Near-infrared fluorescence imaging platform for quantifying in vivo nanoparticle diffusion from drug loaded implants

被引:8
作者
Markovic, Stacey [1 ]
Belz, Jodi [2 ]
Kumar, Rajiv [3 ,4 ,5 ]
Cormack, Robert A. [4 ,5 ]
Sridhar, Srinivas [3 ,4 ,5 ]
Niedre, Mark [1 ]
机构
[1] Northeastern Univ, Dept Elect & Comp Engn, 213B Lake Hall,360 Huntington Ave, Boston, MA 02115 USA
[2] Northeastern Univ, Dept Bioengn, Boston, MA 02115 USA
[3] Northeastern Univ, Dept Phys, Boston, MA 02115 USA
[4] Brigham & Womens Hosp, Dana Farber Canc Inst, Dept Radiat Oncol, 75 Francis St, Boston, MA 02115 USA
[5] Harvard Univ, Sch Med, Boston, MA USA
来源
INTERNATIONAL JOURNAL OF NANOMEDICINE | 2016年 / 11卷
关键词
optical imaging; fluorescence; drug delivery; brachytherapy; treatment monitoring; LOCALIZED PROSTATE-CANCER; MODIFIED SILICA NANOPARTICLES; RADIATION-THERAPY; TISSUE PHANTOM; BRACHYTHERAPY; TRIAL;
D O I
10.2147/IJN.S93324
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Drug loaded implants are a new, versatile technology platform to deliver a localized payload of drugs for various disease models. One example is the implantable nanoplatform for chemo-radiation therapy where inert brachytherapy spacers are replaced by spacers doped with nanoparticles (NPs) loaded with chemotherapeutics and placed directly at the disease site for long-term localized drug delivery. However, it is difficult to directly validate and optimize the diffusion of these doped NPs in in vivo systems. To better study this drug release and diffusion, we developed a custom macroscopic fluorescence imaging system to visualize and quantify fluorescent NP diffusion from spacers in vivo. To validate the platform, we studied the release of free fluorophores, and 30 nm and 200 nm NPs conjugated with the same fluorophores as a model drug, in agar gel phantoms in vitro and in mice in vivo. Our data verified that the diffusion volume was NP size-dependent in all cases. Our near-infrared imaging system provides a method by which NP diffusion from implantable nanoplatform for chemo-radiation therapy spacers can be systematically optimized (eg, particle size or charge) thereby improving treatment efficacy of the platform.
引用
收藏
页码:1213 / 1223
页数:11
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