The application of prodrug-based nano-drug delivery strategy in cancer combination therapy

Yanxiu Ge1, Yakun Ma1, Lingbing Li1

  • 1Department of Pharmaceutics, School of Pharmacy, Shandong University, 44 Wenhuaxi Road, Jinan, Shandong Province 250012, China.

Insights

Prodrug-based nano-drug delivery systems (P-N-DDSs) are revolutionizing cancer treatment by enabling effective combination therapies. These systems combine multiple agents to overcome multidrug resistance and reduce side effects.

Area of Science:

  • Nanomedicine
  • Oncology
  • Drug Delivery Systems

Background:

  • Single-agent cancer therapy often leads to multidrug resistance and severe side effects.
  • Combination therapies targeting multiple signaling pathways are a key research focus.
  • Prodrug-based nano-drug delivery systems (P-N-DDSs) offer a promising platform for advanced cancer treatment.

Purpose of the Study:

  • To review the application of P-N-DDSs in cancer combination therapy.
  • To explore combinations of prodrugs with chemotherapeutics, other agents, and nucleic acids.
  • To discuss the integration of different therapy types, such as chemotherapy and phototherapy, using P-N-DDSs.

Main Methods:

  • Literature review of recent studies on prodrug-based nanoparticulate drug delivery strategies.
  • Analysis of P-N-DDSs employed in various combination cancer therapy approaches.
  • Discussion of case examples demonstrating the feasibility of these technologies.

Main Results:

  • P-N-DDSs are effectively utilized for combining various therapeutic agents for cancer treatment.
  • These systems facilitate the co-delivery of chemotherapeutics, other drugs, and nucleic acids.
  • Combination of chemotherapy with other modalities like phototherapy is feasible using P-N-DDSs.

Conclusions:

  • P-N-DDSs represent a viable and advanced strategy for combination cancer therapy.
  • These systems hold significant potential for overcoming multidrug resistance and improving treatment outcomes.
  • Further research and development in P-N-DDSs are crucial for their clinical translation.

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