Molecular Elucidation of Biological Response to Mesoporous Silica Nanoparticles in Vitro and in Vivo

Cheng Chung Chou, Wei Chen, Yann Hung, Chung Yuan Mou

Research output: Contribution to journalArticlepeer-review

59 Citations (Scopus)


Biomedical applications of mesoporous silica nanoparticles (MSNs) require efficient cellular uptake and low toxicity. The purpose of this study is to investigate the cellular uptake and toxicity of MSNs with different sizes and charges (50, 100, and 250 nm with a positive surface charge and 100 nm with a negative surface charge) exposed to human monocyte-derived macrophages, lung epithelium BEAS-2B cells, and mice using genome-wide gene expression analysis and cellular/animal-level end point tests. We found that MSNs can be taken up into cells through endocytosis in a charge- and size-dependent manner, with positively charged and larger MSNs being more easily taken up into the cells by recruiting more types of endocytotic pathways for more cellular uptake. Moreover, the cytotoxicity of MSNs could be correlated with the amount of MSNs taken up by cells, which positively correlates to the particle size and dosage. Therefore, only positively charged and larger MSNs (≥100 nm) during higher treatment doses (≥500 μg mL-1) resulted in a sufficient accumulation of internalized MSNs in cells to induce significant release of reactive oxygen species (ROS) and oxidative stress, inflammatory gene upregulation through NF-B and AP-1, and eventually autophagy-mediated necrotic cell death. Furthermore, genome-wide gene expression analysis could reflect the above in vitro cellular damages and corresponding in vivo injuries in mice, indicating that specific gene expression footprints may be used for assessing the safety of nanoparticles. The present finding provides some insights into the rational design of effective MSN-based drug/gene delivery systems and biomedical applications.

Original languageEnglish
Pages (from-to)22235-22251
Number of pages17
JournalACS Applied Materials and Interfaces
Issue number27
Publication statusPublished - Jul 12 2017
Externally publishedYes


  • autophagy
  • endocytosis
  • gene expression microarray
  • inflammation
  • mesoporous silica nanoparticles
  • oxidative stress
  • reactive oxygen species (ROS)
  • toxicity

ASJC Scopus subject areas

  • Materials Science(all)


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