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Lyotropic Liquid Crystals Prepared with Biocompatible Ionic Liquids for Improving Transdermal Permeation

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Lyotropic Liquid Crystals Prepared with Biocompatible Ionic Liquids for Improving Transdermal Permeation

国立国会図書館請求記号
Z18-1127
国立国会図書館書誌ID
034369910
資料種別
記事
著者
Koki Haraほか
出版者
東京 : 日本膜学会
出版年
2025-09
資料形態
掲載誌名
膜 = Membrane / 膜編集委員会 編 50(5)=299:2025.9
掲載ページ
p.229-236
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資料種別
記事
著者・編者
Koki Hara
Masahiro Goto
タイトル(掲載誌)
膜 = Membrane / 膜編集委員会 編
巻号年月日等(掲載誌)
50(5)=299:2025.9
掲載巻
50
掲載号
5
掲載通号
299
掲載ページ
229-236
掲載年月日(W3CDTF)
2025-09
ISSN(掲載誌)
0385-1036
ISSN-L(掲載誌)
0385-1036
出版事項(掲載誌)
東京 : 日本膜学会
出版地(国名コード)
JP
本文の言語コード
eng
NDLC
対象利用者
一般
所蔵機関
国立国会図書館
請求記号
Z18-1127
連携機関・データベース
国立国会図書館 : 国立国会図書館雑誌記事索引
書誌ID(NDLBibID)
034369910
整理区分コード
632

デジタル

要約等
Lyotropic liquid crystals (LLCs) have been attracting attention as new transdermal drug delivery carriers because of their high stability compared with that of other liquid carriers, such as emulsions, micelles, and liposomes. However, the transdermal delivery performance of LLCs is not satisfactory because their high viscosity often reduces the permeation rate of the drugs. In the present study, to improve the performance of LLCs as a drug delivery carrier, we have developed an ionic liquid crystal (ILC) formulation by adding an ionic liquid (IL) component as a mesogen, which can enhance transdermal permeation. A biocompatible ionic liquid IL[Cho][Ole], composed of choline and oleic acid, was synthesized for pharmaceutical applications. The ILC formulations loaded with 1 wt% of favipiravir (FAV), which had potential as a therapeutic agent for coronavirus infections, showed excellent stability. In vitro drug permeation experiments using mouse skin indicated that the ILCs enhanced the permeability of FAV. In particular, FAV–ILC–70 (IL[Cho][Ole] : water = 7 : 3 (w/w)), which has a gyroid structure, significantly improved the transdermal delivery of FAV by fluidizing the stratum corneum lipids. These results suggest that liquid crystalline formulations with biocompatible ILs are promising new transdermal drug delivery carriers.
DOI
10.5360/membrane.50.229
オンライン閲覧公開範囲
インターネット公開
連携機関・データベース
科学技術振興機構 : J-STAGE

デジタル

要約等
Lyotropic liquid crystals (LLCs) have been attracting attention as new transdermal drug delivery carriers because of their high stability compared with that of other liquid carriers, such as emulsions, micelles, and liposomes. However, the transdermal delivery performance of LLCs is not satisfactory because their high viscosity often reduces the permeation rate of the drugs. In the present study, to improve the performance of LLCs as a drug delivery carrier, we have developed an ionic liquid crystal (ILC) formulation by adding an ionic liquid (IL) component as a mesogen, which can enhance transdermal permeation. A biocompatible ionic liquid IL[Cho][Ole], composed of choline and oleic acid, was synthesized for pharmaceutical applications. The ILC formulations loaded with 1 wt% of favipiravir (FAV), which had potential as a therapeutic agent for coronavirus infections, showed excellent stability. In vitro drug permeation experiments using mouse skin indicated that the ILCs enhanced the permeability of FAV. In particular, FAV–ILC–70 (IL[Cho][Ole] : water = 7 : 3 (w/w)), which has a gyroid structure, significantly improved the transdermal delivery of FAV by fluidizing the stratum corneum lipids. These results suggest that liquid crystalline formulations with biocompatible ILs are promising new transdermal drug delivery carriers.
連携機関・データベース
国立情報学研究所 : CiNii Research
提供元機関・データベース
Japan Link Center
雑誌記事索引データベース
Crossref
書誌ID(NDLBibID)
034369910