Advances in mesoporous silica nanoparticles for targeted stimuli-responsive drug delivery: an update

被引:148
作者
Castillo, Rafael R. [1 ,2 ,3 ]
Lozano, Daniel [1 ,2 ,3 ]
Gonzalez, Blanca [1 ,2 ,3 ]
Manzano, Miguel [1 ,2 ,3 ]
Izquierdo-Barba, Isabel [1 ,2 ,3 ]
Vallet-Regi, Maria [1 ,2 ,3 ]
机构
[1] Univ Complutense Madrid, Dept Quim Ciencias Farmaceut, Unidad Quim Inorgan & Bionorgan, Madrid, Spain
[2] Hosp 12 Octubre Imas12, Inst Invest Sanitaria, Madrid, Spain
[3] Ctr Invest Biomed Red Bioingn Biomat & Nanomed CI, Madrid, Spain
基金
欧洲研究理事会;
关键词
Mesoporous silica nanoparticles; targeting; stimuli-responsive drug delivery; biomedical applications; IN-VIVO BIODISTRIBUTION; CONTROLLED-RELEASE; CO-DELIVERY; FUNCTIONALIZED NANOPARTICLES; MULTIDRUG-RESISTANCE; COMBINATION THERAPY; PEPTIDE LIGAND; VISIBLE-LIGHT; TUMOR-CELLS; CANCER;
D O I
10.1080/17425247.2019.1598375
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: Mesoporous silica nanoparticles (MSNs) are outstanding nanoplatforms for drug delivery. Herein, the most recent advances to turn MSN-based carriers into minimal side effect drug delivery agents are covered.Areas covered: This review summarizes the scientific advances dealing with MSNs for targeted and stimuli-responsive drug delivery since 2015. Delivery aspects to diseased tissues together with approaches to obtain smart MSNs able to respond to internal or external stimuli and their applications are here described. Special emphasis is done on the combination of two or more stimuli on the same nanoplatform and on combined drug therapy.Expert opinion: The use of MSNs in nanomedicine is a promising research field because they are outstanding platforms for treating different pathologies. This is possible thanks to their structural, chemical, physical and biological properties. However, there are certain issues that should be overcome to improve the suitability of MSNs for clinical applications. All materials must be properly characterized prior to their in vivo evaluation; furthermore, preclinical in vivo studies need to be standardized to demonstrate the MSNs clinical translation potential.
引用
收藏
页码:415 / 439
页数:25
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