Long-term theranostic hydrogel system for solid tumors

Biomaterials. 2012 Mar;33(7):2251-9. doi: 10.1016/j.biomaterials.2011.11.083. Epub 2011 Dec 19.

Abstract

The long-term theranostic hydrogel system for solid tumors was prepared via simple physical mixing, which consisted of three major parts: the thermosensitive/biodegradable poly(organophosphazene) hydrogel, PEGylated cobalt ferrite nanoparticles, and paclitaxel (PTX). The PEGylated cobalt ferrite nanoparticles showed extremely low cytotoxicity due to the surface modification using PEG chains. The long-term theranostic hydrogel system showed adequate properties to be used for long-term MR theragnosis. In particular, the theranostic hydrogel gradually degraded over 28 days, and the PTX was sustainedly released out from the theranostic hydrogel over the same period in vitro. Furthermore, the in vivo efficacy of long-term MR theragnosis using the theranostic hydrogel system was estimated successfully over 3 weeks by using high field (4.7 T) animal MRI and solid tumor-bearing mice. Based on our results, we expect that this system can supply multiple data regarding a) the progress of therapy and b) the treatment processes via one- or two-time i.t. administration for cases in which surgical approaches are difficult to apply. Meanwhile, cancer patients can be free from the pain of multiple surgical treatments and have the advantage of therapy through a simple i.t. administration.

Publication types

  • Evaluation Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antineoplastic Agents* / chemistry
  • Antineoplastic Agents* / metabolism
  • Antineoplastic Agents* / therapeutic use
  • Biocompatible Materials / chemistry
  • Biocompatible Materials / metabolism
  • Cell Line, Tumor
  • Drug Carriers / chemistry
  • Drug Carriers / metabolism
  • Drug Delivery Systems*
  • Humans
  • Hydrogels / chemistry*
  • Hydrogels / metabolism*
  • Materials Testing
  • Metal Nanoparticles / chemistry
  • Mice
  • Mice, Nude
  • Neoplasms, Experimental / drug therapy*
  • Paclitaxel* / chemistry
  • Paclitaxel* / metabolism
  • Paclitaxel* / therapeutic use

Substances

  • Antineoplastic Agents
  • Biocompatible Materials
  • Drug Carriers
  • Hydrogels
  • Paclitaxel