EP0872219B1 - Use of the bio-frequency spectrum in animal embryo-engineering - Google Patents
Use of the bio-frequency spectrum in animal embryo-engineering Download PDFInfo
- Publication number
- EP0872219B1 EP0872219B1 EP95936416A EP95936416A EP0872219B1 EP 0872219 B1 EP0872219 B1 EP 0872219B1 EP 95936416 A EP95936416 A EP 95936416A EP 95936416 A EP95936416 A EP 95936416A EP 0872219 B1 EP0872219 B1 EP 0872219B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- bio
- medium
- embryos
- vitro
- spectrum
- 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.)
- Expired - Lifetime
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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 non-human embryonic engineering.
- embryonic engineering as used in the following description relates to non-human animal embryos only.
- 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 microinjection 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.
- SU-A-1724204 discloses the use of infra-red laser radiation having a particular wavelength during the processing of animal reproduction sperm ;
- SU-A-731 976 discloses a method for improving fertility of lab rodents by subjecting the females to the irradiation of cm band ;
- SU-A-1757676 discloses a method of irradiating the chicken embryos with He-Ne laser having a particular wavelength of 632.8 nm ;
- SU-A-1152583 discloses a method of treatment using pure magnetic field ;
- SU-A-1 402 343 discloses an animal sperm treatment using pure magnetic field and
- US 493 0505 discloses a therapeutic method using a laser having a particular wavelength.
- 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.
- 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 after 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 NaCI 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.
Landscapes
- 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)
Description
components | g/l |
NaCl | 6.55 |
KCl | 0.30 |
CaCl2 · 2H2O | 0.33 |
NaH2PO4 · H2O | 0.11 |
MgCl2 · 6H2O | 0.11 |
NaHCO3 | 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) |
Claims (2)
- A method of applying biofrequency spectrum irradiation to non-human animal embryonic engineering, said bio-frequency spectrum having wavelength ranging from 0.2 µm to 10 cm, said non-human animal embryonic engineering including :(1) in vitro maturation of collected oocytes ;(2) capacitation of spermatozoa ;(3) in vitro culture of embryos
during in vitro fertilization, both oocytes and spermatozoa capacited in vitro are co-cultured in a test tube containing a standard or defined medium and irradiated with bio spectrum generator for 1 to 3 times, from 3 to 25 minutes each time ; the medium temperature during irradiation being not higher than 40°C ;"
during in vitro culture of embryos, potential zygotes are transferred into a standard or defined medium and irradiated with bio-spectrum generator for 3 to 20 minutes ; the medium temperature in this period being not higher than 40°C. - A method according to claim 1, wherein the components of said defined medium are NaCI 6.55 g/l, KCI 0.30 g/l, CaCl2.2H2O 0.33 g/l, NaH2PO4 H2O 0.11 g/l, MgCl2.6H2O 0.11 g/l, NaHCO3 3.10 g/l, glucose 2.5 g/l, sodium pyruvate 0.14 g/l (pyruvate 0.11 g/l), bovine serum albumin 3.00 g/l, sodium salt penicillin 0.031 g/l (50 IU/ml) and 84 mg NaHCO3 is added to 100 ml of said defined medium.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN94118306 | 1994-11-24 | ||
CN 94118306 CN1068195C (en) | 1994-11-24 | 1994-11-24 | Application of biological spectrum in animal embryo engineering and animal |
PCT/CN1995/000087 WO1996015732A1 (en) | 1994-11-24 | 1995-11-02 | Use of the bio-frequency spectrum in animal embryo-engineering |
Publications (3)
Publication Number | Publication Date |
---|---|
EP0872219A1 EP0872219A1 (en) | 1998-10-21 |
EP0872219A4 EP0872219A4 (en) | 1999-02-03 |
EP0872219B1 true EP0872219B1 (en) | 2002-09-18 |
Family
ID=5038758
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP95936416A Expired - Lifetime EP0872219B1 (en) | 1994-11-24 | 1995-11-02 | Use of the bio-frequency spectrum in animal embryo-engineering |
Country Status (6)
Country | Link |
---|---|
EP (1) | EP0872219B1 (en) |
CN (1) | CN1068195C (en) |
AU (1) | AU704690B2 (en) |
CA (1) | CA2207013C (en) |
DE (1) | DE69528295T2 (en) |
WO (1) | WO1996015732A1 (en) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
IL137366A0 (en) * | 2000-07-18 | 2001-07-24 | Shladot Metal Works Ltd | A method for increasing the fertilizing capability of sperm cells |
KR100516881B1 (en) * | 2002-12-13 | 2005-09-27 | (주)아비코아생명공학연구소 | Method for Inactivating Nuclear Chromosomal Materials of Recipient Oocyte for Manufacturing Clone Embryo from Somatic Cell Using X-ray Irradiation |
CN102250832B (en) * | 2011-05-30 | 2012-08-15 | 中国农业大学 | Culture liquid for promoting ectogenesis of frozen embryo after thawing |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
SU731976A1 (en) * | 1975-04-18 | 1980-05-05 | Ленинградский Научно-Исследовательский Институт Радиационной Гигиены | Method for improving fertility of small rodents |
SU1152583A1 (en) * | 1982-03-01 | 1985-04-30 | Кубанский Ордена Трудового Красного Знамени Сельскохозяйственный Институт | Method of insemination of sow |
EP0263192A1 (en) * | 1986-10-03 | 1988-04-13 | HENKEL CORPORATION (a Delaware corp.) | Dicyanoethenyl fatty compounds and derivatives thereof |
SU1402343A1 (en) * | 1985-06-04 | 1988-06-15 | Кубанский сельскохозяйственный институт | Method and apparatus for treatment of sperm of animals |
SU1724204A1 (en) * | 1989-10-09 | 1992-04-07 | Гродненский государственный медицинский институт | Method of boar sperm treatment |
SU1757676A1 (en) * | 1989-11-27 | 1992-08-30 | Горский Сельскохозяйственный Институт | Method for stimulation of specific immunity induction in hens to newcastle disease |
-
1994
- 1994-11-24 CN CN 94118306 patent/CN1068195C/en not_active Expired - Lifetime
-
1995
- 1995-11-02 DE DE69528295T patent/DE69528295T2/en 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/en active IP Right Grant
- 1995-11-02 AU AU38386/95A patent/AU704690B2/en not_active Expired
- 1995-11-02 EP EP95936416A patent/EP0872219B1/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
AU704690B2 (en) | 1999-04-29 |
CA2207013A1 (en) | 1996-05-30 |
EP0872219A1 (en) | 1998-10-21 |
EP0872219A4 (en) | 1999-02-03 |
WO1996015732A1 (en) | 1996-05-30 |
CN1068195C (en) | 2001-07-11 |
AU3838695A (en) | 1996-06-17 |
CA2207013C (en) | 2006-07-11 |
DE69528295D1 (en) | 2002-10-24 |
CN1123131A (en) | 1996-05-29 |
DE69528295T2 (en) | 2003-05-08 |
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