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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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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 |
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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 |
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