• 제목/요약/키워드: Saikosaponin

검색결과 57건 처리시간 0.025초

식물생장조절물질 처리에 따른 시호의 생육특성 (Effect of Application of Plant Growth Regulator on Growth Characteristics in Bupleurum falcatum L.)

  • 이호;김길웅;손태권;이지언;이상철
    • 한국약용작물학회지
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    • 제10권5호
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    • pp.344-352
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    • 2002
  • 본 시험은 국내 재래종 정선시호와 일본에서 도입된 삼도시호를 공시하여 시호의 품질 향상을 위해 식물생장조절제 처리가 시호의 생육 및 saikosaponin 함량에 미치는 요인들을 구명하여 얻어진 결과를 요약하면 다음과 같다. 1. 정선시호는 삼도시호보다 분지수는 적었지만 경수는 많았고, 근경이 굵으며 생근중과 건근중은 무거웠고 지근수도 많은 경향이었다. SSa 및 TSS 함량에서 정선시호가 삼도시호보다 높았고, SSc 함량에서는 정선시호가 삼도시호보다 적었다. 2. 식물생장조절제 처리시기 간에서는 6월에 처리한 것이 7월에 처리한 것보다 경수가 많았고 건근중에서는 유의적인 차이가 없었으나, 6월에 처리한 것이 7월에 처리한 것보다 SSd 함량이 높았다. 3. 식물생장조절제 처리에서 $GA_3$, 10, 50, 100 ppm, IAA 10, 50 ppm, kinetin 50 ppm 지상부 처리에서 지상부 생육을 촉진하였고, kinetin 50 ppm 처리구의 생근중과 건근중은 무처리구보다 무거웠으나 TSS 함량은 무처리구보다 낮았다. $GA_3$, 10 ppm, IAA 10 ppm처리에서 SSa, SSd 및 TSS 함량이 증가되었으며 TSS 함량은 $GA_3$, 50 및 100 ppm에서 높았다. 4. 무처리에 비하여 정선시호는 6월의 $GA_3$, 100 rpm, IAA 10 및 50 ppm, kinetin 10 ppm 처리구에서, 삼도시호는 6월의 $GA_3$, 10 ppm, IAA 10 및 100 ppm 처리구에서 생근중이나 근중은 차이가 없었지만 TSS 함량이 높아 시호생산에 가장 유리한 처리로 판단되었다.

시호(柴胡)의 화경예취(花莖刈取)가 근수량(根收量)과 성분(成分)에 미치는 영향(影響) (Effects of Topping on Growth and Root Yield in Bupleurum falcatum L.)

  • 성재덕;박용진;김금숙;김현태;서형수;김성만
    • 한국약용작물학회지
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    • 제4권2호
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    • pp.153-156
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    • 1996
  • 시호(柴胡) 재래종(在來種)의 화경예취(花莖刈取)가 생육(生育), 건근수량(乾根收量) 및 saikosaponin 함량(含量)에 미치는 영향(影響)을 조사(調査)한 결과(結果)는 다음과 같다. 1. 지상(地上) 50cm 부위 예취시(刈取時)의 생육(生育)은 무예취구(無刈取區)와 비슷하면서 도복(倒伏)이 경감(輕減)되었으며, 근태(根太)가 굵고 건물비율(乾物比率)이 증가(增加)하여 10a당(當) 건근수량(乾根收量)은 무예취(無刈取)보다 19% 증가(增加)하였다. 2. 예취(刈取)에 따른 지상부(地上部)의 경장(莖長), 경태(莖太), 분지수(分枝數)는 감소(減少)하고 분얼수(分?數)는 차(差)가 없었으며 도복(倒伏)이 경감(輕減)되었다. 예취시(刈取時) 지하부(地下部)의 생육(生育)은 7월(月) 16일(日) 예취(刈取)한 것은 근태(根太)와 지근수(枝根數)를 제외(除外)한 모든 형질(形質)이 증가(增加)하였으며, 6월(月) 16일(日)과 7월(月) 16일(日), 2회(回) 예취시(刈取時) 건근수량(乾根收量)은 167kg/10a로서 무처리(無處理)보다 56% 증가(增加)하였다. 3. 예취시기별(刈取時期別) Saikosaponin 함량(含量)은 2회(回) 예취(刈取)가 0. 727%로 가장 높았고, 7월(月) 16일(日) 1회(回) 예취(刈取) > 무예취(無刈取) > 6월(月) 16일(日) 1회(回) 예취(刈取) 의 순(順)이었다.

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Pigment and Saikosoponin Production Through Bioreactor Culture of Carthamus tinctorius and Bupleurum falcatum

  • Wenyuan Gao;Lei Fan;Hahn, Eun-Joo;Paek, Kee-Yoeup
    • Journal of Plant Biotechnology
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    • 제3권1호
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    • pp.1-5
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    • 2001
  • Traditional culture technology of medicinal plants mainly depends on the field culture, which has many problems. With progress of modern culture technology, it has become possible to produce valuable secondary metabolites from medicinal plants. In this paper, we discuss about the pigment and saikosaponin production from too medicinal plants, Carthamus tinctorius and Bupleurum falcatum, through bioreactor culture system. A two-stage bioreactor culture system was established for the production of yellow and red pigments and saikosaponins by cell suspension cultures of Carthamus tinctorius and Bupleurum falcatum. In Carthamus tinctorius, balloon type airlift bioreactors and column type airlift bioreactors were employed for the tell culture and for the pigment production, respectively. The greatest pigment production was obtained on White medium supplemented with 4 mg/L kinetin, high levels of sucrose concentration and photosynthetic photon flux. In Bupleurum falcatum, adventitious roots were cultured in balloon type airlift bioreactors and the root growth was greatest on SH medium containing 5 mg/L IBA and 0.2 mg/L kinetin. HPLC analysis showed that the contents of main active saikosaponins a, c, and d in adventitious roots were almost the same as those in field cultured root.

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광반응 HPLC를 이용한 시호 사포닌의 분석 (Analysis of Saikosaponins by HPLC with Photoreduction Fluorescence Detection)

  • 신영근;조경희;권수진;도영미;황귀서;박정일;박만기
    • 약학회지
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    • 제40권1호
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    • pp.41-45
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    • 1996
  • A high performance liquid chromatography using photoreduction fluorescence detection was described for the analysis of saikosaponins. Saikosaponins were separated on an $NH_2$ column using acetonitrile and aqueous 2-tert-butylanthraquinone(t-BAQ) as mobile phase. Column effluent was passed through a 40cm PTFE capillary tube coiled around a 10W UV lamp to reduce t-BAQ to a highly fluorescent dihydroxyanthracene derivative which was detected by a fluorescence detector. The optimal concentration of t-BAQ was found to be $6{\times}10^{-5}M$ and the optimal reaction time to be 2 seconds. The detection limit for saikosaponin a and d by this method was found to be about 280ng and 80ng. The dynamic linear range was over two orders and the correlation coefficient of the calibration curve of them was 0.998.

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시호의 약리성분 특성 (Medicinal Components in Bupleurum Species)

  • 김관수;이승택;채영암
    • 한국작물학회지
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    • 제41권spc1호
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    • pp.123-144
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    • 1996
  • This review deals briefly with the various medicinal components(mainly saikosaponins), their biological activities and the variation of their contents by different cultivation environment and plant parts in Bupleurum species. Bupleuri radix, a crude drug, is the root of Bupleurum falcatum L. (Korea, Japan), B. chinense(China), and their related species (Umbelliferae). There are over 120 species in Bupleurum genus throughout world, mainly Asian area, and over 5 species in Korea, investigated up to now. These plants contain many physiological active compounds and the principal components are saikosaponins. Major activities of this crude drug and saikosaponins are the anti-inflammatory and antihepatotoxic activities. Saikosaponins and their derivatives in Bupleurum spp. have been chemically studied, isolated and identified over 70 compounds in over 50 species. Other components, physiologically active ones, also have been investigated, which are the groups of lignan, flavonoid, essential oil, polyacetylene, polysaccharide, etc. Saikosaponins belong to the group of triterpenoid saponin chemotaxonomically and occur the accumulation and turnover in plant tissues through secondary metabolism, mevalonic acid pathway. The contents and kinds of saikosaponins and other components in Bupleurum spp. plants are various due to different species and growing environments, as the plant growth characters and yield are various. Most of medicinal plants as well as Bupleurum species are very useful as agricultural products and traditional medicines, and also are very valuable as genetic resources and natural products. So we need to collect, evaluate, preserve, and utilize various medicinal plants, and also to under-stand secondary metabolism and improve the breeding and cultivation techniques for the safe production of crude drugs with high quality and yielding.

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Ultrasonic-assisted Micellar Extraction and Cloud-point Pre-concentration of Major Saikosaponins in Radix Bupleuri using High Performance Liquid Chromatography with Evaporative Light Scattering Detection

  • Suh, Joon-Hyuk;Yang, Dong-Hyug;Han, Sang-Beom
    • Bulletin of the Korean Chemical Society
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    • 제32권8호
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    • pp.2637-2642
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    • 2011
  • A new ultrasonic-assisted micellar extraction and cloud-point pre-concentration method was developed for the determination of major saikosaponins, namely saikosaponins -A, -C and -D, in Radix Bupleuri by high performance liquid chromatography with evaporative light scattering detection (HPLC-ELSD). The non-ionic surfactant Genapol X-080 (oligoethylene glycol monoalkyl ether) was chosen as the extraction additive and parameters affecting the extraction efficiency were optimized. The highest yield was obtained with 10% (w/v) Genapol X-080, a liquid/solid ratio of 200:1 (mL/g) and ultrasonic-assisted extraction for 40 min. In addition, the optimum cloud-point pre-concentration was reached with 10% sodium sulfate and equilibration at $60^{\circ}C$ for 30 min. Separation was achieved on an Ascentis Express C18 column (100 ${\times}$ 4.6 mm i.d., 2.7 ${\mu}M$) using a binary mobile phase composed of 0.1% acetic acid and acetonitrile. Saikosaponins were detected by ELSD, which was operated at a $50^{\circ}C$ drift tube temperature and 3.0 bar nebulizer gas ($N_2$) pressure. The water-based solvent modified with Genapol X-080 showed better extraction efficiency compared to that of the conventional solvent methanol. Recovery of saikosaponins ranged from 93.1 to 101.9%. An environmentally-friendly extraction method was successfully applied to extract and enrich major saikosaponins in Radix Bupleuri.

LC-ESI-MS/MS를 이용한 용담사간탕의 주요 성분 분석 (Quantitative Analysis of the Marker Constituents in Yongdamsagan-Tang using Liquid Chromatography-Electrospray Ionization-Tandem Mass Spectrometry)

  • 서창섭;하혜경
    • 생약학회지
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    • 제48권4호
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    • pp.320-328
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    • 2017
  • Yongdamsagan-tang has been used to treat the urinary disorders, acute- and chronic-urethritis, and cystitis in Korea. In this study, an ultra-performance liquid chromatography-electrospray ionization-mass spectrometry (UPLC-ESI-MS/MS) method was established for simultaneous analysis of the 20 bioactive marker compounds, geniposidic acid, chlorogenic acid, geniposide, liquiritin apioside, acteoside, calceolarioside B, liquiritin, nodakenin, baicalin, liquiritigenin, wogonoside, baicalein, glycyrrhizin, wogonin, glycyrrhizin, wogonin, saikosaponin A, decursin, decursinol angelate, alisol B, alisol B acetate, and pachymic acid in traditional herbal formula, Yongdamsagan-tang. Chromatographic separations of all marker compounds were conducted using a Waters Acquity UPLC BEH $C_{18}$ analytical column ($2.1{\times}100mm$, $1.7{\mu}m$) at $45^{\circ}C$ using a mobile phase of 0.1% (v/v) formic acid in water and acetonitrile with gradient elution. The MS analysis was performed using a Waters ACQUITY TQD LC-MS/MS coupled with an electrospray ionization source in the positive and negative modes. The flow rate was 0.3 mL/min and injection volume was $2.0{\mu}L$. The correlation coefficient of 20 marker compounds in the test ranges was 0.9943-1.0000. The limits of detection and quantification values of the all marker components were 0.11-6.66 and 0.34-19.99 ng/mL, respectively. As a result of the analysis using the optimized LC-ESI-MS/MS method, three compounds, geniposidic acid (from Plantaginis Semen), alisol B (from Alismatis Rhizoma), and pachymic acid (from Poria Sclerotium), were not detected in this sample. While the amounts of the 17 compounds except for the geniposidic acid, alisol B, and pachymic acid were $0.04-548.13{\mu}g/g$ in Yongdamsagan-tang sample. Among these compounds, baicalin, bioactive marker compound of Scutellariae Radix, was detected at the highest amount as a $548.13{\mu}g/g$.