Functionalized liposomes for targeted breast cancer drug delivery

被引:128
作者
Nel, Janske [1 ]
Elkhoury, Kamil [2 ]
Velot, Emilie [3 ]
Bianchi, Arnaud
Acherar, Samir [4 ]
Francius, Gregory [5 ]
Tamayol, Ali [6 ]
Grandemange, Stephanie [7 ]
Arab-Tehrany, Elmira [1 ]
机构
[1] Univ Lorraine, LIBio, F-54000 Nancy, France
[2] CNRS, LAAS, F-31400 Toulouse, France
[3] Univ Lorraine, CNRS, IMoPA, F-54000 Nancy, France
[4] Univ Lorraine, CNRS, LCPM, F-54000 Nancy, France
[5] Univ Lorraine, CNRS, LCPME, F-54000 Nancy, France
[6] Univ Connecticut Hlth Ctr, Dept Biomed Engn, Farmington, CT 06030 USA
[7] Univ Lorraine, CNRS, CRAN, F-54000 Nancy, France
基金
英国科研创新办公室;
关键词
Liposomes; Breast cancer; Anti -cancer agents; Targeted drug delivery; Surface functionalization; Receptor -targeted drug delivery; PHASE-III TRIAL; PHOSPHOLIPASE A(2) ENZYMES; RECEPTOR-RELATED PROTEIN-1; CELL PENETRATING PEPTIDES; PH-SENSITIVE LIPOSOMES; IN-VIVO; TUMOR MICROENVIRONMENT; CO-DELIVERY; MATRIX-METALLOPROTEINASES; CONJUGATED LIPOSOMES;
D O I
10.1016/j.bioactmat.2022.12.027
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
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, trans -membrane 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.
引用
收藏
页码:401 / 437
页数:37
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