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Solvent-Free Fabrication of Biphasic Lipid-Based Microparticles with Tunable Structure

Lipid-based biphasic microparticles are generally produced by long and complex techniques based on double emulsions. In this study, spray congealing was used as a solvent-free fabrication method with improved processability to transform water-in-oil non-aqueous emulsions into spherical solid lipid-b...

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Autores principales: Bertoni, Serena, Albertini, Beatrice, Ronowicz-Pilarczyk, Joanna, Calonghi, Natalia, Passerini, Nadia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8780016/
https://www.ncbi.nlm.nih.gov/pubmed/35056953
http://dx.doi.org/10.3390/pharmaceutics14010054
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author Bertoni, Serena
Albertini, Beatrice
Ronowicz-Pilarczyk, Joanna
Calonghi, Natalia
Passerini, Nadia
author_facet Bertoni, Serena
Albertini, Beatrice
Ronowicz-Pilarczyk, Joanna
Calonghi, Natalia
Passerini, Nadia
author_sort Bertoni, Serena
collection PubMed
description Lipid-based biphasic microparticles are generally produced by long and complex techniques based on double emulsions. In this study, spray congealing was used as a solvent-free fabrication method with improved processability to transform water-in-oil non-aqueous emulsions into spherical solid lipid-based particles with a biphasic structure (b-MPs). Emulsions were prepared by melt emulsification using different compositions of lipids (Dynasan(®)118 and Compritol(®)888 ATO), surfactants (Cetylstearyl alcohol and Span(®)60) and hydrophilic carriers (PEGs, Gelucire(®)48/16 and Poloxamer 188). First, pseudo-ternary phase diagrams were constructed to identify the area corresponding to each emulsion type (coarse emulsion or microemulsion). The hydrophobicity of the lipid mostly affected the interfacial tension, and thus the microstructure of the emulsion. Emulsions were then processed by spray congealing and the obtained b-MPs were characterized in terms of thermal and chemical properties (by DSC and FT-IR), external and internal morphology (by SEM, CLSM and Raman mapping). Solid free-flowing spherical particles (main size range 200–355 µm) with different architectures were successfully produced: microemulsions led to the formation of particles with a homogeneous internal structure, while coarse emulsions generated “multicores-shell” particles consisting of variable size hydrophilic cores evenly distributed within the crystalline lipid phase. Depending on their composition and structure, b-MPs could achieve various release profiles, representing a more versatile system than microparticles based on a single lipid phase. The formulation and technological strategy proposed, provides a feasible and cost-effective way of fabricating b-MPs with tunable internal structure and release behavior.
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spelling pubmed-87800162022-01-22 Solvent-Free Fabrication of Biphasic Lipid-Based Microparticles with Tunable Structure Bertoni, Serena Albertini, Beatrice Ronowicz-Pilarczyk, Joanna Calonghi, Natalia Passerini, Nadia Pharmaceutics Article Lipid-based biphasic microparticles are generally produced by long and complex techniques based on double emulsions. In this study, spray congealing was used as a solvent-free fabrication method with improved processability to transform water-in-oil non-aqueous emulsions into spherical solid lipid-based particles with a biphasic structure (b-MPs). Emulsions were prepared by melt emulsification using different compositions of lipids (Dynasan(®)118 and Compritol(®)888 ATO), surfactants (Cetylstearyl alcohol and Span(®)60) and hydrophilic carriers (PEGs, Gelucire(®)48/16 and Poloxamer 188). First, pseudo-ternary phase diagrams were constructed to identify the area corresponding to each emulsion type (coarse emulsion or microemulsion). The hydrophobicity of the lipid mostly affected the interfacial tension, and thus the microstructure of the emulsion. Emulsions were then processed by spray congealing and the obtained b-MPs were characterized in terms of thermal and chemical properties (by DSC and FT-IR), external and internal morphology (by SEM, CLSM and Raman mapping). Solid free-flowing spherical particles (main size range 200–355 µm) with different architectures were successfully produced: microemulsions led to the formation of particles with a homogeneous internal structure, while coarse emulsions generated “multicores-shell” particles consisting of variable size hydrophilic cores evenly distributed within the crystalline lipid phase. Depending on their composition and structure, b-MPs could achieve various release profiles, representing a more versatile system than microparticles based on a single lipid phase. The formulation and technological strategy proposed, provides a feasible and cost-effective way of fabricating b-MPs with tunable internal structure and release behavior. MDPI 2021-12-27 /pmc/articles/PMC8780016/ /pubmed/35056953 http://dx.doi.org/10.3390/pharmaceutics14010054 Text en © 2021 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
Bertoni, Serena
Albertini, Beatrice
Ronowicz-Pilarczyk, Joanna
Calonghi, Natalia
Passerini, Nadia
Solvent-Free Fabrication of Biphasic Lipid-Based Microparticles with Tunable Structure
title Solvent-Free Fabrication of Biphasic Lipid-Based Microparticles with Tunable Structure
title_full Solvent-Free Fabrication of Biphasic Lipid-Based Microparticles with Tunable Structure
title_fullStr Solvent-Free Fabrication of Biphasic Lipid-Based Microparticles with Tunable Structure
title_full_unstemmed Solvent-Free Fabrication of Biphasic Lipid-Based Microparticles with Tunable Structure
title_short Solvent-Free Fabrication of Biphasic Lipid-Based Microparticles with Tunable Structure
title_sort solvent-free fabrication of biphasic lipid-based microparticles with tunable structure
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8780016/
https://www.ncbi.nlm.nih.gov/pubmed/35056953
http://dx.doi.org/10.3390/pharmaceutics14010054
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