CN101491550A - Compound preparation of red yeast rice extract and coenzyme Q10 and preparation method thereof - Google Patents
Compound preparation of red yeast rice extract and coenzyme Q10 and preparation method thereof Download PDFInfo
- Publication number
- CN101491550A CN101491550A CNA2008100101929A CN200810010192A CN101491550A CN 101491550 A CN101491550 A CN 101491550A CN A2008100101929 A CNA2008100101929 A CN A2008100101929A CN 200810010192 A CN200810010192 A CN 200810010192A CN 101491550 A CN101491550 A CN 101491550A
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- China
- Prior art keywords
- monas cuspurpureus
- cuspurpureus went
- coenzyme
- ubiquinone
- preparation
- Prior art date
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- UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 description 1
- 229960001947 tripalmitin Drugs 0.000 description 1
- 229960004747 ubidecarenone Drugs 0.000 description 1
- 229940040064 ubiquinol Drugs 0.000 description 1
- QNTNKSLOFHEFPK-UPTCCGCDSA-N ubiquinol-10 Chemical compound COC1=C(O)C(C)=C(C\C=C(/C)CC\C=C(/C)CC\C=C(/C)CC\C=C(/C)CC\C=C(/C)CC\C=C(/C)CC\C=C(/C)CC\C=C(/C)CC\C=C(/C)CCC=C(C)C)C(O)=C1OC QNTNKSLOFHEFPK-UPTCCGCDSA-N 0.000 description 1
- 150000003669 ubiquinones Chemical class 0.000 description 1
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 1
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 1
- 239000011782 vitamin Substances 0.000 description 1
- 229940088594 vitamin Drugs 0.000 description 1
- 229930003231 vitamin Natural products 0.000 description 1
- 235000013343 vitamin Nutrition 0.000 description 1
- 150000003722 vitamin derivatives Chemical class 0.000 description 1
- VHBFFQKBGNRLFZ-UHFFFAOYSA-N vitamin p Natural products O1C2=CC=CC=C2C(=O)C=C1C1=CC=CC=C1 VHBFFQKBGNRLFZ-UHFFFAOYSA-N 0.000 description 1
- 239000008802 xuezhikang Substances 0.000 description 1
Landscapes
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
Red rice extract and coenzyme Q10A compound preparation and a preparation method thereof relate to an oral administration red yeast rice extract and coenzyme Q10A compound preparation and a preparation method thereof, which are mainly used for preventing and treating cardiovascular diseases, belong to the technical field of medicines and health care products. The invention adopts the following technical scheme that ingredients of the invention comprise red yeast rice extract and coenzyme Q105-30 parts of red yeast extract and coenzyme Q10The weight portion of the composition is 1-5. The preparation method of the invention comprises the steps of taking various materials according to the weight percentage and taking coenzyme Q10Mixing the oil phase substance with the oil phase substance, heating the oil phase to 70-80 ℃ to dissolve the oil phase substance; get water phase substance sourceDissolving the material and an emulsifier in a water phase, dissolving the red yeast rice extract in the water phase, and heating to 70-80 ℃; and (3) putting the oil phase into the water phase, carrying out high-speed shearing for 1-5 minutes, then putting the oil phase into a high-pressure homogenizer, circulating for 3-6 times under the pressure of 30-100 MPa, and then carrying out spray drying to obtain the compound preparation.
Description
Technical field
The present invention relates to a kind of Monas cuspurpureus Went extract and ubiquinone of oral administration
10Compound preparation and preparation method thereof.Monas cuspurpureus Went extract of the present invention and ubiquinone
10Compound preparation is with Monas cuspurpureus Went medicinal substances extract and ubiquinone
10Be primary raw material, be prepared from, be mainly used in prevention, treatment cardiovascular disease, belong to medicine, health product technology field through certain preparation process.
Background technology
Monas cuspurpureus Went (Monas cuspurpureus Went) is Chinese Chinese medicine material and food, is mainly fermented by Monascus anka Nakazawa et sato.Monas cuspurpureus Went Pseudomonas mycota (Eumycophyta), Ascomycota (Ascomycota), Euascomycetes (Euascomycetes), diffusing ascus Zoopagales (Eurotiales), Monas cuspurpureus Went Cordycepps (Monascaceae), Monas cuspurpureus Went Pseudomonas (Monascus).Being inoculated in Monas cuspurpureus Went that rice fermentation obtains by Monascus anka Nakazawa et sato, to be applied to traditional food painted and as medicinal always.Put down in writing in Ming Dynasty's Compendium of Material Medica: " Monas cuspurpureus Went, warm in nature, sweet in the mouth help digestion and invigorate blood circulation, the dry stomach of spleen invigorating.Wine brewing, the capable medicine gesture of removing blood stasis." from Monas cuspurpureus Went fermentation liquid, find and separate to obtain significantly suppressing the synthetic active substance Monacolin of body inner cholesterol K (he is left alone without help) until Japan's rattan chapter far away; people begin to have given new extensive concern to natural Monas cuspurpureus Went and Monacolin compounds, and the Monacolin compounds has definite effect to blood lipid regulation and cholesterol reducing.Also there are a large amount of monascorubins and various active materials such as ergosterol, unsaturated fatty acid, polysaccharide, saponin, flavone and cellulose in the Monas cuspurpureus Went with antioxidation.A large amount of clinical pharmacologies studies confirm that Monas cuspurpureus Went has significant cholesterol reducing and blood fat at present.U.S. FDA in 1987 the official approval lovastatin (lovastatin, i.e. Monacolin K) be used for clinical.Up to now, the U.S. and Japan etc. have developed a series of statinses such as Lovastatin, Provastatin, Simvastatin and Atorvastatin etc., and its main component is Monacolin (he is left alone without help) compounds.There are Xuezhikang, zhibituo and heart health medicine etc. in China with the blood lipid-lowering medicine and the health food of Monas cuspurpureus Went exploitation.
Ubiquinone
10Have another name called ubiquinone, be also referred to as certain herbaceous plants with big flowers alkene quinone, ubiquinol, vitamin Q, vitamin ubiquinone, English name is Coenzyme Q
10, Ubiquinone, molecular formula is C
59H
90O
4This material be human body from the body material, also extensively be present in organs such as animal hearts, can from animal hearts, extract and obtain, also can be by chemosynthesis, biosynthesis obtains.Ubiquinone
10It is indispensable important physiologically substance in the human body, its chemical constitution characteristics have determined it to have many important physiological function in human body, it is a transmitter substance important in the vital movement, it is the key material of mitochondrial respiratory key rate-limiting reaction, generate at cellular energy, strengthen the biologos aspect and play a significant role.Contain Q in the human body
10Total amount is 500-1500mg, peaks about 20 years old, reduces rapidly then, and 70 years old reduces 57% than 20 years old youngster later on.Discover, in a lot of ill patients, ubiquinone
10Physiological level descends obviously, in the heart failure patient, and ubiquinone in patient's cardiac muscle and the blood
10Content obviously reduces, and replenishes ubiquinone from external source
10After, obviously improve patient symptom.Discover a lot of hypoimmunity patients, its ubiquinone
10Physiological level is lower, replenishes ubiquinone
10After, symptom improves.Modern medicine study finds that his left alone without help class medicine is the HMG-CoA reductase inhibitor, in the time of the performance drug effect, and blocking-up body coenzyme Q
10Biosynthesis, the patient takes his left alone without help class medicine for a long time can cause the body coenzyme Q
10Level reduces, and then causes many related side effects to take place, as hepatorenal damage and muscle damage.As document Ital J Biochem.1995, Jan-Feb; 44 (1): 1-9.Marinari UM, Pronzato MA, Dapino D, Gazzo P, Traverso N, Cottalasso D, Odetti P. and document Proc Natl Acad Sci USA.1990Nov; 87 (22): 8931-4.Folkers K, Langsjoen P, Willis R, RichardsonP, Xia LJ, Ye CQ describes among the Tamagawa H..Therefore, human body replenishes ubiquinone from external source
10Treat various ubiquinones
10Physiological level lowly becomes a kind of feasible clinical treatment method.
Monas cuspurpureus Went and ubiquinone
10All belong to and derive from natural health substance, cardiovascular system is all had health care and therapeutical effect preferably, but physiological action stresses face and mechanism has certain difference, has complementarity, but be independent use substantially in the market.Monas cuspurpureus Went relies on that to contain natural HMG-CoA reductase inhibitor be his left alone without help class component for reducing blood fat and other antioxidant contents, hyperlipidemia and hypercholesterolemia are had strong pharmacological action, but because its main effective ingredient for his left alone without help compounds, will be blocked ubiquinone
10Biosynthesis, influence the body coenzyme Q
10Level, more existing documents have confirmed this point, as H.T.YangYang HT, Lin SH, Huang SY, Chou HJ. is at magazine Br J Nutr 2005; 93:131-135. in described Monas cuspurpureus Went and can reduce the multiple ubiquinone of organizing in the rat body
10Level is so the long-term Monas cuspurpureus Went extract that uses separately may produce certain side effect.In addition owing to ubiquinone among the patient crowd that cardiovascular disease is arranged
10Level is generally low, also needs additionally to replenish ubiquinone
10To normal level.
Summary of the invention
The present invention is exactly at the problems referred to above, provides a kind of and overcomes the side effect hidden danger that single clothes Monas cuspurpureus Went exists, and the Monas cuspurpureus Went and the ubiquinone of cooperative compensating effect are arranged
10Compound preparation and preparation method thereof.
For achieving the above object, the present invention adopts following technical scheme, and the present invention's batching comprises Monas cuspurpureus Went extract, ubiquinone
10, the parts by weight of Monas cuspurpureus Went extract are 5～30 parts, ubiquinone
10Parts by weight be 1～5 part.
Can also add adjuvant and prepare water dispersible stable compound preparation, prepare burden for the Monas cuspurpureus Went extract parts by weight be 5～30 parts, ubiquinone
10Parts by weight be that 1～5 part, the parts by weight of oil phase substance are 5～20 parts of 5～30 parts, the parts by weight of 10～60 parts of the parts by weight of aqueous phase substance, emulsifying agent.
Ubiquinone among the present invention
10Be liposoluble substance, be insoluble in water, relatively poor to light, heat stability, bioavailability is low.Monas cuspurpureus Went extract of the present invention has certain water solublity, and contains the Lip river and cut down his left alone without help and monascorubin, and the monascorubin that is contained is highly stable, has stronger interception, therefore both above-mentioned physicochemical properties be can utilize, microcapsule or nanoparticle are prepared into, fat-soluble ubiquinone with oil-in-water type
10Melt mutually separately or with liposoluble substance, as oil phase, soluble in water with Monas cuspurpureus Went extract and water-soluble substances, as water, under surfactant or emulsifying agent effect, carry out homogenizing and disperse, form nano dispersion fluid, after spray drying or the lyophilization, form water dispersible Monas cuspurpureus Went extract and ubiquinone
10Compound preparation.In this compound preparation, the monascorubin that contains in the Monas cuspurpureus Went extract contains ubiquinone with the common parcel of other adjunct ingredients
10Liposome has improved ubiquinone
10Stability and dissolubility, form and to contain Monas cuspurpureus Went extract and ubiquinone simultaneously
10Compound preparation, and have higher solubility, reached pleasantly surprised effect.
The preparation method of the Chinese medicine Monas cuspurpureus Went extract among the present invention is that employing Monas cuspurpureus Went material with present known technology, adds water or ethanol or methanol and extracts, and obtains after the drying.Mainly contain the Lip river in the Monas cuspurpureus Went extract and cut down compositions such as his left alone without help and monascorubin.Also can directly buy Monas cuspurpureus Went extract from the market.Ubiquinone
10Raw material adopts the commercially available product that meets standards of pharmacopoeia.
Oil phase substance can adopt vegetable oil, fatty glyceride in the adjuvant of the present invention, solid fatty acid any one or theys' mixture, vegetable oil can be any mixture of any one or they of soybean oil, olive oil, rapeseed oil, Petiolus Trachycarpi oil, Oleum Sesami, safflower oil, Semen Maydis oil, perilla oil, fatty glyceride can be monoglyceride, mountain Yu acid glyceride, Palmic acid glyceride, mixed acid glyceride, polyglycerol fatty acid fat is a kind of or their any mixture, and solid fatty acid can be a stearic acid, Palmic acid is a kind of or their mixture.Aqueous phase substance can adopt gelatin, fish glue, arabic gum, any one of sugar and sugar alcohols or their mixture, sugar can be a kind of of lactose, sucrose, mannose, trehalose, maltose or their any mixture, and sugar alcohol can be a kind of of mannitol, sorbitol, xylitol, maltose alcohol or their mixture.Emulsifying agent adopts non-ionic surfactant Tween 20,40,60,80, deoxycholic acid, any one of poloxamer, phospholipid, sucrose fat, fatty acid polyglycol glyceride or their any mixture.
The preparation method of compound preparation of the present invention is got various materials by above-mentioned weight fraction, gets ubiquinone
10, mixing with oil phase substance, heating is warming up to 70～80 ℃ with oil phase substance, makes dissolving; Water intaking phase raw material of substance and emulsifying agent are soluble in the aqueous phase in the material, and above-mentioned Monas cuspurpureus Went extract is dissolved in the aqueous phase substance, are warming up to 70～80 ℃; Oil phase substance is put into aqueous phase substance, carried out high speed shear 1～5 minute, put into high pressure homogenizer then, under 30～100 MPa pressure, circulate 3～6 times, spray drying obtains compound preparation of the present invention then.
The method of homogenizing can adopt the Ultrasonic Pulverization method to substitute, and spray drying can adopt freeze-drying to substitute.
Beneficial effect of the present invention:
The present invention has improved Monas cuspurpureus Went or ubiquinone
10The drug effect of using has been improved the ubiquinone that target of the present invention is used the crowd
10Low physiological level more helps preventing and treating cardiovascular disease, the side effect of having avoided the life-time service Monas cuspurpureus Went extract to cause, because two kinds of materials are formed compound preparation, the patient takes more convenient.Preparation of the present invention is easier dispersing or dissolving in water, ubiquinone
10More stable, and improved bioavailability.
The specific embodiment:
Below description by the specific embodiment the present invention is described in further detail; but this can not be used to limit protection scope of the present invention; those skilled in the art are according to basic thought of the present invention; can make various modifications or improvement; but only otherwise break away from basic thought of the present invention, all within the scope of the present invention.
Embodiment 1
Get ubiquinone
1010g, Monas cuspurpureus Went extract 300g, mix homogeneously.
Embodiment 2
Get ubiquinone
1050g, Monas cuspurpureus Went extract 300g, mix homogeneously.
Embodiment 3:
Get ubiquinone
1010g, soybean oil 25g, glyceryl monostearate 25g mixes, and heat temperature raising to 75 ℃ is standby.Get trehalose 100g, Monas cuspurpureus Went extract 50g, tween (80) 30g is dissolved in the 2000g water jointly, be warming up to 75 ℃, oil phase is joined in the aqueous phase substance, sheared 5 minutes, put into high pressure homogenizer then in the mulser high speed, under 100 MPa pressure, circulate 3 times, spray drying obtains compound preparation of the present invention then.
Emulsifying agent can adopt polysorbas20,40,60, phospholipid, poloxamer, deoxycholic acid to replace.Soybean oil can adopt Semen Maydis oil, olive oil, rapeseed oil, safflower oil, Petiolus Trachycarpi oil, perilla oil to replace.Glyceryl monostearate can adopt Glyceryl Behenate, tripalmitin, mixed acid glyceride to replace.Trehalose can adopt lactose, sucrose, maltose, mannose, mannitol, xylitol, gelatin, fish glue, arabic gum to replace.
Embodiment 4
Get ubiquinone
1010g, Palmic acid glyceride 150g mixes, and heat temperature raising to 75 ℃ is standby.Get lactose 200g, gelatin 100g, Monas cuspurpureus Went extract 300g, phosphatidase 15 0g, poloxamer (188) 100g, deoxycholic acid 50g, be dissolved in jointly in the 5000g water, be warming up to 75 ℃, oil phase substance is joined in the aqueous phase substance, sheared 5 minutes in the mulser high speed, put into high pressure homogenizer then, under 60 MPa pressure, circulate 3 times, spray drying obtains compound preparation of the present invention then.
Embodiment 5
Get ubiquinone
1050g, heat temperature raising to 75 ℃, standby.Get trehalose 300g, fish glue 300g, Monas cuspurpureus Went extract 300g, tween (20) 50g, poloxamer (188) 50g, be dissolved in jointly in the 5000g water, be warming up to 75 ℃, oil phase substance is joined in the aqueous phase substance, sheared 5 minutes in the mulser high speed, Ultrasonic Pulverization is 10 minutes then, and lyophilization then obtains compound preparation of the present invention.
Embodiment 6
Press the compound preparation raw material midbody of embodiment 3 preparations, be prepared into capsule, tablet, granule according to known technology.
Embodiment 7
The sample of embodiment 4 preparations and the sample of embodiment 1 preparation are got in the water dispersible test, and according to concentration 1mg/ml configuration solution, acetonideexample 4 samples can form homogeneous solution, ubiquinone in embodiment 1 sample
10Swim in the solution.
Embodiment 7
Stability test is got the sample and the ubiquinone of the preparation of embodiment 3 methods
10Raw material carries out illumination, high thermal stability test.
1, influence of light test
Get the raw material ubiquinone
10With Monas cuspurpureus Went extract mixture, ubiquinone
10Raw material, and preparation of the present invention placed 10 days under 4000LX light, respectively at 0 day, 5 days, 10 days sampling and measuring, the results are shown in Table 1.
Table 1 light is to ubiquinone
10Influence:
Table 1 shows that light is to ubiquinone
10Considerable influence is arranged, and preparation light stability wherein of the present invention is better than ubiquinone
10Raw material and mixture.
2, temperatures involved test
Get preparation of the present invention and mixture and raw material at 60 ℃, placed 10 days,, the results are shown in Table 2 respectively at 0 day, 5 days, 10 days sampling and measuring.
Table 2 high temperature is to ubiquinone
10Influence (60 ℃):
Table 2 shows that temperatures involved is less.
Embodiment 8
Transfer the blood fat experimental study, experimental technique: the feed high lipid food causes the hyperlipidemia rats model, model is subjected to the reagent thing after setting up, test the 14th day enzymatic assays rat blood serum T-CHOL (TC), serum triglycerides (TG), HDL-C (HPL), the content of low-density lipoprotein cholesterol (LDL).5 administration groups and a high fat matched group and a blank group are established in experiment, the administration group is respectively Monas cuspurpureus Went extract group (0.54g/kg wherein Lip river cut down his left alone without help content be 3.1%), Monas cuspurpureus Went coenzyme Q10 simple mixtures group (5.0g/kg, press embodiment 1 method preparation), the basic, normal, high dosage group of the water dispersible compound preparation of Monas cuspurpureus Went coenzyme Q10 (preparing) by embodiment 4 methods (dosage is respectively 5.0,2.5,0.5g/kg wherein high dose group contain the Lip river to cut down his left alone without help amount consistent with the Monas cuspurpureus Went extract group).The rat feeding normal feedstuff observed for 2 weeks under experimental situation, got blood, surveyed the normal value of TC observation index.Begin each treated animal from formal experiment and fed for 2 weeks, get blood, measure blood fat to determine whether to form hyperlipemia, after hyperlipidemia model is set up, again according to TC level, random packet with high lipid food.Every group 10, when continuing high fat and feed, each organizes equal gastric infusion, and every day 1 time, in continuous 2 weeks, every index is measured in blood sampling in the 14th day.Each treated animal is put to death, and the separating animal's heart is measured coenzyme Q10 content after pre-treatment.The results are shown in following table 3, by the table result as seen, there was no significant difference (P＞0.05) between TC, the TG of each group, HDL, LDL during on-test, when testing 14 days, each administration group can significantly reduce the triglyceride (TG) of hyperlipemia rat, T-CHOL (TC), low-density lipoprotein cholesterol (LDL) content, each is organized blood lipid reducing content effect and is the water dispersible compound recipe of Monas cuspurpureus Went coenzyme Q10＞simple compound capsule＞Monas cuspurpureus Went of Monas cuspurpureus Went coenzyme Q10 in proper order.Animal hearts organizes coenzyme Q10 content to compare with the blank group, and the Monas cuspurpureus Went extract group descends 18%, and the dosage group descends 2% in the water dispersible compound recipe of Monas cuspurpureus Went coenzyme Q10, and the water dispersible compound recipe high dose group of Monas cuspurpureus Went coenzyme Q10 does not descend.
Each administration group of table 3 to the influence of lipid metabolic disorder rat blood serum lipid content (N=10, x ± s, mmol/L)
Annotate: each group compares *: P＜0.05 with model control group
Claims (7)
1, a kind of Monas cuspurpureus Went extract and coenzyme Q10 compound preparation is characterized in that, batching comprises Monas cuspurpureus Went extract, ubiquinone
10, the parts by weight of Monas cuspurpureus Went extract are 5～30 parts, ubiquinone
10Parts by weight be 1～5 part.
2, a kind of Monas cuspurpureus Went extract according to claim 1 and coenzyme Q10 compound preparation, the weight that it is characterized in that Monas cuspurpureus Went extract is 300g, ubiquinone
10Weight be 10g.
3, a kind of Monas cuspurpureus Went extract according to claim 1 and coenzyme Q10 compound preparation, the weight that it is characterized in that Monas cuspurpureus Went extract is 300g, ubiquinone
10Weight be 50g.
4, a kind of Monas cuspurpureus Went extract according to claim 1 and coenzyme Q10 compound preparation is characterized in that in batching adding adjuvant and prepare water dispersible stable compound preparation, prepare burden for the Monas cuspurpureus Went extract parts by weight be 5～30 parts, ubiquinone
10Parts by weight be that 1～5 part, the parts by weight of oil phase substance are 5～20 parts of 5～30 parts, the parts by weight of 10～60 parts of the parts by weight of aqueous phase substance, emulsifying agent.
5, the preparation method of a kind of Monas cuspurpureus Went extract and coenzyme Q10 compound preparation is characterized in that getting by weight ubiquinone
10, mixing with oil phase substance, heating is warming up to 70～80 ℃ with oil phase substance, makes dissolving; Water intaking phase raw material of substance and emulsifying agent are soluble in the aqueous phase in the material, and Monas cuspurpureus Went extract is dissolved in the aqueous phase substance, are warming up to 70～80 ℃; Oil phase substance is put into aqueous phase substance, carried out high speed shear 1～5 minute, put into high pressure homogenizer then, under 30～100 MPa pressure, circulate 3～6 times, spray drying obtains compound preparation of the present invention then.
6, the preparation method of a kind of Monas cuspurpureus Went extract according to claim 5 and coenzyme Q10 compound preparation is characterized in that getting ubiquinone
1010g, soybean oil 25g, glyceryl monostearate 25g mixes, and heat temperature raising to 75 ℃ is standby; Get trehalose 100g, Monas cuspurpureus Went extract 50g, tween 30g is dissolved in the 2000g water jointly, be warming up to 75 ℃, oil phase substance is joined aqueous phase, sheared 5 minutes, put into high pressure homogenizer then in the mulser high speed, under 100 MPa pressure, circulate 3 times, spray drying obtains compound preparation of the present invention then.
7, the preparation method of a kind of Monas cuspurpureus Went extract according to claim 5 and coenzyme Q10 compound preparation is characterized in that getting ubiquinone
1010g, Palmic acid glyceride 150g mixes, and heat temperature raising to 75 ℃ is standby; Get lactose 200g, gelatin 100g, Monas cuspurpureus Went extract 300g, phosphatidase 15 0g, poloxamer 100g, deoxycholic acid 50g, be dissolved in jointly in the 5000g water, be warming up to 75 ℃, oil phase is joined in the aqueous phase substance, sheared 5 minutes in the mulser high speed, put into high pressure homogenizer then, under 60 MPa pressure, circulate 3 times, spray drying obtains compound preparation of the present invention then.
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Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102388971A (en) * | 2011-11-14 | 2012-03-28 | 江苏星驰生物科技有限公司 | Compound bovine colostrums powder |
| CN103613494A (en) * | 2013-11-05 | 2014-03-05 | 广东医学院 | Technology for extracting coenzyme q10 by using Monascus mycelium as raw material and production method |
| IT201700115088A1 (en) * | 2017-10-12 | 2019-04-12 | Pharmanutrition R&D S R L | Powder composition containing fermented red rice with high oral bioavailability |
| CN116035210A (en) * | 2022-12-30 | 2023-05-02 | 广州白云山汉方现代药业有限公司 | Method for solving layering of content and application of method in preparation of plant sterol ester red yeast soft capsules |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4929437A (en) * | 1989-02-02 | 1990-05-29 | Merck & Co., Inc. | Coenzyme Q10 with HMG-CoA reductase inhibitors |
| CA2007983C (en) * | 1989-01-18 | 1996-12-10 | Michael S. Brown | Coenzyme q10 with hmg-coa reductase inhibitors |
| CN1778391A (en) * | 2005-03-07 | 2006-05-31 | 淮北市辉克药业有限公司 | Safety and high-efficient compound hypolipidemic medicine |
-
2008
- 2008-01-22 CN CN2008100101929A patent/CN101491550B/en not_active Expired - Fee Related
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102388971A (en) * | 2011-11-14 | 2012-03-28 | 江苏星驰生物科技有限公司 | Compound bovine colostrums powder |
| CN103613494A (en) * | 2013-11-05 | 2014-03-05 | 广东医学院 | Technology for extracting coenzyme q10 by using Monascus mycelium as raw material and production method |
| CN103613494B (en) * | 2013-11-05 | 2016-02-03 | 广东医学院 | Take Monascus anka Nakazawa et sato filament as technique and the production method that raw material extracts ubiquinone 10 |
| IT201700115088A1 (en) * | 2017-10-12 | 2019-04-12 | Pharmanutrition R&D S R L | Powder composition containing fermented red rice with high oral bioavailability |
| CN116035210A (en) * | 2022-12-30 | 2023-05-02 | 广州白云山汉方现代药业有限公司 | Method for solving layering of content and application of method in preparation of plant sterol ester red yeast soft capsules |
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| CN101491550B (en) | 2011-12-28 |
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