Evidence map›Paper›PMID 28496319›Full record

ArticleInternational journal of nanomedicine2017

In vivo toxicologic study of larger silica nanoparticles in mice.

Wai-Tao Chan, Cheng-Che Liu, Jen-Shiu Chiang Chiau, Shang-Ting Tsai, Chih-Kai Liang, Mei-Lien Cheng, Hung-Chang Lee, Chun-Yun Yeung, Shao-Yi Hou

Abstract read
In one paragraph

Article in International journal of nanomedicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

24 citing papers in PubMed.

  1. Harnessing Silicon and Nanosilicon Formulations withInternational journal of molecular sciences · 2026
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Wai-Tao ChanDepartment of Pediatric Gastroenterology, Hepatology and Nutrition, MacKay Children's Hospital.
Cheng-Che LiuInstitute of Preventive Medicine, National Defense Medical Center, Taipei.
Jen-Shiu Chiang ChiauDepartment of Medical Research, MacKay Memorial Hospital, Hsinchu.
Shang-Ting TsaiGraduate Institute of Biochemical and Biomedical Engineering, National Taipei University of Technology, Taipei.
Chih-Kai LiangGraduate Institute of Biochemical and Biomedical Engineering, National Taipei University of Technology, Taipei.
Mei-Lien ChengDepartment of Medical Research, MacKay Memorial Hospital, Hsinchu.
Hung-Chang LeeDepartment of Pediatrics, MacKay Memorial Hospital, Hsinchu.
Chun-Yun YeungDepartment of Pediatric Gastroenterology, Hepatology and Nutrition, MacKay Children's Hospital.
Shao-Yi HouGraduate Institute of Engineering Technology, National Taipei University of Technology.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Silica nanoparticles (SiNPs) are being studied and used for medical purposes. As nanotechnology grows rapidly, its biosafety and toxicity have frequently raised concerns. However, diverse results have been reported about the safety of SiNPs; several studies reported that smaller particles might exhibit toxic effects to some cell lines, and larger particles of 100 nm were reported to be genotoxic to the cocultured cells. Here, we investigated the in vivo toxicity of SiNPs of 150 nm in various dosages via intravenous administration in mice. The mice were observed for 14 days before blood examination and histopathological assay. All the mice survived and behaved normally after the administration of nanoparticles. No significant weight change was noted. Blood examinations showed no definite systemic dysfunction of organ systems. Histopathological studies of vital organs confirmed no SiNP-related adverse effects. We concluded that 150 nm SiNPs were biocompatible and safe for in vivo use in mice.

Indexed as

AnimalsBlood CellsBrainCell LineHeartLiverLungMaleMice, Inbred BALB CNanoparticlesParticle SizeSilicon DioxideSpleenToxicity TestsSilicon Dioxidein vivomicenanotoxicitysilica nanoparticle

Identifiers

PMID28496319
PMCPMC5417664

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.