CN1307192C - Process of preparing high-purity jasminodin with Cape jasmine fruit - Google Patents

Process of preparing high-purity jasminodin with Cape jasmine fruit Download PDF

Info

Publication number
CN1307192C
CN1307192C CNB2005100261430A CN200510026143A CN1307192C CN 1307192 C CN1307192 C CN 1307192C CN B2005100261430 A CNB2005100261430 A CN B2005100261430A CN 200510026143 A CN200510026143 A CN 200510026143A CN 1307192 C CN1307192 C CN 1307192C
Authority
CN
China
Prior art keywords
cape jasmine
jasminoidin
jasmine fruit
prepare
macroporous adsorbent
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Fee Related
Application number
CNB2005100261430A
Other languages
Chinese (zh)
Other versions
CN1706859A (en
Inventor
范国荣
周婷婷
柴逸峰
吴玉田
洪战英
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Second Military Medical University SMMU
Original Assignee
Second Military Medical University SMMU
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Second Military Medical University SMMU filed Critical Second Military Medical University SMMU
Priority to CNB2005100261430A priority Critical patent/CN1307192C/en
Publication of CN1706859A publication Critical patent/CN1706859A/en
Application granted granted Critical
Publication of CN1307192C publication Critical patent/CN1307192C/en
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Landscapes

  • Medicines Containing Plant Substances (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Saccharide Compounds (AREA)

Abstract

The present invention relates to a method for preparing jasminoidin by using gardenia fruit, which belongs to the technical field of a medicine. Crude gardenia fruit extract is prepared by soaking or reflux by using water or aqueous ethanol solution, processed through macroporous resin, and eluted by respectively using a large amount of water or aqueous ethanol solution with a concentration of 10% to remove strong polar iridoid glycoside components and impurities, and jasminoidinis selectively eluted by using ethanol with a low concentration, and concentrated by pressure reduction to obtain jasminoidin with high purity. The preparation method of the present invention has the advantages of easy operation, low cost high product purity and yield, and no environmental pollution, and is suitable for industrialized production.

Description

A kind of method for preparing high-purity gardenoside with cape jasmine fruit
Technical field
The present invention relates to medical technical field, is a kind of method for preparing high-purity gardenoside from cape jasmine fruit.
Background technology
Cape jasmine has another name called SHANZHIZI, is the fruit of madder wort mountain Cape jasmine Gardenia jasminoides Ellis., and the property bitter cold is nontoxic.The cape jasmine beginning is stated from Shennong's Herbal, has cholagogic, short pancreatic secretion, step-down, calmness, cooling, antimicrobial antiphlogistic effect.The main chemical compositions of cape jasmine is iridoid, flavones, triterpene, organic acid acetic etc., also have d-N.F,USP MANNITOL, sterols, triterpene saponin, long chain alkane, alcohol and pigment etc. in addition, wherein the iridoid glycoside compounds is [Wang Gangli such as its main active ingredient such as jasminoidin, genipin-1-β-D-gentiobiose glycosides, Gardenoside, gardoside, fevervine time glycosides methyl esters, deacetylate psyllium acid methyl esters, cape jasmine thuja acid, gardenin, Chen Dechang etc. Gardenia Ellis plant chemical ingredient progress. CHINA JOURNAL OF CHINESE MATERIA MEDICA, 1996,21 (2): 67; Huang Shengyang. Chinese Gardenia Ellis Study on plants overview. Jiangxi College of Traditional Chinese Medicine journal, 1991,3 (1): 59].Jasminoidin (geniposide) is main iridoid glycoside compound, is the important effective constituent of cape jasmine, and structural formula is as follows:
At present, the traditional method separation and purification jasminoidins such as column chromatography, recrystallization that adopt when preparing jasminoidin with cape jasmine fruit both at home and abroad more, as [Inouye H, et al.Chem Pharm Bull.1970,18 (5): 1066 such as silica gel column chromatography, alumina column chromatography and thin-layer chromatographys; Inouye H, et al.Phytochemistry.1974,13:2219; Endo T, et al.Chem Pharm Bull.1973,21 (12): 2684; The comparison of flourish .TLC of Li Li and column chromatography for separation jasminoidin. Chinese patent medicine .1999,21 (12): 645], these class methods maybe need be used poisonous organic solvent, as chloroform, methyl alcohol, can cause environmental pollution; Or cost height and complex operation, as the neutral alumina filler, cost an arm and a leg.Though also can adopt preparative liquid chromatography to prepare jasminoidin [Wang Lan opens mirror .RP-HPLC preparative chromatography and separates jasminoidin monomer .2003,25 (9): 764], its pre-treating process complex operation is not suitable for large-scale commercial production.There have bibliographical information to adopt macroporous adsorbent resin to separate the jasminoidin cost to be low, do not cause environmental pollution [Lv Maoping, Qiao Qingbin etc. macroporous resin is to the research .2002 of jasminoidin separating effect, 33 (9): 794; CN 1546507A " a kind of Fructus Gardeniae extract and preparation technology thereof and its application "; Jin Rixian, Guo Chunyan etc. the technical study .2005 of jasminoidin in the macroporous adsorbent resin method enrichment cape jasmine, 11 (3): 1], but type of elution commonly used at present has two kinds, one be with behind the water elution directly with the high concentration ethanol wash-out, not only can't remove the iridoid glycoside constituents that polarity is better than jasminoidin slightly, and low-pole impurity is residual more; Two for without washing directly to use the high concentration ethanol wash-out behind the low-concentration ethanol wash-out again, not only can't remove water-soluble impurity, and can introduce more low-pole impurity equally.Therefore, the jasminoidin purity that existing method obtains is lower, still needs to be further purified by above-mentioned traditional separation method, and the application on producing has certain limitation.
Summary of the invention
The invention provides that a kind of preparation technology is simple, the method that from cape jasmine fruit, prepares high-purity gardenoside of low cost and environmentally safe.
The present invention is according to jasminoidin more weak characteristics of relative polarity in the iridoid glycoside constituents, during with purification with macroreticular resin cape jasmine fruit crude extract, earlier with big water gaging and 10% ethanol flush away impurity and the big iridoid glycoside constituents of polarity, low-pole impurity and other iridoid glycosides composition of being introduced with minimizing high concentration ethanol wash-out with 20%~30% ethanol selective elution jasminoidin again.Fact proved that the jasminoidin purity that this simple preparation method obtained is very high, avoided the environmental pollution that causes by other method separation and purification.
The inventive method comprises the steps:
(1) preparation cape jasmine fruit crude extract: routinely dry cape jasmine fruit meal is soaked with water or aqueous ethanolic solution or refluxing extraction 1~3 time, filter, filtrate decompression is concentrated into rare medicinal extract, vacuum-drying gets the cape jasmine fruit crude extract again, and yield is 25%~30%.
(2) prepare jasminoidin: after the above-mentioned cape jasmine fruit crude extract that makes is added the suitable quantity of water suspendible, cross macroporous adsorptive resins.It is colourless that first water respectively and 10% ethanol fully are eluted to elutriant, and water and 10% alcoholic acid elution volume are no less than 4 times of amount of resin usually, discard elutriant, use 20%~30% low-concentration ethanol wash-out again, collect this elutriant, the concentrating under reduced pressure drying promptly gets the jasminoidin powder.Adopt high performance liquid chromatography (HPLC) method that this powder is carried out purity detecting (peak area normalization method) and record jasminoidin purity and be higher than 98%, yield is 0.5%~1.5%.And carry out MS, 1HNMR and 13CNMR analyzes, and carries out structural confirmation according to the gained data, proves jasminoidin.
The present invention adopts macroporous adsorbent resin only with water and low-concentration ethanol wash-out, with low cost, environment is not polluted, in elution process by water and 10% ethanol gradient elution, remove iridoid glycoside compounds and the impurity that depolarization is better than jasminoidin successively by the polarity size, at last not to be higher than 30% low-concentration ethanol selective elution jasminoidin, reduce the interference of low-pole impurity, need not to be further purified and to obtain purity and be higher than 98% jasminoidin, preparation technology is simple, is fit to suitability for industrialized production.
Description of drawings
Fig. 1 is the color atlas of the high performance liquid chromatography (HPLC) of jasminoidin of the present invention
Embodiment
Describe the present invention below in conjunction with embodiment and accompanying drawing.
Embodiment 1:
1. prepare the cape jasmine fruit crude extract: get dry cape jasmine fruit medicinal material coarse powder 500g, measure 50% alcohol reflux 2 times, each 2 hours with 10 times, filter, merging filtrate, 60 ℃ are evaporated to rare medicinal extract, vacuum-drying gets the cape jasmine fruit crude extract, and yield is 26.6%.
2. purifying: get above-mentioned cape jasmine fruit crude extract, add that cumulative volume is 2000ml behind the water suspendible.Join and 1500g is housed on 1300 pretreated macroporous adsorption resin chromatography posts, absorption was 2 hours after last sample finished.With 6000ml water elution (discarding).Use 8000ml 10% ethanol elution (discarding) again, use 6000ml 20% ethanol elution at last, behind the 20% ethanol elution stream part concentrating under reduced pressure, vacuum-drying (60 ℃) gets jasminoidin brown ceramic powder 6.42g, and yield is 1.3%.Adopting high performance liquid chromatography (HPLC) method that this powder is carried out purity detecting (peak area normalization method), to record jasminoidin purity be 98.9%.And carry out MS, 1HNMR and 13CNMR analyzes, and carries out structural confirmation according to the gained data.The HPLC analysis condition is chromatographic column Lichrospher C 18(4.6 * 250mm i.d.5 μ m); Moving phase is acetonitrile: 1% aqueous acetic acid=10: 90; Flow velocity 0.9ml/min; 25 ℃ of column temperatures detect wavelength 238nm.The high-efficient liquid phase chromatogram of jasminoidin is seen Fig. 1 with this understanding, and peak 1 is a jasminoidin.Structure is identified: the jasminoidin that separation is obtained on Varian INOVA-500 type nuclear magnetic resonance analyser and Varian MAT-212 type mass spectrograph, carry out MS, 1HNMR and 13CNMR analyzes, and the result is: UV λ max (nm MeOH): 239.ESI-MS:389(M+1),227,209(M-glu)。 1HNMR(500?MHz,DMSO-d 6)δ:5.12(1H,d,J=7.0Hz,H-1),7.5(1H,brs,H-3),5.6(1H,brs,H-7),4.2(1H,d,J=15.0Hz,H-10),4.0(1H,d,J=14.0Hz,H-10),3.6(3H,s,H-12),4.53(1H,d,J=8.0Hz,H-1′)。 13CNMR(500MHz,DMSO-d 6)δ:95.7(C-1),151.5(C-3),110.9(C-4),45.9(C-5),37.9(C-6),125.4(C-7),144.1(C-8),51(C-9),59.3(C-10),166.9(C-11),34.4(C-12),98.6(C-1′),73.3(C-2′),77.2(C-3′),70(C-4′),76.6(C-5′),61(C-6′)。Confirm as jasminoidin through structure elucidation.
Embodiment 2:
1. preparation cape jasmine fruit crude extract: get dry cape jasmine fruit medicinal material coarse powder 500g, with 10 times of water gaging refluxing extraction 2 times, each 2 hours, filtration, merging filtrate, 60 ℃ are evaporated to rare medicinal extract, and vacuum-drying gets the cape jasmine fruit crude extract, and yield is 28.7%.
2. purifying: get above-mentioned cape jasmine fruit crude extract, add that cumulative volume is 2000ml behind the water suspendible.Join and 1500g is housed on 1300 pretreated macroporous adsorption resin chromatography posts, absorption was 2 hours after last sample finished.With 6000ml water elution (discarding).Use 8000ml 10% ethanol elution (discarding) again, use 4000ml 30% ethanol elution at last, behind the 30% ethanol elution stream part concentrating under reduced pressure, vacuum-drying (60 ℃) gets jasminoidin brown ceramic powder 7.48g, and yield is 1.5%.Adopting high performance liquid chromatography (HPLC) method that this powder is carried out purity detecting (peak area normalization method), to record jasminoidin purity be 98.0%.Jasminoidin structure authentication method, step and result thereof are with embodiment 1.
Embodiment 3:
1. prepare the cape jasmine fruit crude extract: get dry cape jasmine fruit medicinal material coarse powder 500g, extract each 2 hours 2 times with 10 times of amount 50% alcohol immersion, filter, merging filtrate, 60 ℃ are evaporated to rare medicinal extract, vacuum-drying gets the cape jasmine fruit crude extract, and yield is 20.3%.
2. purifying: get above-mentioned cape jasmine fruit crude extract, add that cumulative volume is 2000ml behind the water suspendible.Join and 1500g is housed on pretreated AB-8 macroporous adsorption resin chromatography post, absorption was 2 hours after last sample finished.With 6000ml water elution (discarding).Use 8000ml 10% ethanol elution (discarding) again, use 6000ml 20% ethanol elution at last, behind the 20% ethanol elution stream part concentrating under reduced pressure, vacuum-drying (60 ℃) gets jasminoidin brown ceramic powder 5.36g, and yield is 1.1%.Adopting high performance liquid chromatography (HPLC) method that this powder is carried out purity detecting (peak area normalization method), to record jasminoidin purity be 98.7%.Jasminoidin structure authentication method, step and result thereof are with embodiment 1.
Embodiment 4:
1. prepare the cape jasmine fruit crude extract: get dry cape jasmine fruit medicinal material coarse powder 500g, measure 50% alcohol reflux 2 times, each 2 hours with 10 times, filter, merging filtrate, 60 ℃ are evaporated to rare medicinal extract, vacuum-drying gets the cape jasmine fruit crude extract, and yield is 26.6%.
2. purifying: get above-mentioned cape jasmine fruit crude extract, add that cumulative volume is 2000ml behind the water suspendible.Join and 1500g is housed on pretreated D101 macroporous adsorption resin chromatography post, absorption was 2 hours after last sample finished.With 7000ml water elution (discarding).Use 8000ml 10% ethanol elution (discarding) again, use 5000ml 20% ethanol elution at last, behind the 20% ethanol elution stream part concentrating under reduced pressure, vacuum-drying (60 ℃) gets jasminoidin brown ceramic powder 6.23g, and yield is 1.2%.Adopting high performance liquid chromatography (HPLC) method that this powder is carried out purity detecting (peak area normalization method), to record jasminoidin purity be 98.8%.Jasminoidin structure authentication method, step and result thereof are with embodiment 1.

Claims (8)

1. one kind prepares the method for jasminoidin with cape jasmine fruit, comprises the steps:
(1) preparation cape jasmine fruit crude extract: routinely dry cape jasmine fruit meal is soaked with water or aqueous ethanolic solution or refluxing extraction 1~3 time, filter, filtrate decompression is concentrated into rare medicinal extract, vacuum-drying gets the cape jasmine fruit crude extract again;
(2) purifying: after the above-mentioned cape jasmine fruit crude extract that makes added the suitable quantity of water suspendible, cross macroporous adsorbent resin, it is colourless that first water respectively and 10% ethanol fully are eluted to elutriant, discard elutriant, use 20%~30% low-concentration ethanol wash-out again, collect this elutriant, the concentrating under reduced pressure drying promptly gets jasminoidin.
2. prepare the method for jasminoidin by claim 1 is described with cape jasmine fruit, when it is characterized in that preparing the cape jasmine fruit crude extract, use 50% alcohol reflux.
3. describedly prepare the method for jasminoidin with cape jasmine fruit by claim 1 or 2, when it is characterized in that purifying, water and 10% alcoholic acid elution volume all are no less than 4 times of amount of resin.
4. describedly prepare the method for jasminoidin with cape jasmine fruit by claim 1 or 2, when it is characterized in that purifying, said low-concentration ethanol is 20% ethanol.
5. prepare the method for jasminoidin by claim 3 is described with cape jasmine fruit, when it is characterized in that purifying, said low-concentration ethanol is 20% ethanol.
6. describedly prepare the method for jasminoidin by claim 1 or 2 or 5, it is characterized in that said macroporous adsorbent resin is 1300 or D101 or AB-8 type macroporous adsorbent resin with cape jasmine fruit.
7. prepare the method for jasminoidin by claim 3 is described with cape jasmine fruit, it is characterized in that said macroporous adsorbent resin is 1300 or D101 or AB-8 type macroporous adsorbent resin.
8. prepare the method for jasminoidin by claim 4 is described with cape jasmine fruit, it is characterized in that said macroporous adsorbent resin is 1300 or D101 or AB-8 type macroporous adsorbent resin.
CNB2005100261430A 2005-05-24 2005-05-24 Process of preparing high-purity jasminodin with Cape jasmine fruit Expired - Fee Related CN1307192C (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CNB2005100261430A CN1307192C (en) 2005-05-24 2005-05-24 Process of preparing high-purity jasminodin with Cape jasmine fruit

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CNB2005100261430A CN1307192C (en) 2005-05-24 2005-05-24 Process of preparing high-purity jasminodin with Cape jasmine fruit

Publications (2)

Publication Number Publication Date
CN1706859A CN1706859A (en) 2005-12-14
CN1307192C true CN1307192C (en) 2007-03-28

Family

ID=35580986

Family Applications (1)

Application Number Title Priority Date Filing Date
CNB2005100261430A Expired - Fee Related CN1307192C (en) 2005-05-24 2005-05-24 Process of preparing high-purity jasminodin with Cape jasmine fruit

Country Status (1)

Country Link
CN (1) CN1307192C (en)

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101343297B (en) * 2008-07-08 2011-03-23 陕西科技大学 Method for extracting and purifying gardenoside with absorbent charcoal
CN101407532B (en) * 2008-11-24 2011-12-28 浙江省中药研究所有限公司 Method for preparing gardenin from gardenia
CN101891781A (en) * 2010-07-23 2010-11-24 广西大学 Method for preparing high-purity gardenoside
CN104098632A (en) * 2013-04-10 2014-10-15 江苏康缘药业股份有限公司 Iridoid glycoside compound, and preparation method and application thereof
CN104098631A (en) * 2013-04-10 2014-10-15 江苏康缘药业股份有限公司 Iridoid glycoside compound, and preparation method and application thereof
CN104098630A (en) * 2013-04-11 2014-10-15 江苏康缘药业股份有限公司 Iridoid glycoside compound, and preparation method and application thereof
CN103951718B (en) * 2014-04-12 2016-03-30 云南云药医药研究有限公司 A kind of method preparing high-purity gardenoside and crocin with cape jasmine
CN105566413A (en) * 2016-01-29 2016-05-11 常州市鼎升环保科技有限公司 Separation and purification method for geniposide
CN108047289A (en) * 2017-12-31 2018-05-18 浙江工业大学 A kind of extraction for preparing high-purity gardenoside and process for purification
CN108929350A (en) * 2018-05-25 2018-12-04 无锡济民可信山禾药业股份有限公司 A method of it distills to extract from XINGNAOJING ZHUSHEYE and recycles Gardenoside in waste liquid
CN109223956B (en) * 2018-10-17 2021-06-18 中国人民解放军第二军医大学 Traditional Chinese medicine composition for treating cough and extraction method and application thereof
CN112043759A (en) * 2019-06-06 2020-12-08 南京宸翔医药研究有限责任公司 Method for extracting, separating and purifying multiple components of cape jasmine and pharmaceutical composition thereof
CN112057510B (en) * 2020-09-30 2022-06-10 江西中医药大学 Application of gardenia extract in preparation of medicine for treating ulcerative colitis

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1446818A (en) * 2002-12-27 2003-10-08 成都和康药业有限责任公司 Technique of preparing extract product of Radde Anemone Rhizome extract, and its application in preparing medication of treating cancer
JP2004131633A (en) * 2002-10-11 2004-04-30 Riken Vitamin Co Ltd Method for purifying yellow pigment of gardenia, and purified yellow pigment of gardenia
CN1517326A (en) * 2002-07-12 2004-08-04 范崔生 Capejasmine cycloolefines ether terpene extract and its preparation method and use
CN1546507A (en) * 2003-12-01 2004-11-17 李文军 Cape jasmine extract , its preparing process and application

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1517326A (en) * 2002-07-12 2004-08-04 范崔生 Capejasmine cycloolefines ether terpene extract and its preparation method and use
JP2004131633A (en) * 2002-10-11 2004-04-30 Riken Vitamin Co Ltd Method for purifying yellow pigment of gardenia, and purified yellow pigment of gardenia
CN1446818A (en) * 2002-12-27 2003-10-08 成都和康药业有限责任公司 Technique of preparing extract product of Radde Anemone Rhizome extract, and its application in preparing medication of treating cancer
CN1546507A (en) * 2003-12-01 2004-11-17 李文军 Cape jasmine extract , its preparing process and application

Non-Patent Citations (3)

* Cited by examiner, † Cited by third party
Title
中药栀子提取方法的比较和工艺条件优化 李其兰等,中国医院药学杂志,第24卷第6期 2004 *
中药栀子提取方法的比较和工艺条件优化 李其兰等,中国医院药学杂志,第24卷第6期 2004;栀子苷乙醇提取的方法优化 刘菊芳等,山东中医杂志,第18卷第2期 2004 *
栀子苷乙醇提取的方法优化 刘菊芳等,山东中医杂志,第18卷第2期 2004 *

Also Published As

Publication number Publication date
CN1706859A (en) 2005-12-14

Similar Documents

Publication Publication Date Title
CN1307192C (en) Process of preparing high-purity jasminodin with Cape jasmine fruit
CN101220062A (en) Method for preparing stevioside and rebaudiodside A simultaneously
CN101812098B (en) Method for extracting monotropein monomers from medicinal indianmulberry root
CN105440092B (en) The fast preparation method of flavonoid glycoside in a kind of Extracted From Oil-tea-cake
CN1307191C (en) Process for preparing jasminodin and genipin-1-beta-D-gentiobioside with cape jasmine fruit
CN103739586A (en) Method for extracting diterpenoid compounds from Blumea aromatic DC.
CN109879919B (en) Method for separating and preparing three flavonoid glycosides from spina date seeds
CN1966511A (en) Swertiamarin monomer separation and purification method
CN1289470C (en) Process for rapid preparation of high pure pharmaceutical matters from patrinia villosa juss
CN105017273A (en) Method for extracting, separating and purifying psoralen and isopsoralen from fructus psoraleae
CN1307193C (en) Process of preparing total iridoid glycoside with cape jasmine fruit
CN101220066B (en) Separation purification process of monomeric compound in whitethorn leaf
CN114790222B (en) Flavonoids based on epimedium and preparation method thereof
CN113354697B (en) Method for separating and purifying pectolinarin and linarin
CN105131007A (en) Method for extracting, separating and purifying imperatorin and cnidium lactone from fructus cnidii
CN101891729B (en) Method for extracting high-purity rhamnazin from ford nervilia leaf
CN103497229B (en) Method of preparing flaccid anemone saponins W1 and W3 from rhizome of flaccid anemone
CN1869056A (en) Method of extracting and separating ginseng saponine mixture from ginseng leaf
CN104892702A (en) Method for extracting, separating and purifying two flavonoid glycosides from semen oroxyli
CN1218948C (en) Process for separating and preparing hig purity samguinarine and chelerythrine
CN106668234B (en) Rose extraction and purification process for total flavonoids
CN104496783B (en) A kind of isolation and purification method of 4 '-O-methyl Bavachalcone B monomer
CN110003293B (en) Method for extracting parasitoside from Chinese rose
LU501405B1 (en) Method for preparing acacetin-7-o-glucuronide
CN103073409A (en) Method for separating and purifying emodin in Rhizoma Polygoni Cuspidati

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C14 Grant of patent or utility model
GR01 Patent grant
C17 Cessation of patent right
CF01 Termination of patent right due to non-payment of annual fee

Granted publication date: 20070328

Termination date: 20140524