JP7133564B2 - 油性組成物 - Google Patents
油性組成物 Download PDFInfo
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- JP7133564B2 JP7133564B2 JP2019553794A JP2019553794A JP7133564B2 JP 7133564 B2 JP7133564 B2 JP 7133564B2 JP 2019553794 A JP2019553794 A JP 2019553794A JP 2019553794 A JP2019553794 A JP 2019553794A JP 7133564 B2 JP7133564 B2 JP 7133564B2
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- 235000020944 retinol Nutrition 0.000 description 1
- 239000011607 retinol Substances 0.000 description 1
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- QGNJRVVDBSJHIZ-QHLGVNSISA-N retinyl acetate Chemical compound CC(=O)OC\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C QGNJRVVDBSJHIZ-QHLGVNSISA-N 0.000 description 1
- 235000019173 retinyl acetate Nutrition 0.000 description 1
- 239000011770 retinyl acetate Substances 0.000 description 1
- 229940108325 retinyl palmitate Drugs 0.000 description 1
- 235000019172 retinyl palmitate Nutrition 0.000 description 1
- 239000011769 retinyl palmitate Substances 0.000 description 1
- PYWVYCXTNDRMGF-UHFFFAOYSA-N rhodamine B Chemical compound [Cl-].C=12C=CC(=[N+](CC)CC)C=C2OC2=CC(N(CC)CC)=CC=C2C=1C1=CC=CC=C1C(O)=O PYWVYCXTNDRMGF-UHFFFAOYSA-N 0.000 description 1
- 239000004170 rice bran wax Substances 0.000 description 1
- 235000019384 rice bran wax Nutrition 0.000 description 1
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- 239000012488 sample solution Substances 0.000 description 1
- 108700004121 sarkosyl Proteins 0.000 description 1
- 239000013049 sediment Substances 0.000 description 1
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- 239000012176 shellac wax Substances 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
- 230000037394 skin elasticity Effects 0.000 description 1
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- 239000000344 soap Substances 0.000 description 1
- BTURAGWYSMTVOW-UHFFFAOYSA-M sodium dodecanoate Chemical compound [Na+].CCCCCCCCCCCC([O-])=O BTURAGWYSMTVOW-UHFFFAOYSA-M 0.000 description 1
- 229940010747 sodium hyaluronate Drugs 0.000 description 1
- 229940082004 sodium laurate Drugs 0.000 description 1
- 229940045870 sodium palmitate Drugs 0.000 description 1
- NNMHYFLPFNGQFZ-UHFFFAOYSA-M sodium polyacrylate Chemical compound [Na+].[O-]C(=O)C=C NNMHYFLPFNGQFZ-UHFFFAOYSA-M 0.000 description 1
- YWIVKILSMZOHHF-QJZPQSOGSA-N sodium;(2s,3s,4s,5r,6r)-6-[(2s,3r,4r,5s,6r)-3-acetamido-2-[(2s,3s,4r,5r,6r)-6-[(2r,3r,4r,5s,6r)-3-acetamido-2,5-dihydroxy-6-(hydroxymethyl)oxan-4-yl]oxy-2-carboxy-4,5-dihydroxyoxan-3-yl]oxy-5-hydroxy-6-(hydroxymethyl)oxan-4-yl]oxy-3,4,5-trihydroxyoxane-2- Chemical compound [Na+].CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O)[C@@H]1O[C@H]1[C@H](O)[C@@H](O)[C@H](O[C@H]2[C@@H]([C@@H](O[C@H]3[C@@H]([C@@H](O)[C@H](O)[C@H](O3)C(O)=O)O)[C@H](O)[C@@H](CO)O2)NC(C)=O)[C@@H](C(O)=O)O1 YWIVKILSMZOHHF-QJZPQSOGSA-N 0.000 description 1
- GGXKEBACDBNFAF-UHFFFAOYSA-M sodium;hexadecanoate Chemical compound [Na+].CCCCCCCCCCCCCCCC([O-])=O GGXKEBACDBNFAF-UHFFFAOYSA-M 0.000 description 1
- 235000011069 sorbitan monooleate Nutrition 0.000 description 1
- 239000001593 sorbitan monooleate Substances 0.000 description 1
- 229940035049 sorbitan monooleate Drugs 0.000 description 1
- 235000011076 sorbitan monostearate Nutrition 0.000 description 1
- 239000001587 sorbitan monostearate Substances 0.000 description 1
- 229940035048 sorbitan monostearate Drugs 0.000 description 1
- 229960005078 sorbitan sesquioleate Drugs 0.000 description 1
- 229960002920 sorbitol Drugs 0.000 description 1
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- 230000035882 stress Effects 0.000 description 1
- 238000012916 structural analysis Methods 0.000 description 1
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- 239000000758 substrate Substances 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 229940117986 sulfobetaine Drugs 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 208000024891 symptom Diseases 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 239000001845 taraxacum officinale leaf extract Substances 0.000 description 1
- 229960003080 taurine Drugs 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 229940126585 therapeutic drug Drugs 0.000 description 1
- 239000001585 thymus vulgaris Substances 0.000 description 1
- 239000001430 tilia cordata extract Substances 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 229960001295 tocopherol Drugs 0.000 description 1
- 235000010384 tocopherol Nutrition 0.000 description 1
- 229930003799 tocopherol Natural products 0.000 description 1
- 239000011732 tocopherol Substances 0.000 description 1
- 108010021724 tonin Proteins 0.000 description 1
- 229960000401 tranexamic acid Drugs 0.000 description 1
- GYDJEQRTZSCIOI-LJGSYFOKSA-N tranexamic acid Chemical compound NC[C@H]1CC[C@H](C(O)=O)CC1 GYDJEQRTZSCIOI-LJGSYFOKSA-N 0.000 description 1
- UJMBCXLDXJUMFB-UHFFFAOYSA-K trisodium;5-oxo-1-(4-sulfonatophenyl)-4-[(4-sulfonatophenyl)diazenyl]-4h-pyrazole-3-carboxylate Chemical compound [Na+].[Na+].[Na+].[O-]C(=O)C1=NN(C=2C=CC(=CC=2)S([O-])(=O)=O)C(=O)C1N=NC1=CC=C(S([O-])(=O)=O)C=C1 UJMBCXLDXJUMFB-UHFFFAOYSA-K 0.000 description 1
- 235000013799 ultramarine blue Nutrition 0.000 description 1
- 235000019155 vitamin A Nutrition 0.000 description 1
- 239000011719 vitamin A Substances 0.000 description 1
- NCYCYZXNIZJOKI-UHFFFAOYSA-N vitamin A aldehyde Natural products O=CC=C(C)C=CC=C(C)C=CC1=C(C)CCCC1(C)C NCYCYZXNIZJOKI-UHFFFAOYSA-N 0.000 description 1
- 229940045997 vitamin a Drugs 0.000 description 1
- 150000003722 vitamin derivatives Chemical class 0.000 description 1
- 239000001717 vitis vinifera seed extract Substances 0.000 description 1
- 235000020234 walnut Nutrition 0.000 description 1
- 229920001285 xanthan gum Polymers 0.000 description 1
- 235000010493 xanthan gum Nutrition 0.000 description 1
- 239000000230 xanthan gum Substances 0.000 description 1
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- 235000010447 xylitol Nutrition 0.000 description 1
- 239000000811 xylitol Substances 0.000 description 1
- 229960002675 xylitol Drugs 0.000 description 1
- HEBKCHPVOIAQTA-SCDXWVJYSA-N xylitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)CO HEBKCHPVOIAQTA-SCDXWVJYSA-N 0.000 description 1
- 239000009538 yokuinin Substances 0.000 description 1
- 239000011787 zinc oxide Substances 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
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- GVJHHUAWPYXKBD-IEOSBIPESA-N α-tocopherol Chemical compound OC1=C(C)C(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-IEOSBIPESA-N 0.000 description 1
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Description
この様なペプチド誘導体のエラスターゼ阻害剤として、WS7622Aモノ若しくはジ硫酸エステルをはじめとするペプチド誘導体が知られ(例えば、特許文献4を参照)、かかる薬理作用による虚血性疾患への応用が図られている。また、下記一般式(1)に表される化合物は、WS7622Aと同様に白血球エラスターゼ阻害作用が存することが知られ、皮膚の老化予防又は治療作用(例えば、特許文献5を参照)が報告されている。
本発明は、このような状況下においてなされたものであり、前記一般式(1)に表される化合物、その異性体及び/又はそれらの薬理学的に許容される塩を、化学的安定に組成物に配合する方法を提供することを課題とする。
また、分散系の組成物においては一般に時間が経つと分散成分が沈降してしまうところ、本発明者らは、前記組成物にさらに粉体、固形脂及び/又は半固形脂を含有させることにより、前記一般式(1)に表される化合物、その異性体及び/又はそれらの薬理学的に許容される塩を均一に分散させることができ、経時的な分散安定性を図れることをも見出し、本発明を完成させるに至った。
[1]下記一般式(1)に表される化合物、その異性体及び/又はそれらの薬理学的に許容される塩と、水酸基を0~2個有する油剤とを含有する、油性組成物。
[2]前記水酸基を0~2個有する油剤が、炭化水素油、シリコーン油、及びエステル油からなる群から選択される、[1]に記載の組成物。
[3]前記水酸基を0~2個有する油剤の含有量が、組成物全体の50質量%以上である、[1]又は[2]に記載の組成物。
[4]さらに、油性ゲル化剤を含有する[1]~[3]のいずれかに記載の組成物。
[5]さらに、粉体を含有する、[1]~[4]のいずれかに記載の組成物。
[6]前記粉体の含有量が、組成物全体の0.5~20質量%である、[5]に記載の組成物。
[7]オイルゲル剤型である、[1]~[6]のいずれかに記載の組成物。
[8]固形脂及び/又は半固形脂を組成物全体の5質量%以上含む、[7]に記載の組成物。
[9]実質的に水を含有しない、[1]~[8]のいずれかに記載の組成物。
[10]皮膚外用剤である、[1]~[9]のいずれかに記載の組成物。
前記一般式(1)に表される化合物は、その分子構造中に複数の不斉炭素原子を有する光学活性化合物であるため、その異性体としては、エナンチオマー、ジアステレオマーが存在する。さらに、本発明の前記一般式(1)に表される化合物としては、ラセミ体、エナンチオマー、ジアステレオマー、更には、前記異性体が任意の比率で混合した化合物が存在する。
前記R1に関し好ましいものを具体的に例示すれば、カルボキシメチル基、カルボキシエチル基、カルボキシプロピル基、カルボキシブチル基、メトキシカルボニルメチル基、メトキシカルボニルエチル基、メトキシカルボニルプロピル基、メトキシカルボニルブチル基、エトキシカルボニルメチル基、エトキシカルボニルエチル基、エトキシカルボニルプロピル基、エトキシカルボニルブチル基、プロピルオキシカルボニルメチル基、プロピルオキシカルボニルエチル基、プロピルオキシカルボニルプロピル基、プロピルオキシカルボニルブチル基、ブチルオキシカルボニルメチル基、ブチルオキシカルボニルエチル基、ブチルオキシカルボニルプロピル基、ブチルオキシカルボニルブチル基等が好適に例示出来、より好ましくは、カルボキシメチル基が例示できる。
前記R2及びR3は、それぞれ独立に、好ましいものを具体的に挙げれば、メチル基、エチル基、n-プロピル基、イソプロピル基、n-ブチル基、イソブチル基、sec-ブチル基、tert-ブチル基等が好適に例示出来、より好ましくは、イソプロピル基が好適に例示できる。
なお、KSK32は、別の命名法では、N-[4-[[(カルボキシメチル)アミノ]カルボニル]ベンゾイル]-L-バリル-N-[(RS)-3,3,3-トリフルオロ-1-(1-メチルエチル)-2-オキソプロピル]-L-プロリンアミドとも表記されるが、同一化合物である。
また、本発明の組成物には、前記一般式(1)に表される化合物、その異性体及び/又はそれらの薬理学的に許容される塩より1種又は2種以上を選択し含有させることができる。
十分に発揮することが可能となる。
かかる油剤は、特に限定されないが、炭化水素油、シリコーン油、及びエステル油からなる群から選択されるものである。また、水酸基の数は、0~1個がより好ましく、0個すなわち水酸基を有しないことがさらに好ましい
ここで、水酸基の数は一分子あたりの数をいう。
また、前記一般式(1)に表される化合物、その異性体及び/又はそれらの薬理学的に許容される塩は分解しやすいため、これを含有する組成物において、経時により該化合物の含有量が減少してしまうという問題点が存する。かかる問題点に対して、本発明は水酸基を0~2個有する油剤を分散媒として用いることにより、該化合物を化学的に安定に組成物に配合することができる。
また、本発明の組成物における油剤の総含有量は、通常は組成物全体に対して50質量%以上であり、好ましくは60質量%以上である。
ここで、水酸基を有する油剤としては、例えば、脂肪酸とポリグリセリンとのモノ又はジエステル、脂肪酸と糖アルコールとのエステル、脂肪酸と多糖アルコールとのエステル等が挙げられるがこれらに限定されない。
固形脂や半固形脂を含有させることにより組成物の粘度が大きくなるため、組成物に分散した前記一般式(1)に表される化合物、その異性体及び/又はそれらの薬理学的に許容される塩が、時間が経っても沈降しにくくなり、経時での分散安定性に優れた組成物となり得る。かかる態様は後述のオイルゲル剤型等に好適である。
固形脂及び/又は半固形脂の含有量は総量で、組成物全体の5質量%以上が好ましく、10質量%がより好ましく、20質量%以上がさらに好ましい。また、組成物全体の50質量%以下が好ましく、40質量%以下がより好ましく、30質量%以下がさらに好ましい。
固形脂及び/又は半固形脂としては、植物由来のものとして、カルナウバロウ、モクロウ、キャンデリラロウ、コメヌカロウ、シアバター、アフリカマンゴバター等が挙げられ、動物由来のものとして、ミツロウ、シェラックロウ、イボタロウ等が挙げられ、石油由来のものとして、パラフィンワックス、マイクロクリスタリンワックス等の精製ワックスが挙げられ、鉱物由来のものとしてオゾケライト、セレシン、モンタンワックス等の精製ワックスが挙げられる。ただし、一般に動植物由来の固形脂や半固形脂は、水酸基を有する成分を含みやすいため、石油又は鉱物由来の精製ワックスがより好ましい。なお、これらの固形脂及び/又は半固形脂は単独で又は2種以上組み合わせて用いることができる。
ここで油性ゲル化剤とは、油剤等の油性成分と相溶性のあるゲル化剤をいい、特に限定されないが、12-ヒドロキシステアリン酸、パルミチン酸デキストリン、(パルミチン酸/オクタン酸)デキストリン、ジブチルラウロイルグルタミド、ジメチコンクロスポリマー等を例示できる。
油性ゲル化剤の含有量は、組成物全体の0.5質量%以上が好ましく、2質量%がより好ましく、5質量%以上がさらに好ましい。また、組成物全体の20質量%以下が好ましく、15質量%以下がより好ましく、10質量%以下がさらに好ましい。
本発明の組成物が後述のオイルゲル剤型である場合は、前述の固形脂や半固形脂に加えて又は替えて、油性ゲル化剤を含有することが好ましい。その場合の含有量は、前述の固形脂や半固形脂との合計で組成物全体の5質量%以上が好ましい。
粉体の含有量は、組成物全体の0.5~20質量%が好ましく、1~5質量%がより好ましい。
また、その形状は、特に限定されないが、一般に化粧料等の皮膚外用剤に用いられる球状、半球状、板状などが挙げられ、また多孔性であってもよい。
また、その粒子径は、一般に化粧料等の皮膚外用剤に用いられる程度であればよい。
これらのうち、本発明においては、組成物の分散安定性の観点から、多孔質シリカが特に好ましく挙げられる。
組成物中に水が存在すると、前記一般式(1)に表される化合物、その異性体及び/又はそれらの薬理学的に許容される塩が分解されやすくなり、経時で組成物中の該化合物の残存量が減少してしまう場合があるからである。
本発明においてオイルゲル剤型は、通常は高い粘度を有し流動性が低い状態のものである。例えば、25℃で流動性がないもの、すなわち固形のものが好ましい。また、25℃における粘度が20,000Pa・s以上であることが好ましい。かかる剤型であることにより、前記一般式(1)に表される化合物、その異性体及び/又はそれらの薬理学的に許容される塩が、時間が経っても沈降しにくくなり、経時での分散安定性に優れた組成物となり得る。
美白成分としては、一般的に化粧料に用いられているものであれば特に限定はない。例えば、4-n-ブチルレゾルシノール、アスコルビン酸グルコシド、3-О-エチルアスコルビン酸、トラネキサム酸、アルブチン、エラグ酸、コウジ酸、リノール酸、ニコチン酸アミド、5,5'-ジプロピルビフェニル-2,2'-ジオール、5'-アデニル酸二ナトリウム、トラネキサム酸セチル、4-メトキシサリチル酸カリウム塩、ハイドロキノン、パントテン酸等が挙げられる。
セスキイソステアリン酸ポリグリセリル、ソルビタン脂肪酸エステル類(ソルビタンモノステアレート、セスキオレイン酸ソルビタン等) 、グリセリン脂肪酸エステル類(モノステアリン酸グリセリル等)、プロピレングリコール脂肪酸エステル類(モノステアリン酸プロピレングリコール等)、硬化ヒマシ油誘導体、グリセリンアルキルエーテル、POEソルビタン脂肪酸エステル類(POEソルビタンモノオレエート、モノステアリン酸ポリオキシエチレンソルビタン等)、POEソルビット脂肪酸エステル類(POE-ソルビットモノラウレート等)、POEグリセリン脂肪酸エステル類(POE-グリセリンモノイソステアレート等)、POE脂肪酸エステル類(ポリエチレングリコールモノオレート、POEジステアレート等)、POEアルキルエーテル類(POE2-オクチルドデシルエーテル等)、POEアルキルフェニルエーテル類(POEノニルフェニルエーテル等)、プルロニック型類、POE・POPアルキルエーテル類(POE・POP2-デシルテトラデシルエーテル等)、テトロニック類、POEヒマシ油・硬化ヒマシ油誘導体(POEヒマシ油、POE硬化ヒマシ油等)、ショ糖脂肪酸エステル、アルキルグルコシド等の非イオン界面活性剤類、等が挙げられる。
下記の表1及び2に示す処方に従い、オイルゲル剤形の皮膚外用剤を製造した。すなわち、成分イを95℃にて加熱溶解させ、混合した。さらに95℃下で3000rpm、1分間ディスパーを用いて撹拌しながら、前記混合物に成分ロを添加した。その後脱泡を行い、容器に充填し、冷却固化させ、油性固形化粧料を得た。
(1)KSK32の分解安定性の評価
調製した各油性固形化粧料を60℃で2週間保存した後のKSK32の含有量を測定し、5℃で2週間保存した後のKSK32の含有量を100としたときの割合(残存率)を算出した。残存率が95%以上の場合に分解に対する安定性が◎、95%未満80%以上の場合に安定性が○、80%未満60%以上の場合に安定性が△、60%未満の場合に安定性が×、と評価した。結果を表1及び2に併せて示す。
なお、KSK32の含有量は、化粧料約0.5gを量りとり、移動相にて50mLに希釈したものを試料溶液として高速液体クロマトグラフィー(HPLC)を行い、測定した。
HPLC条件は、カラム;逆相系カラム(3.0×100mm)、カラム温度;室温、移動相;陰イオン系スルホン酸型界面活性剤水溶液/THF25%、pH;3、流速;0.4mL/min.、検知;240nm)。
調製した各油性固形化粧料を40℃で1日間静置した後、KSK32の沈降の有無を目視により観察し、均一に分散している場合に分散安定性が○、沈降が認められた場合に分散安定性が×と評価した。結果を表1及び2に併せて示す。
下記の表3に示す処方に従いクリーム剤型の、表4に示す処方に従いミルク剤型の皮膚外用剤をそれぞれ製造した。すなわち、成分イを95℃にて加熱溶解させ、混合した。さらに95℃下で3000rpm、1分間ディスパーを用いて撹拌しながら、前記混合物に成分ロを添加して、各油性化粧料を得た。
実施例20及び21の油性化粧料についても、前述の試験例の方法でKSK32の分解安定性及び分散安定性が良好であることが確認された。
Claims (9)
- 前記水酸基を有しない油剤が、炭化水素油、シリコーン油、及びエステル油からなる群から選択される、請求項1に記載の組成物。
- さらに、油性ゲル化剤を含有する、請求項1又は2に記載の組成物。
- さらに、粉体を含有する、請求項1~3のいずれか一項に記載の組成物。
- 前記粉体の含有量が、組成物全体の0.5~20質量%である、請求項4に記載の組成物。
- オイルゲル剤型である、請求項1~5のいずれか一項に記載の組成物。
- 固形脂及び/又は半固形脂を組成物全体の5質量%以上含む、請求項6に記載の組成物。
- 水の含有量が組成物全体の0.1質量%以下である、請求項1~7のいずれか一項に記載の組成物。
- 皮膚外用剤である、請求項1~8のいずれか一項に記載の組成物。
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