AU746660B2 - Utilization of natural and/or synthetic quinic acid and/or precursors thereof as insect repellents - Google Patents
Utilization of natural and/or synthetic quinic acid and/or precursors thereof as insect repellents Download PDFInfo
- Publication number
- AU746660B2 AU746660B2 AU35203/99A AU3520399A AU746660B2 AU 746660 B2 AU746660 B2 AU 746660B2 AU 35203/99 A AU35203/99 A AU 35203/99A AU 3520399 A AU3520399 A AU 3520399A AU 746660 B2 AU746660 B2 AU 746660B2
- Authority
- AU
- Australia
- Prior art keywords
- acid
- insects
- natural
- use according
- chinic
- 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.)
- Ceased
Links
- 239000002243 precursor Substances 0.000 title description 8
- 239000000077 insect repellent Substances 0.000 title description 6
- AAWZDTNXLSGCEK-LNVDRNJUSA-N (3r,5r)-1,3,4,5-tetrahydroxycyclohexane-1-carboxylic acid Chemical compound O[C@@H]1CC(O)(C(O)=O)C[C@@H](O)C1O AAWZDTNXLSGCEK-LNVDRNJUSA-N 0.000 title 1
- AAWZDTNXLSGCEK-UHFFFAOYSA-N Cordycepinsaeure Natural products OC1CC(O)(C(O)=O)CC(O)C1O AAWZDTNXLSGCEK-UHFFFAOYSA-N 0.000 title 1
- AAWZDTNXLSGCEK-ZHQZDSKASA-N Quinic acid Natural products O[C@H]1CC(O)(C(O)=O)C[C@H](O)C1O AAWZDTNXLSGCEK-ZHQZDSKASA-N 0.000 title 1
- 241000238631 Hexapoda Species 0.000 claims description 39
- AAWZDTNXLSGCEK-WYWMIBKRSA-N (-)-quinic acid Chemical compound O[C@@H]1C[C@](O)(C(O)=O)C[C@@H](O)[C@H]1O AAWZDTNXLSGCEK-WYWMIBKRSA-N 0.000 claims description 30
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 21
- 230000002940 repellent Effects 0.000 claims description 17
- 239000005871 repellent Substances 0.000 claims description 17
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 12
- 230000000669 biting effect Effects 0.000 claims description 7
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- -1 cremes Substances 0.000 claims description 4
- 241000894007 species Species 0.000 claims description 4
- 239000002253 acid Substances 0.000 claims description 3
- 150000001298 alcohols Chemical class 0.000 claims description 3
- 239000000499 gel Substances 0.000 claims description 3
- 239000006185 dispersion Substances 0.000 claims description 2
- 239000006210 lotion Substances 0.000 claims description 2
- ULWHHBHJGPPBCO-UHFFFAOYSA-N propane-1,1-diol Chemical class CCC(O)O ULWHHBHJGPPBCO-UHFFFAOYSA-N 0.000 claims description 2
- 208000002193 Pain Diseases 0.000 claims 2
- SLSOZIDDEFZSET-UHFFFAOYSA-N carbonic acid;cyclohexane-1,2,3,5-tetrol Chemical compound OC(O)=O.OC1CC(O)C(O)C(O)C1 SLSOZIDDEFZSET-UHFFFAOYSA-N 0.000 claims 2
- 238000005516 engineering process Methods 0.000 claims 1
- 238000012360 testing method Methods 0.000 description 37
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- 239000003995 emulsifying agent Substances 0.000 description 12
- 230000000694 effects Effects 0.000 description 9
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- 238000002474 experimental method Methods 0.000 description 8
- 239000000203 mixture Substances 0.000 description 7
- 239000000126 substance Substances 0.000 description 7
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
- 241001465754 Metazoa Species 0.000 description 6
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 6
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- 230000001681 protective effect Effects 0.000 description 6
- 235000019441 ethanol Nutrition 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 4
- NIQCNGHVCWTJSM-UHFFFAOYSA-N Dimethyl phthalate Chemical compound COC(=O)C1=CC=CC=C1C(=O)OC NIQCNGHVCWTJSM-UHFFFAOYSA-N 0.000 description 4
- 238000001704 evaporation Methods 0.000 description 4
- 210000000245 forearm Anatomy 0.000 description 4
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- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical group CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 3
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- 238000002360 preparation method Methods 0.000 description 3
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- 231100000027 toxicology Toxicity 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- 241000238421 Arthropoda Species 0.000 description 2
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- MMOXZBCLCQITDF-UHFFFAOYSA-N N,N-diethyl-m-toluamide Chemical compound CCN(CC)C(=O)C1=CC=CC(C)=C1 MMOXZBCLCQITDF-UHFFFAOYSA-N 0.000 description 2
- 239000004721 Polyphenylene oxide Substances 0.000 description 2
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 2
- 208000004374 Tick Bites Diseases 0.000 description 2
- 244000078534 Vaccinium myrtillus Species 0.000 description 2
- 208000003152 Yellow Fever Diseases 0.000 description 2
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- 229960001673 diethyltoluamide Drugs 0.000 description 2
- FBSAITBEAPNWJG-UHFFFAOYSA-N dimethyl phthalate Natural products CC(=O)OC1=CC=CC=C1OC(C)=O FBSAITBEAPNWJG-UHFFFAOYSA-N 0.000 description 2
- 229960001826 dimethylphthalate Drugs 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- FKRCODPIKNYEAC-UHFFFAOYSA-N ethyl propionate Chemical compound CCOC(=O)CC FKRCODPIKNYEAC-UHFFFAOYSA-N 0.000 description 2
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- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 2
- 229920000570 polyether Polymers 0.000 description 2
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- KRKNYBCHXYNGOX-UHFFFAOYSA-K Citrate Chemical compound [O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O KRKNYBCHXYNGOX-UHFFFAOYSA-K 0.000 description 1
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- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 1
- 208000001490 Dengue Diseases 0.000 description 1
- 206010012310 Dengue fever Diseases 0.000 description 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
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- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
- 241000257303 Hymenoptera Species 0.000 description 1
- 208000006877 Insect Bites and Stings Diseases 0.000 description 1
- LEVWYRKDKASIDU-IMJSIDKUSA-N L-cystine Chemical compound [O-]C(=O)[C@@H]([NH3+])CSSC[C@H]([NH3+])C([O-])=O LEVWYRKDKASIDU-IMJSIDKUSA-N 0.000 description 1
- ZDXPYRJPNDTMRX-VKHMYHEASA-N L-glutamine Chemical compound OC(=O)[C@@H](N)CCC(N)=O ZDXPYRJPNDTMRX-VKHMYHEASA-N 0.000 description 1
- JVTAAEKCZFNVCJ-UHFFFAOYSA-M Lactate Chemical compound CC(O)C([O-])=O JVTAAEKCZFNVCJ-UHFFFAOYSA-M 0.000 description 1
- 241000948337 Lasius niger Species 0.000 description 1
- 244000178870 Lavandula angustifolia Species 0.000 description 1
- 235000010663 Lavandula angustifolia Nutrition 0.000 description 1
- 229920003266 Leaf® Polymers 0.000 description 1
- 235000007688 Lycopersicon esculentum Nutrition 0.000 description 1
- 239000004907 Macro-emulsion Substances 0.000 description 1
- 244000179970 Monarda didyma Species 0.000 description 1
- 235000010672 Monarda didyma Nutrition 0.000 description 1
- 244000270834 Myristica fragrans Species 0.000 description 1
- 235000009421 Myristica fragrans Nutrition 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 241000694540 Pluvialis Species 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 229920000388 Polyphosphate Polymers 0.000 description 1
- 239000004146 Propane-1,2-diol Substances 0.000 description 1
- 244000171263 Ribes grossularia Species 0.000 description 1
- 235000002357 Ribes grossularia Nutrition 0.000 description 1
- 241001107098 Rubiaceae Species 0.000 description 1
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- 241000533293 Sesbania emerus Species 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- 240000003768 Solanum lycopersicum Species 0.000 description 1
- 229930006000 Sucrose Natural products 0.000 description 1
- 235000021536 Sugar beet Nutrition 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 235000016639 Syzygium aromaticum Nutrition 0.000 description 1
- 244000223014 Syzygium aromaticum Species 0.000 description 1
- 240000001717 Vaccinium macrocarpon Species 0.000 description 1
- 235000012545 Vaccinium macrocarpon Nutrition 0.000 description 1
- 235000017537 Vaccinium myrtillus Nutrition 0.000 description 1
- 235000002118 Vaccinium oxycoccus Nutrition 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 239000002390 adhesive tape Substances 0.000 description 1
- 125000003342 alkenyl group Chemical group 0.000 description 1
- 125000002877 alkyl aryl group Chemical group 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 150000001413 amino acids Chemical class 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 239000012752 auxiliary agent Substances 0.000 description 1
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- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 1
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- 239000008103 glucose Substances 0.000 description 1
- ZDXPYRJPNDTMRX-UHFFFAOYSA-N glutamine Natural products OC(=O)C(N)CCC(N)=O ZDXPYRJPNDTMRX-UHFFFAOYSA-N 0.000 description 1
- 150000004676 glycans Chemical class 0.000 description 1
- KWIUHFFTVRNATP-UHFFFAOYSA-N glycine betaine Chemical group C[N+](C)(C)CC([O-])=O KWIUHFFTVRNATP-UHFFFAOYSA-N 0.000 description 1
- 230000036541 health Effects 0.000 description 1
- 239000003906 humectant Substances 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 208000015181 infectious disease Diseases 0.000 description 1
- 239000001102 lavandula vera Substances 0.000 description 1
- 235000018219 lavender Nutrition 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 201000004792 malaria Diseases 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000000457 mentha pulegium l. herb oil Substances 0.000 description 1
- 239000004530 micro-emulsion Substances 0.000 description 1
- NJTGANWAUPEOAX-UHFFFAOYSA-N molport-023-220-454 Chemical compound OCC(O)CO.OCC(O)CO NJTGANWAUPEOAX-UHFFFAOYSA-N 0.000 description 1
- 125000000896 monocarboxylic acid group Chemical group 0.000 description 1
- 229910052901 montmorillonite Inorganic materials 0.000 description 1
- 230000001459 mortal effect Effects 0.000 description 1
- 229930014626 natural product Natural products 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 230000001473 noxious effect Effects 0.000 description 1
- 239000001702 nutmeg Substances 0.000 description 1
- 239000001814 pectin Substances 0.000 description 1
- 229920001277 pectin Polymers 0.000 description 1
- 235000010987 pectin Nutrition 0.000 description 1
- 229960000490 permethrin Drugs 0.000 description 1
- RLLPVAHGXHCWKJ-UHFFFAOYSA-N permethrin Chemical compound CC1(C)C(C=C(Cl)Cl)C1C(=O)OCC1=CC=CC(OC=2C=CC=CC=2)=C1 RLLPVAHGXHCWKJ-UHFFFAOYSA-N 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- 239000001205 polyphosphate Substances 0.000 description 1
- 235000011176 polyphosphates Nutrition 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
- 239000005017 polysaccharide Substances 0.000 description 1
- 239000013641 positive control Substances 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 235000013772 propylene glycol Nutrition 0.000 description 1
- 125000001453 quaternary ammonium group Chemical group 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000009877 rendering Methods 0.000 description 1
- 230000001846 repelling effect Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 229960004793 sucrose Drugs 0.000 description 1
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Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/36—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/02—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing liquids as carriers, diluents or solvents
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/02—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing liquids as carriers, diluents or solvents
- A01N25/04—Dispersions, emulsions, suspoemulsions, suspension concentrates or gels
Landscapes
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Health & Medical Sciences (AREA)
- Dentistry (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Engineering & Computer Science (AREA)
- Agronomy & Crop Science (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Toxicology (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Chemical & Material Sciences (AREA)
- Dispersion Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
L
Use of natural and/or synthetic chinic acid and/or precursors thereof als insect repellents The present invention relates to an insect repellent against flying, creeping, biting and sucking insects and other related species of articulates (Arthropodes), like mites and ticks (Acarina), as well as spider animals (Arachnida). Such insect repellents are commonly called repellents.
Repellents are chemical substances having a repulsive effect on articulates, particularly on insects, which are noxious and pestering to man and animal.
Their use has a great practical importance in human and veterinary hygiene where they protect man and animal against attacks by bloodsucking, biting or otherwise annoying arthropodes. When repellents have to be applied directly to skin, coat or apparel it is required that these are well tolerated by skin, non-toxic, particularly not resorbable, perspiration and light save and perfect in cosmetic respect. Moreover, the protection of the treated skin areas is to be as broad as possible, i.e. they should act against the largest possible number of harmful and annoying insects.
The practical utilization of repellents and their benefit is exlained solely by the fact that statistically every thirty seconds a person dies from the consequences of insect bites and number and extent of all other consequential manifestations of attacks of insects to man and animal remain unrecordable by number. Therefore only the transfer of dangerous diseases like malaria, yellow fever, dengue fever and filariasis should be refered to as a causal factor for the benefit of repellents.
All repellents so far known present the common chemical-physical property of evaporating more or less quickly at room temperature whereas the intensity and duration of their protective effect depend essentially from two factors: 1. The more volatile a substance, the more intensive its protective effect, in particular shortly after application, however, the duration of its protection is proportionally shorter. In this respect, essential oils and natural compounds comprising these oils should be particularly mentioned and notice should be made how in earlier times they were the only repellents available, like i.e. garlic, pennyroyal oil and the juice of ripe tomatoes resp.
the essential oils citronella, bergamot, eucalyptus, lavender, clove, nutmeg, cinnamon and others.
2. The slower the evaporation proceeds at room temperature, the longer the protective effect lasts. In connection therewith, it should be taken into account that substances which do not evaporate to a sufficient extent cannot establish a durable protective shield capable to disturb to the attracting mechanism of the parasites. These compounds are ill appropriate when not totally unsuitable to be used as repellents.
S:
Consequently, the following ones of the extremely extensive group of repellent acting, synthetic compounds, which are essentially part of the compound classes of amides, alcohols, esters and ethers have proved to be particularly effective and have therefore prevailed on the market: N,Ndiethyl-m-toluamide (DEET), dimethylphthalate (DMP) and butylacetamido .i propionic acid ethyl ester (BAP, 3535) and combinations thereof. Other compounds are not enough effective or involve massive toxicological risks and are only ocasionnally to be found on the market or have already completely gone out. However, for some time past, the medical and in particular the dermatological experts have increasingly debated about the tolerance and the toxicological risks of the above mentioned synthetic repellent active substances since, for reason of their molecular structure, they are able to diffuse through the skin resp. to be resorbed by it.
Therefore, it would be advantageous if at least preferred embodiments of the present invention provide an effective insect repellent based on natural substances and on substances identical to natural substances presenting the minimal toxicological risk and having a high effectivity over a long period.
This may be achieved by the use of natural and/or synthetic chinic acid and/or precursors thereof. Preferably, the chinic acid is dissolved in at least one suitable, toxicologically harmless, natural and/or identical to natural and/or synthetic carrier.
Natural and/or synthetic chinic acid and/or precursors thereof can be used for the protection against creeping, biting, sucking and infecting parasites, particularly insects and related species.
The active substance used in the present invention is chinic acid (1 R; 3R, 4S, 5R)-(1,3,4,5,-tetrahydroxycyclohexane carbonic acid) with the
HO
structure HO COOH and the total formula C 7
H
12 0 6
OH
OH
The molecLilar weight is 192.17.
Preferably, the chinic acid is dissolved in a carrier of natural or synthetic origin, preferably water. The preferred amount of active agent is 0.1 to 50 wt.
of chinic acid in the carrier. An amount of 5 to 30 wt. of chinic acid is particularly preferred.
The carrier used in the present invention can be a mixture of different S. carriers. The use of a mixture of water with glycerol, alcohols or propane diols is particularly preferred. More particularly preferred is the use of a mixture of 0.1 to 50 wt. chinic acid in 50 to 99.1 wt. of a mixture of 0.1 to 99.9 wt. water and 0.1 to 99.9 wt. of the other carrier.
The chinic acid used is prepared according to known methods (extraction and recrystallisation) using its natural sources, chinic bark (Cortex Chinae), different species of chinona (Rubiaceae), coffee- beans, sugar-beets, meadow hay, gooseberrys and blackberrys as well as leafs of bilberrys and cranberrys. Chinic acid can also be prepared synthetically and used.
Precursors of chinic acid can also be used. A preferred precursor is their dehydrated form, the shikimi acid (3,4,5-trihydroxy-l-cyclohexane carbonic acid). In the following all these compounds will be designated chinic acid for simplicity.
In further preferred embodiments 0.1 to 50 wt. of chinic acid and 50 to 99.9 wt.% water, or 0.1 to 50 wt. chinic acid, dissolved in a mixture of glycerol and water or of 1,2-propylene glycol and water, are used. In this case, use of to 30 wt. of chinic acid is particularly preferred. The mixture ratios of the different carriers are as given generally above.
Moreover, chinic acid can be used in the form of an emulsion, dispersion, lotion, creme, gel or solution. For the preparation of these types of applications, the usual methods of preparation can be employed. The usual substances and additives can also be employed. These substances and additives comprise the typically used solvents, solvent accelerators, emulsifiers, solubilizers, wetting agents, anitfoamants, salt formers, buffers, gelatinizing agents, thickening agents, film-forming agents, binders, lubricants, detackifiers, flow regulation agents, humectants resp. desiccants, fillers as well as auxiliary agents, like antioxidants, preservatives, odor correctives and coloring agents.
The wording "emulsion" includes all dispersed systems of two or more liquids not miscible with each other whereby the emulsion components may be compounds solid at room temperature. These emulsions can be macro or micro emulsions. Typically, water-in-oil or oil-in-water emulsions may be used.
For the reduction of the interfacial surface work (work needed for the emulsification) emulsifiers are employed. Emulsifiers are usually surface active compounds, typically with hydrophilic end groups. Typical examples therof comprise: a) anionic emulsifiers, i.e. emulsifiers with carboxylic, sulfonic, sulfate, phosphate, polyphosphate, lactate, citrate, tartrate, glucose or polyglucose end groups; b) cationic emulsifiers, i.e. emulsifiers with amine salt or quaternary ammonium end groups; c) amphoteric and zwitterionic emulsifiers, i.e. emulsifiers with zwitterionic end groups or betain end groups; as well as d) non-ionic emulsifiers, i.e. emulsifiers with alcohol, polyether, glycerol, sorbitol, pentaerythritol, saccharose, acetic acid and/or lactic acid residues as end groups.
All emulsifiers contain additionally lipophilic end groups like alkyl or alkenyl rests, each of which are linear, branched or cyclic as well as aryl or alkylaryl residues.
Further hydrophilic side groups like hydroxyl, ester, sulfamide, amide, amine, polyamide, polyamine, ether, polyether, glycerol, sorbit, pentaerythrite or saccharose end groups can be comprised.
The wording "gels" includes form stable, easily deformable systems being rich in liquids of at least 2 components. Usually these two components are a) a liquid and b) a solid, colloid dispersed compound like gelatine, silicic acid, montmorillonites, bentonites, polysaccharides, polyacrylic acids, pectins etc.
According to the present invention, a completely harmless active substance prepared from natural raw materials is used which can be formulated in equally harmless, cosmetically and pharmaceutically well known and toxicologically totally safe solvents.
Additionally, the use according to the present invention offers in contrary to all other compounds known so far a completely new acting mechanism. This is not a mechanism based on a permanent evaporation cloud extending above the skin and masking the position receptors which are secreted from the skin, the effect of such a mechanism being subject to variations depending on the circumstances. The use of chinic acid according to the present invention blocks in a constant and permanent reaction with precursors permanently produced or secreted and being positioned on the skin and being soluble in the solvent of the repellent the formation of receptors on the skin, the coat or garments lying on top thereof indepently of variations of the surrounding conditions. Said precursors are e.g. ammonia, lactic and butyric acid, carbon dioxide and certain amino acids (like cystine and glutamine). It is thus not an evaporation cloud masking these already formed receptors formed which keeps off parasites but their formation on the skin is already prevented rendering the areas treated therewith unattractive for destructive insects.
The chinic acid used according to the present invention cannot for reason of 'its chemical and physical properties penetrate into the skin. Consequently threre exists no factor of risk for the health.
The following examples will explain the invention.
1. Examples of formulations for use of chinic acid according to the present invention TS 10.00 wt. chinic acid 20.0 wt. water 70.0 wt. 1,2,3-propanetriol (glycerol) TS (II) 5.00 wt. chinic acid a, 57.00wt. water 10.00 wt. Cetylstearyl-polyglycosides 28.00 wt. glycerol TS (III) 2.00 wt. chinic acid 3.00 wt. glycerol 2.00 wt. propane-1,2-diol (1,2-propylene glycol) 3.00 wt. ethanol (ethyl alcohol) 90.00 wt. water 2. Examples of application The repellents and (II) were tested with two different persons whereas a commercial product was used as reference (KIK AKTIV 30 DEET).
Experiment: The right forearm of a test person was treated on an area of about 250 cm 2 with the respective test compound TS or An amount of 2 ml of the respective test compound was equally spread. The treated area of the forearm was sealed on both ends with an insect save adhesive tape and provided with a short plastic tube. The untreated hand was covered with a thick glove and served thus at the same time as a control for the biting activity of the laboratory animals. The left forearm was treated in the same manner with a reference product (REF). As laboratory animals about 300 to 400 yellow fever insects (Aedes aegypti), almost exclusively little females, were employed in a breeding cage of 40x40x40 cm.
For the test, the forearms and the hands, successively, first the left then the right, were kept into the cage with insects and during 10 minutes, the number of insects which: C) a tried to bite through the glove (positive control), b flied closer than 3 cm towards the treated area, c landed and remained sit on the treated area longer than 2 seconds, and d bit into the treated area and sucked blood, was noted.
3. Results: Test person (1) time after duration landing on insects flying landing number of applica- of glove towards insects bites (d) tion exposure TS REF TS REF TS REF TS REF 1h 10min 100 100 0 0 0 0 0 0 2h 10min 100 100 0 0 0 0 0 0 3h 10min 100 100 0 0 0 0 0 0 4h 10min 100 100 0 2 0 0 0 0 10min 100 100 0 4 0 1 0 0 6h 10min 100 100 2 12 0 7 0 0 7h 10min 100 100 1 10 0 3 0 0 8h 10min 100 100 1 8 0 3 0 0 Test person (2) time after duration landing on insects flying landing number of applica- of glove towards insects bites (d) tion exposure TS REF TS REF TS REF TS REF lh 10min 100 100 0 0 0 0 0 0 2h 10min 100 100 0 0 0 0 0 0 3h 10min 100 100 0 0 0 0 0 0 4h 10min 100 100 5 3 1 1 0 0 10min 100 100 8 8 2 1 0 0 6h 10min 100 100 14 10 6 7 0 0 7h 10min 100 100 10 12 4 2 0 0 8h 10min 100 100 8 10 4 6 0 0 The number of insects landing on the gloves was estimated since due to the varying high numbers an exact evaluation was impossible.
The effectivity of a compound results primarily from the ratio of insects landing on the glove and willing to bite to the other values.
The number of biting insects is the decisive factor for the period of effectivity and therewith in the tropics indirectly also for the risk of infection. The tested compounds ensure protection for more than 8 hours. As can be taken from parameters b) and c) there is a certain number of insects even with the utilization of compounds used according to the present invention flying towards and landing; however, they do not bite. A strong repelling effect can be attributed to all tested compounds whereby the TEST PRODUCT (I) showed the best effect. Particularly, the extremely low number of insects flying towards and the fact that not a single insect landed shows the superior effect of the use of chinic acid according to the present invention having an amount of 10% of active substance vis-6-vis the commercial reference ~CrTr
,IV
compound having an amount of 30% of active substance. Therefore, the advantage of preventing the formation of receptors directly on the skin as compared with the covering of receptors is particularly clearly demonstrated.
Even TEST PRODUCT (11) with only one sixth of the content of active substance of the reference results in a comparable effect.
For the verification of these laboratory results a open land experiment was conducted with 20 test persons over a period of 5 days in a river meadow highly burdened with insects and gadflys.
The preparation of the test persons was effectued in the same manner as in the laboratory experiment. The persons who were to be submitted to the tests with insects were exposed exclusively from sunset on at temperatures of from 18 to 28 0 C, relative humidity of from 50 to 95% and wind speeds below 1 m/s and the persons to be submitted to the tests with gadflys were exposed exclusively during the day with the above conditions.
For each experiment, groups of five test persons were formed whereof one person served as an untreated control, 2 persons were treated with the TEST PRODUCT and 2 persons with the REFERENCE. The untreated control served as measurement for the willingness of insects or gadflys to bite and was exposed each time for one minute.
Average values were calculated for all experiments, whereby the insects landing on the gloves were estimated and the insects landing on the remaining protective garment of the test pesons were not taken into consideration.
ST i: L Test results INSECTS, particularly Culex pipiens 1. Average untreated control over 1 min. exposure landing on glove insects flying landing insects number of bites towards 42 42 42 2. Average REFERENCE, exposure 8 hours 10 minutes each, numbers refer to 10 minutes landing on glove insects flying landing insects number of bites towards 120 17 6 0 3. Average TEST PRODUCT exposure as 2.
landing on glove insects flying landing insects number of bites towards 130 4 0 0 The comparison over an average test time of 10 minutes shows that an untreated person would have been bitten theoretically 420 times during that time whereas both the REFERENCE and TP remained without bite.
In a comparison of REF and TP it is again noticeable that the TEST PRODUCT shows a rate of annoyance by far lower (numbers of insects flying towards and landing) and therewith the result of the laboratory experiments could be verified.
-o Test results GADFLYS, particularly Haematopoda pluvialis In this case, only the numbers of bites could be evaluated since gadflys fly towards an area in a stretch without particular search flight, land, bite, suck with lightning speed a drop of blood and start again.
Average of bites of gadflys at 1. untreated control over 1 min. exposure: 2 2. REFERENCE against TEST PRODUCT 10 min. exposure time/ hour, average of all test times 0 Gadfly bites at Time after application REF. TP (I) 1. hours 0.0 0.0 2. hours 0.0 0.0 3. hours 0.1 0.0 4. hours 1.0 0.0 hours 2.0 0.1 6. hours 3.0 This experiment undertaken 12 times during a cross test also shows that the effect of the test product used according to the present invention lasts at least about two hours longer than the effect of the reference commercial product.
For the examination of the effectivness of the repellent effect against ticks as a typical representative of Acarinae which are the by far most dangerous representatives of this genus a five days lasting open land test was conducted. From a house for the protection of animals three shepherd's dogs, male, of almost the same size and the same weight with three dog's masters were provided who walked the dogs daily each time for four hours INC3 through a known tick contaminated area. Constantly, on a daily basis each 1 dog was labelled with K (control), TP and REF. The dog and the leader belonging to it were each treated on the whole surface of their bodies with about 10 ml TEST PRODUCT and REFERENCE. An untreated dog served in each case as control whose masters, although inoculated against FSME, was treated with REFERENCE to encounter the risk of a transfer of borreliosis by possible tick bites.
After each four hour walk daily, the test animals and their masters were thorougly examined for the presence of ticks, these were documented and collected in labeled glasses and observed for another 72 hours.
Results: 1. untreated control during five experiment days 86 ticks, 68 thereof of the genus I.rizinus and 18 of R.sanguineus- whereby the respective stages (adults and nymphs) were not differentiated were found on the dogs. All ticks survived the 72 hours observation afterwards.
On the articles of clothing of the dog's masters, a total of 24 ticks were found, whereby, in comparison to the untreated dog, no tick could be found on the skin of the dog's master or bored into it. The 24 ticks survived the observation time afterwards as well.
2. REFERENCE on the dog a total of 6 ticks were found and on the clothing of the dog's master 19 ticks (adults and nymphs of 21 L.ritinus and 4 R.sanguineus) were found whereby, however, none of them were on the skin or bored into it. All ticks survived the 72 hours observation afterwards. The repellent time (duration of effect) of the reference product can therefore be given as 4 hours whereby, however, the total of 6 ticks would surely have bored into the coat of the dog with a decrease in effect of the product since they survived the observation time afterwards.
V!
3. TEST PRODUCT during the whole 5 days experiment time, no tick was found on the dog.
On the clothing of the dog's masters (all wearing a long-sleeved light shirt and white linen trousers) a total of 5 ticks of the genus I.rizinus were found, 3 of which did not survive the observation time.
After the 72 hours observation time, the total of 110 ticks of the untreated control and the ticks of test product (TP I) were immersed for 5 minutes into TEST PRODUCT according to the instructions of the immersion test of the ectoparasites screening and were all dead 24 hours later. The 25 ticks which survived the observation time of REFERENCE were immersed as above into the reference product for 5 min.and survived additional 72 hours and were then by immersion over 1 min. in TP after additional 24 hours classified as being dead.
That experiment demonstrated that TEST PRODUCT not only shows a protection period against ticks lasting at least 4 hours but also that the ticks were reliably killed after having been brought in contact with the product and that the latter is therefore superior to the ususal in trade, accepted reference as regards the absolute protective effect against tick bites.
As support for the surprisingly occuring mortal effect of the repellent used according to the present invention, the following screenings were conducted with different insects as follows: 1. TEST PRODUCT (111) in comparison with a 2. commercial insect repellent (REFERENCE) comprising as active substance according to the label 0.05 Bio Allethrin and 0.25 Permethrin in a watery emulsion.
j-?'AL 1 Acrylic tubs with L=50 cm, B=30 cm, D=25 cm, whose floors were painted I 1 i with each 1 ml TB (III) and REF, respectively, served as test containers. Both into the containers treated with TB (III) and into the containers treated with REF each 10 test insects were placed onto the floor and after 1 minute contact time transfered into an untreated container and observed for another 48 hours.
Test insects: I. cockroaches (Blatella germanica) II. ants (Lasius niger) Results: Both the test insects brought into contact with TP (III) and those brought into contact with REF were all dead after 48 hours. A further observation over 72 hours brought not any reanimation so that the use of chinic acid according to the present invention shows a comparable effect to the commercially accepted reference product.
In the claims which follow and in the preceding description of the invention, o. except where the context requires otherwise due to express language or necessary implication, the word "comprising", or grammatical variations thereof, S* is used in the sense of "including" i.e. the features specified may be associated with further features in various embodiments of the invention.
0 0
Claims (8)
1. Use of a natural and/or synthetic chinic acid (1,3,4,5-tetrahydroxycyclohexane carbonic acid) and/or shikimi acid as parasite repellents against flying, creeping, stinging, biting and sucking insects.
2. Use according to claim 1 characterized in that the chinic acid is dissolved in at least one appropriate carrier.
3. Use according to claim 2 characterized in that 0.1 to 50 wt.% of chinic acid is dissolved in 50 to 99.9 wt.% carrier.
4. Use according to any one of claims 2 and 3 characterized in that the carrier is water.
5. Use according to any one of claims 2 to 4 characterized in that glycerol, alcohols or propanediols are comprised.
6. Use according to claim 5 characterized in that o* 2 0.1 to 50 wt.% chinic acid, 0.1 to 99.8 wt.% water and 0.1 20 to 99.8 wt.% of a further carrier are comprised. S:
7. Use according to any of claims 1 to 6 in form of emulsions, dispersion, lotions, cremes, gels or solutions.
8. Use of natural and/or synthetic chinic acid (1,3,4,5-tetrahydroxycyclohexane carbonic acid) and/or 25 shikimi acid as parasite repellents against flying, creeping, stinging, biting and sucking insects substantially as herein described with reference to any one of the examples.. Dated this 4th day of January 2002 BIOLINK TECHNOLOGIES AG By their Patent Attorneys GRIFFITH HACK Fellows Institute of Patent and Trade Mark Attorneys of Australia H:\suzannet\Keep\Speci\35203-99.1 CLAIMS.doc 4/01/02
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19812927 | 1998-03-24 | ||
| DE1998112927 DE19812927C1 (en) | 1998-03-24 | 1998-03-24 | Repelling flying, crawling, piercing, biting and sucking pests, including disease vectors such as mosquitoes, from humans and animals |
| PCT/EP1999/001931 WO1999048363A1 (en) | 1998-03-24 | 1999-03-22 | Utilization of natural and/or synthetic quinic acid and/or precursors thereof as insect repellents |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| AU3520399A AU3520399A (en) | 1999-10-18 |
| AU746660B2 true AU746660B2 (en) | 2002-05-02 |
Family
ID=7862140
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU35203/99A Ceased AU746660B2 (en) | 1998-03-24 | 1999-03-22 | Utilization of natural and/or synthetic quinic acid and/or precursors thereof as insect repellents |
Country Status (10)
| Country | Link |
|---|---|
| EP (1) | EP1065926A1 (en) |
| JP (1) | JP2002507549A (en) |
| KR (1) | KR20010034611A (en) |
| CN (1) | CN1298279A (en) |
| AU (1) | AU746660B2 (en) |
| BR (1) | BR9909152A (en) |
| CA (1) | CA2325372A1 (en) |
| DE (1) | DE19812927C1 (en) |
| NO (1) | NO20004708L (en) |
| WO (1) | WO1999048363A1 (en) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE19812927C1 (en) * | 1998-03-24 | 1999-08-12 | Straight Ag | Repelling flying, crawling, piercing, biting and sucking pests, including disease vectors such as mosquitoes, from humans and animals |
| DE19825605A1 (en) * | 1998-06-08 | 1999-12-09 | Straight Ag Zuerich | Use of at least one acid of the citric acid cycle in combination with glycerin as a pesticide |
| DE19961812A1 (en) * | 1999-12-21 | 2001-07-05 | Biolink Technologies Ag Neuhau | Use of at least one fatty acid polydialkanolamide in combination with quinic acid and / or shikimi acid for pest control |
| WO2017027606A1 (en) | 2015-08-10 | 2017-02-16 | Beem Biologics Inc. | Compositions and their use for pest control and to induce plant hormone and gene regulation for improved plant production and defense |
| WO2024038063A1 (en) * | 2022-08-16 | 2024-02-22 | South China Botanical Garden | Pesticidal compositions |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS61291507A (en) * | 1985-06-19 | 1986-12-22 | Hakuyo Kosan Kk | Rodent repellent |
| DE19812927C1 (en) * | 1998-03-24 | 1999-08-12 | Straight Ag | Repelling flying, crawling, piercing, biting and sucking pests, including disease vectors such as mosquitoes, from humans and animals |
-
1998
- 1998-03-24 DE DE1998112927 patent/DE19812927C1/en not_active Expired - Fee Related
-
1999
- 1999-03-22 BR BR9909152-6A patent/BR9909152A/en not_active IP Right Cessation
- 1999-03-22 WO PCT/EP1999/001931 patent/WO1999048363A1/en not_active Ceased
- 1999-03-22 JP JP2000537429A patent/JP2002507549A/en active Pending
- 1999-03-22 CN CN 99805594 patent/CN1298279A/en active Pending
- 1999-03-22 KR KR1020007010463A patent/KR20010034611A/en not_active Ceased
- 1999-03-22 EP EP99916865A patent/EP1065926A1/en not_active Withdrawn
- 1999-03-22 CA CA002325372A patent/CA2325372A1/en not_active Abandoned
- 1999-03-22 AU AU35203/99A patent/AU746660B2/en not_active Ceased
-
2000
- 2000-09-20 NO NO20004708A patent/NO20004708L/en unknown
Non-Patent Citations (1)
| Title |
|---|
| COLE RA ET AL. ANN. APPL. BIOL. (1989) 115, 39-44 * |
Also Published As
| Publication number | Publication date |
|---|---|
| CA2325372A1 (en) | 1999-09-30 |
| JP2002507549A (en) | 2002-03-12 |
| CN1298279A (en) | 2001-06-06 |
| DE19812927C1 (en) | 1999-08-12 |
| EP1065926A1 (en) | 2001-01-10 |
| WO1999048363A1 (en) | 1999-09-30 |
| NO20004708L (en) | 2000-11-24 |
| BR9909152A (en) | 2000-11-28 |
| NO20004708D0 (en) | 2000-09-20 |
| AU3520399A (en) | 1999-10-18 |
| KR20010034611A (en) | 2001-04-25 |
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