CN1883511A - Inclusion compound of ants supercritical extracts and preparation process thereof - Google Patents
Inclusion compound of ants supercritical extracts and preparation process thereof Download PDFInfo
- Publication number
- CN1883511A CN1883511A CNA2006100405959A CN200610040595A CN1883511A CN 1883511 A CN1883511 A CN 1883511A CN A2006100405959 A CNA2006100405959 A CN A2006100405959A CN 200610040595 A CN200610040595 A CN 200610040595A CN 1883511 A CN1883511 A CN 1883511A
- Authority
- CN
- China
- Prior art keywords
- formica fusca
- beta
- oil
- schardinger dextrin
- clathrate
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
Images
Landscapes
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
Disclosed is a kind of clathrate compound of ant super-critical extractant and its preparation. The compound is prepared by crushing drying ants, followed by extracting for 10 to 60min at the pressure of 20 to 36Mpa and temperature of 30 to 60 degree with super-critical extracting method, formulating solution with ant oil and beta-cyclodextric at the molecule ratio of 1:4 to 8, including with colloid grinding method at the temperature of 50 to 80 degree for 20 to 60 min and finally the produced clathrate compound being sieved, washed and dried. The clathrate compound is characterized in good anti-inflammatory and pain-easing effect, stabilization improvement, bad odor shielding, drug utility ratio increase and easy preparation. And the preparation process is simply operated, good in effect and easy to be applied in industrialization.
Description
Technical field
The invention belongs to pharmaceutical field, relate to a kind of clathrate of ants supercritical extracts, the invention still further relates to the preparation technology of the clathrate of this supercritical extract.
Background technology
Formica fusca has another name called XUANJU, is Arthropoda Insecta (Insecta) Hymenoptera (Hymenoptera) Formicidae (Formicidae) animal.The Formica fusca Chinese crude drug mostly is the Polyhachis vicina Roger dry polypide of (Polyrhachis vicina Roger has another name called " ancient cooking vessel dash forward thorniness Formica fusca "), has the kidney invigorating, nourishing the liver, blood circulation promoting and blood stasis dispelling, the effect of wind dispelling cold expelling, be widely used in rheumatoid arthritis in recent years, the treatment of hepatitis B etc.Because Polyhachis vicina Roger complicated component, contain materials such as rich in protein, aminoacid, sugar, fat, multiple alkaloid, steroid compounds, enzyme, terpenes, triterpenes, formic acid, adenosine triphosphate, hormone, vitamin, the composition more complicated, though the curative effect of Polyhachis vicina Roger and preparation thereof is clear and definite, but its mechanism of action, effective substance it be unclear that, and the composition of the extract that different extraction processes obtains and effect are also incomplete same.Therefore, should design corresponding extraction process at different medicinal effects.
Supercritical liquid extraction technique (Superitical Fluid Extraction, be called for short SFE) be a kind of extraction, the isolation technics of rising in 20th century, supercritical fluid has gas, both characteristics of liquid concurrently, density approaches liquid, viscosity and diffusion coefficient approach gas, not only have the solvability suitable, and have good mass-transfer performance with liquid flux.Supercritical liquid extraction technique is exactly a this special nature of utilizing supercritical fluid, under condition of high voltage, supercritical fluid is contacted with solid or liquid mixture to be separated, the operating pressure of regulating system and temperature, extract desired material, method by blood pressure lowering or intensification subsequently, reduce the density of supercritical fluid, make extract obtain separating, this technology has extract at low temperature, the activity of the composition of remaining valid, do not have dissolvent residual and can carry out characteristics such as Selective Separation, is to utilize CO under the supercriticality
2Solvent properties preferably, the extraction separation of the stronger composition of volatility, heat-sensitive substance and liposoluble constituent is had effect preferably, just be subjected to increasing attention, new research, application achievements are constantly come out.
The influence factor of supercritical extraction has fluid ratio, the CO of SFE
2Flow, pressure, time, temperature, comminuted powder granularity etc.Pressure is most important parameter among the SFE.Under the uniform temperature, along with the increase of pressure, fluid density significantly increases, and the dissolubility of solute increases, and extraction efficiency improves.But too high pressure obviously improves production cost, and its extraction yield increases limited.In the SFE process, temperature increases, and has strengthened its diffusivity, makes extract at supercritical CO
2Middle dissolubility increases.Help extraction.But along with the increase of temperature, the dissolubility of impurity also increases, and makes subtractive process complicated, thereby reduces the yield of product.Simultaneous temperature increases, CO
2Fluidic density reduces, and makes to the dissolving power decline of solute, reduces product yield.The extraction time increases, and helps the dissolution equilibrium of effective ingredient in supercritical fluid and the solute, and the time that increases extraction just increases the extraction yield.Owing to behind the extraction certain hour, along with the minimizing of effective ingredient in the solute, increase the extraction time again, the extraction yield increases slowly, and energy consumption increases.And some invalid components also is extracted out more, directly influences the quality of product.
The clathrate technology can make medicine peak time in vivo shorten, promote the medicine absorption in vivo, reaching peak concentration raises, improve bioavailability, and the medicine holdup time is in vivo shortened, and eliminate the half-life shortening, eliminate rapidly, medicine can be detained for a long time when reaching the curative effect of curing the disease in vivo, reduce side effect.The report that adopts inclusion technique that ants supercritical extracts is studied is not arranged at present as yet.
Summary of the invention
The clathrate that the purpose of this invention is to provide a kind of ants supercritical extracts.
Another object of the present invention provides the preparation technology of the clathrate of above-mentioned ants supercritical extracts.
The objective of the invention is to realize by following measures:
A kind of clathrate of ants supercritical extracts, this clathrate prepares through the following steps:
A. with the Formica fusca crushed after being dried, cross 60 mesh sieves; Get an amount of Formica fusca powder and drop in the extraction kettle, regulate extractant CO
2Flow velocity be 10~30L/h, be 20~36Mpa in extracting pressure, extract 10~60min under 30~60 ℃ of conditions of extraction temperature; Regulate extraction-container pressure, separated and collected Formica fusca oil;
B. be that 1: 4~8 ratio is got Formica fusca oil and beta-schardinger dextrin-in host and guest's molecular proportion of Formica fusca oil and beta-schardinger dextrin-;
C. the water that beta-schardinger dextrin-is added weight and be 2~4 times of beta-schardinger dextrin-s grinds evenly, makes the beta-schardinger dextrin-aqueous solution, and adding volume in the Formica fusca oil is the ethanol of Formica fusca oil volume 10~20%, makes Formica fusca oleyl alcohol solution;
D. pour the beta-schardinger dextrin-aqueous solution into colloid mill, regulating suitable mill spacing grinds, drip Formica fusca oleyl alcohol solution in the process of lapping and carry out enclose, control enclose temperature is that 50-80 ℃, enclose time are 20-60 minute, and clathrate is through sucking filtration, washing, dry getting final product.
The clathrate of described ants supercritical extracts, this clathrate prepares by following preferred steps:
A. with the Formica fusca crushed after being dried, cross 60 mesh sieves; Get an amount of Formica fusca powder and drop in the extraction kettle, regulate extractant CO
2Flow velocity be 20L/h, be 36Mpa in extracting pressure, extract 50min under 40 ℃ of conditions of extraction temperature; Regulate extraction-container pressure, separated and collected Formica fusca oil;
Host and guest's molecular proportion b. oily in Formica fusca and beta-schardinger dextrin-is that 1: 6 ratio is got Formica fusca oil and beta-schardinger dextrin-;
C. the water that beta-schardinger dextrin-is added weight and be 2 times of beta-schardinger dextrin-s grinds evenly, makes the beta-schardinger dextrin-aqueous solution, and adding volume in the Formica fusca oil is the ethanol of Formica fusca oil volume 10%, makes Formica fusca oleyl alcohol solution;
D. pour the beta-schardinger dextrin-aqueous solution into colloid mill, regulate suitably the mill spacing and grind, drip Formica fusca oleyl alcohol solution in the process of lapping and carry out enclose, control enclose temperature is that 60 ℃, enclose time are 40 minutes, and clathrate is through sucking filtration, washing, dry getting final product.
The clathrate of above-mentioned ants supercritical extracts, wherein Formica fusca is a Polyhachis vicina Roger.
The preparation technology of the clathrate of described ants supercritical extracts comprises the following steps:
A. with the Formica fusca crushed after being dried, cross 60 mesh sieves; Get an amount of Formica fusca powder and drop in the extraction kettle, regulate extractant CO
2Flow velocity be 10~30L/h, be 20~36Mpa in extracting pressure, extract 10~60min under 30~60 ℃ of conditions of extraction temperature; Regulate extraction-container pressure, separated and collected Formica fusca oil;
B. be that 1: 4~8 ratio is got Formica fusca oil and beta-schardinger dextrin-in host and guest's molecular proportion of Formica fusca oil and beta-schardinger dextrin-;
C. the water that beta-schardinger dextrin-is added weight and be 2~4 times of beta-schardinger dextrin-s grinds evenly, makes the beta-schardinger dextrin-aqueous solution, and adding volume in the Formica fusca oil is the ethanol of Formica fusca oil volume 10~20%, makes Formica fusca oleyl alcohol solution;
D. pour the beta-schardinger dextrin-aqueous solution into colloid mill, regulating suitable mill spacing grinds, drip Formica fusca oleyl alcohol solution in the process of lapping and carry out enclose, control enclose temperature is that 50-80 ℃, enclose time are 20-60 minute, and clathrate is through sucking filtration, washing, dry getting final product.
The extraction process of the clathrate of described ants supercritical extracts comprises following preferred steps:
A. with the Formica fusca crushed after being dried, cross 60 mesh sieves; Get an amount of Formica fusca powder and drop in the extraction kettle, regulate extractant CO
2Flow velocity be 20L/h, be 36Mpa in extracting pressure, extract 50min under 40 ℃ of conditions of extraction temperature; Regulate extraction-container pressure, separated and collected Formica fusca oil;
Host and guest's molecular proportion b. oily in Formica fusca and beta-schardinger dextrin-is that 1: 6 ratio is got Formica fusca oil and beta-schardinger dextrin-;
C. the water that beta-schardinger dextrin-is added weight and be 2 times of beta-schardinger dextrin-s grinds evenly, makes the beta-schardinger dextrin-aqueous solution, and adding volume in the Formica fusca oil is the ethanol of Formica fusca oil volume 10%, makes Formica fusca oleyl alcohol solution;
D. pour the beta-schardinger dextrin-aqueous solution into colloid mill, regulate suitably the mill spacing and grind, drip Formica fusca oleyl alcohol solution in the process of lapping and carry out enclose, control enclose temperature is that 60 ℃, enclose time are 40 minutes, and clathrate is through sucking filtration, washing, dry getting final product.
The preparation technology of the clathrate of above-mentioned ants supercritical extracts, wherein Formica fusca is a Polyhachis vicina Roger.
The extractant of supercritical extraction is generally the CO that concentration is 99.5~99.9% food grade
2
Beneficial effect of the present invention:
The clathrate of ants supercritical extracts provided by the invention has antiinflammatory, analgesic activity preferably.Adopt beta-schardinger dextrin-that the Formica fusca oil through supercritical extraction is carried out enclose, liquid-powderization can be improved its stability and covers bad smell, improve the utilization rate of medicine, be convenient to preparation, improve curative effect.
Adopt the more traditional organic solvent extraction method of method of supercritical carbon dioxide extraction very big advantage all to be arranged at aspects such as product quality, yield and environmental conservation.Extraction process provided by the invention has that extraction temperature is low, the time is short, extract composition advantage more completely.The present invention adopts orthogonal experiment that the enclose condition is screened, and selecting clathrate yield, clathrate oil content, oily utilization rate for use is the index screening optimised process, and it is investigated and studies.Clathrate preparation technology provided by the invention has simple to operate, effective, is easy to advantages such as commercial application.
One, ants supercritical extraction process research
1, uniform experiment design
By trial test, find Formica fusca oil supercritical CO
2The bigger factor of extraction yield influence has extraction kettle pressure, extraction kettle temperature, extraction time, and we select these 3 factors for investigating object.Because factor is 3 o'clock,
Get m=4, n=m+1=5 selects U
5(5
4) uniform designs table, be 3 according to factor, look into corresponding use table, determine wherein the 1st, 2,4, row form U
5(5
4) table arranges even test, factor level sees Table 1, test arrangement and the results are shown in Table 2.
Table 1 uniform Design 3 factors 5 water-glasses
The | Factor | 1 | Factor 2 | Factor 3 |
1 2 3 4 5 | 1 2 3 4 5 | 2 4 1 3 5 | 4 3 2 1 5 |
Table 2 uniform Design experiment and table as a result
The experiment number | Extracting pressure (MPa) | Extraction temperature (℃) | The extraction time (min) | Extraction yield (%) |
1 2 3 4 5 | 20 24 28 32 36 | 45 55 40 50 60 | 40 30 20 10 50 | 10.6 8.1 12.1 8.6 8.4 |
2, supercritical extraction result and date processing are imported computer with the supercritical extraction result, with uniform Design 1.0 softwares the Uniform Design experimental result have been carried out regression analysis, and regressive mathematical model is:
y=189+7.77lnx
1-49.5lnx
2+4.52lnx
3
Coefficient R=0.999
Return significance test: F test value Ft=1538.7>F check marginal value F0.05 (3,1)=215.71 regression equation significance.
Theoretical optimum extraction condition is: X
1=36, X
2=40, X
3=50;
Optimum process condition is: extracting pressure 36Mpa, 40 ℃ of extraction temperature, extraction time 50min.
In the practical application, can do suitable adjustment according to practical situation.
3, extraction process demonstration test
For verifying this result's accuracy, we have done 5 times and have appended confirmatory experiment under optimum condition, the results are shown in Table 3.
Table 3 extraction process demonstration test result
Sample number | Extraction yield (%) | Average extraction yield (%) | RSD(%) |
1 2 3 4 5 | 13.2 13.4 13.9 13.4 13.7 | 13.52 | 2.1 |
The demonstration test presentation of results, stable, feasible, the suitable industrialization production of this extraction process.
Two, pharmacodynamic study of the present invention:
1 experiment material
1.1 instrument
The 4504 type Zu Disi digital stopwatch (Hong Kong Huaxing foundation company limited) that moves; YSD pharmacology physiology is used instrument more; FA1004 type electronic balance (Shanghai Hengping Science Instrument Co., Ltd.); The volume determination instrument; Card punch (diameter 7mm); 501 type ultrathermostats (Shanghai City experimental apparatus head factory).
1.2 medicine and reagent
Ibuprofen (Sino-America Tianjin Shike Pharmaceutical Co., Ltd., lot number: 05040122); Sodium carboxymethyl cellulose (Shanghai chemical reagents corporation of Chinese Medicine group, lot number: F20020928); Acetic acid (AR, Nanjing chemical reagent one factory, lot number: 031110996); Dimethylbenzene (AR, Nanjing chemical reagent factory, lot number: 990305);
Be subjected to reagent (Nanjing Zhongshan Pharmaceutical Co., Ltd. provides):
(1) ants supercritical ant oil (according to embodiment 1 preparation);
(2) ants supercritical ant oil clathrate (according to embodiment 5 preparations).
1.3 laboratory animal
SD rat (body weight: 150~180g; Sex: male)
Kunming mouse (body weight: 18~22g; Sex: male and female half and half)
The unit of providing: Second Military Medical University, PLA's Experimental Animal Center.
Licence: SCXK (Shanghai) 2002-0006.
2 methods and result:
2.1 mice acetic acid twisting method analgesic test
The animal grouping: the difference according to the weight of animals is divided into 4 groups at random, 12 every group.Establish blank group (0.5%CMC-Na solution 0.50ml/10g) respectively, positive drug ibuprofen group, ants supercritical ant oil (hereinafter to be referred as: Formica fusca oil) group, ants supercritical ant oil clathrate are (hereinafter to be referred as group clathrate).
Medication: continuously the i.g. administration is 6 days, and fasting was spent the night in 12 hours, the 7th day again i.g. be administered once front and back administration 7 times altogether, administration volume: 0.50ml/10g.
The test key step: the i.g. administration is 6 days continuously, and fasting 12 hours is freely drunk water.I.g. relative medicine respectively then, after the administration 40min i.p.0.6% acetum 0.20ml/ only, observe and record i.p. acetum after the writhing response number of times of animal in the 15min.Writhing response show as the mouse web portion indent, trunk and back leg are upheld, the arm protuberance.The index of representing pain degree with the number of times that occurs writhing response in the 15min.Each experimental group writhing response number of times average and matched group compares and carry out t check.
Result of the test: result of the test represents that with writhing response number of times in the 15min t-student check the results are shown in Table 4 between statistical test employing group.
Table 4 Formica fusca oil, clathrate are to mouse writhing analgesic test experimental result
Group | Dosage (crude drug amount g/kg) | Number of animals | Writhing response number of times X ± SD |
CMC-Na clathrate Formica fusca oil ibuprofen | --- 1.5 1.5 1.0 | 12 12 12 12 | 38.5±10.4 19.1±3.2 **## 29.7±6.4 * 7.6±6.3 ** |
Annotate:
*: P<0.05,
*: P<0.01, compare with matched group; (t check) compared with the Formica fusca line of oils in ##:P<0.01.
The result shows: relatively there were significant differences (P<0.05 or P<0.01) for the mouse writhing stoichiometric number of clathrate group, Formica fusca line of oils and matched group.Illustrate that clathrate, Formica fusca oil Dichlorodiphenyl Acetate cause the mouse writhing test and have significant analgesia role.Under identical administration (crude drug amount), the body number of turning round of clathrate group obviously is less than the Formica fusca line of oils, and there is significant difference in the two.
The tail method analgesic test 2.2 mice hot water contracts
Animal grouping: with test 2.1
Medication: with test 2.1
The test key step:
The preceding animal of test at first fasting spent the night in 12 hours, freely drank water.The experiment mice tail is immersed 50 ℃ of water bath with thermostatic control 3cm, write down tail incubation period (TFL) that contracts and be threshold of pain index.Twice of administration before measurement (5min at interval), with its average as the basic threshold of pain, reject irritated or blunt animal TFL (<4s or>30s).I.g. relative medicine respectively then, 40min immerses 50 ℃ of water bath with thermostatic control 3cm with the experiment mice tail after the administration, record contracts the tail time again, and with administration before relatively, and calculate the threshold of pain and improve percentage rate (%).
Percentage rate (%)=(TFL-basis TFL after the administration)/basic TFL*100% is improved in the threshold of pain
Result of the test: experimental result improves percentage rate (%) expression with contract tail incubation period (TFL) and the threshold of pain, and the t-student check the results are shown in Table 5 between statistics employing group.
Table 5 Formica fusca oil, clathrate are to the mice hot water tail method analgesic test result that contracts
Group | Dosage (crude drug amount g/kg) | Number of animals | End reaction incubation period (s) (X ± SD) contracts | ||
Before the administration | 40min after the administration | Percentage rate (%) is improved in the threshold of pain | |||
CMC-Na clathrate Formica fusca oil ibuprofen | --- 3.0 3.0 1.0 | 12 12 12 12 | 6.39±0.61 6.41±1.52 6.03±1.61 6.05±1.19 | 7.32±0.72 9.41±1.79 8.30±2.01 9.15±2.19 | 12.44±5.25 48.86±15.51 ** 39.06±17.32 ** 51.40±23.79 ** |
Annotate:
*: P<0.05,
*: P<0.01, compare (t check) with matched group.
The result shows, clathrate, Formica fusca oil can obviously prolong mice hot water and contract tail incubation period (P<0.01, with matched group relatively), show that clathrate, Formica fusca oil have significant analgesia role.Percentage rate is improved greater than Formica fusca oil in the threshold of pain of clathrate.
2.3 mice caused by dimethylbenzene xylene ear swelling inhibitory action test
The animal grouping is with test 2.1
Medication is with test 2.1
The foundation of dimethylbenzene mice ear model and main experimental implementation:
Gastric infusion is after 6 days continuously, and fasting was spent the night in 12 hours.The 7th day again gastric infusion once, 1 hour at interval, evenly be coated with dimethylbenzene 0.05mL on the two sides, front and back of mouse right ear, left ear is left intact.Each group is taken off cervical vertebra execution mice respectively at causing scorching back 60 minutes, cuts ears and lays round auricle in the ears same area respectively with 7mm diameter card punch, and electronic balance claims quality.Calculate swelling degree and inhibitory rate of intumesce, relatively administration group and matched group difference condition.
Observation index:
(1) left auricle quality
(2) cause scorching back auris dextra tablet quality
(3) swelling degree swelling degree (mg)=auris dextra tablet quality-left auricle quality
(4) inhibitory rate of intumesce=(matched group swelling degree-administration group swelling degree)/matched group swelling degree * 100%
Experimental result: experimental result is shown with the swelling kilsyth basalt, be the results are shown in Table 6.T-student check between statistics employing group.
Table 6 Formica fusca extract, clathrate xylol cause the inhibitory action result of the test of mice ear
Group | Dosage (crude drug amount g/kg) | Number of animals | Swelling degree (mg) X ± SD | Inhibitory rate of intumesce (%) |
CMC-Na clathrate Formica fusca oil ibuprofen | --- 3.0 3.0 1.0 | 12 12 12 12 | 8.93±1.49 2.54±0.72**## 3.38±2.12**## 2.15±1.16**## | 0 71.8 68.8 75.5 |
Annotate: (1)
*: P<0.05,
*: P<0.01, compare with matched group; (t check) compared with the Formica fusca line of oils in ##:P<0.01.
The result shows that the ear swelling degree of clathrate group, Formica fusca line of oils and matched group more all have utmost point significant difference (P<0.01).Illustrate that clathrate, Formica fusca oil xylol causes mice ear significant inhibitory effect is arranged.The clathrate group is better than the Formica fusca line of oils.
2.4 carrageenin causes the inhibitory action test of rat toes swelling
The animal grouping is with test 2.1
Medication is with test 2.1
Carrageenin causes the foundation and the experimental implementation of rat toes swelling model:
Gastric infusion is after 6 days continuously, and fasting was spent the night in 12 hours.The displacement of measuring the right back sufficient sole of the foot of rat on the 7th day with sufficient sole of the foot volume determination instrument is as the toes displacement that causes scorching preceding 0h, respectively organize equal gastric infusion then, inject 1% carrageenin 0.05ml so that inflammation immediately in the right back sufficient sole of the foot Intradermal of rat, respectively at causing scorching back 1,2,3,4,5,6h is with sufficient sole of the foot volume determination instrument, measure the displacement (ml) of the right back sufficient sole of the foot of rat, so that the difference of the displacement before and after scorching is represented the swelling degree of the sufficient sole of the foot.
Observation index
(1) right back toes displacement
(2) swelling degree: right back sufficient displacement before the right back sufficient displacement in the scorching back of swelling degree (ml)=cause-cause is scorching
Result of the test: experimental result is shown with the swelling kilsyth basalt, be the results are shown in Table 7.T-student check between statistics employing group.
Table 7 Formica fusca extract A, clathrate on Carrageenan cause the inhibitory action experimental result of the right back toes swelling of rat
Medicine | Dosage (g/kg) | Number of animals | The swelling degree (ml X ± SD) | |||||
1h | 2h | 3h | 4h | 5h | 6h | |||
CMC-Na | --- | 12 | 0.58± 0.20 | 0.70± 0.23 | 0.87± 0.35 | 0.78± 0.26 | 0.81± 0.28 | 0.75± 0.29 |
Clathrate | 2.1 | 12 | 0.19± 0.24 ** | 0.37± 0.16 ** | 0.74± 0.21 | 0.79± 0.13 | 0.73± 0.17 | 0.65± 0.12 |
Formica fusca oil | 2.1 | 12 | 0.25± 0.21 ** | 0.43± 0.15 * | 0.71± 0.25 | 0.75± 0.22 | 0.84± 0.16 | 0.75± 0.14 |
Ibuprofen | 1.0 | 12 | 0.24± 0.14 ** | 0.48± 0.16 * | 0.69± 0.29 | 0.78± 0.15 | 0.75± 0.19 | 0.68± 0.15 |
Annotate: (1)
*: P<0.05,
*: P<0.01, compare (t check) with matched group
The result shows, the inflammation that previous hour after causing inflammation each medicine on Carrageenan causes has certain inhibitory action, Formica fusca clathrate, Formica fusca oil and ibuprofen last, compared with matched group in two hours, the swelling degree all has utmost point significant difference (p<0.01 or p<0.05).But, all no longer can suppress the pedal swelling of rat from causing scorching back three hours.
2.5 conclusion
Polyrhachis its through supercritical CO
2The Formica fusca oil of extraction back gained confirms through pharmacodynamic study: aspect anti-inflammatory and antalgic, have the effect of highly significant, and better through anti-inflammatory pain-stopping effect after the clathrate technical finesse.
Three, the beta-cyclodextrin inclusion compound technology is to the Polyhachis vicina Roger oil inclusion technique project study of supercritical extraction.
Method: adopt orthogonal experimental design method, with the clathrate yield, oil content is an index in clathrate medium oil utilization rate, the clathrate, research host and guest molecular proportion, grinding time, add that water is doubly measured and the ethanol consumption to enclose result's influence.
1. experimental apparatus and reagent
The TM-40 colloid mill, the prosperous general machine-building company limited in Tianjin; UV-2102PC type ultraviolet spectrophotometer, excellent Ni Ke (Shanghai) Instr Ltd.; DZF-1B type vacuum drying oven, the Shanghai medical apparatus and instruments factory of making a leapleap forward; CQX25-06 type ultrasonic cleaner, ultrasonic company limited must be believed in Shanghai; The 95-1 magnetic stirring apparatus, Shanghai Si Le instrument plant; Polyhachis vicina Roger oil is (through supercritical CO
2Extraction, P=36Mpa, T=40 ℃, t=50min) Nanjing Zhongshan Pharmaceutical Co., Ltd. provides by embodiment 1 preparation; Beta-schardinger dextrin-, China Medicine (Group) Shanghai Chemical Reagent Co.,, lot number T20030603; Other reagent is analytical pure.
2. method and result
2.1 the mensuration of Polyhachis vicina Roger oil density: slough moisture in the Polyhachis vicina Roger oil with anhydrous sodium sulfate, according to " " hydrostatic method " measured among 2005 editions appendix VIIA of Chinese pharmacopoeia " relative density algoscopy ", after measured, the density of Polyhachis vicina Roger oil is 0.862g/ml.
2.2 the selection of inclusion method: with clathrate yield, clathrate oil content, oily utilization rate is index, under identical material ratio colloid milling, saturated water solution method, ultrasonic method is compared.
2.2.1 saturated water solution method: get beta-schardinger dextrin-12g, under 60 ℃, be made into saturated solution (seeing Table 8), under constant temperature, slowly add Polyhachis vicina Roger oil 2ml, stir appropriate time, deposit 24h under 4 ℃, sucking filtration, with low amounts of water and washing with alcohol 3 times, 40 ℃ of vacuum dryings promptly get Benexate Hydrochloride.
The solubility table of table 8 beta-schardinger dextrin-
T(℃) | 20 | 40 | 60 | 80 | 100 |
S(g/100ml) | 1.8 | 3.7 | 8.0 | 18.3 | 25.6 |
2.2.2 ultrasonic method: get beta-schardinger dextrin-12g, add triplication water, mix homogeneously slowly adds Polyhachis vicina Roger oil 2ml, ultrasonic (f=40KHz) appropriate time, and all the other are the same.
2.2.3 colloid milling: get beta-schardinger dextrin-12g, add triplication water, mix homogeneously is poured in the colloid mill, regulates mill spacing 5 μ m, and machine (3000r/min) slowly adds Polyhachis vicina Roger oil 2ml, the appropriate time of milling, and all the other are the same.
2.2.4 according to comparative result (seeing Table 9), preferred colloid milling carries out beta-cyclodextrin inclusion compound to Polyhachis vicina Roger oil.
The result of three kinds of different inclusion methods of table 9 relatively
Method | The clathrate yield | The oil utilization rate | The clathrate oil content |
Saturated water solution method ultrasonic method colloid milling | 65.1% 72.7% 75.8% | 63.23% 65.45% 80.37% | 6.94% 7.41% 12.86% |
2.3 Polyhachis vicina Roger oil content assay method in the clathrate
2.3.1 take off the bag choice of Solvent: precision takes by weighing Polyhachis vicina Roger oil Benexate Hydrochloride, the dehydrated alcohol, petroleum ether (30-60), petroleum ether (60-90), dichloromethane, the ethyl acetate that add 20ml respectively, reflux, extract, 30min, relatively take off the bag ability, result: dichloromethane>dehydrated alcohol>petroleum ether (30-60), all the other two kinds of nothings are obviously taken off the bag ability, and dichloromethane obviously is better than dehydrated alcohol, so finally determine with dichloromethane as taking off the bag solvent.
Take by weighing Polyhachis vicina Roger oil Benexate Hydrochloride 2.3.2 take off the selection precision of bag method, add the 20ml dichloromethane respectively, it is 20min that the bag time is taken off in setting, relatively reflux, extract, and supersound extraction are to the influence of measurement result, determine to adopt methylene chloride reflux to extract and take off bag, further investigate the influence of solvent load and return time on this basis, finally determine to take off the bag method and extract 30min for the 30ml methylene chloride reflux to measurement result.
2.3.3UV detection wavelength determination: adopt the method for 2.2.2 item to take off bag clathrate, filter, get filtrate 4ml, be settled to 10ml with dichloromethane, in ultraviolet-visible spectrophotometer scanning (190-600) down, with do not compared by the scanning spectrogram of the Polyhachis vicina Roger oil of enclose, the Polyhachis vicina Roger main body of oil does not change before and after the visible enclose, and determines to calculate with near the absorption maximum peak intensity the 234nm and estimate the enclose result.See Fig. 1,2.
2.3.4 the drafting of standard curve: precision takes by weighing Polyhachis vicina Roger oil 0.5g, with dichloromethane dissolving and be settled to 100ml, be made into the storing solution of 5mg/ml, draw storing solution 1.0,2.5,4.0,5.5 respectively, 7.0ml is settled to 10ml with dichloromethane, measure trap, drawing standard curve (see figure 3) at the 234nm place.Get regression equation: Y=0.3145C+0.0059, R
2=0.9999.
Illustrate that the Polyhachis vicina Roger oil concentration is good in 0.5mg/ml-3.5mg/ml scope internal linear relation.
3. the orthogonal experiment of colloid mill enclose Polyhachis vicina Roger oil
3.1 the preparation method of clathrate: according to the quadrature calendar, get predetermined amount of beta-cyclodextrin, the water that adds regulation times amount grinds evenly, pour in the colloid mill, machine, maintenance speed is 3000r/min, regulating the mill spacing is 5 μ m, slowly drips the Polyhachis vicina Roger oil with an amount of dissolve with ethanol continuously, grinds certain hour, 4 ℃ of following cold preservation 24h, sucking filtration is in 40 ℃ of following vacuum dryings, with low amounts of water and washing with alcohol 3 times, 40 ℃ of return air dryings promptly get clathrate.
3.2 orthogonal experiment design: investigate as can be known by documents and materials and preliminary experiment, the principal element of colloid milling enclose Polyhachis vicina Roger oil has: four factors such as the material ratio of black repeatedly ant oil of plan and beta-schardinger dextrin-, enclose time, amount of water, pure consumption, therefore adopt L
9(3
4) orthogonal array, with clathrate yield, clathrate oil utilization rate, clathrate oil content is evaluation index, and adopting the comprehensive grading method, clathrate yield, clathrate oil utilization rate, clathrate oil content three weight coefficient are respectively 0.2,0.4,0.4, analyze preferred optimum process condition.(factor level is divided and to be seen Table 10, orthogonal experiment arrangement and the results are shown in Table 11)
Table 10 factor level table
Material ratio A (oil: beta-schardinger dextrin-ml/g) | Milling time B (min) | Amount of water C | | |
1 2 3 | 1∶4 1∶6 1∶8 | 20 40 60 | 2 3 4 | 10% 15% 20% |
Clathrate yield, clathrate oil utilization rate, clathrate oil content, comprehensive grading computing formula are as follows:
Clathrate yield=clathrate actual weight/(beta-schardinger dextrin-+throwing oil mass) * 100%
The actual oil content of clathrate oil utilization rate=clathrate/throwing oil mass * 100%
The actual oil content of clathrate oil content=clathrate/clathrate weight * 100%
3.3 the enclose interpretation of result adopts the SPSS13.0 statistical software according to experimental result, and different indexs are carried out intuitive analysis, variance analysis is in conjunction with comprehensive grading method check analysis result.(seeing Table 12-15)
Table 11 Polyhachis vicina Roger oil beta-cyclodextrin inclusion compound orthogonal test table
Test | A | B | C | D | The clathrate yield | The oil utilization rate | Oil content | Comprehensive grading |
Number | (%) | (%) | (%) | |||||
1 2 3 4 5 6 7 8 9 | 1 1 1 2 2 2 3 3 3 | 1 2 3 1 2 3 1 2 3 | 1 2 3 2 3 1 3 1 2 | 1 2 3 3 1 2 2 3 1 | 82.6 86 84.3 87.7 81.4 86.7 84.6 87.4 82.4 | 63.93 74.34 65.97 67.56 80.99 87.17 63.78 99.42 82.32 | 15.92 17.77 16.09 11.23 14.51 14.65 8.5 12.83 11.28 | 84.04 89.63 85.27 84.64 90.06 93.65 81.42 97.96 89.50 |
Bag k1 closes k2 thing k3 and gets R and lead | 252.9 255.8 254.4 0.967 | 254.9 254.8 253.4 0.5 | 256.7 256.1 250.3 2.133 | 246.4 257.3 259.4 4.333 | ||||
The sharp k2 of oil k1 leads R with k3 | 204.24 235.72 245.52 13.760 | 195.27 254.75 235.46 19.827 | 250.52 224.22 210.74 13.260 | 227.24 225.29 232.95 2.553 | ||||
Contain k1 oil k2 and lead k3 R | 49.780 40.300 32.610 5.723 | 35.650 45.110 41.930 3.153 | 43.310 40.280 39.100 1.403 | 41.710 40.830 40.150 0.520 | ||||
Comprehensive k1 closes k2 and gets k3 and divide R | 258.940 268.350 268.880 3.313 | 250.100 277.650 268.420 9.183 | 275.650 263.770 256.750 6.300 | 263.600 264.700 267.870 1.423 |
By Orthogonal experiment results is carried out intuitive analysis as can be known: with the clathrate yield be each factor of index influence D>C>A>B, D, C factor have significant difference, A factor there was no significant difference, best of breed are A
2B
1C
1D
3The results are shown in Table 12.
Table 12 is the variance analysis of index with the clathrate yield
Soruces of variation | Sum of deviation square | Degree of freedom | Mean square | The F value | Significance |
A C D sum of the deviations | 1.402 8.329 32.469 0.469 42.669 | 2 2 2 2 8 | 0.701 4.164 16.234 0.234 | 2.991 17.763 69.246 1.00 | P>0..05 P>0.05 P<0.05 |
F
0.05(2,2)=19
With clathrate oil utilization rate be each factor of index influence B>A>C>D, A, B, C three factors all have significant difference, best of breed is A
3B
2C
1D
3The results are shown in Table 13.
Table 13 is the variance analysis of index with oily utilization rate
Soruces of variation | Sum of deviation square | Degree of freedom | Mean square | The F value | Significance |
A B C sum of the deviations | 310.119 613.912 272.872 10.565 1207.468 | 2 2 2 2 8 | 155.059 306.956 136.436 5.282 | 29.354 58.110 25.829 1.00 | P<0.05 P<0.05 P<0.05 |
F
0.05(2,2)=19
With the clathrate oil content be each factor of index influence A>B>C>D, A, B factor have significant difference, C factor there was no significant difference, best of breed are A
1B
2C
1D
1The results are shown in Table 14.
Table 14 is the variance analysis of index with the oil content
Soruces of variation | Sum of deviation square | Degree of freedom | Mean square | The F value | Significance |
A B C sum of the deviations | 49.279 15.513 3.291 0.406 68.488 | 2 2 2 2 8 | 24.639 7.756 1.645 0.203 | 121.489 38.245 8.113 1.00 | P<0.05 P<0.05 P>0.05 |
F
0.05(2,2)=19
In order more fully to analyze, with comprehensive grading method screening optimised process, concrete computational methods are as follows: in three indexs of Polyhachis vicina Roger oil clathrate, choose the soprano respectively as 100 minutes, all the other by formula calculate: Y
i=100-peak+Yi, since each factor to the influence of clathrate yield less than oil content in oily utilization rate and the clathrate, in conjunction with producing actual requirement, respectively each index is invested different weight coefficients: clathrate yield 0.2, oily utilization rate 0.4, clathrate oil content 0.4, further analyze, the results are shown in Table 2, table 15.Comprehensive grading=clathrate yield score * 0.2+ clathrate oil utilization rate score * 0.4+ clathrate oil content score * 0.4.
Table 15 is the variance analysis (table 9) of index with the comprehensive grading
Soruces of variation | Sum of deviation square | Degree of freedom | Mean square | The F value | Significance |
A B C sum of the deviations | 20.848 131.091 60.847 3.277 216.063 | 2 2 2 2 8 | 10.424 65.545 30.424 1.638 | 6.362 40.005 18.569 1.00 | P>0.05 P<0.05 P>0.05 |
F
0.05(2,2)=19
To clathrate comprehensive grading statistical analysis as a result, by range analysis as can be known, each factor is arranged as B>C>A>D to the size that influences of this index, and B, C factor have significant difference, and A factor there was no significant difference is that the technology of index is A with the integrate score
3B
2C
1D
1, consider the yield of clathrate and oil content this two indexs and production cost of clathrate, be A so establish the enclose optimised process
2B
2C
1D
3Be that the enclose condition is: Polyhachis vicina Roger oil: beta-schardinger dextrin-is 1: 6, and grinding time is 40min, and amount of water is a qdx, alcohol adding amount is 20%, considers factor such as there was no significant difference and production cost between each level of D factor, with D factor 2 class of floating downward, promptly alcohol adding amount is 10%.
3.4 confirmatory experiment is to the horizontal A of the optimised process that optimizes
2B
2C
1D
1, promptly the enclose condition is: Polyhachis vicina Roger oil: beta-schardinger dextrin-is 1: 6, and grinding time is 40min, and amount of water is a qdx, and alcohol adding amount is 10%, carries out three batches of confirmatory experiments, measurement result sees Table 16, illustrates that this process stabilizing is reliable.
Table 16 confirmatory experiment is table as a result
Sequence number | The clathrate yield | The oil utilization | Oil content | |
1 2 3 RSD | 87.3% 86.8% 87.6% 0.46 | 97.3% 96.4% 96.9% 0.47 | 14.52% 14.47% 14.58% 0.38 |
4. clathrate discerns
4.1 difference formula scanning calorimetry (DSC)
Physical mixture to beta-schardinger dextrin-, Polyhachis vicina Roger oil Benexate Hydrochloride, Polyhachis vicina Roger oil, beta-schardinger dextrin-and Polyhachis vicina Roger oil carries out DSC scanning respectively, the results are shown in Figure 4-7.
By collection of illustrative plates we as can be seen: Polyhachis vicina Roger oil has a tangible endothermic peak at 47.5 ℃, beta-schardinger dextrin-is 123.6 ℃ of endothermic peaks, physical mixture is beta-schardinger dextrin-and both stacks of Polyhachis vicina Roger oil, because the beta-schardinger dextrin-endothermic peak is covered the peak of oil, so do not see the endothermic peak of oil, but the beta-schardinger dextrin-endothermic peak is not moved, and clathrate has a tangible endothermic peak at 87.7 ℃, show that Polyhachis vicina Roger oil has formed a kind of new thing phase behind beta-cyclodextrin inclusion compound, bigger moving takes place in its position, proves the formation of clathrate.
5. discuss
5.1 the present invention is by comparing saturated water solution method, ultrasonic method, colloid milling beta-cyclodextrin inclusion compound result, find to adopt colloid milling to carry out enclose, the utilization rate of oil is apparently higher than other two kinds of methods, loss takes place in ant oil in saturated water solution method and the ultrasonic method in the enclose process, thereby influences the enclose result.So the present invention carries out enclose with colloid milling to Polyhachis vicina Roger oil.
5.2 it is to change tooth and decide relative motion between the tooth by taper that colloid milling prepares the principle of Benexate Hydrochloride, effect such as be subjected to shearing, stir, mill when making material by adjustable gap, make the enclose object hit into beta-schardinger dextrin-cavity, thereby reach the enclose effect.Adopt colloid milling to prepare Benexate Hydrochloride enclose time weak point, energy consumption is little, the utilization rate height of product yield and oil, and process conditions are easy to control, are fit to the big production of technology.
5.3 the result learns according to preliminary experiment: chloroform is better than dichloromethane slightly to the dissolubility of Polyhachis vicina Roger oil, consider the zest of chloroform to human body, and dichloromethane can reach more than 90% of chloroform to the solvability of Polyhachis vicina Roger oil, so the present invention adopts dichloromethane to experimentize as solvent.
5.4 adopt steam distillation that clathrate is taken off bag usually, learn through preliminary experiment: adopt steam distillation, its blank response rate is 45%, can not be used for taking off the bag experiment, and employing organic solvent extraction method, its blank response rate can reach 87%, so change the organic solvent extraction method into clathrate is taken off bag.
5.5 adopt ultraviolet spectrophotometry to detect in this experiment, within the range of linearity of Polyhachis vicina Roger oil, calculate the content of clathrate medium oil by the trap value of its maximum absorption band to taking off bag liquid.
5.6 needs in conjunction with industrialized great production, in experimentation, adopt dehydrated alcohol that clathrate is washed, because dehydrated alcohol has certain bag ability of taking off to clathrate, so should be noted that the consumption and the washing times of dehydrated alcohol when clathrate being washed with dehydrated alcohol, consumption is being advisable the clathrate surface coverage, washing times tries not to surpass 3 times, must guard against stirring in the washing process.In actual production, also can not wash and directly add adjuvant therein clathrate, mixing granulation can improve the utilization rate of oil like this.
The result: optimizing optimised process by intuitive analysis, variance analysis is: (Polyhachis vicina Roger oil: beta-schardinger dextrin-) 1: 6, grinding time 40 minutes added 2 times of amounts of water and ethanol consumption 10% to host and guest's molecular proportion.
Conclusion: empirical tests experiment confirm: the technological parameter that optimizes is stable, and is feasible, goes for suitability for industrialized production.
Description of drawings
Fig. 1 takes off bag Polyhachis vicina Roger oil ultraviolet-visible spectrophotometer scintigram.
Fig. 2 is the Polyhachis vicina Roger oil ultraviolet-visible spectrophotometer scintigram of not enclose.
Fig. 3 is a Polyhachis vicina Roger oil content standard curve in the clathrate.
Fig. 4 is a Polyhachis vicina Roger oil DSC scintigram.
Fig. 5 is Polyhachis vicina Roger oil and beta-schardinger dextrin-physical mixture DSC scintigram.
Fig. 6 is a Polyhachis vicina Roger oil Benexate Hydrochloride DSC scintigram.
Fig. 7 is a beta-schardinger dextrin-DSC scintigram.
The specific embodiment
The invention will be further elaborated by the following examples.
With the Polyhachis vicina Roger crushed after being dried, cross 60 mesh sieves; Get 380g Polyhachis vicina Roger powder and drop in the 1L extraction kettle, regulate extractant CO
2Flow velocity be 20L/h, be 36Mpa in extracting pressure, extract 50min under 40 ℃ of conditions of extraction temperature; Regulate extraction-container pressure, separated and collected Polyhachis vicina Roger oil.
Embodiment 2
With the Polyhachis vicina Roger crushed after being dried, cross 60 mesh sieves; Get 400g Polyhachis vicina Roger powder and drop in the 1L extraction kettle, regulate extractant CO
2Flow velocity be 25kg/h, be 28Mpa in extracting pressure, extract 20min under 40 ℃ of conditions of extraction temperature; Regulate extraction-container pressure, separated and collected Polyhachis vicina Roger oil.
Embodiment 3
With the Polyhachis vicina Roger crushed after being dried, cross 60 mesh sieves; Get 400g Polyhachis vicina Roger powder and drop in the 1L extraction kettle, regulate extractant CO
2Flow velocity be 10L/h, be 20Mpa in extracting pressure, extract 40min under 45 ℃ of conditions of extraction temperature; Regulate extraction-container pressure, separated and collected Polyhachis vicina Roger oil.
Embodiment 4
With the Polyhachis vicina Roger crushed after being dried, cross 60 mesh sieves; Get 450g Polyhachis vicina Roger powder and drop in the 1L extraction kettle, regulate extractant CO
2Flow velocity be 30kg/h, be 32Mpa in extracting pressure, extract 60min under 40 ℃ of conditions of extraction temperature; Regulate extraction-container pressure, separated and collected Polyhachis vicina Roger oil.
Embodiment 5
In host and guest's molecular proportion of Polyhachis vicina Roger oil (by embodiment 1 preparation) and beta-schardinger dextrin-is that 1: 6 ratio is got Polyhachis vicina Roger oil and beta-schardinger dextrin-; It is that the water of 2 times of beta-schardinger dextrin-s grinds evenly that beta-schardinger dextrin-is added weight, makes the beta-schardinger dextrin-aqueous solution, and adding volume in the Polyhachis vicina Roger oil is the ethanol of Polyhachis vicina Roger oil volume 10%, makes Polyhachis vicina Roger oleyl alcohol solution; Pour the beta-schardinger dextrin-aqueous solution into colloid mill, machine, maintenance speed is 3000r/min, and regulating the mill spacing is 5 μ m, slowly drip Polyhachis vicina Roger oleyl alcohol solution in the process of lapping continuously and carry out enclose, control enclose temperature is that 60 ℃, enclose time are 50 minutes, 4 ℃ of following cold preservation 24h, sucking filtration, in 40 ℃ of following vacuum dryings, with low amounts of water and washing with alcohol 3 times, 40 ℃ of return air dryings promptly get clathrate.
Embodiment 6
In host and guest's molecular proportion of Polyhachis vicina Roger oil (by embodiment 1 preparation) and beta-schardinger dextrin-is that 1: 8 ratio is got Polyhachis vicina Roger oil and beta-schardinger dextrin-; It is that the water of 3 times of beta-schardinger dextrin-s grinds evenly that beta-schardinger dextrin-is added weight, makes the beta-schardinger dextrin-aqueous solution, and adding volume in the Polyhachis vicina Roger oil is the ethanol of Polyhachis vicina Roger oil volume 15%, makes Polyhachis vicina Roger oleyl alcohol solution; Pour the beta-schardinger dextrin-aqueous solution into colloid mill, machine, maintenance speed is 4000r/min, and regulating the mill spacing is 5 μ m, slowly drip Polyhachis vicina Roger oleyl alcohol solution in the process of lapping continuously and carry out enclose, control enclose temperature is that 55 ℃, enclose time are 60 minutes, 4 ℃ of following cold preservation 24h, sucking filtration, in 40 ℃ of following vacuum dryings, with low amounts of water and washing with alcohol 3 times, 40 ℃ of return air dryings promptly get clathrate.
Embodiment 7
In host and guest's molecular proportion of Polyhachis vicina Roger oil (by embodiment 2 preparation) and beta-schardinger dextrin-is that 1: 6 ratio is got Polyhachis vicina Roger oil and beta-schardinger dextrin-; It is that the water of 4 times of beta-schardinger dextrin-s grinds evenly that beta-schardinger dextrin-is added weight, makes the beta-schardinger dextrin-aqueous solution, and adding volume in the Polyhachis vicina Roger oil is the ethanol of Polyhachis vicina Roger oil volume 20%, makes Polyhachis vicina Roger oleyl alcohol solution; Pour the beta-schardinger dextrin-aqueous solution into colloid mill, machine, maintenance speed is 3000r/min, and regulating the mill spacing is 5 μ m, slowly drip Polyhachis vicina Roger oleyl alcohol solution in the process of lapping continuously and carry out enclose, control enclose temperature is that 70 ℃, enclose time are 20 minutes, 4 ℃ of following cold preservation 24h, sucking filtration, in 40 ℃ of following vacuum dryings, with low amounts of water and washing with alcohol 3 times, 40 ℃ of return air dryings promptly get clathrate.
Embodiment 8
In host and guest's molecular proportion of Polyhachis vicina Roger oil (by embodiment 2 preparation) and beta-schardinger dextrin-is that 1: 4 ratio is got Polyhachis vicina Roger oil and beta-schardinger dextrin-; It is that the water of 2 times of beta-schardinger dextrin-s grinds evenly that beta-schardinger dextrin-is added weight, makes the beta-schardinger dextrin-aqueous solution, and adding volume in the Polyhachis vicina Roger oil is the ethanol of Polyhachis vicina Roger oil volume 10%, makes Polyhachis vicina Roger oleyl alcohol solution; Pour the beta-schardinger dextrin-aqueous solution into colloid mill, machine, maintenance speed is 4000r/min, and regulating the mill spacing is 5 μ m, slowly drip Polyhachis vicina Roger oleyl alcohol solution in the process of lapping continuously and carry out enclose, control enclose temperature is that 50 ℃, enclose time are 45 minutes, 4 ℃ of following cold preservation 24h, sucking filtration, in 40 ℃ of following vacuum dryings, with low amounts of water and washing with alcohol 2 times, 40 ℃ of return air dryings promptly get clathrate.
Embodiment 9
In host and guest's molecular proportion of Polyhachis vicina Roger oil (by embodiment 3 preparation) and beta-schardinger dextrin-is that 1: 5 ratio is got Polyhachis vicina Roger oil and beta-schardinger dextrin-; It is that the water of 3 times of beta-schardinger dextrin-s grinds evenly that beta-schardinger dextrin-is added weight, makes the beta-schardinger dextrin-aqueous solution, and adding volume in the Polyhachis vicina Roger oil is the ethanol of Polyhachis vicina Roger oil volume 15%, makes Polyhachis vicina Roger oleyl alcohol solution; Pour the beta-schardinger dextrin-aqueous solution into colloid mill, machine, maintenance speed is 3000r/min, and regulating the mill spacing is 5 μ m, slowly drip Polyhachis vicina Roger oleyl alcohol solution in the process of lapping continuously and carry out enclose, control enclose temperature is that 65 ℃, enclose time are 30 minutes, 4 ℃ of following cold preservation 24h, sucking filtration, in 40 ℃ of following vacuum dryings, with low amounts of water and washing with alcohol 2 times, 40 ℃ of return air dryings promptly get clathrate.
Embodiment 10
In host and guest's molecular proportion of Polyhachis vicina Roger oil (by embodiment 4 preparation) and beta-schardinger dextrin-is that 1: 7 ratio is got Polyhachis vicina Roger oil and beta-schardinger dextrin-; It is that the water of 4 times of beta-schardinger dextrin-s grinds evenly that beta-schardinger dextrin-is added weight, makes the beta-schardinger dextrin-aqueous solution, and adding volume in the Polyhachis vicina Roger oil is the ethanol of Polyhachis vicina Roger oil volume 20%, makes Polyhachis vicina Roger oleyl alcohol solution; Pour the beta-schardinger dextrin-aqueous solution into colloid mill, machine, maintenance speed is 4000r/min, and regulating the mill spacing is 5 μ m, slowly drip Polyhachis vicina Roger oleyl alcohol solution in the process of lapping continuously and carry out enclose, control enclose temperature is that 65 ℃, enclose time are 40 minutes, 4 ℃ of following cold preservation 24h, sucking filtration, in 40 ℃ of following vacuum dryings, with low amounts of water and washing with alcohol 3 times, 40 ℃ of return air dryings promptly get clathrate.
Claims (6)
1, a kind of clathrate of ants supercritical extracts is characterized in that this clathrate prepares through the following steps:
A. with the Formica fusca crushed after being dried, cross 60 mesh sieves; Get an amount of Formica fusca powder and drop in the extraction kettle, regulate extractant CO
2Flow velocity be 10~30L/h, be 20~36Mpa in extracting pressure, extract 10~60min under 30~60 ℃ of conditions of extraction temperature; Regulate extraction-container pressure, separated and collected Formica fusca oil;
B. be that 1: 4~8 ratio is got Formica fusca oil and beta-schardinger dextrin-in host and guest's molecular proportion of Formica fusca oil and beta-schardinger dextrin-;
C. the water that beta-schardinger dextrin-is added weight and be 2~4 times of beta-schardinger dextrin-s grinds evenly, makes the beta-schardinger dextrin-aqueous solution, and adding volume in the Formica fusca oil is the ethanol of Formica fusca oil volume 10~20%, makes Formica fusca oleyl alcohol solution;
D. pour the beta-schardinger dextrin-aqueous solution into colloid mill, regulating suitable mill spacing grinds, drip Formica fusca oleyl alcohol solution in the process of lapping and carry out enclose, control enclose temperature is that 50-80 ℃, enclose time are 20-60 minute, and clathrate is through sucking filtration, washing, dry getting final product.
2, the clathrate of ants supercritical extracts according to claim 1 is characterized in that this clathrate prepares through the following steps:
A. with the Formica fusca crushed after being dried, cross 60 mesh sieves; Get an amount of Formica fusca powder and drop in the extraction kettle, regulate extractant CO
2Flow velocity be 20L/h, be 36Mpa in extracting pressure, extract 50min under 40 ℃ of conditions of extraction temperature; Regulate extraction-container pressure, separated and collected Formica fusca oil;
Host and guest's molecular proportion b. oily in Formica fusca and beta-schardinger dextrin-is that 1: 6 ratio is got Formica fusca oil and beta-schardinger dextrin-;
C. the water that beta-schardinger dextrin-is added weight and be 2 times of beta-schardinger dextrin-s grinds evenly, makes the beta-schardinger dextrin-aqueous solution, and adding volume in the Formica fusca oil is the ethanol of Formica fusca oil volume 10%, makes Formica fusca oleyl alcohol solution;
D. pour the beta-schardinger dextrin-aqueous solution into colloid mill, regulate suitably the mill spacing and grind, drip Formica fusca oleyl alcohol solution in the process of lapping and carry out enclose, control enclose temperature is that 60 ℃, enclose time are 40 minutes, and clathrate is through sucking filtration, washing, dry getting final product.
3, the clathrate of ants supercritical extracts according to claim 1 and 2 is characterized in that Formica fusca is a Polyhachis vicina Roger.
4, the preparation technology of the clathrate of the described ants supercritical extracts of claim 1 is characterized in that comprising the following steps:
A. with the Formica fusca crushed after being dried, cross 60 mesh sieves; Get an amount of Formica fusca powder and drop in the extraction kettle, regulate extractant CO
2Flow velocity be 10~30L/h, be 20~36Mpa in extracting pressure, extract 10~60min under 30~60 ℃ of conditions of extraction temperature; Regulate extraction-container pressure, separated and collected Formica fusca oil;
B. be that 1: 4~8 ratio is got Formica fusca oil and beta-schardinger dextrin-in host and guest's molecular proportion of Formica fusca oil and beta-schardinger dextrin-;
C. the water that beta-schardinger dextrin-is added weight and be 2~4 times of beta-schardinger dextrin-s grinds evenly, makes the beta-schardinger dextrin-aqueous solution, and adding volume in the Formica fusca oil is the ethanol of Formica fusca oil volume 10~20%, makes Formica fusca oleyl alcohol solution;
D. pour the beta-schardinger dextrin-aqueous solution into colloid mill, regulating suitable mill spacing grinds, drip Formica fusca oleyl alcohol solution in the process of lapping and carry out enclose, control enclose temperature is that 50-80 ℃, enclose time are 20-60 minute, and clathrate is through sucking filtration, washing, dry getting final product.
5, the preparation technology of the clathrate of ants supercritical extracts according to claim 4 is characterized in that comprising the following steps:
A. with the Formica fusca crushed after being dried, cross 60 mesh sieves; Get an amount of Formica fusca powder and drop in the extraction kettle, regulate extractant CO
2Flow velocity be 20L/h, be 36Mpa in extracting pressure, extract 50min under 40 ℃ of conditions of extraction temperature; Regulate extraction-container pressure, separated and collected Formica fusca oil;
Host and guest's molecular proportion b. oily in Formica fusca and beta-schardinger dextrin-is that 1: 6 ratio is got Formica fusca oil and beta-schardinger dextrin-;
C. the water that beta-schardinger dextrin-is added weight and be 2 times of beta-schardinger dextrin-s grinds evenly, makes the beta-schardinger dextrin-aqueous solution, and adding volume in the Formica fusca oil is the ethanol of Formica fusca oil volume 10%, makes Formica fusca oleyl alcohol solution;
D. pour the beta-schardinger dextrin-aqueous solution into colloid mill, regulate suitably the mill spacing and grind, drip Formica fusca oleyl alcohol solution in the process of lapping and carry out enclose, control enclose temperature is that 60 ℃, enclose time are 40 minutes, and clathrate is through sucking filtration, washing, dry getting final product.
6, according to the preparation technology of the clathrate of claim 4 or 5 described ants supercritical extracts, it is characterized in that Formica fusca is a Polyhachis vicina Roger.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CNB2006100405959A CN100381128C (en) | 2006-05-29 | 2006-05-29 | Inclusion compound of ants supercritical extracts and preparation process thereof |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CNB2006100405959A CN100381128C (en) | 2006-05-29 | 2006-05-29 | Inclusion compound of ants supercritical extracts and preparation process thereof |
Publications (2)
Publication Number | Publication Date |
---|---|
CN1883511A true CN1883511A (en) | 2006-12-27 |
CN100381128C CN100381128C (en) | 2008-04-16 |
Family
ID=37581893
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CNB2006100405959A Active CN100381128C (en) | 2006-05-29 | 2006-05-29 | Inclusion compound of ants supercritical extracts and preparation process thereof |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN100381128C (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101810644B (en) * | 2009-07-21 | 2012-01-18 | 黑龙江一辰北药制药有限公司 | Production method of ant essential oil and ant oil soft capsule |
CN107930181A (en) * | 2017-12-24 | 2018-04-20 | 广西南宁秀珀生物科技有限公司 | Ant extraction process based on supercritical carbon dioxide extraction method |
CN103655627B (en) * | 2012-09-07 | 2018-05-29 | 河南科技大学 | The extracting method of fat-soluble active ingredient and Antimicrobial Screening method in insect and arthropod body |
CN108125986A (en) * | 2017-12-24 | 2018-06-08 | 广西南宁秀珀生物科技有限公司 | The extracting method of effective ingredients from ants |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1456303A (en) * | 2003-04-10 | 2003-11-19 | 毛友昌 | Xiaorupi tablets against hyperplasia of mammary glands and preparation thereof |
CN1225528C (en) * | 2004-01-12 | 2005-11-02 | 浙江大学 | Supercritical CO2 extraction process for preparing ant oil |
-
2006
- 2006-05-29 CN CNB2006100405959A patent/CN100381128C/en active Active
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101810644B (en) * | 2009-07-21 | 2012-01-18 | 黑龙江一辰北药制药有限公司 | Production method of ant essential oil and ant oil soft capsule |
CN103655627B (en) * | 2012-09-07 | 2018-05-29 | 河南科技大学 | The extracting method of fat-soluble active ingredient and Antimicrobial Screening method in insect and arthropod body |
CN107930181A (en) * | 2017-12-24 | 2018-04-20 | 广西南宁秀珀生物科技有限公司 | Ant extraction process based on supercritical carbon dioxide extraction method |
CN108125986A (en) * | 2017-12-24 | 2018-06-08 | 广西南宁秀珀生物科技有限公司 | The extracting method of effective ingredients from ants |
Also Published As
Publication number | Publication date |
---|---|
CN100381128C (en) | 2008-04-16 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN101040915A (en) | Method for preparing a Shuanhuanglian injection and the component detecting method | |
CN1883511A (en) | Inclusion compound of ants supercritical extracts and preparation process thereof | |
CN1748740A (en) | Imature bitter orange total flavone and its preparing mthod for its preparation and quality control method | |
CN1876161A (en) | Pharmaceutical formulation and preparing method for breast nodules for treating hyperplasia of mammary glands, and its quality control method | |
CN1843424A (en) | Cassia twig tuckahoe effervescence tablet and preparation method and its quality control method | |
CN1557842A (en) | Process for extracting polygonatum polysaccharides, preparing process for medical preparation and use thereof | |
CN1813860A (en) | Dispersible tablet for clearing away heat of brain and heart and preparation process thereof | |
CN1569884A (en) | Method for preparing astragaloside and its use in preparation of drug for preventing and treating diabetic nephropathy | |
CN1857670A (en) | Medicine for treating hyperplasia of mammary glands and its preparing method | |
CN1562310A (en) | Soft capsule preparation of Tibet medicine 'unique taste' | |
CN1290529C (en) | Medicine for treating gout, hyperuricemia and hyperlipemia and preparation method thereof | |
CN1857588A (en) | Quality control method for Xianlinggubao preparation | |
CN1857385A (en) | Medicine composition for treating cervical spondylosis and its preparing method | |
CN1861106A (en) | Compound isatis root effervescent tablet and its prepn. method | |
CN1827147A (en) | Dispersible tablet with gastrodia tuber for treating headache, its preparation and quality control method | |
CN1850268A (en) | Semen caesalpiniae Chinese medicine preparation for treating cold, its preparing method and quality control method | |
CN1843396A (en) | Oral disintegration tablet for treating coronary heart disease, its preparation process and quality control method | |
CN1562144A (en) | Chinese medicinal composition for treating intestine irritable syndrome and its preparing method | |
CN1686392A (en) | Medicinal composition for treating elytritis, preparation and its quality control method | |
CN1251697C (en) | Composition with functions of regulating immunity and resisting fatigue and its prepn, use and quality control method | |
CN1546129A (en) | Preparing technics of composition of Guizhi and Fuling and its use | |
CN1457852A (en) | A Chinese medicinal composition for treating traumatic injury and pain in chest and hypochondrium, and its preparation method | |
CN1509740A (en) | Chinese medicinal composition for treating atrophic arthritis, preparing method and quality controlling method thereof | |
CN1785287A (en) | Quality control method of child cough and panting preparation | |
CN1903342A (en) | Extractive of flowers and leaves of pseudo-ginseng, prepn. method, quality control method and application thereof |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
C14 | Grant of patent or utility model | ||
GR01 | Patent grant | ||
TR01 | Transfer of patent right | ||
TR01 | Transfer of patent right |
Effective date of registration: 20200525 Address after: 210012 No. 106 Software Avenue, Yuhuatai District, Nanjing City, Jiangsu Province, 2 Blocks 301-8 Patentee after: NANJING SMALL ANT HEALTH SCIENCE RESEARCH INSTITUTE Co.,Ltd. Address before: 210012, Shuanglong street, Yuhuatai District, Jiangsu, Nanjing, 1 Patentee before: NANJING ZHONGSHAN PHARMACEUTICAL Co.,Ltd. |