Phenyl boronic acid-modified lipid nanocarriers of niclosamide for targeting triple-negative breast cancer

被引:27
|
作者
Pindiprolu, Sai Kiran S. S. [1 ]
Krishnamurthy, Praveen T. [1 ]
Ghanta, Venkata Rao [2 ]
Chintamaneni, Pavan Kumar [1 ]
机构
[1] JSS Acad Higher Educ & Res, JSS Coll Pharm, Dept Pharmacol, The Nilgiris 643001, Tamil Nadu, India
[2] GVK Biosci Private Ltd, IDA Nacharam, Synthet Organ Chem Div, Hyderabad 500076, Telangana, India
关键词
metastasis; niclosamide; STAT3; triple-negative breast cancer; tumor relapse; STEM-CELLS; DRUG-DELIVERY; MESENCHYMAL TRANSITION; DIALLYL DISULFIDE; NANOPARTICLES; STAT3; GROWTH; FORMULATION; CONJUGATE; DESIGN;
D O I
10.2217/nnm-2020-0003
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Aim: To study the active targeting efficacy of phenylboronic acid-modified niclosamide solid lipid nanoparticles (PBA-Niclo-SLN) in triple-negative breast cancer (TNBC). Materials & methods: PBA-Niclo-SLNs were formulated by an emulsification-solvent evaporation method using PBA-associated stearylamine (PBSA) as lipid. The drug uptake and the anticancer propensity of PBA-Niclo-SLN were studied in TNBC (MDA-MB231) cells and tumor-bearing mice. Results: PBA-Niclo-SLN formulation resulted in greater antitumor efficacy by inducing G0/G1 cell cycle arrest and apoptosis. Besides, PBA-Niclo-SLN effectively inhibited STAT3, CD44(+)/CD24(-) TNBC stem cell subpopulation, epithelial-mesenchymal transition markers. Besides, PBA-Niclo-SLN selectively accumulated at the tumor site with more significant tumor regression and improved the survivability in TNBC tumor-bearing mice. Conclusion: PBA-Niclo-SLN formulation would be an effective strategy to eradicate TNBC cells (breast cancer stem cells and nonbreast cancer stem cells) efficiently. Graphical abstract
引用
收藏
页码:1551 / 1565
页数:15
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