Development of GE11-Functionalized Liposomes for Doxorubicin and Curcumin Delivery in Breast Cancer Treatment
Juliana Oliveira, Ph.D – Post-doc, Biochemistry, Institute of Biology, University of Campinas; Talita Mendonça, MS – student, Biochemistry, Institute of Biology, University of Campinas (Unicamp); Daniely Paspardelli – undergraduate student, Biochemistry, Institute of Biology, University of Campinas; Eneida de Paula, PhD – Full professor, Biochemistry, Institute of Biology, University of Campinas (Unicamp)
Full professor University of Campinas (Unicamp) Campinas, Sao Paulo, Brazil
Introduction: Breast cancer is the second most prevalent cancer among women worldwide [1]. Conventional therapies are often non-selective, affecting both tumor and healthy tissues, which highlights the need for improved treatment strategies. Liposomes are promising drug delivery systems, as they enhance drug bioavailability, reduce chemoresistance, and enable synergistic effects of actives. Moreover, liposomes functionalized with GE11 peptide, targeting EGFR-overexpressing tumors, allow selective delivery to cancer cells, potentially improving treatment efficacy while minimizing systemic toxicity [2].
Learning Objectives:
Evaluate in vitro efficacy of targeted liposomes for combined anticancer therapy.
Demonstrate advantages of smart drug delivery and drug combinations in breast cancer cells.