Dual delivery of metformin and Y15 from a PLGA scaffold for the treatment of platinum-resistant ovarian cancer

  • Emily Jordan
  • , Marco A. Arriaga
  • , Hannah Obregon
  • , Viviana Villalobos
  • , Manuel A. Duarte
  • , Kristal Garcia
  • , Arkene Levy
  • , Sue Anne Chew

Research output: Contribution to journalArticlepeer-review

Abstract

Aims: Drug-loaded poly(lactic-co-glycolic acid) (PLGA) scaffolds were fabricated using a mold-less technique to investigate whether the combined delivery of both Y15 (FAK inhibitor) and metformin would result in enhanced effects on cell viability compared to the release of each drug alone for the treatment of platinum-resistant ovarian cancer (PROC). Materials & methods: Scaffolds were fabricated using an easy and economical mold-less technique that combined PLGA and the drugs (i.e. metformin and/or Y15) in tetraglycol and injected in PBS, to form a globular morphology. Results: The exposure of cells to metformin and Y15 resulted in a significantly enhanced cytotoxic efficacy compared to single-drug treatment with either metformin or Y15. When the drugs were delivered using the PLGA scaffolds, the combination of the two drugs was significantly more cytotoxic compared to scaffolds containing metformin only and Y15 only. Conclusions: The combination of metformin and Y15 can result in an increase in antitumor activity in PROC cells through apoptosis. The delivery of both drugs from the PLGA biomaterial scaffold allowed for a more enhanced combinational effect compared to the utilization of free drugs (without a scaffold) and should be further explored as a promising treatment of PROC.
Original languageEnglish
Pages (from-to)301-312
Number of pages12
JournalFuture Medicinal Chemistry
Volume17
Issue number3
DOIs
StatePublished - 2025

Bibliographical note

Publisher Copyright:
© 2025 Informa UK Limited, trading as Taylor & Francis Group.

Funding

This work was supported by the National Institute of General Medical Sciences of the National Institutes of Health [grant number 1T34GM137854] and the National Institute of General Medical Sciences of the National Institutes of Health [grant number 1SC3GM135138]. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health.

ASJC Scopus Subject Areas

  • Molecular Medicine
  • Pharmacology
  • Drug Discovery

Keywords

  • biomaterials
  • cytotoxicity
  • focal adhesion kinase
  • Metformin
  • ovarian cancer
  • Y15

Disciplines

  • Pharmacology

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