4.7 Article

In vitro blood cell viability profiling of polymers used in molecular assembly

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SCIENTIFIC REPORTS
卷 7, 期 -, 页码 -

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NATURE PUBLISHING GROUP
DOI: 10.1038/s41598-017-10169-5

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资金

  1. Bio & Medical Technology Development Program of the National Research Foundation of Korea (NRF) - Korean Government [2012M3A9C6050104, 2016M3A9C6917405, 2017R1D1A1A09000510]
  2. Basic Science Research Program of the National Research Foundation of Korea (NRF) - Korean Government [2012M3A9C6050104, 2016M3A9C6917405, 2017R1D1A1A09000510]
  3. Korea Health Technology R&D Project through the Korea Health Industry Development Institute (KHIDI) - Ministry of Health & Welfare, Republic of Korea [HI14C-3266, HI15C-1653]
  4. Korea Health Promotion Institute [HI15C1653020017, HI14C3266030017] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
  5. National Research Foundation of Korea [2016M3A9C6917402, 2017R1D1A1A09000510, 2012M3A9C6050104] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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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 Annexin VFITC/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.

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