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CN106974992A - A kind of composition for increasing bone density and its application - Google Patents

A kind of composition for increasing bone density and its application Download PDF

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Publication number
CN106974992A
CN106974992A CN201710233326.2A CN201710233326A CN106974992A CN 106974992 A CN106974992 A CN 106974992A CN 201710233326 A CN201710233326 A CN 201710233326A CN 106974992 A CN106974992 A CN 106974992A
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weight
parts
concentrate
safflower
composition
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马志新
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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K36/00Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
    • A61K36/18Magnoliophyta (angiosperms)
    • A61K36/88Liliopsida (monocotyledons)
    • A61K36/889Arecaceae, Palmae or Palmaceae (Palm family), e.g. date or coconut palm or palmetto
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/70Carbohydrates; Sugars; Derivatives thereof
    • A61K31/7008Compounds having an amino group directly attached to a carbon atom of the saccharide radical, e.g. D-galactosamine, ranimustine
    • AHUMAN NECESSITIES
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    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/70Carbohydrates; Sugars; Derivatives thereof
    • A61K31/7012Compounds having a free or esterified carboxyl group attached, directly or through a carbon chain, to a carbon atom of the saccharide radical, e.g. glucuronic acid, neuraminic acid
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61K31/70Carbohydrates; Sugars; Derivatives thereof
    • A61K31/715Polysaccharides, i.e. having more than five saccharide radicals attached to each other by glycosidic linkages; Derivatives thereof, e.g. ethers, esters
    • A61K31/716Glucans
    • A61K31/722Chitin, chitosan
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    • A61K36/00Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
    • A61K36/11Pteridophyta or Filicophyta (ferns)
    • A61K36/12Filicopsida or Pteridopsida
    • A61K36/126Drynaria
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    • A61K36/236Ligusticum (licorice-root)
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    • A61K36/32Burseraceae (Frankincense family)
    • A61K36/328Commiphora, e.g. mecca myrrh or balm of Gilead
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    • A61K36/65Paeoniaceae (Peony family), e.g. Chinese peony
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    • A61K36/185Magnoliopsida (dicotyledons)
    • A61K36/71Ranunculaceae (Buttercup family), e.g. larkspur, hepatica, hydrastis, columbine or goldenseal
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    • A61K36/736Prunus, e.g. plum, cherry, peach, apricot or almond
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    • A61K36/75Rutaceae (Rue family)
    • A61K36/758Zanthoxylum, e.g. pricklyash
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    • A61K36/185Magnoliopsida (dicotyledons)
    • A61K36/81Solanaceae (Potato family), e.g. tobacco, nightshade, tomato, belladonna, capsicum or jimsonweed
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    • A61K36/896Liliaceae (Lily family), e.g. daylily, plantain lily, Hyacinth or narcissus
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23VINDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
    • A23V2002/00Food compositions, function of food ingredients or processes for food or foodstuffs
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    • A61K2236/30Extraction of the material
    • A61K2236/33Extraction of the material involving extraction with hydrophilic solvents, e.g. lower alcohols, esters or ketones
    • A61K2236/331Extraction of the material involving extraction with hydrophilic solvents, e.g. lower alcohols, esters or ketones using water, e.g. cold water, infusion, tea, steam distillation or decoction
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    • A61K2236/33Extraction of the material involving extraction with hydrophilic solvents, e.g. lower alcohols, esters or ketones
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Abstract

The invention discloses a kind of composition for increasing bone density and its application; composition includes D-Glucose aldehydic acid, aminohexose, chitosan oligosaccharide, chitosan, taurine amino monose, ginseng, cucumber, frankincense, myrrh, Radix Angelicae Sinensis, safflower, safflower, dragon's blood, peach kernel, muskmelon seed, Soil unit, the rhizome of davallia, the parts by weight of radix cyathulae 30, dipsacus root, pericarpium zanthoxyli, Ligusticum wallichii, native copper, the radix paeoniae rubrathe, almond; the problem of said composition can solve abnormality of bone density, fundamentally can prevent and treat osteoporosis.

Description

A kind of composition for increasing bone density and its application
Technical field
The present invention relates to technical field of compositions, and application of the composition in medicine and health food is prepared.
Background technology
With the growth at people's age, the microcirculation of human body can worse and worse, and many elderly's winter legs and feet can be very cool, also Be it has often been said that:People is old, and pin is first old.The circulation of this explanation body is died down, and local blood flow is reduced, the nutriment in blood Can not the tissue of ample supply in time.Especially because the various nutrition required for the reduction of Blood flow, bone timely can not be obtained To supplement, osteotrophy is caused to lack.The elderly changes due to endocrine, and bone mineral is largely lost in, and long-time osteotrophy is not Good, New bone formation (Gegenbaur's cell) effect is reduced, bone information (osteoclast) effect enhancing, forms osteoporosis.
Osteoporosis is a kind of chronic disease process that is complicated, being produced by many factors, is the common of the elderly Disease, frequently-occurring disease, main clinical manifestation are lumbago, deformity, fracture, Respiratory Disturbances etc., wherein fracture is osteoporosis One of most common and serious complication of disease, the quality of life of strong influence people.
Developing osteoporosis rate is high, and harmfulness is big, is paid much attention to by global medical field, and the World Health Organization will It is classified as one of three big diseases of old people.The current people of the whole world about 200,000,000 suffers from osteoporosis, and its incidence of disease leapt to common disease, multiple The 7th of disease.As aging population becomes clear day by day, especially China can more serious, veteran form in Future population aging Under the situation that society gradually forms, person in middle and old age multiple degenerative disease-osteoporosis and its complication are used as, it has also become One social health problem and the concern for enjoying geriatrist, and the great attention of national governments is caused, therefore will It is set to annual October 20 " international osteoporosis day ".
Osteoporosis is a Complex Diseases, often the result of many factors comprehensive function.Prevent and treat osteoporosis The problem of disease is one sufficiently complex, it is extremely difficult once osteoporosis occur and correcting again.Modern medicine believes that, osteoporosis Disease is a kind of systemic metabolic bone disease, is reduced with bone amount, the Microstructure Fracture of bone is characterized, and causing the fragility of bone increases, Easily fracture.The final purpose of anti-curing osteoporosis is to reduce the generation of fracture, improves the quality of life of the elderly, We can strive for recapturing bone amount, increase bone strength to reach this purpose by delaying and reducing bone loss.It arranges substantially Apply including the sufficient calcium of intake, appropriate physical exertion and prevention bone injury, and give different medicines on this basis and do In advance, it is finally reached the purpose of prevention and treatment fracture.For osteoporosis, at present, the clinical treatment disease is using most The medicines such as estrogen, calcium agent, activated vitamin D, calcitonin and fluoride, although achieve certain curative effect, but western medicine is treated Toxicity adverse reaction be generally existing, such as it is long-term to cause mammary gland and endometrium with the estrogen drugs synthesized Paraplasm, the order use of bis phosphoric acid salt can reduce bone turnover rate, increase bone fragility, and bone can be caused when fluorides are alone Softening, there is allergy in vitamin D class and calcitonin.
The deficiency existed in the treatment relative to doctor trained in Western medicine, traditional Chinese medicine has the excellent of uniqueness in terms of senile osteoporosis is prevented and treated Gesture, while it also avoid the serious side reaction of the western medical treatments such as hormone replacement, has made big in terms of clinical experimental study in recent years Work is measured, there is larger progress.Osteoporosis belongs to " bone withers ", " heumatism " category in traditional Chinese medicine.Traditional Chinese medicine thinks, bone Matter osteoporosis have close relationship with kidney deficiency, insufficiency of the spleen, blood stasis, and wherein kidney deficiency is this sick Etiological, and " multiple deficiency and stasis " are The pathological characteristic of osteoporosis.Therefore, osteoporosis should be basic using kidney in prevention and treatment, based on taste, distinguish Card opinion is controlled, and by invigorating function of kidney and strengthening bone, polishing invigorating the spleen, stagnation resolvation, reaches the purpose of pre- preventing bone rarefaction.Therefore, the present invention is according to the traditional Chinese medical science To the understanding and modern pharmacology of bone, there is provided a kind of pharmaceutical composition with increase bone density effect.
The content of the invention
Therefore, the technical problems to be solved by the invention be provide it is a kind of have increase bone density effect composition and Its preparation method.
In order to solve the above technical problems, the invention provides a kind of composition that there is increase bone density to act on, its raw material Weight is constituted:The parts by weight of cucumber 10-80, the parts by weight of frankincense 2-50, the parts by weight of myrrh 2-50, the weight of Radix Angelicae Sinensis 3-60 Measure part, the parts by weight of safflower 2-30, the parts by weight of safflower 5-50, the parts by weight of dragon's blood 5-50, the parts by weight of peach kernel 3-50, muskmelon seed 10-60 parts by weight, the parts by weight of Soil unit 5-50, the parts by weight of the rhizome of davallia 5-50, radix cyathulae 3--50 parts by weight, the weight of dipsacus root 5-50 Measure part, the parts by weight of pericarpium zanthoxyli 5-50, the parts by weight of Ligusticum wallichii 5-50, the parts by weight of native copper 2-20, the parts by weight of the radix paeoniae rubrathe 5-50, almond 3--50 parts by weight.
It is preferred that, the raw material weight composition of the composition is:50 parts by weight of cucumber, the parts by weight of frankincense 30, system do not have The parts by weight of medicine 30, the parts by weight of Radix Angelicae Sinensis 30, the parts by weight of safflower 20, the parts by weight of safflower 30, the parts by weight of dragon's blood 30, the weight of peach kernel 30 Part, the parts by weight of muskmelon seed 30, the parts by weight of Soil unit 30, the parts by weight of the rhizome of davallia 30, the parts by weight of radix cyathulae 30, the parts by weight of dipsacus root 30, river The parts by weight of green pepper 30, the parts by weight of Ligusticum wallichii 30, the parts by weight of native copper 10, the parts by weight of the radix paeoniae rubrathe 30, the parts by weight of almond 40.
The invention provides a kind of preparation method of composition, comprise the following steps:
(1) Radix Angelicae Sinensis, safflower, safflower are weighed according to selected parts by weight, the mass concentration for adding 10 times of drug weights is 75% ethanol is extracted 2 times, each 1.5h, is merged extract solution and is filtered, and is reclaimed ethanol and is concentrated under reduced pressure into relative density at 60 DEG C 1.20 concentrate I, it is standby;
(2) dragon's blood, peach kernel, muskmelon seed, Soil unit, the rhizome of davallia, radix cyathulae are weighed according to selected parts by weight, adds purifying and carry Take 2 times, add the purified water of 10 times of drug weights to extract 2h for the first time, the purified water of second plus 10 times drug weight extracts 1h, Merge extract solution simultaneously to filter, be concentrated into the concentrate II of relative density 1.15 at 80 DEG C, it is standby;
(3) weigh cucumber according to selected parts by weight, it is frankincense, myrrh, dipsacus root, pericarpium zanthoxyli, Ligusticum wallichii, native copper, red Chinese herbaceous peony, almond, add purified water and extract 2 times, add the purified water of 10 times of drug weights to extract 2h, second plus 10 times of medicines for the first time The purified water of weight extracts 1h, filters, is concentrated under reduced pressure into the concentrate of relative density 1.20 at 60 DEG C, and add 70% ethanol alcohol It is heavy, take supernatant to reclaim ethanol, gained sediment is concentrated under reduced pressure into the concentrate III of relative density 1.15 at 60 DEG C, it is standby;
(4) merge above-mentioned concentrate I, II and III, dry, obtain extract powder, be then made and clinically may be used according to common process The formulation of receiving.
Aforementioned pharmaceutical compositions add customary adjuvant, according to common process be made clinically acceptable capsule, tablet, Granule, mixture, soft extract, pill, electuary, dripping pill, medicinal tea, tincture, vina, beverage, candy or bakery
The invention provides a kind of by above-mentioned pharmaceutical composition addition customary adjuvant, prepared according to common process Pharmaceutical preparation, health food or food.
Medicine or health food with increase bone density effect are being prepared the invention provides above-mentioned pharmaceutical composition Purposes and prepare purposes in the medicine, health food or food of anti-curing osteoporosis.
Beneficial effects of the present invention are as follows:
By changing bone microcirculation, the promoting flow of qi and blood increases Blood flow, while providing sufficient nutrition to bone, promotes Metabolism, improves Bone nutritional condition, improves sclerotin, excludes bone rubbish, repairs the osteocyte of impaired aging, reaches zhuanggu, strong bone, strong Bone increases the purpose of bone density.Due to the increase of CBF in bone, the various nutriments required for bone have been obtained fully Supplement, sclerotin is improved after osteotrophy increase.
Brief description of the drawings
The mouse tibia bone density variation diagram of first group of Normal group of Fig. 1.
The mouse tibia bone density variation diagram of second group of excision both sides ovary group of Fig. 2.
The mouse tibia bone density variation diagram of the 3rd group of excision both sides ovary of Fig. 3 and medication group.
Embodiment
1 prepares composition
The need for present invention experiment, 5 groups of experiments have been carried out according to following table data:
2 preparation methods
(1) ginseng, Radix Angelicae Sinensis, safflower, safflower are weighed according to selected parts by weight, the quality for adding 10 times of drug weights is dense Spend and extracted 2 times for 75% ethanol, each 1.5h merges extract solution and filtered, reclaim ethanol and be concentrated under reduced pressure at 60 DEG C relative The concentrate I of density 1.20, it is standby;
(2) dragon's blood, peach kernel, muskmelon seed, Soil unit, the rhizome of davallia, radix cyathulae are weighed according to selected parts by weight, adds purifying and carry Take 2 times, add the purified water of 10 times of drug weights to extract 2h for the first time, the purified water of second plus 10 times drug weight extracts 1h, Merge extract solution simultaneously to filter, be concentrated into the concentrate II of relative density 1.15 at 80 DEG C, it is standby;
(3) weigh cucumber according to selected parts by weight, it is frankincense, myrrh, dipsacus root, pericarpium zanthoxyli, Ligusticum wallichii, native copper, red Chinese herbaceous peony, almond, add purified water and extract 2 times, add the purified water of 10 times of drug weights to extract 2h, second plus 10 times of medicines for the first time The purified water of weight extracts 1h, filters, is concentrated under reduced pressure into the concentrate of relative density 1.20 at 60 DEG C, and add 70% ethanol alcohol It is heavy, take supernatant to reclaim ethanol, gained sediment is concentrated under reduced pressure into the concentrate III of relative density 1.15 at 60 DEG C, it is standby;
(4) merge above-mentioned concentrate I, II and III, dry, obtain extract powder, D-Glucose aldehydic acid, aminohexose, shell are few Sugar, chitosan, taurine amino monose, are then made clinically acceptable formulation according to common process.
3 rat bone density contrast experiments
(1) animal
SPF grades of SD rats (buying from Beijing Vital River Experimental Animals Technology Co., Ltd.) 60 (about 28 weeks), body weight About 280-300g, is randomly divided into 6 groups, every group 10, wherein being divided into Normal group and medication control group in every group.
(2) experimentation
Under equal conditions fed, administration group is administered according to 1.5% (1500mg/kg) of body weight.Per journal A data are recorded, are fed after completely 90 days, the bone that two sensitive spots of right femur and fl lower end of one group of rat are determined weekly is close Degree.
(3) bone densitometry
U.S.'s HOLOGIG companies QDR-2000 types dual energy X-ray absorptionmetry (coefficient of variation (CV) < 1.0%) is used under anaesthesia Whole body bone mineral content and bone density are scanned, and takes right femur and the sensitive spot of fl lower end two respectively, femur midpoint is measured With the bone density (BMD) of distal end.
(4) experimental data is counted
All data are represented using mean ± standard deviation (X ± SD), are analyzed, compared between group with SPSS statistical softwares With variance analysis, significant difference is examined with q.
(5) result
Left and right side femoral bmd index is apparently higher than control group, and difference has conspicuousness and very significant meaning.
4 ovariectomy mouse are tested
(1) animal
SPF grades of SD Female Rats (buying from Beijing Vital River Experimental Animals Technology Co., Ltd.) 60 (about 16 weeks), body 200g is weighed about, is divided into three groups, first group of operation only cuts off fat, the both sides ovary of second group of excision mouse, the 3rd group of excision mouse Both sides ovary.
(2) same food is fed, the 3rd group of addition composite preparation, is added according to 1.5% (1500mg/kg) of body weight.
(3) after feeding 12 weeks, mouse tibia bone density is determined:
The mouse tibia bone density change of first group of Normal group is not obvious, slightly reduces, such as Fig. 1;
The mouse tibia bone density change of second group of excision both sides ovary group is obvious, hence it is evident that reduction, such as Fig. 2;
The mouse tibia bone density change of 3rd group of excision both sides ovary and medication group is not obvious, hence it is evident that improve, such as Fig. 3.
5 clinical Observation on Bone Mineral Density
(1) samples selection
Criteria of Osteoporosis is used compared with the bone density peak value of local male, is reduced more than 2 standard deviations (SD) For osteoporosis.According to Chinese Adult lumbar spine bmd value, male's peak value was 1.210 ± 0.102g/cm2, at 50~60 years old Age bracket, standard deviation is 0.102, therefore is that osteoporosis is suffered from less than this value using 0.790g/cm2 as Criteria of Osteoporosis Person.
Between case selection in October, -2013 in March, 2013, primary osteoporosis male volunteers 30 are diagnosed as, It is age 61-73 Sui, average 65.2 years old.Treatment group 15, control group 15 are randomly divided into, two groups of ordinary circumstances compare without substantially poor It is different.
(2) instructions of taking
Human oral dosage form is 3g compositions, is taken in the morning and evening, dosage period six months.
(3) process is observed
Two groups of bone density numerical value is measured, administration group bone density averagely improves 12.06%, and control group bone density have dropped 4.58%, there is the raising bone density effect of highly significant.
Group Number BMD (%) before administration BMD (%) after six months BMD rates of change (%)
Administration group 15 72.42±11.32 81.15±11.54 +12.06±5.31
Control group 15 75.22±11.82 71.77±11.66 -4.58±4.13
6 samples are tracked
(1)、ID000427004
Age 72
Sex Female
Height 156cm
Body weight 49kg
First time time of measuring 2011-11-10
First time BMD (g/cm2) 0.4825
Time of measuring after medication 2012-1-12
BMD (g/cm after medication2) 0.5032
(2)、ID02861769
(3)、ID700242064
Birthdate 1945-1-27
Age 66
Sex Female
Height 155cm
Body weight 50kg
First time time of measuring 2011-12-19
First time BMD (g/cm2) 0.431
Time of measuring after medication 2012-2-6
BMD (g/cm after medication2) 0.530
(4)、ID50767298
Birthdate 1953-6-9
Age 58
Sex Female
Height 163cm
Body weight 60kg
First time time of measuring 2012-1-4
First time BMD (g/cm2) 0.806
Time of measuring after medication 2012-2-8
BMD (g/cm after medication2) 0.817
(5)、ID62982
Birthdate 1955-3-15
Age 56
Sex Female
Height 163cm
Body weight 60kg
First time time of measuring 2011-11-10
First time BMD (g/cm2) 0.822
Time of measuring after medication 2011-12-12
BMD (g/cm after medication2) 0.844
(6)、ID18137
Birthdate
Age 67
Sex Female
Height 176cm
Body weight 110kg
First time time of measuring 2011-1-12
First time BMD (g/cm2) 1.014
Time of measuring after medication 2011-12-26
BMD (g/cm after medication2) 1.029
(7)、ID398748
(8)、ID26921
Birthdate 1953-3-19
Age 58
Sex Female
Height 159cm
Body weight 70kg
First time time of measuring 2011-11-10
First time BMD (g/cm2) 0.811
Time of measuring after medication 2012-1-17
BMD (g/cm after medication2) 0.824
(9)、ID20105
Birthdate 1953-3-19
Age 58
Sex Female
Height 159cm
Body weight 71kg
First time time of measuring 2011-11-10
First time BMD (g/cm2) 0.778
Time of measuring after medication 2012-2-2
BMD (g/cm after medication2) 0.824
(10)、ID398748

Claims (7)

1. a kind of increase the composition of bone density, it is characterised in that its raw material weight, which is constituted, is:
The parts by weight of D-Glucose aldehydic acid 5-30, the parts by weight of aminohexose 5-35, the parts by weight of chitosan oligosaccharide 5-50, chitosan 5- 40 parts by weight, ginseng 5-20 amount part, the parts by weight of taurine amino monose 5-50, the parts by weight of cucumber 10-80, frankincense 2- 50 parts by weight, the parts by weight of myrrh 2-50, the parts by weight of Radix Angelicae Sinensis 3-60, the parts by weight of safflower 2-30, the parts by weight of safflower 5-50, The parts by weight of dragon's blood 5-50, the parts by weight of peach kernel 3-50, the parts by weight of muskmelon seed 10-60, the parts by weight of Soil unit 5-50, the rhizome of davallia 5- 50 parts by weight, 10-50 parts of the root bark of Chinese wolf-berry, radix cyathulae 3--50 parts by weight, the parts by weight of dipsacus root 5-50, the parts by weight of pericarpium zanthoxyli 5-50, river The parts by weight of rhizome of chuanxiong 5-50, the parts by weight of native copper 2-20, the parts by weight of the radix paeoniae rubrathe 5-50, almond 3--50 parts by weight.
2. composition according to claim 1, it is characterised in that the raw material weight of the composition, which is constituted, is:D- grapes The parts by weight of uronic acid 20, the parts by weight of aminohexose 20, the parts by weight of chitosan oligosaccharide 20, the parts by weight of chitosan 20, taurine amino monose Sub 50 parts by weight of 20 parts by weight, the parts by weight of ginseng 10, cucumber, the parts by weight of frankincense 30, the parts by weight of myrrh 30, the weight of Radix Angelicae Sinensis 30 Part, the parts by weight of safflower 20, the parts by weight of safflower 30, the parts by weight of dragon's blood 30, the parts by weight of peach kernel 30, the parts by weight of muskmelon seed 30, Soil unit 30 parts by weight, the parts by weight of the rhizome of davallia 30, the parts by weight of the root bark of Chinese wolf-berry 30, the parts by weight of radix cyathulae 30, the parts by weight of dipsacus root 30, the weight of pericarpium zanthoxyli 30 Part, the parts by weight of Ligusticum wallichii 30, the parts by weight of native copper 10, the parts by weight of the radix paeoniae rubrathe 30, the parts by weight of almond 40.
3. a kind of method for preparing composition described in claim 1 or 2, it is characterised in that comprise the following steps:
(1) ginseng, Radix Angelicae Sinensis, safflower, safflower are weighed according to selected parts by weight, the mass concentration for adding 10 times of drug weights is 50-80% ethanol is extracted 1-3 times, each 1-3h, is merged and filtering gained extract solution, is reclaimed ethanol, then subtract gained filtrate Pressure is concentrated into the concentrate I of relative density 1.15-1.25 at 60 DEG C, standby;
(2) dragon's blood, peach kernel, muskmelon seed, Soil unit, the rhizome of davallia, the root bark of Chinese wolf-berry, radix cyathulae are weighed according to selected parts by weight, adds 10 The purified water of times drug weight is extracted 1-3 time, each 1-3 hour, is merged and extract solution obtained by filtering, is then subtracted gained filtrate Pressure is concentrated into the concentrate II of relative density 1.10-1.20 at 80 DEG C, standby;
(3) cucumber, frankincense, myrrh, dipsacus root, pericarpium zanthoxyli, Ligusticum wallichii, native copper, the radix paeoniae rubrathe, apricot are claimed according to selected parts by weight Benevolence, the purified water for adding 10 times of drug weights is extracted 1-3 times, each 1-3 hours, is merged and filtering gained extract solution, by gained Filtrate decompression is concentrated into the concentrate of relative density 1.15-1.25 at 60 DEG C, and adds 50-80% ethanol alcohol precipitations, takes supernatant Ethanol is reclaimed, the concentrate III of relative density 1.10-1.20 at 60 DEG C is concentrated under reduced pressure into, it is standby;
(4) merge above-mentioned concentrate I, II and III, dry, obtain extract powder, add D-Glucose aldehydic acid, aminohexose, shell few Clinically acceptable formulation is made in sugar, chitosan, taurine amino monose, common process.
4. preparation method according to claim 3, it is characterised in that comprise the following steps:
(1) ginseng, Radix Angelicae Sinensis, safflower, safflower are weighed according to selected parts by weight, the mass concentration for adding 10 times of drug weights is 75% ethanol is extracted 2 times, each 1.5h, is merged extract solution and is filtered, and is reclaimed ethanol and is concentrated under reduced pressure into relative density at 60 DEG C 1.20 concentrate I, it is standby;
(2) dragon's blood, peach kernel, muskmelon seed, Soil unit, the rhizome of davallia, the root bark of Chinese wolf-berry, radix cyathulae are weighed according to selected parts by weight, added pure Change and extract 2 times, add the purified water of 10 times of drug weights to extract 2h for the first time, the purified water of second plus 10 times drug weight is extracted 1h, merges extract solution and simultaneously filters, and is concentrated into the concentrate II of relative density 1.15 at 80 DEG C, standby;
(3) cucumber, frankincense, myrrh, dipsacus root, pericarpium zanthoxyli, Ligusticum wallichii, native copper, the radix paeoniae rubrathe, apricot are weighed according to selected parts by weight Benevolence, adds purified water and extracts 2 times, adds the purified water of 10 times of drug weights to extract 2h, second plus 10 times of drug weights for the first time Purified water extract 1h, filter, be concentrated under reduced pressure into the concentrate of relative density 1.20 at 60 DEG C, and add 70% ethanol alcohol precipitation, Take supernatant to reclaim ethanol, gained sediment is concentrated under reduced pressure into the concentrate III of relative density 1.15 at 60 DEG C, it is standby;
(4) merge above-mentioned concentrate I, II and III, dry, obtain extract powder, D-Glucose aldehydic acid, aminohexose, chitosan oligosaccharide, shell Glycan, taurine amino monose, are then made clinically acceptable formulation according to common process.
5. application of the composition in the medicine with increase bone density effect is prepared described in claim 1 or 2.
6. application of the composition in the health food with increase bone density effect is prepared described in claim 1 or 2.
7. application of the composition in the food with increase bone density effect is prepared described in claim 1 or 2.
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