Polypeptide-based materials prepared by ring-opening polymerisation of anionic-based alpha-amino acid N-carboxyanhydrides: A platform for delivery of bioactive-compounds

Polymerisation of a-amino acid N-carboxyanhydrides (NCAs) is one of the most common techniques to prepare synthetic polypeptides. Of special interest are the NCAs derived from a-amino acids, L-aspartic acid and L-glutamic acid, since most investigations have been focused on their use to synthesise m...

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Detalles Bibliográficos
Autores: Tinajero, Ernesto|||0000-0001-5993-8114, Kimmins, Scott D, García-Carvajal, Zaira-Yunuen, Martínez de Ilarduya Sáez de Asteasu, Domingo Antxon|||0000-0001-8105-2168
Tipo de recurso: artículo
Fecha de publicación:2021
País:España
Institución:Universitat Politècnica de Catalunya (UPC)
Repositorio:UPCommons. Portal del coneixement obert de la UPC
Idioma:inglés
OAI Identifier:oai:upcommons.upc.edu:2117/356121
Acceso en línea:https://hdl.handle.net/2117/356121
https://dx.doi.org/10.1016/j.reactfunctpolym.2021.105040
Access Level:acceso abierto
Palabra clave:Copolymers
Polymerization
Drug carriers (Pharmacy)
N-carboxyanhydrides
Ring-opening polymerisation
l-Aspartic acid
l-Glutamic acid
Synthetic copolypeptides
Hybrid copolymers
Excipients
Bioactive-compounds
Copolímers
Polimerització
Àrees temàtiques de la UPC::Enginyeria química
Descripción
Sumario:Polymerisation of a-amino acid N-carboxyanhydrides (NCAs) is one of the most common techniques to prepare synthetic polypeptides. Of special interest are the NCAs derived from a-amino acids, L-aspartic acid and L-glutamic acid, since most investigations have been focused on their use to synthesise multiblock copolypeptides or hybrid synthetic polypeptide-polymers to design excipients suitable for delivery of bioactive compounds. This perspective highlights advantages of using L-aspartic acid and L-glutamic over other natural a-amino acids in that their pendant carboxyl group serves as a reactive handle for coupling a variety of reactive groups, and because the resulting polypeptides have the ability to adopt secondary structures. In addition, recent progress in the ring-opening polymerisation of NCAs will be discussed. Throughout, we provide representative examples that shed light on the NCAs polymerisation process, and we finally share our perspectives concerning the practical use of anionic a-amino acids as building blocks for future investigations.