ID | JOS-fddev.2023.1270584 |
著者:名前 | |
著者:別形式 | Todo, Hiroaki / Niki, Rina / Okada, Akie / Narita, Ibuki / Inamura, Kazuya / Ito, Ayu / Itakura, Shoko / Hijikuro, Ichiro / Sugibayashi, Kenji |
著者:カナ | |
著者:所属 | 城西大学薬学部 / 城西大学薬学部 / 城西大学薬学部 / 城西大学薬学部 / 城西大学薬学部 / 城西大学薬学部 / 城西大学薬学部 / 株式会社ファルネックス / 城西国際大学薬学部 |
著者:所属(別形式) | Josai University, Faculty of Pharmacy and Pharmaceutical Sciences / Josai University, Faculty of Pharmacy and Pharmaceutical Sciences / Josai University, Faculty of Pharmacy and Pharmaceutical Sciences / Josai University, Faculty of Pharmacy and Pharmaceutical Sciences / Josai University, Faculty of Pharmacy and Pharmaceutical Sciences / Josai University, Faculty of Pharmacy and Pharmaceutical Sciences / Josai University, Faculty of Pharmacy and Pharmaceutical Sciences / Farnex Incorporated / Josai International University, Faculty of Pharmaceutical Sciences |
著者版フラグ | publisher |
出版者 | Frontiers |
電子ISSN | 26740850 |
掲載誌名 | |
巻 | 3 |
刊行年月 | 2023-10 |
開始ページ | 1 |
終了ページ | 11 |
コンテンツ作成日 | 2023-08-01 |
コンテンツ修正日 | 2023-09-22 |
コンテンツ登録日 | 2023-10-26 |
識別番号:DOI | info:doi/10.3389/fddev.2023.1270584 |
識別番号:DOI(リンク) | |
抄録 | Non-lamellar liquid crystal (NLLC) structures have gained increasing attention for the controlled release of entrapped drugs. In the present study, an in situ NLLC structure-forming depot formulation through contact with water was developed using a ternary mixture system of soya phosphatidyl choline (SPC), 1, 2-dioleoyl-sn-glycero-3-phosphoglycerol sodium salt (DOPG), and sorbitan trioleate (Span 85), and the long-term release of an entrapped model drug, leuprolide acetate (LA), was investigated using evaluation of in vitro release and in vivo blood concentration–time profiles. Polarized images and small angle X-ray scattering analysis were used to confirm the presence of NLLC structures by contacting the prepared formulation with water. In addition, LA release and blood concentration–time profiles were investigated using in vitro and in vivo experiments, respectively. In situ NLLC constructed formulations by contacting water were achieved using a ternary mixture of SPC, DOPG, and Span 85. In particular, negative curvature was increased with an increase in the amount of Span 85 in the formulation, and an Fd3m structure was obtained with a sustained release of LA. A maintained blood concentration of LA over 21 days was confirmed by subcutaneous (s.c.) administration of the formulation. No retained administered formulation at the injection site was confirmed 28 days after administration without any signs of irritation, inflammation, or other apparent toxicity confirmed by visual observation. This result may be helpful for the development of a lipid-based formulation of peptides and proteins with sustained drug release. |
キーワード | |
注記 | This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
言語 | eng |
資源タイプ | text |
ジャンル | |
フォーマット | application/pdf |
権利 | Copyright © 2023 Todo, Niki, Okada, Narita, Inamura, Ito, Itakura, Hijikuro and Sugibayashi. |
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