CN104352633A - Preparation method of pharmaceutical composition for treating osteoarthrosis - Google Patents
Preparation method of pharmaceutical composition for treating osteoarthrosis Download PDFInfo
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Abstract
The invention belongs to the field of traditional Chinese medicine preparations, and particularly relates to a preparation method of a pharmaceutical composition for treating osteoarthrosis. According to the preparation method disclosed by the invention, the pharmaceutical composition is prepared from rhizoma cibotii, herba epimedii, radix angelicae pubescentis, drynaria rhizome, teasel root, parasitic loranthus, caulis spatholobi, prepared rehmannia root, elecampane, and processed products of olibanum volatile oil, myrrh essential oil and fructus psoraleae as medicines. The pharmaceutical composition prepared by the method is capable of effectively treating osteoarthritis and lumbar muscle degeneration caused by deficiency of the liver and kidneys, qi-stagnation and blood stasis, and vein stagnation, is capable of effectively reducing hepatic toxic side effects of original products, and has relatively good clinical treatment effects.
Description
Technical field
The invention belongs to field of traditional Chinese, be specifically related to a kind of preparation method being used for the treatment of the pharmaceutical composition of osteoarthritis.
Background technology
Osteoarthritis (osteoarthritis, OA) is a kind of common chronic joint diseases, and its major lesions is degeneration and the Secondary cases hyperosteogeny of articular cartilage.Degenerative osteoarthritis refers to a series of degeneratioies that human body occurs, as arthralgia, stiff and limitation of activity etc., is a kind of comprehensive disease.In its crowd more than 50 years old, sickness rate is only second to heart disease, and the sickness rate in over-65s crowd, up to 60-90%, brings particularly to the life of middle-aged and elderly people painful and inconvenient greatly.
Lumbar muscle strain is also modal a kind of pain in pain in the lumbar region disease, is often used as the general name of the chronic low back pain not having organic change.Lumbar muscle strain is caused by a lot of reasons, and the prolonged and repeated outbreak of its pain, waist is ached or distending pain.Clinical manifestation is, hyperkinesia, then pain of bending over for a long time increase the weight of, and straight waist difficulty, sombre, wet weather can increase the weight of disease.
For above-mentioned osteoarthritis and lumbar muscle strain symptom, Chinese patent CN1931277A discloses a kind of pharmaceutical composition for the treatment of osteoarthritis.Described pharmaceutical composition is made up of Rhizoma Cibotii, Herba Epimedii, Radix Angelicae Pubescentis, Rhizoma Drynariae, Radix Dipsaci, Fructus Psoraleae, Herba Taxilli, Caulis Spatholobi, Radix Rehmanniae Preparata, the Radix Aucklandiae, Olibanum, Myrrha 12 taste Chinese medicine, there is liver and kidney tonifying, nourshing blood and promoting blood circulation, relaxing muscles and tendons and activating QI and blood in the collateral, the functions such as regulating QI to relieve pain, be mainly used in deficiency of the liver and kindey, stagnation of QI and blood, the diseases such as the osteoarthritis caused by obstruction of meridians and collaterals, lumbar muscle strain.And animal and clinical trial display, this medicine has definite curative effect to osteoarthritis, lumbar muscle strain, and obtains the favor of extensive patients.
But said medicine finds to there is certain hepatic injury in Clinical practice process, for this reason, under the prerequisite ensureing drug effect, carrying out reducing hepatic injury research to it by process modification is problem in the urgent need to address.
Summary of the invention
For this reason, there is the problem of certain hepatic injury untoward reaction in the medicine that technical problem to be solved by this invention is to treat in prior art osteoarthritis, so develop the damage of a kind of liver toxicity lower, the preparation method that effectively can treat the pharmaceutical composition of osteoarthritis.
For solving the problems of the technologies described above, the preparation method of the pharmaceutical composition for the treatment of osteoarthritis of the present invention, comprises the steps:
(1) get Olibanum 154-520 weight portion, the mixing of Myrrha 154-520 weight portion, add water and carry out vapor distillation extraction, collect volatile oil, add customary adjuvant and make volatile oil clathrate compound, for subsequent use;
(2) get Fructus Psoraleae 154-520 weight portion, extracting in water, after discarding Aqueous extracts, collect medicinal residues, obtain Fructus Psoraleae processed product, for subsequent use;
(3) Rhizoma Cibotii 290-864 weight portion, Herba Epimedii 154-520 weight portion, Radix Angelicae Pubescentis 154-520 weight portion, Rhizoma Drynariae 224-692 weight portion, Radix Dipsaci 290-864 weight portion, Herba Taxilli 290-864 weight portion, Caulis Spatholobi 154-520 weight portion, Radix Rehmanniae Preparata 692-2076 weight portion, Radix Aucklandiae 154-520 weight portion is got, mix with described Fructus Psoraleae processed product for subsequent use, pulverize, add described volatile oil clathrate compound for subsequent use and customary adjuvant, conveniently technique makes clinical acceptable oral formulations.
Further, the preparation method of described pharmaceutical composition, comprises the steps:
(1) get Olibanum 346.1 weight portion, the mixing of Myrrha 346.1 weight portion, add water and carry out vapor distillation extraction, collect volatile oil, add customary adjuvant and make volatile oil clathrate compound, for subsequent use;
(2) get Fructus Psoraleae 346.1 weight portion, extracting in water, after discarding Aqueous extracts, collect medicinal residues, obtain Fructus Psoraleae processed product, for subsequent use;
(3) Rhizoma Cibotii 576.8 weight portion, Herba Epimedii 346.1 weight portion, Radix Angelicae Pubescentis 346.1 weight portion, Rhizoma Drynariae 462.0 weight portion, Radix Dipsaci 576.8 weight portion, Herba Taxilli 576.8 weight portion, Caulis Spatholobi 346.1 weight portion, Radix Rehmanniae Preparata 1384.2 weight portion, the Radix Aucklandiae 346.1 weight portion is got, mix with described Fructus Psoraleae processed product for subsequent use, pulverize, add described volatile oil clathrate compound for subsequent use and customary adjuvant, conveniently technique makes clinical acceptable oral formulations.
Preferably, the preparation method of described pharmaceutical composition, comprises the steps:
(1) get described Olibanum and Myrrha mixing according to selected weight portion, add 8-12 times of water gaging and carry out vapor distillation extraction 8-15 hour, collect volatile oil, add customary adjuvant and make volatile oil clathrate compound, for subsequent use;
(2) get described Fructus Psoraleae according to selected weight portion, add 6-10 times amount water extraction 1-3 time, each 0.5-2 hour, after discarding Aqueous extracts, collect medicinal residues, be drying to obtain Fructus Psoraleae processed product, for subsequent use;
(3) Rhizoma Cibotii, Herba Epimedii, Radix Angelicae Pubescentis, Rhizoma Drynariae, Radix Dipsaci, Herba Taxilli, Caulis Spatholobi, Radix Rehmanniae Preparata, the Radix Aucklandiae is got according to selected weight portion, mix with described Fructus Psoraleae processed product for subsequent use, pulverize, add described volatile oil clathrate compound for subsequent use and customary adjuvant, conveniently technique makes clinical acceptable oral formulations.
More excellent, the preparation method of described pharmaceutical composition, comprises the steps:
(1) get described Olibanum and Myrrha mixing according to selected weight portion, add 10 times of water gagings and carry out vapor distillation and extract 12 hours, collect volatile oil, add customary adjuvant and make volatile oil clathrate compound, for subsequent use;
(2) get described Fructus Psoraleae according to selected weight portion, add 8 times amount water extraction 2 times, each 1 hour, after discarding Aqueous extracts, collect medicinal residues, be drying to obtain Fructus Psoraleae processed product, for subsequent use;
(3) Rhizoma Cibotii, Herba Epimedii, Radix Angelicae Pubescentis, Rhizoma Drynariae, Radix Dipsaci, Herba Taxilli, Caulis Spatholobi, Radix Rehmanniae Preparata, the Radix Aucklandiae is got according to selected weight portion, mix with described Fructus Psoraleae processed product for subsequent use, pulverize, add described volatile oil clathrate compound for subsequent use and customary adjuvant, conveniently technique makes clinical acceptable oral formulations.
In described step (1), the customary adjuvant preparing described volatile oil clathrate compound comprises beta-schardinger dextrin-, water and ethanol.
In described step (1), the mass ratio of described volatile oil, beta-schardinger dextrin-, water and ethanol is 1:8-12:16-24:1-2.
The mass ratio of described volatile oil, beta-schardinger dextrin-, water and ethanol is 1:10:20:1.
Described Olibanum and/or Myrrha are processed with vinegar.
The invention also discloses the pharmaceutical composition prepared by described preparation method, and add customary adjuvant by aforementioned pharmaceutical compositions, conveniently the clinical acceptable oral formulations made of technique.
Preparation method of the present invention is improved on the basis of existing product, the pharmaceutical composition of described treatment osteoarthritis is made up of medical materials such as Fructus Psoraleae, Rhizoma Drynariae, Radix Dipsaci, Herba Epimedii, Radix Angelicae Pubescentis, the Radix Aucklandiae, Caulis Spatholobi and Rhizoma Cibotii, is mainly used in deficiency of the liver and kindey, qi depression to blood stasis, osteoarthritis caused by the resistance of venation numbness and the disease such as lumbar muscle strain.The method of pharmaceutical compositions of the present invention is used as medicine with the volatile oil of Olibanum and Myrrha and Fructus Psoraleae processed product, on the basis keeping existing product drug effect, greatly reduce the liver toxicity side effect of original product further, make product have better medical value and market prospect.
Experimental example
Experimental example 1 pharmacodynamic experiment
1 material
1.1 animal
Hartley Cavia porcellus, regular grade, SD rat, KM mice, SPF level, purchased from Beijing HFK Bio-Technology Co., Ltd., the quality certification number: SCXK (capital) 2009-0004; Raise in Tianjin University Of Traditional Chinese Medicine's Experimental Animal Center, keep Animal House quiet, ventilate, dry, room temperature 18 ~ 25 DEG C, humidity 40% ~ 70%, freely ingests, drinks water.
1.2 by reagent
New technology pill prepared by embodiment 1;
ZHUANGGU GUANJIE WAN, China Resources Sanjiu Medical & Pharmaceutical Co., Ltd..
Experimental administration dosage is with reference to clinical people's dosage of ZHUANGGU GUANJIE WAN: 12g/d, each dosage in experiment all amounts to into corresponding dosage according to different genera animal.
1.3 reagent
Glucosamine hydrochloride capsule (Zhejiang Cheng Yi Pharmaceutical Co., Ltd);
Papain, F127 (Sigma company);
0.5% eosin stains liquid, haematoxylin dyeing liquid (Wu Teng KCC);
Fibroblast collagenase (MMP-1), Fibroblast collagenase inhibitor (TIMP-1) Elisa test kit (Cusabio); TIMP-1 and MMP-3ELISA test kit (Wuhan You Ersheng company); UNIQ-10column Trizol total RNA extraction reagent box (Shanghai Sheng Gong biological engineering limited company); MProm II Reverse Transcription System Reverse Transcriptase kit (Promega); FastStart Universal CYBR Green test kit (Roche); BCA protein detection kit (Beyotime);
Alkali phosphatase (AKP), Bioengineering Research Institute is built up in Nanjing;
Benzalkonium bromide solution, Jingdone district, Jiangxi pharmaceutcal corporation, Ltd;
Benzylpenicillin sodium for injection, middle promise Pharmaceutical (Shijiazhuang) company limited;
Glacial acetic acid, Tianjin Chemical Reagents Factory No.1;
Formaldehyde, Tianjin Fengchuan Chemical Reagent Science & Technology Co., Ltd.;
Dimethylbenzene, Tianjin, Tianjin is by Fine Chemical Co., Ltd.
1.4 instrument
JJ3000 electronic balance, JJ2000 precision electronic balance (Changshu Shuan Jie test instrunment factory);
YLS-Q4 ear swells card punch (Jinan Yi Yan development in science and technology company limited);
HSS-1 (B) thermostatic bath (Chengdu Instruement Factory);
MEK-6318K type cellanalyzer (Nihon Kohden Corporation);
Nucleic acid-protein analyser-DU800, Allegra 64R High-Speed Centrifuge (BeckmanCoulter); Real-time RT-PCR System, Prism7500 (Applied Biosystem); PCR-C1000 type PCR instrument, C1000Touch Thermal Cycler (Bio-Rad); The multi-functional microplate reader of FlexStation3 (Molecular Devices); MODEL 1012 type hybridization case (SHEL LAB); ASP300S Full automatic sealing dewaterer, RM2135 microtome (Leica); BMJ-1 biological tissue embedding machine (Tianjin Aviation Mechano-Electrical Co.); Photomicroscope (OLYMPUS); Ultrasonic Cell Disruptor (UIBRA); MEK-7222K Automatic Blood Cell Analyzer (Japanese photoelectricity industry Zhu Shi people's commune);
IKA/T18 refiner (1KA); KJ-201A type agitator (Jiangsu Kangjian Medical Apparators Co., Ltd.);
QL-901 type turbine mixer (its woods Bel instrument manufacturing company limited of Haimen City);
MilliQ pure water system (Millipore company).
2 methods
2.1 osteoarthritis treatment Effect study
2.1.1 to the therapeutical effect of the spontaneous osteoarthritis of hareley Cavia porcellus
Get hartley Cavia porcellus, female, be divided into model group (matched group) at random, ZHUANGGU GUANJIE WAN group (0.96g/kg) and present composition high dose (1.92g/kg), middle dosage (0.96g/kg), low dosage (0.48g/kg) 5 dosage groups, often organize 10.After the spontaneous osteoarthritis model of 5 monthly age Cavia porcellus is formed, start administration, model group gives respective volume distilled water, successive administration 4 weeks.Observe animal general state every day, claim the weight of animals and appetite on every Mondays, abdominal aortic blood after last administration, detect the content of MMP-1, TIMP-1 in serum.The articular cartilage cut after sacrifice of animal between tibia to femur carries out histopathological examination.
2.1.2 to the treatment of the rat bone arthritis chronica phase of Papain enzyme induction
Select healthy male SD rat, by the chloral hydrate anesthesia of 0.3g/kg body weight lumbar injection 10%, load 4% papain with 35% poloxamer medicine carrying body and make temperature sensitive type in-situ gel controlled release agent (pH5.7), according to 0.05mL (1.6U)/joint dosage, bilateral knee joint injection, be placed in special couveuse by modeling animal knee joint and with lower limb body, under 50 DEG C of environment, insulation effect 2 hours, can cause the damage of cartilage.Randomly draw 3/10 rat and carry out histopathologic examination, check reliability and the success rate of model.
Select the successful osteoarthritis rat of modeling 40, be divided into model group, ZHUANGGU GUANJIE WAN group, the present composition 2.20g/kg, 1.10g/kg and 0.55g/kg dosage group at random, often organize 8.Select healthy male SD rat 8 else, as a control group.ZHUANGGU GUANJIE WAN and the present composition, according to setting dosage gastric infusion, are treated 4 weeks, matched group and model group gavage equal-volume distilled water continuously.
After treatment terminates, anaesthetize by the chloral hydrate of 0.3mL/100g body weight lumbar injection 10%, abdominal aortic blood.Open left knee joint cavity, repeatedly rinse 3 times with 1mL normal saline, collect joint fluid, centrifugal 10 minutes of 3000r/min, get supernatant ,-20 DEG C save backup.With the surface cartilage in pocket knife scraping rat femur articular surface and tibial prosthesis face, weigh, put into 400 μ l Trizol, deposit for subsequent use for-80 DEG C, adopt real-time quantitative RT-PCR method to measure cartilage of rats iNOS, Aggrecan and Collegan II mrna expression.Take whole right knee joint 10% formalin to fix.Measure the content of joint fluid MMP-3 and TIMP-1 by ELISA method, design of primers is in table 1.
Conventional Trizol method extracts total serum IgE, estimates the purity of nucleic acid according to the value of OD260/OD280.Real-time RT-PCR method is adopted to measure cartilage of rats Aggrecan and Collegan-II mrna expression.Get 2-△ △ CT value and carry out data statistics.
Table 1 Real-time RT-PCR primer sequence
Get fixing right knee joint, formalin is removed, replace to 5% salpeter solution and carry out decalcification.Routine paraffin wax embedding, HE dyeing, carry out histopathologic examination under light microscopic.
The data obtained is all added up with SPSS 17.0 software, and data are used
represent, measuring result more all adopts variance analysis between respectively organizing, and P<0.05 is that difference has statistical significance.
2.2 analgesic activity
2.2.1 mouse hot-plate experiment
Select KM mice, female, by it by being only placed on 55 DEG C of metal fever board slots, constant temperature change is in ± 0.5 DEG C, and timing from mice puts into hot plate groove, to lick metapedes for pain indicator reaction.Test advance action thing screening, is less than 5s the response latency or be greater than 30s animal reject, choose qualified KM mice 60, be divided into matched group at random; ZHUANGGU GUANJIE WAN high dose group (3.08g/kg); Present composition high dose group (3.08g/kg), middle dosage group (1.54g/kg), low dose group (0.77g/kg) 5 dosage groups.Administration every day 1 time, matched group gives corresponding dosage distilled water, administration 14 days, measures the pain threshold of mice, the difference between comparative experiments group and matched group with hot plate method (55 DEG C ± 0.5 DEG C).
2.2.2 mice acetic acid twisting is tested
Choose KM mice 60, male and female half and half, grouping, administration are tested with 2.2.1 mouse hot-plate, after last administration 30min, by 0.2mL/ only, lumbar injection 0.7% glacial acetic acid, observes and writhing sum after recording injection in 5-10min, 11-15min and 16-20min time period in the writhing number of times of mice and 15min, the difference between comparative experiments group and matched group.
2.3 antiinflammatory action
2.3.1 the swollen experiment of mice dimethylbenzene ear
Choose KM mice 60, female, grouping, administration are tested with 2.2.1 mouse hot-plate, 30min after last administration, in mouse right ear tow sides even spread 100% dimethylbenzene proinflammatory agent 0.03mL/ only, swelling (mg) is calculated, the difference between comparative experiments group and matched group by the dimethylbenzene ear method that swells.2.3.2 the swollen experiment of rat granuloma
Choose rat 60, male, be divided into matched group at random; ZHUANGGU GUANJIE WAN high dose group (2.20g/kg); Present composition high dose group (2.20g/kg), middle dosage group (1.10g/kg); Low dose group (0.55g/kg) 5 dosage groups.Take rat granuloma to swell model method rat et al. Ke cotton balls, after 24h, according to dosage set continuous gavage 14d, matched group gives respective volume distilled water, administration every day 1 time, after last administration, puts to death animal, cotton balls and granulation tissue are extracted in the lump, weighs, record weight in wet base.Weigh after 60 DEG C of dry 24h, be dry weight, deduct original cotton balls weight, be granulation net weight, compare the difference between administration group and matched group.
3 results
3.1 osteoarthritis treatment effects
3.1.1 to the therapeutical effect of the spontaneous osteoarthritis of hareley Cavia porcellus
Form the Cavia porcellus of spontaneous osteoarthritis, successive administration is after 4 weeks, and body weight there was no significant difference compared with model group of each administration treated animal, MMP-1 and TIMP-1 value is all higher than model group.Histopathological examination shows, and obvious cartilaginous tissue degeneration occurs model group animal knee joint, as not obvious in cartilage four-layer structure, and cells of superficial layer comes off, the phenomenons such as a small amount of cell infiltration and chondrocyte necrosis; Each administration group compares with model group, and knee cartilage regression is all suppressed or delay (see table 2, Fig. 1).
Table 2 ZHUANGGU GUANJIE WAN and the present composition are on the impact of guinea pig serum MMP-1, TIMP-1
3.1.2 to the treatment of the rat bone arthritis chronica phase of Papain enzyme induction
As shown result shown in 3-1, to the osteoarthritis chronic phase rat articular liquid MMP-3 content of Papain enzyme induction higher than Normal group (P < 0.01), the changes of contents of TIMP is not obvious (P > 0.05), and the ratio of MMP-3/TIMP-1 increases, the content of MMP-3 increases (P < 0.01) relatively, with ZHUANGGU GUANJIE WAN 1.10g/kg and new technology 2.20g/kg, 1.10g/kg treatment 4 weeks, MMP-3 content obviously reduces (P < 0.01), the concentration ratio of MMP-3/TIMP-1 trends towards balance.
Table 3-1 ZHUANGGU GUANJIE WAN and the present composition are on the impact of joint fluid MMP-3 and TIMP-1
Note: compare with matched group, * * P<0.01; Compare with model group, #P<0.05, ##P<0.01
As shown result shown in 3-2, OA chronic phase cartilage of rats Collagen II mRNA and Aggrecan mRNA obviously weakens (P < 0.05 or P < 0.01), treat 4 weeks with ZHUANGGU GUANJIE WAN and the present composition, present composition 2.20g/kg dosage group rabbit cartilage Collagen II mrna expression obviously strengthens (P < 0.01), ZHUANGGU GUANJIE WAN 1.10g/kg and present composition 2.20g/kg, 1.10g/kg dosage group Aggrecan mrna expression all obviously strengthens, wherein present composition 1.10g/kg dosage group and model group difference have statistical significance (P < 0.01).Result shows that ZHUANGGU GUANJIE WAN and the present composition can promote the synthesis of Collagen II and Aggrecan, has certain anti-cartilage injury's effect, can delay the process of cartilage degeneration.
Table 3-2 ZHUANGGU GUANJIE WAN and the present composition are on the impact of cartilage CollagenII, AggrecanmRNA
Note: compare with matched group, * P < 0.05, * * P < 0.01; Compare with model group, #P < 0.05, ##p < 0.01
OA rat articular histopathologic examination finds, gross examination of skeletal muscle: ZHUANGGU GUANJIE WAN and present composition treatment group: rat articular pathological changes is slightly lighter than model group.PATHOMORPHOLOGICAL OBSERVATION OF PULLORUM: ZHUANGGU GUANJIE WAN and the present composition 2.20g/kg, 1.10g/kg dosage treatment group: compared with model group, cartilaginous tissue necrosis reduces, and necrotic area remains more chondrocyte, not of uniform size, arrangement disorder, some tufted arrangements.
3.2 analgesic activity
3.2.1 hot-plate display
30min after medicine, compared with matched group, in the pain response time (p<0.01) of the present composition three dosage groups equal energy significant prolongation mice, has good analgesic activity; 60min after medicine, only has the middle dosage group of the present composition to show good analgesic effect (p<0.05); 120min after medicine, each administration group is without analgesic effect (the results are shown in Table 4).
Table 4. ZHUANGGU GUANJIE WAN and the present composition are on the impact in mouse hot-plate pain response time
Note: compare with matched group, through t inspection,
*p<0.05,
*p<0.01,
* *p<0.001
3.2.2 acetic acid twisting experiment
Result shows, and after injecting algogen acetic acid to mice, the present composition three dosage groups all have certain inhibitory action to mouse writhing number of times, and You Yigao, middle dosage analgesic effect are significantly (see table 5).
Table 5. ZHUANGGU GUANJIE WAN and the present composition are on the impact of mice acetic acid twisting number of times
Note: compare with matched group,
*p<0.05,
*p<0.01,
* *p<0.001
3.3 antiinflammatory action
The swollen experiment of mice dimethylbenzene ear and the swollen experiment display of rat granuloma, the present composition can suppress the Mice Auricle topical acute inflammation caused by dimethylbenzene and rat granuloma to swell hypertrophy, effectively reduces the acute inflammation of Mouse and rat and the generation (see table 6,7) of chronic inflammatory disease.
The impact that table 6. ZHUANGGU GUANJIE WAN and the present composition swell on mice caused by dimethylbenzene xylene ear
Note: compare with matched group,
*p<0.05,
*p<0.01,
* *p<0.001.
The impact that table 7. ZHUANGGU GUANJIE WAN and the present composition swell on rat granuloma
Note: compare with matched group,
*p<0.05,
*p<0.01,
* *p<0.001
Experimental example 2 toxicity test
1, materials and methods
1.1 test sample
The present composition prepared by embodiment 1, China Resources Sanjiu Medical & Pharmaceutical Co., Ltd., the black watered pill, gas fragrance, mildly bitter flavor;
1.2 reference substance
ZHUANGGU GUANJIE WAN, China Resources Sanjiu Medical & Pharmaceutical Co., Ltd., the black watered pill, gas fragrance, mildly bitter flavor.1.3 compound method
The present composition and reference substance are without the need to preparation, and according to the body weight measured the last before every animal drugs, determine the dosage (remaining to arithmetic point 1) of every animal, the amount of taking of the present composition should control at theoretical dosage ± 0.2g.Dosage is by raw medicine calculation, and 1 gram of new technology (prepared by embodiment 1) is equivalent to 1.13 grams of crude drugs, and 1 gram of ZHUANGGU GUANJIE WAN is equivalent to 1 gram of crude drug.
2, experimental system
Beagle dog, regular grade, 60, male and female half and half; The animal monthly age: when administration starts, animal was 6 ~ 7 monthly ages; The weight of animals: the weight of animals when administration starts: 5.33-6.67kg (♂), 5.44-7.84kg (♂); Laboratory animal is originated: Beijing Marshall Biotechnology Co., Ltd; Laboratory animal production licence number: SCXK (capital) 2011-0003; The Quality of Experimental Animals quality certification is numbered: 0234473; Production licence signs and issues unit: Science and Technology Commission of Beijing.
3, EXPERIMENTAL DESIGN
3.1 test grouping and dosages
According to the weight of animals that (D-2) before administration measures, select the animal that quarantine is qualified, healthy, body weight is close, use the random number of computer system, animal is carried out section random packet according to sex.Each treated animal dosage and the animal number after dividing into groups see the following form 8:
The each tested treated animal dosage design of table 8
Note:
a: body weight for humans is pressed 60kg and is calculated, and clinical plan dosage is 0.2g/kg/ days (by raw medicine calculation)
Route of administration is oral administration, and administration frequency and cycle are, Per-Hop behavior 6 days, and every day is administered once, successive administration 39 weeks, altogether administration 234 times.
4, living animal Testing index
4.1 general clinical observations
Every morning and afternoon respectively carry out 1 general clinical observation, comprising: cage is looked on and examined animal dead or dying situation, the mental status, behavioral activity, feces character etc.
4.2 Detailed clinical are observed
Carry out Detailed clinical observation once in a week, comprising: the mental status, behavioral activity, skin, by hair, eye, ear, nose, abdominal part, external genitalia, anus, extremity, mouth, foot and breathing etc.
4.3 other parameters are observed
Comprise irregularly the weight of animals, body temperature, Ecg.
4.4 clinical pathology monitorings
Comprise and Testing index after cytometry, coagulation function (prothrombin time (PT), active partial thromboplastin time (APTT), Fibrinogen (FIB)), blood parameters, uroscopy, ophthalmologic examination, animal euthanasia is detected, the corpse of the animal after euthanasia is observed simultaneously, monitor organ weights and routine paraffin wax embedding, section, HE dyeing and microscopic examination are carried out to the Organ and tissue of all animals.
5, data acquisition and statistical analysis
Data acquisition: what protocols call measured needs written notes to suitable form or the direct image data of computer with the data result observed.
Statistical analysis: all statistical analysiss adopt two tail analysis, and statistics level is located at 5% or P≤0.05.The body weight of each treated animal, body temperature, electrocardiogram parameters, cytometry, coagulation function, blood biochemical, the index such as organ weights and organ coefficient all calculate average and the standard deviation of different Group Animals (female animals combines).Above-mentioned data will by following process analysis: first carry out Homogeneity Test with Levene Test to data.If data homogeneous (P ﹥ 0.05), then carry out one factor analysis of variance; If variance analysis significantly (P≤0.05), is then carried out Dunnett ' s and is carried out statistical analysis.If the result of LeveneTest significantly (P≤0.05), then carries out Kruskal-wallis non parametric tests; If Kruskal-wallis non parametric tests result significantly (P≤0.05), then Mann-WhitneyU inspection is adopted to carry out statistical analysis further.When sample number (n) is less than 3, do not carry out statistical analysis.
6, result
6.1 animal deads and dying
Duration of test, there is not dead or dying phenomenon in each treated animal.
6.2 clinical observation
Duration of test, the abnormal response of each administration group is mainly the gastrointestinal reaction after medicine, and concrete condition is as follows:
ZHUANGGU GUANJIE WAN 3g/kg dosage group: 2 animals occur vomiting after medicine first, there is vomiting in other animal visible successively afterwards, vomit as seen after the animal drugs of administration period 7/10, wherein W1 animal occurs that the frequency of vomiting is 9 dogs time, W13 animal occurs that the frequency of vomiting is 1 dog time, all there is not vomiting in W27 animal, W39 animal occurs that the frequency of vomiting is 4 dogs time; There is loose stool in 1 animal (D2) after the 2nd medicine, there is soft stool or loose stool in other animal visible successively afterwards, visible soft stool or loose stool after the animal drugs of administration period 9/10, wherein W1 and W13 animal occurs that the frequency of loose stool or soft stool is 2 dogs time, and soft stool or loose stool all do not appear in W27 and W39 animal.
ZHUANGGU GUANJIE WAN 10g/kg dosage group: 9 animals occur vomiting after medicine first, there is vomiting in other animal visible successively afterwards, vomit as seen after the animal drugs of administration period 10/10, wherein W1, W13, W27 and W39 animal occurs that the frequency of vomiting is respectively 54,25,17 and 12 dogs time; There is loose stool in 1 animal (D2) after the 2nd medicine, there is soft stool or loose stool in other animal visible successively afterwards, visible soft stool or loose stool after the animal drugs of administration period 10/10, wherein W1, W13 and W27 animal occurs that the frequency of soft stool or loose stool is respectively 10,13 and 1 dog time, and soft stool or loose stool do not appear in W39 animal.
Present composition 1g/kg dosage group: during administration, vomiting does not appear in animal, soft stool is there is after 1 animal D5 medicine, there is soft stool or loose stool in other animal visible successively afterwards, visible soft stool or loose stool after the animal drugs of administration period 5/10, wherein W1 animal occurs that the frequency of soft stool or loose stool is 1 dog time, and soft stool or loose stool all do not appear in W13, W27 and W39 animal.
Present composition 3g/kg dosage group: 1 animal occurs vomiting after medicine first, there is vomiting in other animal visible successively afterwards, vomit as seen after the animal drugs of administration period 4/10, wherein W1 animal occurs that the frequency of vomiting is 1 dog time, and vomiting does not appear in W13, W27 and W39 animal; Soft stool is there is after 2 animals the 2nd medicine, there is soft stool or loose stool in other animal visible successively afterwards, visible soft stool or loose stool after the animal drugs of administration period 5/10, wherein W1 animal occurs that the frequency of soft stool or loose stool is 2 dogs time, and soft stool or loose stool all do not appear in W13, W27 and W39 animal.
Present composition 10g/kg dosage group: 1 animal occurs vomiting after medicine first, there is vomiting in other animal visible successively afterwards, vomit as seen after the animal drugs of administration period 10/10, wherein W1, W13, W27 and W39 animal occurs that the frequency of vomiting is respectively 7,2,8 and 2 dogs time; Soft stool is there is in 2 animals after the 2nd medicine, there is soft stool or loose stool in other animal visible successively afterwards, visible soft stool or loose stool after the animal drugs of administration period 10/10, wherein W1 and W13 animal occurs that the frequency of soft stool or loose stool is respectively 9 and 6 dogs time, and soft stool or loose stool all do not appear in W27 and W39 animal.
In addition, visible sialism performance during comprising the Some Animals administration of negative control group, may with stress be relevant; The performances such as Some Animals visible dermis erythema, erubescence, anomalies of conjunctiva, discharge of eye, wound, skin ulceration, movement disorder, the changes such as the wound occurred when being thought of as the change of animal spontaneity or activity, think uncorrelated with administration.
6.3 body weight
Duration of test, compared with same period negative control group, the body weight of ZHUANGGU GUANJIE WAN 10g/kg dosage treated animal D49, D56, D63, D70, D77, D84, D91 and D210 reduces (P≤0.05), and the body weight of all the other each treated animals is there are no the change of toxicological significance; Compared with same period present composition 10g/kg dosage group, the body weight of ZHUANGGU GUANJIE WAN 10g/kg dosage treated animal D49, D56, D63, D70, D77, D84, D91 and D210 reduces (P≤0.05).
Different time points each treated animal body weight change trend is shown in Fig. 2.
6.4 body temperature
Duration of test, the body temperature of all animals has no the change with toxicological significance.
6.5 electrocardiogram
Duration of test, compared with same period negative control group, the QRS time limit of ZHUANGGU GUANJIE WAN 10g/kg dosage group and present composition 10g/kg dosage treated animal D272 shortens.ZHUANGGU GUANJIE WAN 10g/kg dosage group is compared with the QRS time limit of new technology 10g/kg dosage treated animal D272 and is had no difference (P>0.05).
Because the QRS time limit of ZHUANGGU GUANJIE WAN 10g/kg dosage group and present composition 10g/kg dosage treated animal D272 is in reference range, and also have no significant change compared with before medicine, therefore think that this change does not have toxicological significance.
6.6 clinical pathology
6.6.1 cytometry
Related indexes of red blood cells
Duration of test, compared with same period negative control group, the Retic (absolute value) of present composition 10g/kg dosage group D273 raises, and MCH reduces; The MCH of present composition 3g/kg dosage group D273 reduces, and above difference has statistical significance (P≤0.05).
Compared with the dosage ZHUANGGU GUANJIE WAN matched group such as same period, the MCH of present composition 3g/kg dosage treated animal D273 reduces (P≤0.05); Retic (absolute value) and the MCH of present composition 10g/kg dosage treated animal D273 have no significant change (P>0.05).
Because the Retic (absolute value) of present composition 10g/kg dosage treated animal D273 and the MCH of MCH and present composition 3g/kg dosage treated animal D273 is all in reference range, and have no clear and definite time m-reaction relation, therefore think that this change does not have toxicological significance.
Platelet counts
Duration of test, compared with same period negative control group, WBC and Neut (absolute value) of present composition 10g/kg dosage treated animal D184 raises, and the Lymph (absolute value) of D273 raises; The Mono (relative value and absolute value) of ZHUANGGU GUANJIE WAN 10g/kg dosage treated animal D273 raises, and Eos (relative value) reduces, and above difference has statistical significance (P≤0.05).
Compared with the dosage ZHUANGGU GUANJIE WAN matched groups such as the same period, WBC and Neut (absolute value) of present composition 10g/kg dosage treated animal D184 raises, the Mono (relative value and absolute value) of D273 reduces, EOS (relative value) raises, and above difference has statistical significance (P≤0.05).
Due to WBC, Neut (absolute value) of present composition 10g/kg dosage treated animal D184, the Lymph (absolute value) of D273 and the Mono (relative value and absolute value) of ZHUANGGU GUANJIE WAN 10g/kg dosage treated animal D273 and Eos (relative value) is all in reference range, and have no clear and definite time m-reaction relation, therefore think that this change does not have toxicological significance.
Platelet
Duration of test, compared with same period negative control group, the PLT of ZHUANGGU GUANJIE WAN 3g/kg dosage treated animal D91, D184 and D273 raises, and the PLT of ZHUANGGU GUANJIE WAN 10g/kg dosage treated animal D29, D91, D184 and D273 raises; The PLT of present composition 3g/kg and 10g/kg dosage treated animal D29, D91, D184 and D273 raises, and above difference has statistical significance (P≤0.05).
Compared with the dosage present composition group such as same period, the PLT of ZHUANGGU GUANJIE WAN 0g/kg treated animal D273 raises (P≤0.05).
At the end of convalescent period, the regularity change that each administration group platelet shows no obvious abnormalities.
During administration, each treated animal PLT situation of change sees the following form 9:
Each treated animal PLT situation of change during table 9 administration
Note: 1. " * " represents compared with Vehicle controls group, P≤0.05; 2. " ↑ " represents rising
The situation of change prompting of above-mentioned PLT: after administration, ZHUANGGU GUANJIE WAN and the present composition 3,10g/kg dosage treated animal PLT all present and obviously raise phenomenon, and above phenomenon thinks relevant to administration.6.6.2 coagulation function
Duration of test, each administration treated animal Blood Coagulation is there are no the change of toxicological significance.
6.6.3 blood biochemical
Duration of test, with the same period negative control compared with, ALT and ALB of ZHUANGGU GUANJIE WAN 3g/kg dosage treated animal D91 reduces, and ALP raises, and the ALP of D184 raises, ALP and TCH of D273 raises;
ALT, ALB and A/G of ZHUANGGU GUANJIE WAN 10g/kg dosage treated animal D29 decline, TG raises, ALT, AST, ALB, A/G and Cl-of D91 reduce, ALP and TG raises, A/G, BUN, CREA and Cl-of D184 reduce, ALP, GLB and K+ raise, and AST, ALB, A/G, BUN, CREA, Na+ and Cl-of D273 reduce, and ALP, GGT and TG raise;
ALB and A/G of the present composition (prepared by embodiment 1) 1g/kg dosage treated animal D91 and D184 reduces;
The A/G of present composition 3g/kg dosage treated animal D29 reduces, and the ALB of D91 reduces, and the TCH of D184 and D273 raises;
ALT and A/G of present composition 10g/kg dosage treated animal D29 reduces, and GLB raises, and ALT, ALB and A/G of D91 reduce, ALB and A/G of D184 reduces, GLB and TCH raises, ALB and A/G of D273 reduces, TCH raises, and above difference has statistical significance (P≤0.05).All the other blood parameters have no notable difference.
Compared with the dosage present composition (prepared by the embodiment 1) group such as same period, the ALP of ZHUANGGU GUANJIE WAN 3g/kg dosage treated animal D91, D184 and D273 raises, and the TCH of D91 and D184 reduces; The TG of ZHUANGGU GUANJIE WAN 10g/kg dosage treated animal D29 raises, CREA and TCH of D91, D184 and D273 reduces, the Cl-of D91 and D273 reduces, the ALP of D184 and D273 raises, AST, BUN, A/G and Na+ of D273 reduce, GGT raises, and above difference has statistical significance (P≤0.05).
In the blood parameters of above-mentioned appearance change, due to ALT, AST, BUN, CREA, Na
+, K
+and Cl
-all fluctuate in reference range, have no evident regularity change, therefore think uncorrelated with administration.All the other blood parameters situations of change are as following table 10.
Table 10 blood parameters situation of change
Note: " ↓ " represents reduction; " ↑ " represents rising; And compare with the negative control group same period, difference has statistical significance (P≤0.05)
In the data of above-mentioned change, as following table 11 compared with each treated animal is worth with before medicine:
The each treated animal of table 11 and medicine front value contrast
Note: " ↓ " represents reduction; " ↑ " represents rising
Blood parameters situation of change prompting in upper table: during administration, ZHUANGGU GUANJIE WAN 3g/kg and 10g/kg dosage treated animal ALP obviously raises, at the end of the administration of ZHUANGGU GUANJIE WAN 10g/kg dosage treated animal, visible GGT significantly raises, think that the rising of ALP with GGT is relevant with the liver toxicity of ZHUANGGU GUANJIE WAN, though the visible ALP of present composition 10g/kg dosage treated animal D184 raises, have no significant change compared with before medicine; ZHUANGGU GUANJIE WAN 3g/kg and 10g/kg and present composition 3g/kg and the visible TCH of 10/kg dosage treated animal raises, and the visible TG of ZHUANGGU GUANJIE WAN 10g/kg dosage treated animal raises, and thinks that this change is relevant to administration; The visible ALB of each administration group slightly reduces, ZHUANGGU GUANJIE WAN 10g/kg and the visible A/G of the present composition each dosage group reduces, ZHUANGGU GUANJIE WAN and the visible GLB of present composition 10g/kg group raise, in conjunction with combination pathological examination result, think that this change may be relevant to administration, but each dosage group ALB of the present composition has no significant change compared with before administration, the slight reduction of A/G may be relevant with the slight rising of GLP after medicine.
6.7 urinalysis
Duration of test, the uroscopy of each administration treated animal is there are no the change of toxicological significance.
6.8 ophthalmologic examination
Duration of test, each administration treated animal ophthalmologic examination is there are no the change of toxicological significance.
6.9 pathologic finding
Compared with same period negative control group, at the end of the administration phase, ZHUANGGU GUANJIE WAN group 3g/kg dosage treated animal liver weight raises, and ZHUANGGU GUANJIE WAN 10g/kg dosage treated animal liver weight and dirty body are than raising, epididymis weight reduces, and above difference has statistical significance (P≤0.05).
Compared with the dosage present composition (prepared by the embodiment 1) groups such as the same period, ZHUANGGU GUANJIE WAN 3g/kg dosage treated animal liver weight raises, the dirty body of ZHUANGGU GUANJIE WAN 10g/kg dosage treated animal liver is than raising, epididymis weight reduces, and above difference has statistical significance (P≤0.05).
Histological indications shows, and the toxic pathology of the visible liver of ZHUANGGU GUANJIE WAN 10g/kg dosage treated animal changes, therefore in this test, the weight change of ZHUANGGU GUANJIE WAN matched group liver may be relevant to administration.
6.10 gross examination of skeletal muscle
All animal gross examination of skeletal muscle are showed no the obvious exception relevant to medicine.
6.11 histological examination
Microscopic examination showed, the visible Histological change relevant to ZHUANGGU GUANJIE WAN of liver.Successive administration 39 weeks, ZHUANGGU GUANJIE WAN 10g/kg group has the visible Binucleate Hepatocytes of 2/6 animal livers to increase, the visible bile duct proliferation of 1/6 animal, and the visible hepatocellular degeneration of 1/6 animal, recovers after recovering 4 weeks completely; ZHUANGGU GUANJIE WAN 3g/kg group, recovers there is the visible bile duct proliferation of 1/4 animal at the end of 4 weeks.
And the present composition (prepared by embodiment 1) each dosage group has no obviously relevant to new technology Histological change.
Discuss
7.1 toxic reaction analyses
The gastrointestinal reactions such as during administration, present composition group and bone strengthening arthritis matched group are mainly vomitted as seen, soft stool or loose stool, and the body weight of the visible gastrointestinal reaction secondary of bone strengthening arthritis 10g/kg group reduces.
Bone strengthening arthritis matched group 3g/kg and 10g/kg dosage treated animal ALP obviously raises, and at the end of the administration of bone strengthening arthritis matched group 10g/kg dosage treated animal, visible GGT significantly raises, and thinks that the arthritic liver toxicity of the rising of ALP with GGT and bone strengthening is relevant.
Bone strengthening arthritis matched group 3g/kg and 10g/kg and the visible TCH of the present composition (prepared by embodiment 1) 3g/kg and 10g/kg dosage treated animal raises, and the visible TG of bone strengthening arthritis matched group 10g/kg dosage treated animal raises; The visible ALB of bone strengthening arthritis matched group each dosage group slightly reduces, bone strengthening arthritis matched group 10g/kg and the visible A/G of the present composition (prepared by embodiment 1) each dosage group reduces, bone strengthening arthritis and the visible GLB of present composition 10g/kg group raise, think that this change may be relevant to administration, but the slight reduction of the present composition each dosage group A/G may be relevant with the slight rising of GLB.
7.2 toxic reactions compare
During administration, the GI irritation reactions such as the present composition and bone strengthening arthritis matched group are vomitted all as seen, soft stool or loose stool, but under Isodose, occur in the frequency that GI irritation is reacted and the extent of reaction, the arthritic gastrointestinal reaction of bone strengthening is slightly heavy, and bone strengthening arthritis occurs that the body weight of secondary reduces performance; And the present composition 3 and 10g/kg and bone strengthening arthritis contrast 3 and all visible PLT of 10g/kg dosage group raise, but under Isodose, the amplitude that present composition PLT raises is a little less than bone strengthening arthritis.Bone strengthening arthritis contrast 3 and the visible ALP of 10g/kg group obviously raise, and the GGT at the end of the administration of bone strengthening arthritis contrast 10g/kg group raises; The ALP of present composition 10g/kg group D184 raises, but amplitude of variation is little compared with dosage bone strengthening arthritis contrasts such as the same periods; Bone strengthening arthritis 3g/kg and the visible liver weight of 10g/kg dosage group raise, and the reactions such as the visible Binucleate Hepatocytes of liver increases, bile duct proliferation and hepatocellular degeneration, the present composition each dosage group liver has no obvious change.
Toxicity contrast Deng dosage ZHUANGGU GUANJIE WAN and the present composition is listed as follows table 12-14.
The gastrointestinal toxicity contrast of dosage ZHUANGGU GUANJIE WAN such as table 12 grade and the present composition
The liver toxicity contrast of dosage ZHUANGGU GUANJIE WAN such as table 13 grade and the present composition
The index change of dosage ZHUANGGU GUANJIE WAN such as table 14 grade and the present composition
Note: " ↑ " represents rising; And compare with the negative control group same period, difference has statistical significance (P≤0.05)
8 conclusions
Under this experimental condition, the pill of ZHUANGGU GUANJIE WAN contrast and the embodiment of the present invention 1 preparation is adopted to repeat orally to give Beagle dog, Per-Hop behavior 6 days, every day is administered once, successive administration 39 weeks, ZHUANGGU GUANJIE WAN dosage is 3 and 10g/kg respectively, and major toxicity reaction is gastrointestinal reaction (being mainly vomiting, soft stool or loose stool) and hepatic injury; Pill prepared by the embodiment of the present invention 1 is 1,3 and 10g/kg respectively, and major toxicity reaction is gastrointestinal reaction, and gastrointestinal reaction comparatively waits dosage ZHUANGGU GUANJIE WAN (former technique) light, and liver toxicity damage is lower.
Detailed description of the invention
Embodiment 1
[prescription] Rhizoma Cibotii 576.8 grams, Herba Epimedii 346.1 grams, Radix Angelicae Pubescentis 346.1 grams, Rhizoma Drynariae 462.0 grams, Radix Dipsaci 576.8 grams, Herba Taxilli 576.8 grams, Caulis Spatholobi 346.1 grams, Radix Rehmanniae Preparata 1384.2 grams, the Radix Aucklandiae 346.1 grams, Olibanum 346.1 grams, Myrrha 346.1 grams, Fructus Psoraleae 346.1 grams.
[preparation method]
Get described Olibanum and Myrrha mixing according to selected weight, add 10 times of water gagings and carry out vapor distillation and extract 12 hours, collect volatile oil; According to volatile oil: beta-schardinger dextrin-: water: the mass ratio of ethanol is that the ratio of 1:10:20:1 adds adjuvant, and grinding 20min carries out enclose, with inner drying, pulverizing, cross 120 mesh sieves, make volatile oil clathrate compound for 50 DEG C, for subsequent use;
Get described Fructus Psoraleae according to selected weight, add 8 times amount water extraction 2 times, each 1 hour, after discarding Aqueous extracts, collect medicinal residues, be drying to obtain Fructus Psoraleae processed product, for subsequent use;
Get all the other medical materials according to selected weight, mix, pulverize, sieve, add volatile oil clathrate compound and appropriate binding agent with Fructus Psoraleae processed product, mixing, uses water pill, and dry, film coating, to obtain final product.
Embodiment 2
[prescription] Rhizoma Cibotii 290 grams, Herba Epimedii 520 grams, Radix Angelicae Pubescentis 154 grams, Rhizoma Drynariae 692 grams, Radix Dipsaci 290 grams, Herba Taxilli 864 grams, Caulis Spatholobi 154 grams, Radix Rehmanniae Preparata 2076 grams, the Radix Aucklandiae 154 grams, Olibanum 520 grams, Myrrha 154 grams and Fructus Psoraleae 520 grams.
[preparation method]
Get described Olibanum and Myrrha mixing according to selected weight, add 8 times of water gagings and carry out vapor distillation and extract 15 hours, collect volatile oil; According to volatile oil: beta-schardinger dextrin-: water: the mass ratio of ethanol is that the ratio of 1:8:24:1 adds adjuvant, and grinding 20min carries out enclose, with inner drying, pulverizing, makes volatile oil clathrate compound for 50 DEG C, for subsequent use;
Get described Fructus Psoraleae according to selected weight, add 6 times amount water extraction 3 times, each 0.5 hour, after discarding Aqueous extracts, collect medicinal residues, be drying to obtain Fructus Psoraleae processed product for subsequent use;
Get all the other medical materials according to selected weight, mix, pulverize, sieve, add volatile oil clathrate compound and appropriate binding agent with Fructus Psoraleae processed product, mixing, uses water pill, and dry, film coating, to obtain final product.
Embodiment 3
[prescription] Rhizoma Cibotii 864 grams, Herba Epimedii 154 grams, Radix Angelicae Pubescentis 520 grams, Rhizoma Drynariae 224 grams, Radix Dipsaci 864 grams, Herba Taxilli 290 grams, Caulis Spatholobi 520 grams, Radix Rehmanniae Preparata 692 grams, the Radix Aucklandiae 520 grams, Olibanum 154 grams, Myrrha 520 grams and Fructus Psoraleae 154 grams.
[preparation method]
Get described Olibanum and Myrrha mixing according to selected weight, add 12 times of water gagings and carry out vapor distillation and extract 8 hours, collect volatile oil; According to volatile oil: beta-schardinger dextrin-: water: the mass ratio of ethanol is that the ratio of 1:12:16:2 adds adjuvant, and grinding 20min carries out enclose, 50 DEG C with inner drying, pulverizing, make volatile oil clathrate compound, for subsequent use;
Get described Fructus Psoraleae according to selected weight, add 10 times amount water extraction 1 time, 0.5 hour, after discarding Aqueous extracts, collect medicinal residues, be drying to obtain Fructus Psoraleae processed product for subsequent use;
Get all the other medical materials according to selected weight, mix, pulverize, sieve, add volatile oil clathrate compound and appropriate binding agent with Fructus Psoraleae processed product, mixing, uses water pill, and dry, film coating, to obtain final product.
Embodiment 4
[prescription] Rhizoma Cibotii 576.8 grams, Herba Epimedii 346.1 grams, Radix Angelicae Pubescentis 346.1 grams, Rhizoma Drynariae 462.0 grams, Radix Dipsaci 576.8 grams, Herba Taxilli 576.8 grams, Caulis Spatholobi 346.1 grams, Radix Rehmanniae Preparata 1384.2 grams, the Radix Aucklandiae 346.1 grams, Olibanum 346.1 grams, Myrrha 346.1 grams, Fructus Psoraleae 346.1 grams.
[preparation method]
Get described Olibanum and Myrrha mixing according to selected weight, add 10 times of water gagings and carry out vapor distillation and extract 12 hours, collect volatile oil, add customary adjuvant and make volatile oil clathrate compound, for subsequent use;
Get described Fructus Psoraleae according to selected weight, add 8 times amount water extraction 2 times, each 1 hour, after discarding Aqueous extracts, collect medicinal residues, be drying to obtain Fructus Psoraleae processed product for subsequent use;
Get all the other medical materials according to selected weight, mix with described volatile oil clathrate compound and Fructus Psoraleae processed product, pulverize, sieve, add appropriate customary adjuvant, make honeyed pill.
Embodiment 5
[prescription] Rhizoma Cibotii 576.8 grams, Herba Epimedii 346.1 grams, Radix Angelicae Pubescentis 346.1 grams, Rhizoma Drynariae 462.0 grams, Radix Dipsaci 576.8 grams, Herba Taxilli 576.8 grams, Caulis Spatholobi 346.1 grams, Radix Rehmanniae Preparata 1384.2 grams, the Radix Aucklandiae 346.1 grams, Olibanum 346.1 grams, Myrrha 346.1 grams, Fructus Psoraleae 346.1 grams.
[preparation method]
Get described Olibanum and Myrrha mixing according to selected weight, add water and carry out vapor distillation extraction, collect volatile oil, add customary adjuvant and make volatile oil clathrate compound, for subsequent use;
Get described Fructus Psoraleae, extracting in water according to selected weight, collect medicinal residues after discarding Aqueous extracts, be drying to obtain Fructus Psoraleae processed product, for subsequent use;
Get all the other medical materials according to selected weight, mix with described Fructus Psoraleae processed product, pulverize, sieve, add volatile oil clathrate compound and appropriate customary adjuvant, make tablet.
Obviously, above-described embodiment is only for clearly example being described, and the restriction not to embodiment.For those of ordinary skill in the field, can also make other changes in different forms on the basis of the above description.Here exhaustive without the need to also giving all embodiments.And thus the apparent change of extending out or variation be still among the protection domain of the invention.
Accompanying drawing explanation
In order to make content of the present invention be more likely to be clearly understood, below according to a particular embodiment of the invention and by reference to the accompanying drawings, the present invention is further detailed explanation, wherein,
Fig. 1 is H.E dyeing picture (× 200) of each test group to the osteoarthritis rat knee joints cartilaginous tissue effect of Papain enzyme induction; Wherein, A is matched group, B is model group, C is ZHUANGGU GUANJIE WAN group, D-F is respectively embodiment 1 test medicine 2.20,1.10,0.55g/kg group, G be glucosamine matched group;
Fig. 2 is different time points each treated animal body weight change trend in toxicity test.
Claims (10)
1. treat a preparation method for the pharmaceutical composition of osteoarthritis, it is characterized in that, comprise the steps:
(1) get Olibanum 154-520 weight portion, the mixing of Myrrha 154-520 weight portion, add water and carry out vapor distillation extraction, collect volatile oil, add customary adjuvant and make volatile oil clathrate compound, for subsequent use;
(2) get Fructus Psoraleae 154-520 weight portion, extracting in water, after discarding Aqueous extracts, collect medicinal residues, obtain Fructus Psoraleae processed product, for subsequent use;
(3) Rhizoma Cibotii 290-864 weight portion, Herba Epimedii 154-520 weight portion, Radix Angelicae Pubescentis 154-520 weight portion, Rhizoma Drynariae 224-692 weight portion, Radix Dipsaci 290-864 weight portion, Herba Taxilli 290-864 weight portion, Caulis Spatholobi 154-520 weight portion, Radix Rehmanniae Preparata 692-2076 weight portion, Radix Aucklandiae 154-520 weight portion is got, mix with described Fructus Psoraleae processed product for subsequent use, pulverize, add described volatile oil clathrate compound for subsequent use and customary adjuvant, conveniently technique makes clinical acceptable oral formulations.
2. the preparation method of pharmaceutical composition according to claim 1, is characterized in that, comprises the steps:
(1) get Olibanum 346.1 weight portion, the mixing of Myrrha 346.1 weight portion, add water and carry out vapor distillation extraction, collect volatile oil, add customary adjuvant and make volatile oil clathrate compound, for subsequent use;
(2) get Fructus Psoraleae 346.1 weight portion, extracting in water, after discarding Aqueous extracts, collect medicinal residues, obtain Fructus Psoraleae processed product, for subsequent use;
(3) Rhizoma Cibotii 576.8 weight portion, Herba Epimedii 346.1 weight portion, Radix Angelicae Pubescentis 346.1 weight portion, Rhizoma Drynariae 462.0 weight portion, Radix Dipsaci 576.8 weight portion, Herba Taxilli 576.8 weight portion, Caulis Spatholobi 346.1 weight portion, Radix Rehmanniae Preparata 1384.2 weight portion, the Radix Aucklandiae 346.1 weight portion is got, mix with described Fructus Psoraleae processed product for subsequent use, pulverize, add described volatile oil clathrate compound for subsequent use and customary adjuvant, conveniently technique makes clinical acceptable oral formulations.
3. the preparation method of pharmaceutical composition according to claim 1 and 2, is characterized in that, comprises the steps:
(1) get described Olibanum and Myrrha mixing according to selected weight portion, add 8-12 times of water gaging and carry out vapor distillation extraction 8-15 hour, collect volatile oil, add customary adjuvant and make volatile oil clathrate compound, for subsequent use;
(2) get described Fructus Psoraleae according to selected weight portion, add 6-10 times amount water extraction 1-3 time, each 0.5-2 hour, after discarding Aqueous extracts, collect medicinal residues, be drying to obtain Fructus Psoraleae processed product, for subsequent use;
(3) Rhizoma Cibotii, Herba Epimedii, Radix Angelicae Pubescentis, Rhizoma Drynariae, Radix Dipsaci, Herba Taxilli, Caulis Spatholobi, Radix Rehmanniae Preparata, the Radix Aucklandiae is got according to selected weight portion, mix with described Fructus Psoraleae processed product for subsequent use, pulverize, add described volatile oil clathrate compound for subsequent use and customary adjuvant, conveniently technique makes clinical acceptable oral formulations.
4. the preparation method of pharmaceutical composition according to claim 3, is characterized in that, comprises the steps:
(1) get described Olibanum and Myrrha mixing according to selected weight portion, add 10 times of water gagings and carry out vapor distillation and extract 12 hours, collect volatile oil, add customary adjuvant and make volatile oil clathrate compound, for subsequent use;
(2) get described Fructus Psoraleae according to selected weight portion, add 8 times amount water extraction 2 times, each 1 hour, after discarding Aqueous extracts, collect medicinal residues, be drying to obtain Fructus Psoraleae processed product, for subsequent use;
(3) Rhizoma Cibotii, Herba Epimedii, Radix Angelicae Pubescentis, Rhizoma Drynariae, Radix Dipsaci, Herba Taxilli, Caulis Spatholobi, Radix Rehmanniae Preparata, the Radix Aucklandiae is got according to selected weight portion, mix with described Fructus Psoraleae processed product for subsequent use, pulverize, add described volatile oil clathrate compound for subsequent use and customary adjuvant, conveniently technique makes clinical acceptable oral formulations.
5., according to the preparation method of the arbitrary described pharmaceutical composition of claim 1-4, it is characterized in that, in described step (1), the customary adjuvant preparing described volatile oil clathrate compound comprises beta-schardinger dextrin-, water and ethanol.
6. the preparation method of pharmaceutical composition according to claim 5, is characterized in that, in described step (1), the mass ratio of described volatile oil, beta-schardinger dextrin-, water and ethanol is 1:8-12:16-24:1-2.
7. the preparation method of the pharmaceutical composition according to claim 5 or 6, is characterized in that, in described step (1), the mass ratio of described volatile oil, beta-schardinger dextrin-, water and ethanol is 1:10:20:1.
8., according to the preparation method of the arbitrary described pharmaceutical composition of claim 1-7, it is characterized in that, described Olibanum and/or Myrrha are processed with vinegar.
9. the pharmaceutical composition prepared by the arbitrary described preparation method of claim 1-8.
10. add customary adjuvant by pharmaceutical composition described in claim 9, conveniently the clinical acceptable oral formulations made of technique.
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Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN104435314A (en) * | 2014-11-14 | 2015-03-25 | 华润三九医药股份有限公司 | Medicament composition for treating osteoarthrosis and application of medicament composition |
| CN105232621A (en) * | 2014-11-11 | 2016-01-13 | 天津中医药大学 | Processing method of fructus psoraleae medicinal materials, fructus psoraleae extract and pharmaceutical composition |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1931277A (en) * | 2005-10-08 | 2007-03-21 | 周小明 | Osteoarthrosis treating Chinese medicine composition and its prepn process |
-
2014
- 2014-11-14 CN CN201410649898.5A patent/CN104352633B/en active Active
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1931277A (en) * | 2005-10-08 | 2007-03-21 | 周小明 | Osteoarthrosis treating Chinese medicine composition and its prepn process |
Non-Patent Citations (4)
| Title |
|---|
| 周昆等: "壮骨关节丸中肝毒性药材的筛选研究", 《中国药物警戒》 * |
| 周昆等: "补骨脂水提取引起的大鼠肝损害", 《天津中医药大学学报》 * |
| 国家药典委员会编: "《中华人民共和国药典：2010年版：第二增补本》", 30 September 2013, 中国医药科技出版社 * |
| 谈英等: "乳香没药挥发油入药的β-环糊精包合工艺及镇痛作用研究", 《中国药物警戒》 * |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN105232621A (en) * | 2014-11-11 | 2016-01-13 | 天津中医药大学 | Processing method of fructus psoraleae medicinal materials, fructus psoraleae extract and pharmaceutical composition |
| CN104435314A (en) * | 2014-11-14 | 2015-03-25 | 华润三九医药股份有限公司 | Medicament composition for treating osteoarthrosis and application of medicament composition |
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