Tumor CT imaging using targeted nanoparticle delivery for contrast enhancement and tumor inhibition using targeted release of carboplatin nanoparticles via radiotherapy

S. Harada, S. Ehara, K. Ishii, Takahiro Sato, M. Koka, T. Kamiya, K. Sera, S. Goto
{"title":"Tumor CT imaging using targeted nanoparticle delivery for contrast enhancement and tumor inhibition using targeted release of carboplatin nanoparticles via radiotherapy","authors":"S. Harada, S. Ehara, K. Ishii, Takahiro Sato, M. Koka, T. Kamiya, K. Sera, S. Goto","doi":"10.1142/S0129083514400075","DOIUrl":null,"url":null,"abstract":"In this paper, we used microcapsules releasing liposome-protamine-hyaluronic acid nanoparticles (LPH-NP) with/without carboplatin in response to radiation to image and treat MM48 breast cancer in C3He/N mice in two radiation sessions. The micro-particle-induced X-ray emission (PIXE) camera and quantitative PIXE were used to image and measure the release of nanoparticles from the microcapsules. In session one, iopamiron and computed tomography (CT)-detectable microcapsules containing P-selectin and LPH-NP were mixed with a solution of alginate, hyaluronate, ascorbate, and P-selectin. This solution was sprayed into an FeCl2 solution containing VEGFR-1/2 antibodies (Abs). The microcapsules obtained were injected intravenously into mice, and after 9 h, the mice were exposed to 10 or 20 Gy (140 keV) of X-ray radiation. Anti-VEGFR-1/VEGFR-2 microcapsules accumulated around tumors and released P-selectin and the iopamiron-labeled LPH-NP in response to the first radiation. The iopamiron-containing nanoparticles were detected by CT, allowing detection of MM48 tumors by CT. In the second session, the microcapsules released LPH-NH that delivered carboplatin into the tumor cells. This treatment had a significant antitumor effect (P<0.05). The micro-PIXE camera and quantitative PIXE successfully imaged and measured the release of contents from microcapsules. Our results indicate that targeted nanoparticles allow for accurate detection and treatment of tumors.","PeriodicalId":14345,"journal":{"name":"International Journal of PIXE","volume":"9 1","pages":"137-149"},"PeriodicalIF":0.0000,"publicationDate":"2014-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal of PIXE","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1142/S0129083514400075","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

In this paper, we used microcapsules releasing liposome-protamine-hyaluronic acid nanoparticles (LPH-NP) with/without carboplatin in response to radiation to image and treat MM48 breast cancer in C3He/N mice in two radiation sessions. The micro-particle-induced X-ray emission (PIXE) camera and quantitative PIXE were used to image and measure the release of nanoparticles from the microcapsules. In session one, iopamiron and computed tomography (CT)-detectable microcapsules containing P-selectin and LPH-NP were mixed with a solution of alginate, hyaluronate, ascorbate, and P-selectin. This solution was sprayed into an FeCl2 solution containing VEGFR-1/2 antibodies (Abs). The microcapsules obtained were injected intravenously into mice, and after 9 h, the mice were exposed to 10 or 20 Gy (140 keV) of X-ray radiation. Anti-VEGFR-1/VEGFR-2 microcapsules accumulated around tumors and released P-selectin and the iopamiron-labeled LPH-NP in response to the first radiation. The iopamiron-containing nanoparticles were detected by CT, allowing detection of MM48 tumors by CT. In the second session, the microcapsules released LPH-NH that delivered carboplatin into the tumor cells. This treatment had a significant antitumor effect (P<0.05). The micro-PIXE camera and quantitative PIXE successfully imaged and measured the release of contents from microcapsules. Our results indicate that targeted nanoparticles allow for accurate detection and treatment of tumors.
肿瘤CT成像使用靶向纳米颗粒输送增强对比和靶向释放卡铂纳米颗粒通过放疗抑制肿瘤
在本文中,我们使用微胶囊释放脂质体-蛋白蛋白-透明质酸纳米颗粒(LPH-NP),加卡铂或不加卡铂对辐射成像的反应,并在两次放射治疗中治疗C3He/N小鼠的MM48乳腺癌。利用微粒子诱导x射线发射(PIXE)相机和定量x射线发射(PIXE)对微胶囊中纳米粒子的释放进行了成像和测量。在第一阶段,将含有p -选择素和LPH-NP的iopamiron和计算机断层扫描(CT)可检测的微胶囊与海藻酸盐、透明质酸盐、抗坏血酸盐和p -选择素的溶液混合。将该溶液喷洒到含有VEGFR-1/2抗体(Abs)的FeCl2溶液中。将获得的微胶囊静脉注射到小鼠体内,9小时后,将小鼠暴露于10或20 Gy (140 keV)的x射线辐射下。抗vegfr -1/VEGFR-2微胶囊在肿瘤周围积聚,释放p -选择素和iopam铁标记的LPH-NP。CT检测含iopam铁纳米颗粒,实现MM48肿瘤的CT检测。在第二阶段,微胶囊释放LPH-NH,将卡铂递送到肿瘤细胞中。该治疗具有显著的抗肿瘤作用(P<0.05)。微PIXE相机和定量PIXE成功地成像并测量了微胶囊中内容物的释放。我们的研究结果表明,靶向纳米颗粒可以精确检测和治疗肿瘤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信