Designed inorganic porous nanovector with controlled release and MRI features for safe administration of doxorubicin

Tutkimustuotos: Lehtiartikkelivertaisarvioitu

Tutkijat

  • Simo Näkki
  • Julie T.W. Wang
  • Jianwei Wu
  • Li Fan
  • Jimi Rantanen
  • Tuomo Nissinen
  • Mikko I. Kettunen
  • Matilda Backholm

  • Robin Ras

  • Khuloud T. Al-Jamal
  • Vesa Pekka Lehto
  • Wujun Xu

Organisaatiot

  • University of Eastern Finland
  • King’s College London
  • Fourth Military Medical University

Kuvaus

The inability of traditional chemotherapeutics to reach cancer tissue reduces the treatment efficacy and leads to adverse effects. A multifunctional nanovector was developed consisting of porous silicon, superparamagnetic iron oxide, calcium carbonate, doxorubicin and polyethylene glycol. The particles integrate magnetic properties with the capacity to retain drug molecules inside the pore matrix at neutral pH to facilitate drug delivery to tumor tissues. The MRI applicability and pH controlled drug release were examined in vitro together with in-depth material characterization. The in vivo biodistribution and compound safety were verified using A549 lung cancer bearing mice before proceeding to therapeutic experiments using CT26 cancer implanted mice. Loading doxorubicin into the porous nanoparticle negated the adverse side effects encountered after intravenous administration highlighting the particles’ excellent biocompatibility. Furthermore, the multifunctional nanovector induced 77% tumor reduction after intratumoral injection. The anti-tumor effect was comparable with that of free doxorubicin but with significantly alleviated unwanted effects. These results demonstrate that the developed porous silicon-based nanoparticles represent promising multifunctional drug delivery vectors for cancer monitoring and therapy.

Yksityiskohdat

AlkuperäiskieliEnglanti
Sivut327-336
Sivumäärä10
JulkaisuInternational Journal of Pharmaceutics
Vuosikerta554
TilaJulkaistu - 10 tammikuuta 2019
OKM-julkaisutyyppiA1 Julkaistu artikkeli, soviteltu

ID: 30129729