Synthesis and in Vitro Testing of J591 Antibody−Dendrimer Conjugates for Targeted Prostate Cancer Therapy
- 8 October 2004
- journal article
- research article
- Published by American Chemical Society (ACS) in Bioconjugate Chemistry
- Vol. 15 (6) , 1174-1181
- https://doi.org/10.1021/bc0499127
Abstract
Targeted therapeutics using antibodies are an attractive option over conventional cancer chemotherapeutics due to their potential to deliver a therapeutic specifically to cancer tissue without damaging normal tissue. However, there are known problems with immunoconjugates such as decreased immunoreactivity and poor solubility. Using dendrimers as carriers for these agents has the potential to resolve these issues. We synthesized J591 anti-PSMA (prostate specific membrane antigen) antibody dendrimer conjugates containing fluorophores on the dendrimer. The in vitro studies of these conjugates show that they specifically bind to cells expressing PSMA. Confocal microscopy experiments document the binding and internalization of these conjugates. This research encourages the further study of antibody-dendrimer-drug conjugates for use in targeted therapeutics.Keywords
This publication has 6 references indexed in Scilit:
- Site-Specific Conjugation of Boron-Containing Dendrimers to Anti-EGF Receptor Monoclonal Antibody Cetuximab (IMC-C225) and Its Evaluation as a Potential Delivery Agent for Neutron Capture TherapyBioconjugate Chemistry, 2003
- Anti‐tumor effects of toxins targeted to the prostate specific membrane antigenThe Prostate, 2002
- The Synthesis and Testing of Anti-Cancer Therapeutic NanodevicesBiomedical Microdevices, 2001
- Monoclonal antibody-dendrimer conjugates enable radiolabeling of antibody with markedly high specific activity with minimal loss of immunoreactivityEuropean Journal of Nuclear Medicine and Molecular Imaging, 2000
- Terminal Groups in Starburst Dendrimers: Activation and Reactions with ProteinsBioconjugate Chemistry, 1998
- Boronated starburst dendrimer-monoclonal antibody immunoconjugates: Evaluation as a potential delivery system for neutron capture therapyBioconjugate Chemistry, 1994