Oral delivery of diclofenac sodium using a novel solid-in-oil suspension

Hongyu Piao, Noriho Kamiya, Junji Watanabe, Hideakira Yokoyama, Akihiko Hirata, Takeru Fujii, Ichiro Shimizu, Susumu Ito, Masahiro Goto

研究成果: ジャーナルへの寄稿学術誌査読

38 被引用数 (Scopus)

抄録

The present work reports on a new pharmaceutical formulation for oral delivery of diclofenac sodium (DFNa), a non-steroidal anti-inflammatory drug (NSAID). Although DFNa itself is water-soluble at neutral pH, it was readily suspended in soybean oil via complex formation with an edible lipophilic surfactant and a matrix protein. The resulting solid-in-oil (S/O) suspension containing stably encapsulated DFNa in an oil phase markedly reduced the risks for gastrointestinal ulcers upon oral administration even at the LD50 level in rats (ca. 50 mg/kg DFNa). In addition, plasma concentration of DFNa upon administration of an S/O suspension was comparable with that of the aqueous counterpart at the same DFNa dose. These results indicate the potential use of S/O suspensions as novel oil-based pharmaceutical formulations for oral delivery of water-soluble drugs without causing severe mucitis.

本文言語英語
ページ(範囲)159-162
ページ数4
ジャーナルInternational Journal of Pharmaceutics
313
1-2
DOI
出版ステータス出版済み - 4月 26 2006

!!!All Science Journal Classification (ASJC) codes

  • 薬科学

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