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Multifunctional nanocarriers for mammographic quantification of tumor dosing and prognosis of breast cancer therapy

  • Efstathios Karathanasis
  • , Leslie Chan
  • , Sri R. Balusu
  • , Carl J. D'Orsi
  • , Ananth V. Annapragada
  • , Ioannis Sechopoulos
  • , Ravi V. Bellamkonda*
  • *Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

Nanoscale therapeutic interventions are increasingly important elements in the portfolio of cancer therapeutics. The efficacy of nanotherapeutics is dictated, in part, by the access they have to tumors via the leaky tumor vasculature. Yet, the extent of tumor vessel leakiness in individual tumors varies widely resulting in a correspondingly wide tumor dosing and resulting range of responses to therapy. Here we report the design of a multifunctional nanocarrier that simultaneously encapsulates a chemotherapeutic and a contrast agent which enables a personalized nanotherapeutic approach for breast cancer therapy by permitting tracking of the nanocarrier distribution by mammography, a widely used imaging modality. Following systemic administration in a rat breast tumor model, imaging demonstrated a wide range of intratumoral deposition of the nanocarriers, indicating variable tumor vessel leakiness. Notably, specific tumors that exhibited high uptake of the nanocarrier as visualized by imaging were precisely the animals that responded best to the treatment as quantified by low tumor growth and prolonged survival.

Original languageEnglish
Pages (from-to)4815-4822
Number of pages8
JournalBiomaterials
Volume29
Issue number36
DOIs
Publication statusPublished - Dec 2008
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Breast cancer imaging
  • Iodine-doxorubicin-loaded liposome
  • Mutlifunctional nanoparticle
  • Personalized medicine
  • Prediction of chemotherapy
  • n/a OA procedure

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