Redox-Responsive Mesoporous Silica Nanoparticles for Cancer Treatment: Recent Updates

被引:26
|
作者
Gisbert-Garzaran, Miguel [1 ]
Vallet-Regi, Maria [2 ,3 ]
机构
[1] Univ Paris Saclay, CNRS, Inst Galien Paris Saclay, UMR 8612,Fac Pharm, F-92296 Chatenay Malabry, France
[2] Univ Complutense Madrid, Dept Quim Ciencias Farmaceut, Inst Invest Sanitaria Hosp 12 Octubre I 12, Plaza Ramon y Cajal S-N, Madrid 28040, Spain
[3] Networking Res Ctr Bioengn Biomat & Nanomed CIBER, Madrid 28029, Spain
基金
欧洲研究理事会;
关键词
mesoporous silica nanoparticles; redox-responsive; stimuli-responsive; drug delivery; cancer cell targeting; biodegradable nanoparticles; periodic mesoporous organosilica nanoparticles; DRUG-DELIVERY SYSTEM; ORGANOSILICA NANOPARTICLES; CONTROLLED-RELEASE; CO-DELIVERY; TUMOR; NANOCARRIERS; NANOPLATFORM; CARRIERS; SIRNA;
D O I
10.3390/nano11092222
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Mesoporous silica nanoparticles have been widely applied as carriers for cancer treatment. Among the different types of stimuli-responsive drug delivery systems, those sensitive to redox stimuli have attracted much attention. Their relevance arises from the high concentration of reductive species that are found within the cells, compared to bloodstream, which leads to the drug release taking place only inside cells. This review is intended to provide a comprehensive overview of the most recent trends in the design of redox-responsive mesoporous silica nanoparticles. First, a general description of the biological rationale of this stimulus is presented. Then, the different types of gatekeepers that are able to open the pore entrances only upon application of reductive conditions will be introduced. In this sense, we will distinguish among those targeted and those non-targeted toward cancer cells. Finally, a new family of bridged silica nanoparticles able to degrade their structure upon application of this type of stimulus will be presented.
引用
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页数:18
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