Liver Cancer
Copyright ©The Author(s) 2004. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Gastroenterol. Dec 1, 2004; 10(23): 3424-3427
Published online Dec 1, 2004. doi: 10.3748/wjg.v10.i23.3424
Preparation of human hepatocellular carcinoma-targeted liposome microbubbles and their immunological properties
Ai-Na Bian, Yun-Hua Gao, Kai-Bin Tan, Ping Liu, Gong-Jun Zeng, Xin Zhang, Zheng Liu
Ai-Na Bian, Yun-Hua Gao, Kai-Bin Tan, Ping Liu, Gong-Jun Zeng, Xin Zhang, Zheng Liu, Department of Ultrasonic Diagnosis, Xinqiao Hospital the Third Military Medical University, Chongqing 400037, China
Author contributions: All authors contributed equally to the work.
Supported by the National Natural Science Foundation of China, No. 30270384
Correspondence to: Professor. Yun-Hua Gao, Director of Department of Ultrasonic Diagnosis, Xinqiao Hospital, the Third Military Medical University, Chongqing 400037, China. gyhxq@sina.com
Telephone: +86-23-68755631 Fax: +86-23-68755631
Received: December 23, 2003
Revised: January 8, 2004
Accepted: January 15, 2004
Published online: December 1, 2004
Abstract

AIM: To prepare the human hepatocellular carcinoma-(HCC)-targeted liposome microbubbles and to investigate their immunological properties.

METHODS: Human hepatocarcinoma specific monoclonal antibody HAb18 was attached to the surface of home-made liposome microbubbles by static attraction to prepare the targeted liposome microbubbles. The combination of HAb18 with liposome microbubbles was confirmed by the slide agglutination test and immunofluorescent assay. Their immunological activity was measured by ELISA. Rosette formation test, rosette formation blocking test and immun-ofluorescent assay were used to identify the specific binding of targeted liposome microbubbles to SMMC-7721 hepatoma cells, and cytotoxicity assay was used to detect their effect on human hepatocytes.

RESULTS: The targeted liposome microbubbles were positive in the slide agglutination test and immunofluorescent assay. ELISA indicated that the immunological activity of HAb18 on the liposome microbubbles was similar to that of free HAb18. SMMC-7721 cells were surrounded by the targeting liposome microbubbles to form rosettes, while the control SGC-7901 gastric cancer cells were not. Proliferation of SMMC-7721 cells and normal human hepatocytes was not influenced by the targeted liposome microbubbles.

CONCLUSION: The targeted liposome microbubbles with a high specific biological activity have been successfully prepared, which specifically bind to human hepatocarcinoma cells, and are non-cytotoxic to hepatocytes. These results indicate that the liposome microbubbles can be used as a HCC-targeted ultrasound contrast agent that may enhance ultrasound images and thus improve the diagnosis of HCC, especially at the early stage.

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