On-demand drug release and hyperthermia therapy applications of thermoresponsive poly-(NIPAAm-co-HMAAm)/polyurethane core-shell nanofiber mat on non-vascular nitinol stents

Nanomedicine. 2017 Feb;13(2):527-538. doi: 10.1016/j.nano.2016.12.012. Epub 2016 Dec 20.

Abstract

A functional cover made up of core-shell nanofibers with a unique combination of thermoresponsive polymeric shell and stretchable polymeric core for non-vascular nitinol stents that uses an alternating magnetic field (AMF) to induce heat in the stent for hyperthermia therapy and simultaneously release 5-fluorouracil and/or paclitaxel was designed. Varying the ratios of NIPAAm to HMAAm monomer resulted in different LCST properties for the synthesized copolymer and further utilized for an on-demand drug release. Biocompatibility test using NIH-3T3 fibroblast cells indicates that the composite with drug content is biocompatible and the in-vitro cancer cytotoxicity test using ESO26 and OE21 cancer cells proved that the material shows cancer cytotoxic properties via combination of dual drug and hyperthermia therapy. With this functional material, we propose a tailorable and on-demand drug release with more control that can be employed for a combination drug therapy/single drug therapy combined with hyperthermia therapy for cancer cytotoxicity effect.

Keywords: Chemotherapy; Core-shell nanofibers; Drug eluting stents (DES); Hyperthermia; Lower critical solution temperature (LCST); Thermoresponsive polymers.

MeSH terms

  • Drug Liberation*
  • Fibroblasts
  • Humans
  • Hyperthermia, Induced / methods*
  • Nanofibers*
  • Polymers
  • Polyurethanes*
  • Stents
  • Temperature
  • Tumor Cells, Cultured

Substances

  • Polymers
  • Polyurethanes