Cargando…

Development of lipid nanoparticles and liposomes reference materials (II): cytotoxic profiles

Lipid based nanocarriers are one of the most effective drug delivery systems that is evident from the recent COVID-19 mRNA vaccines. The main objective of this study was to evaluate toxicity of six lipid based formulations with three surface charges—anionic, neutral or cationic, to establish certifi...

Descripción completa

Detalles Bibliográficos
Autores principales: Syama, Krishnapriya, Jakubek, Zygmunt J., Chen, Sam, Zaifman, Josh, Tam, Yuen Yi C., Zou, Shan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9610362/
https://www.ncbi.nlm.nih.gov/pubmed/36302886
http://dx.doi.org/10.1038/s41598-022-23013-2
_version_ 1784819250390630400
author Syama, Krishnapriya
Jakubek, Zygmunt J.
Chen, Sam
Zaifman, Josh
Tam, Yuen Yi C.
Zou, Shan
author_facet Syama, Krishnapriya
Jakubek, Zygmunt J.
Chen, Sam
Zaifman, Josh
Tam, Yuen Yi C.
Zou, Shan
author_sort Syama, Krishnapriya
collection PubMed
description Lipid based nanocarriers are one of the most effective drug delivery systems that is evident from the recent COVID-19 mRNA vaccines. The main objective of this study was to evaluate toxicity of six lipid based formulations with three surface charges—anionic, neutral or cationic, to establish certified reference materials (CRMs) for liposomes and siRNA loaded lipid nanoparticles (LNP-siRNA). Cytotoxicity was assessed by a proliferation assay in adherent and non-adherent cell lines. High concentration of three LNP-siRNAs did not affect viability of suspension cells and LNP-siRNAs were non-toxic to adherent cells at conventionally used concentration. Systematic evaluation using multiple vials and repeated test runs of three liposomes and three LNP-siRNA formulations showed no toxicity in HL60 and A549 cells up to 128 and 16 µg/mL, respectively. Extended treatment and low concentration of LNPs did not affect the viability of suspension cells and adherent cells at 96 h. Interestingly, 80% of A549 and HL60 cells in 3D conditions were viable when treated with cationic LNP-siRNA for 48 h. Taken together, anionic, cationic and neutral lipid formulations were non-toxic to cells and may be explored further in order to develop them as drug carriers.
format Online
Article
Text
id pubmed-9610362
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-96103622022-10-28 Development of lipid nanoparticles and liposomes reference materials (II): cytotoxic profiles Syama, Krishnapriya Jakubek, Zygmunt J. Chen, Sam Zaifman, Josh Tam, Yuen Yi C. Zou, Shan Sci Rep Article Lipid based nanocarriers are one of the most effective drug delivery systems that is evident from the recent COVID-19 mRNA vaccines. The main objective of this study was to evaluate toxicity of six lipid based formulations with three surface charges—anionic, neutral or cationic, to establish certified reference materials (CRMs) for liposomes and siRNA loaded lipid nanoparticles (LNP-siRNA). Cytotoxicity was assessed by a proliferation assay in adherent and non-adherent cell lines. High concentration of three LNP-siRNAs did not affect viability of suspension cells and LNP-siRNAs were non-toxic to adherent cells at conventionally used concentration. Systematic evaluation using multiple vials and repeated test runs of three liposomes and three LNP-siRNA formulations showed no toxicity in HL60 and A549 cells up to 128 and 16 µg/mL, respectively. Extended treatment and low concentration of LNPs did not affect the viability of suspension cells and adherent cells at 96 h. Interestingly, 80% of A549 and HL60 cells in 3D conditions were viable when treated with cationic LNP-siRNA for 48 h. Taken together, anionic, cationic and neutral lipid formulations were non-toxic to cells and may be explored further in order to develop them as drug carriers. Nature Publishing Group UK 2022-10-27 /pmc/articles/PMC9610362/ /pubmed/36302886 http://dx.doi.org/10.1038/s41598-022-23013-2 Text en © Crown 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Syama, Krishnapriya
Jakubek, Zygmunt J.
Chen, Sam
Zaifman, Josh
Tam, Yuen Yi C.
Zou, Shan
Development of lipid nanoparticles and liposomes reference materials (II): cytotoxic profiles
title Development of lipid nanoparticles and liposomes reference materials (II): cytotoxic profiles
title_full Development of lipid nanoparticles and liposomes reference materials (II): cytotoxic profiles
title_fullStr Development of lipid nanoparticles and liposomes reference materials (II): cytotoxic profiles
title_full_unstemmed Development of lipid nanoparticles and liposomes reference materials (II): cytotoxic profiles
title_short Development of lipid nanoparticles and liposomes reference materials (II): cytotoxic profiles
title_sort development of lipid nanoparticles and liposomes reference materials (ii): cytotoxic profiles
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9610362/
https://www.ncbi.nlm.nih.gov/pubmed/36302886
http://dx.doi.org/10.1038/s41598-022-23013-2
work_keys_str_mv AT syamakrishnapriya developmentoflipidnanoparticlesandliposomesreferencematerialsiicytotoxicprofiles
AT jakubekzygmuntj developmentoflipidnanoparticlesandliposomesreferencematerialsiicytotoxicprofiles
AT chensam developmentoflipidnanoparticlesandliposomesreferencematerialsiicytotoxicprofiles
AT zaifmanjosh developmentoflipidnanoparticlesandliposomesreferencematerialsiicytotoxicprofiles
AT tamyuenyic developmentoflipidnanoparticlesandliposomesreferencematerialsiicytotoxicprofiles
AT zoushan developmentoflipidnanoparticlesandliposomesreferencematerialsiicytotoxicprofiles