidence. The HPLC-DAD method was validated for specificity, linearity, precision, accuracy, limit of detection, and limit of quantitation. The calibration curve of xanthoangelol had significant linearity (R2 >0.9999). Limit of detection and limit of quantitation 0.018 and 0.059 µg/mL, respectively. The relative standard deviation values of precision test, and intra- and inter-day tests were less than 0.22 and 0.40%, respectively. In the recovery test, the accuracy ranged from 98.98-102.78% with RSD values less than 0.13%. The method validation parameters indicate the applicability of the HPLC method for quality control of food or drug formulations containing L. bicolor.
AbstractList This study was undertaken to determine the characteristics of xanthoangelol, the major chalcone constituent derived from the extracts of different parts of Lespedeza bicolor. Xanthoangelol was isolated from the root extract using column chromatography and used as a standard for quantitative analysis. The structure of the isolated compound was established based on spectroscopic evidence. The HPLC-DAD method was validated for specificity, linearity, precision, accuracy, limit of detection, and limit of quantitation. The calibration curve of xanthoangelol had significant linearity (R2>0.9999). Limit of detection and limit of quantitation 0.018 and 0.059 μg/mL, respectively. The relative standard deviation values of precision test, and intra- and inter-day tests were less than 0.22 and 0.40%, respectively. In the recovery test, the accuracy ranged from 98.98-102.78% with RSD values less than 0.13%. The method validation parameters indicate the applicability of the HPLC method for quality control of food or drug formulations containing L. bicolor. KCI Citation Count: 0
This study was undertaken to determine the characteristics of xanthoangelol, the major chalcone constituent derived from the extracts of different parts of Lespedeza bicolor. Xanthoangelol was isolated from the root extract using column chromatography and used as a standard for quantitative analysis. The structure of the isolated compound was established based on spectroscopic evidence. The HPLC-DAD method was validated for specificity, linearity, precision, accuracy, limit of detection, and limit of quantitation. The calibration curve of xanthoangelol had significant linearity (R2 >0.9999). Limit of detection and limit of quantitation 0.018 and 0.059 µg/mL, respectively. The relative standard deviation values of precision test, and intra- and inter-day tests were less than 0.22 and 0.40%, respectively. In the recovery test, the accuracy ranged from 98.98-102.78% with RSD values less than 0.13%. The method validation parameters indicate the applicability of the HPLC method for quality control of food or drug formulations containing L. bicolor.
This study was undertaken to determine the characteristics of xanthoangelol, the major chalcone constituent derived from the extracts of different parts of Lespedeza bicolor. Xanthoangelol was isolated from the root extract using column chromatography and used as a standard for quantitative analysis. The structure of the isolated compound was established based on spectroscopic evidence. The HPLC-DAD method was validated for specificity, linearity, precision, accuracy, limit of detection, and limit of quantitation. The calibration curve of xanthoangelol had significant linearity (R2>0.9999). Limit of detection and limit of quantitation 0.018 and 0.059 ㎍/mL, respectively. The relative standard deviation values of precision test, and intra- and inter-day tests were less than 0.22 and 0.40%, respectively. In the recovery test, the accuracy ranged from 98.98-102.78% with RSD values less than 0.13%. The method validation parameters indicate the applicability of the HPLC method for quality control of food or drug formulations containing L. bicolor. 본 연구는 싸리나무의 기능성 식의약품 개발을 위해 부위별 최적의 에탄올 추출조건을 탐색하고 HPLC-DAD 분석방법에 대한 밸리데이션을 실시하였다. 싸리나무뿌리 추출물로부터 반복적인 크로마토그래피 기법으로 주요성분을 분리하여 NMR, MS와 같은 기기분석 data를 해석하여 xanthoangelol 화합물임을 확인하였다. Xanthoangelol를 표준물질로 선정하여 HPLC-DAD 분석법이 타당한지를 검토하기 위하여 직선성, 일간 일내 정확성, 정밀성 검출한계 및 정량한계를 확인하는 분석법 밸리데이션을 수행하였다. Xanthoangelol 분석은 ZORBAX Eclipse plus C18 (4.6×150 mm, 5 ㎛) 칼럼과 기울기 용출(gradient elution) 방법으로, 370 nm 파장에서 다른 물질의 간섭 없이 안정되게 분석되는 것을 확인하였다. 기능성 소재로 적용하기에 적합한 물과 에탄올을 이용해 농도별(water, 30, 50, 70, 95% EtOH)로 추출하고 xanthoangelol의 함량을 분석하였으며, 에탄올 비율에 따라 대상 성분의 추출율을 조절함으로써 기능성 바이오 식의약품 원료 개발을 위한 기초 자료로 활용할 수 있을 것으로 생각한다.
Author 오유진(Yu Jin Oh)
김대욱(Dae Wook Kim)
송세규(Se-Kyu Song)
김영수(Yeong-Su Kim)
우현심(Hyun Sim Woo)
조해진(Hae Jin Cho)
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xanthoangelol
HPLC-DAD
Lespdeza bicolor
validation
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SubjectTerms Column chromatography
Columnar structure
Food quality
High performance liquid chromatography
Lespedeza bicolor
Linearity
Liquid chromatography
Quality control
Quantitation
식품과학
Title 싸리나무 추출물의 Xanthoangelol 분리 및 HPLC-DAD 밸리데이션
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