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Effect of Composition and Size on Surface Properties of Anti-Cancer Nanoparticles
Liposomal formulations offer significant advantages as anticancer drug carriers for targeted drug delivery; however, due to their complexity, clinical translation has been challenging. In addition, liposomal product manufacturing has been interrupted in the past, as was the case for Doxil(®) (doxoru...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10487715/ https://www.ncbi.nlm.nih.gov/pubmed/37686222 http://dx.doi.org/10.3390/ijms241713417 |
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author | Mishra, Ina Garrett, Meredith Curry, Stephen Jameson, Jeffrey Kastellorizios, Michail |
author_facet | Mishra, Ina Garrett, Meredith Curry, Stephen Jameson, Jeffrey Kastellorizios, Michail |
author_sort | Mishra, Ina |
collection | PubMed |
description | Liposomal formulations offer significant advantages as anticancer drug carriers for targeted drug delivery; however, due to their complexity, clinical translation has been challenging. In addition, liposomal product manufacturing has been interrupted in the past, as was the case for Doxil(®) (doxorubicin hydrochloride liposome injection). Here, interfacial tension (IFT) measurements were investigated as a potential physicochemical characterization tool to aid in liposomal product characterization during development and manufacturing. A pendant drop method using an optical tensiometer was used to measure the interfacial tension of various analogues of Doxil(®) liposomal suspensions in air and in dodecane. The effect of liposome concentration, formulation (PEG and cholesterol content), presence of encapsulated drug, as well as average particle size was analyzed. It was observed that Doxil(®) analog liposomes demonstrate surfactant-like behavior with a sigmoidal-shape interfacial tension vs. concentration curve. This behavior was heavily dependent on PEG content, with a complete loss of surfactant-like behavior when PEG was removed from the formulation. In addition to interfacial tension, three data analyses were identified as able to distinguish between formulations with variations in PEG, cholesterol, and particle size: (i) polar and non-polar contribution to interfacial tension, (ii) liposomal concentration at which the polar and non-polar components were equal, and (iii) rate of interfacial tension decay after droplet formation, which is indicative of how quickly liposomes migrate from the bulk of the solution to the surface. We demonstrate for the first time that interfacial tension can be used to detect certain liposomal formulation changes, such as PEG content, encapsulated drug presence, and size variability, and may make a useful addition to physicochemical characterization during development and manufacturing of liposomal products. |
format | Online Article Text |
id | pubmed-10487715 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-104877152023-09-09 Effect of Composition and Size on Surface Properties of Anti-Cancer Nanoparticles Mishra, Ina Garrett, Meredith Curry, Stephen Jameson, Jeffrey Kastellorizios, Michail Int J Mol Sci Article Liposomal formulations offer significant advantages as anticancer drug carriers for targeted drug delivery; however, due to their complexity, clinical translation has been challenging. In addition, liposomal product manufacturing has been interrupted in the past, as was the case for Doxil(®) (doxorubicin hydrochloride liposome injection). Here, interfacial tension (IFT) measurements were investigated as a potential physicochemical characterization tool to aid in liposomal product characterization during development and manufacturing. A pendant drop method using an optical tensiometer was used to measure the interfacial tension of various analogues of Doxil(®) liposomal suspensions in air and in dodecane. The effect of liposome concentration, formulation (PEG and cholesterol content), presence of encapsulated drug, as well as average particle size was analyzed. It was observed that Doxil(®) analog liposomes demonstrate surfactant-like behavior with a sigmoidal-shape interfacial tension vs. concentration curve. This behavior was heavily dependent on PEG content, with a complete loss of surfactant-like behavior when PEG was removed from the formulation. In addition to interfacial tension, three data analyses were identified as able to distinguish between formulations with variations in PEG, cholesterol, and particle size: (i) polar and non-polar contribution to interfacial tension, (ii) liposomal concentration at which the polar and non-polar components were equal, and (iii) rate of interfacial tension decay after droplet formation, which is indicative of how quickly liposomes migrate from the bulk of the solution to the surface. We demonstrate for the first time that interfacial tension can be used to detect certain liposomal formulation changes, such as PEG content, encapsulated drug presence, and size variability, and may make a useful addition to physicochemical characterization during development and manufacturing of liposomal products. MDPI 2023-08-30 /pmc/articles/PMC10487715/ /pubmed/37686222 http://dx.doi.org/10.3390/ijms241713417 Text en © 2023 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 Mishra, Ina Garrett, Meredith Curry, Stephen Jameson, Jeffrey Kastellorizios, Michail Effect of Composition and Size on Surface Properties of Anti-Cancer Nanoparticles |
title | Effect of Composition and Size on Surface Properties of Anti-Cancer Nanoparticles |
title_full | Effect of Composition and Size on Surface Properties of Anti-Cancer Nanoparticles |
title_fullStr | Effect of Composition and Size on Surface Properties of Anti-Cancer Nanoparticles |
title_full_unstemmed | Effect of Composition and Size on Surface Properties of Anti-Cancer Nanoparticles |
title_short | Effect of Composition and Size on Surface Properties of Anti-Cancer Nanoparticles |
title_sort | effect of composition and size on surface properties of anti-cancer nanoparticles |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10487715/ https://www.ncbi.nlm.nih.gov/pubmed/37686222 http://dx.doi.org/10.3390/ijms241713417 |
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