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Salicylic Acid Co-Precipitation with Alginate via Supercritical Atomization for Cosmetic Applications

Alginate-based microparticles were produced via supercritical assisted atomization (SAA) with the aim of obtaining a biocompatible and low-cost carrier for the delivery of active compounds in cosmetic applications. Salicylic acid was selected as an active model compound, and it was co-precipitated w...

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Autores principales: Baldino, Lucia, Reverchon, Ernesto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9654882/
https://www.ncbi.nlm.nih.gov/pubmed/36363226
http://dx.doi.org/10.3390/ma15217634
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author Baldino, Lucia
Reverchon, Ernesto
author_facet Baldino, Lucia
Reverchon, Ernesto
author_sort Baldino, Lucia
collection PubMed
description Alginate-based microparticles were produced via supercritical assisted atomization (SAA) with the aim of obtaining a biocompatible and low-cost carrier for the delivery of active compounds in cosmetic applications. Salicylic acid was selected as an active model compound, and it was co-precipitated with alginate via SAA, operating at 82 bar and 80 °C. In particular, the drug-to-polymer weight ratio was fixed at 1/4, whereas polymer concentration was varied from 5 to 20 mg/mL in the starting aqueous solution. Operating in this way, alginate-salicylic acid microparticles were characterized by a mean diameter of 0.72 ± 0.25 µm, and the active compound became amorphous after processing. A salicylic acid encapsulation efficiency close to 100% was reached, and the drug release time from the biopolymeric microparticles was prolonged up to nine times with respect to untreated salicylic acid powder.
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spelling pubmed-96548822022-11-15 Salicylic Acid Co-Precipitation with Alginate via Supercritical Atomization for Cosmetic Applications Baldino, Lucia Reverchon, Ernesto Materials (Basel) Article Alginate-based microparticles were produced via supercritical assisted atomization (SAA) with the aim of obtaining a biocompatible and low-cost carrier for the delivery of active compounds in cosmetic applications. Salicylic acid was selected as an active model compound, and it was co-precipitated with alginate via SAA, operating at 82 bar and 80 °C. In particular, the drug-to-polymer weight ratio was fixed at 1/4, whereas polymer concentration was varied from 5 to 20 mg/mL in the starting aqueous solution. Operating in this way, alginate-salicylic acid microparticles were characterized by a mean diameter of 0.72 ± 0.25 µm, and the active compound became amorphous after processing. A salicylic acid encapsulation efficiency close to 100% was reached, and the drug release time from the biopolymeric microparticles was prolonged up to nine times with respect to untreated salicylic acid powder. MDPI 2022-10-30 /pmc/articles/PMC9654882/ /pubmed/36363226 http://dx.doi.org/10.3390/ma15217634 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Baldino, Lucia
Reverchon, Ernesto
Salicylic Acid Co-Precipitation with Alginate via Supercritical Atomization for Cosmetic Applications
title Salicylic Acid Co-Precipitation with Alginate via Supercritical Atomization for Cosmetic Applications
title_full Salicylic Acid Co-Precipitation with Alginate via Supercritical Atomization for Cosmetic Applications
title_fullStr Salicylic Acid Co-Precipitation with Alginate via Supercritical Atomization for Cosmetic Applications
title_full_unstemmed Salicylic Acid Co-Precipitation with Alginate via Supercritical Atomization for Cosmetic Applications
title_short Salicylic Acid Co-Precipitation with Alginate via Supercritical Atomization for Cosmetic Applications
title_sort salicylic acid co-precipitation with alginate via supercritical atomization for cosmetic applications
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9654882/
https://www.ncbi.nlm.nih.gov/pubmed/36363226
http://dx.doi.org/10.3390/ma15217634
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