Modification of microbial polymers by thiol-ene click reaction: Nanoparticle formation and drug encapsulation

Comb-like amphiphilic polymers were obtained by grafting long paraffinic chains on microbial poly(¿,dl-glutamic acid) and poly(ß,l-malic acid) through two steps, i.e. allylation of the carboxylic side groups followed by UV-initiated thiol-ene click reaction with 1-alkanethiols bearing 8, 12 and 16 c...

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Detalles Bibliográficos
Autores: Lanz, Alberto, Martínez de Ilarduya Sáez de Asteasu, Domingo Antxon|||0000-0001-8105-2168, García Álvarez, Montserrat|||0000-0003-2279-3649, Muñoz Guerra, Sebastián|||0000-0002-4273-2301
Tipo de recurso: artículo
Fecha de publicación:2016
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:2117/90229
Acceso en línea:https://hdl.handle.net/2117/90229
https://dx.doi.org/10.1016/j.reactfunctpolym.2016.07.020
Access Level:acceso abierto
Palabra clave:Biopolymers
Pharmaceutical biotechnology
Poly(¿-glutamic acid)
Poly(ß
l-malic acid)
Click-reaction
Drug encapsulation
Biodegradable nanoparticles
Biopolímers
Sistemes d'administració de medicaments
Biotecnologia farmacèutica
Àrees temàtiques de la UPC::Enginyeria química
Descripción
Sumario:Comb-like amphiphilic polymers were obtained by grafting long paraffinic chains on microbial poly(¿,dl-glutamic acid) and poly(ß,l-malic acid) through two steps, i.e. allylation of the carboxylic side groups followed by UV-initiated thiol-ene click reaction with 1-alkanethiols bearing 8, 12 and 16 carbon atoms, and their characterization was accomplished by 1H NMR, GPC and DSC. The grafted polymers were capable of self-assembling in nanoparticles with diameters in the 80–240 nm range. Incubation in water under physiological conditions led to hydrolysis of the lateral ester bonds followed by scission of the polyamide or polyester main chain. The model drugs, Theophylline and Carbamazepine, were efficiently encapsulated in these systems with much better results attained for the later. Drug release from nanoparticles incubated under physiological conditions occurred with a burst effect and were completely discharged in 24 h. Release profiles recorded from drug-loaded films suggested that the drug was delivered in both cases through a diffusion process.