Engineering combination nanomedicines to overcome cancer resistance

Hina Singh1, Sri Renukadevi Balusamy2, Johan Sukweenadhi3,4

  • 1Division of Biomedical Sciences, School of Medicine, University of California Riverside CA 92521 USA Hina.Singh@medsch.ucr.edu.

RSC Advances
|January 26, 2026
PubMed

Insights

Combination nanomedicine offers coordinated delivery of multiple cancer therapies to improve efficacy and safety. Overcoming clinical translation challenges requires scalable manufacturing and standardized characterization for advanced nanomedicine platforms.

Area of Science:

  • Biomedical Engineering
  • Nanotechnology
  • Oncology

Background:

  • Combination nanomedicine utilizes nanosystems for coordinated delivery of multiple agents, addressing tumor heterogeneity and resistance.
  • Clinical translation of nanomedicine faces hurdles including poor pharmacokinetics, inadequate predictive models, and manufacturing limitations.

Purpose of the Study:

  • To review design principles of co-delivery nanomedicine platforms for cancer therapy.
  • To summarize strategies for integrating diverse therapeutic modalities within nanocarriers.
  • To discuss translational challenges and future directions for combination nanomedicine.

Main Methods:

  • Examination of design principles for liposomal, polymeric, inorganic, hybrid, and biomimetic nanocarriers.
  • Analysis of strategies for combining chemotherapy, immunotherapy, gene/RNA therapies, and physical modalities.
  • Review of stimuli-responsive and actively targeted systems for enhanced tumor delivery.

Main Results:

  • Co-delivery platforms are evaluated based on pharmacokinetics, biodistribution, endosomal escape, and tumor microenvironment interactions.
  • Synergistic therapeutic effects are achieved by integrating multiple treatment modalities.
  • Stimuli-responsive and targeted systems demonstrate potential for precise drug release and tumor accumulation.

Conclusions:

  • Combination nanomedicine holds significant promise for enhancing cancer therapy efficacy and safety.
  • Future efforts must focus on modular, scalable platforms, standardized characterization, and clinically relevant models.
  • Addressing manufacturing, quality control, and regulatory pathways is crucial for successful clinical translation.

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