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In vitro blood cell viability profiling of polymers used in molecular assembly
Biocompatible polymers have been extensively applied to molecular assembly techniques on a micro- and nanoscale to miniaturize functional devices for biomedical uses. However, cytotoxic assessments of developed devices are prone to partially focus on non-specific cells or cells associated with the s...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5573391/ https://www.ncbi.nlm.nih.gov/pubmed/28842713 http://dx.doi.org/10.1038/s41598-017-10169-5 |
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author | Jeong, Hyejoong Hwang, Jangsun Lee, Hwankyu Hammond, Paula T. Choi, Jonghoon Hong, Jinkee |
author_facet | Jeong, Hyejoong Hwang, Jangsun Lee, Hwankyu Hammond, Paula T. Choi, Jonghoon Hong, Jinkee |
author_sort | Jeong, Hyejoong |
collection | PubMed |
description | Biocompatible polymers have been extensively applied to molecular assembly techniques on a micro- and nanoscale to miniaturize functional devices for biomedical uses. However, cytotoxic assessments of developed devices are prone to partially focus on non-specific cells or cells associated with the specific applications. Thereby, since toxicity is dependent on the type of cells and protocols, we do not fully understand the relative toxicities of polymers. Additionally, we need to ensure the blood cell biocompatibility of developed devices prior to that of targeted cells because most of the devices contact the blood before reaching the targeted regions. Motivated by this issue, we focused on screening cytotoxicity of polymers widely used for the layer-by-layer assembly technique using human blood cells. Cytotoxicity at the early stage was investigated on twenty types of polymers (positively charged, negatively charged, or neutral) and ten combination forms via hemolysis, cell viability, and AnnexinV-FITC/PI staining assays. We determined their effects on the cell membrane depending on their surface chemistry by molecular dynamics simulations. Furthermore, the toxicity of LbL-assembled nanofilms was assessed by measuring cell viability. Based on this report, researchers can produce nanofilms that are better suited for drug delivery and biomedical applications by reducing the possible cytotoxicity. |
format | Online Article Text |
id | pubmed-5573391 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55733912017-09-01 In vitro blood cell viability profiling of polymers used in molecular assembly Jeong, Hyejoong Hwang, Jangsun Lee, Hwankyu Hammond, Paula T. Choi, Jonghoon Hong, Jinkee Sci Rep Article Biocompatible polymers have been extensively applied to molecular assembly techniques on a micro- and nanoscale to miniaturize functional devices for biomedical uses. However, cytotoxic assessments of developed devices are prone to partially focus on non-specific cells or cells associated with the specific applications. Thereby, since toxicity is dependent on the type of cells and protocols, we do not fully understand the relative toxicities of polymers. Additionally, we need to ensure the blood cell biocompatibility of developed devices prior to that of targeted cells because most of the devices contact the blood before reaching the targeted regions. Motivated by this issue, we focused on screening cytotoxicity of polymers widely used for the layer-by-layer assembly technique using human blood cells. Cytotoxicity at the early stage was investigated on twenty types of polymers (positively charged, negatively charged, or neutral) and ten combination forms via hemolysis, cell viability, and AnnexinV-FITC/PI staining assays. We determined their effects on the cell membrane depending on their surface chemistry by molecular dynamics simulations. Furthermore, the toxicity of LbL-assembled nanofilms was assessed by measuring cell viability. Based on this report, researchers can produce nanofilms that are better suited for drug delivery and biomedical applications by reducing the possible cytotoxicity. Nature Publishing Group UK 2017-08-25 /pmc/articles/PMC5573391/ /pubmed/28842713 http://dx.doi.org/10.1038/s41598-017-10169-5 Text en © The Author(s) 2017 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Jeong, Hyejoong Hwang, Jangsun Lee, Hwankyu Hammond, Paula T. Choi, Jonghoon Hong, Jinkee In vitro blood cell viability profiling of polymers used in molecular assembly |
title | In vitro blood cell viability profiling of polymers used in molecular assembly |
title_full | In vitro blood cell viability profiling of polymers used in molecular assembly |
title_fullStr | In vitro blood cell viability profiling of polymers used in molecular assembly |
title_full_unstemmed | In vitro blood cell viability profiling of polymers used in molecular assembly |
title_short | In vitro blood cell viability profiling of polymers used in molecular assembly |
title_sort | in vitro blood cell viability profiling of polymers used in molecular assembly |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5573391/ https://www.ncbi.nlm.nih.gov/pubmed/28842713 http://dx.doi.org/10.1038/s41598-017-10169-5 |
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