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Studies On The Acid Degradation Process Of Total Ginsenosides In The Roots Of Panax Ginseng C. A.Mey. And Glycosylation Of Novel Panaxadiol

Posted on:2010-03-16Degree:MasterType:Thesis
Country:ChinaCandidate:R XingFull Text:PDF
GTID:2144360272497588Subject:Medicinal chemistry
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Panax ginseng C.A.Meyer,which is widely used as traditional Chinese medcine,its products are increasingly popular and readily available in pharmacies and health food around the world.Ginsenosides which are the main bioactive components of Panax ginseng,have unique pharmacological activity.In this thesis,the acid degradation process of total ginsenosides in the roots of ginseng,at the same time,the mothed of glycosylation of novel panaxadiol were studied.The sense of this thesis is for the further study of the medicinal value of ginseng,for new drug research reserves compounds basic.1.Literature reviewGinseng as one of the traditional Chinese medicine,it has a long history in our country, ginsenosides were the main effect comoonent,both domestic and foreign scholars were isolated 63 kinds of ginsenosides from ginseng.A large number of studies showed that ginsenosides can suppress tumor cell growing and anti-fatigue,slow aging,improve immunity,improve the cardio- and cerebro-vascular insufficiency and so on.2.Degradation process of total saponins of Panax ginseng rootsIn this paper,we used strong acid(HCl,H2SO4) weak acid(HAc) ethanol solution separately degradation total saponins of Panax ginseng root,the target compound was novel panaxadiol.Through single factor test,we chosed acid type,acid concentration,degradation time and degradation temperature four factors for degradation process researching.The results showed that the optimal conditions for degradation was 80℃,7%sulfuric acid degradation 8 h.Application of the above method on degradation,the degradation was stability,and degradation rate was higher.3.The novel panaxadiol's HPLC researchingWe firstly used HPLC for the content of novel panaxadiol.Chromatographic conditions: Kromasil C18 column(4.6 mm×250 mm,5μm),mobile phase was methanol - water(90:10), flow volume was 1.0 mL/min,detection wavelength was 203 nm,column temperature was 35℃,injection volume was 10μL.On the conditions,the results were the linear range of 0.2~4.0μg and correlation coefficient r was 0.9998.The precision test's RSD was 0.70%,the stability test's RSD was 1.13%,the reproducibility test's RSD was 1.85%,recovery test for 0.42%of RSD. 4.Studied on the novel panaxadiol with amyloidβmolecular simulationIn this paper,we innovatively used molecular docking approach,the target was amyloid 13 protein,taken the novel panaxadiol,protopanoxadiol and ginsenoside-Rg3 as small molecule probes,carried out the molecular simu- lation,in order to put forward a new theory and the possible mechanism of interaction between the two models,the novel panaxadiol and amyloidβprotein,as.well as provided orientation of further study.In this study,two innovative mechanism of drugs were proposed:one mechanism,β-sheet in the horizontal position of the three small molecules,respectively,from the side of amyloidβ,in space there was on steric effects,effectively blockedβ-sheet further formed;mechanism two,β-sheet in the vertical position,separately for the three small molecule amyloidβprotein from one side, constitute a steric inter-layer.The results showed that the horizonta binding energy of novel panaxadiol with amyloidβwas -4.59 kal/mol 1,vertical integration to -6.19 kal/mol.At the same time,the novel panaxadiol's 3-OH part in the internalβ-sheet,modified the 3-OH was the method of stabilization of the novel panaxadiol and amyloidβ.This had the important role on the treating and preventing AD.5.The glycosilation of novel panaxadiolThrough molecular modeling studies,we could conclud that the novel panaxadiol's 3-OH was the role of the target,taken glycosilation can be combined with the protein more stable conducive to prevent theβ-sheet,so as to effectively prevent and treat AD.In this test purpose,the glycosilation of the novel panaxadiol test was studied.The suger donator was 2,3,4,6 - tetra- O- ac etyl-β-D-gluxosyl-trichloroacetic ester imide.The suger acceptor was the novel panaxadiol.,and catalytic agent was TMSOTf.Through the analysis,we coule simply arrive at the novel panaxadiol connected with glucose,but the exact location of the connection had to be further studied.6.The innovative and value of researchingThe novel panaxadiol was new compounds in ginseng root,one of the sapogenins.Acid degradation process and HPLC studies were the firstly.In addition,this article innovatively took technologies in molecular simulation on ginseng,and predicted two mechanisms of novel panaxadiol with amyloidβprotein.Glycosilation of novel panaxadiol was under the molecular simulation guidance.All the results of the study can offer credible foundation for the development of new anti-Alzheimer's disease.
Keywords/Search Tags:novel Panaxadiol, anti-Alzheimer's disease, molecular simulation, glycosilation
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