Oral delivery of peptide drugs using nanoparticles self-assembled by poly(γ-glutamic acid) and a chitosan derivative functionalized by trimethylation

Fwu Long Mi, Yong Yi Wu, Yu Hsin Lin, Kiran Sonaje, Yi Cheng Ho, Chiung Tong Chen, Jyuhn Huarng Juang, Hsing Wen Sung

研究成果: 雜誌貢獻文章同行評審

124 引文 斯高帕斯(Scopus)

摘要

In the study, chitosan (CS) was conjugated with trimethyl groups for the synthesis of N-trimethyl chitosan (TMC) polymers with different degrees of quaternization. Nanoparticles (NPs) self-assembled by the synthesized TMC and poly(γ-glutamic acid) (γ-PGA, TMC/γ-PGA NPs) were prepared for oral delivery of insulin. The loading efficiency and loading content of insulin in TMC/γ-PGA NPs were 73.8 ± 2.9% and 23.5 ± 2.1%, respectively. TMC/γ-PGA NPs had superior stability in a broader pH range to CS/γ-PGA NPs; the in vitro release profiles of insulin from both test NPs were significantly affected by their stability at distinct pH environments. At pH 7.0, CS/γ-PGA NPs became disintegrated, resulting in a rapid release of insulin, which failed to provide an adequate retention of loaded insulin, while the cumulative amount of insulin released from TMC/γ-PGA NPs was significantly reduced. At pH 7.4, TMC/γ-PGA NPs were significantly swelled and a sustained release profile of insulin was observed. Confocal microscopy confirmed that TMC40/γ-PGA NPs opened the tight junctions of Caco-2 cells to allow the transport of insulin along the paracellular pathway. Transepithelial-electrical-resistance measurements and transport studies implied that CS/γ-PGA NPs can be effective as an insulin carrier only in a limited area of the intestinal lumen where the pH values are close to the pKa of CS. In contrast, TMC40/γ-PGA NPs may be a suitable carrier for transmucosal delivery of insulin within the entire intestinal tract.

原文英語
頁(從 - 到)1248-1255
頁數8
期刊Bioconjugate Chemistry
19
發行號6
DOIs
出版狀態已發佈 - 六月 2008
對外發佈

ASJC Scopus subject areas

  • 化學 (全部)
  • 有機化學
  • 臨床生物化學
  • 生物化學、遺傳與分子生物學 (全部)
  • 生物化學

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