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Progressing Towards the Sustainable Development of Cream Formulations

This work aims at providing the assumptions to assist the sustainable development of cream formulations. Specifically, it envisions to rationalize and predict the effect of formulation and process variability on a 1% hydrocortisone cream quality profile, interplaying microstructure properties with p...

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Detalles Bibliográficos
Autores principales: Simões, Ana, Veiga, Francisco, Vitorino, Carla
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7407566/
https://www.ncbi.nlm.nih.gov/pubmed/32659962
http://dx.doi.org/10.3390/pharmaceutics12070647
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author Simões, Ana
Veiga, Francisco
Vitorino, Carla
author_facet Simões, Ana
Veiga, Francisco
Vitorino, Carla
author_sort Simões, Ana
collection PubMed
description This work aims at providing the assumptions to assist the sustainable development of cream formulations. Specifically, it envisions to rationalize and predict the effect of formulation and process variability on a 1% hydrocortisone cream quality profile, interplaying microstructure properties with product performance and stability. This tripartite analysis was supported by a Quality by Design approach, considering a three-factor, three-level Box-Behnken design. Critical material attributes and process parameters were identified from a failure mode, effects, and criticality analysis. The impact of glycerol monostearate amount, isopropyl myristate amount, and homogenization rate on relevant quality attributes was estimated crosswise. The significant variability in product droplet size, viscosity, thixotropic behavior, and viscoelastic properties demonstrated a noteworthy influence on hydrocortisone release profile (112 ± 2–196 ± 7 μg/cm(2)/√h) and permeation behavior (0.16 ± 0.03–0.97 ± 0.08 μg/cm(2)/h), and on the assay, instability index and creaming rate, with values ranging from 81.9 to 120.5%, 0.031 ± 0.012 to 0.28 ± 0.13 and from 0.009 ± 0.000 to 0.38 ± 0.07 μm/s, respectively. The release patterns were not straightforwardly correlated with the permeation behavior. Monitoring the microstructural parameters, through the balanced adjustment of formulation and process variables, is herein highlighted as the key enabler to predict cream performance and stability. Finally, based on quality targets and response constraints, optimal working conditions were successfully attained through the establishment of a design space.
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spelling pubmed-74075662020-08-25 Progressing Towards the Sustainable Development of Cream Formulations Simões, Ana Veiga, Francisco Vitorino, Carla Pharmaceutics Article This work aims at providing the assumptions to assist the sustainable development of cream formulations. Specifically, it envisions to rationalize and predict the effect of formulation and process variability on a 1% hydrocortisone cream quality profile, interplaying microstructure properties with product performance and stability. This tripartite analysis was supported by a Quality by Design approach, considering a three-factor, three-level Box-Behnken design. Critical material attributes and process parameters were identified from a failure mode, effects, and criticality analysis. The impact of glycerol monostearate amount, isopropyl myristate amount, and homogenization rate on relevant quality attributes was estimated crosswise. The significant variability in product droplet size, viscosity, thixotropic behavior, and viscoelastic properties demonstrated a noteworthy influence on hydrocortisone release profile (112 ± 2–196 ± 7 μg/cm(2)/√h) and permeation behavior (0.16 ± 0.03–0.97 ± 0.08 μg/cm(2)/h), and on the assay, instability index and creaming rate, with values ranging from 81.9 to 120.5%, 0.031 ± 0.012 to 0.28 ± 0.13 and from 0.009 ± 0.000 to 0.38 ± 0.07 μm/s, respectively. The release patterns were not straightforwardly correlated with the permeation behavior. Monitoring the microstructural parameters, through the balanced adjustment of formulation and process variables, is herein highlighted as the key enabler to predict cream performance and stability. Finally, based on quality targets and response constraints, optimal working conditions were successfully attained through the establishment of a design space. MDPI 2020-07-09 /pmc/articles/PMC7407566/ /pubmed/32659962 http://dx.doi.org/10.3390/pharmaceutics12070647 Text en © 2020 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
Simões, Ana
Veiga, Francisco
Vitorino, Carla
Progressing Towards the Sustainable Development of Cream Formulations
title Progressing Towards the Sustainable Development of Cream Formulations
title_full Progressing Towards the Sustainable Development of Cream Formulations
title_fullStr Progressing Towards the Sustainable Development of Cream Formulations
title_full_unstemmed Progressing Towards the Sustainable Development of Cream Formulations
title_short Progressing Towards the Sustainable Development of Cream Formulations
title_sort progressing towards the sustainable development of cream formulations
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7407566/
https://www.ncbi.nlm.nih.gov/pubmed/32659962
http://dx.doi.org/10.3390/pharmaceutics12070647
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