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In vivo Biodistribution and Urinary Excretion of Mesoporous Silica Nanoparticles: Effects of Particle Size and PEGylation

He, Qianjun, Zhang, Zhiwen, Gao, Fang, Li, Yaping, Shi, Jianlin·2011·Small

Abstract

The in vivo biodistribution and urinary excretion of spherical mesoporous silica nanoparticles (MSNs) are evaluated by tail‐vein injection in ICR mice, and the effects of the particle size and PEGylation are investigated. The results indicate that both MSNs and PEGylated MSNs of different particle sizes (80–360 nm) distribute mainly in the liver and spleen, a minority of them in the lungs, and a few in the kidney and heart. The PEGylated MSNs of smaller particle size escape more easily from capture by liver, spleen, and lung tissues, possess longer blood‐circulation lifetime, and are more slowly biodegraded and correspondingly have a lower excreted amount of degradation products in the urine. Neither MSNs nor PEGylated MSNs cause tissue toxicity after 1 month in vivo.

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Metadata

Authors
He, Q., Zhang, Z., Gao, F., Li, Y., & Shi, J.
Venue
Small
Publisher
Wiley
Published
2010-12-10
Volume
7
Issue
2
Pages
271-280
ISSN
  • 1613-6810 (ISSN-L)
  • 1613-6829
OpenAlex
W2138861644
Cited by
661
References
2
FWCI
11.47
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: In vivo Biodistribution and Urinary Excretion of Mesoporous Silica Nanoparticles: Effects of Particle Size and PEGylation. https://app.cochat.ai/papers/10.1002/smll.201001459
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He, Q., Zhang, Z., Gao, F., Li, Y., & Shi, J. (2011). In vivo Biodistribution and Urinary Excretion of Mesoporous Silica Nanoparticles: Effects of Particle Size and PEGylation. Small. https://doi.org/10.1002/smll.201001459

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