pH-responsive polymer-liposomes for intracellular drug delivery and tumor extracellular matrix switched-on targeted cancer therapy

Biomaterials. 2014 Jul;35(20):5414-5424. doi: 10.1016/j.biomaterials.2014.03.046. Epub 2014 Apr 4.

Abstract

This study presents a tumor-extracellular matrix pH-induced targeting liposome (ECM-targeting liposomes), crosslinked from methoxy-poly(ethylene glycol)-b-poly(N-2-hydroxypropyl methacrylamide-co-histidine)-cholesterol copolymers and biotin2-polyethylene glycol crosslinkers by hydrogen bonds to overcome the defects of liposomes. In this study, ECM-targeting liposomes were completely investigated their pH-responsibility, drug releasing behaviors, anticancer efficiencies and the time-dependent organ distribution and toxic effects. Experimental results indicate that ECM-targeting liposomes showed rapid drug releasing profiles in acidic conditions. Because the ECM-targeting liposomes accumulated preferentially in tumor, the ECM-targeting liposomes exhibited exceptional anticancer activity in vivo and lower hepatic and renal toxicity. The ECM-targeting liposomes which are switched on the targeting ability in tumor ECM possess potential for future application in anticancer therapy.

Keywords: Cancer therapy; Intracellular drug delivery; Liposomes; Polymers; Tumor ECM-induced targeting.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acrylamides / chemistry*
  • Acrylamides / pharmacokinetics
  • Animals
  • Antineoplastic Agents / chemistry*
  • Antineoplastic Agents / pharmacokinetics
  • Biotin / analogs & derivatives*
  • Biotin / chemistry
  • Biotin / pharmacokinetics
  • Disease Models, Animal
  • Doxorubicin / chemistry
  • Doxorubicin / pharmacokinetics
  • Drug Delivery Systems / methods*
  • Extracellular Matrix / drug effects*
  • Extracellular Matrix / metabolism
  • Female
  • HCT116 Cells
  • Humans
  • Hydrogen-Ion Concentration
  • Liposomes / chemistry*
  • Liposomes / pharmacokinetics
  • Mice
  • Mice, Inbred BALB C
  • Mice, Nude
  • Neoplasms / drug therapy*
  • Polyethylene Glycols / chemistry*
  • Polyethylene Glycols / pharmacokinetics
  • Polymers / chemistry*
  • Polymers / pharmacokinetics
  • Tissue Distribution

Substances

  • Acrylamides
  • Antineoplastic Agents
  • Liposomes
  • Polymers
  • methoxy-poly(ethylene glycol)-b-poly(N-2-hydroxypropyl methacrylamide-co-histidine)cholesterol
  • Polyethylene Glycols
  • Biotin
  • Doxorubicin