Silver Nanoscale Antisense Drug Delivery System for Photoactivated Gene Silencing

被引:109
作者
Brown, Paige K.
Qureshi, Ammar T.
Moll, Alyson N.
Hayes, Daniel J.
Monroe, W. Todd [1 ]
机构
[1] Louisiana State Univ, Baton Rouge, LA 70803 USA
基金
美国国家科学基金会;
关键词
silver nanoparticles; drug delivery; photoactivation; antisense therapeutics; nanomedicine; SCATTERING SUBMICROSCOPIC PARTICLES; HIGHLY FLUORESCENT ANALOGS; GOLD NANOPARTICLES; ENHANCED PHOTOCHEMISTRY; BIOLOGICAL APPLICATIONS; MEDIATED DELIVERY; SINGLE-MOLECULE; NUCLEIC-ACIDS; TRACER LABELS; LIGHT;
D O I
10.1021/nn304868y
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The unique photophysical properties of noble metal nanoparticles contribute to their potential as photoactivated drug delivery vectors. Here we demonstrate the synthesis and characterization of 60-80 nm silver nanoparticles (SNPs) decorated with thiol-terminated photolabile DNA oligonucleotides. In vitro assays and fluorescent confocal microscopy of treated cell cultures show efficient UV-wavelength photoactivation of surface-tethered caged 15152302 antisense oligonucleotides possessing internal photocleavable linkers. As a demonstration of the advantages of these novel nanocarriers, we investigate properties including: enhanced stability to nucleases, increased hybridization activity upon photorelease, and efficient cellular uptake as compared to commercial transfection vectors. Their potential as multicomponent delivery agents for oligonucleotide therapeutics is shown through regulation of ICAM-1 (Intracellular Adhesion Molecule-1) silencing. Our results suggest a means to achieve light-triggered, spatiotemporally controlled gene silencing via nontoxic silver nanocarriers, which hold promise as tailorable platforms for nanomedicine, gene expression studies, and genetic therapies.
引用
收藏
页码:2948 / 2959
页数:12
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