NZ277896A - Anaesthetising aquatic organisms using (iso)eugenol - Google Patents
Anaesthetising aquatic organisms using (iso)eugenolInfo
- Publication number
- NZ277896A NZ277896A NZ277896A NZ27789694A NZ277896A NZ 277896 A NZ277896 A NZ 277896A NZ 277896 A NZ277896 A NZ 277896A NZ 27789694 A NZ27789694 A NZ 27789694A NZ 277896 A NZ277896 A NZ 277896A
- Authority
- NZ
- New Zealand
- Prior art keywords
- organism
- isoeugenol
- amount
- compound
- anaesthetising
- Prior art date
Links
- RRAFCDWBNXTKKO-UHFFFAOYSA-N eugenol Chemical compound COC1=CC(CC=C)=CC=C1O RRAFCDWBNXTKKO-UHFFFAOYSA-N 0.000 title description 10
- NPBVQXIMTZKSBA-UHFFFAOYSA-N Chavibetol Natural products COC1=CC=C(CC=C)C=C1O NPBVQXIMTZKSBA-UHFFFAOYSA-N 0.000 title description 3
- 239000005770 Eugenol Substances 0.000 title description 3
- UVMRYBDEERADNV-UHFFFAOYSA-N Pseudoeugenol Natural products COC1=CC(C(C)=C)=CC=C1O UVMRYBDEERADNV-UHFFFAOYSA-N 0.000 title description 3
- 229960002217 eugenol Drugs 0.000 title description 3
- BJIOGJUNALELMI-UHFFFAOYSA-N trans-isoeugenol Natural products COC1=CC(C=CC)=CC=C1O BJIOGJUNALELMI-UHFFFAOYSA-N 0.000 claims description 53
- BJIOGJUNALELMI-ONEGZZNKSA-N Isoeugenol Natural products COC1=CC(\C=C\C)=CC=C1O BJIOGJUNALELMI-ONEGZZNKSA-N 0.000 claims description 52
- BJIOGJUNALELMI-ARJAWSKDSA-N cis-isoeugenol Chemical compound COC1=CC(\C=C/C)=CC=C1O BJIOGJUNALELMI-ARJAWSKDSA-N 0.000 claims description 52
- 239000000203 mixture Substances 0.000 claims description 46
- 238000000034 method Methods 0.000 claims description 39
- 150000001875 compounds Chemical class 0.000 claims description 32
- 230000003444 anaesthetic effect Effects 0.000 claims description 28
- 230000001624 sedative effect Effects 0.000 claims description 25
- 239000000243 solution Substances 0.000 claims description 21
- 239000004094 surface-active agent Substances 0.000 claims description 21
- 238000003306 harvesting Methods 0.000 claims description 16
- 239000000932 sedative agent Substances 0.000 claims description 12
- ZORQXIQZAOLNGE-UHFFFAOYSA-N 1,1-difluorocyclohexane Chemical compound FC1(F)CCCCC1 ZORQXIQZAOLNGE-UHFFFAOYSA-N 0.000 claims description 6
- 229920003171 Poly (ethylene oxide) Polymers 0.000 claims description 5
- 239000001593 sorbitan monooleate Substances 0.000 claims description 5
- 235000011069 sorbitan monooleate Nutrition 0.000 claims description 5
- 229940035049 sorbitan monooleate Drugs 0.000 claims description 5
- 239000007864 aqueous solution Substances 0.000 claims description 4
- 235000019688 fish Nutrition 0.000 description 23
- 241000251468 Actinopterygii Species 0.000 description 21
- 206010002091 Anaesthesia Diseases 0.000 description 19
- 238000001949 anaesthesia Methods 0.000 description 19
- 230000037005 anaesthesia Effects 0.000 description 19
- 241001465754 Metazoa Species 0.000 description 17
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 16
- 206010039897 Sedation Diseases 0.000 description 13
- 230000036280 sedation Effects 0.000 description 13
- 229940124326 anaesthetic agent Drugs 0.000 description 9
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 9
- 229910052760 oxygen Inorganic materials 0.000 description 9
- 239000001301 oxygen Substances 0.000 description 9
- 206010011224 Cough Diseases 0.000 description 8
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 7
- 241001280377 Oncorhynchus tshawytscha Species 0.000 description 7
- 238000009472 formulation Methods 0.000 description 7
- 235000010482 polyoxyethylene sorbitan monooleate Nutrition 0.000 description 7
- 229920000053 polysorbate 80 Polymers 0.000 description 7
- 238000011084 recovery Methods 0.000 description 7
- 239000013535 sea water Substances 0.000 description 7
- 230000000694 effects Effects 0.000 description 6
- 235000013305 food Nutrition 0.000 description 6
- 230000011514 reflex Effects 0.000 description 6
- 230000009182 swimming Effects 0.000 description 6
- 241001417534 Lutjanidae Species 0.000 description 5
- 238000006243 chemical reaction Methods 0.000 description 5
- 230000000366 juvenile effect Effects 0.000 description 5
- 231100000252 nontoxic Toxicity 0.000 description 5
- 230000003000 nontoxic effect Effects 0.000 description 5
- 239000002244 precipitate Substances 0.000 description 5
- 241000972773 Aulopiformes Species 0.000 description 4
- 238000005273 aeration Methods 0.000 description 4
- 230000008901 benefit Effects 0.000 description 4
- 239000000839 emulsion Substances 0.000 description 4
- 239000002085 irritant Substances 0.000 description 4
- 231100000021 irritant Toxicity 0.000 description 4
- 241000238565 lobster Species 0.000 description 4
- 230000033001 locomotion Effects 0.000 description 4
- 235000019515 salmon Nutrition 0.000 description 4
- 229940125723 sedative agent Drugs 0.000 description 4
- 238000009423 ventilation Methods 0.000 description 4
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 238000009360 aquaculture Methods 0.000 description 3
- 244000144974 aquaculture Species 0.000 description 3
- 231100000673 dose–response relationship Toxicity 0.000 description 3
- 238000002474 experimental method Methods 0.000 description 3
- 239000013505 freshwater Substances 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 239000000244 polyoxyethylene sorbitan monooleate Substances 0.000 description 3
- 229940068968 polysorbate 80 Drugs 0.000 description 3
- 229920006395 saturated elastomer Polymers 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 206010001488 Aggression Diseases 0.000 description 2
- 241000238366 Cephalopoda Species 0.000 description 2
- 241000238557 Decapoda Species 0.000 description 2
- FHFZEKYDSVTYLL-UHFFFAOYSA-N Methomidate Chemical compound COC(=O)C1=CN=CN1C(C)C1=CC=CC=C1 FHFZEKYDSVTYLL-UHFFFAOYSA-N 0.000 description 2
- 241001277085 Pagrus auratus Species 0.000 description 2
- 241000269908 Platichthys flesus Species 0.000 description 2
- 229920001214 Polysorbate 60 Polymers 0.000 description 2
- NWGKJDSIEKMTRX-AAZCQSIUSA-N Sorbitan monooleate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O NWGKJDSIEKMTRX-AAZCQSIUSA-N 0.000 description 2
- 230000006399 behavior Effects 0.000 description 2
- BLFLLBZGZJTVJG-UHFFFAOYSA-N benzocaine Chemical compound CCOC(=O)C1=CC=C(N)C=C1 BLFLLBZGZJTVJG-UHFFFAOYSA-N 0.000 description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 2
- 238000000605 extraction Methods 0.000 description 2
- 210000004945 gill lamellae Anatomy 0.000 description 2
- FJQXCDYVZAHXNS-UHFFFAOYSA-N methadone hydrochloride Chemical compound Cl.C=1C=CC=CC=1C(CC(C)N(C)C)(C(=O)CC)C1=CC=CC=C1 FJQXCDYVZAHXNS-UHFFFAOYSA-N 0.000 description 2
- 229960002047 metomidate Drugs 0.000 description 2
- 229920002113 octoxynol Polymers 0.000 description 2
- 229920000136 polysorbate Polymers 0.000 description 2
- 230000000750 progressive effect Effects 0.000 description 2
- 230000002035 prolonged effect Effects 0.000 description 2
- 230000000384 rearing effect Effects 0.000 description 2
- 230000004044 response Effects 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 235000015170 shellfish Nutrition 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 230000001629 suppression Effects 0.000 description 2
- LSAOROFQQDIDSZ-UHFFFAOYSA-N 2-methoxy-4-prop-1-enylphenol Chemical compound COC1=CC(C=CC)=CC=C1O.COC1=CC(C=CC)=CC=C1O LSAOROFQQDIDSZ-UHFFFAOYSA-N 0.000 description 1
- QCDWFXQBSFUVSP-UHFFFAOYSA-N 2-phenoxyethanol Chemical compound OCCOC1=CC=CC=C1 QCDWFXQBSFUVSP-UHFFFAOYSA-N 0.000 description 1
- 206010067484 Adverse reaction Diseases 0.000 description 1
- 241000424135 Aldrichetta forsteri Species 0.000 description 1
- 241000252073 Anguilliformes Species 0.000 description 1
- 241000473391 Archosargus rhomboidalis Species 0.000 description 1
- 241000237528 Arcidae Species 0.000 description 1
- 241000237519 Bivalvia Species 0.000 description 1
- 241000252229 Carassius auratus Species 0.000 description 1
- 241001609213 Carassius carassius Species 0.000 description 1
- 241000252099 Conger myriaster Species 0.000 description 1
- 241000238424 Crustacea Species 0.000 description 1
- 241000252233 Cyprinus carpio Species 0.000 description 1
- 241000723298 Dicentrarchus labrax Species 0.000 description 1
- 241000237858 Gastropoda Species 0.000 description 1
- 241001489141 Haliotis iris Species 0.000 description 1
- 241000282412 Homo Species 0.000 description 1
- 241000371391 Jasus edwardsii Species 0.000 description 1
- 241001502129 Mullus Species 0.000 description 1
- 241000238413 Octopus Species 0.000 description 1
- 241000277269 Oncorhynchus masou Species 0.000 description 1
- 241000277275 Oncorhynchus mykiss Species 0.000 description 1
- 241000237502 Ostreidae Species 0.000 description 1
- 241000935974 Paralichthys dentatus Species 0.000 description 1
- 241001250103 Paralichthys lethostigma Species 0.000 description 1
- 241000237509 Patinopecten sp. Species 0.000 description 1
- 241000861915 Plecoglossus Species 0.000 description 1
- 241001600434 Plectroglyphidodon lacrymatus Species 0.000 description 1
- 241001529596 Pontinus kuhlii Species 0.000 description 1
- 241001648771 Pseudolabrus Species 0.000 description 1
- 241000287531 Psittacidae Species 0.000 description 1
- 241000231739 Rutilus rutilus Species 0.000 description 1
- 241000975357 Salangichthys microdon Species 0.000 description 1
- 241000277331 Salmonidae Species 0.000 description 1
- 241000269851 Sarda sarda Species 0.000 description 1
- 241001125046 Sardina pilchardus Species 0.000 description 1
- 241000269821 Scombridae Species 0.000 description 1
- 241000238371 Sepiidae Species 0.000 description 1
- 241001658874 Squilla Species 0.000 description 1
- 238000000692 Student's t-test Methods 0.000 description 1
- 235000016639 Syzygium aromaticum Nutrition 0.000 description 1
- 244000223014 Syzygium aromaticum Species 0.000 description 1
- 241001441724 Tetraodontidae Species 0.000 description 1
- 241001441726 Tetraodontiformes Species 0.000 description 1
- 241001504592 Trachurus trachurus Species 0.000 description 1
- 241000894431 Turbinidae Species 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 230000006838 adverse reaction Effects 0.000 description 1
- 230000016571 aggressive behavior Effects 0.000 description 1
- 125000003342 alkenyl group Chemical group 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 125000005530 alkylenedioxy group Chemical group 0.000 description 1
- 238000010171 animal model Methods 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 150000001491 aromatic compounds Chemical class 0.000 description 1
- 229960005274 benzocaine Drugs 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 230000037396 body weight Effects 0.000 description 1
- 238000012656 cationic ring opening polymerization Methods 0.000 description 1
- 235000005911 diet Nutrition 0.000 description 1
- 230000037213 diet Effects 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- NPUKDXXFDDZOKR-LLVKDONJSA-N etomidate Chemical compound CCOC(=O)C1=CN=CN1[C@H](C)C1=CC=CC=C1 NPUKDXXFDDZOKR-LLVKDONJSA-N 0.000 description 1
- 229960001690 etomidate Drugs 0.000 description 1
- 235000013373 food additive Nutrition 0.000 description 1
- 239000002778 food additive Substances 0.000 description 1
- 210000002816 gill Anatomy 0.000 description 1
- 208000014674 injury Diseases 0.000 description 1
- 230000007794 irritation Effects 0.000 description 1
- 235000020640 mackerel Nutrition 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 231100000344 non-irritating Toxicity 0.000 description 1
- 231100001223 noncarcinogenic Toxicity 0.000 description 1
- 235000020636 oyster Nutrition 0.000 description 1
- 229960005323 phenoxyethanol Drugs 0.000 description 1
- 235000011118 potassium hydroxide Nutrition 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 230000007425 progressive decline Effects 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 239000011435 rock Substances 0.000 description 1
- 238000005070 sampling Methods 0.000 description 1
- 235000019512 sardine Nutrition 0.000 description 1
- 235000020637 scallop Nutrition 0.000 description 1
- 239000011343 solid material Substances 0.000 description 1
- 230000024188 startle response Effects 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 238000012353 t test Methods 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 230000001052 transient effect Effects 0.000 description 1
- 230000008733 trauma Effects 0.000 description 1
- FQZJYWMRQDKBQN-UHFFFAOYSA-N tricaine methanesulfonate Chemical compound CS([O-])(=O)=O.CCOC(=O)C1=CC=CC([NH3+])=C1 FQZJYWMRQDKBQN-UHFFFAOYSA-N 0.000 description 1
- 230000007306 turnover Effects 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/075—Ethers or acetals
- A61K31/085—Ethers or acetals having an ether linkage to aromatic ring nuclear carbon
-
- 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
- A01K79/00—Methods or means of catching fish in bulk not provided for in groups A01K69/00 - A01K77/00, e.g. fish pumps; Detection of fish; Whale fishery
- A01K79/02—Methods or means of catching fish in bulk not provided for in groups A01K69/00 - A01K77/00, e.g. fish pumps; Detection of fish; Whale fishery by electrocution
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23K—FODDER
- A23K50/00—Feeding-stuffs specially adapted for particular animals
- A23K50/80—Feeding-stuffs specially adapted for particular animals for aquatic animals, e.g. fish, crustaceans or molluscs
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Polymers & Plastics (AREA)
- Environmental Sciences (AREA)
- Marine Sciences & Fisheries (AREA)
- Animal Husbandry (AREA)
- Pharmacology & Pharmacy (AREA)
- Public Health (AREA)
- Food Science & Technology (AREA)
- Zoology (AREA)
- Medicinal Chemistry (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Veterinary Medicine (AREA)
- Biodiversity & Conservation Biology (AREA)
- Insects & Arthropods (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Catching Or Destruction (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Farming Of Fish And Shellfish (AREA)
Description
New Zealand No. 277896 International No. PCT/NZ94/00148
TO BE ENTERED AFTER ACCEPTANCE AND PUBLICATION
Priority dates: 23.12.1993;3! 10.1994;
Complete Specification Filed: 21.12.1994
Classification:(6) A01K79/00; A61K31/085; A01K61/00
Publication date: 26 August 1998
Journal No.: 1431
NEW ZEALAND PATENTS ACT 1953
COMPLETE SPECIFICATION
Title of Invention:
Methods for sedating and anaesthetising aquatic organisms
Name, address and nationality of applicant(s) as in international application form:
NEW ZEALAND INSTITUTE FOR CROP & FOOD RESEARCH LIMITED, a New Zealand company of Canterbury Agriculture and Science Centre, Ellesmere Road, Lincoln, Canterbury, New Zealand
WO 95/17176 PCT/NZ94/00148
1 -
277896
Methods for sedating and anaesthetising aquatic organisms
FIELD OF THE INVENTION
This invention relates to improved methods for sedating and/or anaesthetising aquatic organisms and to compositions for use in such methods.
BACKGROUND OF THE INVENTION 10 The practice of catching fish or other aquatic organisms usually involves the organisms undergoing some stress. The organisms commonly associate capture with predation and therefore struggle to escape immobilization. This struggle can have a major impact on the post-mortem quality of the tissue of the organism depending upon its duration and at the pre-mortem physical condition of the organism (Lowe, T.E.; Ryder, J.M.; Carragher, 15 J.F.; Wells, R.M.G. 1993: Flesh quality in snapper, Pagrus auratus, affected by capture stress. Journal of Food Science 58: 770-773).
In aquaculture, the cultured organisms are usually individually handled during their life cycle. With excitable fish species such as Chinook Salmon (Oncorhynchus tshawytscha), 20 great care must be taken to ensure that the animals are not bruised, scaled or in any way disfigured or damaged during handling. A natural, undamaged appearance is often a critical factor in determining the final sale price of the fish.
To achieve optimum product quality during harvesting, the organisms must be maintained 25 in a calm state. One approach which has been investigated is the use of anaesthetics during harvesting. Commonly used anaesthetics such as MS-222, 2-phenoxyethanol, benzocaine and more recently, the sedatives etomidate and metomidate (Kreiberg, H. 1992: Metomidate Sedation Minimises Handling Stress in Chinook Salmon. Bulletin of the Aquacultural Association of Canada 92-3: 52-54) have been used to minimise damage 30 during handling but their potential residual toxicity to (or misuse by) humans prevents their use during harvesting.
SUBSTITUTE SHEET
^ WO 95/17176
277896
Non-toxic non-chemical anaesthesia has also been investigated. Commonly used nontoxic alternatives such as cold anaesthesia (Mittal, A.K. and Whitear, M. 1978: A note on cold anaesthesia of poikilotherms. Journal offish Biology: 519-520) or carbonic acid anaesthesia (Post, G. 1979: Carbonic Acid Anaesthesia for Aquatic Organisms. The 5 Progressive Fish Culturist 41(3): 142-144) do induce anaesthesia but can also cause considerable trauma in the process. They are accordingly not appropriate for use in harvesting if the quality of the post-mortem flesh is to be maintained as near pre-mortem as is possible.
It is therefore apparent that a need exists for a readily available non-toxic anaesthetic suitable for use inter alia in the harvesting of aquatic organisms. The ideal chemical anaesthesia for harvesting would be cost-effective, have low irritant qualities and be suitable for use with animals intended for human consumption.
JP 46-23256 discloses a general class of aromatic compounds having the formula
where R1 and R2 are H, OH or an alkoxy group or R1 and R2 are the same lower alkylenedioxy group and R3 is an alkenyl group. These compounds are disclosed as being effective as sedatives/anaesthetics for fish, with some compounds of the class being toxic 25 and others non-toxic.
Two of the compounds covered by the general formula above are 4-allyl-2-methoxyphenol and 4-hydroxy-3-methoxy-l-propenylbenzene which are known as eugenol and isoeugenol respectively. These compounds are non-toxic food grade additives which are approved 30 for human consumption. They are however known irritants (Martindale, the Extra Pharmacopoeia, 29th Edition, Pharmaceutical Press, London) which means that they could be expected to be unsuitable for use as aquatic anaesthetics during harvesting due
SUBSTITUTE SHEET
277
to the tendency of irritants to induce the organisms to struggle, which in turn reduces post-mortem flesh quality.
JP 46-23256 discloses that eugenoi and isoeugenol are effective as aquatic 5 anaesthetics/sedatives at different concentrations. In particular, Table 1 of JP 46-23256 teaches that eugenoi is 100% effective as a fish anaesthetic/sedative at concentrations of 25 rag l"1 (equivalent to ppm) or above, but totally ineffective at a concentration of 12.5 mg l"1, and that isoeugenol is 100% effective at concentrations of or above 25 mg 1"\ partially effective at a concentration of 12.5 mg l"1 and totally ineffective at a 10 concentration of 6.25 mg l"1.
It has now surprisingly been found by the applicants that both eugenoi and isoeugenol are effective aquatic anaesthetics when employed at concentrations which are disclosed in JP 46-23256 as being totally ineffective. It has also been found that at such 15 concentrations the compounds are substantially non-irritants. It is upon these unexpected findings that the present invention is based.
SUMMARY OF THE INVENTION
Accordingly, in a first aspect, this invention provides a method of sedating and/or 20 anaesthetising an aquatic organism comprising the step of contacting said organism with a solution containing a compound of the formula
(where R is CHCHCH3 or CH2CHCH2) in an amount of up to but less than 12.5 mg l'1.
OH
R
SUBSTITUTE SHEET
277896
In a further aspect, the invention provides a method of harvesting an aquatic organism while substantially retaining its pre-mortem flesh quality comprising the steps of : sedating and/or anaesthetising said organism to be harvested by contacting the organism with a solution containing a compound of the formula
(where R is CHCHCH3 or CH2CHCH2) in an amount of up to but less than 12.5 mg l"1 harvesting said organism while sedated and/or anaesthetised.
In yet a further aspect, the invention provides a method of transporting a live aquatic organism comprising the steps of:
sedating and/°.r anaesthetising said organism to be transported by contacting the organism with a solution containing a compound of the formula
OH
(where R is CHCHCH3 or CH2CHCH2) in an amount of up to but less than 12.5 mg l"1; and transporting said organism while sedated and/or anaesthetised.
In each of the above methods, the compound may be either eugenoi or isoeugenol.
OH
R
R
INTELLECTUAL PROPERTY OFFICE OF N.Z
0 5 JUN '398
RECEIVED
In still a further aspect, the present invention provides a sedative and/or anaesthetic aqueous solution for use in sedating and/or anaesthetising an aquatic organism which includes a compound of the formula
OH
OCH.
(where R is CHCHCH3 or CH2CHCH2) in an amount of up to but less than 12.5 mg l*1.
In a final aspect, the invention provides an active composition suitable for use as an aquatic sedative or anaesthetic which comprises, in admixture, an effective amount of a compound of the formula
OH
OCH,
(where R is CHCHCH3 or CH2CHCH2) and an amount of polyethylene oxide sorbitan mono-oleate as a surfactant.
BRIEF DESCRIPTION OF THE DRAWING 25 While the present invention is broadly defined above, it will of course be appreciated by those persons skilled in the art that it is not limited thereto but that it also includes embodiments of which the following description provides examples.
In addition, the invention will be better understood by reference to the accompanying 30 Figure 1 which shows the response of king salmon to nominal concentrations of (a) eugenoi and (b) isoeugenol.
SUBSTITUTE SHEET
277896
DETAILED DESCRIPTION OF THE INVENTION
As summarised above, the present invention is based upon the applicants' surprising finding that the food grade additives eugenoi and isoeugenol can be utilised as aquatic sedatives and/or anaesthetics at concentrations which were previously thought to be 5 totally ineffective. This finding has important consequences for the aquaculture industry, in terms of both the transporting and harvesting of aquatic organisms.
The aquatic organisms to which the methods of the present invention are applied are the so-called primary aquatic organisms which are cold blooded animals living in water and 0 respiring dissolved oxygen. The methods of the present invention are preferably applied to very valuable high grade marketable organisms from an economic point of view. Examples of such organisms include those belonging to the class Pisces such as salmon, trout, char, ayu, carp, crucian carp, goldfish, roach, whitebait, eel, conger eel, sardine, flying fish, sea bass, sea bream, parrot bass, snapper, mackerel, horse mackerel, tuna, 5 bonito, yellowtail, rockfish, fluke, sole, flounder, blowfish, filefish, etc.; those belonging to the class Cephalopoda such as squid, cuttlefish, octopus, etc.; those belonging to the class Pelecypoda such as clam, scallop, ark shell, oyster, etc.; those belonging to the class Gastropoda such as turban shell, abalone, etc.; and those belonging to the class Crustacea such as lobster, prawn, shrimp, crab, squilla, etc.
3
For use in the present invention, the active compounds eugenoi and isoeugenol can be readily obtained from commercial sources. Alternatively, eugenoi can be obtained by conventional extraction techniques from a variety of natural sources such as Oil of Cloves (Claisen, Ann, 418, 113 (1919)), and isoeugenol prepared from eugenoi by heating with 5 a caustic potash (West, J Soc Chem Ind, 59, 275 (1940)).
In the present invention, the active compound (eugenoi or isoeugenol) can be used in pure form or in a mixture. Such a mixture can be a suspension or emulsion of the active compound(s) in water or can be a mixture in which the active compound(s) are dissolved ) in an appropriate alcohol such as ethanol.
SUBSTITUTE SHEET
Alternatively, the active compound be used in the form of a composition which includes a surfactant as described below. Such a composition is preferred.
Subject always to the upper limit of 12.5 mg l"1, the amount of active compound employed 5 in the methods of the invention may vary, depending on whether the active compound is eugenoi or isoeugenol. Where the compound employed is eugenoi, it is preferred that the amount of eugenoi used is from 2-12.5 mg l"1, more preferably from 3-10 mg 1"\ most preferably from 6-8 mg l"1.
In the alternative, where the compound employed is isoeugenol, it is preferred that the amount of isoeugenol used is from 1-10 mg l"1, more preferably from 3-9 mg l"1, most preferably from 5-8.5 mg l"1.
As stated above, it is the applicants preference that the active compound form part of an 15 active composition which includes a surfactant. For use in the methods of the invention, this surfactant could in theory be any commercially available surfactant having suitable properties but is preferably polyethylene oxide sorbitan mono-oleate. The surfactant polyethylene oxide sorbitan mono-oleate is commercially available under the trade name Polysorbate 80, with it being particularly preferred that the form of Polysorbate 80 sold 20 as Liposorb-0-20 (Lipochemicals, Inc., USA) be used.
The applicants have surprisingly found that the use of Liposorb-0-20 results in a composition having superior properties in terms of solubility in water and in terms of stability in aqueous solution over time as compared to compositions including other 25 surfactants (such as Tween 60, Tween 65, Tween 80 and Span 80 (all ICI) and Triton X). In view of this unexpected finding, the active composition comprising eugenoi and/or isoeugenol and polyethylene oxide sorbitan mono-oleate forms yet a further aspect of the invention.
While various proportions of active compound and surfactant can be employed in forming the composition, it is presently preferred that each be included as 50% of the volume of the final composition. The most preferred composition is 50% by volume of isoeugenol
SUBSTITUTE SHEET
PCT/NZS4/00148
(Naarden International, Bussem, The Netherlands) and 50% by volume Liposorb-0-20 (Lipochemicals Inc, USA).
The invention will now be illustrated with reference to the following Examples.
EXAMPLE 1
MATERIALS AND METHODS Experimental animals
Thirty-nine female king salmon (Oncorhynchus tshawytscha) with a mean wet weight of 10 365g (s.d. = 78) were used in this experiment. These animals were sampled from a tank population of 299 animals which had been reared indoors in a 28m3 oval tank from smoltification. The rearing tank was supplied with filtered seawater on a flow-through basis with a typical turnover of one tank volume per 3.5 hours. Auxiliary aeration maintained the dissolved oxygen concentration typically between 85 to 95% of saturation. 15 The salmon were fed ad libitum a 3mm proprietary salmon diet (NRM New Zealand Ltd, Nelson, New Zealand) at a rate up to but not exceeding 2% of body weight per day. For two months prior to the experiment, the food had been distributed into the bubble stream of an air stone positioned immediately adjacent to the tank wall. This facilitated capture and reduced the likelihood of learned net avoidance behaviour.
Animal sampling and test conditions
Each animal was caught in a shallow dip net as it came to the surface adjacent to the tank wall to feed. Once caught, each animal was transferred to an insulated 700 litre tank located within 1 metre of the rearing tank. A lid was then placed on the tank for 25 5 minutes to allow the fish to settle slightly before the anaesthetic doses were added.
Prior to each trial, the tank was thoroughly cleaned and rinsed with fresh water. It was then filled to a depth of 490mm with 500 ± 251 of sand-filtered 34% seawater at a temperature of 14.4 ± 0.5°C. Auxiliary aeration was used to ensure dissolved oxygen 30 saturation at the beginning of each trial. A YSI Model 57 dissolved oxygen meter was used to confirm that dissolved oxygen concentrations remained above 90% saturation during each trial.
SUBSTITUTE SHEET
A Minolta CR-200B Chroma Meter was used to characterise the grey tank colour according to the L*a*b* International Colour System (CIE, 1976) as L* = 55.4; a* = -0/9 and b* = 1.7. Light intensity (400 to 700nm) at the physical centre of the tank was measured using a Licor LI-1000 logger fitted with LI-192SA Underwater Quantum 5 Sensor. The light intensity ranged between 1.2 and 2.3 /*mol s"1 m"2 with the tank lid removed.
Dose-response trials
Five fish were used in seven of the eight dose-response trials with the remaining trial 0 using four (Figure la). For each trial eugenoi (4-allyl-2-methoxyphenol) or isoeugenol (4-hydroxy-3-methoxy-l-propenylbenzene) were dissolved in 200 mis 99.7% ethanol to aid dispersion in seawater. Five trials were undertaken for eugenoi with nominal concentrations of 25.0, 12.5, 8.0, 6.3 and 3.0 ± 0.5 mg l"1 seawater. Three trials were undertaken for isoeugenol with nominal concentrations of 25.0, 8.0 and 3.0 ± f\5 mg l"1 5 seawater. Experimental timing was initiated from the addition of the anaesthetic-ethanol mixture. Mixing of the anaesthetic-ethanol solution and the seawater was achieved by aeration. After 15 seconds mixing, the aeration was stopped to avoid accelerated air-stripping of anaesthetics. Care was taken to disturb the fish as little as possible during the mixing procedure.
0
Dose-response criteria
The responses of the fish to the nominal anaesthetic concentrations were judged against two criteria. The time taken from the addition of the anaesthetic dose to the point where the fish failed to avoid a hand placed in their path gave an empirical estimation of a 5 sedative effect. Animals in this state could be removed from the water but would rouse themselves and slightly struggle if they were not returned to the water within 5 to 10 seconds. Ventilation was often exaggerated and the fish would tend to swim slightly "nose up" near the tank surface. Fish in this stage were characterised as "handleable" for the purposes of this experiment.
3
The time taken from the addition of the anaesthetic dose to the point where the animals were insensible to forced extension of the operculum and contact with the gill lamellae
SUBSTITUTE SHEET
WO 95/17176 PCT/NZ94/00148
gave an indication of an anaesthetic effect. In this state the fish exhibited a loss of equilibrium but weak swimming motions were often present. Ventilation was often erratic and exaggerated at this stage. Fish that had not reached this state would respond within 30 seconds of contact with the gill lamellae with a reflexive "cough".
RESULTS AND DISCUSSION
At all of the concentrations tested, the two anaesthetic formulations generated very similar patterns of behaviour when first introduced into the seawater. Some initial "coughing" was observed and was particularly pronounced with the higher concentrations 10 indicating a transitory period of gill irritation in some cf the animals.
In both anaesthetic formulations, increasing sedation was characterised by a slight increase in swimming speed, moderate ventilation and a progressive decrease in the distance at which the tank walls and water surface were perceived. At the point of 15 "handleability", the animals were often unaware of the tank walls until contact was made. A loud noise could elicit a transient startle response at this level of sedation.
Progression from the point of "handleability" to the loss of the "coughing" reflex is characterised by a progressive loss of equilibrium and effective swimming motions. The 20 fish were insensitive to loud noises and physical restraint. The erratic ventilation observed at this stage slowed and eventually ceased as anaesthesia deepened leaving the fish inert and apparently unresponsive to physical stimuli.
Where the two formulations differ is in the nominal concentration and rate at which the 25 abolition of the "coughing" reflex occurs. Figures 1(a) and (b) illustrate this result. There appears to be no effective or statistical difference between the formulations at a nominal concentration of 25 mg l*1 (t-test, P<0.05). At a nominal concentration of 8.0 mg l"1, the mean time to elimination of the "coughing" reflex was approximately 2.5 times shorter for the isoeugenol formulation. At 3.0 mg l"1 the eugenoi formulation did not produce 30 sufficient depth of anaesthesia to depress the "cough" reflex however the sedated, "handleable", state was easily achieved. At 3.0 mg l"1 nominal concentration isoeugenol produced a loss of equilibrium and weak ineffectual swimming motions but did not
SUBSTITUTE SHEET
WO 95/17176 PCT/NZ94/00148
11 -
produce full suppression of the "cough" reflex. Eugenoi produced a similar effect at a nominal concentration of 6.3 mg l"1.
The reason for the apparent differences in activity between the two formulations is likely 5 to be attributable to differences in the solubility of the active ingredients. In practice, there appears to be little gained from nominal dosages above 12.5 mg l"1 for eugenoi and approximately 8.0 mg l'1 for isoeugenol.
General observations in relation to recovering from the anaesthetics suggest that recovery 10 is rapid when the fish are placed in clean, well aerated water. Typically, when anaesthetized using low to medium concentrations to the point of suppression of the "coughing" reflex, the fish will regain orientation and coordinated swimming within approximately 5 to 15 minutes. In one incidence, approximately 171 (mean weight 578g) king salmon resumed apparently normal feeding within approximately two hours of 15 exposure to 8 mg l"1 isoeugenol for approximately 10 to 30 minutes (Jerrett, Holland and Cleavsr, unpublished results).
EXAMPLE 2
This example reports the applicants observations when 50% by volume isoeugenol is 20 admixed with 50% by volume of various surfactants.
ICI Tween 60
Very viscous solution which solidifies in cold weather (below about 15°C). Gentle heating will liquefy the solid material, ie. placing the. container in a water bath (40°C). 25 Surfactant mixes well with isoeugenol but will solidify again if mixing does not take place quickly. Generally forms the composition as a very viscous mixture. Forms a cloudy white solution in water. A white precipitate forms after 10 minutes and by 20 minutes an emulsion has formed on the bottom of the container with some formation of isoeugenol globules. Will resuspend on shaking.
SUBSTITUTE SHEET
ICI Tween 65
Solid needing direct heating, ie. on a hot plate to liquefy. Mixes well with isoeugenol but does need to be mixed quickly to stop the surfactant solidifying. Forms the composition as a very viscous solution. Mixes with water to form a cloudy solution but does not 5 appear to mix totally. Separation takes place almost immediately. Globules formed on the sides of the bottle. Separates out into two distinct layers, one yellow (isoeugenol) and the other a white precipitate formed after two minutes. Isoeugenol globules form at the top and the bottom of the solution. Some resuspension will occur with prolonged shaking.
ICI Tween 80
Isoeugenol and Tween 80 do not mix together easily. Will eventually (10 mins) blend with gentle mixing. Mixes well on addition to water. After 5 minutes precipitate forms. Some emulsion formed at ten minutes. Will resuspend with a good shake although some 15 globules appear to be left on the side of the container.
ICI Span 80
Mixes well with isoeugenol but separates out immediately on addition to water. 20 Triton X
Solid at room temperature. When melted mixes well with isoeugenol and immediately forms a cloudy solution. Mixes well on addition to water. Separation occurs as very fine precipitate within 10 minutes. Isoeugenol globules formed after 3 hours. Appeared after 5 hours that both the surfactant and isoeugenol had separated out. Resuspension will 25 occur but some globules are left on the side of the container.
Liposorb-0-20
Surfactant is less viscous and mixes relatively easily with isoeugenol. Will mix with a good shake.
Mixture goes into solution well on addition to water. No deposit is left on the side of the bottle. A fine precipitate is formed on the bottom of the container after about 15
SUBSTITUTE SHEET
minutes but this resuspends very easily once disturbed. Three hours before any emulsion is seen on the bottom of the flask. It appeared the isoeugenol did not separate out from the surfactant even when the mixture was left overnight. Total resuspension occurred on shaking.
It can therefore be seen that Liposorb-0-20 confers superior properties upon the ultimate composition in terms of mixability, solubility in water and stability. These advantages are surprising given that Tween 80 (also a polysorbate 80) is not nearly so effective.
EXAMPLE 3
This example demonstrates the effect of the applicants preferred composition (50% by volume isoeugenol and 50% by volume Lipsorb-0-20) on a range of aquatic organisms. In this example, the composition is referred to as AQUI-S and the amount of isoeugenol with which the organisms are contacted is one-half of the AQUI-S dosage. 15 (i) Rainbow trout (Salmo gairdneri)
Dosage Temperature Time for sedation Time for anaesthesia
Recovery
(ii) Rock Lobster (Jasus edwardsii)
Dosage
Temperature pH
Dissolved Oxygen Salinity
Reaction to Introduction Time to Sedation
Time to anaesthesia Recovery
40
17mg l'1 AQUI-S (8.5 mg l"1 isoeugenol) 12.5°C
12 to 16 minutes ; ^
to 40 minutes. More mature fish were the ones that took longer.
Similar to salmon, as reported in Example 1.
17 mg l"1 AQUI-S (8.5 mg l"1 isoeugenol)
.6°C
8.2
Saturated 32.84
No apparent awareness Juvenile 8 to 10 minutes
Adult 10 to 12 minutes
Juvenile 12 to 15 minutes
Adult 15 to 20 minutes
Equilibrium regained and walking/swimming motions regained within 5 minutes of introduction to fresh water. Tail curl was noticeable after 15 minutes of introduction to fresh water. Lobster still remained calm with no avoiciance of handling for a further
SUBSTITUTE SHEET
PCIYNZ94/00148
minutes. At about 1 hour after being removed from the anaesthetic the aggressive behaviour was returning. Examination the next day showed full regaining of aggressive behaviour. Adults and juveniles responded in a similar fashion.
Sedation in this case is defined as the point at which equilibrium is lost and there is no aggression to being handled although the animal is definitely still aware of being handled.
Anaesthesia is defined as the point at which the lobster can be handled with no reaction from the animal. In this state, the tail fans are spread out and there is no reflexive curling in of the tail. When the animal is placed on its back the tail is fully extended.
(iii) Paua (Haliotis iris)
Dosage Temperature pH
Dissolved Oxygen Salinity
Reaction to Introduction Time to Sedation Time to anaesthesia Recovery
17 mg l"1 AQUI-S (8.5 mg l"1 isoeugenol)
.6°C
8.2
Saturated 32.84
Awareness of substance but no apparent adverse reaction, ie. no avoidance.
Juvenile 8 to 10 minutes
Adult 13 to 20 minutes
Juvenile 12
Adult 30 minutes
Appeared to be fully recovered by 6 to 10 minutes after removal from the anaesthetic.
40
(iv)
45
Sedation in this case is defined as the point at which the animal is very slow to right itself after being placed on its back.
Anaesthesia is defined as the point at which the animal has released its hold on the substrate and usually fails completely to right itself after being placed on its back.
Long Finned Eels (Anguillea dieffenbachi)
Dosage 17mg l"1 AQUI-S (8.5mg l"1 isoeugenol)
Temperature Initial temperature 13°C
Final temperature 4°C Dissolved oxygen Saturated
Time to anaesthesia 10 to 15 minutes
Recovery 10 to 12 minutes
SUBSTITUTE SHEET
Anaesthesia is defined as the point at which the eel lost equilibrium and turned over onto its back. No reaction to being handled.
(v) Snapper (Pagrus auratus)
Dosage Temperature Dissolved oxygen Time to sedation Time to anaesthesia Recovery
12mg l"1 AQUI-S (6mg l"1 isoeugenol)
18°C
7.4 mg l'1
to 30 minutes
40 to 50 minutes
to 20 minutes
Sedation is defined as the point at which equilibrium is lost and anaesthesia is the point at which there is no reaction from the snapper upon removal from the water. This is for juvenile snapper weighing approximately 12 grams.
(vi) Yellow Eyed Mullet (Aldrichetta forsteri)
Dosage Temperature Time to sedation Time to anaesthesia Recovery
17 mg l"1 AQUI-S (8.5 mg l"1 isoeugenol) 10°C
9 to 10 minutes 14 to 15 minutes 5 minutes
Flounder (Paralichthys lethostigma) and spotty's (Pseudolabrus celidotus) in the same tank as the mullclt appeared to respond in much the same manner within the same time frame.
Thus, in accordance with the present invention there are provided methods and compositions for sedating/anaesthetising aquatic organisms. Further, and most importantly, the active agents which are responsible for producing the sedating/anaesthetising effect are food grade additives which are non-carcinogenic (Finding of the WHO Expert Committee on Food Additives reported in Martindale, The 35 Extra Pharmacopoeia, 29th Edition), and which are non-irritating to the organism at the concentrations employed.
Those persons skilled in the art will therefore appreciate the advantages of the present invention as well as the many applications to which the methods and compositions of the 40 present invention can be put. As a first example, the methods and compositions can be employed in the harvesting of aquatic organisms for ultimate human consumption. This is particularly so in the case of organisms such as fish which otherwise struggle violently
SUBSTITUTE SHEET
to avoid capture, having a major impact on the post-mortem quality of the tissue. However, when sedated and/or anaesthetised in accordance with the present methods this struggling is at least much reduced, if not eliminated. Further, any residual concentration of eugenoi or isoeugenol in the tissue of the organism following harvesting 5 does not detract from the suitability of the flesh for human consumption.
Additionally, where the aquatic organism is a shellfish, sedation/anaesthetisation of the shellfish greatly eases the extraction of the flesh from the shell.
A further application of the sedation and/or anaesthetic methods and compositions is in the transportation of live aquatic organisms. This is once again particularly the case with fish which are to be transported live to overseas markets and where the natural undamaged appearance of the fish is critical to the market price obtained.
Still a further application of the invention is in the transport of aquatic organisms to a market where the organism is to be sold in a pre-rigor state. By "pre-rigor" it is meant a state in which the tissue of the organism remains alive for a prolonged period following administration of the eugenol/isoeugenol but in which the organism is no longer capable of control of its musculature and from which the organism will not recover. The 20 organism is therefore in a state of "living death".
The advantage of transporting the organism in this f re-rigor state is that the organism need not be transported in its aquatic environment. Instead, the organism can be transported "dry", which represents a considerable reduction in expense over that 25 associated with the transportation of live organisms in their aquatic environment.
Additionally, as the tissue of the organism remains alive until the organism has reached its market, the flesh remains "fresh" and able to command a market premium over flesh from organisms euthanised before transport.
Other applications of the present methods and compositions will be readily apparent to the skilled worker in this art.
SUBSTITUTE SHEET
In addition, the use of lesser amounts of eugenoi and isoeugenol as compared to the amounts previously disclosed as being effective has significant advantages. In particular, the applicants have found that, while effective in sedating/anaesthetising the organisms, the higher concentrations of eugenoi and isoeugenol disclosed in JP 46-23256, do tend 5 to irritate the organism and cause it to exercise more vigorously until such time as the sedative/anaesthetic effect takes hold. This is undesirable in terms of the effect this activity can have on the post-harvest flesh quality of the organism.
Equally, with the higher concentrations, the risk of the flesh becoming "tainted" by the 10 residual levels of eugenoi and isoeugenol is much increased. Again, this is undesirable, particularly where the flesh is to be consumed raw.
Finally, as a matter of simple economics, it is preferable to use lesser amounts of the active compounds to reduce overheads. In a large scale aquaculture operation, this can 15 lead to considerable savings.
It will be appreciated that the above description is provided by way of example only and that the present invention is limited only by the lawful scope of the appended claims.
SUBSTITUTE SHEET
Claims (26)
1. A method of sedating and/or anaesthetising an aquatic organism comprising the step of contacting said organism with a solution containing a compound of the formula OH a (where R is CHCHCH3 or CH2CHCH2) in an amount of up to but less than 12.5 mg l'1.
2. A method of harvesting an aquatic organism while substantially retaining its pre-mortem flesh quality comprising the steps of sedating and/or anaesthetising said organism to be harvested by contacting the organism with a solution containing a compound of the formula OCH; (where R is CHCHCH3 or CH2CHCH2) in an amount of up to but less than 12.5 mg l"1 ; and harvesting said organism while sedated and/or anaesthetised.
3. A method of transporting a live aquatic organism comprising the steps of: sedating and/or anaesthetising said organism to be transported by contacting the organism with a solution containing a compound of the formula OCH, INTELLECTUAL PROPERTY OFFICE | OF N.Z 0 5 JUN 1993 WO 95/17176 PCT/NZ94/OOH8 - 19 - (where R is CHCHCH3 or CH2CHCH2) in an amount of up to but less than 12.5 mg l'1; and transporting said organism while sedated and/or anaesthetised. 5
4. A method according to any one of claims 1 to 3 wherein the compound is eugenoi.
5. A method according to claim 4 wherein said solution contains eugenoi in an amount of from 2 up to but not including 12.5 mg l"1. 10
6. A method according to claim 4 wherein said solution contains eugenoi in an amount of from 3 to 10 mg l'1.
7. A method according to claim 4 wherein said solution contains eugenoi in an amount of from 6 to 8 mg I"1.
8. A method according to any one of claims 1 to 3 wherein the compound is isoeugenol.
9. A method according to claim 8 wherein said solution contains isoeugenol in an 20 amount of from 1 to 10 mg l'1.
10. A method according to claim 8 wherein said solution contains isoeugenol in an amount of from 3 to 9 rng l'1. 25
11. A method according to claim 8 wherein said solution contains isoeugenol in an amount of from 5 to 8.5 mg l'1.
12. A method according to any one of claims 1 to U wherein said solution further includes a surfactant. 15
13. A method according to claim 12 wherein the surfactant i sorbitan mono-oleate surfactant. 0 5 j'Jil £?,3 WO 95/17176 PCT7NZ94/00148 -20-
14. A method according to claim 12 wherein said surfactant is Liposorb-0-20.
15. A sedative and/or anaesthetic aqueous solution for use in sedating and/or anaesthetising an aquatic organism which includes a compound of the formula 10 OCH, (where R is CHCHCH3 or CH2CHCH2) in an amouht of up to but less than 12.5 mg l"1. 15
16. An active composition suitable for use as an aquatic sedative or anaesthetic which comprises, in admixture, an effective amount of a compound of the formula OCH, 20 (where R is CHCHCH3 or CH2CHCH2) and an amount of polyethylene oxide sorbitan mono-oleate as a surfactant.
17. A composition according to claim 16 wherein the compound is eugenoi. 25
18. A composition according to claim 16 wherein the compound is isoeugenol.
19. A composition according to any one of claims 16 to 18 wherein the surfactant is Liposorb-0-20. 30
20. A composition according to claim 19 in which said surfactant is 50% by volume of the total composition. SUBSTITUTE SHEET WO 95/17176 PCT/NZ94/00148 - 21 -
21. A composition according to claim 16 which is 50% by volume isoeugenol and 50% by volume Liposorb-0-20.
22. A method as defined in claim 1 of sedating and/or anaesthetising an aquatic organism substantially as herein described with reference to any example thereof and with or without reference to the accompanying drawings.
23. A method as defined in claim 2 of harvesting an aquatic organism while substantially retaining its pre-morlem flesh quality substantially as herein described with reference to any example thereof and with or without reference to the accompanying drawings.
24. A method as defined in claim 3 of transporting a live aquatic organism substantially as herein described with reference to any example thereof and with or without reference to the accompanying drawings.
25. A sedative and/or anaesthetic aqueous solution as claimed in claim 15 for use in sedating and/or anaesthetising an aquatic organism substantially as herein described with reference to any example tliereof and widi or without reference to the accompanying drawings.
26. An active composition as defined in claim 16 suitable for use as an aquatic sedative or anaesthetic substantially as herein described widi reference to any example thereof and with or without reference to the accompanying drawings. RUSSELL McVEAGH WE8T WALKED A7TORNEYSTOR THE APPLICANT INTELLECTUAL PROPERTY OFFICE OF IM.Z 0 5 JUN ICy
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
NZ277896A NZ277896A (en) | 1993-12-23 | 1994-12-21 | Anaesthetising aquatic organisms using (iso)eugenol |
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
NZ25058593 | 1993-12-23 | ||
NZ26481894 | 1994-10-31 | ||
PCT/NZ1994/000148 WO1995017176A1 (en) | 1993-12-23 | 1994-12-21 | Methods for sedating and anaesthetising aquatic organisms |
NZ277896A NZ277896A (en) | 1993-12-23 | 1994-12-21 | Anaesthetising aquatic organisms using (iso)eugenol |
Publications (1)
Publication Number | Publication Date |
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NZ277896A true NZ277896A (en) | 1998-08-26 |
Family
ID=26651260
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NZ277896A NZ277896A (en) | 1993-12-23 | 1994-12-21 | Anaesthetising aquatic organisms using (iso)eugenol |
Country Status (5)
Country | Link |
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AU (2) | AU1328695A (en) |
CA (1) | CA2178722C (en) |
GB (1) | GB2299757B (en) |
NZ (1) | NZ277896A (en) |
WO (1) | WO1995017176A1 (en) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
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AU7942498A (en) * | 1997-06-04 | 1998-12-21 | Aqui-S (Nz) Limited | Compositions and methods for sedating, anaesthetising and euthanising aquatic organisms |
NZ508087A (en) * | 2000-11-10 | 2003-03-28 | Aqui S Nz Ltd | Compositions and methods for sedating, anaesthetising and euthanasing aquatic organisms using trans isoeugenol |
CN108935252A (en) * | 2018-06-21 | 2018-12-07 | 镇江市绿色农业科技有限公司 | A kind of anesthesia transportation resources of steamed crab |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
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JPS4623256B1 (en) * | 1968-08-01 | 1971-07-02 | ||
JPS60146803A (en) * | 1984-01-06 | 1985-08-02 | Kiyoshi Saotome | Germination and proliferation inhibitor against phytopathogenic bacteria |
JPH02207758A (en) * | 1989-02-09 | 1990-08-17 | Taiyo Kagaku Co Ltd | Feed for pisciculture |
-
1994
- 1994-12-21 NZ NZ277896A patent/NZ277896A/en not_active IP Right Cessation
- 1994-12-21 AU AU13286/95A patent/AU1328695A/en not_active Abandoned
- 1994-12-21 WO PCT/NZ1994/000148 patent/WO1995017176A1/en active Application Filing
- 1994-12-21 CA CA002178722A patent/CA2178722C/en not_active Expired - Lifetime
- 1994-12-21 GB GB9612687A patent/GB2299757B/en not_active Expired - Lifetime
-
1999
- 1999-02-24 AU AU18385/99A patent/AU1838599A/en not_active Abandoned
Also Published As
Publication number | Publication date |
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GB2299757A (en) | 1996-10-16 |
CA2178722C (en) | 2003-06-17 |
AU1838599A (en) | 1999-09-09 |
WO1995017176A1 (en) | 1995-06-29 |
GB9612687D0 (en) | 1996-08-21 |
CA2178722A1 (en) | 1995-06-29 |
AU1328695A (en) | 1995-07-10 |
GB2299757B (en) | 1998-06-17 |
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