Dual temperature/pH-sensitive drug delivery of poly(N-isopropylacrylamide-co-acrylic acid) nanogels conjugated with doxorubicin for potential application in tumor hyperthermia therapy

Colloids Surf B Biointerfaces. 2011 Jun 1;84(2):447-53. doi: 10.1016/j.colsurfb.2011.01.040. Epub 2011 Feb 2.

Abstract

In this paper, a dual temperature/pH-sensitive poly(N-isopropylacrylamide-co-acrylic acid) nanogel (PNA) was prepared and utilized as a drug carrier. The anti-cancer drug doxorubicin (DOX) was covalent bound to PNA via an acid-labile hydrazone linkage. DOX-PNA conjugates had a pH-dependent LCST, which was 41°C and 43°C at pH 5.3 and 6.8 respectively, but higher than 50°C at pH 7.4. The nanogels which were hydrophilic below LCST and changed to hydrophobic state above LCST possessed dual pH/temperature dependent cellular uptake and cytotoxicity. With increasing temperature, the cellular uptake of DOX-PNA was almost no difference at pH 7.4, but enhanced about 43% at pH 6.8. So the cytotoxicity of DOX-PNA also increased in higher temperature and lower pH value. It was able to distinguish tumor extracellular pH from physiological pH under hyperthermia of 43°C, suggesting a great potential for anti-cancer therapy.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acrylamides / chemistry*
  • Antineoplastic Agents / therapeutic use
  • Cell Line, Tumor
  • Doxorubicin / chemistry*
  • Doxorubicin / therapeutic use
  • Drug Delivery Systems*
  • Hep G2 Cells
  • Humans
  • Hydrogen-Ion Concentration
  • Molecular Structure
  • Nanogels
  • Polyethylene Glycols / chemistry*
  • Polyethyleneimine / chemistry*
  • Temperature*

Substances

  • Acrylamides
  • Antineoplastic Agents
  • Nanogels
  • polyethylene glycol polyethyleneimine nanogel
  • Polyethylene Glycols
  • Doxorubicin
  • Polyethyleneimine
  • N-isopropylacrylamide