A review of nanoparticle drug delivery systems responsive to endogenous breast cancer microenvironment

Tengteng Zou1, Wenping Lu2, Yaroslav Mezhuev3

  • 1College of Pharmacy, Jinan University, Guangzhou 510632, PR China.

Insights

Stimuli-responsive nanoparticle drug delivery systems (NDDS) offer targeted breast cancer treatment by leveraging the tumor microenvironment. These systems enhance drug efficacy and reduce side effects for improved therapeutic outcomes.

Area of Science:

  • Biomedical Engineering
  • Oncology
  • Nanotechnology

Background:

  • Breast cancer remains a significant health threat, necessitating novel therapeutic strategies.
  • Nanoparticle drug delivery systems (NDDS) show promise for targeted breast cancer treatment, improving drug bioavailability and reducing toxicity.
  • The tumor microenvironment (TME) presents challenges to NDDS efficacy due to factors like hypoxia, acidosis, and protease activity.

Purpose of the Study:

  • To review the impact of the breast cancer microenvironment on NDDS.
  • To summarize innovative stimuli-responsive NDDS designed to overcome TME challenges.
  • To discuss the potential applications and limitations of these advanced drug delivery systems.

Main Methods:

  • Exploiting endogenous stimuli within the breast cancer TME (hypoxia, acidosis, protease expression) to trigger drug release.
  • Designing NDDS with specific materials, targeting groups, and drug payloads.
  • Analyzing the function of stimuli-responsive NDDS in targeting and drug delivery within the TME.

Main Results:

  • Stimuli-responsive NDDS can be engineered to target breast cancer cells effectively by responding to the unique TME.
  • These systems demonstrate enhanced drug bioavailability and reduced systemic toxicity compared to conventional therapies.
  • The heterogeneity of the breast cancer TME necessitates tailored NDDS designs for optimal therapeutic response.

Conclusions:

  • Stimuli-responsive NDDS represent a promising advancement in breast cancer therapy by utilizing the TME for targeted drug delivery.
  • Further research into material science, targeting strategies, and drug loading is crucial for clinical translation.
  • These systems hold potential for overcoming drug resistance and improving treatment outcomes for breast cancer patients.

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