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Determination of 5-Hydroxymethyl-2-furfural, Albiflorin, Paeoniflorin, Liquiritin, Ferulic Acid, Nodakenin, and Glycyrrhizin by HPLC-PDA, and Evaluation of the Cytotoxicity of Palmul-tang, a Traditional Korean Herbal Medicine
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  • Determination of 5-Hydroxymethyl-2-furfural, Albiflorin, Paeoniflorin, Liquiritin, Ferulic Acid, Nodakenin, and Glycyrrhizin by HPLC-PDA, and Evaluation of the Cytotoxicity of Palmul-tang, a Traditional Korean Herbal Medicine
  • Determination of 5-Hydroxymethyl-2-furfural, Albiflorin, Paeoniflorin, Liquiritin, Ferulic Acid, Nodakenin, and Glycyrrhizin by HPLC-PDA, and Evaluation of the Cytotoxicity of Palmul-tang, a Traditional Korean Herbal Medicine
저자명
Seo. Chang-Seob,Lee. Mee-Young,Lim. Hye-Sun,Kim. Su-Jeong,Ha. Hyekyung,Lee. Jin-Ah,Shin. Hyeun-Kyoo
간행물명
Archives of pharmacal research : a publication of the Pharmaceutical Society of Korea
권/호정보
2012년|35권 1호|pp.101-108 (8 pages)
발행정보
대한약학회
파일정보
정기간행물|ENG|
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이 논문은 한국과학기술정보연구원과 논문 연계를 통해 무료로 제공되는 원문입니다.
서지반출

기타언어초록

A high-performance liquid chromatographic (HPLC) method was developed for quantitative analysis of seven components, 5-hydroxymethyl-2-furaldehyde (1), albiflorin (2), paeoniflorin (3), liquiritin (4), ferulic acid (5), nodakenin (6), and glycyrrhizin (7) of Palmul-tang (PMT), a traditional Korean medicine. HPLC analysis was performed using a Gemini C18 column at $40^{circ}C$, and photodiode array (PDA) detection at 230 nm, 254 nm, 280 nm, 320 nm, and 330 nm was used for quantification of the seven components in PMT. The mobile phase was a gradient flow composed of two solvent systems. Solvent A was 1.0% (v/v) aqueous acetic acid and solvent B was acetonitrile containing 1.0% (v/v) acetic acid. Calibration curves were acquired with $r^2$ values > 0.9998, and the relative standard deviations (RSDs, %) for intra- and inter-day precision were both less than 6.0%. The recovery of each component was in the range of 90.66-103.79%, with a RSD less than 5.0%. The contents of the seven components in PMT range form 0.61-6.21 mg/g. Additionally, we investigated the cytotoxicity of the extract against the RBL-1 and BEAS-2B cell lines, as well as splenocytes.