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METHOD OF TRANSDERMALLY ABSORBING HYDROPHILIC DRUG
专利权人:
KYUSHU UNIV;国立大学法人九州大学;NISSAN CHEM CORP;日産化学株式会社
发明人:
GOTO MASAHIRO,後藤 雅宏,IMOTO TAKAYUKI,井本 鷹行,IWAMA TAKEHISA,岩間 武久,MIYAJI NOBUHIDE,宮地 伸英
申请号:
JP2019031758
公开号:
JP2019116484A
申请日:
2019.02.25
申请国别(地区):
JP
年份:
2019
代理人:
摘要:
To provide methods of transdermally absorbing a hydrophilic drug that is intended to increase not only feeling of use but also the percutaneous absorption properties, by using a low molecule gelling agent.SOLUTION: Provided is a method of transdermally absorbing a hydrophilic drug, characterized by using a lipid peptide type compound consisting of at least one of a compound represented by the formula (1) and an analogue compound thereof or a pharmaceutically usable salt thereof. (Where, Rrepresents an aliphatic group of C9-23; Rrepresents H, or an alkyl group of C1 to C4 which may have a branched chain of C1 to 2; Rrepresents -(CH)-X group, n represents a number of 1-4, and X represents an amino group, a guanidino group, a -CONHgroup, or a 5- or 6-membered ring which may have 1 to 3 N or a fused heterocyclic ring composed of a 5-membered ring and a 6-membered ring.)SELECTED DRAWING: None【課題】低分子ゲル化剤を用い、使用感のみならず経皮吸収性の向上を図った親水性薬物を経皮吸収させる方法の提供。【解決手段】式(1)で表される化合物並びにその類似化合物又はその薬学的に使用可能な塩のうちの少なくとも一種からなる脂質ペプチド型化合物を用いることを特徴とする、親水性薬物を経皮吸収させる方法。(式中、R1はC9~23の脂肪族基、R2はH、又はC1~2の分枝鎖を有し得るC1~4のアルキル基、R3は-(CH2)n-X基、nは1~4の数、Xはアミノ基、グアニジノ基、-CONH2基、又はNを1~3個有し得る5員環若しくは6員環又は5員環と6員環から構成される縮合複素環を表す。)【選択図】なし
来源网站:
中国工程科技知识中心
来源网址:
http://www.ckcest.cn/home/

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