CN101759770A - Method for extracting transfer factor from chicken spleen - Google Patents
Method for extracting transfer factor from chicken spleen Download PDFInfo
- Publication number
- CN101759770A CN101759770A CN200810154336A CN200810154336A CN101759770A CN 101759770 A CN101759770 A CN 101759770A CN 200810154336 A CN200810154336 A CN 200810154336A CN 200810154336 A CN200810154336 A CN 200810154336A CN 101759770 A CN101759770 A CN 101759770A
- Authority
- CN
- China
- Prior art keywords
- transfer factor
- spleen
- distilled water
- filtration
- animal
- 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.)
- Pending
Links
Landscapes
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
Abstract
The invention provides a method for extracting transfer factor from chicken spleen, which includes the steps of organizing, cell breakage by a high pressure homogenizer, flocculant sediment, millipore membrane filtration, ultrafiltration with ultrafilter membrane. The flocculant is added during cell breakage process to enable protein in the solution to precipitate, and the solution becomes clear, the blockage of hollow fiber ultrafilter columns is reduced during ultrafiltration process. The method can greatly shorten the production cycle, saves large quantity of human and material resources, improves the productivity of transfer factor and provides feasible approaches for industrial and large scale production.
Description
Technical field
The invention belongs to field of veterinary, particularly relate to a kind of method of from the animal spleen, extracting transfer factor.What summary of the invention of the present invention related generally to is the method for extracting transfer factor from chicken spleen.
Background technology
(transfer factor TF) is a kind of material that can shift sensitization information that the T lymphocyte discharges to transfer factor, and it can give acceptor with the cellular immunization information transfer of donor specifically, thereby strengthens the immunologic function of acceptor.TF finds so far that from the fifties Chinese scholars is all carried out big quantity research to this, and is introduced in animal doctor's immunity and the clinical treatment in 1979, and it has become a kind of widely used enhancing immunity preparation abroad at present.
Because transfer factor do not have species specificity, therefore the source of transfer factor is comparatively extensive clinically, human common clinically have people's transfer factor, pig transfer factor, ox transfer factor, sheep transfer factor, goose, monkey transfer factor etc.At present livestock and poultry go up common have ox transfer factor, pig transfer factor, chicken transfer factor.Fowl poultry spleen is the refuse in the course of processing, therefore extremely wide application and development prospect is arranged, and has become the focus of transfer factor research.
Transfer factor be molecular weight less than 10000, the small-molecule mixture of the heterogencity of biologically active, its inclusion comprises total free aminoacids (16-18 kind), metallic elements such as nucleic acid, polypeptide and K, Na, Ca, Mg, Zn.Physicochemical property in the various TF, moiety difference is little, but content has than big-difference.
On immunology, TF can be divided into specific transfer factor and non-specific transfer factor two big classes.Extract again behind certain specific pathogen infection of specific transfer factor system employing or immune crowd, the animal and contain the active transfer factor of this antigen-specific, present clinical hepatitis B virus special transfer factor, various tomour specific transfer factor, epidemic haemorrhagic fever virus transfer factor, cloth Salmonella transfer factor, simplexvirus transfer factor, encephalitis B transfer factor, the tubercule bacillus transfer factor etc. used.Non-specific transfer factor is meant with what nature crowd or animal white corpuscle extracted to have an active transfer factor of panimmunity, immunity function that can non-specific adjusting body, thus improve the resistibility of body or the immune effect of vaccine.
Cellular immunization mainly realizes by the T lymphocyte, report transfer factor such as Wang Jianwen can strengthen the lymphocytic ratio of the young cock T of Luo Man, Ma Fenglong etc. discover that with chicken spleen transfer factor and newcastle disease I be that injection can significantly improve lymphocytic transformation efficiency to seedling to fryer simultaneously, proof chicken spleen TF has promoter action to the cellular immunization of chicken, can promote the lymphocytic propagation of T with ripe, the cellullar immunologic response ability of enhancing body.
Early stage classical transfer factor mechanism research trial just finds that transfer factor has the activity of transmitting the specific cell immunologic information, and the performance of the stimulation of antigenic information and animal body immunologic function has directly and gets in touch.Existing numerous data confirm, but transfer factor activated lymphocyte E acceptor, the formation number of increase E rosette.Therefore immunologic information is transferred to the acceptor lymphocyte by TF, make cell obtain this immunologic information and produce the antigenic acceptor of identification specificity, when this kind antigen exists, this specific recognition acceptor will combine with specific antigens and trigger the recipient cell activation, causes its height differentiation and proliferation from strengthening lymphocytic activity.
After high winter jasmine was waited research report chicken injection TF, inoculation egg-decreasing syndrome inactivated vaccine can significantly improve the antibody titers of chicken body.Discovery chicken TF living vaccines such as Ma Fenglong and oil-emulsion inactivated vaccine all have synergy when head exempts from booster immunization, can significantly improve the humoral immunoresponse(HI) ability of immunization chicken, produce higher titer antibody, and prolong the antibody peak period, make it to keep the less time.Because the X lymphocyte is realizing that the humoral immunization function needs T lymphocytic auxiliary, generally believe that at present transfer factor mainly is an immunity function of regulating body by the T lymphocyte to the influence of humoral immunization.
Liu Runzhen etc. prepare specificity spleen transfer factor after utilizing canine penton vaccine immunity pig, can significantly strengthen mouse E rosette forming rate and peritoneal macrophage activate the phagocytic capacity.Chen Dekun etc. discover, to healthy mice injection and oral pig spleen transfer factor can strengthen the peripheral blood neutrophil leucocyte to staphylococcic phagocytic rate and peritoneal macrophage to erythrocytic phagocytic rate.Therefore, transfer factor also has enhancement to the non-specific immunity function of body.
Fan Zhenqing etc. discover, the heavy exponential of leukocyte count, lymphocyte percentage and spleen of the oral and injection TF mouse that is caused by hydrocortisone capable of blocking descends.The immunosuppression Rabbit Model that Miao Naifa adopts endoxan to set up is carried out the pig spleen transfer factor and is promoted the white corpuscle experiment, and injection back 3d is that visible total white blood cells rises rapidly, and 5d can reach the climax, and trend is normal behind the 8d.After inferring that thus TF enters body as immunoactivator, can make hemopoietic system produce a large amount of white corpuscles at short notice, the while activated lymphocyte, increase the t helper cell generation and discharge more lymphokine, thereby promote T lymphocyte growth and division performance to resist the effect of radiation, anti-immunosuppression, raise immunity.
The oral 0.5-1.0ML transfer factor of report chick such as Wang Jianwen raw product is not compared with taking the transfer factor group behind the 7d, and weightening finish is obvious, and oral transfer factor group chickens' extract is refreshing active, and feather is glossy.Jiang Qingyan etc. find that in test injection spleen transfer factor has obvious effects to the yellow chicken weightening finish in Guangdong.The normal growth of animal body is grown generally by T3, T4 and GH coordinated regulation and is finished.GH mainly promotes tissue growth, and T3, T4 mainly promote the differentiation of organ, tissue, and the growth promoting function of GH needs an amount of T3, the existence of T4.In this test, the TF chicken group of injection different concns is blood T4 when 8 ages in week, and the GH level all is significantly higher than control group, infers that thus the inherent mechanism that the spleen transfer factor promotes the yellow chicken in Guangdong to grow is relevant with the rising of blood T4, GH level.
Along with improving constantly of mass-producing, intensification degree cultured in modernization, virus disease has become puzzlement raiser's a great problem at present.Existing general solution is exactly immunity, yet for various reasons, can cause immuning failure unavoidably sometimes, breaks out atypical transmissible disease, brings certain difficulty for diagnosis and treatment.Behind immuning failure, often rely on antibiotic therapy, caused the increase of Resistant strain and the generation of cross infection.Transfer factor is sent out as a kind of cellular immunization and is answered toughener, can play an important role aspect disease preventing and treating, improves the immune effect after the immunity, effectively improves the resistance against diseases of body.
Present existing transfer factor technology after normally the fat in the spleen of animal and great vessels being picked out, is organized and is smashed to pieces, behind the multigelation, obtains the process cost height by the semi-permeable membranes dialysis.In addition, the conventional Laurence method that adopts promptly utilizes twice this method of dialysis method recovery transfer factor simple to operate, but production cycle farm labourer preface loaded down with trivial details (production cycle needs 20 days approximately), length consuming time is wasted a large amount of manpower and materials.Therefore these methods all are difficult to carry out large-scale industrialization production.
Therefore, need a kind of quick, efficient and economic method of from the animal spleen, obtaining transfer factor, to satisfy present suitability for industrialized production.
Summary of the invention
The object of the invention is to provide a kind of method of obtaining transfer factor from the animal spleen, comprising:
1) with refrigerated animal spleen 1000g, be cut into small pieces after cleaning with distilled water, add 1000ml distilled water, rub with tissue mashing machine;
2) high pressure homogenizer (60MPa) carries out cytoclasis, adds flocculation agent 160ml simultaneously;
3) under 4 ℃, with 7000 rev/mins, centrifugal 15 minutes, go precipitation, stay supernatant liquor;
4) supernatant liquor filters with millipore filtration, carries out ultrafiltration with ultra-filtration membrane then, is the stoste that contains transfer factor.
The transfer factor that contains expection in the stoste is removed the preparation of virus back according to the national drug management method then.
In a specific embodiments, described distilled water is the former distilled water that reduces phlegm and internal heat.
In another embodiment, described flocculation agent is a medicinal alcohol.
In another embodiment, the described millipore filtration preferred 0.22 μ m in footpath.
In another embodiment, the preferred molecular weight cut-off of described ultra-filtration membrane is 5000 daltonian ultra-filtration membranes.
In another embodiment, described animal is a bird, preferred chicken.
Term:
" pyrogen " means the pyrogenic substance that can cause the rising of warm blooded animal abnormal body temperature by microorganisms.It comprises bacillary pyrogen, endogenous polymer pyrogen, the low molecule pyrogen of endogenous and chemical pyrogen etc.Here " pyrogen " of indication mainly is meant bacillary pyrogen, is meta-bolites, bacterium corpse and the intracellular toxin of some bacterium.What the pyrogenicity ability was the strongest is the product of gram negative bacillus, secondly is gram-positive bacillus class, gram positive coccus then a little less than, mould, yeast even virus also can produce pyrogen.Pyrogen is the many pure mixtures that form with protein bound of phosphatide normally.The many alcohol of phosphatide are active centre of mixture, and pyrogenic action is the strongest.Its chemical constitution is because of the different differences to some extent of bacterial classification.Molecular weight is 5 * 104～5 * 105, and the big more pyrogenic action of molecular weight is also strong more.
The former method of reducing phlegm and internal heat comprises:
1. pyroprocess: the resistance toheat of pyrogen is good, and 60 ℃ of heating 1h destruction that is not decomposed do not degrade for 100 ℃, but 180 ℃ of 3～4h, 200 ℃ of 60min or 250 ℃ of 30～45min can make pyrogen thoroughly destroy.Therefore the syringe that uses when used container and other apparatus and injection in heat-resisting article such as glasswork, metal products, the production process etc. all can adopt this method to destroy pyrogen.But under normally used injection pressure sterilizing condition, be not enough to destroy pyrogen.
2. absorption method: pyrogen can be by absorption such as gac, asbestos, white boles in the aqueous solution and is removed.Because activated carbon property is stable, adsorptivity has concurrently by force and helps filter and decolorization, thus be widely used in injection production, but should note adsorbing the loss of the main ingredient that soup causes.
3. ultrafiltration process: the pyrogen molecular weight is 1 * 10
6About, volume is less, and about 1～5nm can pass through general filter and millipore filtration, but adopts ultrafiltration process as being removed with 3.0～15nm ultra-filtration membrane.
4. distillation method: pyrogen can be water-soluble but non-volatile, but can enter with the droplet of water vapour in the water for injection, when therefore preparing water for injection, pyrogen in the former water can be removed through distillation, but needs repeatedly distillation, and be added with every the foam device, single distills that often effect is undesirable.
5. acid-base method: pyrogen can be destroyed by strong acid, highly basic, strong oxidizer.Glass Containers and apparatus such as dosing destroy pyrogen with available potassium bichromate sulfuric acid cleaning liquor or dilute sodium hydroxide processing such as glassware, infusion bottles.
Other: comprise that ion exchange method, gel filter method, reverse osmosis method etc.
Beneficial effect
1. the present invention is in leaching process, and broken back uses high pressure homogenizer to carry out broken wall once more, makes tissue or entocyte fully be released;
2. added flocculation agent at broken wall simultaneously, made protein precipitation in the solution, the solution becomes clarification, in the process of ultrafiltration, reduced stop up the Hollow Fiber Ultrafiltration post may;
3. adopt production transfer factor of the present invention, the production cycle shortens greatly, makes to carry out the method that cell wall breaking, semi-permeable membranes are dialysed by the method for traditional multigelation, and the production cycle shortens about 20 days; And adopt the transfer factor production cycle of the inventive method preparation only to need about 7 days, saved lot of manpower and material resources;
4. improved the production efficiency of transfer factor, the method of tradition multigelation is carried out the method that cell wall breaking, semi-permeable membranes are dialysed, the transfer factor stoste of producing, it is stoste 2000ml about 2.0mg/mL that every 1000g spleen is produced content approximately, to produce content approximately be stoste 1000ml about 7.0mg/mL and adopt the present invention to produce every 1000g spleen, and amounting to output increases by 175%.
Embodiment
The present invention will be further described below in conjunction with embodiment.
Embodiment 1: the preparation of transfer factor
1, cut and pluck, clean: will melt is that the animal spleen that partly freezes attitude is removed fat and blood vessel, and accurate weighing 1kg is with no thermal source distilled water water cleaning 3 times.
2, rub: the spleen after the grease removal takes by weighing in the mincer and just twists 3 times, does not have thermal source distilled water with adding 1000ml in the spleen that rubs, and puts into and smashs cylinder to pieces, smart strand.
3, grind: the spleen slurry of smashing to pieces is put into colloidal mill with its grinding, make homogenate.
4, cytoclasis: with above-mentioned spleen homogenate, in high pressure homogenizer, pressure 60MPa carries out homogeneous, makes homogenate.
5, high-pressure homogeneous good homogenate is added medicinal alcohol 160ml, put in the refrigerated centrifuge, 7000 rev/mins, centrifugal 15 minutes, 4 ℃ of Centrifugal Environment temperature discarded sediment, collected supernatant liquor.
6, supernatant liquor filters with the millipore filtration of 0.22 μ m, is that 5000 dalton's ultra-filtration membranes carry out ultrafiltration with molecular weight cut-off then, is stoste.
Embodiment 2: to the detection of the transfer factor of prepared of the present invention
Transfer factor stoste to embodiment 1 described prepared is carried out following detection according to National Drug Administration, national drug standards WS1-XG-036-2000:
1, appearance character is little yellow clear liquid, meets the appearance character of transfer factor solution.
2, the amino acid identification is positive reaction.
3, ultraviolet spectrophotometry: above-mentioned gained sample ABS
260/ ABS
280＞2.0.
4, the pH value is between 6.0～7.5.
5,20% sulphosalicylic acid detects: above-mentioned gained sample does not have muddiness and deposited phenomenon, illustrates that albumen test all becomes negative, and it does not contain macro-molecular protein.
6, high molecular weight material detects, and does not have absorption peak before the Regular Insulin appearance time, and illustrating does not have the macromole that is higher than molecular weight 6000 in this product.
7, total free aminoacids detects: this product aminoacids content 11mg among every 1ml.
7, transfer factor determination of activity: can make its function of receptors of thymus gland T cellular-restoring that takes off behind the E acceptor according to transfer factor, thus the biological activity of reaction transfer factor.The percentage that above-mentioned gained sample forms the E rosette is respectively 29.4%, 28.9%, and comparison increases by 15.8%, 15.2% (P≤0.01) respectively according to group.
8, bacteriological analysis: no aerobic, anaerobism, saprophytic microorganism and fungi exist in the above-mentioned gained sample.
9, supersensitivity, toxicity test: get 10 of healthy mices, male and female half and half, oral this product concentrated solution, be equivalent to 100 times of normal oral dosage, observe the variation of the viability of small white mouse, the result: do not have any allergy, toxic reaction, also do not have any dead appearance, illustrate that this product is safe, does not have any toxicity and side effect.
10, nucleic acid content is measured: above-mentioned gained sample is measured nucleic acid content through orcin method and is respectively 587.02 μ g/mL, 582.29 μ g/mL.
11, determining content of peptides: above-mentioned gained sample is measured content of peptides through the Lowry method and is respectively: 6.85mg/mL, 7.02mg/mL.
By the foregoing description, we find the chicken spleen transfer factor content height that extracted, and production process is simple, the production efficiency height.Institute's production transfer factor stoste meets the standard code of national code simultaneously.Therefore production method of the present invention can be produced popularization on a large scale.
Claims (6)
1. method of obtaining transfer factor from the animal spleen comprises:
1) with refrigerated animal spleen 1000g, be cut into small pieces after cleaning with distilled water, add 1000ml distilled water, rub with tissue mashing machine;
2) high pressure homogenizer (60MPa) carries out cytoclasis, adds flocculation agent 100-200ml simultaneously;
3) under 4 ℃, with 7000 rev/mins, centrifugal 15 minutes, go precipitation, stay supernatant liquor;
4) supernatant liquor filters with millipore filtration, carries out ultrafiltration with ultra-filtration membrane then, is the stoste that contains transfer factor.
2. the process of claim 1 wherein that described distilled water is the former distilled water that reduces phlegm and internal heat.
3. claim 1 or 2 method, wherein said flocculation agent is medicinal alcohol 160ml.
4. each method in the claim 1 to 3, the wherein said millipore filtration preferred 0.22 μ m in footpath.
5. each method in the claim 1 to 4, the preferred molecular weight cut-off of wherein said ultra-filtration membrane is 5000 daltonian ultra-filtration membranes.
6. each method in the claim 1 to 5, wherein said animal is a bird, preferred chicken.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN200810154336A CN101759770A (en) | 2008-12-23 | 2008-12-23 | Method for extracting transfer factor from chicken spleen |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN200810154336A CN101759770A (en) | 2008-12-23 | 2008-12-23 | Method for extracting transfer factor from chicken spleen |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN101759770A true CN101759770A (en) | 2010-06-30 |
Family
ID=42491166
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN200810154336A Pending CN101759770A (en) | 2008-12-23 | 2008-12-23 | Method for extracting transfer factor from chicken spleen |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN101759770A (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102078329A (en) * | 2011-01-26 | 2011-06-01 | 天津农学院 | Method for preparing concentration-controllable broiler spleen transfer factor oral solution |
| CN102453088A (en) * | 2010-10-22 | 2012-05-16 | 曹吉祥 | Anti-chicken infectious bursal disease specific transfer factor and preparation method thereof |
| CN105030827A (en) * | 2015-07-14 | 2015-11-11 | 天津瑞普生物技术股份有限公司 | Transfer factor and application thereof |
-
2008
- 2008-12-23 CN CN200810154336A patent/CN101759770A/en active Pending
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102453088A (en) * | 2010-10-22 | 2012-05-16 | 曹吉祥 | Anti-chicken infectious bursal disease specific transfer factor and preparation method thereof |
| CN102078329A (en) * | 2011-01-26 | 2011-06-01 | 天津农学院 | Method for preparing concentration-controllable broiler spleen transfer factor oral solution |
| CN102078329B (en) * | 2011-01-26 | 2012-12-12 | 天津农学院 | Method for preparing concentration-controllable broiler spleen transfer factor oral solution |
| CN105030827A (en) * | 2015-07-14 | 2015-11-11 | 天津瑞普生物技术股份有限公司 | Transfer factor and application thereof |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN101475626B (en) | Method for extracting transfer factor from pig spleen | |
| CN103585626B (en) | Preparation method for newcastle disease and infectious bursal disease bigeminal composite inactivated vaccine | |
| CN103479995A (en) | Preparation method of mycoplasma gallisepticum and mycoplasma synoviae bivalent inactivated vaccine | |
| CN103432158B (en) | A kind of polysaccharide compound preventing and treating diarrhea of pigs and purposes | |
| CN103550244B (en) | A kind of Chinese herbal medicine compound polysaccharide and application with collaboration enhancing body fluid and immunization of cell | |
| CN111500482B (en) | Clostridium perfringens type A strain of sheep, inactivated vaccine and vaccine preparation method | |
| CN115772550A (en) | Preparation method of straw mushroom polypeptide with antioxidant activity and liver protection effect | |
| CN101240313A (en) | Method for preparing collagen peptide | |
| CN101690811B (en) | Concentrated freeze-dried yolk antibody composite preparation for infectious bursal disease and preparation process thereof | |
| CN103160555A (en) | Culture medium, culture method and application of high-yield exotoxin of clostridium perfringens | |
| CN101690813B (en) | Concentrated freeze-dried yolk antibody composite preparation for Newcastle disease and preparation process thereof | |
| CN101759770A (en) | Method for extracting transfer factor from chicken spleen | |
| CN102167726A (en) | Method for separating and extracting active polypeptide and immune ribonucleic acid by utilizing blood and spleen of animal | |
| CN101757029A (en) | Method for extracting transfer factors from cattle spleen | |
| CN103191422A (en) | Triple oral vaccine for cultivating marine fishes as well as preparation method and use method thereof | |
| CN1454901A (en) | Gynaecological anti-infective specificity IgY and its combined preparation | |
| CN104888209A (en) | B-group epidemic neisseria meningitidis recombinant protein vaccine and preparing method thereof | |
| CN102716481A (en) | Immunoadjuvant of oral vaccine for tilapia and use thereof | |
| JP6648279B2 (en) | Immune enhancer, foot-and-mouth disease inactivated vaccine and method for producing the same | |
| CN102286408A (en) | Bacillus amyloliquefaciens WH3, and preparation method and application thereof | |
| CN109943507B (en) | Preparation method and application of veterinary A-type clostridium perfringens toxin | |
| Xu et al. | Preparation and determination of immunological activities of anti-HBV egg yolk extraction | |
| CN111926049A (en) | Soybean meal antibacterial peptide and preparation method and application thereof | |
| CN101492492A (en) | Transfer factor for dog, preparation method and application thereof | |
| CN105713855A (en) | Strains, application of strains, vaccine and preparation method of vaccine |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C02 | Deemed withdrawal of patent application after publication (patent law 2001) | ||
| WD01 | Invention patent application deemed withdrawn after publication |
Open date: 20100630 |