CN103463624A - Bone joint composite nutrient supplement and preparation method thereof - Google Patents
Bone joint composite nutrient supplement and preparation method thereof Download PDFInfo
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- CN103463624A CN103463624A CN2013104286681A CN201310428668A CN103463624A CN 103463624 A CN103463624 A CN 103463624A CN 2013104286681 A CN2013104286681 A CN 2013104286681A CN 201310428668 A CN201310428668 A CN 201310428668A CN 103463624 A CN103463624 A CN 103463624A
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- osteoarthrosis
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- olibanum
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- nourishing energizing
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- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
The invention discloses a bone joint composite nutrient supplement and a preparation method thereof. The bone joint composite nutrient supplement comprises the following components in parts by weight: 350-600 parts of glucosamine hydrochloride, 350-450 parts of chondroitin/MSM (methyl sulfonyl methane) mixture and 16-60 parts of traditional Chinese medicine extract, wherein the chondroitin/MSM mixture comprises chondroitin sulfate, dimethyl sulfone, collagen, frankincense and hyaluronic acid according to weight part of 2:3:1:1:3, the extraction process of the traditional Chinese medicine extract comprises the steps of smashing clean traditional Chinese medicinal materials, heating and back flowing for 2-3 hours by a low solubility ethyl alcohol solution, extracting for 3 times, combining the extracting solutions, after purification, concentrating, and drying at low temperature. The bone joint composite nutrient supplement not only can improve various arthritis and symptoms caused by arthritis, but also can improve various symptoms caused by osteoporosis.
Description
Technical field
the invention belongs to nutriment health preparation technical field, more specifically say a kind of osteoarthrosis composite nourishing energizing agent and preparation method thereof.
Background technology
osteoarthritis very common joint disease in the diseases of middle-and old-aged person, it can cause arthralgia and ankylosis, can cause to middle-older patient, cause certain handicapped.The traditional treatment joint disease, comprise common gonarthritis, cervical spondylosis, prolapse of lumbar intervertebral disc, hyperosteogeny (bony spur), scapulohumeral periarthritis etc., mainly contains the methods such as naturopathy, operative treatment, Drug therapy.These methods can only the respite symptom, can not reach the purpose of basic treatment.The life-time service drug side effect is large simultaneously, and untoward reaction is serious, and especially hormone medicine, can bring out the more serious diseases such as hypertension, diabetes, glaucoma, and can draw backlash after drug withdrawal, causes symptom further to increase the weight of.For a long time, due to the understanding lacked the pathogenic basic reason of joint disease, the treatment of joint disease is always for symptom treatments such as pain, swelling, be in the refractory condition originally of taking stopgap measures, in the time for the treatment of, disease continues development, finally cause joint deformity, tetanic, function completely loses, and is paralyzed in bed, and can't take care of oneself.Scientific research proves, and osteoarthritis (also claiming osteoarthritis) is a kind of known joint degenerative disease, and its basic reason is destruction and the forfeiture of articular cartilage, and in brief, arthritis-disease is in joint, and root is at cartilage.Therefore, the correct effective method for the treatment of joint disease is to repair damaged articular cartilage, supplements glucosamine, bone collagen (II collagen type) and chondroitin sulfate etc. simultaneously, and antiinflammatory, analgesia, reparation chondrocyte, settle at one go.At present, in worldwide, glucosamine, bone collagen, chondroitin sulfate be as the supplementary targetedly of articular cartilage, by medical circle be known as can the thorough improvement joint disease the specificity preparation.Glucosamine, bone collagen, chondroitin sulfate are all the natural components be present in articular cartilage, research worker is thought, they can be by promoting that Human Osteoarthritis forms new articular cartilage, slow down the forfeiture of articular cartilage, can also the alleviating pain symptom, keep the motility of joint motions.
Summary of the invention
it not only can be used as the health food of prevention osteoarticular injury, the poor disease of human synovial fluid and exhaustion and the anti-ageing diet nutritional supplement of waiting for a long time osteoarthrosis nutrition enhancer of the present invention, and, through further clinical practice exploitation, can be made into the specific medicament for the treatment of osteoarthritis.
the invention discloses a kind of osteoarthrosis composite nourishing energizing agent for this reason, it is characterized in that it is comprised of glucosamine hydrochoride, chrondroitin/MSM mixture, Chinese medicine extract, wherein glucosamine hydrochoride: chrondroitin/MSM mixture: the ratio of weight and number of Chinese medicine extract is 350-600 part: 350-450 part: 16-60 part; It take described chrondroitin/MSM mixture ratio of weight and number by chondroitin sulfate, dimethyl sulfone, collagen protein, Olibanum, hyaluronic acid and forms as 2:3:1:1:3; Described Chinese medicine extract refers to Olibanum extract or/and Herba Epimedii.
chinese medicine extract of the present invention refers to: clean Olibanum or Herba Epimedii pulverized, with ethanol (35%-60%) vlil 2-3 hour, extracted three times, and merge extractive liquid,, after carrying out purification process, concentrated, oven drying at low temperature gets final product.
osteoarthrosis composite nourishing energizing agent of the present invention, wherein the molecular weight of collagen protein is 1000 dalton.Hyaluronic acid refers to molecular weight from 5,000 to 2,000 ten thousand Dao Er, preferably clear matter acid 5000 molecular weight Dao Er.
osteoarthrosis composite nourishing energizing agent of the present invention refers to oral formulations.Preferred tablet or capsule.
its each component content of the preferred oral formulations tablet of the present invention:
glucosamine hydrochoride: 350mg---600mg chrondroitin mixture: 350mg--450mg
chinese medicine extract: 16mg---60mg calcium phosphate: 0.1mg-8mg
sodium borate 7mg-20mg vitamin C 13mg-26mg
manganese sulfate 1---4mg methylcellulose 1-4mg
burnt sugar coloring 1-4mg microcrystalline Cellulose 2-6mg
silica 1--3mg titanium dioxide 1-5mg
magnesium stearate 1--4mg palm wax 0.3---2mg;
it take described chrondroitin/MSM mixture ratio of weight and number by chondroitin sulfate, dimethyl sulfone, collagen protein, Olibanum, hyaluronic acid and forms as 2:3:1:1:3; Described Chinese medicine extract refers to Olibanum extract or/and Herba Epimedii.
the tablet each component content be more preferably:
glucosamine hydrochoride 500mg/ sheet chrondroitin/MSM design of mixture 396mg/ sheet
chinese medicine extract: 33.3mg calcium phosphate: 4mg
sodium borate: 13.3mg vitamin C: 60mg
manganese sulfate: 2mg methylcellulose: 3mg
burnt sugar coloring: 2mg microcrystalline Cellulose: 3mg
silicon dioxide: 3mg titanium dioxide: 4mg
magnesium stearate: 3mg palm wax: 0.8mg;
it take described chrondroitin/MSM mixture ratio of weight and number by chondroitin sulfate, dimethyl sulfone, collagen protein, Olibanum, hyaluronic acid and forms as 2:3:11:3; Described Chinese medicine extract refers to Olibanum extract or/and Herba Epimedii.Leaching process: clean Olibanum or Herba Epimedii are pulverized, with ethanol (35%-60%) vlil 2-3 hour, extracted three times, merge extractive liquid,, after carrying out purification process, concentrated, oven drying at low temperature, standby.
chondroitin sulfate is the acidic mucopolysaccharide obtained from the extraction of the cartilages such as mammal trachea.It has the clarification lipid, improves the body function of detoxification, the effects such as diuresis and analgesia (having commercially available).
in every 3 of osteoarthrosis nutrition enhancer of the present invention, add: glucosamine hydrochoride 1500mg, chrondroitin/MSM design of mixture 1250mg, Olibanum extract 100mg.
through pharmacological evaluation, confirm: Herba Epimedii has the effect while of androgen sample, and Herba Epimedii can also suppress vasomotor center, and the expansion peripheral vessels, make the blood pressure drops Herba Epimedii be mainly used in clinically treating joint disease.Add Herba Epimedii extract and can improve old people's hormonal readiness, blood vessel dilating, promote the repair of cartilage growth.
through pharmacological evaluation, confirm: Olibanum extract can antiphlogistic antibacterial, contributes to alleviate arthralgia, improve aspect knee comfortableness and activeness effective.
osteoarthrosis composite nourishing energizing agent of the present invention, wherein the molecular weight of collagen protein is 1000 dalton.Hyaluronic acid refers to molecular weight from 5,000 to 2,000 ten thousand Dao Er, and preferably clear matter acid molecule amount is 5000 Dao Er.Described osteoarthrosis nutrition enhancer refers to oral formulations, for example tablet or capsule.
oral formulations of the present invention refers to its each component content of tablet:
glucosamine hydrochoride: 350mg--600mg ossein mixture: 350mg--450mg
olibanum extract or Herba Epimedii extract: 16mg-60mg calcium phosphate: 0.1mg--8mg
sodium borate 7mg-20mg vitamin C 13mg--26mg
manganese sulfate 1--4mg methylcellulose 1-4mg
burnt sugar coloring 1-4mg microcrystalline Cellulose 2-6mg
silica 1--3mg titanium dioxide 1-5mg
magnesium stearate 1--4mg palm wax 0.3---2mg;
tablet test report:
Sequence number | Detection material | Requirement | Actual measurement |
1 | Glucosamine hydrochoride | 350mg-600mg | 510mg |
2 | Chrondroitin/MSM design of mixture (chondroitin sulfate, dimethyl sulfone (MSM), collagen protein, Olibanum, hyaluronic acid), | 350mg-450mg | 398mg |
3 | Olibanum extract | 16mg---60mg | 35.3mg |
4 | Calcium phosphate | 0.1mg—8mg | 4 |
5 | Sodium borate | 7mg—20mg | 17.3mg |
6 | Vitamin C | 13mg----26mg | 68mg |
7 | Manganese sulfate | 1 mg ----4mg | 2mg |
8 | Methylcellulose | 1 mg—4mg | 3mg |
9 | Burnt sugar coloring | 1 mg--—4mg | 2mg |
10 | Microcrystalline Cellulose | 2 mg ---6mg | 3mg |
11 | Silicon dioxide | 1 mg ---3mg | 3mg |
12 | Titanium dioxide | 1 mg—5mg | 4mg |
13 | Magnesium stearate | 1 mg ---4mg | 3mg |
14 | Palm wax | 0.3 mg ---2mg | 0.8mg |
another typical formula of the present invention is as follows:
composition: glucosamine hydrochoride chrondroitin/design of mixture (chondroitin sulfate, collagen protein, Olibanum, hyaluronic acid), Herba Epimedii extract, Olibanum extract, vitamin C, manganese sulfate, methylcellulose, burnt sugar coloring, microcrystalline Cellulose, silicon dioxide, titanium dioxide, magnesium stearate, palm wax calcium phosphate;
each component content:
glucosamine hydrochoride: 350mg-600mg/ sheet chrondroitin mixture: 350mg-450mg/ sheet
herba Epimedii extract: 0.3--0.85mg/ sheet Olibanum extract: 16mg-60mg/ sheet
sodium borate 7mg--20mg/ sheet vitamin C 13mg--26mg/ sheet
manganese sulfate: 1 mg-4mg/ sheet methylcellulose 1mg-4mg/ sheet
burnt sugar coloring 1mg-4mg/ sheet microcrystalline Cellulose 2 mg-6mg/ sheets
silica 1 mg-3mg/ sheet titanium dioxide 1mg-5mg/ sheet
magnesium stearate 1 mg-4mg/ sheet palm wax 0.3mg-2mg/ sheet
calcium phosphate: 0.1mg--8mg/ sheet;
it take ratio of weight and number as chondroitin sulfate by chondroitin sulfate, dimethyl sulfone, collagen protein, Olibanum, hyaluronic acid described chrondroitin/MSM mixture: dimethyl sulfone: collagen protein: Olibanum: hyaluronic acid 2:3:1:1:3 forms survey report:
Sequence number | Detection material | Requirement | Actual measurement |
1 | Glucosamine hydrochoride | 350mg---600mg | 510mg |
2 | Chrondroitin/MSM design of mixture (be take ratio of weight and number as chondroitin sulfate: dimethyl sulfone: collagen protein: Olibanum: hyaluronic acid 2:3:1:1:3) | 350mg----450mg | 398mg |
3 | Herba Epimedii extract | 0.3 mg ---0.85mg | 70mg |
4 | Olibanum extract | 16mg---60mg | 35.3mg |
5 | Sodium borate | 7mg—20mg | 17.3mg |
6 | Vitamin C | 13mg----26mg | 68mg |
8 | Manganese sulfate | 1 mg ----4mg | 2mg |
9 | Methylcellulose | 1 mg—4mg | 3mg |
10 | Burnt sugar coloring | 1 mg--—4mg | 2mg |
11 | Microcrystalline Cellulose | 2 mg ---6mg | 3mg |
12 | Silicon dioxide | 1 mg ---3mg | 3mg |
13 | Titanium dioxide | 1 mg—5mg | 4mg |
14 | Magnesium stearate | 1 mg ---4mg | 3mg |
15 | Palm wax | 0.3 mg ---2mg | 0.8mg |
16 | Calcium phosphate | 0.1mg—8mg | 4 |
the preparation method of osteoarthrosis composite nourishing energizing agent of the present invention, adopt conventional method for preparing tablet thereof, for example can say various raw material mix homogeneously, add appropriate 10% hydroxypropyl methylcellulose solution to granulate, drying, then add carboxymethyl starch sodium etc., magnesium stearate, mix, tabletting.
the present invention further discloses the application of osteoarthrosis composite nourishing energizing agent in improving Senile degenerative osteopathia medicine, particularly improve the application in medicine for treating osteoporosis.
below provide the pharmacological experimental data that the present invention improves the osteoarthrosis composite nourishing energizing agent, and concrete pharmacodynamics and toxicity test result be summarized as follows:
one, pharmacodynamics test:
1, osteoarthrosis composite nourishing energizing agent on Carrageenan of the present invention causes the swollen inhibitory action (arthritis test) of rat foot:
osteoarthrosis composite nourishing energizing agent on Carrageenan of the present invention cause rat foot swollen inhibitory action arranged, result of the test shows, the osteoarthrosis composite nourishing energizing agent is 25,50 and during 100mg/kg in dosage, respectively at after administration 0.5,1,2,3 and 4 hour, the rat foot being swollen to rise all has obvious inhibitory action (P<0.01), and positive control drug glucosamine hydrochloride (50mg/kg) has identical inhibitory action (P<0.01).
, osteoarthrosis composite nourishing energizing agent of the present invention is to the analgesic activity (acetic acid twisting test) of mice:
result of the test shows, the oral osteoarthrosis composite nourishing energizing agent of the present invention of mice, at dosage, be 25,50 and during 100mg/kg, the mice pain that Dichlorodiphenyl Acetate causes all has inhibitory action in various degree, compare (P<0.05,0.05 and 0.01) with model group, with contrasting, medicine glucosamine hydrochloride (50mg/kg) effect is suitable.
, osteoarthrosis nutrition enhancer of the present invention is to the refrigeration function (endotoxin pyrogenic) of rabbit:
result of the test shows, the rabbit gavage gives osteoarthrosis nutrition enhancer 50 of the present invention and 100mg/kg, all can suppress rabbit and raise (P<0.05), and inhibitory action continues 1~2 hour, and with contrast, medicine glucosamine hydrochloride (50mg/kg) effect is suitable.
mice with Cmax, oral administration gavage osteoarthrosis composite nourishing energizing agent of the present invention 2g/kg of maximum administration volume after, the mental status is good, autonomic activities is normal, breathe, heart rate is normal, Continuous Observation one week, body weight gain is normal, have no any toxic reaction, without the phenomena of mortality.Therefore, the median lethal dose(LD 50) LD of bone osteoarthrosis composite nourishing energizing agent gastric infusion of the present invention
50
2g/kg.
the clinical trial situation that osteoarthrosis composite nourishing energizing agent prepared by the present invention carries out is as follows:
the index of osteopathia rehabilitation:
1. alleviating pain; 2. anti-inflammation detumescence; 3. keep muscular strength, function of joint; 4. prevention/correct deformity;
5. improve the ADL ability; 6. Saving cortilage, maintain or increase range of motion; 7. no longer recurrence after rehabilitation.
observation item:
1, clinical observation: leading indicator is the parameters for observation on effect total points, and this total points is according to playing the cumulative gained of ankylosis scoring in articular pain, level walking pain, rest pain, morning.Wherein level walking bitterly mark and rest pain scoring according to the VAS pain scores, and play the ankylosis scoring in articular pain and morning according to the scoring of testing program standards of grading (light according to the order of severity, in, heavily be respectively 0,1,2 minutes)
2, lab index: after reaching treatment before treatment, 4,8,12wk does respectively blood, urine, just conventional, electrocardiogram, liver, renal function, blood glucose inspection.
method: 192 routine morning, middle knee osteoarthritis patient are divided into 3 groups at random:
experimental group 64 examples, take 2 courses for the treatment of of osteoarthrosis nutrition enhancer, every day consumption 3.3 grams;
matched group 64 examples give the oral hydrochloride glucosamine 2 courses for the treatment of, every day consumption 3.3 grams;
blank group 64 examples, only used placebo.
result of the test is as following table:
the therapeutic evaluation of table 1 treatment situation improvement rate relatively
discuss:
d-glucosamine is one of main constituent of picked-up formation cartilage proteoglycan, can relax the pain because of arthronosos deformans, and prevents continuing of deterioration.Chondroitin sulfate have the smooth effect in joint that keeps, and participates in manufacturing skeleton.Dimethyl sulfone can be safeguarded the balance of human-body biological element sulphur, by blood circulation and channel invigorating, promotes the conveying of nutrient substance and functional component, the action and efficacy of strengthening D-glucosamine chrondroitin.Collagen protein is the skeleton in skeleton, promotes the basic of osteanagenesis.The dietary supplement that contains single D-glucosamine composition can only relax the osteopathia symptom, can not farthest cure osteopathia, only has by the interaction between them, and the success rate of curing osteopathia just can farthest be improved.Above-mentioned experiment shows:
(1) the taking dose matched group is compared with experimental group, takes the same dosage of D-glucosamine and nutrition enhancer.
(2) the therapeutic effect matched group is compared with experimental group, and general effect is better than the matched group of single use D-glucosamine.。
(3) classical symptom improves main manifestations for greatly shortening time and the pain degree of deadlock in morning, the mobility in increase joint.
conclusion:
the blocking-up inflammation develops, repairs impaired synovial membrane and cartilage, is the important step of curing joint disease.Result shows: the osteoarthrosis nutrition enhancer of taking synthetic prescription will obviously be better than taking merely the dietary supplement of D-glucosamine composition to the therapeutic effect of osteopathia.
embodiment
below in conjunction with embodiment, the present invention is described, the scheme of embodiment described here, do not limit the present invention, one of skill in the art can make improvements and change according to spirit of the present invention, described these improvement and variation all should be considered as within the scope of the invention, and scope of the present invention and essence are limited by claim.Active component Herba Epimedii extract used, Olibanum extract have commercially available, also can be by the method preparation of embodiment.
glucosamine hydrochoride is bought in ZHEJIANG AOXING BIOTECHNOLOGY CO., LTD.
chondroitin sulfate is bought in the precious bio tech ltd of Shandong benefit.
dimethyl sulfone is bought in Wuhan Yi Huacheng Chemical Industry Science Co., Ltd.
collagen protein is bought in holy day science and technology of Tianjin gold limitedcompany
.
hyaluronic acid is bought in Hubei Yuancheng Pharmaceutical Co., Ltd..
embodiment 1
glucosamine hydrochoride 500mg/ sheet
chrondroitin/MSM design of mixture (be take ratio of weight and number as chondroitin sulfate: dimethyl sulfone: collagen protein: Olibanum: hyaluronic acid 2:3:1:1:3) 396mg/ sheet
olibanum extract: 33.3mg calcium phosphate: 4mg sodium borate: 13.3mg
vitamin C: 60mg manganese sulfate: 2mg methylcellulose: 3mg
burnt sugar coloring: 2mg microcrystalline Cellulose: 3mg silicon dioxide: 3mg
titanium dioxide: 4mg magnesium stearate: 3mg palm wax: 0.8mg.
olibanum extract: refer to clean Olibanum, with hanging down solubility 60% ethanol (w/w) vlil 2 hours, extract three times, merge extractive liquid,, after carrying out purification process, concentrated, oven drying at low temperature gets final product.
embodiment 2
glucosamine hydrochoride 500mg/ sheet chrondroitin/MSM design of mixture 396mg/ sheet
herba Epimedii extract: 33.3mg calcium phosphate: 4mg sodium borate: 13.3mg
vitamin C: 60mg manganese sulfate: 2mg methylcellulose: 3mg
burnt sugar coloring: 2mg microcrystalline Cellulose: 3mg silicon dioxide: 3mg
titanium dioxide: 4mg magnesium stearate: 3mg palm wax: 0.8mg;
it is by take ratio of weight and number as chondroitin sulfate for described chrondroitin/MSM mixture: dimethyl sulfone: collagen protein: Olibanum: hyaluronic acid 2:3:1:1:3.
herba Epimedii extract: refer to clean Olibanum, with hanging down solubility 40% ethanol (w/w) vlil 3 hours, extract three times, merge extractive liquid,, after carrying out purification process, concentrated, oven drying at low temperature gets final product.
embodiment 3
glucosamine hydrochoride 500mg/ sheet
chrondroitin/MSM design of mixture 396mg/ sheet
herba Epimedii extract: 60.5mg Olibanum extract: 33.3mg sodium borate: 13.3mg
vitamin C: 60mg manganese sulfate: 2mg methylcellulose: 3mg
burnt sugar coloring: 2mg microcrystalline Cellulose: 3mg silicon dioxide: 3mg
titanium dioxide: 4mg magnesium stearate: 3mg palm wax: 0.8mg
calcium phosphate: 4mg.
it is by take ratio of weight and number as chondroitin sulfate for described chrondroitin/MSM mixture: dimethyl sulfone: collagen protein: Olibanum: hyaluronic acid 2:3:1:1:3.
herba Epimedii extract: refer to clean Herba Epimedii, with hanging down solubility ethanol (35%) vlil 3 hours, extract three times, merge extractive liquid,, after carrying out purification process, concentrated, oven drying at low temperature gets final product.
olibanum extract: refer to clean Olibanum, with hanging down solubility ethanol (35%) vlil 2 hours, extract three times, merge extractive liquid,, after carrying out purification process, concentrated, oven drying at low temperature gets final product.
embodiment 4
the preparation of embodiment 1-3 tablet:
By the above-mentioned raw materials mix homogeneously, add appropriate 10% hydroxypropyl methylcellulose solution to granulate, drying, then add carboxymethyl starch sodium, magnesium stearate, mix, tabletting.
Claims (9)
1. an osteoarthrosis composite nourishing energizing agent, it is characterized in that it is comprised of glucosamine hydrochoride, chrondroitin/MSM mixture, Chinese medicine extract, wherein glucosamine hydrochoride: chrondroitin/MSM mixture: the ratio of weight and number of Chinese medicine extract is 350-600 part: 350-450 part: 16-60 part; It take ratio of weight and number as chondroitin sulfate by chondroitin sulfate, dimethyl sulfone, collagen protein, Olibanum, hyaluronic acid described chrondroitin/MSM mixture: dimethyl sulfone: collagen protein: Olibanum: hyaluronic acid 2:3:1:1:3 forms; Described Chinese medicine extract refers to Olibanum extract or/and Herba Epimedii extract.
2. osteoarthrosis composite nourishing energizing agent claimed in claim 1, Chinese medicine extract wherein refers to pulverizes clean Olibanum or Herba Epimedii, with 35%-60% alcoholic solution reflux 2-3 hour, extract three times, merge extractive liquid,, after carrying out purification process, concentrated, oven drying at low temperature gets final product.
3. osteoarthrosis composite nourishing energizing agent claimed in claim 1, wherein the molecular weight of collagen protein is 1000 dalton.
4. osteoarthrosis composite nourishing energizing agent claimed in claim 1, hyaluronic acid wherein refers to molecular weight from 5,000 to 2,000 ten thousand Dao Er.
5. osteoarthrosis composite nourishing energizing agent claimed in claim 4, it is 5000 Dao Er that hyaluronic acid wherein refers to molecular weight.
6. osteoarthrosis composite nourishing energizing agent claimed in claim 1, hardening agent wherein refers to oral formulations.
7. osteoarthrosis composite nourishing energizing agent claimed in claim 6, oral formulations wherein refers to tablet or capsule.
8. the described osteoarthrosis composite nourishing energizing agent of claim 1 improves the application in Senile degenerative osteopathia medicine in preparation.
9. the described osteoarthrosis composite nourishing energizing agent of claim 1 improves the application in medicine for treating osteoporosis in preparation.
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Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN105770864A (en) * | 2016-04-08 | 2016-07-20 | 杭州合研科技有限公司 | Composition with function of relieving joint inflammation pain |
CN106072651A (en) * | 2016-07-19 | 2016-11-09 | 山东明仁福瑞达制药股份有限公司 | A kind of have compositions increasing bone density, anti-inflammatory and analgesic effect and preparation method thereof |
CN110946874A (en) * | 2019-12-27 | 2020-04-03 | 华熙生物科技股份有限公司 | Hyaluronic acid composition for relieving osteoarthritis |
CN111280447A (en) * | 2018-12-07 | 2020-06-16 | 解冰 | Composite nanometer preparation for treating and recovering bone joint function and preparation method thereof |
CN112826925A (en) * | 2021-04-12 | 2021-05-25 | 仕医堂(吉林)生物药业有限公司 | Traditional Chinese medicine liquid for treating osteoarticular diseases and preparation method thereof |
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Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1364464A (en) * | 2002-01-29 | 2002-08-21 | 郑刚 | Aminoglucose hydrochloride medicinal composition |
CN1771046A (en) * | 2003-04-11 | 2006-05-10 | 协和发酵工业株式会社 | Preventive or therapeutic agent for arthritis |
US20080138417A1 (en) * | 2006-11-22 | 2008-06-12 | Charles Grigsby | Topical Composition And Method Of Forming |
WO2009153200A1 (en) * | 2008-06-18 | 2009-12-23 | Gertrud Langhoff | Preparation containing glucosamine and/or chondroitin for prophylaxis and treatment of arthrosis and for supporting the immune system |
CN101961110A (en) * | 2010-10-14 | 2011-02-02 | 马宏达 | Preparation method of functional food for nourishing cartilage and resisting joint inflammation |
CN103039997A (en) * | 2013-01-11 | 2013-04-17 | 湖南映荷生物科技有限公司 | Health-care food composition for increasing bone mineral density and preparation method |
-
2013
- 2013-09-22 CN CN2013104286681A patent/CN103463624A/en active Pending
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1364464A (en) * | 2002-01-29 | 2002-08-21 | 郑刚 | Aminoglucose hydrochloride medicinal composition |
CN1771046A (en) * | 2003-04-11 | 2006-05-10 | 协和发酵工业株式会社 | Preventive or therapeutic agent for arthritis |
US20080138417A1 (en) * | 2006-11-22 | 2008-06-12 | Charles Grigsby | Topical Composition And Method Of Forming |
WO2009153200A1 (en) * | 2008-06-18 | 2009-12-23 | Gertrud Langhoff | Preparation containing glucosamine and/or chondroitin for prophylaxis and treatment of arthrosis and for supporting the immune system |
CN101961110A (en) * | 2010-10-14 | 2011-02-02 | 马宏达 | Preparation method of functional food for nourishing cartilage and resisting joint inflammation |
CN103039997A (en) * | 2013-01-11 | 2013-04-17 | 湖南映荷生物科技有限公司 | Health-care food composition for increasing bone mineral density and preparation method |
Non-Patent Citations (2)
Title |
---|
J. E. DECHANT 等: ""Effects of glucosamine hydrochloride and chondroitin sulphate, alone and in combination, on normal and interleukin-1 conditioned equine articular cartilage explant metabolism"", 《EQUINE VETERINARY JOURNAL》, vol. 37, no. 3, 31 May 2005 (2005-05-31), pages 227 - 231 * |
无: ""自然之宝葡萄糖胺软骨素MSM复合营养片"", 《百度百科》, 16 January 2012 (2012-01-16) * |
Cited By (10)
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CN106072651B (en) * | 2016-07-19 | 2019-08-23 | 山东明仁福瑞达制药股份有限公司 | It is a kind of with increasing bone density, composition of anti-inflammatory and analgesic effect and preparation method thereof |
CN111280447A (en) * | 2018-12-07 | 2020-06-16 | 解冰 | Composite nanometer preparation for treating and recovering bone joint function and preparation method thereof |
CN110946874A (en) * | 2019-12-27 | 2020-04-03 | 华熙生物科技股份有限公司 | Hyaluronic acid composition for relieving osteoarthritis |
CN112826925A (en) * | 2021-04-12 | 2021-05-25 | 仕医堂(吉林)生物药业有限公司 | Traditional Chinese medicine liquid for treating osteoarticular diseases and preparation method thereof |
CN112826925B (en) * | 2021-04-12 | 2022-09-06 | 仕医堂(吉林)生物药业有限公司 | Traditional Chinese medicine liquid for treating osteoarticular diseases and preparation method thereof |
CN113662739A (en) * | 2021-08-20 | 2021-11-19 | 刘浩泉 | Ice compress and manufacturing method thereof |
CN116726141A (en) * | 2023-08-09 | 2023-09-12 | 华润圣海健康科技有限公司 | Composition for preventing and relieving osteoarthropathy and application thereof |
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