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1.
Jiang‐Tao Chen Hai‐Zhou Li Dong Wang Ying‐Jun Zhang Chong‐Ren Yang 《Helvetica chimica acta》2006,89(7):1442-1448
Three new dammarane monodesmosides, named notoginsenosides Ft1 ( 1 ), Ft2 ( 2 ), and Ft3 ( 3 ), together with three known ginsenosides, were obtained from a mild acidic hydrolysis of the saponins from notoginseng (Panax notoginseng (Burk .) F. H. Chen ) leaves. Their structures were elucidated to be (3β,12β,20R)‐12,20‐dihydroxydammar‐24‐en‐3‐yl O‐β‐D ‐xylopyranosyl‐(1 → 2)‐O‐β‐D ‐glucopyranosyl‐(1 → 2)‐β‐D ‐glucopyranoside ( 1 ), (3β,12β)‐12,20,25‐trihydroxydammaran‐3‐yl O‐β‐D ‐xylopyranosyl‐(1 → 2)‐O‐β‐D ‐glucopyranosyl‐(1 → 2)‐β‐D ‐glucopyranoside ( 2 ), and (3β,12β,24ξ)‐12,20,24‐trihydroxydammar‐25‐en‐3‐yl O‐β‐D ‐xylopyranosyl‐(1 → 2)‐O‐β‐D ‐glucopyranosyl‐(1 → 2)‐β‐D ‐glucopyranoside ( 3 ), by means of spectroscopic evidences. The known ginsenosides Rh2 and Rg3 4 – 6 were obtained as the major products from this acidic deglycosylation. 相似文献
2.
Ionic liquid and aqueous two‐phase extraction based on salting‐out coupled with high‐performance liquid chromatography for the determination of seven rare ginsenosides in Xue‐Sai‐Tong injection 下载免费PDF全文
Lan‐Jie Li Yong‐Ri Jin Xiao‐Zhong Wang Ying Liu Qian Wu Xiao‐Lei Shi Xu‐Wen Li 《Journal of separation science》2015,38(17):3055-3062
A method of ionic liquid salt aqueous two‐phase extraction coupled with high‐performance liquid chromatography has been developed for the analysis of seven rare ginsenosides including Rg6, F4, 20(S)‐Rg3, 20(R)‐Rg3, Rk3, Rk1, and Rg5 in Xue‐Sai‐Tong injection. The injection was mixed with ionic liquid 1‐butyl‐3‐methylimidazolium bromide aqueous solution, and a mixture was obtained. With the addition of sodium dodecyl sulfate and dipotassium phosphate into the mixture, the aqueous two‐phase mixture was formed after ultrasonic treatment and centrifuged. Rare ginsenosides were extracted into the upper phase. To obtain a high extraction factors, various influences were considered systematically, such as the volume of ionic liquid, the category and amount of salts, the amount of sodium dodecyl sulfate, the pH value of system, and the time of ultrasonic treatment. Under the optimal condition, rare ginsenosides in Xue‐Sai‐Tong injection were enriched and detected, the recoveries of seven rare ginsenosides ranged from 90.05 to 112.55%, while relative standard deviations were lower than 2.50%. The developed method was reliable, rapid and sensitive for the determination of seven rare ginsenosides in the injections. 相似文献
3.
This study compared eight major ginsenosides (Rg1, Rg2, Rf, Re, Rd, Rc, Rb1 and Rb2) between Panax sokpayensis and Panax bipinnatifidus collected from Sikkim Himalaya, India. High-performance liquid chromatographic analysis revealed that all major ginsenosides were present in the rhizomes of P. sokpayensis except ginsenoside Rc, whereas ginsenoside Rf, Rc and Rb2 were not detected in P. bipinnatifidus. 相似文献
4.
Isolation of dammarane saponins from Panax notoginseng by high-speed counter-current chromatography 总被引:7,自引:0,他引:7
The Chinese phytomedicinal formulation Sanqi Zongdai Pian, traditionally prepared from crude extracts from roots of Panax notoginseng (Araliaceae), contains highly polar dammarane saponins which were separated at a preparative scale using high-speed counter-current chromatography (HSCCC). In each operation, 283 mg methanolic extract of five tablets was separated and yielded pure 157, 17, 13 and 56 mg of ginsenoside-Rb1, notoginsenoside-R1, ginsenoside-Re and ginsenoside-Rg1, respectively, n-hexane-n-butanol-water (3:4:7, v/v/v) was used for the two-phase solvent system of the HSCCC separation. The chemical structures of three ginsenosides and one notoginsenoside were elaborated by means of electrospray ionization MS-MS and NMR analysis. 相似文献
5.
6.
Jianing Mi Min Zhang Hongyang Zhang Yuerong Wang Shikun Wu Ping Hu 《Journal of separation science》2013,36(3):593-601
A high‐efficient and environmental‐friendly method for the preparation of ginsenosides from Radix Ginseng using the method of coupling of ultrasound‐assisted extraction with expanded bed adsorption is described. Based on the optimal extraction conditions screened by surface response methodology, ginsenosides were extracted and adsorbed, then eluted by the two‐step elution protocol. The comparison results between the coupling of ultrasound‐assisted extraction with expanded bed adsorption method and conventional method showed that the former was better than the latter in both process efficiency and greenness. The process efficiency and energy efficiency of the coupling of ultrasound‐assisted extraction with expanded bed adsorption method rapidly increased by 1.4‐fold and 18.5‐fold of the conventional method, while the environmental cost and CO2 emission of the conventional method were 12.9‐fold and 17.0‐fold of the new method. Furthermore, the theoretical model for the extraction of targets was derived. The results revealed that the theoretical model suitably described the process of preparing ginsenosides by the coupling of ultrasound‐assisted extraction with expanded bed adsorption system. 相似文献
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8.
A new extraction method for ginsenosides from ginseng roots, ginseng leaves and ginseng drug preparations by Sep-Pak C18 cartridges has been studied. Ginsenoside extraction by Sep-Pak cartridges is a rapid, efficient, reproducible method. In addition, the extracts were analyzed by high performance thin layer chromatography (HPTLC) and reverse phase high performance liquid chromatography (HPLC). The major components of ginseng saponins were effectively separated using an ODS-120T column. 相似文献
9.
A robust method based on high-performance liquid chromatography (HPLC) with ultraviolet (UV) detection has been developed
for simultaneous determination of six important ginsenosides (Rg1, Re, Rb1, Rc, Rb2, and Rd) in pharmaceutical preparations.
For sample preparation, simple and efficient extraction by ultrasonication, combined with solid-phase extraction (SPE) for
clean-up, was effective without consuming large amounts of solvent. Chromatographic separation was performed on an ODS column
with optimized gradient elution by means of a dual-solvent-pumping system. The validated method results in excellent separation,
and quantitative determination is highly precise and accurate. The problem of co-elution of ginsenosides Rg1 and Re is also
solved, with good resolution (RS approx. 1.5). Intraday variation was between 0.2 and 4.4% and interday variation was between 0.4 and 6.5% (n=5 for both). The accuracy was satisfactory—in the range 93.9 to 103.4% from replicate evaluation at three different spiking
concentrations. Overall limits of detection based on a typical injection volume of 5 μL were from 1.16 to 1.58 ng μL−1. The validated method enabled complete assessment for quality control of ginseng samples. The technique may be performed
with less sample preparation and, consequently, reduced possibility of sample loss. 相似文献
10.
Lou DW Saito Y Zarzycki PK Ogawa M Jinno K 《Analytical and bioanalytical chemistry》2006,385(1):96-104
An improved high-performance liquid chromatographic method for separation of a number of ginsenosides has been developed.
The influence of temperature (from 0 to 25°C) on the retention and separation of the ginsenosides was studied by applying
a binary mobile phase (acetonitrile/water, 82:18 v/v) and a diol column (LiChrospher 100 Diol). The column temperature is
one of the more important parameters for the retention and separation of the components investigated. Selected thermodynamic
parameters, including changes of enthalpy (ΔH°) and entropy (ΔS°), were estimated from linear van’t Hoff plots, and possible retention mechanisms were discussed. Moreover, the best separation
conditions were selected based on optimization criteria including maximum retention time (t
R max), minimum resolution (R
s
min), and relative resolution product (r). Temperature regions close to 14°C offered the highest selectivity and almost equal distribution of the ginsenosides peaks
across the chromatogram. Under such isocratic conditions, excellent separation of chromatographic standards and selected ginseng
samples was achieved in less than 16 min. 相似文献