Multifunctional calcium-based nanocarriers for synergistic treatment of triple-negative breast cancer

被引:2
|
作者
Martins, Sara A. [1 ,2 ]
Costa, Rui R. [1 ,2 ]
Brito, Alexandra [1 ,2 ]
Reis, Rui L. [1 ,2 ]
Alves, Natalia M. [2 ]
Pashkuleva, Iva [1 ,2 ]
Costa, Diana Soares da [1 ,2 ]
机构
[1] Univ Minho, I3Bs Res Inst Biomat Biodegradables & Biomimet, Headquarters European Inst Excellence Tissue Engn, 3Bs Res Grp, AvePk, P-4805017 Barco Gmr, Portugal
[2] PT Govt Associate Lab, ICVS 3Bs, Guimaraes, Portugal
关键词
Core/shell nanoparticles; Breast cancer; Calcium overload; Hyaluronic acid; Cell spheroids; Doxorubicin; DELIVERY; MICROCAPSULES; IMAGE;
D O I
10.1016/j.jcis.2024.06.159
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Targeted breast cancer therapies hold the potential to improve the efficiency of drug delivery to the pathology site without impacting the viability and function of healthy cells. Herein, we developed multifunctional nanocarriers that target simultaneously several downstream signaling processes in triple negative breast cancer cells. The system comprises pH sensitive CaCO3 nanoparticles (NPs) as carriers of the anticancer drug doxorubicin (DOX). The NPs were coated in a layer-by-layer (LbL) fashion using poly-L-lysine and hyaluronic acid to target receptors overexpressed in breast cancer (e.g. CD44, RHAMM). Spheroids of the triple-negative Hs578T cell line were used as a 3D model to assess the therapeutic potential of this system. Our results showed that the NPs act via a synergistic mechanism that combines Ca2+ overload causing cell calcification and DNA damage by DOX. The LbL coating was crucial for the protection of the healthy cells, i.e. it provides NPs with targeting capacity. The
引用
收藏
页码:500 / 512
页数:13
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