Nanostructured lipid carriers in cancer therapy: Advances in passive and active targeting strategies

  • 0Department of Pharmaceutics and Pharmaceutical Technology, College of Pharmacy, University of Sharjah 27272 Sharjah, United Arab Emirates; Research Institute of Medical & Health Sciences, University of Sharjah 27272 Sharjah, United Arab Emirates.

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Summary

This summary is machine-generated.

Nanostructured lipid carriers (NLCs) offer enhanced drug delivery for cancer therapy. These carriers improve tumor targeting through passive and active strategies, advancing precision oncology.

Area Of Science

  • Biomedical Engineering
  • Nanotechnology
  • Oncology

Background

  • Nanostructured lipid carriers (NLCs) are advanced drug delivery systems with improved drug solubility, stability, and controlled release capabilities.
  • NLCs are increasingly explored for cancer therapy, focusing on passive and active tumor targeting to enhance treatment efficacy.
  • Precision oncology aims to tailor cancer treatments to individual patients, requiring sophisticated drug delivery platforms.

Purpose Of The Study

  • To comprehensively review the application of NLCs in cancer therapy, emphasizing passive and active targeting strategies.
  • To analyze how NLC formulation, targeting methods, and stimuli-responsive designs impact therapeutic outcomes in oncology.
  • To discuss the potential of NLCs as a versatile platform for advancing targeted cancer treatment.

Main Methods

  • Literature review of recent studies on NLC formulation, targeting mechanisms, and therapeutic applications in cancer.
  • Analysis of passive targeting via the enhanced permeability and retention (EPR) effect and active targeting using ligand-mediated approaches.
  • Examination of lymphatic-targeting and stimuli-responsive NLCs for improved drug delivery and site-specific release.

Main Results

  • NLCs facilitate enhanced tumor-specific drug delivery through both passive (EPR effect) and active (ligand-mediated) targeting.
  • Lymphatic-targeting NLCs show potential for improved delivery to metastatic sites, while stimuli-responsive NLCs enable controlled release.
  • Advances in NLC composition and functionalization significantly impact drug loading, biodistribution, and therapeutic efficacy.

Conclusions

  • NLCs represent a highly adaptable and promising platform for precision cancer therapy.
  • Optimization of NLC formulation, functionalization, and clinical translation is crucial for realizing their full potential in targeted oncology.
  • Continued research into NLCs can lead to more effective and personalized cancer treatment strategies.

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