Figure - PMC

Skip to main content

An official website of the United States government

Here's how you know

Here's how you know

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you've safely connected to the .gov website. Share sensitive information only on official, secure websites.

View full-text article in PMC

. 2015 Nov 30;107(1):60–67. doi: 10.1111/cas.12841

Search in PMC
Search in PubMed
View in NLM Catalog
Add to search

© 2015 The Authors. Cancer Science published by Wiley Publishing Asia Pty Ltd on behalf of Japanese Cancer Association.

This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.

PMC Copyright notice

Ex vivo accumulation of ¹¹¹In‐encapsulated liposomes at several time points among four human ovarian cancer xenografted tumors. (a) Ex vivo analysis at each time point revealed significantly higher accumulation levels in Caov‐3 and SK‐OV‐3 tumors than those in KURAMOCHI and TOV‐112D tumors at 72 h after injection. Six to 11 mice were used for analysis in each group at each time point. (b) Accumulation of ¹¹¹In‐encapsulated liposomes in an individual mouse at 72 h after injection. Most notably, among all four tumor types analyzed, only SK‐OV‐3 displayed a wide range of variation. *P < 0.05. %AD/g, % of administered dose/gram of organ.