JP2021516659A - 抗菌組成物 - Google Patents
抗菌組成物 Download PDFInfo
- Publication number
- JP2021516659A JP2021516659A JP2020536579A JP2020536579A JP2021516659A JP 2021516659 A JP2021516659 A JP 2021516659A JP 2020536579 A JP2020536579 A JP 2020536579A JP 2020536579 A JP2020536579 A JP 2020536579A JP 2021516659 A JP2021516659 A JP 2021516659A
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- JP
- Japan
- Prior art keywords
- composition
- effective amount
- alternatively
- antibacterial
- antibacterial effect
- Prior art date
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- 108090000623 proteins and genes Proteins 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
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- 239000012429 reaction media Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 230000010076 replication Effects 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 238000012552 review Methods 0.000 description 1
- 239000006254 rheological additive Substances 0.000 description 1
- 230000035807 sensation Effects 0.000 description 1
- 235000019615 sensations Nutrition 0.000 description 1
- 238000013207 serial dilution Methods 0.000 description 1
- 239000002884 skin cream Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000001694 spray drying Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 230000001954 sterilising effect Effects 0.000 description 1
- 238000004659 sterilization and disinfection Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 230000001629 suppression Effects 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- QJVXKWHHAMZTBY-GCPOEHJPSA-N syringin Chemical compound COC1=CC(\C=C\CO)=CC(OC)=C1O[C@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 QJVXKWHHAMZTBY-GCPOEHJPSA-N 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- CRDAMVZIKSXKFV-UHFFFAOYSA-N trans-Farnesol Natural products CC(C)=CCCC(C)=CCCC(C)=CCO CRDAMVZIKSXKFV-UHFFFAOYSA-N 0.000 description 1
- URAYPUMNDPQOKB-UHFFFAOYSA-N triacetin Chemical compound CC(=O)OCC(OC(C)=O)COC(C)=O URAYPUMNDPQOKB-UHFFFAOYSA-N 0.000 description 1
- ICUTUKXCWQYESQ-UHFFFAOYSA-N triclocarban Chemical compound C1=CC(Cl)=CC=C1NC(=O)NC1=CC=C(Cl)C(Cl)=C1 ICUTUKXCWQYESQ-UHFFFAOYSA-N 0.000 description 1
- 229960001325 triclocarban Drugs 0.000 description 1
- 239000001069 triethyl citrate Substances 0.000 description 1
- VMYFZRTXGLUXMZ-UHFFFAOYSA-N triethyl citrate Natural products CCOC(=O)C(O)(C(=O)OCC)C(=O)OCC VMYFZRTXGLUXMZ-UHFFFAOYSA-N 0.000 description 1
- 235000013769 triethyl citrate Nutrition 0.000 description 1
- 150000004043 trisaccharides Chemical class 0.000 description 1
- 239000006150 trypticase soy agar Substances 0.000 description 1
- MWOOGOJBHIARFG-UHFFFAOYSA-N vanillin Chemical compound COC1=CC(C=O)=CC=C1O MWOOGOJBHIARFG-UHFFFAOYSA-N 0.000 description 1
- FGQOOHJZONJGDT-UHFFFAOYSA-N vanillin Natural products COC1=CC(O)=CC(C=O)=C1 FGQOOHJZONJGDT-UHFFFAOYSA-N 0.000 description 1
- 235000012141 vanillin Nutrition 0.000 description 1
- 239000012808 vapor phase Substances 0.000 description 1
- RGVQNSFGUOIKFF-UHFFFAOYSA-N verdyl acetate Chemical compound C12CC=CC2C2CC(OC(=O)C)C1C2 RGVQNSFGUOIKFF-UHFFFAOYSA-N 0.000 description 1
- 239000004034 viscosity adjusting agent Substances 0.000 description 1
- 239000011782 vitamin Substances 0.000 description 1
- 229940088594 vitamin Drugs 0.000 description 1
- 229930003231 vitamin Natural products 0.000 description 1
- 235000013343 vitamin Nutrition 0.000 description 1
- 239000000341 volatile oil Substances 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 239000010457 zeolite Substances 0.000 description 1
- 229930007845 β-thujaplicin Natural products 0.000 description 1
Images
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- 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
- A01N49/00—Biocides, pest repellants or attractants, or plant growth regulators, containing compounds containing the group, wherein m+n>=1, both X together may also mean —Y— or a direct carbon-to-carbon bond, and the carbon atoms marked with an asterisk are not part of any ring system other than that which may be formed by the atoms X, the carbon atoms in square brackets being part of any acyclic or cyclic structure, or the group, wherein A means a carbon atom or Y, n>=0, and not more than one of these carbon atoms being a member of the same ring system, e.g. juvenile insect hormones or mimics thereof
-
- 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
- A01N31/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic oxygen or sulfur compounds
- A01N31/04—Oxygen or sulfur attached to an aliphatic side-chain of a carbocyclic ring system
-
- A—HUMAN NECESSITIES
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- 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
- A01N31/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic oxygen or sulfur compounds
- A01N31/02—Acyclic compounds
-
- 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
- A01N31/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic oxygen or sulfur compounds
- A01N31/06—Oxygen or sulfur directly attached to a cycloaliphatic ring system
-
- 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
- A01N31/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic oxygen or sulfur compounds
- A01N31/08—Oxygen or sulfur directly attached to an aromatic ring system
-
- 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
- A01N31/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic oxygen or sulfur compounds
- A01N31/08—Oxygen or sulfur directly attached to an aromatic ring system
- A01N31/16—Oxygen or sulfur directly attached to an aromatic ring system with two or more oxygen or sulfur atoms directly attached to the same aromatic ring system
-
- 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
- A01N35/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having two bonds to hetero atoms with at the most one bond to halogen, e.g. aldehyde radical
- A01N35/04—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having two bonds to hetero atoms with at the most one bond to halogen, e.g. aldehyde radical containing aldehyde or keto groups, or thio analogues thereof, directly attached to an aromatic ring system, e.g. acetophenone; Derivatives thereof, e.g. acetals
-
- 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
- A01N37/02—Saturated carboxylic acids or thio analogues thereof; Derivatives thereof
-
- 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
- A01N43/04—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom
- A01N43/06—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings
- A01N43/08—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings with oxygen as the ring hetero atom
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- 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
- A01N43/04—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom
- A01N43/14—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom six-membered rings
- A01N43/16—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom six-membered rings with oxygen as the ring hetero atom
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- A—HUMAN NECESSITIES
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- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
- A01N43/24—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with two or more hetero atoms
- A01N43/26—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with two or more hetero atoms five-membered rings
- A01N43/28—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with two or more hetero atoms five-membered rings with two hetero atoms in positions 1,3
- A01N43/30—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with two or more hetero atoms five-membered rings with two hetero atoms in positions 1,3 with two oxygen atoms in positions 1,3, condensed with a carbocyclic ring
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Abstract
Description
本出願は、2018年3月20日に提出された国際特許出願番号PCT/CN2018/079526の優先権を主張し、その内容全体が、全体として参照により本明細書に組み込まれる。
本開示は、抗菌組成物および抗菌剤としてのその使用、または抗菌活性香料組成物およびコンシューマー製品の製造のためのその使用の分野に関する。
衛生は、その最も完全な意味では、単なる「清潔さ」を超えて、製品、プロセスおよびデバイスに加えて、安全で健康的な環境を生じさせかつ育む全ての環境および実践、ライフスタイル習慣および前提を含む広大な主題である。特に、衛生は、健康を維持しかつ疾病の蔓延を妨げるための助けとなる条件および実践を指し、したがって、この健康の維持に関連する実践の具体的なセット、たとえば環境の清浄化、器機、手指衛生、水および衛生設備の滅菌または医療廃棄物の安全な処分を含む。
一態様では、本開示は、香料成分を含む組成物を提供し、この組成物は、以下からなる群から選択される:
i. 3−(1,3−ベンゾジオキソール−5−イル)−2−メチルプロパナール(以後「ヘリオプロパナール」)、(Z)−3,7−ジメチル−2,6−オクタジエン−1−オール(以後「ネロール」)、フェニルヘキサノール、および3,7−ジメチル−3−オクタノール(以後「テトラリノール」);
ii. 4−メトキシベンズアルデヒド(以後「アニスアルデヒド」)、1,3−ベンゾジオキソール−5−カルバルデヒド(以後「ヘリオトロピン」)、および2−(4−メチルシクロヘキサ−3−エン−1−イル)プロパン−2−オール(以後「テルピネオール」);
iii. アニスアルデヒド、ヘリオトロピン、テルピネオール、およびヘリオプロパナール;
iv. γ−ドデカラクトン(以後「デカール」)、2−メトキシ−4−(プロパ−1−エン−1−イル)フェノール(以後「イソオイゲノール」)、(S)−(−)−(4−イソプロペニル−1−シクロヘキセニル)メタノール(以後「ペリコロール」)、およびテトラリノール;
v. フェニルヘキサノール、テルピネオール、およびイソオイゲノール;
vi. フェニルヘキサノール、テルピネオール、イソオイゲノール、および2H−クロメン−2−オン(以後「クマリン」);
vii. 2−メトキシ−4−(プロパ−2−エン−1−イル)フェノール(以後「オイゲノールF」)、フェニルヘキサノール、およびジメチルフェニルエチルカルビノール(以後「カルビノールミュゲ」);および
viii. オイゲノールF、フェニルヘキサノール、カルビノールミュゲ、および酢酸ベンジル、
ここで、これらの香料成分は、抗菌効果を提供するために十分な量で組成物中に存在する。
以下の説明では、例により示されている、実施することができる具体的な実施態様を参照する。これらの実施態様は、当業者が、ここに記載された発明を実施することができるほど詳細に記載されており、他の実施態様が利用されてよく、ここに示された態様の範囲から逸脱することなく論理的な変更を行ってよいと解釈される。したがって、例示的な実施態様の以下の記載は、限定的な意味にとるべきでなく、ここに示された多様な態様の範囲は、添付の特許請求の範囲によって定義される。
D=Dm[fa/(1−fa)]l/m
式中、
Dは、一定程度の効果(fa)を有する用量であり;
Dmは、50%効果用量であり;
mは、用量−効果の関係の形を表す係数である。
Dは、x%の効果を有する「単独の」薬剤jであり、
Djは、x%の効果を有する「組み合わせた」薬剤jの用量である。
i. ヘリオプロパナール、ネロール、フェニルヘキサノール、およびテトラリノール;
ii. アニスアルデヒド、ヘリオトロピン、およびテルピネオール;
iii. アニスアルデヒド、ヘリオトロピン、テルピネオール、およびヘリオプロパナール;
iv. デカール、イソオイゲノール、ペリコロール、およびテトラリノール;
v. フェニルヘキサノール、テルピネオール、およびイソオイゲノール;
vi. フェニルヘキサノール、テルピネオール、イソオイゲノール、およびクマリン;
vii. オイゲノールF、フェニルヘキサノール、およびカルビノールミュゲ;および
viii. オイゲノールF、フェニルヘキサノール、カルビノールミュゲ、および酢酸ベンジル、
ここで、これらの香料成分は、抗菌効果を提供するために十分な量で組成物中に存在する。
i. ヘリオプロパナール、ネロール、フェニルヘキサノール、およびテトラリノール;
ii. アニスアルデヒド、ヘリオトロピン、およびテルピネオール;
iii. アニスアルデヒド、ヘリオトロピン、テルピネオール、およびヘリオプロパナール;
iv. デカール、イソオイゲノール、ペリコロール、およびテトラリノール;
v. フェニルヘキサノール、テルピネオール、およびイソオイゲノール;
vi.フェニルヘキサノール、テルピネオール、イソオイゲノール、およびクマリン;
vii. オイゲノールF、フェニルヘキサノール、およびカルビノールミュゲ;および
viii. オイゲノールF、フェニルヘキサノール、カルビノールミュゲ、および酢酸ベンジル、
ここで、これらの香料成分は、抗菌効果を提供するために十分な量で組成物中に存在する。
・ アルデヒド成分: デカナール、ドデカナール、2−メチル−ウンデカナール、10−ウンデセナール、オクタナールおよび/またはノネナール;
・ 芳香性薬草成分:ユーカリ油、カンファー、ユーカリプトール、メントールおよび/またはα−ピネン;
・ バルサム成分: クマリン、エチルバニリンおよび/またはバニリン;
・ シトラス成分:ジヒドロミルセノール、シトラール、オレンジ油、酢酸リナリル、シトロネリルニトリル、オレンジテルペン、リモネン、1−P−メンテン−8−イルアセテートおよび/または1,4(8)−P−メタンジエン;
・ フローラル成分:ジヒドロジャスモン酸メチル、リナロール、シトロネロール、フェニルエタノール、3−(4−tert−ブチルフェニル)−2−メチルプロパナール、ヘキシルシンナムアルデヒド、酢酸ベンジル、サリチル酸ベンジル、テトラヒドロ−2−イソブチル−4−メチル−4(2H)−ピラノール、β−イオノン、2−(メチルアミノ)安息香酸メチル、(E)−3−メチル−4−(2,6,6−トリメチル−2−シクロヘキセン−1−イル)−3−ブテン−2−オン、サリチル酸ヘキシル、3,7−ジメチル−1,6−ノナジエン−3−オール、3−(4−イソプロピルフェニル)−2−メチルプロパナール、酢酸ベルジル(verdyl acetate)、ゲラニオール、P−メンタ−1−エン−8−オール、4−(1,1−ジメチルエチル)−1−シクロヘキシルアセテート、1,1−ジメチル−2−フェニルエチルアセテート、4−シクロヘキシル−2−メチル−2−ブタノール、サリチル酸アミル、高シス型のジヒドロジャスモン酸メチル、3−メチル−5−フェニル−1−ペンタノール、プロピオン酸ベルジル(verdyl proprionate)、酢酸ゲラニル、テトラヒドロリナロール、シス−7−P−メンタノール、プロピル(S)−2−(1,1−ジメチルプロポキシ)プロパノアート、2−メトキシナフタレン、2,2,2−トリクロロ−1−フェニルエチルアセテート、4/3−(4−ヒドロキシ−4−メチルペンチル)−3−シクロヘキセン−1−カルバルデヒド、アミルシンナムアルデヒド、4−フェニル−2−ブタノン、酢酸イソノニル、4−(1,1−ジメチルエチル)−1−シクロヘキシルアセテート、イソブチル酸ベルジル(verdyl isobutyrate)および/またはメチルイオノン異性体の混合物;
・ フルーティ成分:ガンマ ウンガンマ−ドデカラクトンアセトン、4−デカノリド、エチル2−メチル−ペンタノアート、酢酸ヘキシル、エチル2−メチルブタノアート、γ−ノナラクトン、アリルヘプタノアート、2−フェノキシエチルイソブチラート、エチル2−メチル−1,3−ジオキソラン−2−アセテートおよび/またはジエチル1,4−シクロヘキサンジカルボキシラート;
・ グリーン成分:2,4−ジメチル−3−シクロヘキセン−1−カルバルデヒド、2−tert−ブチル−1−シクロヘキシルアセテート、スチルアリルアセテート、アリル(2−メチルブトキシ)アセテート、4−メチル−3−デセン−5−オール、ジフェニルエーテル、(Z)−3−ヘキセン−1−オールおよび/または1−(5,5−ジメチル−1−シクロヘキセン−1−イル)−4−ペンテン−1−オン;
・ ムスク成分:1,4−ジオキサ−5,17−シクロペンタデカンジオン、ペンタデセノリド、3−メチル−5−シクロペンタデセン−1−オン、1,3,4,6,7,8−ヘキサヒドロ−4,6,6,7,8,8−ヘキサメチル−シクロペンタ−g−2−ベンゾピラン、(1S,1′R)−2−[1−(3′,3′−ジメチル−1′−シクロヘキシル)エトキシ]−2−メチルプロピルプロパノアート、ペンタデカノリドおよび/または(1S,1′R)−[1−(3′,3′−ジメチル−1′−シクロヘキシル)エトキシカルボニル]メチルプロパノアート;
・ ウッディ成分:1−(オクタヒドロ−2,3,8,8−テトラメチル−2−ナフタレニル)−1−エタノン、パチュリ油、パチュリ油のテルペン画分、(1′R,E)−2−エチル−4−(2′,2′,3′−トリメチル−3′−シクロペンテン−1′−イル)−2−ブテン−1−オール、2−エチル−4−(2,2,3−トリメチル−3−シクロペンテン−1−イル)−2−ブテン−1−オール、メチルセドリルケトン、5−(2,2,3−トリメチル−3−シクロペンテニル)−3−メチルペンタン−2−オール、1−(2,3,8,8−テトラメチル−1,2,3,4,6,7,8,8a−オクタヒドロナフタレン−2−イル)エタン−1−オンおよび/または酢酸イソボルニル;
・ 他の成分(たとえばアンバー、パウダリースパイシーまたはウォータリー):ドデカヒドロ−3a,6,6,9a−テトラメチル−ナフト[2,1−b]フランおよびその任意の立体異性体、ヘリオトロピン、アニスアルデヒド、オイゲノール、シンナムアルデヒド、チョウジ油、3−(1,3−ベンゾジオキソール−5−イル)−2−メチルプロパナールおよび/または3−(3−イソプロピル−1−フェニル)ブタナール。
実施例1:細菌懸濁液の準備およびBCT試験
C.キセロシス(C. xerosis):C.キセロシス(C. xerosis)ATCC 373株の懸濁液を以下のように準備した:保存培養(−80℃で保存)を解凍し、0.5%Tween80を有するトリプティックソイ寒天培地(TSA−TW80)上で継代培養し、37℃で48hインキュベートした。初代培養を、TSA−TW80上で再び継代培養し、二次培養を準備した。二次培養の単一コロニーを選択し、0.5%Tween80を有するブレインハートインフュージョンブロス(BHI−TW80)30mlに接種するために使用した。接種したブロスを、37℃で180rpmで24hインキュベートした。24h培養のアリコート(1ml)を、新しいBHI−TW80ブロス培地30ml内に接種し、37℃で180rpmで48hインキュベートした。48h培養のアリコート(2〜3ml)を、4つの新しいBHI−TW80ブロス培地50ml内に接種し、37℃で180rpmで4〜6hインキュベートした。OD600nmが1.6の目標値に到達した際に、細胞を5000rpmで10分間遠心分離により収穫し、次いで109〜1010cfu/mLの濃度で同じ新しいBHI−TW80内に再懸濁させた。この懸濁液を、BCT試験のための細菌懸濁液として使用した。
実施例3:デオドラントベース中の「A4」で示された組成物のインビボ効果
Claims (15)
- 組成物であって、
前記組成物は香料成分を含み;
前記組成物は、
i. ヘリオプロパナール、ネロール、フェニルヘキサノール、およびテトラリノール;
ii. アニスアルデヒド、ヘリオトロピン、およびテルピネオール;
iii. アニスアルデヒド、ヘリオトロピン、テルピネオール、およびヘリオプロパナール;
iv. デカール、イソオイゲノール、ペリコロール、およびテトラリノール;
v. フェニルヘキサノール、テルピネオール、およびイソオイゲノール;
vi. フェニルヘキサノール、テルピネオール、イソオイゲノール、およびクマリン;
vii. オイゲノールF、フェニルヘキサノール、およびカルビノールミュゲ;および
viii. オイゲノールF、フェニルヘキサノール、カルビノールミュゲ、および酢酸ベンジル、
からなる群から選択され、
前記香料成分は、抗菌効果を提供するために十分な量で前記組成物中に存在する、組成物。 - 微生物を含む基材を、抗菌効果を提供するための有効量の請求項1記載の組成物で処理することを含む、方法。
- ヘリオプロパナール、ネロール、フェニルヘキサノール、およびテトラリノールの比率が、6:3:5:6である、請求項1記載の組成物。
- アニスアルデヒド、ヘリオトロピン、およびテルピネオールの比率が、13:20:3である、請求項1記載の組成物。
- アニスアルデヒド、ヘリオトロピン、テルピネオール、およびヘリオプロパナールの比率が、13:20:3:20である、請求項1記載の組成物。
- デカール、イソオイゲノール、ペリコロール、およびテトラリノールの比率が、2:1:5:2である、請求項1記載の組成物。
- フェニルヘキサノール、テルピネオール、およびイソオイゲノールの比率が、2:5:5である、請求項1記載の組成物。
- フェニルヘキサノール、テルピネオール、イソオイゲノール、およびクマリンの比率が、5:1:1:2である、請求項1記載の組成物。
- オイゲノールF、フェニルヘキサノール、およびカルビノールミュゲの比率が、1:5:10である、請求項1記載の組成物。
- オイゲノールF、フェニルヘキサノール、カルビノールミュゲ、および酢酸ベンジルの比率が、1:5:10:10である、請求項1記載の組成物。
- 香料担体、香料補助成分、およびこれら混合物、ならびに任意に少なくとも一つの香料助剤からなる群から選択される少なくとも一つの成分をさらに含む、請求項1記載の組成物。
- 前記組成物が、香料、ファブリックケア製品、ボディケア製品、化粧品、スキンケア製品、エアケア製品、およびホームケア製品からなる群から選択されるコンシューマー製品として配合される、請求項1記載の組成物。
- 前記コンシューマー製品が、ファインパフューム、スプラッシュもしくはオードパフューム、コロン、シェービングもしくはアフターシェービングローション、液体もしくは固形洗剤、ファブリック柔軟剤、ファブリックリフレッシャー、アイロン水、紙、漂白剤、カーペットクリーナー、カーテンケア製品、シャンプー、カラーリング調製剤、カラーケア製品、ヘアシェイプ製品、デンタルケア製品、消毒剤、インティメートケア製品、ヘアスプレー、バニッシングクリーム、デオドラントもしくは制汗剤、脱毛剤、タンニングもしくは日焼け製品、ネイル製品、スキンクレンジング、メーキャップ、賦香石鹸、シャワーもしくはバスムース、オイルもしくはジェル、またはフット/ハンドケア製品、衛生製品、エアフレッシュナー、「すぐに使える」粉末エアフレッシュナー、カビ取り剤、家具ケア、拭き取り用品、食器用洗剤もしくは硬質表面用洗剤、レザーケア製品、カーケア製品からなる群から選択される、請求項12記載の組成物。
- 前記組成物が、細菌細胞の不活性化による抗菌効果を提供する、請求項1記載の組成物。
- 前記抗菌効果が、コリネバクテリウム・キセロシス(Corynebacterium xerosis)、シュードモナス・エルギノーザ(Pseudomonas aeruginosa)、サモネラ・エンテリカ(Salmonella enterica)、スタフィロコッカス・ヘモリチカス(Staphylococcus haemolyticus)、スタフィロコッカス・アウレウス(Staphylococcus aureus)およびエシェリキア・コリ(Escherichia coli)からなる群から選択される細菌株の増殖阻害である、請求項14記載の組成物。
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Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2003510343A (ja) * | 1999-10-04 | 2003-03-18 | フイルメニツヒ ソシエテ アノニム | 抗菌性付香組成物 |
JP2004513153A (ja) * | 2000-11-09 | 2004-04-30 | イェルク・ペーター・シューア | Gras香料またはその誘導体を含む殺菌性組成物を含有する薬物 |
JP2009132665A (ja) * | 2007-12-03 | 2009-06-18 | Kao Corp | 非接触型防カビ剤組成物 |
JP2010530855A (ja) * | 2007-06-22 | 2010-09-16 | ジボダン エス エー | 桂皮酸またはアニス酸およびベンズアルデヒド(誘導体)を含む保存料非含有の組成物 |
WO2018024886A2 (en) * | 2016-08-05 | 2018-02-08 | Firmenich Sa | Antimicrobial composition |
Family Cites Families (20)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH05271073A (ja) | 1992-02-10 | 1993-10-19 | Takasago Internatl Corp | 抗緑膿菌剤 |
CH690263A5 (fr) * | 1996-04-03 | 2000-06-30 | Firmenich & Cie | Composition parfumante présentant une activité antimicrobienne et procédé de parfumage. |
EP0841391A1 (en) * | 1996-11-07 | 1998-05-13 | The Procter & Gamble Company | Perfume compositions |
US5861546A (en) * | 1997-08-20 | 1999-01-19 | Sagi; Nehemiah Hemi | Intelligent gas flow measurement and leak detection apparatus |
US6319958B1 (en) * | 1998-06-22 | 2001-11-20 | Wisconsin Alumni Research Foundation | Method of sensitizing microbial cells to antimicrobial compound |
FR2801811B1 (fr) | 1999-12-06 | 2002-05-03 | Gerard Habar | Procede de fabrication de microcapsules portant des charges cationiques |
US6495512B1 (en) * | 2000-06-23 | 2002-12-17 | International Flavors & Fragrances Inc. | Salicylaldehyde-containing composition having antimicrobial and fragrancing properties and process for using same |
JP2004018470A (ja) * | 2002-06-18 | 2004-01-22 | Takasago Internatl Corp | 抗菌香料組成物および口臭抑制香料組成物ならびにそれらを含有する口腔用組成物 |
US7655613B2 (en) * | 2004-10-20 | 2010-02-02 | Firmenich Sa | Solubilizing systems for flavors and fragrances |
WO2005079573A1 (en) | 2004-02-24 | 2005-09-01 | Givaudan Sa | Antifungal compositions |
GB0425305D0 (en) * | 2004-11-17 | 2004-12-15 | Givaudan Sa | Bactericidal formulations |
US20080253976A1 (en) * | 2007-04-16 | 2008-10-16 | Douglas Craig Scott | Personal Care Compositions Comprising An Antimicrobial Blend of Essential Oils or Constituents Thereof |
US8362077B2 (en) * | 2008-08-15 | 2013-01-29 | Pibed Limited | Chemical compositions for skin care emulsions and heavy duty hand cleansers |
CA2801143C (en) | 2009-09-24 | 2017-09-26 | Unilever Plc | Disinfecting agent comprising eugenol, terpineol and thymol |
BR112013018933A2 (pt) * | 2011-02-10 | 2016-09-13 | Unilever Nv | composições antiviral, antisséptica líquida, e sólida para a lavagem pessoal, de limpeza sólida e líquida da superfície rígida, antimicrobiana, higienizadora de mãos, método de desinfecção de uma superfície e utilização de uma composição |
MX354483B (es) | 2011-12-06 | 2018-03-07 | Unilever Nv | Composición antimicrobiana. |
EP2759199A1 (en) * | 2013-01-28 | 2014-07-30 | Unilever N.V. | A method of providing antimicrobial action and a synergistic antimicrobial composition thereof |
CA2974825C (en) * | 2015-02-02 | 2023-08-01 | Johnson & Johnson Consumer Inc. | Perfume compositions |
CN106109263B (zh) * | 2016-07-06 | 2018-11-13 | 上海应用技术学院 | 一种长效留香东方花香型香水及其制备方法 |
JP7038718B2 (ja) * | 2016-12-22 | 2022-03-18 | フイルメニツヒ ソシエテ アノニム | 密度均衡化された、影響力の大きい香料マイクロカプセル |
-
2019
- 2019-03-18 WO PCT/EP2019/056727 patent/WO2019179953A2/en unknown
- 2019-03-18 JP JP2020536579A patent/JP7520715B2/ja active Active
- 2019-03-18 CN CN202210112745.1A patent/CN114586782B/zh active Active
- 2019-03-18 US US16/954,332 patent/US11785945B2/en active Active
- 2019-03-18 CN CN201980010972.XA patent/CN111669971B/zh active Active
- 2019-03-18 EP EP19717759.5A patent/EP3706573A2/en active Pending
- 2019-03-18 CN CN202410326128.0A patent/CN118415168A/zh active Pending
-
2023
- 2023-09-11 US US18/244,377 patent/US20240000078A1/en active Pending
-
2024
- 2024-02-26 JP JP2024026615A patent/JP2024063074A/ja active Pending
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2003510343A (ja) * | 1999-10-04 | 2003-03-18 | フイルメニツヒ ソシエテ アノニム | 抗菌性付香組成物 |
JP2004513153A (ja) * | 2000-11-09 | 2004-04-30 | イェルク・ペーター・シューア | Gras香料またはその誘導体を含む殺菌性組成物を含有する薬物 |
JP2010530855A (ja) * | 2007-06-22 | 2010-09-16 | ジボダン エス エー | 桂皮酸またはアニス酸およびベンズアルデヒド(誘導体)を含む保存料非含有の組成物 |
JP2009132665A (ja) * | 2007-12-03 | 2009-06-18 | Kao Corp | 非接触型防カビ剤組成物 |
WO2018024886A2 (en) * | 2016-08-05 | 2018-02-08 | Firmenich Sa | Antimicrobial composition |
Non-Patent Citations (1)
Title |
---|
BIOLOGICAL AND PHARMACEUTICAL BULLETIN, vol. 32, no. 6, JPN6023009377, 2009, pages 1114 - 1117, ISSN: 0005179781 * |
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