Diatomite biosilica nanocarriers for siRNA transport inside cancer cells

被引:90
作者
Rea, Ilaria [1 ]
Martucci, Nicola M. [2 ]
De Stefano, Luca [1 ]
Ruggiero, Immacolata [2 ]
Terracciano, Monica [1 ,3 ]
Dardano, Principia [1 ]
Migliaccio, Nunzia [2 ]
Arcari, Paolo [2 ]
Tate, Rosarita [4 ]
Rendina, Ivo [1 ]
Lamberti, Annalisa [2 ]
机构
[1] CNR, Inst Microelect & Microsyst, I-80125 Naples, Italy
[2] Univ Naples Federico II, Dept Mol Med & Med Biotechnol, Naples, Italy
[3] Univ Naples Federico II, Dept Pharm, Naples, Italy
[4] CNR, Inst Genet & Biophys, I-80125 Naples, Italy
来源
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS | 2014年 / 1840卷 / 12期
关键词
Diatomite; Porous material; Surface modification; Photoluminescence; Nanovector; Drug delivery; MESOPOROUS SILICA NANOPARTICLES; DELIVERY; MICROPARTICLES; PURIFICATION; PRINCIPLES; RELEASE; RNA;
D O I
10.1016/j.bbagen.2014.09.009
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Background: Diatomite is a natural porous biomaterial of sedimentary origin, formed by fragments of diatom siliceous skeletons, called "frustules". Due to large availability in many areas of the world, chemical stability, and non-toxicity, these fossil structures have been widespread used in lot of industrial applications, such as food production, water extracting agent, production of cosmetics and pharmaceutics. However, diatomite is surprisingly still rarely used in biomedical applications. In this work, we exploit diatomite nanoparticles for small interfering ribonucleic acid (siRNA) transport inside human epidermoid cancer cells (H1355). Methods: Morphology and composition of diatomite microfrustules (average size lower than 40 mu m) are investigated by scanning electron microscopy equipped by energy dispersive X-ray spectroscopy, Fourier transform infrared analysis, and photoluminescence measurements. Nanometric porous particles (average size lower than 450 nm) are obtained by mechanical crushing, sonication, and filtering of micrometric frustules. siRNA bioconjugation is performed on both micrometric and nanometric fragments by silanization. Results: In-vitro experiments show very low toxicity on exposure of the cells to diatomite nanoparticle concentration up to 300 mu g/ml for 72 h. Confocal microscopy imaging performed on cancer cells incubated with siRNA conjugated nanoparticles demonstrates a cytoplasmatic localization of vectors. Gene silencing by delivered siRNA is also demonstrated. Conclusion: Our studies endorse diatomite nanoparticles as non-toxic nanocarriers for siRNA transport in cancer cells. General significance: siRNA is a powerful molecular tool for cancer treatment but its delivery is inefficient due to the difficulty to penetrate the cell membrane. siRNA-diatomite nanoconjugate may be well suited for delivery of therapeutic to cancer cells. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:3393 / 3403
页数:11
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