Nanoparticle-Based Brachytherapy Spacers for Delivery of Localized Combined Chemoradiation Therapy

被引:23
作者
Kumar, Rajiv [1 ,3 ,4 ]
Belz, Jodi [1 ]
Markovic, Stacey [2 ]
Jadhav, Tej [1 ]
Fowle, William [1 ]
Niedre, Mark [2 ]
Cormack, Robert [3 ,4 ]
Makrigiorgos, Mike G. [3 ,4 ]
Sridhar, Srinivas [1 ,3 ,4 ]
机构
[1] Northeastern Univ, Nanomed Sci & Technol Ctr, Boston, MA 02115 USA
[2] Northeastern Univ, Dept Elect & Comp Engn, Boston, MA 02115 USA
[3] Brigham & Womens Hosp, Dana Farber Canc Inst, Dept Radiat Oncol, Boston, MA 02115 USA
[4] Harvard Univ, Sch Med, Boston, MA USA
来源
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS | 2015年 / 91卷 / 02期
关键词
CONFORMAL RADIATION-THERAPY; RISK PROSTATE-CANCER; SILICA NANOPARTICLES; DRUG-DELIVERY; IN-VITRO; PLGA NANOPARTICLES; PHARMACOKINETICS; TRIAL;
D O I
10.1016/j.ijrobp.2014.10.041
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: In radiation therapy (RT), brachytherapy-inert source spacers are commonly used in clinical practice to achieve high spatial accuracy. These implanted devices are critical technical components of precise radiation delivery but provide no direct therapeutic benefits. Methods and Materials: Here we have fabricated implantable nanoplatforms or chemoradiation therapy (INCeRT) spacers loaded with silica nanoparticles (SNPs) conjugated containing a drug, to act as a slow-release drug depot for simultaneous localized chemoradiation therapy. The spacers are made of poly(lactic-co-glycolic) acid (PLGA) as matrix and are physically identical in size to the commercially available brachytherapy spacers (5 mm x 0.8 mm). The silica nanoparticles, 250 nm in diameter, were conjugated with near infrared fluorophore Cy7.5 as a model drug, and the INCeRT spacers were characterized in terms of size, morphology, and composition using different instrumentation techniques. The spacers were further doped with an anticancer drug, docetaxel. We evaluated the in vivo stability, biocompatibility, and biodegradation of these spacers in live mouse tissues. Results: The electron microscopy studies showed that nanoparticles were distributed throughout the spacers. These INCeRT spacers remained stable and can be tracked by the use of optical fluorescence. In vivo optical imaging studies showed a slow diffusion of nanoparticles from the spacer to the adjacent tissue in contrast to the control Cy7.5-PLGA spacer, which showed rapid disintegration in a few days with a burst release of Cy7.5. The docetaxel spacers showed suppression of tumor growth in contrast to control mice over 16 days. Conclusions: The imaging with the Cy7.5 spacer and therapeutic efficacy with docetaxel spacers supports the hypothesis that INCeRT spacers can be used for delivering the drugs in a slow, sustained manner in conjunction with brachytherapy, in contrast to the rapid clearance of the drugs when administered systemically. The results demonstrate that these spacers with tailored release profiles have potential in improving the combined therapeutic efficacy of chemoradiation therapy. (C) 2015 Elsevier Inc.
引用
收藏
页码:393 / 400
页数:8
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