CN100455294C - Process for preparing chick embryo element - Google Patents
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- CN100455294C CN100455294C CNB2005100179953A CN200510017995A CN100455294C CN 100455294 C CN100455294 C CN 100455294C CN B2005100179953 A CNB2005100179953 A CN B2005100179953A CN 200510017995 A CN200510017995 A CN 200510017995A CN 100455294 C CN100455294 C CN 100455294C
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Abstract
The present invention discloses a method for preparing a chicken embryo extractive having high biological activity, which comprises the steps that the surface of a zygote of a chicken finely selected is disinfected after the zygote is conventionally incubated for 10 to 13 days; the egg shell is removed to take a chicken embryo; the chicken embryo is pulverized at low temperature; sterile purified water is added to the pulverized chicken embryo to be pulped; the pulp is centrifugated at 4 DEG C to obtain supernatant fluid; then the supernatant fluid is filtered by a hollow fiber ultrafiltration device having the interception of more than 800000 dalton to obtain an ultrafiltrate; the ultrafiltrate is processed to obtain white-like loose blocks after being frozen and dried, namely chicken embryo extractives, or the ultrafiltrate is ultrafiltered and concentrated to the certain concentration to be directly and aseptically subpackaged and preserved, namely a chicken embryo extractive solution. The chicken embryo extractives prepared by the present invention contain various nutrient components of amino acid, small molecule polypeptide, growth regulation factor, ribonucleic acid, nucleic acid derivative, etc. Because the low-temperature preparation process and modern biological separation technology are adopted, high biological activity of multiple active substances in the chicken embryo is kept.
Description
One. technical field:
The present invention relates to a kind of preparation method of embryo's element, particularly relate to a kind of preparation method with higher bioactive chick embryo element.
Two. background technology:
Chick embryo element is one group of growth-stimulating factor with high bioactivity, nerve growth factor, active polysaccharide, active polypeptide, the small-molecule mixture of several amino acids and other nutrient substance that enrich, they have the elite composition of growth promotion and activation physiological function, energy human activin histiocyte, activation tissue organ function, regulate the various immunity of human body, improve the ability of human body resist the disease, and delaying sanility, wherein contained growth-stimulating factor can increase moisture content of skin, promote epithelial metabolism, application through certain hour, can delay the skin corium aging, atrophy, make dermal layer of the skin full, and can increase the epidermis water content, make epidermis smooth moist.
The primary raw material of chick embryo element is an Embryo Gallus domesticus, is with fertilized eggs (being chicken oosperm), a kind of animal embryo that cultivates by hatching artificial or chicken itself.According to the growth course of having introduced Embryo Gallus domesticus in " chick embryo development collection of illustrative plates " (Jiang Xidong work, Science Press publish nineteen eighty-three): " played pearl, the yellow middle reaches of flake on the 1st; ' Fructus Pruni pseudocerasi ' on the two rises, and heart begins to move; Blood vessel became on 3rd, and ' mosquito ' is in Huang; Decided the position on the 4th, sample is little Aranea seemingly, Great Wall Software's bone on the five, and eye shows single pearl; Placenta Hominis was moving on 6th, end to end Cheng Shuanzhu; Sank in the albumen in 7th from shell; The limit mouth was hard on 8th, and tire is in the egg middle reaches; Mouth was regardless of on 9th, reversed end to end; Apparent hollow billet on the ten, blood vessel beginning overstriking; 11 ventral seta are complete, and allantois closes up entirely; 12 staple lengths are neat, and fish hawk is clearly demarcated up and down; Go out up to 21 chickens "; chicken oosperm can be by sophisticated little chicken individuals of a unicellular bud in short 21 days; huge variation has taken place chicken oosperm during this period; supervene a large amount of growth-stimulating factors, nerve growth factor, active polysaccharide, active polypeptide, several amino acids and other abundant nutrient substance in this change procedure, so as to supporting the g and D of newborn living individual.
Embryo Gallus domesticus is after blood vessel all forms, like the non-meat of meat,, be the highest active embryo of nutrition like the non-egg of egg, be called as since ancient times " popular tonic product ", it contains 18 seed amino acids, vitamin of rich in protein, needed by human body and to human body beneficial's trace element.Though the food therapy value of Embryo Gallus domesticus is very high, but people's eating method is science not very, stillborn fetus egg, kemp egg that the source of Embryo Gallus domesticus is cleared up from the egg hatching process often, hesitate to discard, twice laid, boiling and eating such as: the embryo that checkmates (i.e. hair egg), have also add Chinese medicine boiling eat be used to cure the disease, diseases prevention, the somebody is processed into canned food with it.According to surveying and determination, stillborn fetus egg and kemp egg almost absolutely can be found pathogenic bacterias such as escherichia coli, staphylococcus, and inedibility is so people have just turned one's attention in the research of preparation chick embryo element.Chinese invention patent CN 1226401A, application number is 98100528.4, denomination of invention is: disclosing a kind of in " ' phoenix tire ' health food and preparation method thereof " is the health food of primary raw material with fresh and alive Embryo Gallus domesticus, egg yolk, it by live, embryo is that 7～9 days Embryo Gallus domesticus, egg yolk is dosed a certain proportion of distilled water and an amount of salt age, stirring, steaming and decocting, quantitatively packing, capping, sterilization, packing form; Chinese invention patent CN 1324625A, application number is 00107555.1, denomination of invention is: the preparation technology who discloses a kind of chick embryo element in " manufacture method of chicken embryo essence ", it is active Embryo Gallus domesticus to be added Chinese medicine transform into liquid, by concentrating resulting essence serial product.Embryo's class preparation of these two kinds of patented methods and the preparation of existing other technologies, the room temperature separating and extracting process that adopt more, the effective ingredient that is extracted is so-called " nutrient substance " such as aminoacid, trace element, because under the temperature of room temperature, even method such as enzymolysis, high-temperature sterilization, polypeptide, protein lose activity because of factors such as the broken bosom of space structure, chain interruption, enzyme hydrolysiss mostly, thereby become " dead matter ".Also there is not at present to keep the report of the relevant technologies of higher bioactive chick embryo element.
Three. summary of the invention:
The objective of the invention is: overcome the deficiencies in the prior art, a kind of preparation method that adopts temperature production process and modern bioseparation technology to keep higher bioactive chick embryo element is provided.
Technical scheme of the present invention is:
A kind of preparation method of chick embryo element comprises selected chicken oosperm and hatching, comprises following concrete steps:
A. selected chicken oosperm, surperficial conventional decontamination, conventional incubation 10～13 days;
B. will hatch good germ cell surface and carry out routine disinfection, and remove eggshell and take out Embryo Gallus domesticus, Embryo Gallus domesticus will be put into refrigerator-freezer, under≤-20 ℃ temperature conditions, freezing 0.5～5 hour, then Embryo Gallus domesticus be pulverized;
C. the Embryo Gallus domesticus after will pulverizing is pulled an oar, and adds the sterile water for injection that 3～5 times of Embryo Gallus domesticus volumes are chilled to 0～4 ℃ in advance during making beating in Embryo Gallus domesticus, stirs under 60～80 rev/mins mixing speed 5～10 minutes;
D. the Embryo Gallus domesticus of pulping is carried out 3～5 times multigelation, freezing temperature is-26～-28 ℃, and each freezing time is 0.5～5 hour, melts naturally under the room temperature condition;
E. the Embryo Gallus domesticus of multigelation slurry is poured in the centrifuge under≤4 ℃ of temperature conditions, under 3000～10000 rev/mins speed conditions centrifugal 10～30 minutes, obtained supernatant;
F. supernatant is crossed the ultrafiltration post of molecular cut off more than 800000 dalton, got ultrafiltrate;
G. with obtaining the loose lumps material of off-white color after the ultrafiltrate lyophilization, be described chick embryo element, or, be chick embryo element solution the direct aseptic subpackaged preservation behind ultrafiltration and concentration of above-mentioned ultrafiltrate;
H. relative humidity less than 30% environment in, resulting chick embryo element or chick embryo element solution inserted in the hermetic container keeps in Dark Place, with standby.
The preparation method of described chick embryo element, wherein said selected chicken oosperm is selected from egg type chicken fertilized eggs, and in 3～7 days puerperal, egg size is at 110～120 grams, profile rule, not damaged.
The preparation method of described chick embryo element, wherein the parameters optimization in the conventional incubation method is:
1. incubation temperature: the 1st～10 day 37.8 ℃, the 10th～13 day 37.6 ℃;
2. hatch humidity: relative humidity is about 60%;
3. ventilation: keep the airborne oxygen content of hatching box more than 21%;
4. egg-turning: egg-turning was 1 time in per 1～2 hour;
5. hatch to 11～14 days, remove eggshell behind the taking-up incubated egg and take out Embryo Gallus domesticus.
The method that described Embryo Gallus domesticus is pulverized is: fresh Embryo Gallus domesticus is placed low temperature refrigerator, laying temperature sensor probe in the middle of Embryo Gallus domesticus, after all samples temperature is frozen to-26～-28 ℃, refreeze 1～2.5 hour, use size reduction machinery that it is crushed to 40～100 orders then.
Described multigelation is that the slurry of the Embryo Gallus domesticus after the making beating is placed-30 ℃ low temperature refrigerator, after sample being refrigerated to-26～-28 ℃, freezing 1～3 hour, place then when being melted up to the frozen water coexistence under the room temperature condition naturally, place-30 ℃ of low temperature refrigerators again, sample is refrigerated to-26～-28 ℃, freezing 1～3 hour, so multigelation was 3～5 times.
Described hyperfiltration process is that the Embryo Gallus domesticus after centrifugal slurry supernatant is crossed hollow fiber membrane ultrafiltration device more than molecular cut off 800000 dalton, molecular cut off obtains molecular weight smaller or equal to 800000 daltonian ultrafiltrates greater than the composition of 800000 dalton part.
The cryodesiccated method of described ultrafiltrate is that resulting ultrafiltrate is placed aseptic rustless steel pallet, charging thickness≤1.5 centimetre, put into sterilization in advance, in the freeze dryer lyophilizing cabin after the pre-cooling, regulate the lyophilizing parameter, above-mentioned ultrafiltrate evenly is refrigerated to below-40 ℃, start vacuum pump and lobe pump in the freeze dryer vacuum system then successively, regulate vacuum below 6.5～13Pa, kept 2～3 hours, start the heating system in the freeze dryer then, attention and maintenance vacuum are below 6.5～13Pa in the heating process, and the material maximum temperature must not surpass 35 ℃ during heating, be stabilized in 35 ℃ when being heated to temperature of charge, vacustat is when 8Pa is following, kept 1～3 hour, and can shut down, discharging, the loose lumps thing of resulting yellow-white is chick embryo element.
The conventional adjuvant that chick embryo element is dosed medically can be made tablet, or capsule, or oral liquid, or cosmetics, or health product.Described capsule is a soft capsule.
Positive beneficial effect of the present invention is:
1. the preparation method of chick embryo element of the present invention has kept the various bioactive substances in the Embryo Gallus domesticus.Embryo's class preparation of existing other technologies preparation, the room temperature separating and extracting process that adopt more, the effective ingredient that is extracted is an aminoacid, trace element etc. so-called " nutrient substance ", because under the temperature of room temperature, even enzymolysis, methods such as high-temperature sterilization, polypeptide, protein is mostly because of the broken bosom of space structure, chain interruption, factors such as enzyme hydrolysis and losing activity, thereby become " dead matter ", owing to adopted temperature production process and modern bioseparation technology, the various nutrient substance in the Embryo Gallus domesticus have not only been kept, various bioactive substances in the Embryo Gallus domesticus have also been kept, the chick embryo element of being produced is " active material ", not only the nutrition body can also promote the metabolism of body tissue, and regulating action is played in the immunity of body.
2. the chick embryo element that preparation method obtained of chick embryo element of the present invention is one group of growth-stimulating factor with high bioactivity, nerve growth factor, active polysaccharide, active polypeptide, the small-molecule mixture of several amino acids and other nutrient substance that enrich, they have the elite composition of growth promotion and activation physiological function, energy human activin histiocyte, activation tissue organ function, regulate the various immunity of human body, improve the ability of human body resist the disease, and delaying sanility, wherein contained " allantoin " and growth-stimulating factor can increase moisture content of skin, promote epithelial metabolism, application through certain hour, can delay the skin corium aging, atrophy, make dermal layer of the skin full, and can increase the epidermis water content, make epidermis smooth moist.Owing to adopted temperature production process and modern bioseparation technology to keep than high bioactivity, the high bioactivity chick embryo element that is obtained can be widely used in preparing industries such as high-activity biological medicine, functional food and cosmetics.
3. the chick embryo element that preparation method obtained of chick embryo element of the present invention has oxidation resistance preferably, can improve the activity of SOD in the subacute aging model mouse blood of D-galactose significantly, reduces MDA concentration in the serum, suppresses the formation of liver lipofuscin.
4. the chick embryo element that preparation method obtained of chick embryo element of the present invention can significantly improve or adjust the metabolism of senile cell, improves the vitality of cell, delays the process of body and skin aging.
A. the physicochemical property and the quality standard of the chick embryo element that preparation method obtained of chick embryo element of the present invention:
1. originate: chick embryo element is from 10～13 days Embryo Gallus domesticus of chicken oosperm conventional incubation, adopts extract at low temperature, the resulting molecular weight of separation method less than 10 * 10
6Albumen, polypeptide, aminoacid, hormone, constant and the trace element of adjusting body growth or the like.
2. character:
2.1. lyophilizing chick embryo element powder: off-white color, little bloom end, have and draw moistly, the Embryo Gallus domesticus special odor is arranged; The liquid chick embryo element: yellow or little yellow clear liquid has the Embryo Gallus domesticus special odor.
2.2. this product is water-soluble, is insoluble to various organic solvents.
3. differentiate: get the about 10mg of lyophilizing chick embryo element powder, use the 50ml dissolved in distilled water, or it is an amount of to get chick embryo element solution, is diluted to 0.2mg/ml, these two kinds of solution are as testing sample solution.
3.1. get testing sample solution 1ml and pH5.0, the 0.2mol/L citrate buffer solution fully mixes, and adds ninhydrin reagent 1ml then, fully mixes, 100 ℃ of heating 10min should show bluish violet.
3.2. it is an amount of to get testing sample solution, carries out wavelength-trap scanning with ultraviolet spectrophotometer, near 280nm maximum absorption band should be arranged.
4. content of beary metal:
4.1. content of beary metal (ppm) :≤20
4.2. arsenic salt content (ppm) :≤2
5. loss on drying:
Get lyophilizing chick embryo element powder 0.5g, the accurate title, decide, at P
2O
5(accurate again title is fixed behind 2.67～5.34Pa) the dry 24h, and subtracting weight loss must not surpass 4% decompression down.
6. assay:
Get and freeze in chick embryo element powder or chick embryo element liquid in right amount, measure nitrogen content, be scaled protein content with micro-Kjeldahl, should be greater than 90% of labelled amount.
7. microbial check:
7.1. bacterial population: bacterial population in every 1g lyophilizing chick embryo element powder:＜1000; Bacterial population in every 1ml chick embryo element stock solution:＜100/ml
7.2. yeast: mycete, yeast in every 1g lyophilizing chick embryo element powder:＜100/g; Mycete, yeast in every 1ml chick embryo element stock solution:＜100/ml
7.3. the large intestine dust is uncommon: must not detect/g (solid), or: must not detect/ml (liquid)
7.4. coliform:＜100/g (solid)
Coliform:＜10/ml (liquid)
8. determination of activity:
8.1. get 30 of Kunming mouses, male and female half and half, body weight 16～18g, be divided into three groups at random, first group of (chick embryo element group) mice gavages chick embryo element with 10.0g/kg dosage every day, second group (model group) and the 3rd group of (normal group) mice all gavage the equal-volume normal saline, continuous irrigation stomach 14 days.In giving chick embryo element beginning in the 10th day, first and second group mouse peritoneal is injected the cyclophosphamide (Cy) of 60mg/kg, and continuous 4 days, the 3rd group of mice injected the equivalent normal saline as blank with approach.Irritate harmonization of the stomach injection Cy after 2 hours last day, put to death animal, weigh, cut open rapidly and get thymus, spleen tissue, remove the blood of its surface attachment with the filter paper suction, on precision torsion balance, claim its weight in wet base immediately, with every 10g body weight to the mg number of thymus and spleen as thymus index and index and spleen index, the thymus index and the index and spleen index that compare chick embryo element group and model group, the chick embryo element group should exceed than the thymus index of model group more than 20%, and the chick embryo element group should exceed more than 30% than the index and spleen index of model group.
8.2. get 30 of mices, male and female half and half are divided into chick embryo element group, model group and normal group at random.Preceding two treated animal every Mus nape every day subcutaneous injection 5%D-galactose 0.5ml, the latter, injected 10 days as blank continuously with approach injection equal-volume normal saline.In beginning (continuation injection of d-galactose) in the 11st day, chick embryo element group mice gavaged chick embryo element by body weight 10g/kg, and model group and normal group all gavage the equal-volume normal saline, and successive administration and modeling are 30 days again.Last was irritated the harmonization of the stomach injection of d-galactose after 2 hours, weighed, and eye socket is got blood, required to measure blood SOD, MDA according to SOD, the operation of MDA test kit.Chick embryo element group mouse blood SOD average activity should be higher more than 20% than model group; Chick embryo element group mouse blood MDA average level should be lower more than 30% than model group.
B. the chick embryo element beautifying and anti-aging is regulated the experimentation of immunity:
Chick embryo element has the effects such as immunocompetence that kidney tonifying, essence replenishing, replenishing QI to invigorate the spleen, blood-supplementing blood-nourishing, looks improving and the skin nourishing, raising are in inhibitory state.Adopt artificial aged animal model, observe chick embryo element some aging index, immunoregulatory influence.
1. experiment material
1.1. medicine and reagent: chick embryo element meets the quality standard that researcher proposes;
Tetraethoxypropane (TAP), Switzerland FluKa product;
SOD, MDA measures test kit, and Nanjing is built up bio-engineering research and is provided;
D-galactose (D-gal) and all the other reagent are commercially available homemade biochemical reagents or analytical pure chemical reagent.
1.2. animal: healthy Kunming mouse, body weight 20 ± 2g, male and female half and half, effluent south medical university zoopery center provides.
2. method and result
2.1.D-the subacute aging model facture of galactose: get 30 of mices, male and female half and half are divided into chick embryo element group, model group and normal group at random.Preceding two treated animal every Mus nape every day subcutaneous injection 5%D-galactose 0.5ml, the latter, injected 10 days as blank continuously with approach injection equal-volume normal saline.In beginning (continuation injection of d-galactose) in the 11st day, chick embryo element group mice gavaged chick embryo element by body weight 5g/kg, and model group and normal group all gavage the equal-volume normal saline, and successive administration and modeling are 30 days again.Last was irritated the harmonization of the stomach injection of d-galactose after 2 hours, weighed, and eye socket is got blood, is used for biochemical measurement; Get liver and weigh, make homogenate, standby; Peel off skin and tail tendon, standby.
2.2. superoxide dismutase in the blood (SOD) determination of activity: SOD measures according to the operation of test kit description and requires and computational methods are carried out, detailed results is referring to table 1:
Table 1: chick embryo element is to (the x ± s) of the active influence of SOD in the aging model mouse blood
| Group | Number of animals (n) | 5%D-gal (ml/ only) | Chick embryo element (g/kg) | Whole blood SOD (μ/ml) |
| The chick embryo element group | 10 | 0.5 | 5.0 | 397.44±52.46 ** |
| Model group | 10 | 0.5 | - | 301.3610±48.52 |
| Normal group | 10 | - | - | 516.88±73.42 |
Compare with model group:
*P＜0.01
As shown in Table 1, can obviously the raise vigor of SOD in the mouse blood of chick embryo element, with the poor heteropole of model group significantly (P＜0.01), its climbing reaches 22.75%.
2.3. serum malonaldehyde (MDA) is measured: eye socket is got blood, separation of serum requires and computational methods are carried out according to the operation of test kit description, and detailed results is referring to table 2:
Table 2: chick embryo element is to the influence of MDA content in the aging model mice serum (x ± s)
| Group | Number of animals (n) | 5%D-gal (ml/ only) | Chick embryo element (g/kg) | MDA concentration (MDA nM/ml) |
| The chick embryo element group | 10 | 0.5 | 5.0 | 4.78±0.93 ** |
| Model group | 10 | 0.5 | - | 11.62±0.94 |
| Normal group | 10 | - | - | 3.64±0.51 |
Compare with model group:
*P＜0.01
The result shows that MDA content is significantly higher than normal group level (P＜0.01) in the model group mice serum, and the oral administration chick embryo element is after 40 days, and MDA content obviously descends (P＜0.01) in the serum, and the be formed with obvious suppression effect of chick embryo element to MDA is described.
2.4. liver lipofuscin (LF) Determination on content: with chloroform-methanol (2: 1) preparation liver homogenate, use spectrofluorophotometer at excitation wavelength 360nm with reference to people's methods such as Sohal, emission wavelength 430nm place surveys its fluorescent value, with quinine sulfate as standard control, calculate the content of its LF, detailed results is referring to table 3:
Table 3: chick embryo element is to the influence of aging model mouse liver LF content (x ± s)
| Group | Number of animals (n) | Dosage (g/kg) | 5%D-gal (ml/ only) | Liver L F content (μ/g wet tissue) |
| The chick embryo element group | 10 | 0.5 | 5.0 | 135.07±9.77 ** |
| Model group | 10 | 0.5 | - | 177.71±9.55 |
| Normal group | 10 | - | - | 132.43±8.34 |
Compare with model group:
*P＜0.01
Presentation of results, model group mice and normal group relatively, its liver lipofuscin content significantly rise (P＜0.01), and the oral administration chick embryo element is after 40 days, its lipofuscin content descends obviously (P＜0.01), and as seen, chick embryo element has the effect that lipofuscin forms that suppresses.
2.5. the mensuration of hydroxyproline content in skin and the tail tendon: get skin or the tail tendon of mice, shred, mix.Precision takes by weighing 10mg, makes sample liquid with 6MHCl dissolving, surveys record OD value at 721 spectrophotometer 561nm wavelength places, and hydroxyproline content organizes contained hydroxyproline milligram numerical table to show with per hundred milligrams, and detailed results is referring to table 4:
Table 4: chick embryo element is to the influence of hydroxyproline content in aging model mouse skin and the tail tendon (x ± s)
Compare with model group:
*P＜0.01
The result shows that chick embryo element group and model group compare, and hydroxyproline content obviously raises (P＜0.05, P＜0.01) in skin and the tail tendon, and the prompting chick embryo element can significantly increase the elasticity of hydroxyproline content and skin.
2.6. influence: get 30 of Kunming mouses to immunologic hypofunction mouse immune organ weight, male and female half and half, body weight 16～18g, be divided into three groups at random, first group of (chick embryo element group) mice gavages chick embryo element with 5.0g/kg dosage every day, second group (model group) and the 3rd group of (normal group) mice all gavage the equal-volume normal saline, continuous irrigation stomach 14 days, giving chick embryo element beginning in the 10th day, the cyclophosphamide (Cy) of first and second group mouse peritoneal injection 60mg/kg, continuous 4 days, the 3rd group of mice injected the equivalent normal saline as blank with approach.Irritate harmonization of the stomach injection Cy after 2 hours last day, put to death animal, weigh, cut open rapidly and get thymus, spleen tissue, inhale with filter paper and remove the blood of its surface attachment, claim its weight in wet base immediately on precision torsion balance, detailed results is referring to table 5:
Table 5: chick embryo element is to immunologic hypofunction mouse immune organ weight's influence (x ± s), (n=10)
| Group | 5%D-gal (ml/ only) | Chick embryo element (g/kg) | Thymus index (mg/10g) | Spleen index (mg/10g) |
| The chick embryo element group | 0.5 | 5.0 | 18.25±2.14 ** | 47.22±5.97 ** |
| The Cy group | 0.5 | - | 12.87±1.42 | 31.74±5.02 |
| Normal group | - | - | 20.89±2.49 | 50.33±6.76 |
Compare with the Cy group:
*P＜0.01
As known from Table 5, chick embryo element group and Cy group compare, and its thymus index and spleen index obviously raise (P＜0.01, P＜0.01), illustrate that chick embryo element improves significantly for immune organ weight and the immunologic function degression tool thereof that cyclophosphamide causes.
2.7. influence: get 20 of Kunming mouses to model of blood dificiency mouse red blood cell and hemoglobin, body weight 18～22g, male and female half and half, be divided into two groups at random, measure each Mus administration proerythrocyte (RBC) and hemoglobin (Hb) value earlier, after the afterbody depletion method causes losing blood property model of blood dificiency (RBC, Hb all are starkly lower than normal value) then, irritate stomach chick embryo element or normal saline respectively every day, successive administration 14 days, last gives chick embryo element after 2 hours, RBC and Hb value are surveyed in afterbody blood sampling, and detailed results is referring to table 6:
Table 6: chick embryo element is to the influence of model of blood dificiency mouse red blood cell and hemoglobin (x ± s)
| Group | Number of animals (n) | Dosage (g/kg or ml/kg) | RBC increment (ten thousand/mm3) | Hb rise in value (g%) |
| The chick embryo element group | 10 | 5.0 | 366.41±37.78 ** | 4.45±0.61 ** |
| The normal saline group | 10 | 10.0 | 224.73±39.32 | 3.21±0.49 |
Compare with normal saline:
*P＜0.01
As seen from Table 6, take blood deficiency mice RBC and the Hb value of chick embryo element after 14 days and be significantly higher than normal saline group (P all＜0.01), illustrate that this product has blood tonification effect preferably.
3. conclusion and discussion:
Have oxidation resistance preferably 3.1. originally experimental results show that chick embryo element, can improve the activity of SOD in the subacute aging model mouse blood of D-galactose significantly, reduce MDA concentration in the serum, suppress the formation of liver lipofuscin.The results suggest chick embryo element can significantly improve or adjust the metabolism of senile cell, improves the vitality of cell, delays the process of body and skin aging.Lipofuscin (LF) and MDA are the ageing products of interior free yl reaction, they increase with advancing age, superoxide dismutase (SOD) then is the main enzyme that body is removed free radical, it with age and active the reduction, so both all are one of important biochemical indicators of mankind aging.In addition, free radical still causes old and feeble major reasons such as skin collagen polymerization, reduction elasticity.
3.2. this experimental result shows, give the heavy dose of D-galactose of mouse subcutaneous injection 40 days continuously, can make the hydroxyproline in mouse skin and the tail tendon significantly be lower than normal mouse, its hydroxyproline content rebound significantly after taking chick embryo element, this prompting chick embryo element has the effect that prevents skin aging, and this may be relevant with the effect that improves collagen content, increase skin elasticity.Modern study confirms, along with increasing age, the collagen albumen solubility significantly descends in the body, because it is old and feeble, the interchain covalent cross-linking degree of body collagen protein polypeptide increases, and makes the skin stiff few elasticity that becomes, and permeability is low, the collagenic supersession rate reduces, and the free peptide in the collagen tissue or the hydroxyproline content of binding peptide are reduced.
3.3. this laboratory observation arrives, cyclophosphamide (Cy) can cause immune function of mice low, and can make the immune organ weight index decreased.Chick embryo element can antagonism Cy immunosuppressive action, protection mouse thymus and spleen are avoided the infringement of Cy, illustrate that this product has the effect of raise immunity.Be accompanied by the growth at age, human immunologic function is also being faded.Observe proof to removing thymus Mus aged animal model, immunologic function degression is a key factor of body aging, and human body immunity improving power just makes body exempt the invasion and attack of many pathogen, just make body strengthen monitoring and removing, thereby reduced the generation of disease mutant cell.Its result is strong body and defying age.
3.4. this experiment adopts Mus tail depletion method to cause losing blood property of mice model of blood dificiency, has observed the influence of chick embryo element to blood deficiency mouse red blood cell (RBC) and hemoglobin (Hb), the result shows that this product can be improved the Anemia of blood deficiency mice significantly.The prompting chick embryo element has the effect of benefiting vital QI and blood, skin care skin Caring.The traditional Chinese medical science thinks that QI and blood is the material base of vital movement.QI and blood is filled Sheng, not only can show as energetic, radiant, the colour of skin is beautiful, and can also have good health and a long life, in case deficiency of both QI and blood, then inevitable complexion is withered, pachylosis, wrinkle increase, weak and sickly.So the relation of QI and blood and life-span, skin is very close.
C. the conventional formulation of the prepared chick embryo element of the present invention is:
1. tablet: with the chick embryo element is major ingredient, is aided with the conventional adjuvant of relevant tablet, and every contains chick embryo element 0.5g, is grown up each 1～2, every day 1～2 time;
2. capsule: with the chick embryo element is major ingredient, is aided with the conventional adjuvant of relevant capsule, and every capsules contains chick embryo element 0.5g, is grown up each 1～2, every day 1～2 time;
3. soft capsule: with the chick embryo element is major ingredient, is aided with polyunsaturated vegetable oil, and every soft capsule contains chick embryo element 0.5g, is grown up each 1～2, every day 1～2 time;
4. oral liquid: with the chick embryo element is major ingredient, is aided with antiseptic, correctives, is mixed with 500mg: 10ml/ bottle concentration oral liquid, be grown up each 1～2 bottle, every day 1～2 time.
5. cosmetics: with the chick embryo element is major ingredient, and emulsifying in suitable cosmetics emulsifiable paste base material is aided with suitable antiseptic and spice, can make the cream type chick embryo element cosmetics of different flavor; Also chick embryo element can be dissolved in suitable liquid, be aided with relevant auxiliary materials, spice, antiseptic and produce the liquid dosage form skincare liquid.
D. chick embryo element oral dose:
Experimental results show that the chick embryo element avirulence that the present invention is prepared, safety range reaches food stage, calculates that according to the zoopery effective dose per day for adults 0.5g can tell on, and escalated dose is to 2g every day, and effect will be better; According to the composition reasoning,, do not use the chick embryo element oral formulations to the egg allergy sufferers.
Four. the specific embodiment:
Embodiment one: selected do not have a fresh chicken oosperm of additive in violation of rules and regulations, places commercially available full-automatic hatching egg machine inner pallet, regulates parameters then: 1. incubation temperature: the 1st～10 day 37.8 ℃, the 10th～13 day 37.6 ℃; 2. hatch humidity: relative humidity 60%; 3. the ventilation coefficient 4～6; 4. egg-turning: egg-turning was 1 time in per 1.5 hours; 5. hatch to 14 days rules.Remove eggshell taking-up Embryo Gallus domesticus rapidly after taking out incubated egg, this fresh Embryo Gallus domesticus is shredded to 1～3 centimetre of big fine grained chippings with chipper, put into cleaning rustless steel pallet, place low temperature refrigerator, laying temperature sensor probe in the middle of Embryo Gallus domesticus, after all samples temperature is frozen to-26～-28 ℃, refreeze 1 hour, use the efficient universal pulverizer to be crushed to 80 orders then; Embryo Gallus domesticus after pulverizing is added 3 times of volumes be chilled to pure water about 2 ℃, 60 rev/mins of stirrings suspendible slurrying in 5 minutes in advance in proper container; This Embryo Gallus domesticus slurry is placed low temperature refrigerator, after sample temperature freezes to-26～-28 ℃, refreeze 1 hour, put then when being melted up to the frozen water coexistence under the room temperature condition naturally, put low temperature refrigerator again, after sample temperature freezes to-26～-28 ℃, refreeze 1 hour, so multigelation is 5 times; After Embryo Gallus domesticus behind multigelation slurry melted, place refrigerated centrifuge, attemperation control make the rotor chamber temperature remain on+4 ℃, 10000 rev/mins are centrifugal 10 minutes; With the careful sucking-off of the slurry supernatant of the Embryo Gallus domesticus after centrifugal, place aseptic rustless steel container, by the above hollow fiber membrane ultrafiltration device of molecular cut off 800,000 dalton, obtain ultrafiltrate rapidly; This ultrafiltrate is placed aseptic rustless steel pallet, and 1.5 centimetres of thickness of charging are put into the freeze dryer lyophilizing cabin after sterilization, the pre-cooling in advance; Regulate the lyophilizing parameter, set freeze-drying curve; Above-mentioned ultrafiltrate evenly is refrigerated to-40 ℃; Start freeze dryer then, the vacuum pump of vacuum system, lobe pump is opened successively, regulate vacuum below 13Pa, when vacuum remains on below the 13Pa after constant 1 hour, start the freeze dryer heating system, attention and maintenance vacuum are still below 13Pa in the heating process, the material maximum temperature must not be above 35 ℃ during heating, be stabilized in 35 ℃ when being heated to temperature of charge, vacustat kept 2 hours when 8Pa is following, can shut down, discharging, the loose lumps thing of resulting yellow-white is chick embryo element, and this chick embryo element is inserted lucifuge stored refrigerated in the hermetic container immediately, and is standby.
Embodiment two: selected do not have a fresh chicken oosperm of additive in violation of rules and regulations, places commercially available full-automatic hatching egg machine inner pallet, regulates parameters then: 1. incubation temperature: the 1st～10 day 37.8 ℃, the 10th～13 day 37.6 ℃; 2. hatch humidity: relative humidity 60%; 3. the ventilation coefficient 4～6; 4. egg-turning: egg-turning was 1 time in per 1 hour; 5. hatch to rule taking-up in 12 days; Remove eggshell taking-up Embryo Gallus domesticus rapidly after taking out incubated egg; This fresh Embryo Gallus domesticus is shredded to 1～3 centimetre of big fine grained chippings with chipper, put into cleaning rustless steel pallet, place low temperature refrigerator, laying temperature sensor probe in the middle of Embryo Gallus domesticus, after all samples temperature is frozen to-26～-28 ℃, refreeze 2.5 hours, use the efficient universal pulverizer to be crushed to 80 orders then; Embryo Gallus domesticus after pulverizing is added 4 times of volumes be chilled to pure water about 1 ℃, 80 rev/mins of stirrings suspendible slurrying in 8 minutes in advance in proper container; This Embryo Gallus domesticus slurry is placed low temperature refrigerator, after sample temperature freezes to-26～-28 ℃, refreeze 2.5 hours, put then when being melted up to the frozen water coexistence under the room temperature condition naturally, put low temperature refrigerator again, after sample temperature freezes to-26～-28 ℃, refreeze 2.5 hours, so multigelation is 3 times; After Embryo Gallus domesticus behind multigelation slurry melted, place refrigerated centrifuge, attemperation control make the rotor chamber temperature remain on+1 ℃～+ 4 ℃, 3000 rev/mins are centrifugal 30 minutes; With the careful sucking-off of the slurry supernatant of the Embryo Gallus domesticus after centrifugal, place aseptic rustless steel container, by the above hollow fiber membrane ultrafiltration device of molecular cut off 800000 dalton, obtain ultrafiltrate rapidly; This ultrafiltrate is placed aseptic rustless steel pallet, and charging thickness is less than 1.2 centimetres, puts in advance the freeze dryer lyophilizing cabin after sterilization, the pre-cooling; Regulate the lyophilizing parameter: above-mentioned ultrafiltrate evenly is refrigerated to-40 ℃; Start the vacuum pump vacuum of freeze dryer vacuum system then and below 30Pa, start lobe pump, kept the vacuum 5.6Pa～13Pa of system about 1.5 hours; Start the freeze dryer heating system then, the material maximum temperature must not be above 35 ℃ during heating, and keep vacuum below 13Pa, be stabilized in 35 ℃ when being heated to temperature of charge, vacustat kept 2.5 hours when 8Pa is following, shutdown, discharging, the loose lumps thing of resulting yellow-white is chick embryo element, and this chick embryo element is inserted lucifuge stored refrigerated in the hermetic container immediately, and is standby.
Embodiment three: selected do not have a fresh germ cell of the kind chicken of additive forage feed in violation of rules and regulations, places commercially available full-automatic hatching egg machine inner pallet, regulates parameters then: 1. incubation temperature: the 1st～10 day 37.8 ℃, the 10th～13 day 37.6 ℃; 2. hatch humidity: relative humidity 60%; 3. the ventilation coefficient 4; 4. egg-turning: egg-turning was 1 time in per 1 hour; 5. hatch to rule taking-up in 13 days; Remove eggshell taking-up Embryo Gallus domesticus rapidly after taking out incubated egg; This fresh Embryo Gallus domesticus is put into refrigerator-freezer be refrigerated to about-1 ℃, chopping is put into cleaning rustless steel pallet to 1～3 centimetre of big fine grained chippings, places low temperature refrigerator to be refrigerated to about-20 ℃, refreezes 3 hours, uses the efficient universal pulverizer to be crushed to 100 orders then; Embryo Gallus domesticus after pulverizing is added 5 times of volumes be chilled to sterile distilled water about 1 ℃, 70 rev/mins of stirrings suspendible slurrying in 10 minutes in advance in proper container; Place low temperature refrigerator to be refrigerated to about-28 ℃ in this Embryo Gallus domesticus slurry, refreeze 3 hours, when rearmounted room temperature is melted up to the frozen water coexistence naturally, puts low temperature refrigerator again and be refrigerated to about-28 ℃, refreeze 3 hours, multigelation 4 times; After the thawing of the slurry of the Embryo Gallus domesticus behind the multigelation, place the considerable low-temperature centrifuge, regulate the rotor chamber temperature at+4 ℃, 8000 rev/mins are centrifugal 20 minutes; With the careful sucking-off of the slurry supernatant of the Embryo Gallus domesticus after centrifugal, place aseptic rustless steel container, by the above hollow fiber membrane ultrafiltration device of molecular cut off 800000 dalton, obtain ultrafiltrate rapidly; This ultrafiltrate is concentrated by the method for freezing again, when 1/3 of simmer down to original volume is measured, insert airtight sterile chamber freezing (26 ℃～-40 ℃) and preserve, standby.
Claims (9)
1. the preparation method of a chick embryo element comprises selected chicken oosperm and hatching, it is characterized in that, comprises following concrete steps:
A. selected chicken oosperm, surperficial conventional decontamination, conventional incubation 10～13 days, described selected chicken oosperm are meant selects egg type chicken fertilized eggs for use, and in 3～7 days puerperal, egg size is at 110～120 grams, profile rule, not damaged;
B. will hatch good germ cell surface and carry out routine disinfection, and remove eggshell and take out Embryo Gallus domesticus, Embryo Gallus domesticus will be put into refrigerator-freezer, under≤-20 ℃ temperature conditions, freezing 0.5～5 hour, then Embryo Gallus domesticus be pulverized;
C. the Embryo Gallus domesticus after will pulverizing is pulled an oar, and adds the sterile water for injection that 3～5 times of Embryo Gallus domesticus volumes are chilled to 0～4 ℃ in advance during making beating in Embryo Gallus domesticus, stirs under 60～80 rev/mins mixing speed 5～10 minutes;
D. the Embryo Gallus domesticus of pulping is carried out 3～5 times multigelation, freezing temperature is-26～-28 ℃, and each freezing time is 0.5～5 hour, melts naturally under the room temperature condition;
E. the Embryo Gallus domesticus of multigelation slurry is poured in the centrifuge under≤4 ℃ of temperature conditions, under 3000～10000 rev/mins speed conditions centrifugal 10～30 minutes, obtained supernatant;
F. supernatant is crossed the ultrafiltration post of molecular cut off more than 800000 dalton, got ultrafiltrate;
G. with obtaining the loose lumps material of off-white color after the ultrafiltrate lyophilization, be described chick embryo element, or, be chick embryo element solution the direct aseptic subpackaged preservation behind ultrafiltration and concentration of above-mentioned ultrafiltrate;
H. relative humidity less than 30% environment in, resulting chick embryo element or chick embryo element solution inserted in the hermetic container keeps in Dark Place, with standby.
2. the preparation method of chick embryo element according to claim 1, it is characterized in that: the hatching parameter in the described conventional incubation method is:
1. incubation temperature: the 1st～10 day 37.8 ℃, the 10th～13 day 37.6 ℃;
2. hatch humidity: relative humidity is about 60%;
3. ventilation: keep the airborne oxygen content of hatching box more than 21%;
4. egg-turning: egg-turning was 1 time in per 1～2 hour;
5. hatch to 11～14 days, remove eggshell behind the taking-up incubated egg and take out Embryo Gallus domesticus.
3. the preparation method of chick embryo element according to claim 1, it is characterized in that: the method that described Embryo Gallus domesticus is pulverized is: fresh Embryo Gallus domesticus is placed low temperature refrigerator, laying temperature sensor probe in the middle of Embryo Gallus domesticus, after all samples temperature is frozen to-26～-28 ℃, refreeze 1～2.5 hour, use size reduction machinery that it is crushed to 40～100 orders then.
4. the preparation method of chick embryo element according to claim 1, it is characterized in that: described multigelation is that the slurry of the Embryo Gallus domesticus after the making beating is placed-30 ℃ low temperature refrigerator, after sample being refrigerated to-26～-28 ℃, freezing 1～3 hour, place then when being melted up to the frozen water coexistence under the room temperature condition naturally, place-30 ℃ of low temperature refrigerators again, sample is refrigerated to-26～-28 ℃, freezing 1～3 hour, so multigelation was 3～5 times.
5. the preparation method of chick embryo element according to claim 1, it is characterized in that: described hyperfiltration process is that the Embryo Gallus domesticus after centrifugal slurry supernatant is crossed hollow fiber membrane ultrafiltration device more than molecular cut off 800000 dalton, molecular cut off obtains molecular weight smaller or equal to 800000 daltonian ultrafiltrates greater than the composition of 800000 dalton part.
6. the preparation method of chick embryo element according to claim 1, it is characterized in that: the cryodesiccated method of described ultrafiltrate is that resulting ultrafiltrate is placed aseptic rustless steel pallet, charging thickness≤1.5 centimetre, put into sterilization in advance, in the freeze dryer lyophilizing cabin after the pre-cooling, regulate the lyophilizing parameter, above-mentioned ultrafiltrate evenly is refrigerated to below-40 ℃, start vacuum pump and lobe pump in the freeze dryer vacuum system then successively, regulate vacuum below 6.5～13Pa, kept 2～3 hours, start the heating system in the freeze dryer then, attention and maintenance vacuum are below 6.5～13Pa in the heating process, the material maximum temperature must not be above 35 ℃ during heating, be stabilized in 35 ℃ when being heated to temperature of charge, vacustat kept 1～3 hour when 8Pa is following, i.e. shutdown, discharging, the loose lumps thing of resulting yellow-white is chick embryo element.
7. according to the preparation method of any described chick embryo element of claim of claim 1～6, it is characterized in that: the conventional adjuvant that described chick embryo element adds is medically made tablet, or capsule, or oral liquid.
8. the preparation method of chick embryo element according to claim 7, it is characterized in that: described capsule is a soft capsule.
9. according to the preparation method of any described chick embryo element of claim of claim 1～6, it is characterized in that: the conventional adjuvant that described chick embryo element adds is medically made cosmetics, or health product.
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| JP2010505884A (en) * | 2006-10-12 | 2010-02-25 | ユナイテッド パラゴン アソシエイツ インコーポレイテッド | Method for preparing components of fertilized eggs |
| CN102028199B (en) * | 2010-11-08 | 2012-10-03 | 河南科技大学 | Health-care capsule of chicken embryo egg and processing technique thereof |
| CN102525867B (en) * | 2012-01-16 | 2013-07-31 | 上海得高实业有限公司 | Chick embryo essence freeze-dried powder and preparation method and application thereof |
| CN103012584A (en) * | 2012-12-28 | 2013-04-03 | 江南大学 | Preparation method of chicken embryo hybrid peptide with high angiotensin-converting enzyme inhibitory activity |
| CN102987411A (en) * | 2012-12-28 | 2013-03-27 | 黑龙江新曙光牧业集团有限公司 | Preparation method for fast and efficient absorption early-stage high-activity life source essence powder |
| CN103262939A (en) * | 2013-05-23 | 2013-08-28 | 江南大学 | Preparation method of antioxidant activity mixed peptide originated from chick embryo |
| CN103301088B (en) * | 2013-07-03 | 2016-02-10 | 金莲英 | A kind of chick embryo polysaccharide capsule preparation and preparation method thereof |
| CN105851747A (en) * | 2016-04-05 | 2016-08-17 | 江苏强农农业技术服务有限公司 | Lepidium meyenii health-care beverage capable of beautifying features and resisting ageing and preparation method of lepidium meyenii health-care beverage |
| CN106138101B (en) * | 2016-08-08 | 2019-09-17 | 山东宏济堂制药集团股份有限公司 | A kind of preparation method of chicken embryo placenta extract |
| CN106562994A (en) * | 2016-10-26 | 2017-04-19 | 谢培增 | Preparation method for preparing duck embryos and application of duck embryos |
| CN106692735A (en) * | 2016-10-26 | 2017-05-24 | 沈会强 | Production method and application of oat embryo extract |
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| CN114569636A (en) * | 2020-12-02 | 2022-06-03 | 西南交通大学 | Processed chicken embryo, and its preparation method and application |
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