JP2020128363A - 皮膚外用組成物 - Google Patents
皮膚外用組成物 Download PDFInfo
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- JP2020128363A JP2020128363A JP2019107022A JP2019107022A JP2020128363A JP 2020128363 A JP2020128363 A JP 2020128363A JP 2019107022 A JP2019107022 A JP 2019107022A JP 2019107022 A JP2019107022 A JP 2019107022A JP 2020128363 A JP2020128363 A JP 2020128363A
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Abstract
Description
項1.
(A)水溶性多糖類、(B)ニコチン酸アミド3質量%以上、及び(C)両親媒性成分を含有する、皮膚外用組成物。
項2.
前記(B)成分の含有量が、3〜20質量%である、項1に記載の皮膚外用組成物。
項3.
前記(C)成分が、ホスホリルコリン含有ポリマー、二価カルボン酸エステル、炭素数5〜10のアルカンジオール及び下記化学式(I)で表されるアルキレンオキシド誘導体からなる群より選ばれる1種又は2種以上である、項1又は2に記載の皮膚外用組成物:
Z−{O(AO)a(EO)b−(BO)cH}n (I)
(式中
nは1〜9の整数であり;
Zは、水素原子、又は炭素数1〜30のヒドロキシ化合物からn個のヒドロキシ基を除去することによって得られる基であり;
AOは3〜4個の炭素原子を有するオキシアルキレン基であり;
EOはオキシエチレン基であり;
BOは4個の炭素原子を有するオキシアルキレン基であり;
a、b、及びcはそれぞれAO、EO、及びBOの平均付加モル数であって、それぞれ独立して0〜200であり;a、b、及びcが全て0になることはなく;
AO及びEOはランダム状に付加しても、ブロック状に付加してもよく;
nが2以上の場合は、複数のa、b、及びcはそれぞれ同一でも異なってもよく;
Zが水素原子の場合は、nは1である)。
項4.
前記(A)成分が、ガム類、ヘパリン類似物質、アルギン酸類、寒天、ペクチン、プルラン、及びマンナンからなる群より選ばれる1種又は2種以上である、請求項1〜3のいずれか一項に記載の皮膚外用組成物。
項5.
前記化学式(I)において、Zが、水素原子、又は、炭素数4〜24のアルキルモノアルコール、グリセリン、トリメチロールプロパン、エリスリトール、ペンタエリスリトール、アルキルグルコシド、ジグリセリン、キシリトール、ジペンタエリスリトール、ソルビトール、イノシトール、スクロース、トレハロース、マルチトール、若しくは炭素数1〜30のヒドロキシ化合物から、n個のヒドロキシ基を除去することによって得られる基である、項3又は4に記載の皮膚外用組成物。
本発明の(A)成分として皮膚外用組成物に含まれる水溶性多糖類は、天然由来の物質であっても、化学合成によって得られる物質であってもよい。
本発明の皮膚外用組成物には市販品を用いてもよく、特に限定されないが、例えばKELCOGEL CG−LA、KELCOGEL CG−HA、ケルコゲルHM、ケルコゲルDGA(以上、CP Kelco U.S社製)等が使用できる。
(A)成分の総含有量は、使用感を良好とする観点から、皮膚外用組成物の全量に対して、好ましくは5質量%以下、より好ましくは3質量%以下、更に好ましくは2質量%以下、更により好ましくは1.5質量%以下、特に好ましくは1.2質量%以下である。
(A)成分の総含有量は、皮膚外用組成物全量に対して、好ましくは0.005〜5質量%、より好ましくは0.01〜3質量%、更に好ましくは0.05〜2質量%、更により好ましくは0.1〜1.5質量%である。
(A)成分のうち、寒天の含有量は、特に限定されず、皮膚外用組成物全量に対して、好ましくは0.01〜3質量%、より好ましくは0.05〜2質量%、更に好ましくは、0.1〜1.5質量%である。
本発明の(B)成分として皮膚外用組成物に含まれるニコチン酸アミドは、ニコチン酸(ビタミンB3/ナイアシン)のアミド化合物であり、水溶性ビタミンである。ニコチン酸は、天然物からの抽出物であっても良いし、公知の方法によって合成した物でも良い。具体的には、第17改正日本薬局方に収載されているものを用いることができる。血行促進作用や、肌荒れ改善作用の他、メラニン生成抑制作用や美白効果が知られている。
(B)成分の含有量は、製剤の安定性と使用感を良好とする観点から、皮膚外用組成物全量に対して、好ましくは20質量%以下、より好ましくは15質量%以下、更に好ましくは10質量%以下、更により好ましくは8質量%以下である。
(B)成分の含有量は、皮膚外用組成物全量に対して、好ましくは、3〜20質量%、より好ましくは3〜15質量%、更に好ましくは3〜10質量%である、更により好ましくは3〜8質量%である。
本発明の(C)成分として皮膚外用組成物に含まれる両親媒性成分は、一つの分子内に親水基と疎水基(親油基)の両方が存在し、その結果水相と油相(有機相)のいずれにも親和性がある化合物全般を指す。
(式中
nは1〜9の整数であり;
Zは、水素原子、又は炭素数1〜30のヒドロキシ化合物からn個のヒドロキシ基を除去することによって得られる基であり;
AOは3〜4個の炭素原子を有するオキシアルキレン基であり;
EOはオキシエチレン基であり;
BOは4個の炭素原子を有するオキシアルキレン基であり;
a、b、及びcはそれぞれAO、EO、及びBOの平均付加モル数であって、それぞれ独立して0〜200であり;a、b及びcが全て0になることはなく;
AO及びEOはランダム状に付加しても、ブロック状に付加してもよく;
nが2以上の場合は、複数のa、b、及びcはそれぞれ同一でも異なってもよく;
Zが水素原子の場合は、nは1である)。
BOは炭素数4のオキシアルキレン基であり、例としてはオキシブチレン基(オキシn−ブチレン基、オキシイソブチレン基、オキシt−ブチレン基)、オキシテトラメチレン基等が挙げられる。BOは、好ましくはオキシブチレン基である。
中でも、ポリオキシエチレングリセリルエーテル、ポリオキシプロピレングリセリルエーテル、ポリオキシエチレンポリオキシプロピレングリセリルエーテル、ポリオキシブチレンポリオキシエチレンポリオキシプロピレングリセリルエーテル、ポリオキシブチレンポリオキシエチレンポリオキシプロピレンアルキルグルコシド、ポリオキシエチレンポリオキシプロピレンアルキルグルコシド、ポリオキシエチレンアルキルグルコシド、ポリオキシプロピレンアルキルグルコシド、ポリオキシプロピレンアルキルエーテル、ポリオキシエチレンポリオキシプロピレンアルキルエーテル、ポリオキシプロピレンソルビット、ポリオキシエチレンソルビット、ポリオキシエチレンポリオキシプロピレンソルビット、ポリオキシプロピレンエリスリトールエーテル、ポリオキシエチレンエリスリトールエーテル、ポリオキシエチレンペンタエリスリトールエーテル、ポリオキシエチレンポリオキシプロピレンエリスリトールエーテル、ポリオキシプロピレンペンタエリスリトールエーテル、ポリオキシブチレンポリオキシエチレンペンタエリスリトールエーテル、ポリオキシエチレンポリオキシプロピレンペンタエリスリトールエーテル、ポリオキシエチレンジグリセリルエーテル、ポリオキシプロピレンジグリセリルエーテル、ポリオキシエチレンポリオキシプロピレンジグリセリルエーテル、ポリオキシブチレンポリオキシエチレンポリオキシプロピレンジグリセリルエーテル、ポリオキシエチレントリメチロールプロパン、ポリオキシプロピレントリメチロールプロパン、ポリオキシエチレンポリオキシプロピレントリメチロールプロパン、ポリオキシプロピレングリコール、ポリオキシエチレンポリオキシプロピレングリコール、ポリオキシブチレンポリオキシエチレンポリオキシプロピレングリコール、ポリオキシエチレンキシリトール、ポリオキシプロピレンキシリトール、ポリオキシエチレンポリオキシプロピレンキシリトール、ポリオキシエチレンポリオキシプロピレンジペンタエリスリトール、ポリオキシエチレンジペンタエリスリトール、ポリオキシプロピレジペンタエリスリトール、ポリオキシエチレンイノシトール、ポリオキシプロピレンイノシトール、ポリオキシエチレンポリオキシプロピレンイノシトール、ポリオキシエチレンスクロースエーテル、ポリオキシプロピレンスクロースエーテル、ポリオキシエチレンポリオキシプロピレンスクロースエーテル、ポリオキシエチレントレハロースエーテル、ポリオキシプロピレントレハロースエーテル、ポリオキシエチレンポリオキシプロピレントレハロースエーテル、ポリオキシエチレンマルチトールエーテル、ポリオキシプロピレンマルチトールエーテル、及びポリオキシエチレンポリオキシプロピレンマルチトールエーテルからなる群より選ばれる1種又は2種以上が好ましく、
ポリオキシエチレングリセリルエーテル、ポリオキシプロピレングリセリルエーテル、ポリオキシエチレンポリオキシプロピレングリセリルエーテル、ポリオキシブチレンポリオキシエチレンポリオキシプロピレングリセリルエーテル、ポリオキシブチレンポリオキシエチレンポリオキシプロピレンアルキルグルコシド、ポリオキシエチレンアルキルグルコシド、ポリオキシプロピレンアルキルグルコシド、ポリオキシプロピレンアルキルエーテル、ポリオキシエチレンポリオキシプロピレンアルキルエーテル、ポリオキシプロピレンソルビット、ポリオキシエチレンソルビット、ポリオキシエチレンポリオキシプロピレンソルビット、ポリオキシエチレンポリオキシプロピレンペンタエリスリトールエーテル、ポリオキシプロピレンペンタエリスリトールエーテル、ポリオキシエチレンペンタエリスリトールエーテル、ポリオキシブチレンポリオキシエチレンペンタエリスリトールエーテル、ポリオキシエチレンジグリセリルエーテル、ポリオキシプロピレンジグリセリルエーテル、ポリオキシエチレンポリオキシプロピレンジグリセリルエーテル、ポリオキシブチレンポリオキシエチレンポリオキシプロピレンジグリセリルエーテル、ポリオキシエチレンポリオキシプロピレントリメチロールプロパン、ポリオキシプロピレングリコール、ポリオキシエチレンポリオキシプロピレングリコール、及びポリオキシブチレンポリオキシエチレンポリオキシプロピレングリコール、からなる群より選ばれる1種又は2種以上がより好ましく、
ポリオキシエチレングリセリルエーテル、ポリオキシプロピレングリセリルエーテル、ポリオキシエチレンポリオキシプロピレングリセリルエーテル、ポリオキシブチレンポリオキシエチレンポリオキシプロピレングリセリルエーテル、ポリオキシエチレンポリオキシプロピレンアルキルエーテル、ポリオキシプロピレンアルキルエーテル、ポリオキシブチレンポリオキシエチレンポリオキシプロピレンアルキルグルコシド、ポリオキシエチレンアルキルグルコシド、ポリオキシプロピレンアルキルグルコシド、ポリオキシプロピレンソルビット、ポリオキシエチレンポリオキシプロピレンソルビット、ポリオキシエチレンポリオキシプロピレンペンタエリスリトールエーテル、ポリオキシブチレンポリオキシエチレンペンタエリスリトールエーテル、ポリオキシエチレンジグリセリルエーテル、ポリオキシプロピレンジグリセリルエーテル、ポリオキシエチレンポリオキシプロピレンジグリセリルエーテル、ポリオキシブチレンポリオキシエチレンポリオキシプロピレンジグリセリルエーテル、ポリオキシプロピレングリコール、ポリオキシエチレンポリオキシプロピレングリコール、及びポリオキシブチレンポリオキシエチレンポリオキシプロピレングリコール、からなる群より選ばれる1種又は2種以上が更に好ましく、
ポリオキシエチレングリセリルエーテル、ポリオキシプロピレングリセリルエーテル、ポリオキシエチレンポリオキシプロピレングリセリルエーテル、ポリオキシブチレンポリオキシエチレンポリオキシプロピレングリセリルエーテル、ポリオキシブチレンポリオキシエチレンポリオキシプロピレンアルキルグルコシド、ポリオキシプロピレンアルキルグルコシド、ポリオキシエチレンジグリセリルエーテル、ポリオキシプロピレンジグリセリルエーテル、ポリオキシエチレンポリオキシプロピレンジグリセリルエーテル、ポリオキシブチレンポリオキシエチレンポリオキシプロピレンジグリセリルエーテルからなる群より選ばれる1種又は2種以上が更により好ましい。
アルキレンオキシド誘導体の市販品としては、本発明の効果を顕著に奏する観点から、ユニルーブ50MB−26、ユニルーブ50MB−168、ユニオールHS−1600D、プロノン#208、プロノン#124P、ユニオールD−2000、マクビオブライドMG−10E、マクビオブライドMG−20E、マクビオブライドMG−10P、マクビオブライドMG−20P、ウィルブライドMG2070、ユニルーブ5TP−300KB、ユニルーブ50TG−32、ウィルブライドS-753、ユニオックスG−1200、ユニルーブDGP−700、ユニルーブDGP−950、SY−DP14、SY−DP9、ニューポールGP−1000、ニューポールSP−750、ニューポールPE−68、ニューポールPE−78、ニューポールGEP−2800、NIKKOL SG−G2424、及びエマルゲンPP−290からなる群より選ばれる1種又は2種以上であることが好ましく、
ウィルブライドS−753、ユニオールHS−1600D、プロノン#208、プロノン#124P、ユニオールD−2000、マクビオブライドMG−10E、マクビオブライドMG−20E、マクビオブライドMG−10P、マクビオブライドMG−20P、ウィルブライドMG2070、ユニオックスG−1200、ユニルーブ50TG−32、ユニルーブDGP−700、ユニルーブDGP−950、SY−DP14、SY−DP9、ニューポールGP−1000、ニューポールSP−750、ニューポールPE−68、ニューポールPE−78、ニューポールGEP−2800、NIKKOL SG−G2424、及びエマルゲンPP−290からなる群より選ばれる1種又は2種以上であることがより好ましく、
ウィルブライドS−753、マクビオブライドMG−20P、及びマクビオブライドMG−10P、ユニルーブDGP−700、ユニルーブDGP−950、SY−DP14、SY−DP9、からなる群より選ばれる1種又は2種以上であることが更に好ましく、
ウィルブライドS−753、ユニルーブDGP−700、ユニルーブDGP−950、SY−DP14、及びSY−DP9からなる群より選ばれる1種又は2種以上であることが更により好ましい。
また、市販品としては、特に限定されないが、コハク酸ジエトキシエチル(CRODAMOL DES)、コハク酸ジエチルヘキシル(CRODAMOL OSU)(いずれもクローダジャパン(株)製)、Neosolue−Aqua・Neosolue−AquaS((エイコサン二酸/テトラデカン二酸)ポリグリセリル−10)、Neosolue−Aqulio(シクロヘキサンジカルボン酸ビスエトキシジグリコール)(いずれも日本精化(株)製)が利用できる。
(C)成分の総含有量は、製剤の安定性を良好とする観点から、皮膚外用組成物の全量に対して、好ましくは20質量%以下、より好ましくは15質量%以下、更に好ましくは12質量%以下、更により好ましくは10質量%以下、さらにより好ましくは8質量%以下である。
(C)成分の総含有量は、皮膚外用組成物の全量に対して、好ましくは0.001〜20質量%、より好ましくは0.005〜15質量%、更に好ましくは0.01〜12質量%、更により好ましくは0.05〜10質量%、特に好ましくは0.1〜8質量%である。
本発明の皮膚外用組成物には、前述した(A)〜(C)成分以外に、他の有用な作用を付加するため、紫外線散乱剤、紫外線吸収剤、DNA損傷の予防及び/又は修復作用を有する成分、美白成分、抗炎症成分、抗菌成分、殺菌成分、清涼化剤、有機酸、抗糖化成分、細胞賦活化成分、収斂成分、抗酸化成分、老化防止成分、保湿成分、多価アルコール、角質柔軟成分、ビタミン類、血行促進成分、皮脂吸着成分、ペプチド又はその誘導体、アミノ酸又はその誘導体等の各種成分を、1種又は2種以上組み合わせて配合してもよい。これらの各成分としては、医薬品、医薬部外品、化粧品分野などにおいて使用され得るものであれば特に限定されず、任意のものを適宜選択し使用することができる。また、以下の複数の成分に該当するものは、それらのうちの任意の効能の成分として添加できるものとする。
BB/100、Tinosorb S(BASF社製)、Uvasorb HEB、ユビナール T150(BASF社製)、Heliosun OTZ(O’Laughlin Industries 社製)、Parsol SLX(DSMニュートリションジャパン社製)、Parsol 340(DSMニュートリションジャパン社製)、エスカロール597(アシュランドジャパン社製)、Parsol HS(DSMニュートリションジャパン社製)、Eusolex232(Merk社製)、NeoHeliopanAP(ハーマン&レイマー社製)、ユビナールM40、エスカロール567アシュランドジャパン社製)、ユビナールMS40(BASF社製)、SEESORB107(シプロ化成社製)、SEESORB100(シプロ化成社製)、SEESORB106(シプロ化成社製)を挙げることができる
プラセンタ;アルブチン;コウジ酸;フィチン酸;トラネキサム酸;ハイドロキノン;アスコルビン酸、アスコルビン酸ナトリウム、アスコルビン酸リン酸エステルナトリウム、アスコルビン酸リン酸エステルマグネシウム、テトラ2−ヘキシルデカン酸アスコルビル、2−O−エチルアスコルビン酸、3−O−エチルアスコルビン酸、アスコルビン酸グルコシド;ビタミンA油;イリス根エキス、アーモンド油、アロエベラエキス、アセロラエキス、エイジツエキス、オウゴンエキス、オトギリソウエキス、オドリコソウエキス、海藻エキス、カッコンエキス、カミツレエキス、シャクヤクエキス、ソウハクヒエキス、ダイズエキス、チャエキス、シロチャエキス、トウキンセンカ、ハマメリス、ヨクイニン、ハトムギエキス、ホップエキス、プルーン抽出液、カンゾウエキス、油溶性カンゾウエキス、シモツケソウエキス、ムラサキシキブエキス、アルピニアカツマダイ種子エキス、グレープフルーツエキス、イザヨイバラエキス、レモンエキス、キウイエキス、マツエキス、ニーム葉エキス、アーティチョークエキス、スギナエキス、オオバクエキス、メマツヨイグサエキス、月見草油、ビルベリー葉エキス、ヒメフウロエキス、アッケシソウエキス、セイヨウシロヤナギエキス、ツボクサエキス、及びサンシュユ果実エキスからなる群より選ばれる1種又は2種以上がより好ましい。
中でも、サリチル酸、塩化ベンザルコニウム、エタノール、塩化セチルピリジニウム、塩化セチルトリメチルアンモニウム、グルコン酸、イソプロピルメチルフェノール、パラベン、フェノキシエタノール、塩化セチルピリジニウム、ジンクピリチオン、クロロブタノール、エチルヘキシルグリセリン、ブチルカルバミン酸ヨウ化プロピニル、カプリルヒドロキサム酸、ソルビン酸、β−グリチルレチン酸、ローズマリーエキス、ユーカリエキスからなる群より選ばれる1種又は2種以上が好ましい。抗菌成分又は殺菌成分を配合する場合、その含有量は、皮膚への使用感や効果を考慮して適宜選択できるが、本発明の皮膚外用組成物の全量に対して、例えば、約0.0003〜10質量%、好ましくは、約0.001〜5質量%である。
中でも、アクリル酸メタクリル酸アルキル共重合体、ヒドロキシエチルセルロース、ヒドロキシプロピルセルロース、ヒドロキシプロピルメチルセルロース、カルボキシビニルポリマー、ジメチルジステアリルアンモニウムヘクトライト、(アクリル酸ヒドロキシエチル/アクリロイルジメチルタウリンNa)コポリマー、(アクリロイルジメチルタウリンアンモニウム/ビニルピロリドン)コポリマーが好ましい。
本発明の皮膚外用組成物の粘度(25℃)は、1〜500000mPa・sの範囲内であれば、特に限定されないが、本発明の効果を顕著に奏する観点から、好ましくは、2〜500000mPa・s、より好ましくは、5〜450000mPa・s、更に好ましくは、100〜400000mPa・s、更により好ましくは、200〜300000mPa・s、特に好ましくは、500〜300000mPa・s、である。主に、添加成分である増粘剤の種類や含有量を適宜選択することにより、このような粘度の皮膚外用組成物を得ることができる。
η=KB × T/ω
η:液体の粘度(mPa・s)
KB:装置定数(rad/cm3)
ω:角速度(rad/s)
T:円筒面に作用するトルク(10−7N・m)
本発明の皮膚外用組成物は、通常pH2.0〜9.0の液性を備えていればよいが、皮膚や粘膜に対する低刺激性、及び皮膚使用感の良さという観点から、好ましくは、pH3.0〜8.5、より好ましくは、pH4.0〜8.0である。
本発明の皮膚外用組成物の製造方法は特に限定されず、上記(A)〜(C)成分の他、前記のその他の成分等を適宜選択、配合して、常法により、必要により乳化を行って、製造することができる。
本発明の皮膚外用組成物の性状は、特に限定されず、液体状、流動状、又は半固形状とすることができる。また製剤形態としては、例えば、液剤、懸濁剤、乳剤、クリーム剤、乳液、軟膏剤、ゲル剤、リニメント剤、ローション剤、エアゾール剤、スプレー剤、不織布に薬液を含浸させたシート剤などの製剤とすることができる。中でも、液剤、乳剤、クリーム剤、乳液、軟膏剤、ゲル剤、ローション剤、又はシート剤が好適であり、クリーム剤、乳液、ゲル剤、ローション剤、又はシート剤が特に好適である。なお、乳剤やクリーム剤、軟膏剤のように、油性基剤と水性基剤とを含む場合は、W/O型でもO/W型でもよいが、本発明の皮膚外用組成物の適度な増粘性を確保する観点、及び使用感(べたつき、のび、しっとり感、みずみずしさ、浸透感等)の観点からO/W型がより好ましい。
医薬部外品又は化粧品用の外用組成物とする場合の用途としては具体的には、例えば、化粧水、乳液、ジェル、クリーム、美容液、日焼け止め化粧料、パック、マスク、ハンドクリーム、オールインワンゲル、オールインワンクリーム、ボディローション、及びボディークリームのような基礎化粧料;並びに洗顔料、ハンドソープ、メイク落とし、ボディーシャンプー、シャンプー、リンス、及びトリートメントのような洗浄用化粧料、ファンデーション、化粧下地、BBクリーム、CCクリーム等のフェイスメイクアップ用化粧料;リップクリーム、リップライナー等の口唇化粧料;毛髪用のヘアリンス、ヘアートリートメント、ヘアコンディショナー、ヘアジェル、ヘアムース、ヘアミスト、ヘアローション、スタイリング剤のような毛髪用化粧料などが挙げられる。これらの中でも皮膚用の外用組成物が特に好ましい。すなわち、本発明の外用組成物は、医薬品、医薬部外品、又は化粧品用の皮膚外用組成物とすることができる。皮膚外用組成物の製剤形態は、本発明の外用組成物の場合と同じである。また、使用可能な基剤又は担体、添加剤、及び有効成分、並びにそれらの好ましいものは、本発明の外用組成物の場合と同じである。
本発明の皮膚外用組成物は、使用目的及び用途に応じ、適宜選択した形状、材質の容器に収容し、使用することができる。具体的な容器としては、例えば、スプレータイプ、ボトルタイプ、チューブタイプ、ジャータイプ、スポイドタイプ、ディスペンサータイプ、スティックタイプ、パウチ袋、及びチアパックなどが例示される。本発明の皮膚外用組成物は、容器からの出しやすさの観点で、好ましい状態で用いることができるため、高濃度のニコチン酸アミドを含有する製剤設計の自由度を高めることができる。すなわち、高濃度のニコチン酸アミド含有製剤であっても、ジャーはもちろん、スプレー、ボトル、チューブやディスペンサーなど多種多様な容器にて容易に使用することが可能となる。
本発明の皮膚外用組成物は、ニコチン酸アミドの生理活性を期待して、血行促進、抗炎症、セラミド合成促進の目的で、好適に使用できる。さらに美白、抗シワ、アンチエイジングの効果も期待でき、美白剤、日焼け止め剤などを含めて、多機能な製剤として有用である。本発明の皮膚外用組成物は、用途などに応じて1日あたり1回から数回に分けて、公知あるいは慣用されている用法・用量にて使用することができる。
下記表1に示す組成のサンプルを調製した。各サンプルをガラス瓶に20mL充填し、60℃で1週間保存した(常温で1年の保存に相当)。保存前後のサンプルの粘度をB型粘度計(BL形)(型式TV−10M、東機産業(株)製)を用い、比較例1−1、1−2及び実施例1−1〜3ではM3ロータ、それ以外はM2ロータを用いて、25℃で6rpmの回転数にて1分間測定した。そして、粘度低下率を下記式により求めた。結果を同じ表1に示す。
<粘度低下率>
粘度低下率(%) = (保存前粘度 − 保存後粘度)/保存前粘度 × 100
下記表2に示す組成のサンプルを調製した。各サンプルをガラス瓶に20mL充填し、60℃で1週間保存した(常温で1年の保存に相当)。25℃にて恒常化後、保存前後のサンプルの粘度をB型粘度計(BL形)(型式TV−10M、東機産業(株)製)を用い、M3ロータを用いて、25℃で6rpmの回転数にて1分間測定した。そして、試験例1と同様の式で粘度低下率を求めた。結果を同じ表2に示す。
下記表3、4に示す組成のサンプルを調製した。各サンプルをガラス瓶に20mL充填し、25℃において、国際照明委員会(CIE)が定める標準光源であるD65蛍光ランプの光を4500lx/hで合計120万lxとなるまで照射した。照射前後のサンプルの粘度を、B型粘度計(BL形)(型式TV−10M、東機産業(株)製)を用い、M3ロータを用いて、25℃で6rpmの回転数にて1分間測定した。そして、粘度低下率を下記式により求めた。結果を同じ表3、4にそれぞれ示す。
<粘度低下率>
粘度低下率(%) = (照射前粘度 − 照射後粘度)/照射前粘度 × 100
下記表5に示す組成のサンプルを調製した。各サンプルをガラス瓶に20mL充填し、35℃において、サンテストXLS+(東洋精機社製、1700W キセノン空冷ランプ光源)を用いて、紫外光を照度765W/m2で72時間照射した。同時にアルミ箔で遮光したサンプル(コントロール)にも照射を行い、25℃にて恒常化後、両サンプルの粘度を、B型粘度計(BL形)(型式TV−10M、東機産業(株)製)を用い、比較例4−3〜4及び実施例4−4ではM4ロータを用い、それ以外はM3ロータを用いて、25℃で6rpmの回転数にて1分間測定した。そして、粘度低下率を下記式により求めた。結果を同じ表5に示す。
<粘度低下率>
粘度低下率(%) = (コントロールサンプル粘度 − 照射サンプル粘度)/コントロールサンプル粘度 × 100
以下の表6〜31の処方に基づいて、本発明の皮膚外用組成物(製剤例1〜26)を調製した。
Claims (5)
- (A)水溶性多糖類、(B)ニコチン酸アミド3質量%以上、及び(C)両親媒性成分を含有する、皮膚外用組成物。
- 前記(B)成分の含有量が、3〜20質量%である、請求項1に記載の皮膚外用組成物。
- 前記(C)成分が、ホスホリルコリン含有ポリマー、二価カルボン酸エステル、炭素数5〜10のアルカンジオール及び下記化学式(I)で表されるアルキレンオキシド誘導体からなる群より選ばれる1種又は2種以上である、請求項1又は2に記載の皮膚外用組成物:
Z−{O(AO)a(EO)b−(BO)cH}n (I)
(式中
nは1〜9の整数であり;
Zは、水素原子、又は炭素数1〜30のヒドロキシ化合物からn個のヒドロキシ基を除去することによって得られる基であり;
AOは3〜4個の炭素原子を有するオキシアルキレン基であり;
EOはオキシエチレン基であり;
BOは4個の炭素原子を有するオキシアルキレン基であり;
a、b、及びcはそれぞれAO、EO、及びBOの平均付加モル数であって、それぞれ独立して0〜200であり;a、b、及びcが全て0になることはなく;
AO及びEOはランダム状に付加しても、ブロック状に付加してもよく;
nが2以上の場合は、複数のa、b、及びcはそれぞれ同一でも異なってもよく;
Zが水素原子の場合は、nは1である)。 - 前記(A)成分が、ガム類、ヘパリン類似物質、アルギン酸類、寒天、ペクチン、プルラン、及びマンナンからなる群より選ばれる1種又は2種以上である、請求項1〜3のいずれか一項に記載の皮膚外用組成物。
- 前記化学式(I)において、Zが、水素原子、又は、炭素数4〜24のアルキルモノアルコール、グリセリン、トリメチロールプロパン、エリスリトール、ペンタエリスリトール、アルキルグルコシド、ジグリセリン、キシリトール、ジペンタエリスリトール、ソルビトール、イノシトール、スクロース、トレハロース、マルチトール若しくは炭素数1〜30のヒドロキシ化合物から、n個のヒドロキシ基を除去することによって得られる基である、請求項3又は4に記載の皮膚外用組成物。
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