CN1265802C - Effective extract of Chinese silkuine bark with cardotonic function and its preparing process and uasge - Google Patents

Effective extract of Chinese silkuine bark with cardotonic function and its preparing process and uasge Download PDF

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CN1265802C
CN1265802C CN 200410019975 CN200410019975A CN1265802C CN 1265802 C CN1265802 C CN 1265802C CN 200410019975 CN200410019975 CN 200410019975 CN 200410019975 A CN200410019975 A CN 200410019975A CN 1265802 C CN1265802 C CN 1265802C
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cortex periplocae
macroporous resin
bark
cardiotonic
effective extract
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CN1593503A (en
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张伯礼
刘虹
高秀梅
潘桂湘
郭俊华
朱晓薇
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Tasly Pharmaceutical Group Co Ltd
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TIANJIN COLLEGE OF TRADITIONAL CHINESE MEDICINE
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Abstract

The present invention discloses an effective extract of Chinese silkvine bark with a cardiotonic function, a preparing process thereof and a usage thereof. The preparing process comprises: the extraction of the medicinal material Chinese silkvine bark: the medicinal material Chinese silkvine bark is extracted with alcohol with concentration of 40% to 80% or methanol with the concentration of 40% to 100% as an extraction solvent, the solvent is steamed after extraction, and the solute is thinned by water and filtered or centrifuged to obtain the settled water solution of the Chinese silkvine bark; (2) the adsorptive separation of macroporous resin: the water solution of the Chinese silkvine bark is adsorbed with the macroporous resin, the macroporous resin is eluted with alcohol with volume 2 to 10 times greater than that of a resin bed, and the eluent is collected, concentrated and dried to obtain the effect extract of Chinese silkvine bark with a cardiotonic function. Isolated heart perfusion experiments show that under the conditions of constant-pressure and constant-flow perfusion, the effect extract of Chinese silkvine bark can obviously increase the left ventricular systolic pressure of the isolated heart of a rat, can increase the maximum upstroke velocity of intraventricular pressure and can lower left-ventricular end-diastolic pressure to improve heart functions; the effect extract of Chinese silkvine bark has the cardiotonic function and can be applied to the preparation of medicines for treating acute congestive heart failure and chronic congestive heart failure.

Description

Cortex Periplocae cardiotonic effective extract and preparation method
Technical field
The invention belongs to medical technical field, be specifically related to a kind of Chinese medicine effective extract of acute and chronic congestive heart failure, preparation method of effective extract for the treatment of.
Background technology
Cortex Periplocae is the dry root bark of asclepiadaceae plant P. sepium Bunge, and the traditional Chinese medical science thinks that it has the effect of wind-damp dispelling, bone and muscle strengthening, is mainly used in anemofrigid-damp arthralgia, soreness of the waist and knees, shortness of breath and palpitation, edema of lower limbs etc.Because of Cortex Periplocae has heart tonifying and diuretic effect concurrently, other Chinese medicine composition compound recipe of the normal and QI invigorating of Cortex Periplocae, warming YANG, blood stasis dispelling, diuretic in recent years, be applied to the clinical treatment of CHF, as the compound recipe SHENGMAI YIN, heart tonifying drink, stilbene add electuary, periploca sepium mixture, heart failure spirit etc.From its preparation technology, be the compound recipe that whole part is used as medicine.Cardiac glycoside composition glucoperiplocymarin does not obtain enrichment in the Cortex Periplocae; The content of glucoperiplocymarin can not be controlled effectively.
Japan scholar Seiichi Sakama (Seiichi Sakama, et al.Constituents of Chinese Crude Drug " Wujiapi " I.Studies on the Aglycones of Steroidal Glycosides of Pei-Wujiapi (1) .Chem.Pharm.Bull, 1968,16 (2): 326) in the disclosed technology, the extraction of Cortex Periplocae is to be solvent with 95% ethanol, and is lower to the extraction efficiency of glucoperiplocymarin.Have nothing to do in the report of Cortex Periplocae extraction process the report that also has nothing to do and prepare in the effective extract of Cortex Periplocae cardiotonic thereafter.
Summary of the invention
The objective of the invention is to overcome deficiency of the prior art, a kind of Cortex Periplocae cardiotonic effective extract is provided.
Another object of the present invention provides a kind of preparation method of Cortex Periplocae cardiotonic effective extract.
Technical scheme of the present invention is summarized as follows:
Cortex Periplocae cardiotonic effective extract is to be prepared from following method:
(1) extraction of Cortex Periplocae medical material: with concentration of volume percent is that 40%~80% ethanol or 40%~100% methanol serve as to extract solvent, and Cortex Periplocae is extracted, and boils off solvent after the extraction, thin up after-filtration or centrifugal, clarifying Cortex Periplocae aqueous solution;
(2) macroporous resin adsorption is separated: the Cortex Periplocae aqueous solution is through macroporous resin adsorption, and with 2~10 times of resin bed volume of ethanol eluting, described alcoholic acid concentration of volume percent is 50%~95%, collect eluent, concentrate, after the drying, promptly get Cortex Periplocae cardiotonic effective extract.
A kind of preparation method of Cortex Periplocae cardiotonic effective extract comprises the steps:
(1) extraction of Cortex Periplocae medical material: with concentration of volume percent is that 40%~80% ethanol or 40%~100% methanol serve as to extract solvent, and Cortex Periplocae is extracted, and boils off solvent after the extraction, thin up after-filtration or centrifugal, clarifying Cortex Periplocae aqueous solution;
(2) macroporous resin adsorption is separated: the Cortex Periplocae aqueous solution is through macroporous resin adsorption, and with 2~10 times of resin bed volume of ethanol eluting, described alcoholic acid concentration of volume percent is 50%~95%, collect eluent, concentrate, after the drying, promptly get Cortex Periplocae cardiotonic effective extract.
In the leaching process of Cortex Periplocae medical material, extract the concentration of volume percent of etoh solvent and be advisable, preferably 60% with 50%~70%.
In the macroporous resin adsorption separation process, the alcoholic acid concentration of volume percent of eluting solvent is advisable with 60%~70%.
Described macroporous resin is non-polar macroporous resin or low pole macroporous resin.
Described non-polar macroporous resin is to be the macroporous resin of skeleton with styrene or ethyl styrene or α-Jia Jibenyixi.
Described low pole macroporous resin is to be the macroporous resin of skeleton with styrene.
The Cortex Periplocae aqueous solution is after macroporous resin adsorption in the described step (2), and preferably first concentration of volume percent with 1~4 times of resin bed volume is 10%~30% ethanol prewashing, reuse 60%~70% ethanol elution.
A kind of Cortex Periplocae cardiotonic effective extract of the present invention can compositions the mode of form by oral administration be applied to the patient who needs this treatment.Be used for when oral, can be made into conventional solid preparation such as tablet, granule or capsule etc.
Various dosage form of the present invention can be by the conventional production method preparation of pharmaceutical field.A kind of Cortex Periplocae cardiotonic effective extract is mixed with one or more carriers, be made into required dosage form then.
The isolated heart perfusion experiment proves: under constant voltage, the constant current perfusion condition, can significantly the raise left ventricular systolic pressure of isolated rat heart of Cortex Periplocae effective extract, increase the maximum climbing speed of intraventricular pressure, improve cardiac function, have cardiotonic thereby reduce left ventricular end-diastolic pressure; And the prewashing position does not have this effect.
Use a kind of Cortex Periplocae cardiotonic effective extract of method preparation of the present invention, removed the crude drug Cortex Periplocae with irrelevant saccharide, aminoacid, polypeptide, inorganic salt and other impurity of cardiotonic, enrichment heart tonifying composition glucoperiplocymarin, especially after 10%~30% ethanol prewashing, concentration effect is better; And greatly reduce paste-forming rate.The present invention improves dosage form for the dosage that reduces medicine, improves curative effect, and it is significant to be convenient to quality control.The present invention extracts fully glucoperiplocymarin with 40%~80% ethanol extraction; Can once finish the enrichment of remove impurity and effective ingredient with macroporous resin.This method cost is low, and is simple to operate, with practical value.
Description of drawings
Fig. 1 is the chromatogram of Cortex Periplocae effective extract;
Fig. 2 is the chromatogram at macroporous resin prewashing position;
Fig. 3 is that the Cortex Periplocae effective extract influences the isolated rat heart left ventricular systolic pressure;
Fig. 4 is that the Cortex Periplocae effective extract influences the isolated rat heart left ventricular diastolic pressure;
Fig. 5 is that the Cortex Periplocae effective extract is to the indoor maximum climbing speed influence of isolated rat heart;
Fig. 6 is that the Cortex Periplocae effective extract is to the indoor maximum fall off rate influence of isolated rat heart.
The specific embodiment
Below in conjunction with embodiment, the present invention is further illustrated:
Embodiment 1
(1) extraction of Cortex Periplocae medical material: it is 80% alcoholic solution that the 500g Cortex Periplocae adds the 3000mL concentration of volume percent, reflux, extract, 3 times, each 2 hours, merge extractive liquid,, be evaporated to about 400mL, add 600mL water dilution after-filtration, get clarifying Cortex Periplocae aqueous solution;
(2) macroporous resin adsorption is separated: with the Cortex Periplocae aqueous solution good 800mL D of pretreatment 101After macroporous resin (production of the Tianjin insecticide factory) absorption, wash with 800mL earlier, the back ethanol prewashing of 800mL 30%, reuse 1600mL 95% ethanol elution, with the eluent evaporated under reduced pressure, vacuum drying gets Cortex Periplocae cardiotonic effective extract 17.5 grams, paste-forming rate is 3.5%, and the shared mass percent of its glucoperiplocymarin is 3.18%.(if the Cortex Periplocae aqueous solution that extracts is without macroporous resin treatment, and its paste-forming rate is 21.3%, and the shared mass percent of glucoperiplocymarin is 0.52%).
The chromatogram of Cortex Periplocae effective extract is seen Fig. 1, and 1 is the glucoperiplocymarin peak among the figure; The chromatogram at prewashing position is seen Fig. 2, no glucoperiplocymarin peak among the figure.
Embodiment 2
The Cortex Periplocae effective extract is to the influence of isolated heart cardiac function
Choose 24 of healthy rats, be divided into 3 groups at random: be respectively blank group, Cortex Periplocae effective extract A group, Cortex Periplocae prewashing position B group, every group 8, the rat sacrificed by decapitation is taken out heart rapidly, place 4 ℃ of K-H liquid, discharge remained blood gently, heart is connected to Langendorff system perfusion device and fixes the beginning perfusion with silk thread, perfusate is kept 37 ℃, and feeds 95% oxygen.Connect electrocardioelectrode, after treating that electrocardio steadily, perfusion pressure is adjusted in about 46 ± 3mmHg, perfusion flow is adjusted in 6.00 ± 0.06ml/min and carries out the constant pressure and flow perfusion, left ventricular systolic pressure (LVSP), left ventricular end-diastolic pressure (LVEDP), maximum the climbing speed (± dp/dt of intraventricular pressure before the record administration of stable back Max), heart rate (HR), slowly inject with Krebs-Henseleit liquid dissolved medicinal liquid through dosing holes, A, B group is pressed the disposable administration of 40mg crude drug/heart respectively; Blank group is given the Krebs-Henseleit liquid/heart with volume, above-mentioned every index in 10 minutes before the record administration and after the administration.
Krebs-Henseleit liquid, it consists of (mmol/L): NaCl 118,, KCl 4.7, MgSO 47H 2O 1.2,, CaCl 22.0,, NaHCO 320, KH 2PO 41.2,, glucose 11.1, pH value 7.2-7.4.
Result data sees Table 1 and table 2, accompanying drawing 3, accompanying drawing 4, accompanying drawing 5 and accompanying drawing 6.
The result shows: under constant voltage, constant current perfusion condition, and can significantly the raise LVSP of isolated rat heart of Cortex Periplocae effective extract A, increase ± dp/dt MaxThereby, reduce LVEDP and improve cardiac function, have cardiotonic: Cortex Periplocae prewashing position B does not have this effect; A, B all do not make significant difference to the rat heart rate.
Embodiment 3
(1) extraction of Cortex Periplocae medical material: it is 40% alcoholic solution that the 500g Cortex Periplocae adds the 4000mL concentration of volume percent, carries out percolation and extracts, and extracting solution is evaporated to about 500mL, adds 500mL water dilution after-filtration, gets clarifying Cortex Periplocae aqueous solution;
(2) macroporous resin adsorption is separated: the Cortex Periplocae aqueous solution is adsorbed with the good 800mL AB-8 macroporous resin (Chemical Plant of Nankai Univ.'s production) of pretreatment, with 8000mL 50% ethanol elution, with eluent evaporated under reduced pressure solvent, get effective extract 31.0 grams of Cortex Periplocae cardiotonic, paste-forming rate 6.2%, the shared mass percent of its glucoperiplocymarin is 1.65%.
Embodiment 4
(1) extraction of Cortex Periplocae medical material: it is 70% alcoholic solution that the 500g Cortex Periplocae adds the 4000mL concentration of volume percent, and reflux, extract, 2.5 hours is extracted 2 times, merge extractive liquid,, be evaporated to about 300mL, add 700mL water dilution after-filtration, get clarifying Cortex Periplocae aqueous solution;
(2) macroporous resin adsorption is separated: with the Cortex Periplocae aqueous solution good 800mL D of pretreatment 301Macroporous resin (production of Tianjin insecticide factory) absorption with 3200mL 70% ethanol elution, evaporated under reduced pressure solvent, gets effective extract 33.6 grams of Cortex Periplocae cardiotonic, and paste-forming rate is 6.7%, and the shared mass percent of its glucoperiplocymarin is 1.57%.
Embodiment 5
(1) extraction of Cortex Periplocae medical material: it is 50% alcoholic solution merceration that the 500g Cortex Periplocae adds the 4000mL concentration of volume percent, and extracting solution is evaporated to about 300mL, adds 700mL water dilution after-filtration, gets clarifying Cortex Periplocae aqueous solution;
(2) macroporous resin adsorption is separated: the Cortex Periplocae aqueous solution is adsorbed with the good HPD100 macroporous resin of pretreatment (Cangzhou precious grace chemical industry company limited is produced), with 3200mL 70% ethanol elution, the evaporated under reduced pressure solvent, get effective extract 31.6 grams of Cortex Periplocae cardiotonic, paste-forming rate is 6.3%, and the shared mass percent of its glucoperiplocymarin is 1.73%.
Embodiment 6
(1) extraction of Cortex Periplocae medical material: it is that 40% methanol solution carries out the percolation extraction that the 500g Cortex Periplocae adds the 8000mL concentration of volume percent, and extracting solution is evaporated to about 400mL, adds 700mL water dilution after-filtration, gets clarifying Cortex Periplocae aqueous solution;
(2) macroporous resin adsorption is separated: after the Cortex Periplocae aqueous solution is tried 102 (productions of Shanghai chemical reagent work) absorption with good the going up of pretreatment, wash with 800mL earlier, the back ethanol prewashing of 3200mL 10%, reuse 8000mL 50% ethanol elution, with the eluent evaporated under reduced pressure, vacuum drying gets Cortex Periplocae cardiotonic effective extract 17.4 grams, paste-forming rate is 3.5%, and the shared mass percent of its glucoperiplocymarin is 3.72%.
Embodiment 7
(1) extraction of Cortex Periplocae medical material: the 500g Cortex Periplocae adds the 3000mL methanol solution, reflux, extract, 3 times, each 2 hours, merge extractive liquid, was evaporated to driedly, adds 800mL water dilution after-filtration, clarifying Cortex Periplocae aqueous solution;
(2) macroporous resin adsorption is separated: with the Cortex Periplocae aqueous solution good D of pretreatment 201After macroporous resin (production of Tianjin insecticide factory) adsorbs, earlier with the 1600mL washing, the back ethanol prewashing of 1600mL 30%, reuse 8000mL 60% ethanol elution, with the eluent evaporated under reduced pressure, vacuum drying gets Cortex Periplocae cardiotonic effective extract 15.8 grams.Paste-forming rate is 3.2%, and the shared mass percent of its glucoperiplocymarin is 3.87%.
When practical operation, the non-polar macroporous resin model that can also select for use is: D 101(Tianjin insecticide factory); HPD 100, or HPD 300 (Cangzhou precious grace chemical industry company limited); GDX-104 (production of Tianjin reagent two factories); SIP-1100, or SIP-1200, or SIP-1300, or SIP-1400 (Shanghai Institute of Pharmaceutical Industry); Last examination 101, or go up examination 102, or go up examination 401, or go up examination 402 (Shanghai chemical reagent works); Nanjing University 3520, or D1, or D, or Dm2, Dm5 (Chemical Plant of Nankai Univ.) or the like.The model of eligible low pole macroporous resin is: D 201Or D 101(Tianjin insecticide factory); AB-8 (Chemical Plant of Nankai Univ.); HPD 500, HPD 400 (Cangzhou precious grace chemical industry company limited); D201, D301 (Tianjin insecticide factory) or the like.In addition, can also select for use external Diaion (HP10, HP20, HP21), Amberlite (XAD-1, XAD-2).
Embodiment 8
Make tablet (1000 slice prescription):
Cortex Periplocae cardiotonic effective extract 125g
Lactose 250g
Microcrystalline Cellulose 105g
Sodium Hydroxymethyl Stalcs 15g
5%PVPK 30Solution 100ml
Aspartame 5g
Magnesium stearate 2g
Preparation method: remove PVPK 30Outside the solution, it is standby that above supplementary material is all crossed 100 mesh sieves.With Cortex Periplocae cardiotonic effective extract, lactose, microcrystalline Cellulose, Sodium Hydroxymethyl Stalcs and aspartame mix homogeneously.Use PVPK 30Solution system soft material, 16 mesh sieves are granulated, 60 ℃ of dryings and granulate.Granule behind the granulate adds magnesium stearate, mix homogeneously, tabletting.Every heavily about 0.5 gram of sheet.It is the 0.125g/ sheet that perfume (or spice) adds sheet cardiotonic effective extract content.
Usage and consumption: oral, twice, one time on the one a slice.
Embodiment 9
Make capsule (1000 prescriptions):
Cortex Periplocae cardiotonic effective extract 64g
Lactose 170g
Microcrystalline Cellulose 100g
Sodium Hydroxymethyl Stalcs 8g
5%PVPK 30Solution 80ml
Aspartame 5g
Magnesium stearate 1g
Micropowder silica gel 2g
Preparation method: remove PVPK 30Outside the solution, it is standby that above supplementary material is all crossed 100 mesh sieves.With Cortex Periplocae cardiotonic effective extract, lactose, microcrystalline Cellulose, Sodium Hydroxymethyl Stalcs and aspartame mix homogeneously.Use PVPK 30Solution system soft material, 20 mesh sieves are granulated, 60 ℃ of dryings and granulate.Granule behind the granulate adds magnesium stearate and micropowder silica gel, mix homogeneously, the capsule of packing into No. 1.Heavily about 0.35 gram of every capsules.It is the 0.064g/ grain that perfume (or spice) adds sheet cardiotonic effective extract content.
Usage and consumption: oral, one day twice, once two.
Table 1 Cortex Periplocae effective extract is to isolated rat heart LVSP (mmHg), LVEDP (mmHg) ,+dp/dtmax (mmHgs -1) ,-dp/dtmax (mmHgs -1) influence (x ± s)
Group Before the administration After the administration
1min 2min 3min 4min 5min 10min
Blank group n=8 LVSP LVEDP +dp/dt max -dp/dt max 73.88±8.93 - 0.84±4.65 1018.40±195.94 - -68.55±134.19 - 75.10±9.56 (101.61±2.76) 1.62±4.90 1040.69±187.32 (102.36±4.09) -628.86±134.93 (103.50±4.01) 74.67±7.78 (101.37±5.08) 1.13±5.09 1032.66±168.11 (101.95±6.92) -626.94±150.02 (102.92±8.98) 74.21±7.52 (100.83±6.05) 1.65±5.52 1014.76±161.99 (100.33±8.88) -619.66±146.60 (101.81±9.55) 74.98±7.12 (102.02±7.45) 2.10±6.00 1020.49±145.89 (101.30±10.22) -626.87±144.70 (103.32±10.86) 74.18±7.38 (100.89±7.30) 2.47±6.38 1009.99±149.99 (100.23±11.01) -623.57±147.37 (102.65±11.26) 75.07±12.29 (101.45±9.13) 1.38±6.14 1032.44±221.01 (101.06±9.02) -636.32±183.83 (103.16±14.91)
A group n=8 1.36mg medicine/heart LVSP LVEDP +dp/dt max -dp/dt max 72.30±11.78 - 2.54±4.91 967.86±195.29 - -569.98±140.74 - 88.24±16.89 * (121.66±8.50) *** 1.74±9.67 1167.00±253.79 (120.59±8.66) *** -692.21±201.75 (121.41±12.99) *** 87.03±22.78 (119.18±13.68) ** 1.27±9.39 1145.44±249.72 (118.79±13.22) ** -692.08±208.24 (121.37±16.76) ** 81.10±13.60 (112.37±6.91) ** 2.67±9.51 1063.92±151.76 (112.02±15.37) * -636.95±124.37 (113.81±14.02) * 78.05±9.11 (108.85±8.34) 3.34±8.88 1019.40±122.25 (107.92±17.13) -605.00±82.17 (109.51±17.79) 78.76±12.27 (109.92±13.44) 4.22±8.25 1004.82±129.79 (106.72±19.79) -583.12±71.20 (106.74±23.18) 78.51±12.20 (110.14±17.58) 4.27±8.79 1075.95±304.15 (118.48±56.90) -665.52±193.19 (124.23±54.89)
B group n=8 0.78mg medicine/heart LVSP LVEDP +dp/dt max -dp/dt max 71.32±8.58 - 2.72±2.74 977.66±124.72 - -619.32±95.84 - 74.18±10.00 # (104.03±7.24) ### 2.08±2.51 1026.45±130.98 (105.19±7.55) ### -646.07±105.29 (104.48±8.41) ### 73.81±10.62 (103.37±7.26) ## 2.11±2.57 1022.88±136.03 (104.74±7.32) ## -649.83±94.98 (105.28±7.65) # 72.94±10.76 (102.04±6.14) ## 2.45±3.10 1011.04±141.58 (103.39±6.59) -643.53±98.29 (104.13±7.26) 72.77±10.83 (101.75±5.24) 2.89±3.56 1002.37±137.69 (102.50±5.90) -643.10±95.63 (104.06±6.44) 73.81±12.72 (102.95±6.58) 3.42±4.59 1012.24±155.79 (103.30±5.86) -647.70±101.28 (104.72±6.93) 75.03±12.92 (104.93±11.41) 3.34±3.94 1017.73±138.23 (104.33±10.23) -656.69±77.10 (107.06±12.90)
The F value LVSP LVEDP +dp/dt max -dp/dt max 0.144 - 0.485 0.187 - 0.344 - 0.137 (21.689) 0.011 1.231 (15.497) 0.368 (9.518) 3.113 (8.598) 0.056 1.020 (7.079) 0.350 (5.765) 1.897 (7.911) 0.053 0.302 (2.462) 0.078 (2.852) 1.294 (2.543) 0.074 0.045 (0.690) 0.238 (0.576) 0.672 (1.938) 0.142 0.005 (0.462) 0.690 (0.141) 0.498 (0.878) 0.400 0.137 (0.600) 0.070 (0.886)
Annotate: 1. with the blank group than * P<0.05, * * P<0.01, * * * P<0.001: with the A group than #P<0.05, ##P<0.01, ###P<0.001
2. numerical value is numerical value before each time numerical value/administration in the bracket *100 each numerical value rising relative value who obtains.
Table 2 Cortex Periplocae Radicis extract is to isolated rat heart heart rate (HR/timesmin -1) influence (n=8) (x ± s)
Group Before the administration After the administration
1min 2min 3min 4min 5min 10min
Blank group A group B group F value 165.18±50.83 175.07±36.01 174.71±44.47 0.144 155.71±48.30 169.14±18.10 164.25±40.90 0.256 155.52±44.06 158.42±20.85 170.94±40.84 0.399 154.56±40.60 161.96±16.23 167.62±35.15 0.327 150.89±41.29 167.86±14.16 155.03±43.16 0.498 159.29±44.26 165.26±17.79 153.80±43.58 0.190 156.44±36.76 165.30±17.06 158.90±44.11 0.143

Claims (8)

1. Cortex Periplocae cardiotonic effective extract is characterized in that being prepared from following method:
(1) extraction of Cortex Periplocae medical material: with concentration of volume percent is that 40%~80% ethanol or 40%~100% methanol serve as to extract solvent, and Cortex Periplocae is extracted, and boils off solvent after the extraction, thin up after-filtration or centrifugal, clarifying Cortex Periplocae aqueous solution;
(2) macroporous resin adsorption is separated: the Cortex Periplocae aqueous solution is through macroporous resin adsorption, and with 2~10 times of resin bed volume of ethanol eluting, described alcoholic acid concentration of volume percent is 50%~95%, collect eluent, concentrate, after the drying, promptly get Cortex Periplocae cardiotonic effective extract.
2. the preparation method of a Cortex Periplocae cardiotonic effective extract is characterized in that comprising the steps:
(1) extraction of Cortex Periplocae medical material: with concentration of volume percent is that 40%~80% ethanol or 40%~100% methanol serve as to extract solvent, and Cortex Periplocae is extracted, and boils off solvent after the extraction, thin up after-filtration or centrifugal, clarifying Cortex Periplocae aqueous solution;
(2) macroporous resin adsorption is separated: the Cortex Periplocae aqueous solution is through macroporous resin adsorption, and with 2~10 times of resin bed volume of ethanol eluting, described alcoholic acid concentration of volume percent is 50%~95%, collect eluent, concentrate, after the drying, promptly get Cortex Periplocae cardiotonic effective extract.
3. the preparation method of a kind of Cortex Periplocae cardiotonic effective extract according to claim 2, the concentration that it is characterized in that described extraction etoh solvent is 50%~70%.
4. the preparation method of a kind of Cortex Periplocae cardiotonic effective extract according to claim 2 is characterized in that described eluting solvent concentration of ethanol is 60%~70%.
5. the preparation method of a kind of Cortex Periplocae cardiotonic effective extract according to claim 2 is characterized in that described macroporous resin is non-polar macroporous resin or low pole macroporous resin.
6. the preparation method of a kind of Cortex Periplocae cardiotonic effective extract according to claim 5 is characterized in that described non-polar macroporous resin is is the macroporous resin of skeleton with styrene or ethyl styrene or α-Jia Jibenyixi.
7. the preparation method of a kind of Cortex Periplocae cardiotonic effective extract according to claim 5 is characterized in that described low pole macroporous resin is is the macroporous resin of skeleton with styrene.
8. the preparation method of a kind of Cortex Periplocae cardiotonic effective extract according to claim 2, it is characterized in that the Cortex Periplocae aqueous solution is after macroporous resin adsorption in the described step (2), with the prewashing of 1~4 times of resin bed volume of ethanol, described alcoholic acid concentration of volume percent is 10%~30%.
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