Relative study between anti-EGFR and GE-11 peptide conjugated gold nanoparticles for in vivo targeting in pancreatic cancer [abstract]

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Relative study between anti-EGFR and GE-11 peptide conjugated gold nanoparticles for in vivo targeting in pancreatic cancer [abstract]

Please use this identifier to cite or link to this item: http://hdl.handle.net/10355/9779

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Title: Relative study between anti-EGFR and GE-11 peptide conjugated gold nanoparticles for in vivo targeting in pancreatic cancer [abstract]
Author: Chanda, Nripen; Zambre, Ajit; Shukla, Ravi; Mukharjee, Priyabrata; Mukhopadhyay, Debabrata; Boote, Evan; Kannan, Raghuraman; Katti, Kattesh V.
Keywords: cancer treatment
diagnostic medicine
Date: 2010-10-07
Abstract: Pancreatic cancer is the fourth leading cause of cancer related deaths in the United States due to its severe aggressiveness and lethal malignancy. Epidermal Growth Factor Receptor (EGFR) is over expressed in more than 95% of human pancreatic cancer patients. A number of peptides and monoclonal antibodies have been developed to target the EGFR in pancreatic cancer. Our research has focused on developing EGFR targeting biomolecule conjugated gold nanoparticles for the diagnosis and staging of various cancers. In this study, we have synthesized a series of Antibody EGFR and EGFR-peptide (GE-11) conjugated AuNPs. We investigated the in vivo EGFR targeting characteristics of these conjugates in pancreatic tumor bearing SCID mice models. Our investigation has provided evidence that the peptide conjugated AuNPs have high in vivo mobility and targets pancreatic tumor effectively. We have also established that the EGFR-peptide-AuNP conjugates serve as better X-ray contrast agents for early detection of pancreatic cancer in mice models. The details of this comparative study will be presented in this poster. INVENTOR(S): Nripen Chanda; Ajit Zambre; Ravi Shukla; Priyabrata Mukharjee; Debabrata Mukhopadhyay; Evan Boote; Raghuraman Kannan; Kattesh V. Katti CONTACT INFO: Paul Hippenmeyer, Ph.D., M.B.A.; hippenmeyerp@missouri.edu; (573)-882-0470
URI: http://hdl.handle.net/10355/9779

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