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利用中子俘获放射自显影术,通过聚乙二醇结合脂质体使硼化合物在肿瘤中蓄积。

Accumulation of boron compounds to tumor with polyethylene-glycol binding liposome by using neutron capture autoradiography.

作者信息

Yanagië Hironobu, Ogura Koichi, Takagi Kenji, Maruyama Kazuo, Matsumoto Toshio, Sakurai Yoshinori, Skvarc Jure, Illic Radomir, Kuhne Guido, Hisa Tomoyuki, Yoshizaki Iwao, Kono Kenji, Furuya Yoshitaka, Sugiyama Hirotaka, Kobayashi Hisao, Ono Koji, Nakagawa Keiichi, Eriguchi Masazumi

机构信息

Project of Tumor Metastasis Inhibition, Research Center for Advanced Science & Technology, The University of Tokyo, 4-6-1 Komaba, Meguro-ku, Tokyo 153-8904, Japan.

出版信息

Appl Radiat Isot. 2004 Oct;61(4):639-46. doi: 10.1016/j.apradiso.2004.03.109.

Abstract

The cytotoxic effect of boron neutron capture therapy (BNCT) is due to a nuclear reaction between 10B and thermal neutrons. It is necessary to accumulate the 10B atoms to the tumor cells selectively for effective BNCT. In order to achieve an accurate measurement of 10B concentrations in the biological samples, we employed a technique of neutron capture autoradiography (NCAR) of the sliced whole-body samples of tumor bearing mice using CR-39 plastic track detectors. The CR-39 detectors attached with samples were exposed to thermal neutrons in the thermal column of the TRIGA II reactor at the Institute for Atomic Energy, Rikkyo University and thermal neutron facility of Paul Scherer Institute(PSI). We obtained NCAR images for mice injected intravenously by 10B-PEG liposome, 10B-transferrin-PEG liposome, or 10B-bare liposome. The 10B concentrations in the tumor tissue of mice were estimated by means of alpha-track density measurements. In this study, we can increase the accumulation of 10B atoms in the tumor tissues by binding polyethylene-glycol chains to the surface of liposome, which increase the retention in the blood flow and escape the phagocytosis by reticulo-endothelial systems. Therefore, we will be able to apply NCAR technique for selection of effective 10B carrier in BNCT for cancer.

摘要

硼中子俘获疗法(BNCT)的细胞毒性作用源于硼 - 10(¹⁰B)与热中子之间的核反应。为了实现有效的BNCT,有必要将¹⁰B原子选择性地积累到肿瘤细胞中。为了准确测量生物样品中的¹⁰B浓度,我们采用了一种技术,即使用CR - 39塑料径迹探测器对荷瘤小鼠的全身切片样本进行中子俘获放射自显影(NCAR)。附着有样品的CR - 39探测器在立教大学原子能研究所的TRIGA II反应堆热柱以及保罗·谢尔研究所(PSI)的热中子设施中暴露于热中子。我们获得了通过静脉注射¹⁰B - PEG脂质体、¹⁰B - 转铁蛋白 - PEG脂质体或¹⁰B裸脂质体的小鼠的NCAR图像。通过α径迹密度测量来估计小鼠肿瘤组织中的¹⁰B浓度。在本研究中,我们可以通过将聚乙二醇链结合到脂质体表面来增加¹⁰B原子在肿瘤组织中的积累,这会增加其在血流中的滞留并逃避网状内皮系统的吞噬作用。因此,我们将能够应用NCAR技术来选择用于癌症BNCT的有效¹⁰B载体。

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