JP5940731B2 - S−アリル−l−システインを有効成分として含む眼疾患予防または治療用組成物、およびこれを含む医薬製剤 - Google Patents
S−アリル−l−システインを有効成分として含む眼疾患予防または治療用組成物、およびこれを含む医薬製剤 Download PDFInfo
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- JP5940731B2 JP5940731B2 JP2015527392A JP2015527392A JP5940731B2 JP 5940731 B2 JP5940731 B2 JP 5940731B2 JP 2015527392 A JP2015527392 A JP 2015527392A JP 2015527392 A JP2015527392 A JP 2015527392A JP 5940731 B2 JP5940731 B2 JP 5940731B2
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
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Description
本発明の他の目的は、前記眼疾患予防または治療用組成物を用いて製造した医薬製剤を提供することにある。
前記眼疾患は、加齢性黄斑変性または網膜変性疾患であってもよい。
前記眼疾患予防または治療用組成物は、前記S−アリル−L−システインを5〜99.9重量%で含んでもよい。
前記眼疾患予防または治療用組成物は、抗炎症剤または抗酸化剤をさらに含んでもよい。
以下、本発明をさらに詳細に説明する。
前記眼疾患は加齢性黄斑変性または網膜変性疾患であってもよい。
前記眼疾患予防または治療用組成物は、抗炎症剤または抗酸化剤をさらに含んでもよい。
また、前記眼疾患予防または治療用組成物を含む医薬製剤は、眼疾患の予防または治療効果を奏する。
本発明の実験および分析に使用された網膜色素上皮細胞株(Arising retinal pigment epithelia cell line、ARPE−19:ATCC no.CRL−2302)は、分譲を受け(ARPE−19、American Type Culture Collection、Manassas VA)、従来の文献に記述された方法で継代培養した(Sparrow, J. Retal., Α2Ε, a1ipofuscinfluorophore, in human retinal pigmented epithelial cells in culture. Invest Ophthalmol Vis Sci 1999, 40(12), 2988-95)。
細胞を実験に使用する際には、5×10個の細胞数で6−well plateに接種(seeding)して実験に使用した。
青色光によって酸化したA2Eに対するS−アリル−L−システイン(S-allyl-cysteine)の酸化抑制能実験
青色光によって酸化したA2Eに対するS−アリル−L−システイン(S-allyl-cysteine)の酸化抑制能を測定するために、100μMのΑ2ΕをPBS(phosphate buffered saline)に最終濃度が20μMとなるように溶解させ、96−well plateにそれぞれ200μLずつ添加した後、この溶液に陰性対照群および陽性対照群(ルテイン:20μΜ)または所定の濃度(S-allyl-cysteine:1、10、100μΜ)で希釈された試料を添加した。
B={Abs. of A2E+sample)−Abs. of sample}−
{(Abs. of A2E+sample+blue light)−
(Abs. of sample−Abs. of sample+blue light)}
A2Eの蓄積したヒトの網膜色素上皮細胞株(ARPE−19)における青色光によるアポトーシスに対するS−アリル−システイン(S-allyl-cysteine)の細胞保護能の実験
青色光によって酸化したA2Eに対するS−アリル−L−システイン(S-allyl-cysteine)の酸化抑制能
本発明のS−アリル−L−システインのA2Eに対する酸化抑制能を確認するために、実験例1と同様の方法によって青色光を照射した後、酸化A2Eの濃度を測定し、図1に示した。
Claims (6)
- S−アリル−L−システイン、その薬学的に許容される塩、またはそれらの溶媒和物または水和物を有効成分として含み、網膜色素上皮細胞内のN−レチニリデン−N−レチニル−エタノールアミン(A2E)の光酸化を抑制することを特徴とする、乾性加齢性黄斑変性予防または治療用組成物。
- 前記眼疾患予防または治療用組成物が前記S−アリル−L−システインを5〜99.9重量%で含むことを特徴とする、請求項1に記載の乾性加齢性黄斑変性予防または治療用組成物。
- 前記S−アリル−L−システインは、ネギ属(Allium genus)植物から分離精製されたもの、合成されたもの、および発酵によって製造されたものよりなる群から選ばれたいずれかであることを特徴とする、請求項1に記載の乾性加齢性黄斑変性予防または治療用組成物。
- 前記眼疾患予防または治療用組成物が抗炎症剤または抗酸化剤をさらに含むことを特徴とする、請求項1に記載の乾性加齢性黄斑変性予防または治療用組成物。
- 前記抗炎症剤は、イブプロフェン(ibuprofen)、ケトプロフェン(ketoprofen)、フルルビプロフェン(flurbiprofen)、フェノプロフェン(feno-profen)、ナプロキセン(naproxen)、ピキシカム(piroxicam)、テキノシカム(tenoxicam)、イソキシカム(isoxicam)、メロキシカム(meloxicam)、インドメタシン(indomethacin)、アセクロフェナク(aceclofenac)、ジクロフェナク(diclofenac)、およびこれらの組み合わせよりなる群から選ばれたいずれか一つであり、
前記抗酸化剤は、ビタミンA、ビタミンC、ビタミンE、カロチノイド、亜鉛、銅、鉄、マンガン、ルテイン、ゼアキサンチン、セレニウム、グルタチオン(GHS)、リコピン、およびこれらの組み合わせよりなる群から選ばれたいずれか一つであることを特徴とする、請求項4に記載の乾性加齢性黄斑変性予防または治療用組成物。 - 請求項1に記載の乾性加齢性黄斑変性予防または治療用組成物を含む経口投与用製剤、粘膜適用製剤、注射剤、吸入剤および外用剤よりなる群から選ばれる医薬製剤。
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KR10-2012-0089857 | 2012-08-17 | ||
KR1020120089857A KR101423631B1 (ko) | 2012-08-17 | 2012-08-17 | 에스-알릴엘-시스테인을 유효성분으로 포함하는 안질환 예방 또는 치료용 조성물 및 이를 포함하는 의약제제 |
PCT/KR2013/007420 WO2014027865A1 (ko) | 2012-08-17 | 2013-08-19 | 에스-알릴엘-시스테인을 유효성분으로 포함하는 안진환 예방 또는 치료용 조성물 및 이를 포함하는 의약제제 |
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TWI715864B (zh) * | 2018-09-05 | 2021-01-11 | 趙效明 | 用於預防或治療由視網膜缺血引起的疾病、病症或病況的方法 |
KR102165845B1 (ko) * | 2018-09-18 | 2020-10-15 | 안국건강 주식회사 | 청색광에 의한 눈피로 개선용 조성물 |
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JP2875308B2 (ja) | 1989-11-22 | 1999-03-31 | 湧永製薬株式会社 | S−アリルシステイン高濃度含有組成物の製造方法 |
US5596011A (en) * | 1995-04-06 | 1997-01-21 | Repine; Karen M. | Method for the treatment of macular degeneration |
US6866864B2 (en) * | 2000-03-20 | 2005-03-15 | Ahmed Mousa | Compositions and methods of use in the treatment of angiogenesis and vascular-related disorders |
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CN104540506A (zh) | 2015-04-22 |
US20150231100A1 (en) | 2015-08-20 |
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JP2015528825A (ja) | 2015-10-01 |
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US9326960B2 (en) | 2016-05-03 |
KR20140023659A (ko) | 2014-02-27 |
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