CN1395922A - Theopolyphenol composition for injection and its preparing process - Google Patents
Theopolyphenol composition for injection and its preparing process Download PDFInfo
- Publication number
- CN1395922A CN1395922A CN02137817.7A CN02137817A CN1395922A CN 1395922 A CN1395922 A CN 1395922A CN 02137817 A CN02137817 A CN 02137817A CN 1395922 A CN1395922 A CN 1395922A
- Authority
- CN
- China
- Prior art keywords
- injection
- tea polyphenols
- composition
- theopolyphenol
- cyclodextrin
- 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.)
- Granted
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 41
- 238000002347 injection Methods 0.000 title claims abstract description 33
- 239000007924 injection Substances 0.000 title claims abstract description 33
- 238000000034 method Methods 0.000 title claims description 26
- 229920000858 Cyclodextrin Polymers 0.000 claims abstract description 23
- 239000002994 raw material Substances 0.000 claims abstract description 22
- 239000007788 liquid Substances 0.000 claims abstract description 15
- -1 hydroxypropyl cyclo dextrin Chemical compound 0.000 claims abstract description 14
- HFHDHCJBZVLPGP-UHFFFAOYSA-N schardinger α-dextrin Chemical compound O1C(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(O)C2O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC2C(O)C(O)C1OC2CO HFHDHCJBZVLPGP-UHFFFAOYSA-N 0.000 claims abstract description 13
- 239000000463 material Substances 0.000 claims abstract description 10
- NZAQRZWBQUIBSF-UHFFFAOYSA-N 4-(4-sulfobutoxy)butane-1-sulfonic acid Chemical compound OS(=O)(=O)CCCCOCCCCS(O)(=O)=O NZAQRZWBQUIBSF-UHFFFAOYSA-N 0.000 claims abstract description 8
- 239000000284 extract Substances 0.000 claims abstract description 7
- 239000000843 powder Substances 0.000 claims abstract description 7
- 238000005342 ion exchange Methods 0.000 claims abstract description 5
- 150000008442 polyphenolic compounds Chemical class 0.000 claims description 80
- 235000013824 polyphenols Nutrition 0.000 claims description 80
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 48
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 38
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 claims description 38
- 238000001914 filtration Methods 0.000 claims description 37
- 239000000243 solution Substances 0.000 claims description 29
- 238000003756 stirring Methods 0.000 claims description 22
- 239000008215 water for injection Substances 0.000 claims description 21
- 230000033228 biological regulation Effects 0.000 claims description 19
- 239000011780 sodium chloride Substances 0.000 claims description 19
- 239000012141 concentrate Substances 0.000 claims description 17
- 238000002360 preparation method Methods 0.000 claims description 17
- 238000004108 freeze drying Methods 0.000 claims description 16
- 239000002671 adjuvant Substances 0.000 claims description 15
- 238000000108 ultra-filtration Methods 0.000 claims description 15
- FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 claims description 13
- 229930195725 Mannitol Natural products 0.000 claims description 13
- 239000000594 mannitol Substances 0.000 claims description 13
- 235000010355 mannitol Nutrition 0.000 claims description 13
- 230000000274 adsorptive effect Effects 0.000 claims description 11
- 229920000036 polyvinylpyrrolidone Polymers 0.000 claims description 11
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 claims description 11
- 239000011347 resin Substances 0.000 claims description 11
- 229920005989 resin Polymers 0.000 claims description 11
- 230000001954 sterilising effect Effects 0.000 claims description 11
- 238000010438 heat treatment Methods 0.000 claims description 10
- 239000000049 pigment Substances 0.000 claims description 10
- 239000001267 polyvinylpyrrolidone Substances 0.000 claims description 10
- 238000004659 sterilization and disinfection Methods 0.000 claims description 10
- 241001597008 Nomeidae Species 0.000 claims description 9
- 238000007789 sealing Methods 0.000 claims description 9
- 229920003088 hydroxypropyl methyl cellulose Polymers 0.000 claims description 8
- 235000010979 hydroxypropyl methyl cellulose Nutrition 0.000 claims description 8
- 238000001694 spray drying Methods 0.000 claims description 8
- 239000001866 hydroxypropyl methyl cellulose Substances 0.000 claims description 7
- UFVKGYZPFZQRLF-UHFFFAOYSA-N hydroxypropyl methyl cellulose Chemical compound OC1C(O)C(OC)OC(CO)C1OC1C(O)C(O)C(OC2C(C(O)C(OC3C(C(O)C(O)C(CO)O3)O)C(CO)O2)O)C(CO)O1 UFVKGYZPFZQRLF-UHFFFAOYSA-N 0.000 claims description 7
- 229920001223 polyethylene glycol Polymers 0.000 claims description 6
- 238000001291 vacuum drying Methods 0.000 claims description 6
- 239000002202 Polyethylene glycol Substances 0.000 claims description 5
- 230000009514 concussion Effects 0.000 claims description 5
- 239000000546 pharmaceutical excipient Substances 0.000 claims description 5
- 239000012047 saturated solution Substances 0.000 claims description 5
- 239000001116 FEMA 4028 Substances 0.000 claims description 4
- WHGYBXFWUBPSRW-FOUAGVGXSA-N beta-cyclodextrin Chemical compound OC[C@H]([C@H]([C@@H]([C@H]1O)O)O[C@H]2O[C@@H]([C@@H](O[C@H]3O[C@H](CO)[C@H]([C@@H]([C@H]3O)O)O[C@H]3O[C@H](CO)[C@H]([C@@H]([C@H]3O)O)O[C@H]3O[C@H](CO)[C@H]([C@@H]([C@H]3O)O)O[C@H]3O[C@H](CO)[C@H]([C@@H]([C@H]3O)O)O3)[C@H](O)[C@H]2O)CO)O[C@@H]1O[C@H]1[C@H](O)[C@@H](O)[C@@H]3O[C@@H]1CO WHGYBXFWUBPSRW-FOUAGVGXSA-N 0.000 claims description 4
- 235000011175 beta-cyclodextrine Nutrition 0.000 claims description 4
- 229960004853 betadex Drugs 0.000 claims description 4
- 235000018927 edible plant Nutrition 0.000 claims description 4
- 235000002639 sodium chloride Nutrition 0.000 claims description 4
- 239000004372 Polyvinyl alcohol Substances 0.000 claims description 3
- 238000005498 polishing Methods 0.000 claims description 3
- 229920002451 polyvinyl alcohol Polymers 0.000 claims description 3
- 235000019422 polyvinyl alcohol Nutrition 0.000 claims description 3
- 238000012545 processing Methods 0.000 claims description 3
- 239000007921 spray Substances 0.000 claims description 3
- 238000010521 absorption reaction Methods 0.000 claims description 2
- DPXJVFZANSGRMM-UHFFFAOYSA-N acetic acid;2,3,4,5,6-pentahydroxyhexanal;sodium Chemical compound [Na].CC(O)=O.OCC(O)C(O)C(O)C(O)C=O DPXJVFZANSGRMM-UHFFFAOYSA-N 0.000 claims description 2
- 239000001768 carboxy methyl cellulose Substances 0.000 claims description 2
- 229940124531 pharmaceutical excipient Drugs 0.000 claims description 2
- 235000019812 sodium carboxymethyl cellulose Nutrition 0.000 claims description 2
- 229920001027 sodium carboxymethylcellulose Polymers 0.000 claims description 2
- 241001122767 Theaceae Species 0.000 claims 10
- 238000000227 grinding Methods 0.000 claims 1
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- 229920002689 polyvinyl acetate Polymers 0.000 claims 1
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- 239000004375 Dextrin Substances 0.000 abstract description 2
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- 239000000654 additive Substances 0.000 abstract 1
- 230000000996 additive effect Effects 0.000 abstract 1
- 238000007670 refining Methods 0.000 abstract 1
- 244000269722 Thea sinensis Species 0.000 description 79
- 235000013616 tea Nutrition 0.000 description 79
- 239000012528 membrane Substances 0.000 description 19
- ADRVNXBAWSRFAJ-UHFFFAOYSA-N catechin Natural products OC1Cc2cc(O)cc(O)c2OC1c3ccc(O)c(O)c3 ADRVNXBAWSRFAJ-UHFFFAOYSA-N 0.000 description 16
- 235000005487 catechin Nutrition 0.000 description 16
- 239000012982 microporous membrane Substances 0.000 description 15
- 229950001002 cianidanol Drugs 0.000 description 14
- PFTAWBLQPZVEMU-DZGCQCFKSA-N (+)-catechin Chemical compound C1([C@H]2OC3=CC(O)=CC(O)=C3C[C@@H]2O)=CC=C(O)C(O)=C1 PFTAWBLQPZVEMU-DZGCQCFKSA-N 0.000 description 13
- 230000004927 fusion Effects 0.000 description 13
- XMOCLSLCDHWDHP-IUODEOHRSA-N epi-Gallocatechin Chemical compound C1([C@H]2OC3=CC(O)=CC(O)=C3C[C@H]2O)=CC(O)=C(O)C(O)=C1 XMOCLSLCDHWDHP-IUODEOHRSA-N 0.000 description 12
- ZEACOKJOQLAYTD-UHFFFAOYSA-N flavan-3,3',4,4',5,5',7-heptol Chemical compound OC1C(O)C2=C(O)C=C(O)C=C2OC1C1=CC(O)=C(O)C(O)=C1 ZEACOKJOQLAYTD-UHFFFAOYSA-N 0.000 description 12
- ODLHGICHYURWBS-FOSILIAISA-N molport-023-220-444 Chemical compound CC(O)COC[C@@H]([C@@H]([C@H]([C@@H]1O)O)O[C@@H]2O[C@H]([C@H](O[C@@H]3O[C@@H](COCC(C)O)[C@@H]([C@H]([C@@H]3O)O)O[C@@H]3O[C@@H](COCC(C)O)[C@@H]([C@H]([C@@H]3O)O)O[C@@H]3O[C@@H](COCC(C)O)[C@@H]([C@H]([C@@H]3O)O)O[C@@H]3O[C@@H](COCC(C)O)[C@@H]([C@H]([C@@H]3O)O)O3)[C@@H](O)[C@@H]2O)COCC(O)C)O[C@H]1O[C@@H]1[C@@H](O)[C@H](O)[C@H]3O[C@H]1COCC(C)O ODLHGICHYURWBS-FOSILIAISA-N 0.000 description 12
- WMBWREPUVVBILR-WIYYLYMNSA-N (-)-Epigallocatechin-3-o-gallate Chemical compound O([C@@H]1CC2=C(O)C=C(C=C2O[C@@H]1C=1C=C(O)C(O)=C(O)C=1)O)C(=O)C1=CC(O)=C(O)C(O)=C1 WMBWREPUVVBILR-WIYYLYMNSA-N 0.000 description 9
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 9
- WMBWREPUVVBILR-UHFFFAOYSA-N GCG Natural products C=1C(O)=C(O)C(O)=CC=1C1OC2=CC(O)=CC(O)=C2CC1OC(=O)C1=CC(O)=C(O)C(O)=C1 WMBWREPUVVBILR-UHFFFAOYSA-N 0.000 description 9
- PFTAWBLQPZVEMU-ZFWWWQNUSA-N (+)-epicatechin Natural products C1([C@@H]2OC3=CC(O)=CC(O)=C3C[C@@H]2O)=CC=C(O)C(O)=C1 PFTAWBLQPZVEMU-ZFWWWQNUSA-N 0.000 description 8
- 239000003814 drug Substances 0.000 description 8
- LPTRNLNOHUVQMS-UHFFFAOYSA-N epicatechin Natural products Cc1cc(O)cc2OC(C(O)Cc12)c1ccc(O)c(O)c1 LPTRNLNOHUVQMS-UHFFFAOYSA-N 0.000 description 8
- 235000012734 epicatechin Nutrition 0.000 description 8
- PFTAWBLQPZVEMU-UKRRQHHQSA-N (-)-epicatechin Chemical compound C1([C@H]2OC3=CC(O)=CC(O)=C3C[C@H]2O)=CC=C(O)C(O)=C1 PFTAWBLQPZVEMU-UKRRQHHQSA-N 0.000 description 6
- XMOCLSLCDHWDHP-UHFFFAOYSA-N L-Epigallocatechin Natural products OC1CC2=C(O)C=C(O)C=C2OC1C1=CC(O)=C(O)C(O)=C1 XMOCLSLCDHWDHP-UHFFFAOYSA-N 0.000 description 6
- GAMYVSCDDLXAQW-AOIWZFSPSA-N Thermopsosid Natural products O(C)c1c(O)ccc(C=2Oc3c(c(O)cc(O[C@H]4[C@H](O)[C@@H](O)[C@H](O)[C@H](CO)O4)c3)C(=O)C=2)c1 GAMYVSCDDLXAQW-AOIWZFSPSA-N 0.000 description 6
- 229930014669 anthocyanidin Natural products 0.000 description 6
- 150000001452 anthocyanidin derivatives Chemical class 0.000 description 6
- 235000008758 anthocyanidins Nutrition 0.000 description 6
- YTJJRAWFHJBAMT-UHFFFAOYSA-N depside Natural products OC(=O)CC1=C(O)C=C(O)C=C1OC(=O)C1=CC=C(O)C(O)=C1 YTJJRAWFHJBAMT-UHFFFAOYSA-N 0.000 description 6
- DZYNKLUGCOSVKS-UHFFFAOYSA-N epigallocatechin Natural products OC1Cc2cc(O)cc(O)c2OC1c3cc(O)c(O)c(O)c3 DZYNKLUGCOSVKS-UHFFFAOYSA-N 0.000 description 6
- 229930003944 flavone Natural products 0.000 description 6
- 150000002212 flavone derivatives Chemical class 0.000 description 6
- 235000011949 flavones Nutrition 0.000 description 6
- HVQAJTFOCKOKIN-UHFFFAOYSA-N flavonol Natural products O1C2=CC=CC=C2C(=O)C(O)=C1C1=CC=CC=C1 HVQAJTFOCKOKIN-UHFFFAOYSA-N 0.000 description 6
- 150000002216 flavonol derivatives Chemical class 0.000 description 6
- 235000011957 flavonols Nutrition 0.000 description 6
- 239000004615 ingredient Substances 0.000 description 6
- 239000003094 microcapsule Substances 0.000 description 6
- 230000003647 oxidation Effects 0.000 description 6
- 238000007254 oxidation reaction Methods 0.000 description 6
- 150000002989 phenols Chemical class 0.000 description 6
- VHBFFQKBGNRLFZ-UHFFFAOYSA-N vitamin p Natural products O1C2=CC=CC=C2C(=O)C=C1C1=CC=CC=C1 VHBFFQKBGNRLFZ-UHFFFAOYSA-N 0.000 description 6
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- NWUYHJFMYQTDRP-UHFFFAOYSA-N 1,2-bis(ethenyl)benzene;1-ethenyl-2-ethylbenzene;styrene Chemical compound C=CC1=CC=CC=C1.CCC1=CC=CC=C1C=C.C=CC1=CC=CC=C1C=C NWUYHJFMYQTDRP-UHFFFAOYSA-N 0.000 description 3
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- LNTHITQWFMADLM-UHFFFAOYSA-N anhydrous gallic acid Natural products OC(=O)C1=CC(O)=C(O)C(O)=C1 LNTHITQWFMADLM-UHFFFAOYSA-N 0.000 description 2
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- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 1
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- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
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Landscapes
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
A theopolyphenol injection is prepared from hydroxypropyl cyclo dextrin or sulfobutylether cyclo dextrin and theopolyphenol or theapigment through refining the theopolyphenol extract by ion exchange to obtain the raw material for injection, preparing composition for injection from the said material, the said tyclo dextrin and additive, and preparing liquid injection or powder injection.
Description
Technical field
The present invention relates to a kind of Theopolyphenol composition for injection or be called tea polyphenols and the molecular microcapsule of water soluble cyclodextrin derivant, and the preparation method of this tea polyphenols compositions (or molecular microcapsule) injection.
Background technology
Tea polyphenols (Tea polyphenol TP) is the polyphenol compound that extracts from Folium Camelliae sinensis.Be divided into four classes by its chemical constitution, comprise catechin, flavone and flavonols, leucoanthocyanidin and anthocyanidin, phenols and depside.Wherein most important composition is the multiple catechin (Catechins) of flavanol compound, accounts for 60%～80% of TP total amount.The research of tea polyphenols starts from the eighties, enters the nineties and forms climax, and is in the ascendant so far.Both at home and abroad a large amount of work has been carried out in aspects such as the mechanism of action of tea polyphenols, clinical pharmacology, effective ingredient, studies show that, 18 times of the VE of the oxidation resistance of tea polyphenols, be VC 3-10 doubly.This strong reducing power of tea polyphenols can be removed generation, the activity of lipoxygenase inhibitor and the peroxidation of lipid of free radical, blocking-up N-nitroso compound in vivo; Inhibition is because of the infringement of lipid peroxidation due to the Radical Metabolism disorder of in-vivo tissue week; Improve the activity of enzymes such as SOD; Can also prevent and suppress to poison cell and wash infection effect that cell sees and mutation-resisting functional etc., making it embody superior therapeutic efficiency preventing and treating all many-sides such as cardiovascular disease, defying age, cancer-resisting, antiinflammatory be antibacterial, is the medicine that the utmost point has clinical future.Shortcomings such as but it is bigger than normal that the tea polyphenols clinical oral administration exists dosage, easily decomposed by gastrointestinal tract, and bioavailability is lower, and experiment in vitro result and interior curative effect gap are bigger.Intramuscular administration has the bioavailability of improving active component, avoids the degraded of the intestines and stomach environment to effective ingredient, can significantly improve the curative effect of medicine.But because the strong reducing property of tea polyphenols, extremely unstable, easy oxidation discoloration in environment such as soda acid, air.The water at normal temperature dissolubility is less etc.Everything causes adopting product clarity and less stable in preparation or short-term put procedure of common process and prescription, and injection type adopts common process and the no feasibility of prescription.This ingredient stability has become pharmaceutical preparation, and especially the major obstacle of liquid preparation exploitation listing has seriously restricted the performance and the industrialization development of tea polyphenols clinical efficacy.
Summary of the invention
The water-soluble composition that the purpose of this invention is to provide a kind of tea polyphenols, said composition should solve the problem of the unstable easy oxidation discoloration of TP, solves simultaneously to strengthen its water miscible problem.The effective ingredient of tea polyphenols should be very stable in this compositions, and easily dissolving, so that on this basis, and the tea polyphenols injection of preparation liquid drugs injection or powder aciculiform formula.The present invention also will provide this preparation of compositions method.The present invention is applicable to from green tea and extracts, content is 50～99% all kinds of tea polyphenols extracts; Each component in the tea polyphenols, " tea polyphenols component " is meant: catechin (+C), epicatechin (EC), epigallo catechin (EGC), Galla Turcica (Galla Helepensis) acyl epicatechin (ECG), the plain constituents of the main youngster bitter edible plant such as epigallocatechin gallate (EGCG) (EGCG), the oxidation product tea pigment of tea polyphenols etc.; The mixture of tea polyphenols and tea pigment (following general designation or abbreviation " tea polyphenols ").
The technical scheme that realizes above-mentioned purpose is: Theopolyphenol composition for injection is characterized in that: include the derivant of tea polyphenols or its component or tea pigment and water soluble Beta-cyclodextrin, and, mol ratio is 1: 0.5～10.Recommending mol ratio is 1: 1～5.In this compositions, the cavity-like structure of the derivant of new type water-solubility cyclodextrin and tea polyphenols form molecular microcapsule, and the tea polyphenols molecule is isolated, and play stable, promotion dissolution, thereby increase the clarity of its solution.Make after the compositions, also can alleviate the stimulation of medicine, and improve bioavailability of medicament body.Here said tea polyphenols comprises: extraction, content are 50～99% all kinds of tea polyphenols extracts from green tea; Each component in the tea polyphenols, " tea polyphenols component " is meant: catechin (+C), epicatechin (EC), epigallo catechin (EGC), Galla Turcica (Galla Helepensis) acyl epicatechin (ECG), epigallocatechin gallate (EGCG) main catechin compositions such as (EGCG), the oxidation product tea pigment of tea polyphenols etc.; The mixture of tea polyphenols and tea pigment.The derivant of the water soluble Beta-cyclodextrin here can be hydroxypropyl cyclodextrin (HP-β-CD) or sulfobutyl ether cyclodextrin (SBE-β-CD).From microcosmic, also this compositions can be regarded as a kind of tea polyphenols molecular microcapsule, the molecule of tea polyphenols is formed molecular microcapsule by the cavity-like molecule of water soluble cyclodextrin derivant parcel, and the tea polyphenols molecule is played a protective role.Can include the molecule, the microcapsule that both molecule forms of derivant of molecule, the new type water-solubility cyclodextrin of tea polyphenols or its component or tea pigment in the composition of this compositions, and above each mixture of ingredients.
The technology of preparation said composition may further comprise the steps:
1, the tea polyphenols extract is dissolved in an amount of ethanol or the water for injection,
2, adopt ion exchange, absorption, ultrafiltration, method such as concentrate to be refined into the pin material liquid; Or
Do or lyophilizing is refined into satisfactory pin raw material through spraying,
3, with the tea polyphenols pin with raw material or tea polyphenols pin with material liquid and hydroxypropyl cyclodextrin or sulfobutyl ether ring
Dextrin also adds proper pharmaceutical excipients, by saturated solution method, stirs or ultrasonic or concussion or adopt and grind
Processing such as mill method, spray drying or lyophilization prepare composition for injection,
4, content preparation in accordance with regulations is standby by filtering,
5, behind the fill sealing by fusing, aqueous injection is made in sterilization; Perhaps, after aseptic filtration, fill is frozen
Do or spray and do, make injectable powder.
When preparation aqueous injection or injectable powder, the adjuvant that aforesaid liquid is added can be one or more in the following composition: tween 80, sodium carboxymethyl cellulose, polyvinylpyrrolidone (PVP), Polyethylene Glycol (PEG), polyvinyl alcohol (PVA), sodium chloride, hydroxypropyl methylcellulose (HPMC), mannitol, lactose.
The prioritization scheme of said method has:
When tea polyphenols is dissolved into 50～70% ethanol in the first step, can little heating and stirring.
Adopt in second step that macroporous adsorptive resins separates, to filter, be evaporated to proportion be 1.02～1.04 pin material liquid to ultrafilter membrane (5K).
Adopt tea polyphenols in the third step: hydroxypropyl cyclodextrin or sulfobutyl ether cyclodextrin mol ratio are 1: 1, or with the tea polyphenols pin with material liquid and weight ratio be 1: 3.5; Pharmaceutic adjuvant is recommended to use polyvinylpyrrolidone, sodium chloride, mannitol; Technology recommend with saturated solution method (time of two kinds of mixed stirrings of solution or concussion, recommend 0～70 ℃ 1～3 hour, 0～70 ℃ is ultrasonic 60～90 minutes.), polishing (adopting the operation of colloid mill or ball mill), a sublimed method is recommended in spray drying or lyophilization: pre-freeze-34～-38 ° ,-38 ° to-17 ℃ intensification vacuum dryings are 14～20 hours in the intensification dry run, at 10 to 15 ℃ of vacuum dryings 8～10 hours again.The intensification lyophilization, vacuum＞0.1mmHg.
Coarse filtration in the 4th step, fine straining adopt medium size sand filtration rod, No. 4 or No. 6 incipient fusion filters, 0.8um microporous filter membrane.
Sterilization is 100 ℃ of flowing steam sterilizations 30 minutes in the 5th step.
The water-soluble composition of tea polyphenols of the present invention, utilize physics, chemical method impels catechin molecule and cyclodextrin derivative to form super molecule inclusion compound, the molecule of catechin or its group enter in the ring cavity of water soluble cyclodextrin derivant, and by various chemical bonds formation supermolecules, catechin stability is obviously strengthened, because it is hydrophobic in the cyclodextrin derivative, outer hydrophilic characteristics as a result, the water solublity of supermolecule is significantly improved, and this programme has solved the problem of the unstable easy oxidation discoloration of TP simultaneously, strengthen its water miscible problem, alleviate medicine to the problem of body stimulation and the problem that improves bioavailability of medicament.In compositions of the present invention, the effective ingredient of tea polyphenols is very stable, and easily dissolving, and the tea polyphenols injection of Zhi Bei liquid drugs injection or powder aciculiform formula uses very convenient on this basis.Preparation method of composition provided by the invention has been finished the design of the production technology of this new product, and is simple and practical, is easy to promote.
The specific embodiment
Embodiment 1 prescription tea polyphenols 20gHP
2-β-CD 80g sodium chloride 4.3g water for injection adds to 1000ml
Get tea polyphenol raw materials (comprising catechin, flavone and flavonols, leucoanthocyanidin and anthocyanidin, phenols and depside), 70% alcohol dissolving is filtered, and concentrates, add in 10 liters of pure water, stir, filter, by macroporous adsorptive resins, PH4.8 acetate solution eluting, filtering with microporous membrane, 50 ℃ are evaporated to proportion 1.03, add 20% (w/v) HP-b-CD solution and other adjuvant, and 60 ℃ were stirred 1 hour, 10～20 ℃ are stirred after 3 hours content dosing in accordance with regulations, G
3Number incipient fusion filter bulb coarse filtration, 0.8um microporous filter membrane fine straining.The fill sealing by fusing.100 ℃ of flowing steam sterilizations 30 minutes promptly.
Embodiment 2 prescription tea polyphenols 20gHP
2-β-CD 80g polyvinylpyrrolidone (PVP), 5.7g sodium chloride 4.3g water for injection adds to 1000ml
Get tea polyphenol raw materials, 70% dissolve with ethanol filters, concentrate, add in 10 liters of pure water, stir, filter, by macroporous adsorptive resins, PH4.8 acetate solution eluting, filtering with microporous membrane, the 10K ultrafiltration membrance filter, 50 ℃ are evaporated to proportion 1.03, add 20% (w/v) HP-b-CD solution and polyvinylpyrrolidone (PVP), 60 ℃ were stirred 1 hour, and 10～20 ℃ were stirred after 3 hours, content dosing in accordance with regulations, G
3Number incipient fusion filter bulb coarse filtration, 0.8um microporous filter membrane fine straining.The fill sealing by fusing.100 ℃ of flowing steam sterilizations 30 minutes promptly.
Embodiment 3 prescription tea polyphenols 20gHP
2-β-CD 80g sodium chloride 4.3g mannitol 3.9g water for injection adds to 1000ml
Get tea polyphenol raw materials, 70% dissolve with ethanol filters, concentrate, add in 10 liters of pure water, stir, filter, by macroporous adsorptive resins, PH4.8 acetate solution eluting, filtering with microporous membrane, the 10K ultrafiltration membrance filter, 50 ℃ are evaporated to proportion 1.03, add 20% (w/v) HP-b-CD solution and other adjuvant, 60 ℃ were stirred 1 hour, and 10-20 ℃ was stirred after 3 hours, content dosing in accordance with regulations, G
3Number incipient fusion filter bulb coarse filtration, 0.8um microporous filter membrane fine straining.Fill, fill.Lyophilization 28 hours, tamponade is sealed promptly.
Embodiment 4 prescription tea polyphenols 14gSBE
7-β-CD 100g mannitol 3.6g water for injection adds to 1000ml
Get tea polyphenol raw materials, 30% alcohol dissolving is filtered, concentrate, add in 8 liters of pure water, stir, filter, by cation exchange resin column, the 0.8um filtering with microporous membrane, the 10K ultrafiltration membrance filter, 50 ℃ are evaporated to proportion 1.03, add 20% (w/v) SBE-b-CD solution, 60-80 ℃ of ultrasonic place 0.5 hour, 10-20 ℃ of supersound process added mannitol after 2 hours, content dosing in accordance with regulations, G
6Number incipient fusion filter bulb coarse filtration, 0.8um microporous filter membrane fine straining.Fill.Lyophilization, tamponade is sealed promptly.
Embodiment 5 prescription tea polyphenols 20gHP
2-β-CD 120g hydroxypropyl methylcellulose HPMCk15 6g sodium chloride 4.3g water for injection adds to 1000ml
Get tea polyphenol raw materials, 70% dissolve with ethanol filters, and concentrates, and adds in 10 liters of pure water, stirs, filter, and by macroporous adsorptive resins, PH4.8 acetate solution eluting, 0.8um filtering with microporous membrane, 5K ultrafiltration membrance filter, spray drying.
Get HP
2-β-CD adds 5 times of water gagings, and put in the colloid mill, and add tea polyphenols and other adjuvant, the mixing of fully milling, machine intimate residual fraction water repeatedly cleans on a small quantity, and washing liquid is incorporated pastel into, and decompress filter gets white powder body.With water for injection in accordance with regulations after the dosing, G
6Number sintered glass filter-bulb aseptic filtration, 0.8um microporous filter membrane fine straining.Fill.Lyophilization 28 hours, tamponade is sealed promptly.
Embodiment 6 prescription tea polyphenols 20gSBE
7-β-CD 150gPVP
K305g sodium chloride 4.3g tween 80 1.5 waters for injection add to 1000ml
Get tea polyphenol raw materials, 70% alcohol dissolving is filtered, and concentrates, add in 15 liters of pure water, stir, filter, pass through macroporous adsorptive resins, PH5.4 acetate buffer solution eluting, the 0.8um filtering with microporous membrane, the 10K ultrafiltration membrance filter, 50 ℃ are evaporated to proportion 1.02 (50 ℃).Add 30% (w/v) SBE-b-CD solution and PVP
K30, 60 ℃ jolt 25min, stop heating, continue to jolt to room temperature, 10-20 ℃ jolt 4 hours after, add other adjuvant, with water for injection in accordance with regulations after the dosing, G
3Number sintered glass filter-bulb coarse filtration, 0.8um microporous filter membrane fine straining.The fill sealing by fusing.Pressure sterilizing 90-115 ℃, 6.86 * 10
4P, 30 minutes, promptly.
Embodiment 7 prescription tea polyphenols 20gHP
2-β-CD 120g hydroxypropyl methylcellulose HPMCk4m 6.4g lactose 9.2g sodium chloride 3.5g water for injection adds to 1000ml
Get tea polyphenol raw materials, 70% dissolve with ethanol filters, concentrate, and by silica gel column chromatography, PH4.8 acetate solution-30% ethanol elution, eluent 0.8um filtering with microporous membrane,, 50 ℃ are evaporated to proportion 1.02 (50 ℃).Add 30% (w/v) HP-b-CD solution and other adjuvant, 60 ℃ were stirred after 1 hour, and heat treatment 15min (115 ℃, 6.86 * 10
4P), stop heating, continue to be stirred to room temperature, 10-20 ℃ was stirred after 4 hours, with water for injection in accordance with regulations after the dosing, and G
6Number sintered glass filter-bulb coarse filtration, 0.8um microporous filter membrane fine straining.The 5K ultrafiltration membrance filter, fill.Lyophilization 28 hours, tamponade is sealed promptly.
Embodiment 8 prescription tea polyphenols tea pigment mixture 20gHP
2-β-CD 120g hydroxypropyl methylcellulose HPMCk4m 6.4g sodium chloride 3.5g water for injection adds to 1000ml
Get raw material, 70% dissolve with ethanol filters, concentrate, and by ion exchange column, eluent 0.8um filtering with microporous membrane, 50 ℃ are evaporated to proportion 1.02 (50 ℃).Add 30% (w/v) HP-b-CD solution and other adjuvant, 60 ℃ were stirred after 1 hour, and heat treatment 15min (115 ℃, 6.86 * 10
4P), stop heating, continue to be stirred to room temperature, 10-20 ℃ was stirred after 4 hours, with water for injection in accordance with regulations after the dosing, and G
6Number sintered glass filter-bulb coarse filtration, 0.8um microporous filter membrane fine straining.The 5K ultrafiltration membrance filter, spray drying, packing, tamponade is sealed promptly.
Embodiment 9 prescription tea pigment mixture 33gHP
2-β-CD 80gSBE
7-β-CD 100g hydroxypropyl methylcellulose HPMCk4m 6.4g sodium chloride 3.5g water for injection adds to 1000ml
Get raw material, 70% dissolve with ethanol filters, concentrate, and by ion exchange column, eluent 0.8um filtering with microporous membrane, 50 ℃ are evaporated to proportion 1.02 (50 ℃).Add 30% (w/v) HP-b-CD solution and other adjuvant, 60 ℃ were stirred after 1 hour, and heat treatment 15min (115 ℃, 6.86 * 10
4P), stop heating, continue to be stirred to room temperature, 10-20 ℃ was stirred after 4 hours, with water for injection in accordance with regulations after the dosing, and G
6Number sintered glass filter-bulb coarse filtration, 0.8um microporous filter membrane fine straining.The 5K ultrafiltration membrance filter, spray drying, packing, tamponade is sealed promptly.
Embodiment 10 prescription tea polyphenols 20gHP
2-β-CD 80g sodium chloride 4.3g water for injection adds to 1000ml
Get tea polyphenol raw materials (comprising catechin, flavone and flavonols, leucoanthocyanidin and anthocyanidin, phenols and depside), 70% dissolve with ethanol filters, and concentrates, add in 10 liters of pure water, stir, filter, by macroporous adsorptive resins, PH4.8 acetate solution eluting, filtering with microporous membrane, 50 ℃ are evaporated to proportion 1.03, add 20% (w/v) HP-b-CD solution and other adjuvant, and 60 ℃ were stirred 1 hour, 10-20 ℃ is stirred after 3 hours content dosing in accordance with regulations, G
3Number incipient fusion filter bulb coarse filtration, 0.8um microporous filter membrane fine straining.The fill sealing by fusing.100 ℃ of flowing steam sterilizations 30 minutes promptly.
Embodiment 11 prescription tea polyphenols 20gSBE-β-CD 100g sodium chloride 4.3g waters for injection add to 1000ml
Get tea polyphenol raw materials (comprising catechin, flavone and flavonols, leucoanthocyanidin and anthocyanidin, phenols and depside), 70% alcohol dissolving is filtered, and concentrates, add in 10 liters of pure water, stir, filter, by macroporous adsorptive resins, PH4.8 acetate solution eluting, filtering with microporous membrane, 50 ℃ are evaporated to proportion 1.03, add 20% (w/v) HP-b-CD solution and other adjuvant, and 60 ℃ were stirred 1 hour, 10-20 ℃ is stirred after 3 hours content dosing in accordance with regulations, G
3Number incipient fusion filter bulb coarse filtration, 0.8um microporous filter membrane fine straining.The fill sealing by fusing.100 ℃ of flowing steam sterilizations 30 minutes promptly.
Embodiment 12 prescription tea polyphenols 20gHP
2-β-CD 80g sodium chloride 4.3g water for injection adds to 1000ml
Get tea polyphenol raw materials (comprising youngster bitter edible plant element, flavone and flavonols, leucoanthocyanidin and anthocyanidin, phenols and depside), 70% dissolve with ethanol filters, and concentrates, add in 10 liters of pure water, stir, filter, by macroporous adsorptive resins, PH4.8 acetate solution eluting, filtering with microporous membrane, 50 ℃ are evaporated to proportion 1.03, add 20% (w/v) HP-b-CD solution and other adjuvant, and 60 ℃ were stirred 1 hour, 10-20 ℃ is stirred after 3 hours content dosing in accordance with regulations, G
3Number incipient fusion filter bulb coarse filtration, 0.8um microporous filter membrane fine straining.The fill sealing by fusing.100 ℃ of flowing steam sterilizations 30 minutes promptly.
Embodiment 13 prescription tea polyphenols 20gSBE-β-CD 100g Polyethylene Glycol (PEG) 3.9g sodium chloride 4.3g waters for injection add to 1000ml
Get tea polyphenol raw materials (comprising catechin, flavone and flavonols, leucoanthocyanidin and anthocyanidin, phenols and depside), 70% dissolve with ethanol filters, and concentrates, add in 10 liters of pure water, stir, filter, by macroporous adsorptive resins, PH4.8 acetate solution eluting, filtering with microporous membrane, 50 ℃ are evaporated to proportion 1.03, add 20% (w/v) HP-b-CD solution and other adjuvant, and 60 ℃ were stirred 1 hour, 10-20 ℃ is stirred after 3 hours content dosing in accordance with regulations, G
3Number incipient fusion filter bulb coarse filtration, 0.8um microporous filter membrane fine straining.The fill sealing by fusing.100 ℃ of flowing steam sterilizations 30 minutes promptly.
Embodiment 14 prescription tea polyphenols, tea pigment mixture 14gSBE
7-β-CD 100g mannitol 3.6g water for injection adds to 1000ml
Get tea polyphenol raw materials, 30% alcohol dissolving is filtered, concentrate, add in 8 liters of pure water, stir, filter, by cation exchange resin column, the 0.8um filtering with microporous membrane, the 10K ultrafiltration membrance filter, 50 ℃ are evaporated to proportion 1.03, add 20% (w/v) SBE-b-CD solution, 60-80 ℃ of supersound process 0.5 hour, 10-20 ℃ of supersound process added mannitol after 2 hours, content dosing in accordance with regulations, G
6Number incipient fusion filter bulb coarse filtration, 0.8um microporous filter membrane fine straining.Fill.Lyophilization, tamponade is sealed promptly.
Embodiment 15 prescription table nutgall catechin gallic acid ester (EGCG) 0.2gHP
2-β-CD 80g sodium chloride 4.3g mannitol 3.9g water for injection adds to 1000ml
Get raw material, dissolve with ethanol adds in the pure water, stirs, and filters, and adds 20% (w/v) HP-b-CD solution and other adjuvant, and 60 ℃ were stirred 1 hour, and 10-20 ℃ is stirred after 3 hours content dosing in accordance with regulations, G
3Number incipient fusion filter bulb coarse filtration, 0.8um microporous filter membrane fine straining.The 10K ultrafiltration membrance filter, fill.Lyophilization 28 hours, tamponade is sealed promptly.
Embodiment 16 prescription table catechins (EC), epigallo catechin (EGC), Galla Turcica (Galla Helepensis) acyl epicatechin (ECG), the plain epicatechol gallate 5 kinds of main catechin mixture 0.2gHP such as (EGCG) of the epigallocatechin gallate bitter edible plant
2-β-CD 80g sodium chloride 4.3g mannitol 3.9g water for injection adds to 1000ml
Get raw material, 70% dissolve with ethanol adds in the pure water, stirs, and adds 20% (w/v) HP-b-CD solution and other adjuvant, and 60 ℃ were stirred 1 hour, and 10-20 ℃ is stirred after 3 hours content dosing in accordance with regulations, G
3Number incipient fusion filter bulb coarse filtration, 0.8um microporous filter membrane fine straining.The 10K ultrafiltration membrance filter, fill.Lyophilization 28 hours, tamponade is sealed promptly.
Embodiment 17 prescription tea polyphenols 14gSBE
7-β-CD 60gHP
2-β-CD 50g mannitol 3.6g water for injection adds to 1000ml
Get tea polyphenol raw materials, 30% alcohol dissolving is filtered, concentrate, add in 8 liters of pure water, stir, filter, by cation exchange resin column, the 0.8um filtering with microporous membrane, the 10K ultrafiltration membrance filter, 50 ℃ are evaporated to proportion 1.03, add 20% (w/v) SBE-b-CD solution, 60-80 ℃ of supersound process 0.5 hour, 10-20 ℃ of supersound process added mannitol after 2 hours, content dosing in accordance with regulations, G
6Number incipient fusion filter bulb coarse filtration, 0.8um microporous filter membrane fine straining.Fill.Lyophilization, tamponade is sealed promptly.
Claims (10)
1, a kind of injection bitter edible plant polyphenol compositions is characterized in that: include the derivant of tea polyphenols or its component or tea pigment and water soluble Beta-cyclodextrin, mol ratio is 1: 0.5～10.
2, according to the described Theopolyphenol composition for injection of claim 1, it is characterized in that: the derivant of said water soluble Beta-cyclodextrin is hydroxypropyl cyclodextrin or sulfobutyl ether cyclodextrin.
3, according to claim 1 or 2 described Theopolyphenol composition for injection, it is characterized in that: the mol ratio of two components is 1: 1～5.
4, according to the described Theopolyphenol composition for injection of claim 3, it is characterized in that: the mol ratio of two components is 1: 1.
5, the preparation method of the described Theopolyphenol composition for injection of one of a kind of claim 1～3 may further comprise the steps:
The tea polyphenols extract is dissolved in an amount of ethanol or the water for injection,
Method is refined into the pin material liquid to adopt ion exchange, absorption, ultrafiltration, concentrate etc.; Or through spray
Dried or lyophilizing is refined into satisfactory pin raw material,
Use material liquid and hydroxypropyl cyclodextrin or sulfobutyl ether ring to stick with paste with raw material or tea polyphenols pin on the tea polyphenols pin
Essence is also added proper pharmaceutical excipients, by saturated solution method, stirs or ultrasonic or concussion or employing grinding
Processing such as method, spray drying or lyophilization prepare composition for injection,
Content preparation in accordance with regulations, standby by filtering,
Behind the fill sealing by fusing, aqueous injection is made in sterilization; Perhaps, after aseptic filtration, fill, lyophilizing
Or spray is dried, makes injectable powder.
6, according to the preparation method of the described Theopolyphenol composition for injection of claim 5, it is characterized in that: when tea polyphenols is dissolved into 50～70% ethanol in the first step, little heating and stirring.
7, according to the preparation method of claim 5 or 6 described Theopolyphenol composition for injection, it is characterized in that: adopting macroporous adsorptive resins separation, ultrafiltration membrance filter in second step, being evaporated to proportion is 1.02～1.04 pin material liquid.
8, according to the preparation method of claim 5 or 6 described Theopolyphenol composition for injection, it is characterized in that: adopt tea polyphenols in the third step: hydroxypropyl cyclodextrin or sulfobutyl ether cyclodextrin mol ratio are 1: 1, or with the tea polyphenols pin with material liquid and weight ratio be 1: 3.5; Pharmaceutic adjuvant is a polyvinylpyrrolidone, sodium chloride, mannitol; The process using saturated solution method, two kinds of mixed stirrings of solution or concussion, at 0～70 ℃, or 0～70 ℃ ultrasonic 60-90 minute, or polishing operation, a sublimed method is adopted in spray drying or lyophilization: pre-freeze-34～-38 °, in the intensification dry run-38 ° to-17 ℃ of intensification vacuum dryings, in 10 to 15 ℃ of vacuum dryings again, lyophilization.
9, according to the preparation method of the described Theopolyphenol composition for injection of claim 7, it is characterized in that: adopt tea polyphenols in the third step: hydroxypropyl cyclodextrin or sulfobutyl ether cyclodextrin mol ratio are 1: 1, or with the tea polyphenols pin with material liquid and weight ratio be 1: 3.5; Pharmaceutic adjuvant is a polyvinylpyrrolidone, sodium chloride, mannitol; The process using saturated solution method, two kinds of mixed stirrings of solution or concussion, at 0～70 ℃, or 0～70 ℃ ultrasonic 60-90 minute, or polishing operation, a sublimed method is adopted in spray drying or lyophilization: pre-freeze-34～-38 °, in the intensification dry run-38 ° to-17 ℃ of intensification vacuum dryings, in 10 to 15 ℃ of vacuum dryings again, lyophilization.
10, according to the preparation method of the described Theopolyphenol composition for injection of claim 9, it is characterized in that: before stirring waits processing, add high polymer adjuvant: sodium carboxymethyl cellulose, polyvinylpyrrolidone PVP, Polyethylene Glycol PEG, PVAC polyvinylalcohol, sodium chloride, hydroxypropyl methylcellulose HPMC, or take heating, pressurized treatments simultaneously.
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| CN107982514B (en) * | 2017-12-12 | 2021-08-27 | 苏州卫生职业技术学院 | Multifunctional tea polyphenol health product and preparation process thereof |
| CN109924390A (en) * | 2019-03-19 | 2019-06-25 | 浙江工商大学 | It is a kind of biology crude antistaling agent preparation method and its application in sturgeon caviar |
| CN109924390B (en) * | 2019-03-19 | 2022-01-14 | 浙江工商大学 | Preparation method of biological natural preservative and application of biological natural preservative in sturgeon caviar |
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