Assessing Lipid Nanoparticle Protein Corona Formation and Cytocompatibility

Lipid nanoparticles(LNPs) represent an emerging new modality for mRNA delivery. Following administration and interaction with blood constituents, LNPs form a corona complex consisting of proteins adsorbed on the surface altering their stability, biological identity, and fate. Cytocompatibility of th...

Full description

Bibliographic Details
Main Authors: Rand Abdulrahman, Huda Ibrahem, Amna Mahmood, Kevin Edward Treacher, Robin Bruno Capomaccio, Catherine Vasey, Yvonne Perrie, Zahra Rattray
Format: Article
Language:English
Published: University of Huddersfield Press 2023-12-01
Series:British Journal of Pharmacy
Subjects:
Online Access:https://www.bjpharm.org.uk/article/1398/galley/1030/view/
_version_ 1827380684800393216
author Rand Abdulrahman
Huda Ibrahem
Amna Mahmood
Kevin Edward Treacher
Robin Bruno Capomaccio
Catherine Vasey
Yvonne Perrie
Zahra Rattray
author_facet Rand Abdulrahman
Huda Ibrahem
Amna Mahmood
Kevin Edward Treacher
Robin Bruno Capomaccio
Catherine Vasey
Yvonne Perrie
Zahra Rattray
author_sort Rand Abdulrahman
collection DOAJ
description Lipid nanoparticles(LNPs) represent an emerging new modality for mRNA delivery. Following administration and interaction with blood constituents, LNPs form a corona complex consisting of proteins adsorbed on the surface altering their stability, biological identity, and fate. Cytocompatibility of the LNPs is an important factor when considering their safety efficacy in delivering the encapsulated drug dose, lipid choice and the specific target cells. The aim of this study was to investigate the changes in LNP physical parameters in physiologically-relevant media. Key attributes such as particle size, polydispersity index and zeta-potential were measured using Dynamic Light Scattering (DLS) and Nanoparticle Tracking Analysis (NTA). Cytocompatibility was assessed via CellTiter-Glo® assay. Following 24-hour incubation of LNPs with Bovine Serum Albumin (BSA), the LNP z-average increased from 92.4 (± 49.0) nm to 131.4 (± 64.9) nm indicating interaction between LNPs and BSA. A decrease in percentage cell viability was demonstrated with increased lipid concentration for MCF-7 and A549 cell lines. This work shows changes in LNP physicochemical properties in the presence of protein and biologically relevant conditions consistent with protein surface adsorption. The cytocompatibility of LNPs can be associated with the type of lipids used in the synthesis of LNPs.
first_indexed 2024-03-08T13:37:35Z
format Article
id doaj.art-9f3ab08241654b64a92d9deea72d6112
institution Directory Open Access Journal
issn 2058-8356
language English
last_indexed 2024-03-08T13:37:35Z
publishDate 2023-12-01
publisher University of Huddersfield Press
record_format Article
series British Journal of Pharmacy
spelling doaj.art-9f3ab08241654b64a92d9deea72d61122024-01-16T15:17:54ZengUniversity of Huddersfield PressBritish Journal of Pharmacy2058-83562023-12-018210.5920/bjpharm.1398Assessing Lipid Nanoparticle Protein Corona Formation and CytocompatibilityRand AbdulrahmanHuda Ibrahem 0Amna Mahmood 1Kevin Edward Treacher2https://orcid.org/0000-0002-8705-3476Robin Bruno Capomaccio3Catherine Vasey4Yvonne Perrie5Zahra Rattray6University of StrathclydeUniversity of StrathclydeAstraZenecaAstraZenecaUniversity of NottinghamUniversity of StrathclydeUniversity of StrathclydeLipid nanoparticles(LNPs) represent an emerging new modality for mRNA delivery. Following administration and interaction with blood constituents, LNPs form a corona complex consisting of proteins adsorbed on the surface altering their stability, biological identity, and fate. Cytocompatibility of the LNPs is an important factor when considering their safety efficacy in delivering the encapsulated drug dose, lipid choice and the specific target cells. The aim of this study was to investigate the changes in LNP physical parameters in physiologically-relevant media. Key attributes such as particle size, polydispersity index and zeta-potential were measured using Dynamic Light Scattering (DLS) and Nanoparticle Tracking Analysis (NTA). Cytocompatibility was assessed via CellTiter-Glo® assay. Following 24-hour incubation of LNPs with Bovine Serum Albumin (BSA), the LNP z-average increased from 92.4 (± 49.0) nm to 131.4 (± 64.9) nm indicating interaction between LNPs and BSA. A decrease in percentage cell viability was demonstrated with increased lipid concentration for MCF-7 and A549 cell lines. This work shows changes in LNP physicochemical properties in the presence of protein and biologically relevant conditions consistent with protein surface adsorption. The cytocompatibility of LNPs can be associated with the type of lipids used in the synthesis of LNPs.https://www.bjpharm.org.uk/article/1398/galley/1030/view/lipid nanoparticlesanalysisprotein coronacytocompatibility
spellingShingle Rand Abdulrahman
Huda Ibrahem
Amna Mahmood
Kevin Edward Treacher
Robin Bruno Capomaccio
Catherine Vasey
Yvonne Perrie
Zahra Rattray
Assessing Lipid Nanoparticle Protein Corona Formation and Cytocompatibility
British Journal of Pharmacy
lipid nanoparticles
analysis
protein corona
cytocompatibility
title Assessing Lipid Nanoparticle Protein Corona Formation and Cytocompatibility
title_full Assessing Lipid Nanoparticle Protein Corona Formation and Cytocompatibility
title_fullStr Assessing Lipid Nanoparticle Protein Corona Formation and Cytocompatibility
title_full_unstemmed Assessing Lipid Nanoparticle Protein Corona Formation and Cytocompatibility
title_short Assessing Lipid Nanoparticle Protein Corona Formation and Cytocompatibility
title_sort assessing lipid nanoparticle protein corona formation and cytocompatibility
topic lipid nanoparticles
analysis
protein corona
cytocompatibility
url https://www.bjpharm.org.uk/article/1398/galley/1030/view/
work_keys_str_mv AT randabdulrahman assessinglipidnanoparticleproteincoronaformationandcytocompatibility
AT hudaibrahem assessinglipidnanoparticleproteincoronaformationandcytocompatibility
AT amnamahmood assessinglipidnanoparticleproteincoronaformationandcytocompatibility
AT kevinedwardtreacher assessinglipidnanoparticleproteincoronaformationandcytocompatibility
AT robinbrunocapomaccio assessinglipidnanoparticleproteincoronaformationandcytocompatibility
AT catherinevasey assessinglipidnanoparticleproteincoronaformationandcytocompatibility
AT yvonneperrie assessinglipidnanoparticleproteincoronaformationandcytocompatibility
AT zahrarattray assessinglipidnanoparticleproteincoronaformationandcytocompatibility