SPANosomes as Delivery Vehicles for Small Interfering RNA (siRNA)

被引:35
作者
Zhou, Chenguang [1 ,5 ]
Mao, Yicheng [1 ,5 ]
Sugimoto, Yasuro [2 ]
Zhang, Yue [1 ,4 ]
Kanthamneni, Naveen [1 ]
Yu, Bo [3 ,5 ]
Brueggemeier, Robert W. [2 ]
Lee, L. James [3 ,5 ]
Lee, Robert J. [1 ,5 ]
机构
[1] Ohio State Univ, Coll Pharm, Div Pharmaceut, Columbus, OH 43210 USA
[2] Ohio State Univ, Div Med Chem & Pharmacognosy, Coll Pharm, Columbus, OH 43210 USA
[3] Ohio State Univ, Dept Chem & Biomol Engn, Columbus, OH 43210 USA
[4] Nankai Univ, Coll Pharm, Tianjin 300071, Peoples R China
[5] Ohio State Univ, NSF Nanoscale Sci & Engn Ctr NSEC Affordable Nano, Columbus, OH 43210 USA
基金
美国国家科学基金会;
关键词
drug delivery; nanoparticles; surfactant vesicles; siRNA; molecular beacon; LIPID-LIKE MATERIALS; CATIONIC LIPOSOMES; GENE DELIVERY; INTRACELLULAR TRAFFICKING; TRANSFECTION; EFFICIENT; NIOSOMES; CELLS; THERAPEUTICS; COMPLEXES;
D O I
10.1021/mp200426h
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Nonionic surfactant vesicles, or SPANosomes (SPs), comprised of cationic lipid and sorbitan monooleate (Span 80) were synthesized and evaluated as small interfering RNA (siRNA) vectors. The SPs had a mean diameter of less than 100 nm and exhibited excellent colloidal stability. The SP/siRNA complexes possessed a slightly positive zeta potential of 12 mV and demonstrated a high siRNA incorporation efficiency of greater than 80%. Cryogenic transmission electron microscopy (cryo-TEM) imaging of the SP/siRNA indicated a predominantly core shell structure. The SP/siRNA complexes were shown to efficiently and specifically silence expression of both green fluorescent protein (GFP) (66% knockdown) and aromatase (77% knockdown) genes in breast cancer cell lines. In addition, the cellular trafficking pathway of the SP/siRNA was investigated by confocal microscopy using molecular beacons as probes for cytosolic delivery. The results showed efficient endosomal escape and cytosolic delivery of the siRNA cargo following internalization of the SP/siRNA complexes. In conclusion, Span 80 is a potent helper lipid, and the SPs are promising vehicles for siRNA delivery.
引用
收藏
页码:201 / 210
页数:10
相关论文
共 52 条
[1]   A combinatorial library of lipid-like materials for delivery of RNAi therapeutics [J].
Akinc, Akin ;
Zumbuehl, Andreas ;
Goldberg, Michael ;
Leshchiner, Elizaveta S. ;
Busini, Valentina ;
Hossain, Naushad ;
Bacallado, Sergio A. ;
Nguyen, David N. ;
Fuller, Jason ;
Alvarez, Rene ;
Borodovsky, Anna ;
Borland, Todd ;
Constien, Rainer ;
de Fougerolles, Antonin ;
Dorkin, J. Robert ;
Jayaprakash, K. Narayanannair ;
Jayaraman, Muthusamy ;
John, Matthias ;
Koteliansky, Victor ;
Manoharan, Muthiah ;
Nechev, Lubomir ;
Qin, June ;
Racie, Timothy ;
Raitcheva, Denitza ;
Rajeev, Kallanthottathil G. ;
Sah, Dinah W. Y. ;
Soutschek, Juergen ;
Toudjarska, Ivanka ;
Vornlocher, Hans-Peter ;
Zimmermann, Tracy S. ;
Langer, Robert ;
Anderson, Daniel G. .
NATURE BIOTECHNOLOGY, 2008, 26 (05) :561-569
[2]   Mechanistic investigation of poly(ethylene imine)-based siRNA delivery: Disulfide bonds boost intracellular release of the cargo [J].
Breunig, Miriam ;
Hozsa, Constantin ;
Lungwitz, Uta ;
Watanabe, Kazuo ;
Umeda, Isao ;
Kato, Hiroyuki ;
Goepferich, Achim .
JOURNAL OF CONTROLLED RELEASE, 2008, 130 (01) :57-63
[3]   Aromatase and COX in breast cancer:: Enzyme inhibitors and beyond [J].
Brueggemeier, Robert W. ;
Su, Bin ;
Sugimoto, Yasuro ;
Diaz-Cruz, Edgar S. ;
Davis, Danyetta D. .
JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 2007, 106 (1-5) :16-23
[4]   Selective regulation of aromatase expression for drug discovery [J].
Brueggemeier, Robert W. ;
Su, Bin ;
Darby, Michael V. ;
Sugimoto, Yasuro .
JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 2010, 118 (4-5) :207-210
[5]   RNAi therapeutics: a potential new class of pharmaceutical drugs [J].
Bumcrot, David ;
Manoharan, Muthiah ;
Koteliansky, Victor ;
Sah, Dinah W. Y. .
NATURE CHEMICAL BIOLOGY, 2006, 2 (12) :711-719
[6]   Efficient cytosolic delivery of molecular beacon conjugates and flow cytometric analysis of target RNA [J].
Chen, Antony K. ;
Behlke, Mark A. ;
Tsourkas, Andrew .
NUCLEIC ACIDS RESEARCH, 2008, 36 (12)
[7]   An efficient and low immunostimulatory nanoparticle formulation for systemic siRNA delivery to the tumor [J].
Chono, Sumio ;
Li, Shyh-Dar ;
Conwell, Christine C. ;
Huang, Leaf .
JOURNAL OF CONTROLLED RELEASE, 2008, 131 (01) :64-69
[8]   Advanced transfection with Lipofectamine 2000 reagent: primary neurons, siRNA, and high-throughput applications [J].
Dalby, B ;
Cates, S ;
Harris, A ;
Ohki, EC ;
Tilkins, ML ;
Price, PJ ;
Ciccarone, VC .
METHODS, 2004, 33 (02) :95-103
[9]   Self-assembled lamellar complexes of siRNA with lipidic aminoglycoside derivatives promote efficient siRNA delivery and interference [J].
Desigaux, Lea ;
Sainlos, Matthieu ;
Lambert, Olivier ;
Chevre, Raphael ;
Letrou-Bonneval, Emilie ;
Vigneron, Jean-Pierre ;
Lehn, Pierre ;
Lehn, Jean-Marie ;
Pitard, Bruno .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2007, 104 (42) :16534-16539
[10]   The silent treatment: siRNAs as small molecule drugs [J].
Dykxhoorn, DM ;
Palliser, D ;
Lieberman, J .
GENE THERAPY, 2006, 13 (06) :541-552