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Ujita, Hitomi Department of Dental Anesthesiology, Okayama University Hospital
Higuchi, Hitoshi Department of Dental Anesthesiology, Okayama University Hospital ORCID Kaken ID
Nishioka, Yukiko Department of Dental Anesthesiology, Okayama University Hospital
Miyake, Saki Department of Dental Anesthesiology and Special Care Dentistry, Okayama University Graduate of Medicine, Dentistry and Pharmaceutical Sciences
Sato, Riko Department of Dental Anesthesiology and Special Care Dentistry, Okayama University Graduate of Medicine, Dentistry and Pharmaceutical Sciences
Miyawaki, Takuya Department of Dental Anesthesiology and Special Care Dentistry, Okayama University Graduate of Medicine, Dentistry and Pharmaceutical Sciences Kaken ID publons
Abstract
Background/Objectives: Propofol is frequently used as an intravenous anesthetic and is rapidly metabolized. Therefore, if it could be administered non-invasively (e.g., orally) as premedication, it might hasten emergence from anesthesia, thereby improving patient safety. However, it undergoes extensive first-pass metabolism in the liver and intestines, limiting the route for premedication. We evaluated whether intranasal delivery of a propofol-encapsulated liposome solution improves systemic exposure and bioavailability in rabbits. Methods: A propofol-encapsulated liposome solution was administered to rabbits via the intravenous, oral, and intranasal routes. Blood propofol concentrations were measured for up to 60 min after administration and the area under the concentration–time curve (AUC0–60) and bioavailability of the propofol-encapsulated liposome solution were compared with those of the non-encapsulated propofol formulation. The differences were tested by two-way analysis of variance (ANOVA) with Šidák’s post hoc multiple-comparisons test and the Mann–Whitney test (α = 0.05). Results: The AUC0–60 for blood propofol concentrations after intravenous administration was significantly higher with the propofol-encapsulated liposome solution than with the non-encapsulated propofol formulation (3038.8 ± 661.5 vs. 1929.8 ± 58.2 ng·min/mL; p = 0.0286). By contrast, no increase in blood propofol concentrations was observed after oral administration, whereas intranasal administration increased blood propofol concentrations and yielded significantly higher bioavailability compared with the non-encapsulated propofol formulation (16.4 ± 7.3% vs. 2.0 ± 1.2%; p = 0.0286). Conclusions: The findings of the present study suggest that intranasal liposomal propofol increased systemic availability compared with a non-encapsulated formulation, supporting further evaluation as a candidate premedication approach for propofol.
Keywords
liposome
propofol
bioavailability
intranasal administration
Published Date
2025-11-09
Publication Title
Pharmaceutics
Volume
volume17
Issue
issue11
Publisher
MDPI AG
Start Page
1446
ISSN
1999-4923
Content Type
Journal Article
language
English
OAI-PMH Set
岡山大学
Copyright Holders
© 2025 by the authors.
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DOI
Related Url
isVersionOf https://doi.org/10.3390/pharmaceutics17111446
License
https://creativecommons.org/licenses/by/4.0/
Citation
Ujita, H.; Higuchi, H.; Nishioka, Y.; Miyake, S.; Sato, R.; Miyawaki, T. Development of Propofol-Encapsulated Liposomes and the Effect of Intranasal Administration on Bioavailability in Rabbits. Pharmaceutics 2025, 17, 1446. https://doi.org/10.3390/pharmaceutics17111446
助成情報
23K16224: 臨床応用可能なプロポフォール封入リポソーム製剤開発のための生物学的利用能の検討 ( 独立行政法人日本学術振興会 / Japan Society for the Promotion of Science )