Hyperbranched and hiperfunctionalized materials from dendritic chemistry.

MARCELO CALDERÓN; MIRIAM STRUMIA

REVISTA LATINOAMERICANA DE METALURGIA Y MATERIALES

Universidad de Caracas

Lugar: Caracas; Año: 2013 vol. 33 p. 2 - 14

0255-6952

Dendritic molecules are highly ordered, regularly branched, and monodisperse macromolecules. Due to their unique and well-defined macromolecular structure they are attractive scaffolds for a variety of high-end applications and constitute a fascinating nanoscale toolkit. They are of great interest to both, nano and polymer science, as building blocks due to their unique macromolecular properties. In recent years, research in the field of dendritic chemistry has experienced an exponential development in academic and technological areas and such macromolecular structures have also been extensively explored in materials science, specifically in biomedical areas. The unique advantages offered by dendritic architectures over conventional macromolecules and polymers are the presence of multiple functional groups and their amenability to further chemical modification, extremely low molecular weight dispersity, low solution viscosity, reduced molecular entanglement, and nanoscopic size within the range of 1 to 10 nm. The objective of this review is to show the advantage of the dendritic structures, their main properties, and to reflect on their development and use in various science applications. Particular emphasis will be place on biomedical and nanomedicine applications. Therefore, key examples will be discussed to illustrate the main principles involved in dendritic chemistry, and the applications of the dendritic structures at the interfaces between chemistry, biology and biomedicine.