Classifications

• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61D—VETERINARY INSTRUMENTS, IMPLEMENTS, TOOLS, OR METHODS
  • A61D19/00—Instruments or methods for reproduction or fertilisation
  • A61D19/04—Instruments or methods for reproduction or fertilisation for embryo transplantation

Definitions

• the present invention relates to biological engineering, particularly to the application of bio-spectrum embryonic engineering.
• the fundamental researches and technical development on animal embryonic engineering have achieved great progress in recent years.
• the researches on embryonic engineering are moving quickly from the stage of laboratory test to practicalization and commercialization.
• the animal embryonic engineering mainly includes production of embryos in vitro, cryo-preservation of embryos and micro-manipulation of embryos, etc.
• the development of the technique for production of embryos in vitro can make full use of animal genetic resources, accelerate improvement of animal gene.
• the technique can overcome infertility of some rare animals and preserve resources of rare animals.
• the technique can also supply embryos for production of gene transfer in animals and embryos' sexing. However, the production efficiency and the qualities of embryos produced in vitro are lower. The rate of pregnancy is also lower by embryo transfer.
• Cryo-preservation of animal embryos is the key technique, which affect whether or not the technique of embryo transfer can be put into practical use.
• the animal embryos reservoir can be established to facilitate the transportation and exchange of animal breed resources internationally.
• the cryo-preservation There are two internationally acceptable methods of cryo-preserving embryos. One is the slow freezing method, the other is the cryo-preservation.
• the survival rate of frozen/thawed embryos produced in vitro is about 65%, and the pregnant rate of the frozen/thawed embryos is decreased 20% than the fresh embryos.
• Micro-manipulation of embryos consists of sexing of embryos, embryos'cloning including embryo bisection and nuclear transfer, and gene transfer.
• the aim of sexing of embryos is to produce defined sexual offspring. Cloning of embryos can produce many identical offspring from an outstanding animal embryo, improving the reproduction efficiency and speeding the animal breeding.
• Gene transfer animals can be produced by micro-injection and sperm mediated method. The aim of gene transfer technique is to speed up the growth rate and increase resistance to diseases of animals, improve quality of animal production, and therefore supply many valuable medicines for human beings. However, the efficiency of micro-manipulation is very low because the embryos will definitely be injured.
• the invention is based on the following understandings. Very few people have conducted research on the regulation of reproductive and growth abilities of animals with physical method, especially application of physical method to embryos' engineering for resolving technical problems
• the inventor recognized that all living matter has chemical and physical characteristics at the same time.
• the living matter has special physical characteristics such as electric charge in cells, etc.
• the interactions between the substances in living matter which have electric charges and the electromagnetic field in environment can be produced when electromagnetic field in environment and some main physical characteristics of living matter have the same characteristics. The interactions can influence the molecules, atoms and electrons at the same time to produce significant biologic effects. For example, tissues and cells can grow and develop normally in the chemical and physical environment of a living body.
• the growth and development of tissues and cells are decreased significantly when they are separated from the living body, although many kinds of chemical protecting materials and nutritive materials are used for improving the culture conditions.
• the inventor further recognized that the growth ability of tissues and cells in culture condition will be improved by applying a simulated bio-spectrum which is a weak electromagnetic field. So, it has significant meanings to apply the simulated bio-spectrum to embryos' engineering. The bio-spectrum will help improve the reproductive ability, growth speed and resistance to diseases of the animals.
• the object of the invention is to induce irradiation bio-effects by applying the bio-spectrum to animal embryos engineering and animals, which includes:
• the object of the present invention is realized by the following technical solutions.
• Thawed embryos deposited in a culture medium are irradiated with bio-spectrum generator for 3 20 minutes. During irradiation the medium temperature is not higher than 40 °C.
• embryos are deposited in a culture medium and are irradiated with bio-spectrum generator for 3-25 minutes. In order to get stronger effects, embryos are irradiated with bio-spectrum generator for 3-25 minutes before micro-manipulation. During irradiation the medium temperature is not higher that 40 °C.
• Animals are irradiated with bio-spectrum generator once or twice every day, for 30-60 minutes each time. During irradiation, the surface temperature of the animals is kept not higher than 45 °C. The results will be better when conventional techniques of animal reproduction, development and growth, are used together with the irradiation such as all kinds of gonadotrophin.
• Parts or whole bodies of animals are irradiated with bio-spectrum generator for 1-3 times every day, 6-60 minutes each time. During irradiation the temperature of the part irradiated is not higher than 45 °C.
• the survival rate of embryos after frozen/thawed increases by at least 16% and the pregnant rate of transferred embryos could be also significantly improved.
• the oocytes are collected from donor cows by ordinary methods, and than put in common medium or special medium for maturation. During maturation, oocytes are irradiated with bio-spectrum device (model WS-101D) for 15 minutes (at weak level). The temperature should be kept at 38-40 °C by adjusting the distance between embryo container and irradiation device.
• bio-spectrum device model WS-101D
• the special medium is made according to the procedure of Brackett et al.
• the receipt of the special medium is as follows: components g/l NaCl 6.55 KCl 0.30 CaCl 2 ⁇ 2H 2 O 0.33 NaH 2 PO 4 ⁇ H 2 O 0.11 MgCl 2 ⁇ 6H 2 O 0.11 NaHCO 3 3.10 Glucose 2.25 Bovine Serum Albumin 3.00 Sodium Pyruvate (or Pyruvate) 0.14(or 0.11) Na-Penicillin 0.031(50 IU/ml)
• the medium needs to be sterilized by filtration afier the components have dissolved completely in 1000 ml water. This medium is required to equilibrate in the incubator at 38 °C in 59% CO 2 in the air.
• the osmolality of this medium is about 300 mOsm/kg H 2 O.
• the special medium is made by addition of 84 mg NaHCO 3 to 100 ml so-prepared sulotion.
• the m-HIS is made by addition of 34 mg NaCl to 10 ml medium.
• the fresh semen is firstly treated following the procedure of Bracktt et al. Semen is pre-diluted with special medium (350g). After centrifugation, the sperm pellet is re-suspended with m-HIS medium and put in water bath of 38 °C for 15 minutes. After another centrifugation, the sperm pellet is re-suspended with special medium in a tube for irradiation with bio-spectrum device at weak level for 10 minutes. During irradiation, the temperature of medium should be kept at 38-40 °C by adjusting the distance between the tube and irradiation device
• the in-vitro matured oocytes and in-vitro capacitated sperm are put in the special medium in a tube for irradiation with bio-spectrum device for 20 minutes.
• the tube is put in CO 2 incubator for one hour culture at 38 °C.
• the tube is irradiated with bio-spectrum again for 18 minutes and again put in incubator for 5-hour culture.
• weak level is used and the temperature of medium is kept at 38-40 °C by adjusting the distance between the tube and irradiation device.
• the in-vitro fertilized eggs are put in the special medium for irradiation with BIO-SPECTRUM for 25 minutes. Weak level is used. During irradiation the temperature of medium is kept at 38-40 °C by adjusting the distance between the medium container and irradiation device.
• Bovine embryos are put in special medium for irradiation with bio-spectrum for 15 minutes.
• the weak level is used.
• the temperature of medium is kept at 38-40 °C by adjusting the distance between the medium container and irradiation device.
• the cryo-protectant is added following the procedure of the Japanese Journal of Animal Reproduction (28:150-153,1982).
• the embryos are transferred step by step in PBS plus 20% CS and 0.18,0.33,0.75,0.88,1.0M Glycerol, respectively, each step for 5 minutes.
• the embryos are put in freezing medium (PBS plus 20% CS and 1.0M Glycerol) for 30 minutes and then placed in 0.5 ml straw.
• the straws are cooled in a freezer to -7 °C at a speed of 1 °C /min., then artificially seeded, slowly cooled at -0.3 °C/min. to -35 °C and cooled at -0.1 °C/min. to -36 °C, then plunged into liquid nitrogen (-196 °C) and stored.
• Embryo thawing the straws are took out from nitrogen and inserted into 21 °C water bath, slightly shaken until the ice is melted. The speed of thawing is 360 °C/min. After thawing the cryo-protectant is removed by holding embryos each step in reverse of adding cryo-protectant. Then embryos are placed in the special medium for irradiation with bio-spectrum for 20 minutes. Weak level is used. During irradiation the temperature of medium is kept at 38-40 °C by adjusting the distance between the medium container and the irradiation device.
• the 0.25 ml straw is used to take in 100 ⁇ l S-PBS medium, 20 ⁇ l air, 6 ⁇ l EFS medium, 6 ⁇ l air, 40 ⁇ l EFS medium with embryos after 3 minutes equilibration in EFS medium at the room temperature, 6 ⁇ l air, 6 ⁇ l EFS medium, 15 ⁇ l air and 20 ⁇ l S-PBS medium in turn. Then the end of straws is sealed using hot forceps.
• the straws are took out from nitrogen and inserted into 20 °C water bath, slightly shaken until the ice melted. Then embryos are quickly flushed out from straws with 0.5ml S-PBS medium, then transferred to S-PBS medium, 5 minutes later, embryos are transferred to m-PBS medium. After washing three times in the special medium, the embryos are irradiated with BIO-SPECTRUM for 10 minutes. Weak level is used. The temperature of medium is kept at 38-40 °C by adjusting the distance between the medium container and the irradiation device.
• S-PBS medium The receipt of S-PBS medium is as follows: Components g/l NaCl 8 KCl 0.2 NaH 2 PO 4 1.15 KH 2 PO 4 0.2 CaCl 2 0.1 MgCl ⁇ 6H 2 O 0.1 Sodium pyruvate 0.036 Glucose 1 Penicillin 100IU/ml Streptomycin 0.05 g/l Glycerol 0.5M
• EPS medium is 0.5M sucrose solution (EF medium) which contains 30% polysucrose.
• EFS medium is made by mixture of ethylene (40%) and EF medium (60%).
• Embryo splitting The rat, goat and bovine embryo Is split by metal knife following the procedure of matsu Moto Katsu Ya et al. (Japanese Journal of Animal Reproduction).
• the micro-surgical blade made from razor is fixed with a micro-manipulator.
• the embryos are put in the culture medium for irradiation with bio-spectrum for 15 minutes. After irradiation, the embryos are held in a droplet of 0.5ml PBS plus 20% FCS on the center of the plastic dish (diameter 8cm, height 1 cm).
• the micro-surgical bisection is performed using a micro-manipulation unit consisting of an inverted microscope.
• hemi-embryos are put in the culture medium for irradiation with BIO-SPECTRUM for 30 minutes. Weak level is used. During irradiation the temperature of medium is kept at 38-40 °C by adjusting the distance between the medium container and the irradiation device.
• Sex Identification The sex of the embryo can be accurately determined through sampling several cells from the embryo. After sampling, the embryo is partly damaged, and the viability decreases. The viability of the embryo can be raised with the treatment of bio-spectrum for 20 minutes (Model WS-101D).
• mice are used as experimental animals. Female mice are randomly divided into 2 groups, A and B, 20 in each group. Group A is irradiated with bio-spectrum, group B is used as control group without irradiation of bio-spectrum. Both group A and group B are under the same experimental conditions, each treatment had 2 replicates, 10 mice per replicate.
• the mice in group A are irradiated with bio-spectrum for 20 minutes once a day at fixed time, the model of bio-spectrum machine is WS-101, made by Zhoulin Bio-Spectrum Company, high level is used. The temperature over the mouse back is controlled under 38 °C, the mice are irradiated for 10 times in 10 days.
• WS-101 Bio-Spectrum Health Care Device made in Beijing Zhoulin-Bio-Spectrum Company is used for irradiating the abdomen of lambs with diarrhea once a day, 20 minutes each time. Totally for 2-4 days, while high level is used and the surface temperature of the part being irradiated is not more than 45 °C, the diarrhea could be controlled and the results are obvious.
• bio-spectrum would apply to many objects in bio-engineering besides the above examples according to main aspects of the invention. It could not only solve many buffing problems in areas of both embryonic engineering and bio-engineering, but also simplify the complex and difficult techniques in the areas. So there will be other embodiments in the area of bio-engineering and these embodiments will fall into the protection scope of this invention.

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• Health & Medical Sciences (AREA)
• Life Sciences & Earth Sciences (AREA)
• Veterinary Medicine (AREA)
• Wood Science & Technology (AREA)
• Engineering & Computer Science (AREA)
• Reproductive Health (AREA)
• Transplantation (AREA)
• Zoology (AREA)
• Animal Behavior & Ethology (AREA)
• General Health & Medical Sciences (AREA)
• Public Health (AREA)
• Micro-Organisms Or Cultivation Processes Thereof (AREA)
• Agricultural Chemicals And Associated Chemicals (AREA)
• Medicines Containing Material From Animals Or Micro-Organisms (AREA)

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• 1994
  • 1994-11-24 CN CN 94118306 patent/CN1068195C/zh not_active Expired - Lifetime
• 1995
  • 1995-11-02 DE DE69528295T patent/DE69528295T2/de not_active Expired - Lifetime
  • 1995-11-02 CA CA002207013A patent/CA2207013C/en not_active Expired - Lifetime
  • 1995-11-02 WO PCT/CN1995/000087 patent/WO1996015732A1/zh active IP Right Grant
  • 1995-11-02 AU AU38386/95A patent/AU704690B2/en not_active Expired
  • 1995-11-02 EP EP95936416A patent/EP0872219B1/de not_active Expired - Lifetime

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