Original Article
Copyright ©2010 Baishideng. All rights reserved.
World J Gastroenterol. May 7, 2010; 16(17): 2120-2128
Published online May 7, 2010. doi: 10.3748/wjg.v16.i17.2120
Direct in vivo injection of 131I-GMS and its distribution and excretion in rabbit
Yu Ma, Yi Wan, Dong-Hui Luo, Li-Geng Duan, Lin Li, Chuan-Qin Xia, Xiao-Li Chen
Yu Ma, Yi Wan, Li-Geng Duan, Xiao-Li Chen, The Research Unit of Hepato-Bilio-Pancreatology and Department of Hepatic Surgery, West China Hospital of Sichuan University, Chengdu 610041, Sichuan Province, China
Dong-Hui Luo, Chuan-Qin Xia, College of Chemistry, Sichuan University, Chengdu 610041, Sichuan Province, China
Lin Li, Department of Nuclear Medicine and The National Key Discipline of Medical Imaging and Nuclear Medicine, West China Hospital of Sichuan University, Chengdu 610041, Sichuan Province, China
Author contributions: Chen XL, Li L, Xia CQ and Ma Y designed the research; Ma Y, Wan Y, Luo DH and Duan LG performed the research; Ma Y and Chen XL analyzed the data and wrote the paper; Xia CQ, Li L, Wan Y and Luo DH wrote part of the paper.
Supported by Grant from the Science & Technology Pillar Program of Sichuan Province, China, No. 2009SZ184
Correspondence to: Xiao-Li Chen, MD, Professor, The Research Unit of Hepato-Bilio-Pancreatology and Department of Hepatic Surgery, West China Hospital of Sichuan University, Chengdu 610041, Sichuan Province, China. zean_z@yahoo.com.cn
Telephone: +86-28-85422868 Fax: +86-28-85534151
Received: November 29, 2009
Revised: January 3, 2010
Accepted: January 10, 2010
Published online: May 7, 2010
Abstract

AIM: To explore the distribution and metabolism of 131I-gelatin microspheres (131I-GMSs) in rabbits after direct injection into rabbits’ livers.

METHODS: Twenty-eight healthy New Zealand rabbits were divided into seven groups, with four rabbits per group. Each rabbit’s hepatic lobes were directly injected with 41.336 ± 5.106 MBq 131I-GMSs. Each day after 131I-GMSs administration, 4 rabbits were randomly selected, and 250 μL of serum was collected for γ count. Hepatic and thyroid functions were tested on days 1, 4, 8, 16, 24, 32, 48 and 64 after 131I-GMSs administration. Single-photon emission computed tomography (SPECT) was taken for each group on days 0, 1, 4, 8, 16, 24, 32, 48, 64 after 131I-GMSs administration. A group of rabbits were sacrificed respectively on days 1, 4, 16, 24, 32, 48, 64 after 131I-GMSs administration. Their livers were taken out for histological examination.

RESULTS: After 131I-GMSs administration, the nuclide was collected in the hepatic area with microspheres. The radiation could be detected on day 48 after 131I-GMSs administration, and radiography could be seen in thyroid areas in SPECT on days 4, 8, 16 and 24. One day after 131I-GMSs administration, the liver function was damaged but recovered 4 d later. Eight days after 131I-GMSs administration, the levels of free triiodothyronine and free thyroxin were reduced, which restored to normal levels on day 16. Histological examination showed that the microspheres were degraded to different degrees at 24, 32 and 48 d after 131I-GMSs administration. The surrounding parts of injection points were in fibrous sheathing. No microspheres were detected in histological examination on day 64 after 131I-GMSs administration.

CONCLUSION: Direct in vivo injection of 131I-GMSs is safe in rabbits. It may be a promising method for treatment of malignant tumors.

Keywords: 131I; Label; Gelatin microspheres; Animal; Rabbit; Hepatic; Direct injection