JP6817225B2 - 液状冷却組成物 - Google Patents
液状冷却組成物 Download PDFInfo
- Publication number
- JP6817225B2 JP6817225B2 JP2017559418A JP2017559418A JP6817225B2 JP 6817225 B2 JP6817225 B2 JP 6817225B2 JP 2017559418 A JP2017559418 A JP 2017559418A JP 2017559418 A JP2017559418 A JP 2017559418A JP 6817225 B2 JP6817225 B2 JP 6817225B2
- Authority
- JP
- Japan
- Prior art keywords
- menthol
- acid
- weight
- acetate
- composition
- 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.)
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- NOOLISFMXDJSKH-UHFFFAOYSA-N DL-menthol Natural products CC(C)C1CCC(C)CC1O NOOLISFMXDJSKH-UHFFFAOYSA-N 0.000 claims description 44
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- 229940043810 zinc pyrithione Drugs 0.000 description 1
- GAWWVVGZMLGEIW-GNNYBVKZSA-L zinc ricinoleate Chemical compound [Zn+2].CCCCCC[C@@H](O)C\C=C/CCCCCCCC([O-])=O.CCCCCC[C@@H](O)C\C=C/CCCCCCCC([O-])=O GAWWVVGZMLGEIW-GNNYBVKZSA-L 0.000 description 1
- 229940100530 zinc ricinoleate Drugs 0.000 description 1
- PICXIOQBANWBIZ-UHFFFAOYSA-N zinc;1-oxidopyridine-2-thione Chemical compound [Zn+2].[O-]N1C=CC=CC1=S.[O-]N1C=CC=CC1=S PICXIOQBANWBIZ-UHFFFAOYSA-N 0.000 description 1
- UOXSXMSTSYWNMH-UHFFFAOYSA-L zinc;2-aminoacetate Chemical compound [Zn+2].NCC([O-])=O.NCC([O-])=O UOXSXMSTSYWNMH-UHFFFAOYSA-L 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
- OENHQHLEOONYIE-JLTXGRSLSA-N β-Carotene Chemical compound CC=1CCCC(C)(C)C=1\C=C\C(\C)=C\C=C\C(\C)=C\C=C\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C OENHQHLEOONYIE-JLTXGRSLSA-N 0.000 description 1
- QUEDXNHFTDJVIY-UHFFFAOYSA-N γ-tocopherol Chemical class OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1 QUEDXNHFTDJVIY-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/34—Alcohols
-
- 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
- A61K31/045—Hydroxy compounds, e.g. alcohols; Salts thereof, e.g. alcoholates
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
- A61K8/11—Encapsulated compositions
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/37—Esters of carboxylic acids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/48—Preparations in capsules, e.g. of gelatin, of chocolate
- A61K9/4841—Filling excipients; Inactive ingredients
- A61K9/4858—Organic compounds
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q11/00—Preparations for care of the teeth, of the oral cavity or of dentures; Dentifrices, e.g. toothpastes; Mouth rinses
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/20—Chemical, physico-chemical or functional or structural properties of the composition as a whole
- A61K2800/24—Thermal properties
- A61K2800/244—Endothermic; Cooling; Cooling sensation
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
- A61K2800/59—Mixtures
- A61K2800/592—Mixtures of compounds complementing their respective functions
- A61K2800/5922—At least two compounds being classified in the same subclass of A61K8/18
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Epidemiology (AREA)
- Birds (AREA)
- Emergency Medicine (AREA)
- Dermatology (AREA)
- Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Oral & Maxillofacial Surgery (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Rheumatology (AREA)
- Pain & Pain Management (AREA)
- Cosmetics (AREA)
- Medicinal Preparation (AREA)
Description
(a)L-メントール、
(b)D-メントール、および
(c)イソメントール、メンチルアセテート(L)、メンチルアセテート(D)、メンチルアセテート(イソ)、酢酸メンチルラクテート(イソ)および酢酸メンチルラクテート(ネオ)からなる群から選択される少なくとも1つのさらなる冷却剤
を含む、
但し、前記成分(c)がイソメントールを表す場合、前記組成物はアルカンジオールを含まない、
組成物である。
(a)約35〜約55重量%のL-メントール、
(b)約25〜約40重量%のD-メントール、および
(c)約15〜約30重量%のイソメントール、メンチルアセテート(L)、メンチルアセテート(D)、メンチルアセテート(イソ)、酢酸メンチルラクテート(イソ)および酢酸メンチルラクテート(ネオ)またはそれらの混合物
を含むことを特徴とする、
但し、全ての量の合計は100重量%である、
組成物である。
(a)L-メントール、
(b)D-メントール、および
(c)メンチルアセテート(L)、
を含む、
但し、前記組成物はアルカンジオールとイソメントールを同時に含まない、
好ましくは、
(a)50〜55重量%のL-メントール、
(b)25〜35重量%のD-メントール、および
(c)18〜23重量%のメンチルアセテート(L)
を含むことを特徴とする、
但し、全ての量の合計は100重量%である、
組成物である。
(a)L-メントール、
(b)D-メントール、
(c1)メンチルアセテート(L)、さらに
(c2)メンチルアセテート(D)、さらに
(c3)メンチルアセテート(イソ)、およびさらに
(c4)メンチルアセテート(ネオ、イソ)、
好ましくは:
(a)50〜55重量%のL-メントール、
(b)25〜35重量%のD-メントール、
(c1)8〜12重量%のメンチルアセテート(L)、
(c2)8〜12重量%のメンチルアセテート(D)、
(c3)0.1〜1重量%のメンチルアセテート(イソ)、および
(c4)0.1〜1重量%のメンチルアセテート(ネオ、イソ)
を含むことを特徴とする、
但し、全ての量の合計は100重量%である、
組成物である。
(a)L-メントール、
(b)D-メントール、
(c1)メンチルアセテート(L)、およびさらに
(c2)、イソメントール
好ましくは:
(a)35〜45重量%のL-メントール、
(b)35〜45重量%のD-メントール、
(c1)15〜25重量%のメンチルアセテート(L)、および
(c2)2〜8重量%のイソメントール
を含むことを特徴とする、
但し、全ての量の合計は100重量%である、
組成物である。
(a)L-メントール、
(b)D-メントール、
(c1)メンチルアセテート(L)、さらに、
(c2)イソメントール、さらに
(c3)メンチルアセテート(D)、さらに
(c4)メンチルアセテート(イソ)、およびさらに
(c5)メンチルアセテート(ネオ、イソ)、
好ましくは:
(a)35〜45重量%のL-メントール、
(b)35〜45重量%のD-メントール、
(c1)8〜12重量%のメンチルアセテート(L)、
(c2)2〜8重量%のイソメントール、
(c3)8〜12重量%のメンチルアセテート(D)、
(c4)0.1〜1重量%のメンチルアセテート(イソ)、および
(c5)0.1〜1重量%のメンチルアセテート(ネオ、イソ)
を含むことを特徴とする、
但し、全ての量の合計は100重量%である、
組成物である。
・直鎖C8〜22脂肪族アルコールへの、C12〜22脂肪酸への、アルキル基中に8〜15個の炭素原子を含むアルキルフェノールへの、およびアルキル基中に8〜22個の炭素原子を含むアルキルアミンへの2〜30モルのエチレンオキシドおよび/または0〜5モルのプロピレンオキシドの付加生成物;
・アルキル(アルケニル)基に8〜22個の炭素原子を含むアルキルおよび/またはアルケニルオリゴグリコシドおよびそれらのエトキシル化類似体;
・ヒマシ油および/または硬化ヒマシ油への1〜15モルのエチレンオキシドの付加生成物;
・ヒマシ油および/または水素化ヒマシ油への15〜60モルのエチレンオキシドの付加生成物;
・12〜22個の炭素原子を含む不飽和の、直鎖状または飽和の、分岐した脂肪酸および/または3〜18個の炭素原子を含むヒドロキシカルボン酸とのグリセロールおよび/またはソルビタンの部分エステルならびに1〜30モルのエチレンオキシドへのそれらの付加生成物;
・飽和および/または不飽和の、12〜22個の炭素原子を含む直鎖状または分岐の脂肪酸および/または3〜18個の炭素原子を含むヒドロキシカルボン酸とのポリグリセロール(2〜8の平均自己縮合度)、ポリエチレングリコール(分子量400〜5000)、トリメチロールプロパン、ペンタエリスリトール、糖アルコール(例えば、ソルビトール)、アルキルグルコシド(例えば、メチルグルコシド、ブチルグルコシド、ラウリルグルコシド)およびポリグルコシド(例えば、セルロース)の部分エステル、ならびに1〜30モルのエチレンオキシドへのそれらの付加生成物;
・ペンタエリスリトール、脂肪酸、クエン酸および脂肪族アルコールの混成エステルおよび/または6〜22個の炭素原子を有する脂肪酸、メチルグルコースおよびポリオール、好ましくはグリセロールまたはポリグリセロールの混成エステル;
・モノ−、ジ−およびトリアルキルホスフェートおよびモノ−、ジ−および/またはトリ−PEG−アルキルホスフェートおよびそれらの塩;
・ウールワックスアルコール;
・ポリシロキサン/ポリアルキル/ポリエーテル・コポリマーおよび対応する誘導体;
・ブロックコポリマー、例えば、ポリエチレングリコール−30ジポリヒドロキシステアレート;
・ポリマー乳化剤、例えばGoodrichのPemulenタイプ(TR−1、TR−2)またはBASFのCosmedia(登録商標) SP;
・ポリアルキレングリコールおよび
・グリセロールカーボネート。
1FEMAは「風味とエキス工業会(Flavor and Extracts Manufacturers Association)」の略で、GRASは「一般的に安全とみなされている(Generally Regarded As Safe)」と定義される。FEMA GRAS評価はそのように示された物質は標準的な方法に従って試験され、毒性学的に安全とみなされていることを意味する。
・3−ベンジリデンカンファまたは3−ベンジリデンノルカンファおよびそれらの誘導体、例えば、3−(4−メチルベンジリデン)カンファ;
・4−アミノ安息香酸誘導体、好ましくは4−(ジメチルアミノ)安息香酸−2−エチルヘキシルエステル、4−(ジメチルアミノ)安息香酸−2−オクチルエステルおよび4−(ジメチルアミノ)安息香酸アミルエステル;
・桂皮酸のエステル、好ましくは4−メトキシ桂皮酸2−エチルヘキシルエステル、4−メトキシ桂皮酸プロピルエステル、4−メトキシ桂皮酸イソアミルエステル、2−シアノ−3,3−フェニル桂皮酸−2−エチルヘキシルエステル(オクトクリレン);
・サリチル酸のエステル、好ましくはサリチル酸−2−エチルヘキシルエステル、サリチル酸−4−イソプロピルベンジルエステル、サリチル酸ホモメンチルエステル;
・ベンゾフェノン誘導体、好ましくは2−ヒドロキシ−4−メトキシベンゾフェノン、2−ヒドロキシ−4−メトキシ−4’−メチルベンゾフェノン、2,2’−ジヒドロキシ−4−メトキシベンゾフェノン;
・ベンザルマロン酸のエステル、好ましくは4−メトキシベンザルマロン酸ジ−2−エチルヘキシルエステル;
・トリアジン誘導体、例えば、2,4,6−トリアニリノ−(p−カルボ−2’−エチル−1’−ヘキシルオキシ)−1,3,5−トリアジンおよびオクチルトリアゾンまたはジオクチルブタミドトリアゾン(Uvasorb(登録商標) HEB)など;
・プロパン−1,3−ジオン、例えば、1−(4−tert−ブチルフェニル)−3−(4’−メトキシフェニル)プロパン−1,3−ジオン;
・ケトトリシクロ(5.2.1.0)デカン誘導体。
・2−フェニルベンズイミダゾール−5−スルホン酸およびそのアルカリ金属、アルカリ土類金属、アンモニウム、アルカリアンモニウム、アルカノールアンモニウム、およびグルコアンモニウム(glucammonium)塩;
・1H−ベンズイミダゾール−4,6−ジスルホン酸、2,2’−(1,4−フェニレン)ビス−二ナトリウム塩(Neo Heliopan(登録商標) AP)
・ベンゾフェノンのスルホン酸誘導体、好ましくは2−ヒドロキシ−4−メトキシベンゾフェノン−5−スルホン酸およびその塩;
・3−ベンジリデンカンファのスルホン酸誘導体、例えば、4−(2−オキソ−3−ボルニリデンメチル)ベンゼンスルホン酸および2−メチル−5−(2−オキソ−3−ボルニリデン)スルホン酸およびそれらの塩など。
・収れん活性成分、
・油成分、
・非イオン性乳化剤、
・補助乳化剤、
・稠度因子、
・例えば、増粘剤または錯化剤などの形態の賦形剤、および/または
・非水性溶媒、例えば、エタノール、プロピレングリコールおよび/またはグリセロールなど。
・炎症抑制性、皮膚保護性または香りの良い精油、
・合成皮膚保護剤および/または
・油溶性香油。
・防腐剤および抗菌剤、例えば、p−ヒドロキシ安息香酸メチル/エチルまたはプロピルエステル、ソルビン酸ナトリウム、安息香酸ナトリウム、ブロモクロロフェン、フェニルサリチル酸エステル、チモールなど;
・抗歯石剤、具体的には、有機リン酸エステル、例えば、1−ヒドロキシエタン−1,1−ジホスホン酸、1−ホスホノプロパン−1,2,3−トリカルボン酸など、およびその他の、例えば、米国特許第3,488,419号明細書、独国特許出願公開第2224430号明細書および独国特許出願公開第2343196 A1号明細書から知られる抗歯石剤など;
・他の虫歯予防物質、例えば、フッ化ナトリウム、モノフルオロリン酸ナトリウム、フッ化第一スズなど;
・甘味料、例えば、サッカリンナトリウム、シクラミン酸ナトリウム、スクロース、ラクトース、マルトース、フルクトースまたはAspartame(登録商標)(L−α−アスパルチル−L−フェニルアラニン−メチルエステル)、ステビア抽出物およびそれらの甘味化合物、特に、レバウジオシドなど;
・追加の芳香剤、例えば、ユーカリ油、アニス油、ウイキョウ油、キャラウェイ油、酢酸メチル、桂皮アルデヒド、アネトール、バニリン、チモールならびにこれらと他の天然および合成芳香剤との混合物など;
・顔料、例えば、二酸化チタンなど;
・着色剤;
・緩衝物質、例えば、第一、第二または第三のアルカリ金属のリン酸塩またはクエン酸/クエン酸ナトリウムなど;
・創傷治癒および炎症抑制物質、例えば、アラントイン、尿素、アズレン、カモミール活性成分およびアセチルサリチル酸の誘導体など。
・グリセロール;
・アルキレングリコール、例えば、エチレングリコール、ジエチレングリコール、プロピレングリコール、ブチレングリコール、ヘキシレングリコール、および平均分子量100〜1,000ダルトンのポリエチレングリコールなど;
・自己縮合度1.5〜10の工業用オリゴグリセロール混合物、例えば、ジグリセロール含量40〜50重量%の工業用ジグリセロール混合物など;
・メチロール化合物、例えば、特にトリメチロールエタン、トリメチロールプロパン、トリメチロールブタン、ペンタエリスリトールおよびジペンタエリスリトールなど;
・低級アルキルグルコシド、特に、アルキル基において1〜8個の炭素原子を含有するもの、例えば、メチルおよびブチルグルコシドなど;
・5〜12個の炭素原子を含有する糖アルコール、例えば、ソルビトールまたはマンニトールなど;
・5〜12個の炭素原子を含有する糖、例えば、グルコースまたはスクロースなど;
・アミノ糖、例えば、グルカミンなど;
・ジアルコールアミン、例えば、ジエタノールアミンまたは2−アミノプロパン−1,3−ジオールなど。
(a)ゲル形成剤、カチオン性ポリマーおよび活性剤からなるマトリックスを調製し、
(b)任意に、そのマトリックスを油相中に分散させ、
(c)分散したマトリックスをアニオン性ポリマーの水溶液で処理し、任意にこの工程でこの油相を除去すること。
本発明のさらなる主題は、皮膚または粘膜をある量の液状冷却組成物と接触させることによってそれらを冷却または鎮静化するための非治療的方法に関する。特にこれは、上述の化粧品用の組成物のいずれか1つを局所に適用することによって達成され得る。
Claims (13)
- 液状冷却組成物であって、
(a)L-メントール、
(b)D-メントールおよび
(c)メンチルアセテート(L)
を含む、
但し、前記組成物はアルカンジオールとイソメントールを同時に含まない、
組成物。 - 前記組成物は、
(a)50〜55重量%のL-メントール、
(b)25〜35重量%のD-メントールおよび
(c)18〜23重量%のメンチルアセテート(L)
を含むことを特徴とする、
但し、全ての量の合計は100重量%である、
請求項1に記載の前記組成物。 - 前記組成物は、
(a)L-メントール、
(b)D-メントール、
(c1)メンチルアセテート(L)、さらに
(c2)メンチルアセテート(D)、さらに
(c3)メンチルアセテート(イソ)およびさらに
(c4)メンチルアセテート(ネオ、イソ)
を含むことを特徴とする、請求項1に記載の前記組成物。 - 前記組成物は、
(a)50〜55重量%のL-メントール、
(b)25〜35重量%のD-メントール、
(c1)8〜12重量%のメンチルアセテート(L)、
(c2)8〜12重量%のメンチルアセテート(D)、
(c3)0.1〜1重量%のメンチルアセテート(イソ)および
(c4)0.1〜1重量%のメンチルアセテート(ネオ、イソ)
を含むことを特徴とする、
但し、全ての量の合計は100重量%である、
請求項3に記載の前記組成物。 - 前記組成物は、
(a)L-メントール、
(b)D-メントール、
(c1)メンチルアセテート(L)、およびさらに
(c2)イソメントール
を含むことを特徴とする、請求項1に記載の前記組成物。 - 前記組成物は、
(a)35〜45重量%のL-メントール、
(b)35〜45重量%のD-メントール、
(c1)15〜25重量%のメンチルアセテート(L)、および
(c2)2〜8重量%のイソメントール
を含むことを特徴とする、
但し、全ての量の合計は100重量%である、
請求項5に記載の前記組成物。 - 前記組成物は、
(a)L-メントール、
(b)D-メントール、
(c1)メンチルアセテート(L)、さらに、
(c2)イソメントール、さらに
(c3)メンチルアセテート(D)、さらに
(c4)メンチルアセテート(イソ)およびさらに
(c5)メンチルアセテート(ネオ、イソ)
を含むことを特徴とする、請求項1に記載の前記組成物。 - 前記組成物は、
(a)35〜45重量%のL-メントール、
(b)35〜45重量%のD-メントール、
(c1)8〜12重量%のメンチルアセテート(L)、
(c2)2〜8重量%のイソメントール、
(c3)8〜12重量%のメンチルアセテート(D)、
(c4)0.1〜1重量%のメンチルアセテート(イソ)、および
(c5)0.1〜1重量%のメンチルアセテート(ネオ、イソ)
を含むことを特徴とする、
但し、全ての量の合計は100重量%である、
請求項7に記載の前記組成物。 - 請求項1に記載の液状冷却組成物を含有する、化粧品用および/または皮膚科学的および/または医薬用の組成物。
- 0.1〜10重量%の量で前記液状冷却組成物を含有することを特徴とする、請求項9に記載の前記組成物。
- 請求項1に記載の液状冷却組成物を含有する、カプセル。
- ある量の請求項1に記載の液状冷却組成物と皮膚および粘膜を接触させることにより、前記皮膚および粘膜を冷却しかつ沈静化するための非治療的方法。
- 化粧品用および/または皮膚科学用および/または医薬用の組成物の製造のための、請求項1に記載の液状冷却組成物の使用。
Applications Claiming Priority (3)
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EP15167910.7 | 2015-05-15 | ||
EP15167910.7A EP3093002B1 (de) | 2015-05-15 | 2015-05-15 | Flüssige kühlstoffzubereitungen |
PCT/EP2016/060474 WO2016184731A1 (de) | 2015-05-15 | 2016-05-10 | Flüssige kühlstoffzubereitungen |
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JP2020215703A Division JP2021059582A (ja) | 2015-05-15 | 2020-12-24 | 液状冷却組成物 |
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JP6817225B2 true JP6817225B2 (ja) | 2021-01-20 |
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JP2017559418A Active JP6817225B2 (ja) | 2015-05-15 | 2016-05-10 | 液状冷却組成物 |
JP2020215703A Pending JP2021059582A (ja) | 2015-05-15 | 2020-12-24 | 液状冷却組成物 |
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US (1) | US10722434B2 (ja) |
EP (2) | EP3093002B1 (ja) |
JP (2) | JP6817225B2 (ja) |
CN (1) | CN107787218B (ja) |
MY (1) | MY181484A (ja) |
WO (1) | WO2016184731A1 (ja) |
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JPWO2020184479A1 (ja) * | 2019-03-08 | 2020-09-17 | ||
EP4259287A1 (en) | 2020-12-09 | 2023-10-18 | Symrise AG | A method for fighting microorganisms using menthol derivatives |
CN115154661A (zh) * | 2022-07-29 | 2022-10-11 | 广州莱度品牌管理有限公司 | 一种仿生角质膜的制备方法 |
CN117547471B (zh) * | 2024-01-11 | 2024-05-03 | 万华化学集团股份有限公司 | 一种具有改善的凉感透发性的l薄荷醇组合物及其应用 |
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-
2015
- 2015-05-15 EP EP15167910.7A patent/EP3093002B1/de active Active
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2016
- 2016-05-10 EP EP16721435.2A patent/EP3294262B1/de active Active
- 2016-05-10 JP JP2017559418A patent/JP6817225B2/ja active Active
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- 2016-05-10 US US15/574,010 patent/US10722434B2/en active Active
- 2016-05-10 CN CN201680037345.1A patent/CN107787218B/zh active Active
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JP2018515538A (ja) | 2018-06-14 |
EP3093002A1 (de) | 2016-11-16 |
EP3294262A1 (de) | 2018-03-21 |
CN107787218B (zh) | 2021-07-02 |
MY181484A (en) | 2020-12-23 |
US20190175465A1 (en) | 2019-06-13 |
WO2016184731A1 (de) | 2016-11-24 |
EP3093002B1 (de) | 2018-04-25 |
CN107787218A (zh) | 2018-03-09 |
EP3294262B1 (de) | 2020-09-16 |
JP2021059582A (ja) | 2021-04-15 |
US10722434B2 (en) | 2020-07-28 |
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