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Title: | Multivalent ligand: Design principle for targeted therapeutic delivery approach |
Authors: | Chittasupho C. |
Keywords: | antibody antibody conjugate arginylglycylaspartic acid cancer vaccine carbohydrate cephalosporin cisplatin cytotoxic T lymphocyte antigen 4 antibody dendrimer doxorubicin ligand macrogol multivalent ligand nanoparticle peptide polyamidoamine polyglactin polymer single chain fragment variable antibody tumor antigen tumor vaccine unclassified drug very late activation antigen 4 vitronectin receptor autoimmune disease binding affinity binding site breast cancer cancer immunotherapy concentration (parameters) conformational transition controlled drug release density drug delivery system drug half life encapsulation enthalpy entropy human IC 50 immunogenicity ligand binding molecular interaction molecularly targeted therapy nonhuman priority journal protein multimerization review T lymphocyte activation thermodynamics Animals Binding Sites Drug Delivery Systems Drug Design Humans Ligands Thermodynamics |
Issue Date: | 2012 |
Abstract: | Multivalent interactions of biological molecules play an important role in many biochemical events. A multivalent ligand comprises of multiple copies of ligands conjugated to scaffolds, allowing the simultaneous binding of multivalent ligands to multiple binding sites or receptors. Many research groups have successfully designed and synthesized multivalent ligands to increase the binding affinity, avidity and specificity of the ligand to the receptor. A multimeric ligand is a promising option for the specific treatment of diseases. In this review, the factors affecting multivalent interactions, including the size and shape of the ligand, geometry and an arrangement of ligands on the scaffold, linker length, thermodynamic, and kinetics of the interactions are discussed. Examples of the multivalent ligand applications for therapeutic delivery are also summarized. © 2012 Future Science Ltd. |
URI: | https://ir.swu.ac.th/jspui/handle/123456789/14274 https://www.scopus.com/inward/record.uri?eid=2-s2.0-84867940749&doi=10.4155%2ftde.12.99&partnerID=40&md5=7dacdc19cbff1ce1c4410b6d7493ae1c |
ISSN: | 20415990 |
Appears in Collections: | Scopus 1983-2021 |
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