Facile Synthesis of Monodispersed Mesoporous Silica Nanoparticles with Ultralarge Pores and Their Application in Gene Delivery

被引:315
作者
Kim, Mi-Hee [1 ]
Na, Hee-Kyung [1 ]
Kim, Young-Kwan [1 ]
Ryoo, Soo-Ryoon [1 ]
Cho, Hae Sung [1 ]
Lee, Kyung Eun [3 ]
Jeon, Hyesung [3 ]
Ryoo, Ryong [1 ,2 ]
Min, Dal-Hee [1 ]
机构
[1] Korea Adv Inst Sci & Technol, Dept Chem, Taejon 305701, South Korea
[2] Korea Adv Inst Sci & Technol, Grad Sch Nanosci & Technol WCU, Taejon 305701, South Korea
[3] Korea Inst Sci & Technol, Biomed Res Ctr, Seoul 136791, South Korea
关键词
biocompatibility; gene delivery; large pores; plasmid; porous silica nanoparticle; SICKLE-CELL-DISEASE; PLASMID DNA; VECTORS; THERAPY; SPHERES;
D O I
10.1021/nn103130q
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Among various nanoparticles, the silica nanoparticle (SiNP) is an attractive candidate as a gene delivery carrier due to advantages such as availability in porous forms for encapsulation of drugs and genes, large surface area to load biomacromolecules, biocompatibility, storage stability, and easy preparation in large quantity with low cost. Here, we report on a facile synthesis of monodispersed mesoporous silica nanoparticles (MMSN) possessing very large pores (> 15 nm) and application of the nanoparticles to plasmid DNA delivery to human cells. The aminated MMSN with large pores provided a higher loading capacity for plasmids than those with small pores (similar to 2 nm), and the complex of MMSN with plasmid DNA readily entered Into cells without supplementary polymers such as cationic dendrimers. Furthermore, MMSN with large pores could efficiently protect plasmids from nuclease-mediated degradation and showed much higher transfection efficiency of the plasmids encoding luciferase and green fluorescent protein. (pLuc, pGFP) compared to MMSN with small pores (similar to 2 nm).
引用
收藏
页码:3568 / 3576
页数:9
相关论文
共 34 条
[1]   Modular protein engineering for non-viral gene therapy [J].
Arís, A ;
Villaverde, A .
TRENDS IN BIOTECHNOLOGY, 2004, 22 (07) :371-377
[2]   Genetic correction of sickle cell disease: Insights using transgenic mouse models [J].
Blouin, MJ ;
Beauchemin, H ;
Wright, A ;
De Paepe, M ;
Sorette, M ;
Bleau, AM ;
Nakamoto, B ;
Ou, CN ;
Stamatoyannopoulos, G ;
Trudel, M .
NATURE MEDICINE, 2000, 6 (02) :177-182
[3]   Encapsulation of nucleic acids and opportunities for cancer treatment [J].
Brannon-Peppas, Lisa ;
Ghosn, Bilal ;
Roy, Krishnendu ;
Cornetta, Kenneth .
PHARMACEUTICAL RESEARCH, 2007, 24 (04) :618-627
[4]   Gene Therapy for Cancer Treatment: Past, Present and Future [J].
Cross, Deanna ;
Burmester, James K. .
CLINICAL MEDICINE & RESEARCH, 2006, 4 (03) :218-227
[5]   Cationic polymer based gene delivery systems [J].
De Smedt, SC ;
Demeester, J ;
Hennink, WE .
PHARMACEUTICAL RESEARCH, 2000, 17 (02) :113-126
[6]  
DERIUS AM, 2007, BIOCONJUGATE CHEM, V18, P1391
[7]   Cationic lipid-mediated gene transfer: effect of serum on cellular uptake and intracellular fate of lipopolyamine/DNA complexes [J].
Escriou, V ;
Ciolina, C ;
Lacroix, F ;
Byk, G ;
Scherman, D ;
Wils, P .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 1998, 1368 (02) :276-288
[8]   A calcium phosphate-based gene delivery system [J].
Fu, HH ;
Hu, YH ;
McNelis, T ;
Hollinger, JO .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART A, 2005, 74A (01) :40-48
[9]   Carbon nanotube delivery of the GFP gene into mammalian cells [J].
Gao, LZ ;
Nie, L ;
Wang, TH ;
Qin, YJ ;
Guo, ZX ;
Yang, DL ;
Yan, XY .
CHEMBIOCHEM, 2006, 7 (02) :239-242
[10]   Efficient Gene Delivery Vectors by Tuning the Surface Charge Density of Amino Acid-Functionalized Gold Nanoparticles [J].
Ghosh, Partha S. ;
Kim, Chae-Kyu ;
Han, Gang ;
Forbes, Neil S. ;
Rotello, Vincent M. .
ACS NANO, 2008, 2 (11) :2213-2218