4.7 Article

A comprehensive assessment of the biocompatibility of Magnetospirillum gryphiswaldense MSR-1 bacterial magnetosomes in vitro and in vivo

期刊

TOXICOLOGY
卷 462, 期 -, 页码 -

出版社

ELSEVIER IRELAND LTD
DOI: 10.1016/j.tox.2021.152949

关键词

bacterial magnetosomes (BMs); biocompatibility; hemocompatibility; cytotoxicity; inflammation; reactive oxygen species (ROS)

资金

  1. Strategic Priority Research Program of the Chinese Academy of Sciences [XDB36000000]
  2. National Natural Science Foundation [32027801]

向作者/读者索取更多资源

BM shows good biocompatibility, but may have an impact on immune response at excessive concentrations, leading to activation of the complement system and inhibition of lymphocyte proliferation; BM can induce reactive oxygen species (ROS) production in macrophages in a dose-dependent manner, but only causes cell membrane damage and cell cycle arrest at high concentrations, approximately 40 times the clinical dosage.
Bacterial magnetosomes (BMs) are iron oxide nanoparticles synthesized naturally by magnetotactic bacteria, made up of nano-sized inorganic crystals enclosed by a lipid bilayer membrane. Due to several superior characteristics, such as the narrow size distribution, uniform morphology, high purity and crystallinity, single magnetic domain as well as easy surface modification, increasing biomedical and biotechnological applications of BMs have been developed. The attracted wide attentions raise the urge for the evaluation of safety and toxicity. In this work, we performed a rather comprehensive and systematic assessment of in vitro and in vivo toxicity of BMs from MSR-1, including the cytotoxicity, mice bodyweights, blood test, organ coefficients, inflammation, and hemocompatibility study. We found that BMs have good biocompatibility except for influences on the immune response as demonstrated by enhanced activation of the complement system and inhibition of lymphocyte proliferation when used with an excessive concentration. BMs induced the production of reactive oxygen species (ROS) in macrophages at a dose-dependent manner but did not cause cell membrane damage and cell cycle arrest until the concentration is approximately 40 times the clinical dosage. We anticipate our work will guide modifications of BMs and expand their future applications.

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