Abstract
The monoclonal antibody, mAb 2C5, recognizing the surface of numerous tumor, but not normal, cells via their surface-bound nucelosomes, was coupled onto sterically protected poly(ethylene glycol) liposomes. In this study, the development of different mAb 2C5-targeted formulations, like radiolabeled liposomes for gamma imaging of tumors and doxorubicin-containing liposomes for cancer chemotherapy, is described. Our data demonstrate the enhanced in vitro anticancer activities and the evident tumor-avid in vivo biodistribution, confirming the superior tumor-selectivity of the mAb 2C5-modified liposomes. This report reveals the eminent potential for this tumor-targeting strategy, with mAb 2C5, in improving the delivery of drugs and imaging agents into various tumors.
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Acknowledgments
This research was supported by the NIH grant R01-EB02995 to Vladimir P. Torchilin. We thank Dr. B.-A. Khaw of Northeastern University for his valuable help with the γ-scintigraphic imaging studies.
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Surface attachment of the anticancer monoclonal antibody 2C5 to liposomes, on-top of their PEG shield, allows for enhanced targeted delivery of entrapped drugs or contrasts to a wide variety of tumors.
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Elbayoumi, T.A., Torchilin, V.P. Tumor-Targeted Immuno-liposomes for Delivery of Chemotherapeutics and Diagnostics. J Pharm Innov 3, 51–58 (2008). https://doi.org/10.1007/s12247-008-9021-7
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DOI: https://doi.org/10.1007/s12247-008-9021-7