USH2119H1 - Acoustic fusion of aquatic animal tissue cells with biological agents - Google Patents
Acoustic fusion of aquatic animal tissue cells with biological agents Download PDFInfo
- Publication number
- USH2119H1 USH2119H1 US08/971,839 US97183997A USH2119H US H2119 H1 USH2119 H1 US H2119H1 US 97183997 A US97183997 A US 97183997A US H2119 H USH2119 H US H2119H
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- United States
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- treatment zone
- water
- tissue cells
- acoustic field
- biological agent
- Prior art date
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- Abandoned
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- 239000003124 biologic agent Substances 0.000 title claims abstract description 14
- 241001465754 Metazoa Species 0.000 title claims description 10
- 230000004927 fusion Effects 0.000 title description 5
- 238000011282 treatment Methods 0.000 claims abstract description 49
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 19
- 238000001802 infusion Methods 0.000 claims abstract description 13
- 238000000034 method Methods 0.000 claims description 19
- 150000001875 compounds Chemical class 0.000 claims description 13
- 241000251468 Actinopterygii Species 0.000 claims description 7
- 238000010521 absorption reaction Methods 0.000 claims description 6
- 230000001105 regulatory effect Effects 0.000 claims description 5
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 4
- DEGAKNSWVGKMLS-UHFFFAOYSA-N calcein Chemical compound O1C(=O)C2=CC=CC=C2C21C1=CC(CN(CC(O)=O)CC(O)=O)=C(O)C=C1OC1=C2C=C(CN(CC(O)=O)CC(=O)O)C(O)=C1 DEGAKNSWVGKMLS-UHFFFAOYSA-N 0.000 claims description 4
- 235000013601 eggs Nutrition 0.000 claims description 4
- 229960002378 oftasceine Drugs 0.000 claims description 4
- IWVCMVBTMGNXQD-UHFFFAOYSA-N terramycin dehydrate Natural products C1=CC=C2C(O)(C)C3C(O)C4C(N(C)C)C(O)=C(C(N)=O)C(=O)C4(O)C(O)=C3C(=O)C2=C1O IWVCMVBTMGNXQD-UHFFFAOYSA-N 0.000 claims description 4
- 238000012546 transfer Methods 0.000 claims description 2
- 230000001276 controlling effect Effects 0.000 claims 2
- 238000001816 cooling Methods 0.000 claims 1
- 230000001939 inductive effect Effects 0.000 claims 1
- 238000012423 maintenance Methods 0.000 claims 1
- 230000009466 transformation Effects 0.000 claims 1
- 238000012545 processing Methods 0.000 abstract description 4
- 210000001519 tissue Anatomy 0.000 description 13
- 239000003795 chemical substances by application Substances 0.000 description 4
- 238000002604 ultrasonography Methods 0.000 description 4
- 238000010586 diagram Methods 0.000 description 3
- 239000013535 sea water Substances 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- 241000277275 Oncorhynchus mykiss Species 0.000 description 2
- 238000004520 electroporation Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- XIAYFENBYCWHGY-UHFFFAOYSA-N 2-[2,7-bis[[bis(carboxymethyl)amino]methyl]-3-hydroxy-6-oxoxanthen-9-yl]benzoic acid Chemical compound C=12C=C(CN(CC(O)=O)CC(O)=O)C(=O)C=C2OC=2C=C(O)C(CN(CC(O)=O)CC(=O)O)=CC=2C=1C1=CC=CC=C1C(O)=O XIAYFENBYCWHGY-UHFFFAOYSA-N 0.000 description 1
- 241000894006 Bacteria Species 0.000 description 1
- KIPLYOUQVMMOHB-MXWBXKMOSA-L [Ca++].CN(C)[C@H]1[C@@H]2[C@@H](O)[C@H]3C(=C([O-])[C@]2(O)C(=O)C(C(N)=O)=C1O)C(=O)c1c(O)cccc1[C@@]3(C)O.CN(C)[C@H]1[C@@H]2[C@@H](O)[C@H]3C(=C([O-])[C@]2(O)C(=O)C(C(N)=O)=C1O)C(=O)c1c(O)cccc1[C@@]3(C)O Chemical compound [Ca++].CN(C)[C@H]1[C@@H]2[C@@H](O)[C@H]3C(=C([O-])[C@]2(O)C(=O)C(C(N)=O)=C1O)C(=O)c1c(O)cccc1[C@@]3(C)O.CN(C)[C@H]1[C@@H]2[C@@H](O)[C@H]3C(=C([O-])[C@]2(O)C(=O)C(C(N)=O)=C1O)C(=O)c1c(O)cccc1[C@@]3(C)O KIPLYOUQVMMOHB-MXWBXKMOSA-L 0.000 description 1
- 230000003321 amplification Effects 0.000 description 1
- 239000012620 biological material Substances 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 239000013043 chemical agent Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000002826 coolant Substances 0.000 description 1
- 230000005684 electric field Effects 0.000 description 1
- HFGPZNIAWCZYJU-UHFFFAOYSA-N lead zirconate titanate Chemical compound [O-2].[O-2].[O-2].[O-2].[O-2].[Ti+4].[Zr+4].[Pb+2] HFGPZNIAWCZYJU-UHFFFAOYSA-N 0.000 description 1
- 210000004379 membrane Anatomy 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 230000001617 migratory effect Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 210000004400 mucous membrane Anatomy 0.000 description 1
- 238000003199 nucleic acid amplification method Methods 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000011253 protective coating Substances 0.000 description 1
- 229940063650 terramycin Drugs 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N13/00—Treatment of microorganisms or enzymes with electrical or wave energy, e.g. magnetism, sonic waves
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
- C12N15/09—Recombinant DNA-technology
- C12N15/63—Introduction of foreign genetic material using vectors; Vectors; Use of hosts therefor; Regulation of expression
- C12N15/79—Vectors or expression systems specially adapted for eukaryotic hosts
- C12N15/85—Vectors or expression systems specially adapted for eukaryotic hosts for animal cells
- C12N15/8509—Vectors or expression systems specially adapted for eukaryotic hosts for animal cells for producing genetically modified animals, e.g. transgenic
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
- C12N15/09—Recombinant DNA-technology
- C12N15/87—Introduction of foreign genetic material using processes not otherwise provided for, e.g. co-transformation
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01K—ANIMAL HUSBANDRY; AVICULTURE; APICULTURE; PISCICULTURE; FISHING; REARING OR BREEDING ANIMALS, NOT OTHERWISE PROVIDED FOR; NEW BREEDS OF ANIMALS
- A01K2217/00—Genetically modified animals
- A01K2217/05—Animals comprising random inserted nucleic acids (transgenic)
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01K—ANIMAL HUSBANDRY; AVICULTURE; APICULTURE; PISCICULTURE; FISHING; REARING OR BREEDING ANIMALS, NOT OTHERWISE PROVIDED FOR; NEW BREEDS OF ANIMALS
- A01K2227/00—Animals characterised by species
- A01K2227/40—Fish
Definitions
- the present invention relates in general to the perforation of living cells during delivery thereto of biological agents for various purposes including tagging and DNA infusion.
- a process for transfer of chemical agents within some surrounding medium through living tissue referred to as poration is well known in the art as disclosed for example in U.S. Pat. No. 5,128,257 to Baer.
- Such process involves generation of electrical energy forming an electrical field between electrodes within which electroporation occurs.
- the generation of an ultra-sound acoustic field within which different chemical compounds are administered by delivery to the tissue cells of aquatic animals or their eggs for fish farm treatment purposes is disclosed in U.S. Pat. No. 5,076,208 to Zohar et al.
- large numbers of aquatic animals are serviced by poration and fusion of their tissue cells with certain biological compounds transferred from solution within an underwater treatment zone.
- the poration and infusion process is performed within the treatment zone under an acoustic energy field of limited duration produced by amplification of a steady state electrical power signal converted into ultrasound waves within a cavitation frequency range establishing the acoustic field within the treatment zone.
- the tissue cells after being so treated are extracted from the treatment zone.
- FIG. 1 is a block diagram schematically illustrating the process or method of the present invention
- FIG. 2 is a partial section view and block diagram illustrating transducer conversion apparatus associated with the method depicted in FIG. 1 ;
- FIG. 3 is a graphical illustration of processing parameters from which maximized treatment duration is obtained.
- FIG. 1 diagrams the aquatic animal treatment method of the present invention, generally referred to by reference numeral 10 .
- the tissue cells 12 of aquatic animals to be treated such as migratory fish including rainbow trout as denoted in FIG. 1
- a biological agent 14 by insonification which includes perforation and fusion performed within an underwater zone 16 during periods of limited duration so as to accommodate treatment of large populations of the aquatic animals.
- the agent 14 is of a commonly used type from a group of tagging compounds including calcein (Fluorexine) and oxytetracyline hydrochloride (Terramycin) forming a solution with the water in the treatment zone 16 from which it is transferred to tissue cells such as the larvae and/or eggs of the fish being tagged. After completion of such treatment the tissue cells are removed from the treatment zone 16 and may undergo further processing such as washing so as to extract unfused agents from the treated tissues 20 .
- calcein Fruorexine
- oxytetracyline hydrochloride Teerramycin
- treatment within zone 16 is performed in response to establishment of an acoustic field therein by generation 22 of acoustic waves as denoted in FIG. 1 and under certain conditions established by water flow rate and temperature by controls 24 for inflow and temperature and controlled outflow 26 from the treatment zone 16 .
- Timing of treatments within zone 16 are regulated by treatment duration control 28 applied to acoustic field energy generation 22 and controls 24 as also denoted in FIG. 1 .
- treatment efficiency pursuant to the present invention is maximized by so limiting the treatment duration.
- the parameters of method 10 associated with the generation 22 of acoustic field waves for performance of the treatment were obtained in connection with the use of apparatus as depicted in FIG. 2 showing treatment zone 16 enclosed by a cylindrical shaped transducer 30 within which water is confined.
- Such transducer 30 is of a piezoelectric type made of materials such as lead zirconium titanate ceramic (PZT), covered by a water protective coating 32 .
- PZT lead zirconium titanate ceramic
- Such transducer 30 converts electrical energy supplied thereto into ultrasound energy in the form of acoustic waves 34 as symbolically denoted in FIG. 2 , establishing the acoustic field within the water treatment zone 16 .
- the electrical energy was converted by the transducer 30 into a steady state AC signal of approximately 40 kHz within a cavitation frequency range derived from a signal generator 36 and amplified to a voltage level of approximately 200 volts by a power amplifier 38 as denoted in FIG. 2 .
- Such AC signal may be either continuous or pulsed having a selected duty cycle.
- test tube 40 onto which the acoustic waves 34 are focussed as shown in FIG. 2 , mixed with a body of seawater 39 having agent 14 dissolved therein.
- Such treatment was maximized by passage of a continuous flow of water from a coolant supply 42 to maintain the body of seawater 39 chilled to a predetermined constant temperature of 10° C., while air was injected into the seawater within the test tube by flow from air supply 44 forming bubbles therein during a limited treatment duration between 5 and 30 minutes.
- the test tube 40 was made of an acoustically transparent plastic material so as to accommodate exposure of its contents to the acoustic field generated during experimental treatment within zone 16 as hereinbefore described.
- Curved 52 in FIG. 3 depicts the variation in absorption by infusion of a tagging compound type of agent 14 into fish tissue cells as denoted on the vertical scale 46 for different concentrations of such tagging compound (calcein) as denoted on horizontal scale 48 during a 5 minute treatment duration.
- Such graphically depicted treatment reached maximized absorption at a peak point 50 on curve 52 , for the same concentration of the tagging compound corresponding to a maximized absorption peak 54 on curve 56 for a 30 minute treatment duration. Accordingly, treatment is maximized by limiting its duration between 5 and 30 minutes under the conditions of flow, temperature and acoustic field energy within the treatment zone 16 as hereinbefore specified.
- the transducer 30 may be replaced by a flat or curved plate type of transducer with which an unconfined body of water has the acoustic field disposed therein in contact with the transducer. Also, frequencies other than 40 kHz for the electrical energy converted to ultrasound energy by the transducer may be utilized, as long as it is within the cavitation frequency range.
- the fusion treatment was performed under the conditions described herein at a relatively high delivery rate causing detachment of the mucous membrane of the fish larvae. Such membrane is expected to grow back on the fish being tagged if maintained in a clean environment by washing for an adequate period of time following fusion treatment. Treatment for purposes other than tagging, such as DNA infusion, may be achieved by the present invention because of its capability for penetration of single living cells under the conditions described herein.
- the method of the present invention is therefore applicable to single cell organisms such as bacteria as well as plant cells.
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- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Zoology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Wood Science & Technology (AREA)
- Biotechnology (AREA)
- General Engineering & Computer Science (AREA)
- Biomedical Technology (AREA)
- Microbiology (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- Physics & Mathematics (AREA)
- Biophysics (AREA)
- Molecular Biology (AREA)
- Plant Pathology (AREA)
- Veterinary Medicine (AREA)
- Surgical Instruments (AREA)
- Farming Of Fish And Shellfish (AREA)
Abstract
Biological agents in solution within an underwater treatment zone are transferred by infusion to living cells under an acoustic energy field of limited duration and certain accompanying water flow and temperature conditions to maximize processing efficiency.
Description
The present invention relates in general to the perforation of living cells during delivery thereto of biological agents for various purposes including tagging and DNA infusion.
A process for transfer of chemical agents within some surrounding medium through living tissue referred to as poration, is well known in the art as disclosed for example in U.S. Pat. No. 5,128,257 to Baer. Generally, such process involves generation of electrical energy forming an electrical field between electrodes within which electroporation occurs. The generation of an ultra-sound acoustic field within which different chemical compounds are administered by delivery to the tissue cells of aquatic animals or their eggs for fish farm treatment purposes, is disclosed in U.S. Pat. No. 5,076,208 to Zohar et al. However, infusion of animal tissue cells with biological agents such as tagging compounds was heretofore performed by electroporation subject to various disadvantages such as tissue cell disruption by high voltage and reduced processing efficiency because of limits imposed on the number of tissue cells capable of being simultaneously processed. It is therefore an important object of the present invention to provide an improved process for infusion of biological material into living tissue cells of relatively large aquatic animal populations within underwater environments with improved efficiency.
In accordance with the present invention, large numbers of aquatic animals are serviced by poration and fusion of their tissue cells with certain biological compounds transferred from solution within an underwater treatment zone. The poration and infusion process is performed within the treatment zone under an acoustic energy field of limited duration produced by amplification of a steady state electrical power signal converted into ultrasound waves within a cavitation frequency range establishing the acoustic field within the treatment zone. The tissue cells after being so treated are extracted from the treatment zone.
A more complete appreciation of the invention and many of its attendant advantages will be readily appreciated as the same becomes better understood by reference to the following detailed description when considered in connection with the accompanying drawing wherein:
Referring now to the drawing in detail, FIG. 1 diagrams the aquatic animal treatment method of the present invention, generally referred to by reference numeral 10. Pursuant to such method, the tissue cells 12 of aquatic animals to be treated such as migratory fish including rainbow trout as denoted in FIG. 1 , are to be fused with a biological agent 14 by insonification which includes perforation and fusion performed within an underwater zone 16 during periods of limited duration so as to accommodate treatment of large populations of the aquatic animals. The agent 14 according to one embodiment is of a commonly used type from a group of tagging compounds including calcein (Fluorexine) and oxytetracyline hydrochloride (Terramycin) forming a solution with the water in the treatment zone 16 from which it is transferred to tissue cells such as the larvae and/or eggs of the fish being tagged. After completion of such treatment the tissue cells are removed from the treatment zone 16 and may undergo further processing such as washing so as to extract unfused agents from the treated tissues 20.
The foregoing referred to treatment within zone 16 is performed in response to establishment of an acoustic field therein by generation 22 of acoustic waves as denoted in FIG. 1 and under certain conditions established by water flow rate and temperature by controls 24 for inflow and temperature and controlled outflow 26 from the treatment zone 16. Timing of treatments within zone 16 are regulated by treatment duration control 28 applied to acoustic field energy generation 22 and controls 24 as also denoted in FIG. 1. As hereinafter indicated, treatment efficiency pursuant to the present invention is maximized by so limiting the treatment duration.
The parameters of method 10 associated with the generation 22 of acoustic field waves for performance of the treatment, were obtained in connection with the use of apparatus as depicted in FIG. 2 showing treatment zone 16 enclosed by a cylindrical shaped transducer 30 within which water is confined. Such transducer 30 is of a piezoelectric type made of materials such as lead zirconium titanate ceramic (PZT), covered by a water protective coating 32. Such transducer 30 converts electrical energy supplied thereto into ultrasound energy in the form of acoustic waves 34 as symbolically denoted in FIG. 2 , establishing the acoustic field within the water treatment zone 16. The electrical energy was converted by the transducer 30 into a steady state AC signal of approximately 40 kHz within a cavitation frequency range derived from a signal generator 36 and amplified to a voltage level of approximately 200 volts by a power amplifier 38 as denoted in FIG. 2. Such AC signal may be either continuous or pulsed having a selected duty cycle.
Fish eggs and/or larvae obtained from rainbow trout were exposed during experimental treatment to the foregoing described acoustic field within zone 16 by placement into a test tube 40, onto which the acoustic waves 34 are focussed as shown in FIG. 2 , mixed with a body of seawater 39 having agent 14 dissolved therein. Such treatment was maximized by passage of a continuous flow of water from a coolant supply 42 to maintain the body of seawater 39 chilled to a predetermined constant temperature of 10° C., while air was injected into the seawater within the test tube by flow from air supply 44 forming bubbles therein during a limited treatment duration between 5 and 30 minutes. The test tube 40 was made of an acoustically transparent plastic material so as to accommodate exposure of its contents to the acoustic field generated during experimental treatment within zone 16 as hereinbefore described.
From the foregoing referred to experimentation, various parameters of the method 10 were determined as graphically diagrammed in FIG. 3. Curved 52 in FIG. 3 depicts the variation in absorption by infusion of a tagging compound type of agent 14 into fish tissue cells as denoted on the vertical scale 46 for different concentrations of such tagging compound (calcein) as denoted on horizontal scale 48 during a 5 minute treatment duration. Such graphically depicted treatment reached maximized absorption at a peak point 50 on curve 52, for the same concentration of the tagging compound corresponding to a maximized absorption peak 54 on curve 56 for a 30 minute treatment duration. Accordingly, treatment is maximized by limiting its duration between 5 and 30 minutes under the conditions of flow, temperature and acoustic field energy within the treatment zone 16 as hereinbefore specified.
It should be understood that the transducer 30 may be replaced by a flat or curved plate type of transducer with which an unconfined body of water has the acoustic field disposed therein in contact with the transducer. Also, frequencies other than 40 kHz for the electrical energy converted to ultrasound energy by the transducer may be utilized, as long as it is within the cavitation frequency range. The fusion treatment was performed under the conditions described herein at a relatively high delivery rate causing detachment of the mucous membrane of the fish larvae. Such membrane is expected to grow back on the fish being tagged if maintained in a clean environment by washing for an adequate period of time following fusion treatment. Treatment for purposes other than tagging, such as DNA infusion, may be achieved by the present invention because of its capability for penetration of single living cells under the conditions described herein. The method of the present invention is therefore applicable to single cell organisms such as bacteria as well as plant cells.
Obviously, other modifications and variations of the present invention may be possible in light of the foregoing teachings. It is therefore to be understood that within the scope of the appended claims the invention may be practiced otherwise than as specifically described.
Claims (12)
1. A method of treating aquatic animals by infusion of tissue cells thereof with a biological agent dissolved within a body of water in a treatment zone within which said infusion is performed, the improvement residing in the steps of: establishing an acoustic field of limited duration within said treatment zone during which said biological agent is transferred to the tissue cells; and regulating conditions of the body of water within the treatment zone to establish a constant temperature therein during said limited duration of the acoustic field under which said infusion occurs for absorption of the biological agent into the tissue cells.
2. The improvement as defined in claim 1 wherein said step of establishing an acoustic field comprises the steps of: generating steady state electrical signal energy having a frequency within a cavitation range; amplifying the steady state electrical signal energy to an operative voltage level and converting said amplified electrical signal energy into acoustical energy for producing said acoustic field within the treatment zone.
3. The improvement as defined in claim 2 wherein said biological agent is selected from a group of tagging compounds consisting of calcein and oxytetracyline hydrochloride.
4. The improvement as defined in claim 3 wherein said limited duration of the acoustic field is between 5 and 30 minutes during which said absorption of the biological agent in the tissue cells is maximized.
5. The method as defined in claim 4 wherein tissue cells consist of eggs and larvae of fish as the aquatic animals.
6. The improvement as defined in claim 1 wherein said step of regulating conditions of the body of water within the treatment zone includes: controlling flow rate of the water through said treatment zone; and cooling the body of water within the treatment zone for maintenance thereof at said constant temperature.
7. The improvement as defined in claim 1 wherein said biological agent is selected from a group including tagging and DNA transformation compounds.
8. A method applied to living cells for infusion with a biological agent within a water solution in an underwater treatment zone, comprising the steps of: generating steady state electrical signal energy within a cavitation frequency range amplified to a predetermined voltage level; converting said amplified electrical signal energy into acoustical energy for establishment of an acoustic field focussed on the living cells within said underwater treatment zone and regulating conditions within the treatment zone during said establishment of the acoustic field therein for transfer of the biological agent from the water solution to the living cells by controlling flow of water through said underwater treatment zone; and maintaining the water within said treatment zone at a constant temperature during said establishing of the acoustic field for a period of limited duration.
9. The method as defined in claim 8 wherein said constant temperature is 10° C. and said period of limited duration is between 5 and 30 minutes.
10. The method as defined in claim 9 wherein said biological agent is selected from a group of tagging compounds consisting of calcein and oxytetracyline hydrochloride.
11. The method as defined in claim 10 wherein said electrical signal energy has a frequency of approximately 40 kHz and said predetermined voltage level of the amplified signal energy is approximately 200 volts.
12. A method for treatment of living tissue cells by infusion of a tagging compound selected from the group consisting of calcein and oxytetracyline hydrochloride into the tissue cells from a body of water within which the tagging compound is dissolved, the improvement residing in the steps of: establishing an acoustic field within said treatment zone during a period of limited duration of 5 to 30 minutes; and inducing flow of said body of water through the treatment zone during said period of limited duration at a flow rate regulated to maintain a constant temperature of 10° C. within the treatment zone under which said infusion occurs to maximize absorption of the tagging compound within the living tissue cells.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
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US08/971,839 USH2119H1 (en) | 1997-11-17 | 1997-11-17 | Acoustic fusion of aquatic animal tissue cells with biological agents |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
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US08/971,839 USH2119H1 (en) | 1997-11-17 | 1997-11-17 | Acoustic fusion of aquatic animal tissue cells with biological agents |
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USH2119H1 true USH2119H1 (en) | 2005-06-07 |
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US08/971,839 Abandoned USH2119H1 (en) | 1997-11-17 | 1997-11-17 | Acoustic fusion of aquatic animal tissue cells with biological agents |
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Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20060036196A1 (en) * | 2004-03-16 | 2006-02-16 | Wolfgang Schaden | Method of shockwave treating fish and shellfish |
EP3756473A1 (en) * | 2019-06-25 | 2020-12-30 | Centro De Ciências Do Mar Do Algarve | System and process of modulating nutritional supplementation in fish for improving growth rate by using low-frequency ultrasounds |
CN114403064A (en) * | 2022-03-09 | 2022-04-29 | 中国水产科学研究院黄海水产研究所 | Shell OTC marking method suitable for shellfish living bodies |
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1997
- 1997-11-17 US US08/971,839 patent/USH2119H1/en not_active Abandoned
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Cited By (4)
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US20060036196A1 (en) * | 2004-03-16 | 2006-02-16 | Wolfgang Schaden | Method of shockwave treating fish and shellfish |
US7578796B2 (en) * | 2004-10-22 | 2009-08-25 | General Patent Llc | Method of shockwave treating fish and shellfish |
EP3756473A1 (en) * | 2019-06-25 | 2020-12-30 | Centro De Ciências Do Mar Do Algarve | System and process of modulating nutritional supplementation in fish for improving growth rate by using low-frequency ultrasounds |
CN114403064A (en) * | 2022-03-09 | 2022-04-29 | 中国水产科学研究院黄海水产研究所 | Shell OTC marking method suitable for shellfish living bodies |
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