Enhanced combination cancer therapy using lipid-calcium carbonate/phosphate nanoparticles as a targeted delivery platform

被引:16
|
作者
Wu, Yilun [1 ]
Gu, Wenyi [1 ]
Xu, Zhi Ping [1 ]
机构
[1] Univ Queensland, Australian Inst Bioengn & Nanotechnol, St Lucia, Qld 4072, Australia
基金
澳大利亚研究理事会;
关键词
cell apoptosis; cell cycle arrest; combination therapy; lipid-coated calcium carbonate/phosphate; melanoma; CELL-CYCLE; IN-VIVO; PHOSPHATE NANOPARTICLES; OXIDATIVE INACTIVATION; MALIGNANT-MELANOMA; ANTICANCER DRUGS; NONVIRAL VECTORS; FOLIC-ACID; MITOCHONDRIAL; SUCCINATE;
D O I
10.2217/nnm-2018-0252
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: Melanoma, the most life-threatening skin cancer, requires more effective therapies. Methodology: A new folic acid (FA) receptor-targeted lipid-coated calcium carbonate/phosphate (LCCP) nanoparticle was synthesized, incorporating two often-used therapeutics, cell death siRNA and alpha-tocopheryl succinate. Results: The nanoparticles were spherical, with an average size of 40 nm. The nanoparticles exhibited a high gene/drug loading efficiency (60%), with folic acid-enhanced cellular uptake. The nanoparticles with both therapeutics enhanced inhibition of B16F0 melanoma cell growth, showing a moderate synergistic effect. The mechanism of the inhibition is associated with induction of cell apoptosis and cell cycle arrest at G1 phase. Conclusion: Our data indicate that lipid-coated calcium carbonate/phosphate nanoparticles are a potential platform for targeted therapy for melanoma.
引用
收藏
页码:77 / 92
页数:16
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