Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Mishra, Ina, Garrett, Meredith, Curry, Stephen, Jameson, Jeffrey, Kastellorizios, Michail
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
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
_version_ 1785103306427727872
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
work_keys_str_mv AT mishraina effectofcompositionandsizeonsurfacepropertiesofanticancernanoparticles
AT garrettmeredith effectofcompositionandsizeonsurfacepropertiesofanticancernanoparticles
AT currystephen effectofcompositionandsizeonsurfacepropertiesofanticancernanoparticles
AT jamesonjeffrey effectofcompositionandsizeonsurfacepropertiesofanticancernanoparticles
AT kastelloriziosmichail effectofcompositionandsizeonsurfacepropertiesofanticancernanoparticles