238 resultados para Electrospray (ESI)


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采用液相色谱-电喷雾质谱联用(HPLC-ESI-MSn)技术,对北五味子与南五味子中木脂素类成分进行了系统研究.通过HPLC-ESI-MS技术,获得了相应化合物的保留时间、紫外光谱和分子量等信息,利用电喷雾多级串联质谱技术(ESI-MSn),获得了相应化合物的结构信息.研究结果表明,北五味子与南五味子的主要木脂素成分除5个共有成分外其它成分差异较大,并且其共有成分含量差别较大.在此基础上,建立了简便、快速的北五味子与南五味子药材分析鉴定的新方法.

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Four different methods were used to process fresh ginseng into red ginseng in this paper. The contents of AFG in these red ginseng were determined by ESI-MS. The results show that the indirect steaming method plays an important role in increasing the AFG content, while soakage in vinegar alone has no effect on it.

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利用电喷雾串联质谱方法(ESI-MS/MSn)和内标法分析麻黄附子甘草汤方剂中二萜类生物碱种类和含量的变化,通过拆方研究了麻黄、甘草对附子生物碱的影响规律,揭示了麻黄附子甘草汤的配伍内涵。研究表明,麻黄、甘草单独与炮附子配伍时能够通过化学和物理作用减少热解型单酯型生物碱的含量,并生成脂型生物碱,但方剂组合后有效成分热解型单酯型生物碱的含量增加。结合初步药效学实验表明,热解型单酯型生物碱是具有明显的抗炎作用,说明炮附子在复方中发挥抗炎作用的主要成分可能为热解型单酯型生物碱,同时复方的整体配伍利于有效成分的转化。

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利用电喷雾质谱(ESI-MS)法建立龙胆质谱指纹图谱,研究其中代表性裂环烯醚萜苷类成分的ESI-MS规律。采用甲醇超声法提取龙胆中裂环烯醚萜苷类成分,在正离子方式检测模式下直接进样,应用一级全扫描质谱建立其特征图谱。运用化学模式识别方法对图谱数据进行分析,发现秋季龙胆样品的聚集程度优于春季龙胆样品,根据春季、秋季药材样品的差异,可以对采收期进行区分;裂环烯醚萜苷类成分在二级质谱中易发生脱水、乙酰基、葡萄糖基等。电喷雾质谱法的精密度、稳定性、重现性均符合要求,且具有特征性强、分析速度快、样品用量少等优点。

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采用紫外可见分光光度法、ESI-MS(电喷雾质谱)与HPLC-UV(高效液相色谱)测定技术分析了等离子体种子处理机处理人参种子对所栽培人参中人参皂苷含量的影响。结果发现,人参种子受到等离子体与梯度磁场综合作用处理后,培育出的人参其总皂苷含量随磁化电流强度的改变呈现近似的正态分布。其中,在磁化线圈电流强度为1.1~1.5 A处理种子后,栽培的人参中总皂苷含量较高。建立了电喷雾质谱分析人参提取物中人参皂苷的半定量方法,方法便捷地反映了未处理及处理后的人参种子所栽培的人参中皂苷成分的含量变化。

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Aconite alkaloids in two kinds of processed Radix Aconiti Kusnezoffii(RAK) were analyzed by ESI-MS.The results indicate that there are not diester-alkaloids detected in the two kinds of processed RAK by comparison with crude RAK,which show that both steaming process and boiling process decrease toxicity.As the same time,a simple,rapid and sensitive method is provided to analyze aconite alkaloids in different sorts of processed RAK using ESI-MS.

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The ESI-MS analytical method was established for studying the alkaloids content in the decoctions of Radix aconiti combined with Bulbus Fritillariae Thunbergii or bulbus fritillariae Cirrhosae.For the co-decoctions of Radix aconiti combined with Thunberg Fritillary Bulb contains more diester-alkaloids than that of co-decoctions of Radix aconiti combined with Bulbus Fritillariae Cirrhosae.When Radix aconiti was combined with Thunberg Fritillary Bulb,diester-alkaloids were mainly dissolved in water.But diester-alkaloids were mainly converted into lipo-alkaloids when Radix aconiti was combined with Bulbus Fritillariae Cirrhosae.

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Five different processed methods for ginseng were used transferred ginsenosides with large molecule mass into low polar ginsenosides.The contents of low polar ginsenosides in these ginseng products were determined by ESI-MS.The results show that the high pressure steaming method make for increasing the concent of low polar ginsenosides,while soakage in vinegar is not good comparing with it.

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首次采用LC/ESI-MSn方法对乌头碱灌胃给药后不同时间内家兔尿液中的乌头碱代谢产物进对比研究。经与空白尿样对照发现,在0~4h和4~8h两个时间段,家兔尿液中除乌头碱(AC)原形外,均含有相同的代谢产物,但相对含量差别很大。通过总离子流色谱图(TIC)可以发现3个主要代谢产物(M1,M2,M4)。分别测定了各代谢产物的准分子离子及其各级碎片离子,与AC在ESI-MSn条件下的质谱碎裂规律相比较,并参考AC体内代谢文献,推断尿液中的主要代谢产物M1为16-O-去甲基乌头碱;M2和M4的m/z均为616,为同分异构体,结构还需要进一步的确认。

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The velvet antler polypeptide CNT14 was extracted and purified by gel filtration, ion exchange chromatography and RP C, which showed a single peak in HPLC chromatography and a single band in SDS-PAGE. The molecular weight measured by MALDI/TOF/MS spectrum was 1479. 9028. The polypeptide consisted mostly of Glu, Leu, Val, Pro. The amino acid sequence of the polypeptide was detected with ESI-MS/ MS, and the sequence was E-P-T-V-L-D-E-V-C-L-A-H-G-P. The experiments of biological activity of polypeptide CNT14 in vivo were carried out, and the results show that CNT14 has stimulant effects on the growth of rat HT22 cells. Then we produced the polypeptide CNT14 according the amino acid sequence by solid phase synthesis, confirmed the sequence of the polypeptide to be consistent with the amino acid sequence of polypeptide CNT14 which was separated from the velvet antler.

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A high performance liquid chroatography-electrospray ionization-mass spectrometric method was developed for analysis and identification of ginsenosides from the decoction of ginseng, ginseng with trogopteroum feces and ginseng with semen raphani. Ten ginsenosides were separated and detected. The content variation of these ginsenosides was researched. The experimental results showed, that ginsenosides were less in compatible decoction than in separate one expect Ro. the stripping of ginsenosides were restrained by semen raphani and during combination of ginseng with trogopteroum feces, the precipitates were produced by ginsenosides.

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利用电喷雾质谱方法(ESI-MS)分析了附子加辅料(甘草)炮制前后水煎液中二萜类生物碱在种类和含量方面的变化,通过加入内标化合物,建立了电喷雾质谱的半定量分析方法。此方法具有快速、准确、灵敏的特点,能够更加全面地反映中药配伍炮制过程中多种化学成分的含量变化,并能根据电喷雾串联质谱的分析结果鉴定配伍后产生的新的化学成分,在共煎液中的次乌头碱、中乌头碱和乌头碱的相对含量分别是单煎液中的5.67%、4.05%和4.88%。通过研究附子与甘草的单煎液、共煎液以及药渣中化学成分的变化,揭示了甘草作为辅料,在炮制过程中对附子减毒作用机理。

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虎眼万年青(Ornithogalum caudatum Ait)俗名珍珠草,为百合科虎眼万年青属多年生草本植物.其原产非洲南部,我国北方有栽培.民间用其全草或球茎入药,主要用于消炎和抗癌.从该属植物中曾分离得到胆甾烷苷和降胆甾烷苷类成分.

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Traditional Chinese Medicine (TCM) based on natural products is one important part of the Chinese civilization.Owing to the complexity of the composition,the study on medical effective components and curative effects are very difficult;Fuzi (Radix Aconiti Lateralis Praeparata) has been widely used for cardiotonic and analgesics in China,however,the component-aconitine in which is very toxic and may cause some side-effect.This paper reported the application of electrospray iohization mass spectrometric(ESIMS) technique on study of the compound prescriptions containing fuzi,Renshensini concoction and Baweidihuang concoction,to explore the mechanism of synergy between fuzi and other herbs.From chemical point of view,the detoxification mechanism can be attributed to the hydrolysis of the solubility of toxic diester-alkaloids from concoctions of fuzi.Radix Glycyrrhizae Praeparata,Rhizoma Zingiberis,Radix Ginsengp promote the hydrolysis to produce the less toxic monoester-alkaloids and Fructus Corni reduce the solubility of hypaconitine from fuzi.

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A simple route for the preparation of lipo-alkaloid is presented. When aconitine or one of its analogues is heated with a fatty acid for 20 min at 100degreesC in water, the C-8 acetyl group of aconitine is displaced by along chain fatty acyl group. The structures of the products were characterized by electrospray ionization tandem mass spectrometry.