Literature DB >> 28334507

Comparative study of cytotoxicity and genotoxicity of commercial Jeffamines® and polyethylenimine in CHO-K1 cells.

Leniher Castan1, Cristiano José da Silva1, Eduardo Ferreira Molina1, Raquel Alves Dos Santos1.   

Abstract

Jeffamines® are a family of polymers containing primary amine groups attached to the extremities of polyether backbone which can be used as biomaterials. They have been used in combination with polyethylenimine (PEI) to improve biocompatibility in drug and gene delivery systems. Despite these facts, very few studies have been done on cytotoxicity and genotoxicity of pure Jeffamines® or compared with PEI. The present study aimed to evaluate and compare the cytotoxic and genotoxic effects of Jeffamines® and PEI in CHO-K1 cells. Specifically, polypropylene oxide 2000 (PPO 2000, Jeffamine® D series), polyethylene oxide 1900 (PEO 1900, Jeffamine® ED series), branched 25 kDa PEI, and linear 20 kDa PEI were evaluated at different concentrations. Cell viability and proliferation were assessed by 2,3-bis-(2-methoxy-4-nitro-5-sulfophenyl)-2H-tetrazolium-5-carboxanilide (XTT) and 5-bromo-2'-deoxyuridine (BrdU) assays, respectively. Genotoxicity was evaluated using single cell gel electrophoresis assay and the cytokinesis-blocked micronucleus assay. PPO 2000 was the most cytotoxic Jeffamine® , whereas PEO 1900 did not caused significant cell death at any tested concentration. Branched PEI was more cytotoxic than linear PEI (LPEI) and both were more cytotoxic than Jeffamines® . Only PPO 2000 induced DNA damage when evaluated in comet assay probably due to its cytotoxicity. PPO 2000, PEO 1900, and PEI did not increase the frequency of micronuclei when tested at sub-cytotoxic concentrations. This work provides new insights about biocompatibility of Jeffamines® and PEI and suggests the genotoxicological safety for further investigations of PEO 1900 in drug and gene delivery systems.
© 2017 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater, 106B: 742-750, 2018. © 2017 Wiley Periodicals, Inc.

Entities:  

Keywords:  biocompatibility; cationic polymers; cytotoxicity; genotoxicity; non-viral vectors

Mesh:

Substances:

Year:  2017        PMID: 28334507     DOI: 10.1002/jbm.b.33882

Source DB:  PubMed          Journal:  J Biomed Mater Res B Appl Biomater        ISSN: 1552-4973            Impact factor:   3.368


  4 in total

1.  Polymeric Nanoparticles Based on Tyrosine-Modified, Low Molecular Weight Polyethylenimines for siRNA Delivery.

Authors:  Alexander Ewe; Sandra Noske; Michael Karimov; Achim Aigner
Journal:  Pharmaceutics       Date:  2019-11-12       Impact factor: 6.321

2.  Targeting Human Osteoarthritic Chondrocytes with Ligand Directed Bacteriophage-Based Particles.

Authors:  Aitthiphon Chongchai; Sajee Waramit; Tunchanok Wongwichai; Jirawan Kampangtip; Thanyaluck Phitak; Prachya Kongtawelert; Amin Hajitou; Keittisak Suwan; Peraphan Pothacharoen
Journal:  Viruses       Date:  2021-11-23       Impact factor: 5.048

3.  Strategies for accelerating osteogenesis through nanoparticle-based DNA/mitochondrial damage repair.

Authors:  Hye Jin Kim; Hui Bang Cho; Sujin Lee; Jiyon Lyu; Hye-Ryoung Kim; Sujeong Lee; Ji-In Park; Keun-Hong Park
Journal:  Theranostics       Date:  2022-08-29       Impact factor: 11.600

4.  Shaping Rolling Circle Amplification Products into DNA Nanoparticles by Incorporation of Modified Nucleotides and Their Application to In Vitro and In Vivo Delivery of a Photosensitizer.

Authors:  Kyoung-Ran Kim; Pascal Röthlisberger; Seong Jae Kang; Kihwan Nam; Sangyoup Lee; Marcel Hollenstein; Dae-Ro Ahn
Journal:  Molecules       Date:  2018-07-23       Impact factor: 4.411

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.