Papers

Peer-reviewed
Feb, 2015

Augmented EPR effect by photo-triggered tumor vascular treatment improved therapeutic efficacy of liposomal paclitaxel in mice bearing tumors with low permeable vasculature

JOURNAL OF CONTROLLED RELEASE
  • Tomoya Araki
  • ,
  • Ken-ichi Ogawara
  • ,
  • Haruka Suzuki
  • ,
  • Rie Kawai
  • ,
  • Taka-ichi Watanabe
  • ,
  • Tsutomu Ono
  • ,
  • Kazutaka Higaki

Volume
200
Number
First page
106
Last page
114
Language
English
Publishing type
Research paper (scientific journal)
DOI
10.1016/j.jconrel.2014.12.038
Publisher
ELSEVIER SCIENCE BV

The effects of photo-triggered tumor vascular treatment (PVT) on the structural and functional properties of tumor vasculature were assessed in Colon-26 (C26) and B16/BL6 (B16) tumor-bearing mice. Furthermore, anti-tumor efficacy of subsequently injected PEG liposomal paclitaxel (PL-PTX) was also evaluated. As a photosensitizer, a hydrophobic porphyrin derivative was used and formulated in polymeric nanoparticle composed of polyethylene glycol-block-polylactic acid to avoid its non-specific in vivo disposition. In the mice bearing C26 with high permeable vasculature, the prominent anti-tumor activity was confirmed by PVT alone, but the subsequently injected PL-PTX did not show any additive effect. PVT itself initially induced apoptotic cell death of tumor vascular endothelial cells and platelet aggregation, which would have subsequently induced apoptosis of C26 tumor cells surrounding the vasculature. On the other hand, in the mice bearing B16 with low permeable vasculature, PVT enhanced the anti-tumor activity of subsequently injected PL-PTX, which would be attributed to the tumor disposition amount and area of PEG liposomes enhanced by PVT. These results clearly indicated that the treatment would have made it possible to provide more efficient extravasation of PL-PTX, leading to its more potent anti-tumor effect. (C) 2015 Elsevier B.V. All rights reserved.

Link information
DOI
https://doi.org/10.1016/j.jconrel.2014.12.038
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000348456900012&DestApp=WOS_CPL
ID information
  • DOI : 10.1016/j.jconrel.2014.12.038
  • ISSN : 0168-3659
  • eISSN : 1873-4995
  • Web of Science ID : WOS:000348456900012

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