論文

査読有り
2015年5月

Overcoming the polyethylene glycol dilemma via pathological environment-sensitive change of the surface property of nanoparticles for cellular entry

JOURNAL OF CONTROLLED RELEASE
  • Susumu Hama
  • ,
  • Shoko Itakura
  • ,
  • Mayumi Nakai
  • ,
  • Kayoko Nakayama
  • ,
  • Satoshi Morimoto
  • ,
  • Satoko Suzuki
  • ,
  • Kentaro Kogure

206
開始ページ
67
終了ページ
74
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1016/j.jconrel.2015.03.011
出版者・発行元
ELSEVIER SCIENCE BV

Modification with polyethylene glycol (PEG) is currently considered an important strategy for anti-cancer drug delivery, because PEGylated-nanoparticles would be effectively delivered to tumor tissue by enhanced permeation and retention effects. However, PEGylation suppresses the cellular uptake of nanoparticles (NPs) to target cells (known as the PEG dilemma). Here, we propose a novel strategy, namely conferring a pathological environment-sensitive property of nanoparticles for overcoming the PEG dilemma. Specifically, although nanoparticles have an overall negative surface charge to avoid interactions with biogenic substances in blood circulation, inversion of surface charge (to positive) at the pH of the tumor microenvironment may allow the nanoparticles to be taken up by cancer cells. To prove this concept, charge-invertible nanoparticles modified with novel slightly acidic pH-sensitive peptide (SAPSP-NPs) were developed. The negatively-charged SAPSP-NPs were delivered to tumor tissue, and were successfully taken up by cancer cells upon inversion of the surface charge to positive at intratumoral pH. SAPSP-NPs may serve as an alternative carrier to the PEGylated NP for anticancer drug delivery. (C) 2015 Elsevier B.V. All rights reserved.

リンク情報
DOI
https://doi.org/10.1016/j.jconrel.2015.03.011
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000353361400007&DestApp=WOS_CPL
ID情報
  • DOI : 10.1016/j.jconrel.2015.03.011
  • ISSN : 0168-3659
  • eISSN : 1873-4995
  • Web of Science ID : WOS:000353361400007

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