Development of an UPLC-DAD Method for Simultaneous Analysis of Eight Marker Compounds of Bulhwangeumjeonggi-san

UPLC-DAD를 이용한 불환금정기산의 다성분 동시분석법 개발

  • Lee, Kyung-hee (Department of Oriental Pharmacy and Wonkwang-Oriental Medicines Research Institute, College of Pharmacy, Wonkwang University) ;
  • Lamichhane, Ramakanta (Department of Oriental Pharmacy and Wonkwang-Oriental Medicines Research Institute, College of Pharmacy, Wonkwang University) ;
  • Kumar, Sharma Dipak (Department of Oriental Pharmacy and Wonkwang-Oriental Medicines Research Institute, College of Pharmacy, Wonkwang University) ;
  • Raj, Pandeya Prakash (Department of Oriental Pharmacy and Wonkwang-Oriental Medicines Research Institute, College of Pharmacy, Wonkwang University) ;
  • Kim, Se-Gun (Department of Agricultural Biology, National Institute of Agricultural Science, Rural Development Administration) ;
  • Jung, Hyun-Ju (Department of Oriental Pharmacy and Wonkwang-Oriental Medicines Research Institute, College of Pharmacy, Wonkwang University)
  • Received : 2016.08.16
  • Accepted : 2016.10.13
  • Published : 2016.12.30

Abstract

Bulhwangeumjeonggisan (BHGJGS) is a traditional herbal formulation generally used in the treatment of cold and gastritis. BHGJGS consists of eight herbal plants; Atractylodis Rhizoma, Magnoliae Cortex, Citri Pericarpium, Glycyrrhizae Radix, Agastachis Herba, Pinelliae Rhizoma, Zingiberis Rhizoma and Zizyphi Fructus. Complete standardization of this formulation has not been done yet. So, a simple and accurate method was developed and validated using Ultra Performance Liquid Chromatography (UPLC) with Diode Array Detector (DAD) for the standardization of BHGJGS. UPLC conditions were optimized using a c18 RP-Amide column with mobile phase; 0.1% phosphate buffer and acetonitrile, detection wavelength; 210 and 325 nm. The linearities of calibration curves were acceptable ($R^2$>0.9994), and the limit of detection and quantification were within the ranges of 0.011-0.091 and $0.034-0.277{\mu}g/ml$ respectively. The relative standard deviation (RSD) of intra- and inter-day precisions were under 3.61%. The RSD of repeatability was under 0.68 %. The results of recovery test were 94.4-107.9%, and the RSD were under 4.6%. The developed method was used to find the contents of standard constituents in BHGJGS mix extract powder, and two commercial formulation (A and B). The data show that the developed method was specific, sensitive, accurate, and precise for analysis of BHGJGS components.

Keywords

References

  1. 김성조, 정두채, 권기태, 김용우, 윤상헌, 이중근, 김은주 (2001) 다빈도한약재 소비형태 및 가격구조 실태조사 연구. 32-37. 식품의약품안전처. 청원.
  2. 조재국, 김남순, 도세록, 이연희, 윤강재, 박진한, 장동현, 천재영, 김화영, 이난희, 유형석, 서성우 (2011) 한방의료이용 및 한약소비 실태조사. 87-136. 한국보건사회연구원. 서울.
  3. 허준, 현대성인병예방연구회 (1993) 동의보감. 682. 민중서원, 서울
  4. 황도연, 남산당편집국 (1992) 증맥 방약합편. 140. 남산당, 서울.
  5. Im, S. U. (1990) An experimental research of the efficancy of Boolwhangumjeonggisan. J. Int. Korean Med. 11: 15-27.
  6. Huh, I. M. (1990) Experimental studies on the efficacy of Pyungwee-san, Hyang-sapyungwee-san and Bulwhangumchungglsan. 경희한의대논문집. 13: 427-461
  7. Lim, K. M. (2006) Effect of Bulhwangeumjeonggi-san on cytokine levels of muse Th1/Th2 cells and anti-allergic activity in Ovalbumin-sensitized allergic inflammation model. Korean J. Oriental physiology & Pathology 20: 1467-1476.
  8. 식품의약품안전처 (2012) 대한약전외한약(생약)규격집 제4개정. 1077-1078. 식품의약품안전처. 청원.
  9. 식품의약품안전처 (2012) 의약품등 시험방법 밸리데이션 가이드라인. 5-15. 식품의약품안전처. 청원.
  10. 식품의약품안전처 (2010) 생약(한약)제제의 성분 프로파일 설정 가이드라인. 9-23. 식품의약품안전처. 청원.
  11. Kim, H. G., Kim, Y. A, Cheon, J. M. and Go, B. S. (2003) Pattern analysis of Agastachis Herba and Pogostemonis Herba. Kor. J. Pharmacogn. 34: 274-277.
  12. Jo, J. E., Lee, A Y., Kim, H. S., Moon, B. C., Choi, G. Y., Ji, Y. U. and Kim, H. K. (2013) Content Comparative Analysis and Classification for Piniellia ternate, P. pedatisecta and Typhonium flagelliforme by HPLC-PDA analysis. Kor. J. Herbology. 28: 95-101.
  13. Im, D. S., You, S. C. and Chi, H. J. (1988) Phytochemical Study on the Rhizome of Atractylodes japonica from Korea. Kor. J. Pharmacogn. 19: 228-232.