Stimuli-responsive nanotherapeutics for precision drug delivery and cancer therapy

Wiley Interdiscip Rev Nanomed Nanobiotechnol. 2019 Jan;11(1):e1527. doi: 10.1002/wnan.1527. Epub 2018 May 4.

Abstract

Cancer remains one of the world's leading causes of death. However, most conventional chemotherapeutic drugs only show a narrow therapeutic window in patients because of their inability to discriminate cancer cells from healthy cells. Nanoparticle-based therapeutics (termed nanotherapeutics) have emerged as potential solutions to mitigate many obstacles posed by these free drugs. Deep insights into knowledge of the tumor microenvironment and materials science make it possible to construct nanotherapeutics that are able to release cargoes in response to a variety of internal stimuli and external triggers. Therefore, such highly sophisticated nanosystems could help impede the premature release of toxic drugs in the blood circulation or healthy tissues, thus enhancing the safety profiles of encapsulated drugs. In this context, this review offers a comprehensive overview of several specific stimuli, including internal stimuli (e.g., pH, temperature, enzyme, redox, and H2 O2 ) and external stimuli (e.g., magnetic, photo, and ultrasound). We envision that applications of these smart nanotherapeutics can benefit cancer patients and provide a good chance for clinical translation of many nanoparticle formulas. This article is categorized under: Therapeutic Approaches and Drug Discovery > Nanomedicine for Oncologic Disease Diagnostic Tools > Diagnostic Nanodevices Diagnostic Tools > in vitro Nanoparticle-Based Sensing.

Keywords: cancer therapy; external triggers; nanotherapeutics; targeting delivery; tumor microenvironment.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Drug Delivery Systems*
  • Humans
  • Nanoparticles / administration & dosage
  • Nanoparticles / therapeutic use*
  • Neoplasms / drug therapy*
  • Oxidation-Reduction
  • Reactive Oxygen Species / metabolism
  • Tumor Microenvironment

Substances

  • Reactive Oxygen Species