Newly Emerging Theranostic Agents for Simultaneous Cancertargeted Imaging and Therapy

Shenglin Luo, Xiaochao Yang, Chunmeng Shi1

  • 1Institute of Combined Injury, State Key Laboratory of Trauma, Burns and Combined Injury, Chongqing Engineering Research Center for Nanomedicine, Department of Preventive Medicine, Third Military Medical University, Chongqing, 400038, China. shicm@sina.com.

Current Medicinal Chemistry
|December 24, 2015
PubMed

Insights

Multifunctional theranostic agents integrate cancer diagnosis and therapy. This review covers current and emerging strategies for developing these agents, focusing on their preparation, promises, and challenges for clinical use.

Area of Science:

  • Oncology
  • Nanotechnology
  • Drug Delivery

Background:

  • Personalized oncology increasingly utilizes theranostic agents for integrated tumor diagnosis and therapy.
  • Current strategies involve chemical conjugation or nanoplatforms for targeted cancer treatment and detection.

Purpose of the Study:

  • To review existing and novel approaches for preparing multifunctional cancer theranostic agents.
  • To highlight the potential benefits and limitations of each preparation strategy.
  • To provide insights for developing clinically applicable cancer theranostic agents.

Main Methods:

  • Review of chemical conjugation methods linking drugs, contrast agents, and targeting ligands.
  • Analysis of nanoplatform-based strategies utilizing nanoparticles for targeted delivery and therapy.
  • Exploration of emerging approaches using multifunctional small molecules.

Main Results:

  • Chemical conjugation offers a direct route for combining therapeutic and diagnostic functionalities.
  • Nanoplatforms leverage the enhanced permeability and retention (EPR) effect or ligand conjugation for targeted action.
  • Multifunctional small molecules represent a novel and promising strategy for theranostic agent development.

Conclusions:

  • Both conjugation and nanoplatform approaches have distinct advantages and challenges for clinical translation.
  • Emerging strategies using small molecules show significant potential for creating efficient and specific cancer theranostic agents.
  • Further research is needed to optimize these agents for widespread clinical adoption in cancer therapy.