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

Hyejoong Jeong, Jangsun Hwang, Hwankyu Lee, Paula T. Hammond, Jonghoon Choi, Jinkee Hong

Research output: Contribution to journalArticlepeer-review

38 Citations (Scopus)

Abstract

Biocompatible polymers have been extensively applied to molecular assembly techniques on a micro- A nd 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.

Original languageEnglish
Article number9481
JournalScientific reports
Volume7
Issue number1
DOIs
Publication statusPublished - 2017 Dec 1

Bibliographical note

Funding Information:
This research was supported by the Bio & Medical Technology Development Program and Basic Science Research Program of the National Research Foundation of Korea (NRF), funded by the Korean Government (Grants 2012M3A9C6050104 & 2016M3A9C6917405 & 2017R1D1A1A09000510). Additionally, this research was supported by a grant of the Korea Health Technology R&D Project through the Korea Health Industry Development Institute (KHIDI), funded by the Ministry of Health & Welfare, Republic of Korea (Grant HI14C-3266, HI15C-1653).

All Science Journal Classification (ASJC) codes

  • General

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