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Functionalized liposomes for targeted breast cancer drug delivery.
Nel, Janske; Elkhoury, Kamil; Velot, Émilie; Bianchi, Arnaud; Acherar, Samir; Francius, Grégory; Tamayol, Ali; Grandemange, Stéphanie; Arab-Tehrany, Elmira.
Affiliation
  • Nel J; Université de Lorraine, LIBio, F-54000, Nancy, France.
  • Elkhoury K; LAAS-CNRS, F-31400, Toulouse, France.
  • Velot É; Université de Lorraine, CNRS, IMoPA, F-54000, Nancy, France.
  • Bianchi A; Université de Lorraine, CNRS, IMoPA, F-54000, Nancy, France.
  • Acherar S; Université de Lorraine, CNRS, LCPM, F-54000, Nancy, France.
  • Francius G; Université de Lorraine, CNRS, LCPME, F-54000, Nancy, France.
  • Tamayol A; Department of Biomedical Engineering, University of Connecticut Health Center, Farmington, CT, 06030, USA.
  • Grandemange S; Université de Lorraine, CNRS, CRAN, F-54000, Nancy, France.
  • Arab-Tehrany E; Université de Lorraine, LIBio, F-54000, Nancy, France.
Bioact Mater ; 24: 401-437, 2023 Jun.
Article in En | MEDLINE | ID: mdl-36632508
ABSTRACT
Despite the exceptional progress in breast cancer pathogenesis, prognosis, diagnosis, and treatment strategies, it remains a prominent cause of female mortality worldwide. Additionally, although chemotherapies are effective, they are associated with critical limitations, most notably their lack of specificity resulting in systemic toxicity and the eventual development of multi-drug resistance (MDR) cancer cells. Liposomes have proven to be an invaluable drug delivery system but of the multitudes of liposomal systems developed every year only a few have been approved for clinical use, none of which employ active targeting. In this review, we summarize the most recent strategies in development for actively targeted liposomal drug delivery systems for surface, transmembrane and internal cell receptors, enzymes, direct cell targeting and dual-targeting of breast cancer and breast cancer-associated cells, e.g., cancer stem cells, cells associated with the tumor microenvironment, etc.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Bioact Mater Year: 2023 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Bioact Mater Year: 2023 Document type: Article Affiliation country: