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Article Name:  Research update of Matrine Oxymatrine.Lighiyellow Sophora Root.
Key Words:  Lighiyellow Sophora Root.Matrine.M.F.C15H24N2O.98%Oxymatrine.M.F.C15H24N2O2.98%.Sophora Alkaloids Tannate.14%By Titration.Total Matrines.70%By Titration.Lighiyellow Sophora Root Extract
Article Link:  http://www.mdidea.com/products/herbextract/sophoraal/research.html

Research update of Matrine Oxymatrine.Lighiyellow Sophora Root.


  seminal trace...Lighiyellow Sophora Root.Matrine.M.F.C15H24N2O.98%Oxymatrine.M.F.C15H24N2O2.98%.Sophora Alkaloids Tannate.14%By Titration.Total Matrines.70%By Titration.Lighiyellow Sophora Root Extract...


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   Phytochemical info of Matrine Oxymatrine.Lighiyellow Sophora Root.:

 Product Name:
 Synonym:
 Definition: Lighiyellow Sophora Root Extract are majorly composed of
 Chemical information disclosed as following table:
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   Research Update of Matrine Oxymatrine.Lighiyellow Sophora Root.

   Supercritical fluid extraction of quinolizidine alkaloids from Sophora flavescens Ait. and purification by high-speed counter-current chromatography.:J Chromatogr A. 2007 Jan 27;Ling JY, Zhang GY, Cui ZJ, Zhang CK.State Key Laboratory of Microbial Technology, Shandong University, Jinan 250100, China.

 Supercritical fluid extraction (SFE) was used to extract quinolizidine alkaloids from Sophora flavescens Ait. (Kushen). An orthogonal test L(9)(3)(4) including pressure, temperature, flow rate of CO(2) and the amount of modifier was performed to get the optimal conditions. The process was then scaled up by 30 times with a preparative SFE system under 25MPa, 50 degrees C and a flow rate of CO(2) (2l/min) and the amount of modifier (0.04ml/min). The crude extracts were separated and purified by high-speed counter-current chromatography (HSCCC) with a two-phase solvent system composed of chloroform-methanol-2.3x10(-2)M NaH(2)PO(4) (27.5:20:12.5, v/v), and the collected fractions were analyzed by high-performance liquid chromatography (HPLC). Three kinds of quinolizidine alkaloids were obtained, yielding 10.02mg of matrine, 22.07mg of oxysophocarpine and 79.93mg of oxymatrine with purities of 95.6, 95.8, 99.6% in one-step separation, respectively.

   Quinolizidine alkaloids with anti-HBV activity from Sophora tonkinensis.:Planta Med. 2006 Jul;72(9):854-6. Epub 2006 Jun 19.Ding PL, Huang H, Zhou P, Chen DF.Department of Pharmacognosy, School of Pharmacy, Fudan University, Shanghai, P. R. China.[PMID: 16783704]

 A new matrine-type alkaloid, (-)-14 beta-hydroxyoxymatrine (1), was isolated from the roots and rhizomes of Sophora tonkinensis Gapnep. (Leguminosae), together with five known matrine-type alkaloids, (-)-14 beta-hydroxymatrine (2), (+)-oxymatrine (3), (+)-matrine (4), (+)-sophoranol (5), and (-)-5 alpha-hydroxysophocarpine ( 6), as well as with two known cytisine-type alkaloids, (-)-cytisine (7) and (-)- N-methylcytisine (8). Their structures were elucidated by spectroscopic methods. Compounds 1, 5 and 7 showed potent anti-HBV activity with an inhibitory potency against HBsAg secretion of 22.6 %, 31.1 % and 33.2 %, and against HBeAg secretion of 30.4 %, 26.3 % and 27.8 %, respectively.

   Constituents in the alkaloid fraction of Kushen decoction.:Zhongguo Zhong Yao Za Zhi. 2006 Apr;31(7):557-60.Liu B, Shi RB.School of Chinese Pharmacology, Beijing University of Traditional Chinese Medicine, Beijing 100102, China. liubinyn67@163.com.[PMID: 16780157]

 OBJECTIVE: To study the chemical constituents of the alkaloid fraction of Kushen decoction. METHOD: Constituents were isolated by different kinds of column chromatography and their structures were elucidated with spectral methods. RESULT: Eight compounds were isolated and identified as matrine (I), sophoridine (II), sophocarpine (III), sophoramine (IV), oxymatrine (V), oxysophocarpine (VI), aloperine (VII) and sparteine (VIII). CONCLUSION: All these compounds were isolated from Kushen decoction for the first time. Aloperine was found firstly in Sophora flavescens, or Scutellaria baicalensis, or Rehmannia glutinosa which constituted Kushen decoction.

   Determination and pharmacokinetic study of oxymatrine and its metabolite matrine in human plasma by liquid chromatography tandem mass spectrometry.:J Pharm Biomed Anal. 2006 Jun 7;41(3):918-24. Epub 2006 Feb 24.Wu XL, Hang TJ, Shen JP, Zhang YD. Department of Pharmaceutical Analysis, China Pharmaceutical University, Nanjing 210009, PR China.[PMID: 16500065]

 There is little information about the pharmacokinetics of oxymatrine (OMT) and its metabolite matrine (MT) after i.v. administration of OMT in human. Therefore a specific and sensitive liquid chromatography tandem mass spectrometry (LC-MS/MS) method was established for the determination and pharmacokinetic study of OMT and its metabolite MT in human plasma after i.v. infusion administration of 600 mg of OMT in 100 ml of 5% glucose injection in 0.5 h. The analysis was carried out on a Lichrospher-CN column (250 mmx4.6 mm, i.d., 5 microm, Merck) with mobile phase of methanol-ammonium acetate (20 mmol/l; 85:15, v/v) pumped at a flow rate of 1.0 ml/min. The tandem mass detection was made with electrospray ionization in positive ion selected reaction monitoring mode, with argon collision-induced dissociation ion transitions m/z 265.2 to m/z 265.2 for OMT at 25 eV, m/z 249.2 to m/z 249.2 for MT at 25 eV and m/z 340.2 to m/z 324.0 at 35 eV for the internal standard (papaverine), respectively. The assay was validated to be accurate and precise for the analysis in the concentration range of 1.0-40,000 ng/ml for both OMT and MT with the LOD being 0.5 and 0.2 ng/ml, respectively, when 0.25 ml of human plasma sample was processed with papaverine as internal standard. The pharmacokinetic study was made with 10 healthy male Chinese subjects. The plasma concentration time profiles of OMT and MT obtained were best fitted with two-compartment and one-compartment models, respectively. The main pharmacokinetic parameters found for OMT and MT after i.v. infusion were as follows: Cmax (20,519+/-7581) and (247+/-45) ng/ml, Tmax (0.5+/-0.1) and (5.6+/-1.7) h, AUC0-t (20,360+/-5205) and (3817+/-610) ng h/ml, AUC0-infinity (20,436+/-5188) and (3841+/-615) ng h/ml, t1/2 (2.17+/-0.49) and (9.43+/-0.62) h, respectively. The CL/F and Vd/F of OMT were (43.8+/-10.8) l h-1 and (70.1+/-26.6) l, respectively. Therefore only a small amount of OMT was reduced to MT following i.v. administration of OMT judged by the AUCs.

   A sensitive and specific HPLC-MS method for the determination of sophoridine, sophocarpine and matrine in rabbit plasma.:Anal Bioanal Chem. 2005 Aug;382(7):1595-600. Epub 2005 Jul 5.Wu YJ, Chen JJ, Cheng YY.Department of Chinese Medicine Science and Engineering, College of Pharmaceutical Sciences, Zhejiang University, Hangzhou 310027, P.R. China. yjwu@zju.edu.cn

 A sensitive and specific method was developed for the determination of sophoridine (SRI), sophocarpine (SC) and matrine (MT) in rabbit plasma by HPLC-MS. After an administration of Kuhuang by injection, blood samples were collected and extracted with methanol. The extract solutions were analysed by HPLC-MS method. The separation was performed on a ZORBAX Extend-C18 column using methanol/water/diethylamine (50:50:0.07, v/v/v) as mobile phase. The quinolizidine alkaloids were detected by using mass spectrometry in the SIM mode. There was a good linear relationship between peak area and concentration of analytes over the concentration range of 13.2-995.0 ng mL(-1) for SRI, 7.0-530.0 ng mL(-1) for SC and 8.8-655.0 ng mL(-1) for MT, respectively. The absolute recovery of this method was more than 57% for SRI, 87% for SC and 91% for MT. The accuracy of assay was more than 90%. The limits of detection (LODs) were 6.8 ng mL(-1) for SRI, 3.5 ng mL(-1) for SC and 4.2 ng mL(-1) for MT, respectively. The limits of quantitation (LOQs) were 13.2 ng mL(-1) for SRI, 7.0 ng mL(-1) for SC and 8.8 ng mL(-1) for MT, respectively. The intra-day and inter-day coefficients of variation (RSDs) were less than 10.1, 6.3 and 5.8% for SRI, SC and MT, respectively. The developed method was applied to determine the concentration-time profiles of SRI, SC and MT in rabbit plasma after injection of Kuhuang.
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   Recent research progress of anti-tumor mechnism matrine.:Zhongguo Zhong Yao Za Zhi. 2004 Feb;29(2):115-8.Zhang MJ, Huang J.The Second Affiliative Hospital of Zhejiang University, Hangzhou 310009, China. zmj2146@zju.edu.cn

 Matrine, as an active component of Chinese traditional medicine, has a great effect on anti-inflammation, anti-arrhythmia and anti-fibrosis of liver cell. But the recent evidences indicate that matrine also plays an important role in anti-tumor, such as inhibiting proliferation, inducing differation and apoptosis, reducing invasion and metastasis of tumor cell. In the review we summarized the recent research progress of anti-tumor mechanism of matrine.

   Simultaneous determination of oxymatrine and its active metabolite matrine in dog plasma by liquid chromatography-mass spectrometry and its application to pharmacokinetic studies.:J Chromatogr B Analyt Technol Biomed Life Sci. 2005 Mar 25;817(2):319-25.Wang S, Wang G, Li X, Sun J, Ma R, Sheng L.Key Lab of Drug Metabolism and Pharmacokinetics, China Pharmaceutical University, Nanjing 210009, China.[PMID: 15687001]

 A simple, rapid and reliable method was developed for the quantification of oxymatrine (OMT) and its metabolite matrine (MT) in beagle dog plasma using a liquid-liquid extraction procedure followed by liquid chromatography-electrospray ionization mass spectrometric (LC-ESI-MS) analysis. Extend-C18 column (2.1 mm i.d. x 50 mm, 5 microm) with a C18 guard column (2.1 mm i.d. x 12.5 mm) was used as the analytical column. Linear detection responses were obtained for OMT concentration ranging from 5 to 4000 ng/ml and for MT concentration ranging from 5 to 2000 ng/ml. The precision and accuracy data, based on intra- and inter-day variations over 5 days, were lower than 5%. The limit of quantitation for OMT and MT were 2 and 1 ng/ml, respectively, and their recoveries were greater than 90%. Pharmacokinetic data of OMT and its active metabolite MT obtained with this method following a single oral dose of 300 mg OMT capsules to six beagle dogs was also reported for the first time.
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  Scientific References:

  1.Matrine Oxymatrine.Lighiyellow Sophora Root.
  2.Research update of Matrine Oxymatrine.Lighiyellow Sophora Root.


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   Lighiyellow Sophora Root.Matrine.M.F.C15H24N2O.98%Oxymatrine.M.F.C15H24N2O2.98%.Sophora Alkaloids Tannate.14%By Titration.Total Matrines.70%By Titration.Lighiyellow Sophora Root Extract photo picture image  Lighiyellow Sophora Root.Matrine.M.F.C15H24N2O.98%Oxymatrine.M.F.C15H24N2O2.98%.Sophora Alkaloids Tannate.14%By Titration.Total Matrines.70%By Titration.Lighiyellow Sophora Root Extract photo picture image  

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  Claims:  Information this web site presented is meant for Nutritional Benefit and as an educational starting point only, for use in maintenance and promotion good health in cooperation with a common knowledge base reference...Furthermore,it based solely on the traditional and historic use or legend of a given herb from the garden of Adonis. Although every effort has been made to ensure its accurate, please note that some info may be outdated by more recent scientific developments......

  Pharmakon Warning:  The order of knowledge is not the transparent order of forms and ideas,as one might be tempted retrospectively to interpret it; it is the antidote....(Dissemination,Plato's Pharmacy,II.The Ingredients:Phantasms,Festivals,and Paints;138cf. Jacques Derrida.).

  And as it happens,the technique of imitation,along with the production of the simulacrum,has always been in Plato's eyes manifestly magical,thaumaturgical:......and the same things appear bent and straight to those who view them in water and out,or concave and convex,owing to similar errors of vision about colors, and there is obviously every confusion of this sort in our souls.And so scene painting (skiagraphia) in its exploitation of this weakness of four nature falls nothing short of witchcraft (thaumatopoia), and so do jugglery and many other such contrivances.(Republic X,602c-d;cf.also 607c).




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