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  1. 110 医歯薬学総合研究科 = Graduate School of Biomedical Sciences
  2. 110 学術雑誌論文 = Articles in academic journal

One-step formation of plasmid DNA–loaded lipid–inorganic salt nanoparticles optimized via two-step design of experiments

http://hdl.handle.net/10069/0002003515
http://hdl.handle.net/10069/0002003515
a1888c30-c876-4b6e-9ed7-9f255660a5a0
名前 / ファイル ライセンス アクション
EJPB219_114955.pdf EJPB219_114955.pdf (1.7 MB)
 Download is available from 2026/12/9.
アイテムタイプ 学術雑誌論文 / Journal Article(1)
公開日 2025-12-18
タイトル
タイトル One-step formation of plasmid DNA–loaded lipid–inorganic salt nanoparticles optimized via two-step design of experiments
言語 en
言語
言語 eng
キーワード
言語 en
主題Scheme Other
主題 Gene delivery
キーワード
言語 en
主題Scheme Other
主題 Plasmid DNA
キーワード
言語 en
主題Scheme Other
主題 Lipids
キーワード
言語 en
主題Scheme Other
主題 Calcium carbonate
キーワード
言語 en
主題Scheme Other
主題 Nanoparticles
キーワード
言語 en
主題Scheme Other
主題 Design of experiments
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_6501
資源タイプ journal article
著者 Kato, Riku

× Kato, Riku

en Kato, Riku

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Fumoto, Shintaro

× Fumoto, Shintaro

en Fumoto, Shintaro

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Muttil, Pavan

× Muttil, Pavan

en Muttil, Pavan

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Okami, Kazuya

× Okami, Kazuya

en Okami, Kazuya

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Yamashita, Mana

× Yamashita, Mana

en Yamashita, Mana

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Koyanagi, Hayato

× Koyanagi, Hayato

en Koyanagi, Hayato

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Miyamoto, Hirotaka

× Miyamoto, Hirotaka

en Miyamoto, Hirotaka

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Kawakami, Shigeru

× Kawakami, Shigeru

en Kawakami, Shigeru

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Nishida, Koyo

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en Nishida, Koyo

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抄録
内容記述タイプ Abstract
内容記述 For successful gene delivery, researchers need to consider multiple processes, such as the endosomal escape of cargos. The preparation of highly functional systems is complicated. Here, we developed a simplified preparation method for plasmid DNA–loaded galactosylated lipid–inorganic salt nanoparticles, which adopts a one-step alcohol injection method for the formation of lipid nanoparticles. The nanoparticles were designed to have a core of plasmid DNA with inorganic salts consisting of calcium carbonate and phosphate for endosomal escape and a lipid shell for the stable formation of nanoparticles. The formulation and process parameters were optimized using a two-step design of experiments, that is, a definitive screening design followed by a central composite design. We successfully established uniform nanoparticles of 120 nm in size based on micropipette mixing. Transfection efficiency of the nanoparticles prepared via micropipette mixing was equivalent to that of a commercially available transfection reagent in human hepatocellular carcinoma HepG2 cells. Using a microfluidic device, the nanoparticle size was decreased to 70 nm, while a high transfection efficiency was maintained in HepG2 cells. Moreover, the effect of inorganic salts on the nanoparticle transfection efficiency was evaluated. Notably, the formation of a calcium carbonate core was crucial for achieving an effective endosomal escape and a high transfection efficiency. Overall, this study provides valuable information for the design and simplified preparation of lipid–inorganic salt nanoparticles for efficient gene delivery.
言語 en
書誌情報 en : European Journal of Pharmaceutics and Biopharmaceutics

巻 219, p. art. no. 114955, 発行日 2025-12-09
出版者
出版者 Elsevier B.V.
言語 en
ISSN
収録物識別子タイプ ISSN
収録物識別子 09396411
DOI
関連タイプ isVersionOf
識別子タイプ DOI
関連識別子 https://doi.org/10.1016/j.ejpb.2025.114955
権利
権利情報 © 2025 Elsevier B.V. This manuscript version is made available under the CC-BY-NC-ND 4.0 license https://creativecommons.org/licenses/by-nc-nd/4.0/.
言語 en
著者版フラグ
出版タイプ AM
出版タイプResource http://purl.org/coar/version/c_ab4af688f83e57aa
引用
内容記述タイプ Other
内容記述 European Journal of Pharmaceutics and Biopharmaceutics, 219, art. no. 114955; 2025
言語 en
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