CN105456426A - Medicinal composition for treating systemic lupus erythematosus - Google Patents
Medicinal composition for treating systemic lupus erythematosus Download PDFInfo
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- CN105456426A CN105456426A CN201511001664.0A CN201511001664A CN105456426A CN 105456426 A CN105456426 A CN 105456426A CN 201511001664 A CN201511001664 A CN 201511001664A CN 105456426 A CN105456426 A CN 105456426A
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Abstract
The invention discloses a medicinal composition for treating systemic lupus erythematosus, belonging to the technical field of traditional Chinese medicine. The medicinal composition is prepared from the following raw herbal materials: herba portulacae, ginseng, indigo naturalis, coptis chinensis, radix puerariae, henry clematis root, poria cocos, honeysuckle stem, yerbadetajo herb, lotus plumule, fructus gardeniae and liquorice. The medicinal composition has a function of remarkably adjusting the activity of T cell subset and has the advantages of fast effect and short treatment course in treating systemic lupus erythematosus; and moreover, the medicinal composition realizes a therapeutical effect on vasculitis with a remarkable curative effect and is safe and reliable and has a broad prospect in clinical application.
Description
Technical field
The invention belongs to technical field of Chinese medicines, particularly relate to a kind of pharmaceutical composition of systemic lupus erythematosus.
Background technology
Systemic lupus erythematosus (sle), a kind of diffusivity, systemic autoimmune diseases, mainly involve mucocutaneous, skeletal muscle, kidney and central nervous system, multiple organ and the systems such as lung, heart, blood can also be involved simultaneously, show various clinical symptoms, in serum, multiple autoantibody and crucial immunological abnormality can be detected.It is careful that treatment for systemic lupus erythematosus (sle) needs, and only has radical cure systemic lupus erythematosus (sle) just can avoid complication.Wherein common with the complication of cardiovascular system.The hematological of lupus erythematosus is the most common with vasculitis, with extremity, patient often occurs that large stretch of cicatrix petechia of unknown cause is for main clinical manifestation, if do not find timely and treat and develop as one pleases, the limb end of finger tip, toe point will be caused to occur the serious consequence such as depression and ulcer necrosis.Current Western medicine cannot effective systemic lupus erythematosus, although Western medicine can control generation and the development of disease to a certain extent, but adverse effect is obvious, after drug withdrawal, the state of an illness easily recurs, and there is more side effect, therefore, there is great demand in the Chinese medicine of people to effective systemic lupus erythematosus.
Chinese patent application 201310241251.4 discloses a kind of pharmaceutical composition being used for the treatment of systemic lupus erythematosus (sle), and this pharmaceutical composition is obtained by following raw material: Cornu Bubali, Radix Arnebiae (Radix Lithospermi), Ramulus Euonymi, Mirabilitum crystallina part, Cortex Moutan, Caulis Sargentodoxae, the Fructus Kochiae, Rhizoma Paridis, Radix Rumicis Japonici are followed and Fructus Litseae.This pharmaceutical composition can effectively improve lupus erythematosus patients clinical symptoms, but is not very remarkable for the vasculitic effect of complication of systemic lupus erythematosus.
Summary of the invention
The technical problem to be solved in the present invention is to provide a kind of pharmaceutical composition of systemic lupus erythematosus, this pharmaceutical composition can the misery that causes to patient of mitigation system lupus erythematosus and complication vasculitis thereof, it is evident in efficacy, safe and reliable, has wide potential applicability in clinical practice.
Technical scheme of the present invention is: the pharmaceutical composition of systemic lupus erythematosus, and this pharmaceutical composition is made up of the raw material of following weight portion: Herba Portulacae 10-25 part, Radix Ginseng 9-20 part, Indigo Naturalis 8-15 part, Rhizoma Coptidis 8-15 part, Radix Puerariae 6-12 part, Radix Clematidis Henryi 6-12 part, Poria 3-9 part, Caulis Lonicerae 3-9 part, Herba Ecliptae 3-9 part, Plumula Nelumbinis 2-6 part, Fructus Gardeniae 3-6 part and Radix Glycyrrhizae 1-10 part.
Preferably, described pharmaceutical composition is made up of the raw material of following weight portion: Herba Portulacae 10 parts, Radix Ginseng 9 parts, Indigo Naturalis 8 parts, Rhizoma Coptidis 8 parts, Radix Puerariae 6 parts, Radix Clematidis Henryi 6 parts, 3 parts, Poria, Caulis Lonicerae 3 parts, Herba Ecliptae 3 parts, Plumula Nelumbinis 2 parts, Fructus Gardeniae 3 parts and 1 part, Radix Glycyrrhizae.
Preferably, described pharmaceutical composition is made up of the raw material of following weight portion: Herba Portulacae 20 parts, Radix Ginseng 15 parts, Indigo Naturalis 12 parts, Rhizoma Coptidis 12 parts, Radix Puerariae 9 parts, Radix Clematidis Henryi 9 parts, 6 parts, Poria, Caulis Lonicerae 6 parts, Herba Ecliptae 6 parts, Plumula Nelumbinis 4 parts, Fructus Gardeniae 4 parts and 5 parts, Radix Glycyrrhizae.
Preferably, described pharmaceutical composition is made up of the raw material of following weight portion: Herba Portulacae 25 parts, Radix Ginseng 20 parts, Indigo Naturalis 15 parts, Rhizoma Coptidis 15 parts, Radix Puerariae 12 parts, Radix Clematidis Henryi 12 parts, 9 parts, Poria, Caulis Lonicerae 9 parts, Herba Ecliptae 9 parts, Plumula Nelumbinis 6 parts, Fructus Gardeniae 6 parts and 10 parts, Radix Glycyrrhizae.
Correspondingly, present invention also offers the preparation method of the pharmaceutical composition of described systemic lupus erythematosus, the preparation method of described pharmaceutical composition comprises the steps:
(1): get Herba Portulacae, wash away impurity, crushed after being dried, cross 80-100 mesh sieve, adding medical material gross weight 6-10 times amount volume fraction is the ethanol of 60-85%, microwave extraction 15-25 minute, microwave power is 300-500W, and Extracting temperature is 45-60 DEG C, filters and retains Herba Portulacae filtering residue, the extractum that relative density is 1.10-1.25 is surveyed, obtained Herba portulacae extract at filtrate reduced in volume to 60 DEG C;
(2): get Radix Ginseng, Indigo Naturalis, Rhizoma Coptidis, Radix Puerariae, Radix Clematidis Henryi, Poria, Caulis Lonicerae, Herba Ecliptae, Plumula Nelumbinis, Fructus Gardeniae and Radix Glycyrrhizae, wash away impurity, after dry, mixing is ground into coarse powder, merge with above-mentioned Herba Portulacae filtering residue, add the purified water of medical material total amount 6-12 times amount, soak 20-30 minute, reflux, extract, 1-3 time, each 3-6 hour, filter, merging filtrate, the extractum that relative density is 1.10-1.25 is surveyed at filtrate reduced in volume to 60 DEG C, cooling, slowly add ethanol while stirring to alcohol content for reaching 45-60%, 4 DEG C of standing 12-24 hour, filter and retain filtering residue, obtain filtrate A,
(3): the filtering residue obtained in (2) slowly being added while stirring its weight 3-6 times amount volume fraction is the ethanol of 45-60%, 4 DEG C of standing 3-6 hour, filter, obtain liquor B and filtering residue; Filtering residue uses the washing with alcohol 1-2 time of 45-60% again, collects and merges cleaning mixture;
(4): merge described filtrate A, liquor B and cleaning mixture, the extractum that relative density is 1.10-1.25 is surveyed under being evaporated to 60 DEG C of conditions after mixing;
(5): extractum obtained in described Herba portulacae extract and (4) is merged, stir, vacuum belt type drying is carried out at 60 DEG C of temperature, drying pressure is 0.02-0.08MPa, charging rate is 12L/h, and material strip transfer rate is 28cm/min, is pulverized by dry extract after drying, cross 100-200 mesh sieve, to obtain final product.
Preferably, described pharmaceutical composition is made into powder, tablet or capsule.
Source, the nature and flavor of the present invention's component used, return through and effect:
Herba Portulacae: this product is portulacaceous plant Herba Portulacae; Sour in the mouth, cold in nature; Clearing away heat-damp and promoting diuresis, removing pathogenic heat from blood and toxic substance from the body.
Radix Ginseng: this product is the dry root of Araliaceae Radix Ginseng; Sweet in the mouth, micro-hardship, property is put down; Return spleen, lung, heart channel; Strongly invigorating primordial QI, multiple arteries and veins takes off admittedly, and invigorating the spleen to benefit the lung, promotes the production of body fluid, and calms the nerves.
Indigo Naturalis: this product is acanthaceous vegetable acanthaceous indigo, the leaf of polygonaceae plant polygonum tinctorium ait. or cruciferae isatis or stem and leaf be through processing obtained dried powder or agglomerate; Cold in nature, salty in the mouth; Return Liver Channel; Heat-clearing and toxic substances removing, blood cooling and ecchymoses removing, pathogenic fire purging is calmed the frightened.
Rhizoma Coptidis: this product is the dry rhizome of ranunculaceae plant Rhizoma Coptidis; Bitter in the mouth, cold in nature; GUIXIN, spleen, stomach, liver, gallbladder, large intestine channel; Heat clearing and damp drying, eliminating fire and detoxication.
Radix Puerariae: this product is the dry root of legume pueraria lobata or Radix Puerariae rattan; Cool in nature, gas is put down, sweet in the mouth; Heat clearing away, pathogenic fire reducing, toxin expelling.
Radix Clematidis Henryi: this product is root or the leaf of cohosh henry clematis; Acrid in the mouth, hardship, cool in nature; GUIXIN, lung, stomach warp; Heat-clearing and toxic substances removing, eliminating phlegm and relieving cough, promoting flow of QI and blood, pain relieving.
Poria: this product is the dry sclerotia of On Polyporaceae Poria; Sweet in the mouth, light, property is put down; GUIXIN, lung, spleen, kidney channel; Promoting diuresis to eliminate damp pathogen, spleen invigorating mind calming.
Caulis Lonicerae: this product is the dry stem branch of caprifoliaceae plant Radix Ophiopogonis; Sweet in the mouth, cold in nature; Attach to the lung and stomach meridians; Heat-clearing and toxic substances removing, dispelling wind dredging collateral.
Herba Ecliptae: this product is the dry aerial parts of feverfew Eclipta prostrata; Sweet in the mouth, cold in nature; Return kidney, Liver Channel; Nourishing the liver and kidney, cooling blood for hemostasis.
Plumula Nelumbinis: this product is the green radicle (Plumula Nelumbinis) in the middle of the mature seed of nymphaeaceae plant lotus; Bitter in the mouth, cold in nature; GUIXIN, kidney channel; Clear away heart-fire, reduce phlegm and internal heat, hemostasis, arresting seminal emission.
Fructus Gardeniae: this product is the dry mature fruit of Maguireothamnus speciosus Fructus Gardeniae; Property bitter, taste is trembled with fear; GUIXIN, lung, tri-jiao channel; Pathogenic fire purging relieving restlessness, clearing away heat and promoting diuresis, removing pathogenic heat from blood and toxic substance from the body.
Radix Glycyrrhizae: this product is the dry root of glycyrrhizic legume, Glycyrrhiza inflata Bat. or Glycyrrhiza glabra L.; Sweet in the mouth, property is put down; GUIXIN, lung, spleen, stomach warp; Invigorating the spleen and replenishing QI, heat-clearing and toxic substances removing, expelling phlegm for arresting cough, relieving spasm to stop pain, coordinating the actions of various ingredients in a prescription.
Compared with prior art, the present invention has following technical advantage:
(1) compared with current chemotherapeutic agent, pharmaceutical composition of the present invention is natural pure Chinese medicinal preparation, and untoward reaction and side effect significantly reduce, and pharmaceutical composition effect of the present invention is comprehensive, and medication effect is better, improves the quality of life of patient.
(2) in pharmaceutical composition of the present invention containing multi-medicament component, can effective systemic lupus erythematosus by synergism, and can significantly reduce systemic lupus erythematosus disease, the compliance of raising patient.
Therefore, the present invention also this pharmaceutical composition claimed preparing the application in medicament for treating systemic lupus erythematosus.
Detailed description of the invention
It will be understood by those skilled in the art that technology disclosed in following examples represents the technology playing good action in the practice of the invention of the present inventor's discovery.But, many changes can be made in disclosed specific embodiments, and still obtain same or analogous result, and not depart from the spirit and scope of the present invention.
Embodiment 1:
The embodiment of the present invention 1 pharmaceutical composition is made up of the raw material of following weight portion: Herba Portulacae 10 parts, Radix Ginseng 9 parts, Indigo Naturalis 8 parts, Rhizoma Coptidis 8 parts, Radix Puerariae 6 parts, Radix Clematidis Henryi 6 parts, 3 parts, Poria, Caulis Lonicerae 3 parts, Herba Ecliptae 3 parts, Plumula Nelumbinis 2 parts, Fructus Gardeniae 3 parts and 1 part, Radix Glycyrrhizae.
Preparation method is as follows:
(1): get Herba Portulacae, wash away impurity, crushed after being dried, cross 90 mesh sieves, adding medical material gross weight 8 times amount volume fraction is the ethanol of 75%, microwave extraction 20 minutes, microwave power is 400W, and Extracting temperature is 50 DEG C, filters and retains Herba Portulacae filtering residue, the extractum that relative density is 1.20 is surveyed, obtained Herba portulacae extract at filtrate reduced in volume to 60 DEG C;
(2): get Radix Ginseng, Indigo Naturalis, Rhizoma Coptidis, Radix Puerariae, Radix Clematidis Henryi, Poria, Caulis Lonicerae, Herba Ecliptae, Plumula Nelumbinis, Fructus Gardeniae and Radix Glycyrrhizae, wash away impurity, after dry, mixing is ground into coarse powder, merge with above-mentioned Herba Portulacae filtering residue, add the purified water of medical material total amount 9 times amount, soak 25 minutes, reflux, extract, 2 times, each 4 hours, filter, merging filtrate, surveys the extractum that relative density is 1.20 at filtrate reduced in volume to 60 DEG C, cooling, slowly add ethanol while stirring to alcohol content for reaching 50%, 4 DEG C leave standstill 24 hours, filter and retain filtering residue, obtaining filtrate A;
(3): the filtering residue obtained in (2) slowly being added while stirring its weight 4 times amount volume fraction is the ethanol of 50%, 4 DEG C leave standstill 4 hours, filter, obtain liquor B and filtering residue; Filtering residue uses the washing with alcohol 2 times of 50% again, collects and merges cleaning mixture;
(4): merge described filtrate A, liquor B and cleaning mixture, the extractum that relative density is 1.20 is surveyed under being evaporated to 60 DEG C of conditions after mixing;
(5): extractum obtained in described Herba portulacae extract and (4) is merged, stirs, at 60 DEG C of temperature, carry out vacuum belt type drying, drying pressure is 0.05MPa, and charging rate is 12L/h, and material strip transfer rate is 28cm/min, after drying, dry extract is pulverized, cross 100 mesh sieves, to obtain final product.
Embodiment 2:
The embodiment of the present invention 2 pharmaceutical composition is made up of the raw material of following weight portion: Herba Portulacae 20 parts, Radix Ginseng 15 parts, Indigo Naturalis 12 parts, Rhizoma Coptidis 12 parts, Radix Puerariae 9 parts, Radix Clematidis Henryi 9 parts, 6 parts, Poria, Caulis Lonicerae 6 parts, Herba Ecliptae 6 parts, Plumula Nelumbinis 4 parts, Fructus Gardeniae 4 parts and 5 parts, Radix Glycyrrhizae.
Preparation method is with embodiment 1.
Embodiment 3:
The embodiment of the present invention 3 pharmaceutical composition is made up of the raw material of following weight portion: Herba Portulacae 25 parts, Radix Ginseng 20 parts, Indigo Naturalis 15 parts, Rhizoma Coptidis 15 parts, Radix Puerariae 12 parts, Radix Clematidis Henryi 12 parts, 9 parts, Poria, Caulis Lonicerae 9 parts, Herba Ecliptae 9 parts, Plumula Nelumbinis 6 parts, Fructus Gardeniae 6 parts and 10 parts, Radix Glycyrrhizae.
Preparation method is with embodiment 1.
Pharmaceutical composition of the present invention is on the impact of systemic lupus erythematosus (sle) MRL/lpr mice
1. experiment material
1.1 laboratory animal
7 week age Healthy female kunming mice 12,7 week age, systemic lupus erythematosus (sle) (SLE) MRL/lpr female mice 60, was provided by Guangdong Medical Lab Animal Center.
1.2 Experimental agents
(1) pharmaceutical composition for preparing of the embodiment of the present invention 1, embodiment 2;
(2) prednisone acetate tablets (LanZhou FoCi Pharmacy Co., Ltd, the accurate word H62020884 of traditional Chinese medicines).
2. experiment grouping
7 week age, Healthy female kunming mice 12 was blank group, systemic lupus erythematosus (sle) (SLE) MRL/lpr female mice in 96 7 week age is divided into 8 groups at random by body weight, often organize 12, to be respectively in SLE model group, the embodiment of the present invention 1 high dose group, the embodiment of the present invention 1 dosage group, the embodiment of the present invention 2 low dose group and positive controls in dosage group, the embodiment of the present invention 1 low dose group, the embodiment of the present invention 2 high dose group, the embodiment of the present invention 2.
After all mice adaptabilities raise one week, each group of rat gives corresponding tested material by following dosage gavage: the high, medium and low dosage of the pharmaceutical composition that the other gavage embodiment of the present invention 1 of high, medium and low dosage component, embodiment 2 prepare, is respectively 6.0g/kg, 3.0g/kg and 1.5g/kg; The prednisone acetate tablets (LanZhou FoCi Pharmacy Co., Ltd, the accurate word H62020884 of traditional Chinese medicines) of positive controls gavage 1.5g/kg, blank group and SLE model group are with isopyknic distilled water gavage.
All test group administration every day 1 time, successive administration 25 days, gets blood for subsequent use, wins spleen at the end of administration.
3. experimental technique and result
3.1 pharmaceutical compositions of the present invention are on the impact of SLE T lymphocyte subsets in spleen of mice immunized
The preparation of PBS liquid: take 8.5gNaCl, 0.2gKCl, 2.85gNa
2hPO
412H
2o and 0.27gKH
2pO
4, with after 1L distilled water standardize solution and get final product;
The preparation of erythrocyte cracked liquid: take tris20.594g and be dissolved in 500-700ml distilled water, then adjust pH7.65 to 1L with 1MHCl, be mixed with tris solution; Again by 0.83%NH
4cl and tris solution in 9:1 ratio mixing after and get final product;
The preparation of Single-cell suspensions: the spleen of each group of mice is put into the culture dish filling cold PBS liquid and cleans, 3mlPBS grinding is added in glass homogenizer, filter with 200 order stainless (steel) wires again, centrifugal for Splenic vessel liquid with rotating speed 1500rpm/min centrifugal 10 minutes, abandon supernatant, and add erythrocyte cracked liquid 2.5ml, mixing, leave standstill and after 5 minutes, add PBS liquid 2ml termination lytic response again, with 1500rpm/min centrifugal 10 minutes again, abandoning supernatant, adds PBS after washing three times, under fluorescence microscope, calculate cell number with PBS.Above operation all need on ice.
Use above Single-cell suspensions, after meter cell number, cell concentration is adjusted to 5 × 10
6cells/ml.Each group is got a wherein mouse boosting cell sample and is done subgroup analysis, and the mouse boosting cell sample of adjusted concentration is added flow cytometry dedicated pipe, and two pipes prepared by every mouse boosting cell sample, and often pipe adds sample 100 μ l.
5 μ l anti-mouse fluorescent-tagged mAbs CD3(FITC are added at the first pipe containing sample dedicated pipe) and 3 μ l anti-mouse fluorescent-tagged mAbs CD4(PE), the second pipe adds 5 μ lCD3(FITC) and 3 μ l anti-mouse fluorescent-tagged mAbs CD8(PE).Room temperature black out hatches 30min, and each pipe adds 500 μ l sheath fluids, vibration mixing.Carry out upper machine analysis.Experimental result is in table 1.
Table 1 the present invention is on the impact of SLE T lymphocyte subsets in spleen of mice immunized
As shown in Table 1, contrast with blank group, SLE mouse model group CD
3+cD
4+lymphocyte level significantly declines, SLE mouse model group CD
3+cD
8+lymphocyte level significantly rises.Contrast with SLE model group, pharmaceutical composition of the present invention and positive controls can make SLE mice CD
3+cD
4+t lymphocyte significantly rises, and makes CD
3+cD
8+t lymphocyte significantly declines, and wherein the high dose group effect of pharmaceutical composition is better.And CD
3+cD
4+lymphocyte is helper T lymphocyte (Th), CD
3+cD
8+lymphocyte mainly plays inhibition regulating action, therefore shows, pharmaceutical composition of the present invention can correct the imbalance state of SLE mouse T cell subgroup.
3.2 pharmaceutical compositions of the present invention are on the impact of serum IL-10, anti-ds-DNA antibody content
By test kit operating instruction operational approach, adopt IL-10, anti-ds-DNA antibody test kit (Shanghai Ke Feng biological reagent company limited), measure the content of each group of mice serum IL-10, anti-ds-DNA antibody, experimental result is in table 2.
Table 2 the present invention is on the impact of SLE mice serum IL-10, anti-ds-DNA antibody content
Note: compare with blank group,
*p<0.05,
*p<0.01; Compare with SLE model group,
#p<0.05,
##p<0.01; Compare with positive controls,
△p<0.05.
As shown in Table 2, compared with blank group, IL-10 and the anti-ds-DNA antibody level of SLE model mice obviously raise; Compared with SLE model group, SLE mice serum IL-10 and the anti-ds-DNA antibody level content of the high, medium and low dosage group of pharmaceutical composition of the present invention significantly reduce, wherein drug regimen object height, middle dosage group effect are very significantly and be better than positive controls, and embodiment 2 groups is particularly remarkable.This shows, medicine of the present invention is remarkable for SLE mice therapeutic effect.
3.3 pharmaceutical compositions of the present invention are on the impact of SLE mouse retention microalbumin content
The collection of specimen and detection: in the 20th day mice is put in metabolic cage respectively and raises, collect 12 hours overnight urine, accurate recording urine volume.After sodium azide process, centrifugal (2000r/min) 10min, measures the mice urine 2ml of storage, and each group adds bromophenol blue (0.231mmol/L) developer 1ml, and mixing (preventing bubble), measures absorbance A with ultraviolet spectrophotometer under 600nm.The content size of absorbance A reflection microdose urine protein, A value is less, and microdose urine protein content is lower.
Experimental data carries out statistical procedures in accordance with the following methods: adopt SPSS10.0 statistical software, calculate data with mean ± standard deviation (
) represent, many groups data compares employing variance analysis, compares and adopt t inspection in group.With p<0.05 for there being statistical significance.Experimental result is in table 3.
Table 3 pharmaceutical composition of the present invention on the impact of SLE mouse retention microalbumin content (
)
Note: compare with blank group,
*p<0.05,
*p<0.01; Compare with SLE model group,
#p<0.05,
##p<0.01; Compare with positive controls,
△p<0.05.
As shown in Table 3, compared with SLE model group, the high, medium and low dosage group of pharmaceutical composition of the present invention all significantly can reduce albuminous content in SLE mice urine, and pharmaceutical composition high dose group effect particularly significantly and be better than positive drug.This shows further, and pharmaceutical composition of the present invention has outstanding therapeutic effect for the damage of SLE mouse kidney.
Owing to describing the present invention by above preferred embodiment, in spirit of the present invention and/or scope, any for replacement/of the present invention or combination implement the present invention, be all apparent for a person skilled in the art, and be included among the present invention.
Claims (5)
1. the pharmaceutical composition of a systemic lupus erythematosus, it is characterized in that, described pharmaceutical composition is made up of the raw material of following weight portion: Herba Portulacae 10-25 part, Radix Ginseng 9-20 part, Indigo Naturalis 8-15 part, Rhizoma Coptidis 8-15 part, Radix Puerariae 6-12 part, Radix Clematidis Henryi 6-12 part, Poria 3-9 part, Caulis Lonicerae 3-9 part, Herba Ecliptae 3-9 part, Plumula Nelumbinis 2-6 part, Fructus Gardeniae 3-6 part and Radix Glycyrrhizae 1-10 part.
2. the pharmaceutical composition of systemic lupus erythematosus as claimed in claim 1, it is characterized in that, described pharmaceutical composition is made up of the raw material of following weight portion: Herba Portulacae 10 parts, Radix Ginseng 9 parts, Indigo Naturalis 8 parts, Rhizoma Coptidis 8 parts, Radix Puerariae 6 parts, Radix Clematidis Henryi 6 parts, 3 parts, Poria, Caulis Lonicerae 3 parts, Herba Ecliptae 3 parts, Plumula Nelumbinis 2 parts, Fructus Gardeniae 3 parts and 1 part, Radix Glycyrrhizae.
3. the pharmaceutical composition of systemic lupus erythematosus as claimed in claim 1, it is characterized in that, described pharmaceutical composition is made up of the raw material of following weight portion: Herba Portulacae 20 parts, Radix Ginseng 15 parts, Indigo Naturalis 12 parts, Rhizoma Coptidis 12 parts, Radix Puerariae 9 parts, Radix Clematidis Henryi 9 parts, 6 parts, Poria, Caulis Lonicerae 6 parts, Herba Ecliptae 6 parts, Plumula Nelumbinis 4 parts, Fructus Gardeniae 4 parts and 5 parts, Radix Glycyrrhizae.
4. the pharmaceutical composition of systemic lupus erythematosus as claimed in claim 1, it is characterized in that, described pharmaceutical composition is made up of the raw material of following weight portion: Herba Portulacae 25 parts, Radix Ginseng 20 parts, Indigo Naturalis 15 parts, Rhizoma Coptidis 15 parts, Radix Puerariae 12 parts, Radix Clematidis Henryi 12 parts, 9 parts, Poria, Caulis Lonicerae 9 parts, Herba Ecliptae 9 parts, Plumula Nelumbinis 6 parts, Fructus Gardeniae 6 parts and 10 parts, Radix Glycyrrhizae.
5. the pharmaceutical composition of the systemic lupus erythematosus as described in any one of claim 1-4, is characterized in that: described pharmaceutical composition is made into powder, tablet or capsule.
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2015
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