Summary of the invention
It is perfect to the purpose of this invention is to provide a kind of purifying process, quality controllable cudrania tricuspidata extract, its preparation method and application.
The inventor attempts through the exploration to various method for distilling; And to the mainly analysis and research of flavone component in the extract that meets medicinal requirements of various method for distilling acquisitions, having summed up with kaempferol-7-O-β-D-glycoside and Quercetin-7-O-β-D-glycoside is the perfect production technology of a cover of quality control index.It is evident in efficacy to utilize production technology of the present invention to obtain cudrania tricuspidata extract, and quality controllability is good, very is fit to suitability for industrialized production.
First aspect present invention discloses a kind of cudrania tricuspidata extract, and the weight ratio of the kaempferol in the extract-7-O-β-D-glycoside and Quercetin-7-O-β-D-glycoside is 1:0.6-1.1; Preferred 1:0.65-0.82 is the basis with the extract weight, and the total flavones percentage by weight is 1.5-51%; Preferred 16-51%, wherein kaempferol-7-O-β-D-glycoside percentage by weight is 0.3-20%, preferred 2-19%; Quercetin-7-O-β-D-glycoside percentage by weight is 0.2-15%, preferred 1.4-14%, and satisfactory extract obtains through preparation technology of the present invention.
7-glucose-kaempferol glycoside (populnin) is the present known unique flavonoid glycoside composition that is used for the Quality Control of Lignum Cudraniae tricuspidatae preparation, and this all has report in patent application document CN1515294 and CN1726962.Quercetin-7-O-glycoside is another flavonoid glycoside composition of Lignum Cudraniae tricuspidatae, and the inventor also obtains this material in effective ingredient separates.Retrieval finds still do not have the report that other plant contains nimbecetin-7-O-glycoside and Quercetin-70 glycoside binary simultaneously so far according to system documentation.This inventor thought to significantly improve Quality Control project specificity if can in Lignum Cudraniae tricuspidatae and preparation Quality Control thereof, detect above-mentioned binary simultaneously, and enlarged effective ingredient and control the size, help further improving the quality control system of Lignum Cudraniae tricuspidatae and preparation thereof.
The determination of total flavonoids employing is the UV method of contrast with kaempferol-7-O-β-D-glycoside in the cudrania tricuspidata extract of the present invention, and kaempferol-7-O-β-D-glycoside and Quercetin-7-O-β-D-glycoside content adopts the HPLC method to measure respectively.
Second aspect present invention discloses the method for preparing of above-mentioned cudrania tricuspidata extract, comprises the following steps:
A) Lignum Cudraniae tricuspidatae extraction process: get the Lignum Cudraniae tricuspidatae medical material, with 5-10 times of 0%-70% alcohol-water solution to initial medical material weight, reflux, extract, 2-4 time, each 1-5 hours, merge extractive liquid, was evaporated to relative density 1.06-1.07 (70 ℃ ± 10);
B) Lignum Cudraniae tricuspidatae purifying process: the extraction concentrated solution that step a is made; Cross one polyamide is housed chromatographic column, through 3-6 times to the water washing of column volume amount, with 1-4 times of 20-50% ethanol gradient elutions to the column volume amount; (having chosen 20%, 30%, 40% and 50% Concentraton gradient among the embodiment) collected 30-50% ethanol stream part; Concentrating under reduced pressure, vacuum drying obtains extract powder.
Alcohol in the above-mentioned alcohol-water solution is selected from lower aliphatic alcohols, like methanol, ethanol, propanol etc.
Preferable, preferred 40-80 orders of polyamide.The weight of the polyamide of adorning is 1/3-1/8 of initial medical material weight in the chromatographic column.
Improved, after above-mentioned steps b obtains polyamide chromatographic column 30-50% ethanol stream part concentrated solution, after one gel is housed chromatographic column; 50% washing with alcohol through 4-8 column volume amounts; 95% ethanol elution of reuse 4-8 column volume amounts is collected 95% ethanol stream part, concentrating under reduced pressure; Vacuum drying obtains extract powder.
Preferable, above-mentioned gel is a glucose gel, preferred hydroxypropyl glucose gel.The weight of the gel of adorning is that the upper prop concentrated solution is always measured (being dry weight) 10-50 times admittedly in the chromatographic column.
Further improved, before abovementioned steps b, the extraction concentrated solution that earlier step a is made cross one macroporous resin is housed chromatographic column; Through 3-6 times to the water washing of resin bed volume; With 2-4 times of 20-80% alcoholic solution gradient elutions (having chosen 20%, 40%, 60% and 80% Concentraton gradient among the embodiment), collect 40-60% ethanol stream part, concentrating under reduced pressure to the resin bed volume; Obtain concentrated solution; With polyamide chromatographic column on the concentrated solution, carry out purification by abovementioned steps b or improvement project again, finally obtain extract powder.
Preferable, macroporous resin hangs down polarity in being, and the weight of the macroporous resin of adorning is 1/2-1/4 of initial medical material weight in the chromatographic column.
Among the present invention, the concentration of various alcohol is percent by volume.
Research shows that the extract that above-mentioned three kinds of technologies obtain all can reach the technical specification of aforementioned kaempferol-7-O-β-D-glycoside and Quercetin-7-O-β-D-glycoside.
The third aspect of the invention openly is used to prepare the antitumor pharmaceutical formulation with above-mentioned cudrania tricuspidata extract.Said pharmaceutical formulation comprises dosage forms such as granule, tablet, capsule, dry syrup or freeze-dried powder.
Fourth aspect present invention discloses a kind of pharmaceutical composition, is made up of the above-mentioned cudrania tricuspidata extract and the pharmaceutic adjuvant of treatment effective dose, and the weight ratio of cudrania tricuspidata extract and pharmaceutic adjuvant is 3-8:7-2.
Pharmaceutic adjuvant according to the invention is preparation solid preparation adjuvant commonly used, as: starch, dextrin, lactose, microcrystalline Cellulose, low-substituted hydroxypropyl cellulose, sucrose, sorbitol, mannitol, glycine, carboxymethyl starch sodium, magnesium stearate, Pulvis Talci, soluble starch, maltodextrin, micropowder silica gel and correctives etc.
Adopt Lignum Cudraniae tricuspidatae extraction process purifying process of the present invention perfect, technic index is sound, cudrania tricuspidata extract of the present invention and all kinds of preparation thereof, and active component is controlled, and antitumous effect is remarkable, has wide market application prospect.
The specific embodiment
Further set forth the present invention below in conjunction with embodiment.Should be understood that these embodiment only are used to explain the present invention, and unrestricted scope of the present invention.
Each assay method of the present invention is following:
Determination of total flavonoids:
With kaempferol-7-O-β-D-glycoside is contrast, adopts the UV standard measure to measure, and step is following:
(1) configuration kaempferol-7-O-β-D-glycoside reference substance solution;
(2) preparation standard curve;
(3) supply the test agent formulations prepared from solutions: precision takes by weighing or measures an amount of Lignum Cudraniae tricuspidatae powder or extract or preparation, processes sample through conventional extraction or dissolution process;
(4) algoscopy: add AlCl at sample solution
3And before and after the liquor kalii acetici, use the trap of spectrophotometric determination 408nm wavelength respectively, and with the weight that the difference of both traps is read kaempferol the need testing solution-70-β-D-glycoside from standard curve, calculate, promptly get.
Quercetin-7-O-β-D-glycoside assay:
Adopt the HPLC method to measure, operating procedure is carried out according to HPLC (appendix VID of Chinese Pharmacopoeia version in 2005):
(1) chromatographic condition and system suitability test: filler closes silica gel for the octadecylsilane base; Mobile phase is that volume ratio is methanol-water solution or the aqueous acetic acid of methanol-percent by volume 0.3% or the trifluoroacetic acid aqueous solution of methanol-percent by volume 0.1% of 38:62; The detection wavelength is 257nm; Number of theoretical plate is pressed Quercetin-7-O-β-D-glycoside and is calculated, and should be not less than 1000;
(2) configuration Quercetin 7-O-β-D-glycoside reference substance solution;
(3) supply the test agent formulations prepared from solutions: precision takes by weighing or measures an amount of Lignum Cudraniae tricuspidatae powder or extract or preparation, extracts or dissolution process through conventional, uses the macroporous resin column purification process earlier, obtains through filtering with microporous membrane again;
(4) algoscopy: precision is accurate respectively draws reference substance solution and supplies test agent solution 5-15 μ l, and the injection chromatograph of liquid is measured, and promptly gets.
Kaempferol-7-O-β-D-glycoside assay:
Adopt the HPLC method to measure, operating procedure is carried out according to HPLC (appendix VID of Chinese Pharmacopoeia version in 2005):
(1) chromatographic condition and system suitability test: filler closes silica gel for the octadecylsilane base, and mobile phase is methanol-water solution or the aqueous acetic acid of methanol-0.3% or the trifluoroacetic acid aqueous solution of methanol-0.1% of volume ratio 44:56; The detection wavelength is 265nm, and number of theoretical plate is pressed kaempferol-7-O-β-D-glycoside and calculated, and should be not less than 1000;
(2) configuration kaempferol-7-O-β-D-glycoside reference substance solution;
(3) supply the test agent preparation: precision takes by weighing or measures an amount of Lignum Cudraniae tricuspidatae powder or extract or preparation, extracts or dissolution process through conventional, uses the macroporous resin column purification process earlier, obtains through filtering with microporous membrane again;
(4) algoscopy: accurate respectively reference substance solution and the confession test agent solution 5-15 μ l of drawing, inject chromatograph of liquid, measure, promptly get.
Quercetin in embodiment 1 Lignum Cudraniae tricuspidatae-7-O-β-D-glycoside
With the separating and differentiate of kaempferol-7-O-β-D-glycoside
The Lignum Cudraniae tricuspidatae of water or rare alcohol extraction of learning from else's experience extracts concentrated solution; Directly cross the macroporous resin column of a water processing, after the abundant eluting of water is clean, with 30%~95% alcoholic solution gradient elution; To 30%~50% ethanol stream part part of collecting; After concentrating, a last silicagel column is with ethyl acetate-methanol (0~30% methanol) gradient elution; Eluent is a detection means with the TLC method; The unfolding condition that silica gel tlc detects: ethyl acetate-acetone-formic acid-water (5:3:0.5:0.5), color condition: spray AlCl3 ethanol liquid, thin plate volatilizes the back and desires separated component whether on the position identical with Quercetin-7-O-β-D glycoside or kaempferol-7-O-β-D-glycoside contrast chromatograph inspecting under the 365nm fluorescent; Showing has identical yellow-green fluorescence speckle, has and then confirms as the stream part that contains Quercetin-70-β-D-glycoside or kaempferol-7-O-β-D-glycoside.
Merge the stream part that contains kaempferol 7-O-β-D-glycoside and Quercetin-7-O-β-D-glycoside respectively; After the stream part of being rich in kaempferol-7-O-β D glycoside and Quercetin-7-O-β-D-glycoside concentrates respectively; Make eluent with methanol; Repeatedly cross gel column and separate, collect the isolating kaempferol of desire-7-O-β-D-glycoside and Quercetin 7-O-β D glycoside.The kaempferol that obtains-7-O-β D glycoside and Quercetin-7-O-β D glycoside bullion prepare liquid phase through anti-phase respectively and are further purified and separate, and refining back two reference substance purity reaches 98% (HPLC normalization method).
Kaempferol-7-O-β-D-glycoside and Quercetin-7-O-β-D-glycoside chemical constitution is confirmed through UV, EI-MS, ESI-MS, H-NMR and C-NMR spectrum analysis research.
Identify: separated kaempferol-7-O-β-D-glycoside: pale yellow powder (MeOH), mp.259~261 ℃ (not proofreading and correct), uv absorption λ
Max(MeOH): 252,265 and 369nm.Mass spectrum: EIM/Z286 (strong peak, glycoside unit quasi-molecular ions), 448 (faint, molecular ion peaks), ESI (M-1)/Z447.2 (highest peak), (M+1)/and Z449.0 (highest peak), theoretical molecular 448.37.Nuclear magnetic resonance, NMR: 1H-NMR (DMSO-d6) δ (ppm): 5.11 (1H, protons on the glycoside key), 6.38 (1H, d, C6-H), 6.77 (1H; D, C8-H), 6.90 (2H, d, C3 '-H; C5 '-H), 8.04 (2H, d, C2 '-H, C6 ' H), 9.53 (1H; C3-OH), 10.13 (1H, C4 '-OH), 12.45 (1H, C5-OH); 13C-NMR (DMSO-d6) δ (ppm) data are seen table 1.Uv absorption, mass spectrum and hydrogen, nuclear magnetic resonance of carbon data and kaempferol-7-O-β-D-glycoside literature value (Zhang Yuehua; Ren Wanwei; Wan Shuwen etc. Lignum Cudraniae tricuspidatae chemical constitution study [J]. medical industry (3): 15,1980) all corresponding coincideing, the wherein data and the consistent (K.R.Markham of literature value height of carbon spectrum; B.Ternal; R.Stanley, H.Geiger and T.J.Mabry CARBON-13NMRSTUDIES OF FLAVONOIDS-III [J] .Tetrahedron.1978,34:1389-1397).
Separated Quercetin-7-O-β-D-glycoside: pale yellow powder (MeOH), mp.219 ~ 223 ℃ (not proofreading and correct), uv absorption λ
Max(MeOH): 208,257 and 375nm.Mass spectrum: ESI (M-1)/Z463.24 (highest peak), theoretical molecular 464.37.Nuclear magnetic resonance, NMR: 1H-NMR (DMSO-d6) δ (ppm): 5.15 (1H, d, protons on the glycoside key), 6.41 (1H, d, C6-H), 6.76 (1H; D, C8-H), 6.91 (1H, d, C5 '-H), 7.55 (1H; Dd, C2 '-H), 7.71 (1H, d, C6 '-H), 9.10 (3H; M, and C3, C3 ', C4 '-OH), 12.47 (1H, s, C5-OH); 13C-NMR (DMSO-d6) δ (ppm) data are seen table 1.Mass spectrum and hydrogen, nuclear magnetic resonance of carbon data and Quercetin-7-O-β-D-glycoside literature value (Zhang Xiaofeng, Hu Bailin, Zhou Bingnan. the active substance research [J] of Tibetan medicine Heterostemonous Biebersteinia. Acta Pharmaceutica Sinica.1995,30 (3): 211-214) all corresponding coincideing.The determination data of carbon spectrum and document (K.R.Markham, B.Ternal, R.Stanley, H.Geiger and T.J.Mabry CARBON-13NMR STUDIES OF FLAVONOIDS-III [J] .Tetrahedron.1978,34:1389-1397) highly consistent.
Table 1. compound I (kaempferol-7-O-β-D-glycoside)
And II (Quercetin-7-O-β-D-glycoside)
13The chemical shift data (ppm) that C-NMR measures
Confirm that through above-mentioned test from Lignum Cudraniae tricuspidatae, separating the chemical compound that obtains is respectively kaempferol-7-O-β-D-glycoside and Quercetin 7O-β-D-glycoside, purity reaches 98%.This experiment has also been explained and contained kaempferol-7-O-β D-glycoside and Quercetin-7-O-β-D-glycoside in the Lignum Cudraniae tricuspidatae simultaneously.
The preparation of embodiment 2-5 cudrania tricuspidata extracts (crossing the polyamide chromatographic column)
Extraction process: 100kg Lignum Cudraniae tricuspidatae fritter, with 5-10 times of 0%-70% alcohol-water solution to initial medical material weight, reflux, extract, 2 times, each 1-5 hours, merge extractive liquid,, being evaporated to medicinal liquid does not have the alcohol flavor.
Purifying process: concentrated solution is crossed one polyamide (60 orders are housed; Traditional Chinese medicines group) chromatographic column, through 3-6 times to the water washing of column volume amount, with 1-4 times of 20%, 30%, 40% and 50% ethanol gradient elutions to the column volume amount; Collect 30-50% ethanol stream part; Concentrating under reduced pressure, vacuum drying obtains extract powder.
The result that the extraction process parameter is selected and obtained:
Composition one: kaempferol-7-O-β-D-glycoside;
Composition two: Quercetin-7-O-β-D-glycoside
The preparation of embodiment 6 cudrania tricuspidata extracts (crossing polyamide and gel chromatography column)
Get polyamide chromatographic column 30-50% ethanol stream part partial concentration liquid that embodiment 3 obtains, gel (Sephadex LH-20, chromatographic column Pharmacia) are housed after one; Through 50% washing with alcohol of 4-8 column volume amounts, 95% ethanol elution of reuse 4-8 column volume amounts is collected 95% ethanol stream part; Concentrating under reduced pressure, vacuum drying obtains extract powder 120g; Wherein, general flavone content 37%, kaempferol-7-O-β-D-glycoside 9%; Quercetin-7-O-β-D-glycoside 6%, the weight ratio of kaempferol-7-O-β-D-glycoside and Quercetin-7-O-β-D-glycoside is 1:0.66.
The preparation of embodiment 7 cudrania tricuspidata extracts (crossing polyamide and macroporous resin chromatographic column)
Get extracting section concentrated solution that embodiment 3 extraction processes make cross one neutral macroporous resin (HPD-100, precious grace chemical industry) be housed chromatographic column, through 3-6 times to the water washing of resin bed volume; With 2-4 times of 20%, 40%, 60% and 80% alcoholic solution gradient elutions, collect 40-60% ethanol stream part, concentrating under reduced pressure to the resin bed volume; Vacuum drying obtains extract powder 600g, wherein; General flavone content 29%; Kaempferol-7-O-β-D-glycoside 6.8%, Quercetin-7-O-β-D-glycoside 5.1%, the weight ratio of kaempferol-7-O-β-D-glycoside and Quercetin-7-O-β-D-glycoside is 1:0.75.
The preparation of embodiment 8 cudrania tricuspidata extracts (crossing polyamide, macroporous resin and gel chromatography column)
Get 30-50% ethanol stream part partial concentration liquid behind the mistakes polyamide chromatographic column that embodiment 7 obtains, cross one gel is housed chromatographic column, 50% washing with alcohol of 4-8 times of column volume amounts of warp; 95% ethanol elution of 4-8 times of column volume amounts of reuse is collected 95% ethanol stream part, concentrating under reduced pressure; Vacuum drying obtains extract powder 90g, wherein; General flavone content 51%; Kaempferol-7-O-β-D-glycoside 19%, Quercetin-7-O-β-D-glycoside 14%, the weight ratio of kaempferol-7-O-β-D-glycoside and Quercetin-7-O-β-D-glycoside is 1:0.74.
The preparation of embodiment 9 tablets
Get the dry extract (flavones content 18%) 45% that embodiment 3 makes, add microcrystalline Cellulose 35%, low-substituted hydroxypropyl cellulose 8%; Starch 8%, mixing granulation, in add micropowder silica gel, magnesium stearate each 0.5%; Tabletting, film coating 3%, above-mentioned percentage ratio is weight percentage.The heavy 0.5g of sheet, every contains flavone 40mg, kaempferol-7-O-β-D-glycoside 4.5mg wherein, Quercetin-7-O-β-D-glycoside 4.0mg.
Embodiment 10 capsular preparations
Get the extract powder (general flavone content 18%) 60% that embodiment 3 makes, dextrin 20%, starch 10% mix, and other gets 10% amount starch slurrying, is used for wet granulation, dry back filling capsule, and above-mentioned percentage ratio is weight percentage.The heavy 0.4g of grain, every contains total flavones 40mg, kaempferol-7-O-β-D-glycoside 5.0mg wherein, Quercetin-7-O-β-D-glycoside 4.0mg.
The preparation of embodiment 11 injectable powder
Get the extract powder 50g that embodiment 8 makes, add glucose 50g, with the dissolving of 1000ml aquesterilisa, sterilising filtration divides to be filled in the bottle, every bottle of 2ml, and lyophilization then, sealing promptly gets.Every bottle of powder pin contains total flavones 50mg, kaempferol-7-O-β-D-glycoside 19mg, Quercetin-7-O-β-D-glycoside 14mg.
Embodiment 12 anti-tumor activity tests (intestinal cancer)
1. receive the reagent thing: cudrania tricuspidata extract
The cudrania tricuspidata extract of sample 1: embodiment 3
The cudrania tricuspidata extract of sample 2: embodiment 6
The cudrania tricuspidata extract of sample 3: embodiment 7
The cudrania tricuspidata extract of sample 4: embodiment 8
2. tumor cell line: HCT-116 (humanized's colorectal cancer, The National Center for Drug Screening).
3. experimental technique: leech acyl rhodamine B (Sulforhodamine B, SRB) protein staining method.Be 72 hours action time.
4. experimental result: see table 1.
Table 1. Lignum Cudraniae tricuspidatae extracts the suppression ratio (%) of 1~4 couple of people HCT-116 of sample growth of tumour cell
5. experiment conclusion
The growth activity that Lignum Cudraniae tricuspidatae extracts 1~4 couple of people HCT-116 of sample intestinal cancer has the obvious suppression effect.
Embodiment 13 anti-tumor activity tests (gastric cancer)
1. receive the reagent thing: cudrania tricuspidata extract sample 1~4 (with embodiment 12)
2. tumor cell line: HGC-7901 (humanized's gastric cancer, The National Center for Drug Screening).
3. experimental technique: leech acyl rhodamine B (Sulforhodamine B, SRB) protein staining method.Be 72 hours action time.
4. experimental result: see table 2.
Table 2. Lignum Cudraniae tricuspidatae extracts the suppression ratio (%) of 1~5 couple of people HGC-7901 of sample growth of tumour cell
5. experiment conclusion: the growth activity that Lignum Cudraniae tricuspidatae extracts 1~5 couple of people HGC-7901 of sample gastric cancer has the obvious suppression effect.
Above-mentioned test shows, cudrania tricuspidata extract of the present invention and all kinds of preparation thereof, and its active component is controlled, and antitumous effect is remarkable, has wide market application prospect.
Embodiment 14 toxicologic studies
4 sample samples for embodiment 12; Carried out maximum dosage-feeding mensuration: extract is irritated stomach respectively by three dose groups at double and is given mice; Wherein the dosage of sample 2 is respectively 0.4,0.8 and 1.6g/kg, and the suitable crude drug 500g/kg of its maximum dose level is 100 times of clinical using dosage; Tangible toxicity is not also found in none death of animal as a result.