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Tuning the morphology of block copolymer-based pH-triggered nanoplatforms as driven by changes in molecular weight and protocol of manufacturing

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Autor(es):
de Oliveira, Fernando A. ; Batista, Carin C. S. ; Albuquerque, Lindomar J. C. ; Cernoch, Peter ; Steinhart, Milos ; Sincari, Vladimir ; Jager, Alessandro ; Jager, Eliezer ; Giacomelli, Fernando C.
Número total de Autores: 9
Tipo de documento: Artigo Científico
Fonte: Journal of Colloid and Interface Science; v. 635, p. 11-pg., 2023-04-01.
Resumo

The ability to tune size and morphology of self-assemblies is particularly relevant in the development of delivery systems. By tailoring such structural parameters, one can provide larger cargo spaces or produce nanocarriers that can be loaded by hydrophilic and hydrophobic molecules starting ideally from the same polymer building unit. We herein demonstrate that the morphology of block copolymer-based pHtriggered nanoplatforms produced from poly(2-methyl-2-oxazoline)m-b-poly[2-(diisopropylamino)ethyl methacrylate]n (PMeOxm-b-PDPAn) is remarkably influenced by the overall molecular weight of the block copolymer, and by the selected method used to produce the self-assemblies. Polymeric vesicles were produced by nanoprecipitation using a block copolymer of relatively low molecular weight (Mn ti 10 kg.mol-1). Very exciting though, despite the high hydrophobic weight ratio (wPDPA > 0.70), this method conducted to the formation of core-shell nanoparticles when block copolymers of higher molecular weight were used, thus suggesting that the fast (few seconds) self-assembly procedure is controlled by kinetics rather than thermodynamics. We further demonstrated the formation of vesicular structures using longer chains via the solvent-switch approach when the "switching" to the bad solvent is performed in a time scale of a few hours (approximately 3 hs). We accordingly demonstrate that using fairly simple methods one can easily tailor the morphology of such block copolymer self-assemblies, thereby producing a variety of structurally different pH-triggered nanoplatforms via a kinetic or thermodynamically-controlled process. This is certainly attractive towards the development of nanotechnology-based cargo delivery systems. (c) 2022 Elsevier Inc. All rights reserved. (AU)

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Beneficiário:Carin Cristina da Silva Batista
Modalidade de apoio: Bolsas no Brasil - Doutorado
Processo FAPESP: 16/23844-8 - Vesículas poliméricas biodegradáveis e sensíveis ao pH para encapsulação de BIOMACROMOLÉCULAS
Beneficiário:Lindomar Jose Calumby Albuquerque
Modalidade de apoio: Bolsas no Brasil - Doutorado
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Beneficiário:Fernando Augusto de Oliveira
Modalidade de apoio: Bolsas no Brasil - Doutorado
Processo FAPESP: 19/06634-8 - Vesículas poliméricas sensíveis a estímulos ambientais como plataformas alternativas em terapias contra o câncer
Beneficiário:Fernando Carlos Giacomelli
Modalidade de apoio: Auxílio à Pesquisa - Regular
Processo FAPESP: 21/12071-6 - Arquitetando coloides via interações supramoleculares: de fundamentos a aplicações
Beneficiário:Watson Loh
Modalidade de apoio: Auxílio à Pesquisa - Temático