JP5025985B2 - 抗菌剤及びこれを含有する抗菌性組成物 - Google Patents
抗菌剤及びこれを含有する抗菌性組成物 Download PDFInfo
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- JP5025985B2 JP5025985B2 JP2006123696A JP2006123696A JP5025985B2 JP 5025985 B2 JP5025985 B2 JP 5025985B2 JP 2006123696 A JP2006123696 A JP 2006123696A JP 2006123696 A JP2006123696 A JP 2006123696A JP 5025985 B2 JP5025985 B2 JP 5025985B2
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- Prior art keywords
- extract
- zinc
- acid
- antibacterial
- mass
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- JLQFVGYYVXALAG-CFEVTAHFSA-N yasmin 28 Chemical compound OC1=CC=C2[C@H]3CC[C@](C)([C@](CC4)(O)C#C)[C@@H]4[C@@H]3CCC2=C1.C([C@]12[C@H]3C[C@H]3[C@H]3[C@H]4[C@@H]([C@]5(CCC(=O)C=C5[C@@H]5C[C@@H]54)C)CC[C@@]31C)CC(=O)O2 JLQFVGYYVXALAG-CFEVTAHFSA-N 0.000 description 1
- 239000012138 yeast extract Substances 0.000 description 1
- 239000009538 yokuinin Substances 0.000 description 1
- 239000001231 zea mays silk Substances 0.000 description 1
- 239000004246 zinc acetate Substances 0.000 description 1
- 229960000314 zinc acetate Drugs 0.000 description 1
- 229940062776 zinc aspartate Drugs 0.000 description 1
- 239000011746 zinc citrate Substances 0.000 description 1
- 235000006076 zinc citrate Nutrition 0.000 description 1
- 229940068475 zinc citrate Drugs 0.000 description 1
- 229940098697 zinc laurate Drugs 0.000 description 1
- 229940105125 zinc myristate Drugs 0.000 description 1
- 229940012185 zinc palmitate Drugs 0.000 description 1
- 229940032991 zinc picolinate Drugs 0.000 description 1
- 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
- 229910052984 zinc sulfide Inorganic materials 0.000 description 1
- 229940063789 zinc sulfide Drugs 0.000 description 1
- 229940118257 zinc undecylenate Drugs 0.000 description 1
- POEVDIARYKIEGF-CEOVSRFSSA-L zinc;(2s)-2-aminobutanedioate;hydron Chemical compound [Zn+2].[O-]C(=O)[C@@H](N)CC(O)=O.[O-]C(=O)[C@@H](N)CC(O)=O POEVDIARYKIEGF-CEOVSRFSSA-L 0.000 description 1
- UHVMMEOXYDMDKI-JKYCWFKZSA-L zinc;1-(5-cyanopyridin-2-yl)-3-[(1s,2s)-2-(6-fluoro-2-hydroxy-3-propanoylphenyl)cyclopropyl]urea;diacetate Chemical compound [Zn+2].CC([O-])=O.CC([O-])=O.CCC(=O)C1=CC=C(F)C([C@H]2[C@H](C2)NC(=O)NC=2N=CC(=CC=2)C#N)=C1O UHVMMEOXYDMDKI-JKYCWFKZSA-L 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
- GPYYEEJOMCKTPR-UHFFFAOYSA-L zinc;dodecanoate Chemical compound [Zn+2].CCCCCCCCCCCC([O-])=O.CCCCCCCCCCCC([O-])=O GPYYEEJOMCKTPR-UHFFFAOYSA-L 0.000 description 1
- GJAPSKMAVXDBIU-UHFFFAOYSA-L zinc;hexadecanoate Chemical compound [Zn+2].CCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCC([O-])=O GJAPSKMAVXDBIU-UHFFFAOYSA-L 0.000 description 1
- NHVUUBRKFZWXRN-UHFFFAOYSA-L zinc;pyridine-2-carboxylate Chemical compound C=1C=CC=NC=1C(=O)O[Zn]OC(=O)C1=CC=CC=N1 NHVUUBRKFZWXRN-UHFFFAOYSA-L 0.000 description 1
- DRDVZXDWVBGGMH-UHFFFAOYSA-N zinc;sulfide Chemical compound [S-2].[Zn+2] DRDVZXDWVBGGMH-UHFFFAOYSA-N 0.000 description 1
- GBFLQPIIIRJQLU-UHFFFAOYSA-L zinc;tetradecanoate Chemical compound [Zn+2].CCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCC([O-])=O GBFLQPIIIRJQLU-UHFFFAOYSA-L 0.000 description 1
- 239000001243 zingiber officinale rosc. root absolute Substances 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
Landscapes
- Cosmetics (AREA)
- Detergent Compositions (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Description
で表されるアルコールとグリセリンとを脱水縮合反応させる方法、一般式(3)で表されるアルコールと1−クロロ−2,3−プロパンジオールとを脱塩酸反応させる方法、一般式(3)で表されるアルコールとエピクロルヒドリンとを反応させた後、得られたグリシジルエーテル化合物を加水分解する方法、一般式(3)で表されるアルコールとグリシドールとを反応させる方法、一般式(3)で表されるアルコールとアリルクロライド又はアリルブロマイドとを反応させた後、過酸化水素等で酸化させ、得られたグリシジルエーテル化合物を加水分解する方法、下記の一般式(4)
で表される化合物とグリセリンとを脱ハロゲン化水素反応させる方法が挙げられる。これらの方法によって得られる化合物は、一般式(1)と(2)の混合物である場合が多いが、反応触媒によって一般式(1)と(2)の生成の割合が異なる。また、グリセリンを使用する反応においては、グリセリンを低級脂肪酸で部分的にエステル化したものを使用して上記の反応を行い、反応終了後にケン化する方法や、グリセリンをメチルエチルケトン等でケタール化反応を行った後に上記の反応を行い、反応終了後にケタールをはずす方法を行うことにより、一般式(1)と(2)の生成の割合を大きく変えることもできる。
なお、一般式(2)は以下の通りである。
A成分(本発明品)
(A−1)3−シクロヘキシロキシ−1,2−プロパンジオール
(A−2)3−(4−メチルシクロヘキシロキシ)−1,2−プロパンジオール
(A−3)3−(4−t−ブチルシクロヘキシロキシ)−1,2−プロパンジオール
(A−4)3−シクロヘキシルメトキシ−1,2−プロパンジオール
(A−5)3−シクロへキシロキシ−1,2−プロパンジオールと2−シクロヘキシロキシ−1,3−プロパンジオールの1:1(モル比)混合物
キレート剤(B成分):
(B−1)エチレンジアミンテトラ酢酸2ナトリウム
(B−2)グルタミン酸ジ酢酸4ナトリウム
低分子量ポリオール(C成分):
(C−1)1,3−ブタンジオール
(C−2)グリセリン
窒素含有ノニオン界面活性剤(D成分):
(D−1)ヤシ脂肪酸モノエタノールアミド
(D−2)ラウラミドプロピルアミンオキシド(3−ドデシルアミドプロピル−N,N−ジメチルアミンオキシド)
(D−3)POE(3)ラウリルアミン
窒素含有両性界面活性剤(E成分):
(E−1)ヤシ油脂肪酸アミドエチルヒドロキシエチルグリシンナトリウム(ココアンホ酢酸ナトリウム)
植物由来エキス(F成分):
(F−1)カミツレエキス
(F−2)ハマメリスエキス
(F−3)褐藻エキス
亜鉛化合物(G成分):
(G−1)硫酸亜鉛
(G−2)p−フェノールスルホン酸亜鉛
なお、(F−1)〜(F−3)の植物由来エキスは水や有機溶媒を含有する液体であるが、実験に際しては、これらの水分や有機溶媒を除去した固形分を基準として配合した。
(H−1)3−n−オクトキシ−1,2−プロパンジオール
(H−2)1,2−デカンジオール
(H−3)1−(2−ヒドロキシエトキシ)−2−デカノール
(H−4)メチルパラベン
抗菌性試験(最小発育濃度)−1(単品での評価)
ブイヨン培地で前培養した菌液を用いて、107レベルに調整した菌液を、0.27mlマイクロプレートに入れ、10240〜0.625μg/mlの間で各種濃度に調整した上記A〜C成分を0.03ml添加してよく撹拌した。この混合溶液を37℃で24時間培養し、培養終了後、マイクロプレートの濁度を測定し、被験菌の生育を阻止した防腐剤の最低濃度を最小発育濃度(MIC)とした。なお、使用した菌類以下の通りである。結果を表1に示した。
菌1:Bacillus subtilis IFO3134 (枯草菌)
菌2:Escherichia coli ATCC14948 (大腸菌)
菌3:Staphylococcus aureus IFO13276 (黄色ブド ウ球菌)
なお、A−2〜A−4は参考例である。
抗菌性試験(最小発育濃度)−2(併用系での評価)
上記試験で各種濃度に希釈したA成分100質量部に対して、同濃度に希釈したB〜F成分を下表の割合で配合してMICを測定した。ただし、MICの数字はA成分の濃度で表わしてあり、B〜F成分を配合したことによる抗菌性の相乗効果を確認している。結果を表2に記した。
皮膚刺激性試験
上記化合物について、皮膚刺激性をパッチテストにより評価した。即ち、上記化合物100mgをパッチテスト用絆創膏のガーゼ部に塗布し、上腕部裏側に貼付した。48時間後に絆創膏を剥がし、3時間放置した後、目視で紅斑の有無を観察した。試験は40人について行い、以下の基準で評価を行った。結果を表3に示した。
(評価基準)
◎:紅斑が出た人がいなかった。
○:紅斑が出た人が1〜3人いた。
△:紅斑が出た人が4〜7人いた。
×:紅斑が出た人が8人以上いた。
使用感試験
下記の配合で化粧水を調製した。女性モニター20人に、洗顔後、顔面に化粧水を塗布して、下記の基準で、使用感を評価した。結果を表5に記した。
○:全員が塗布部分に違和感を感じず、使用感が優れている。
△:1〜3人が塗布部分に違和感を感じ、使用感がやや劣っている。
×:4人以上が塗布部分に違和感を感じ、使用感が劣っている。
Claims (9)
- (A)成分として請求項1に記載の抗菌剤および、以下の(B)〜(G)成分、
(B)キレート剤、
(C)一般式(1)以外の、分子量50〜1000である低分子ポリオール、
(D)窒素含有ノニオン界面活性剤
(E)窒素含有両性界面活性剤
(G)亜鉛化合物
からなる群から選択される1種または2種以上の成分を含有することを特徴とする、抗菌性組成物であって、
該(G)亜鉛化合物は、硫酸亜鉛、塩化亜鉛、グルコン酸亜鉛、臭化亜鉛、硝酸亜鉛、塩化亜鉛アンモニウム、硫酸亜鉛アルミニウム、硫酸亜鉛カリウムおよびヨウ化亜鉛からなる群から選択される1種又は2種以上である、抗菌性組成物。 - (A)成分100質量部に対して、(B)成分のキレート剤が0.5〜500質量部であることを特徴とする、請求項2に記載の抗菌性組成物。
- (A)成分100質量部に対して、(C)成分の低分子ポリオールが0.5〜500質量部であることを特徴とする、請求項2に記載の抗菌性組成物。
- (A)成分100質量部に対して、(D)成分の窒素含有ノニオン界面活性剤が0.5〜500質量部であることを特徴とする、請求項2に記載の抗菌性組成物。
- (A)成分100質量部に対して、(E)成分の窒素含有両性界面活性剤が0.5〜500質量部であることを特徴とする、請求項2に記載の抗菌性組成物。
- (A)成分100質量部に対して、(G)成分の亜鉛化合物が0.02〜10質量部であることを特徴とする、請求項2に記載の抗菌性組成物。
- 請求項1の抗菌剤または請求項2〜7のいずれか1項に記載の抗菌性組成物を含有することを特徴とする化粧料。
- 請求項1の抗菌剤または請求項2〜7のいずれか1項に記載の抗菌性組成物を含有することを特徴とする洗浄剤。
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| US9981069B2 (en) | 2007-06-20 | 2018-05-29 | The Trustees Of Columbia University In The City Of New York | Bio-film resistant surfaces |
| US9511040B2 (en) | 2007-06-20 | 2016-12-06 | The Trustees Of Columbia University In The City Of New York | Skin and surface disinfectant compositions containing botanicals |
| US9687429B2 (en) | 2007-06-20 | 2017-06-27 | The Trustees Of Columbia University In The City Of New York | Antimicrobial compositions containing low concentrations of botanicals |
| JP4638963B2 (ja) * | 2008-04-07 | 2011-02-23 | 敏 新川 | 痩身用化粧品組成物 |
| BR112012004153A2 (pt) * | 2009-08-26 | 2016-03-22 | Basf Se | uso de um diol, corpo moldado biocidamente acabado, e, preparação líquida |
| IN2014CN04034A (ja) * | 2011-11-03 | 2015-10-23 | Univ Columbia | |
| AU2012332495B2 (en) | 2011-11-03 | 2017-06-08 | The Trustees Of Columbia University In The City Of New York | Composition with sustained antimicrobial activity |
| US9968101B2 (en) | 2011-11-03 | 2018-05-15 | The Trustees Of Columbia University In The City Of New York | Botanical antimicrobial compositions |
| WO2013086094A1 (en) | 2011-12-06 | 2013-06-13 | The Trustees Of Columbia University In The City Of New York | Broad spectrum natural preservative composition |
| JP2015515997A (ja) * | 2012-05-08 | 2015-06-04 | メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツングMerck Patent Gesellschaft mit beschraenkter Haftung | 抗微生物特性を有するシクロヘキサノールエーテルの使用 |
| CN110225739B (zh) | 2016-11-28 | 2022-03-15 | 宝丽化成工业有限公司 | 皱纹改善剂 |
| US20190380933A1 (en) * | 2017-02-03 | 2019-12-19 | Adeka Corporation | Method for improving storage stability of cosmetic |
| JP7735632B2 (ja) * | 2019-04-24 | 2025-09-09 | 株式会社日本抗菌総合研究所 | 抗菌性組成物、薬液及び薬液の製造方法 |
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