JP7487443B2 - 粘膜上皮適用組成物 - Google Patents
粘膜上皮適用組成物 Download PDFInfo
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- JP7487443B2 JP7487443B2 JP2019178899A JP2019178899A JP7487443B2 JP 7487443 B2 JP7487443 B2 JP 7487443B2 JP 2019178899 A JP2019178899 A JP 2019178899A JP 2019178899 A JP2019178899 A JP 2019178899A JP 7487443 B2 JP7487443 B2 JP 7487443B2
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Landscapes
- Coloring Foods And Improving Nutritive Qualities (AREA)
- Medicinal Preparation (AREA)
- Cosmetics (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Description
特許文献1には、有効成分と、油脂又は多糖類とを含有するゲル状組成物(具体的には、ハイドロゲルビーズ(油脂含量40%))にかかる発明が記載されている。この発明によれば、含有する有効成分に対し高い徐放性を有し、また比重の調製により経口投与された場合の胃内滞留性を高めることが可能であることが記載されている。
[1] 油系増粘剤、油脂、及び、有効成分を含み、実質的に水を含有しない、粘膜上皮適用組成物。
[2] ゾル状、ゲル状、ペースト状、又は、クリーム状である、[1]の組成物。
[3] 25℃及びせん断速度10(1/s)における粘度が100mPa・s~20000mPa・sであるか、又は25℃でのゲル強度が800N/m2~51000N/m2である、[1]又は[2]の組成物。
[4] 油系増粘剤がポリグリセリン脂肪酸エステルである、[1]~[3]のいずれかの組成物。
[5] 有効成分が脂溶性有効成分である、[1]~[4]のいずれかの組成物。
[6] 脂溶性有効成分がメントール、ビタミンE、ビタミンA、ビタミンK、ビタミンD、ショウガオール、又は、サンショオールである、[5]の組成物。
[7] 水分含量が1質量%以下である、[1]~[5]のいずれかの組成物。
[8] 粘膜上皮が、眼、耳、鼻、口、呼吸器、消化管、泌尿器、生殖器からなる群より選ばれた少なくとも1種の粘膜上皮である、[1]~[7]のいずれかの組成物。
[9] 経口組成物である、[1]~[7]のいずれかの組成物。
[10] カプセル化又はコーティング化された形態を有する、[9]の組成物。
<1.口粘膜>
1.組成物の調製
下記表1の組成にしたがって、油系増粘剤(ポリグリセリン脂肪酸エステル(製品名:TAISET AD(太陽化学株式会社)))を含む実施例1の組成物、油系増粘剤及び水系増粘剤をいずれも含まない比較例1の組成物、ならびに、水系増粘剤(キサンタンガム)を含む比較例2の組成物を調製した。表中の各成分の量は質量比にて示される。
25℃及びせん断速度10(1/s)における粘度を測定したところ、750mPa・sであった。また、25℃でのゲル強度を測定したところ、2500N/m2であった。
実施例1、比較例1、及び比較例2の各組成物について、パネラー5名により、経口摂取した後に、口腔にて感じられる有効成分による冷涼感を、「0:感じない」から、「10:感じる」の10点満点で点数付けを行い、摂取後0分~35分まで経時的に評価した。
各組成物について、官能実験の結果を図1に示す。結果はパネラー5名の点数の平均値を示す。
油系増粘剤を含む実施例1の組成物は、ゲル化剤を含まない比較例1の組成物と比べて、摂取直後より冷涼感が強く感じられた。また、油系増粘剤を含む実施例1の組成物は、油系増粘剤及び水系増粘剤のいずれも含まない比較例1の組成物、及び、水系増粘剤を含む比較例2の組成物と比べて長時間にわたり冷涼感が感じられた。
1.組成物の調製
下記表2の組成にしたがって、油系増粘剤(ポリグリセリン脂肪酸エステル(製品名:TAISET AD(太陽化学株式会社)))を含む実施例2の組成物、油系増粘剤及び水系増粘剤をいずれも含まない比較例3の組成物、ならびに、水系増粘剤(キサンタンガム)を含む比較例4の組成物を調製した。表中の各成分の量は質量比にて示される。
実施例2、比較例3、及び比較例4の各組成物について、パネラー5名により、鼻粘膜に適用した後に感じられる有効成分による冷涼感を、「0:感じない」から、「10:感じる」の10点満点で点数付けを行い、適用後0分~50分まで経時的に評価した。
各組成物について、官能実験の結果を図2に示す。結果はパネラー5名の点数の平均値を示す。
Claims (7)
- 油系増粘剤、液状の油脂、及び、脂溶性有効成分を含み、実質的に水を含有しない、ゾル状、ペースト状、又は、クリーム状である粘膜上皮適用組成物であって、
油系増粘剤がポリグリセリン脂肪酸エステルであり、
液状の油脂を80.0質量%~99.5質量%の範囲より適宜選択される量で含み、
油系増粘剤が液状の油脂をゲル化して、25℃及びせん断速度10(1/s)における粘度が100mPa・s~20000mPa・sであるか、又は25℃でのゲル強度が800N/m 2 ~51000N/m 2 である、組成物。 - 25℃及びせん断速度10(1/s)における粘度が750mPa・sであるか、又は25℃でのゲル強度が2500N/m 2 である、請求項1に記載の組成物。
- 脂溶性有効成分がメントール、ビタミンE、ビタミンA、ビタミンK、ビタミンD、ショウガオール、又は、サンショオールである、請求項1又は2に記載の組成物。
- 水分含量が1質量%以下である、請求項1~3のいずれか1項に記載の組成物。
- 粘膜上皮が、眼、耳、鼻、口、呼吸器、消化管、泌尿器、生殖器からなる群より選ばれた少なくとも1種の粘膜上皮である、請求項1~4のいずれか1項に記載の組成物。
- 経口組成物である、請求項1~5のいずれか1項に記載の組成物。
- カプセル化又はコーティング化された形態を有する、請求項6に記載の組成物。
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