Advancing Ovarian Cancer Therapeutics: The Role of Targeted Drug Delivery Systems

Int J Nanomedicine. 2024 Sep 10:19:9351-9370. doi: 10.2147/IJN.S478313. eCollection 2024.

Abstract

Ovarian cancer (OC) is the most lethal reproductive system cancer and a leading cause of cancer-related death. The high mortality rate and poor prognosis of OC are primarily due to its tendency for extensive abdominal metastasis, late diagnosis in advanced stages, an immunosuppressive tumor microenvironment, significant adverse reactions to first-line chemotherapy, and the development of chemoresistance. Current adjuvant chemotherapies face challenges such as poor targeting, low efficacy, and significant side effects. Targeted drug delivery systems (TDDSs) are designed to deliver drugs precisely to the tumor site to enhance efficacy and minimize side effects. This review highlights recent advancements in the use of TDDSs for OC therapies, including drug conjugate delivery systems, nanoparticle drug delivery systems, and hydrogel drug delivery systems. The focus is on employing TDDS to conduct direct, effective, and safer interventions in OC through methods such as targeted tumor recognition and controlled drug release, either independently or in combination. This review also discusses the prospects and challenges for further development of TDDSs. Undoubtedly, the use of TDDSs shows promise in the battle against OCs.

Keywords: drug conjugates; hydrogel; nanoparticle; ovarian cancer; targeted drug delivery.

Publication types

  • Review

MeSH terms

  • Animals
  • Antineoplastic Agents* / administration & dosage
  • Antineoplastic Agents* / chemistry
  • Drug Delivery Systems* / methods
  • Female
  • Humans
  • Hydrogels / chemistry
  • Nanoparticle Drug Delivery System / chemistry
  • Nanoparticles / chemistry
  • Ovarian Neoplasms* / drug therapy
  • Tumor Microenvironment / drug effects

Substances

  • Antineoplastic Agents
  • Hydrogels
  • Nanoparticle Drug Delivery System

Grants and funding

This work was supported by the National Natural Science Foundation of China (82002750 to Mo Chen) and the Shanghai Pujiang Programme (23PJD009 to Mo Chen). The funding source provided financial support for the study and did not have any other involvement in this study.