Studies on the Distribution and Radioimmunoimaging of ^(99m)Tc-Labeled 5-Fluorouracil Loaded Immunological Nanoparticles in Tissues and Human Gastric Carcinoma Xenografts

作     者：Kaihong Huang Jianhua Liu Zhaohua Zhu Xuexian Li Xianping Lu 

作者机构：Institute of Gastroenterology Departmentof Nuclear Medicine the 2nd Affiliated Hospital of Sun Yat-sen University Guangzhou510120 China. 

出 版 物：《Chinese Journal of Clinical Oncology》 (中国肿瘤临床（英文版）)

年 卷 期：2007年第4卷第5期

页      面：307-312页

核心收录：

学科分类：1002[医学-临床医学] 100214[医学-肿瘤学] 10[医学] 

基　　金：the grants as fol-lows:The Problems-Tackling Program in Sci-ence and Technology of Guangzhou City,Chi-na(No.2003 Z 3-E0381) National Foundationof Natural Science,China(No.30670951) Guangdong Foundation of Natural Science,Guangdong,China(No.06021322) TheProblems-Tackling Program in Science andTechnology of Guangdong Province,China(No.2005 B31211002) 

主　　题：radionuclide imaging gastric carcinoma monoclonal antibody nanoparticles 

摘      要：OBJECTIVE To explore the method of preparation of 99m↑Tc labeled AntiVEGF McAb 5-FU loaded polylactic acid nanoparticles （99m↑TC-5-FU-Ab-NPs）, and investigate the biological distribution of the nanoparticles in human gastric carcinoma xenografts. METHODS Anti-VEGF monoclonal antibodyes （MCAB）in 5-FU-Ab-NPs were labeled with 99m↑Tc using a modified Schwarz method. After isolation of the 99m↑TC-5-FU-Ab-NPs using a Sephadex G-250 column, the labeling percentage and radiochemical purity were determined using paper chromatography. The immunocempetence of the 99m↑TC-5-FU-Ab-NPs as tumor markers was determined using ELISA and immunohistochemistry. 99m↑TC-5-FU-Ab-NPs （experimental group）, 99m↑Tc-labelled murine multiclonal IgG loaded polylactic acid and nanoparticles （control group） were injected via the tail vein into SCID mice bearing human gastric carcinoma. A radio-immunity ECT image was developed at 2 and 6 h after the injection. Following the ECT imaging, the mice were sacrificed, their tissue and tumor radioactivity distribution determined, and percentage of the injected-dose per gram （%ID/g） and tumor/ nontumor （T/NT） ratio calculated. High performance liquid chromatography （HPLC） was used to determine the 5-FU concentration in the tumor tissue and blood in the mice of both groups. RESULTS The percentage of 99m↑TC-5-FU-Ab-NPs labeling was 90%-95%. There was no obvious decrease in the antibody activity before and after labeling. The radio-immuno-imaging （RII） showed that the tumor image had developed 2 h after injection of the 99m↑TC-5-FU-Ab-NPs, and with time it was clearer at the 6th hour following the injection. The %lD/g of the tumor tissue at both 2 h and 6 h after the injection was significantly higher compared to the control group. The tumor %lD/g and the tumor to blood activity ratio （TB） of the experimental group at 6 h following the injection increased compared to that at 2 h, and at the same time, 5-FU concentration in the tumor of the experimental gro