Co-delivery of genes and drugs with nanostructured calcium carbonate for cancer therapy

被引:49
|
作者
Chen, Si [1 ]
Zhao, Dong [1 ]
Li, Feng [1 ]
Zhuo, Ren-Xi [1 ]
Cheng, Si-Xue [1 ]
机构
[1] Wuhan Univ, Dept Chem, Key Lab Biomed Polymers, Minist Educ, Wuhan 430072, Peoples R China
基金
中国国家自然科学基金;
关键词
P53; DOXORUBICIN; EXPRESSION; APOPTOSIS; VECTORS; TP53; DNA;
D O I
10.1039/c1ra00527h
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
By using a CaCO3 co-precipitation technique, p53 expression plasmids and doxorubicin hydrochloride (DOX) were encapsulated in nano-sized CaCO3/DNA/DOX co-precipitates for co-delivery of genes and drugs. Under a certain Ca2+/CO32- ratio in the co-precipitation, both plasmid DNA and drugs could be loaded in the CaCO3/DNA/DOX nanoparticles with high encapsulation efficiency. The in vitro cell inhibition of the CaCO3/DNA/DOX nanoparticles was evaluated in HeLa cells by a MTT assay. The results showed the simultaneous treatment by gene and drug could induce cell apoptosis and completely inhibit the cell proliferation. The CaCO3/DNA/DOX nanoparticles exhibited a high cell inhibition rate of about 75%, indicating that the CaCO3/DNA/DOX nanoparticles could effectively mediate gene transfection and deliver the drug to the cells. Compared with the gene delivery system (CaCO3/DNA nanoparticles) or the free drug DOX, the co-delivery system (CaCO3/DNA/DOX nanoparticles) exhibits enhanced cell inhibition rate. The calcium carbonate based approach has great potential in the preparation of gene and drug co-delivery systems, and the CaCO3/DNA/DOX nanoparticles have promising applications in cancer treatment.
引用
收藏
页码:1820 / 1826
页数:7
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