Cargando…

Retinol-Containing Graft Copolymers for Delivery of Skin-Curing Agents

The new polymeric systems for delivery in cosmetology applications were prepared using self-assembling amphiphilic graft copolymers. The synthesis based on “click” chemistry reaction included grafting of azide-functionalized polyethylene glycol (PEG-N(3)) onto multifunctional polymethacrylates conta...

Descripción completa

Detalles Bibliográficos
Autores principales: Odrobińska, Justyna, Niesyto, Katarzyna, Erfurt, Karol, Siewniak, Agnieszka, Mielańczyk, Anna, Neugebauer, Dorota
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6722771/
https://www.ncbi.nlm.nih.gov/pubmed/31382359
http://dx.doi.org/10.3390/pharmaceutics11080378
_version_ 1783448616665350144
author Odrobińska, Justyna
Niesyto, Katarzyna
Erfurt, Karol
Siewniak, Agnieszka
Mielańczyk, Anna
Neugebauer, Dorota
author_facet Odrobińska, Justyna
Niesyto, Katarzyna
Erfurt, Karol
Siewniak, Agnieszka
Mielańczyk, Anna
Neugebauer, Dorota
author_sort Odrobińska, Justyna
collection PubMed
description The new polymeric systems for delivery in cosmetology applications were prepared using self-assembling amphiphilic graft copolymers. The synthesis based on “click” chemistry reaction included grafting of azide-functionalized polyethylene glycol (PEG-N(3)) onto multifunctional polymethacrylates containing alkyne units. The latter ones were obtained via atom transfer radical polymerization (ATRP) of alkyne-functionalized monomers, e.g., ester of hexynoic acid and 2-hydroxyethyl methacrylate (AlHEMA) with methyl methacrylate (MMA), using bromoester-modified retinol (RETBr) as the initiator. Varying the content of alkyne moieties adjusted by initial monomer ratios of AlHEMA/MMA was advantageous for the achievement of a well-defined grafting degree. The designed amphiphilic graft copolymers P((HEMA-graft-PEG)-co-MMA), showing tendency to micellization in aqueous solution at room temperature, were encapsulated with arbutin (ARB) or vitamin C (VitC) with high efficiencies (>50%). In vitro experiments carried out in the phosphate-buffered saline solution (PBS) at pH 7.4 indicated the maximum release of ARB after at least 20 min and VitC within 10 min. The fast release of the selected antioxidants and skin-lightening agents by these micellar systems is satisfactory for applications in cosmetology, where they can be used as the components of masks, creams, and wraps.
format Online
Article
Text
id pubmed-6722771
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-67227712019-09-10 Retinol-Containing Graft Copolymers for Delivery of Skin-Curing Agents Odrobińska, Justyna Niesyto, Katarzyna Erfurt, Karol Siewniak, Agnieszka Mielańczyk, Anna Neugebauer, Dorota Pharmaceutics Article The new polymeric systems for delivery in cosmetology applications were prepared using self-assembling amphiphilic graft copolymers. The synthesis based on “click” chemistry reaction included grafting of azide-functionalized polyethylene glycol (PEG-N(3)) onto multifunctional polymethacrylates containing alkyne units. The latter ones were obtained via atom transfer radical polymerization (ATRP) of alkyne-functionalized monomers, e.g., ester of hexynoic acid and 2-hydroxyethyl methacrylate (AlHEMA) with methyl methacrylate (MMA), using bromoester-modified retinol (RETBr) as the initiator. Varying the content of alkyne moieties adjusted by initial monomer ratios of AlHEMA/MMA was advantageous for the achievement of a well-defined grafting degree. The designed amphiphilic graft copolymers P((HEMA-graft-PEG)-co-MMA), showing tendency to micellization in aqueous solution at room temperature, were encapsulated with arbutin (ARB) or vitamin C (VitC) with high efficiencies (>50%). In vitro experiments carried out in the phosphate-buffered saline solution (PBS) at pH 7.4 indicated the maximum release of ARB after at least 20 min and VitC within 10 min. The fast release of the selected antioxidants and skin-lightening agents by these micellar systems is satisfactory for applications in cosmetology, where they can be used as the components of masks, creams, and wraps. MDPI 2019-08-02 /pmc/articles/PMC6722771/ /pubmed/31382359 http://dx.doi.org/10.3390/pharmaceutics11080378 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Odrobińska, Justyna
Niesyto, Katarzyna
Erfurt, Karol
Siewniak, Agnieszka
Mielańczyk, Anna
Neugebauer, Dorota
Retinol-Containing Graft Copolymers for Delivery of Skin-Curing Agents
title Retinol-Containing Graft Copolymers for Delivery of Skin-Curing Agents
title_full Retinol-Containing Graft Copolymers for Delivery of Skin-Curing Agents
title_fullStr Retinol-Containing Graft Copolymers for Delivery of Skin-Curing Agents
title_full_unstemmed Retinol-Containing Graft Copolymers for Delivery of Skin-Curing Agents
title_short Retinol-Containing Graft Copolymers for Delivery of Skin-Curing Agents
title_sort retinol-containing graft copolymers for delivery of skin-curing agents
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6722771/
https://www.ncbi.nlm.nih.gov/pubmed/31382359
http://dx.doi.org/10.3390/pharmaceutics11080378
work_keys_str_mv AT odrobinskajustyna retinolcontaininggraftcopolymersfordeliveryofskincuringagents
AT niesytokatarzyna retinolcontaininggraftcopolymersfordeliveryofskincuringagents
AT erfurtkarol retinolcontaininggraftcopolymersfordeliveryofskincuringagents
AT siewniakagnieszka retinolcontaininggraftcopolymersfordeliveryofskincuringagents
AT mielanczykanna retinolcontaininggraftcopolymersfordeliveryofskincuringagents
AT neugebauerdorota retinolcontaininggraftcopolymersfordeliveryofskincuringagents