Evidence map›Paper›PMID 27998138›Full record

ArticleACS applied materials & interfaces2016

Differential Protein Adsorption and Cellular Uptake of Silica Nanoparticles Based on Size and Porosity.

Jiban Saikia, Mostafa Yazdimamaghani, Seyyed Pouya Hadipour Moghaddam, Hamidreza Ghandehari

Abstract read
In one paragraph

Article in ACS applied materials & interfaces, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed, 1 pooled it
–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

39 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
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  5. Effects of silica nanoparticles with varied physicochemical properties on the survival and functionality of saturated macrophages.Journal of controlled release : official journal of the Controlled Release Society · 2025
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  14. The nanotopography of SiONanoscale · 2021
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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

4 authors.

Jiban SaikiaUtah Center for Nanomedicine, Nano Institute of Utah, §Department of Pharmaceutics and Pharmaceutical Chemistry, and ∥Department of Bioengineering, University of Utah , Salt Lake City, Utah 84112, United States.
Mostafa YazdimamaghaniUtah Center for Nanomedicine, Nano Institute of Utah, §Department of Pharmaceutics and Pharmaceutical Chemistry, and ∥Department of Bioengineering, University of Utah , Salt Lake City, Utah 84112, United States.
Seyyed Pouya Hadipour MoghaddamUtah Center for Nanomedicine, Nano Institute of Utah, §Department of Pharmaceutics and Pharmaceutical Chemistry, and ∥Department of Bioengineering, University of Utah , Salt Lake City, Utah 84112, United States.
Hamidreza GhandehariUtah Center for Nanomedicine, Nano Institute of Utah, §Department of Pharmaceutics and Pharmaceutical Chemistry, and ∥Department of Bioengineering, University of Utah , Salt Lake City, Utah 84112, United States.

Funding

BIOLOGICAL FATE AND BIOCOMPATIBILITY OF SILICA-BASED NANOCONSTRUCTSR01ES024681 · NIEHS · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI Hamid Ghandehari · 2014 to 2026
$4.1M
NIEHS NIH HHS R01 ES024681
6 · The paper itself

Abstract

Slight alterations in nanoparticles' surface properties can significantly influence the corona composition which may alter their interaction with the biological milieu. Size and porosity of silica nanoparticles (SNPs) are known to be predominant factors influencing their dose-dependent toxicity. Little is known however about the extent and type of protein adsorption on SNPs as a function of physicochemical properties and the role this might play on mechanisms of cellular uptake and toxicity. In this work we investigated the influence of size and porosity of SNPs on protein adsorption, cellular uptake, and toxicity in RAW 264.7 macrophages. Toxicity of the SNPs was found to be concentration dependent, and the formation of the protein corona mitigated toxicity for all particles. Detailed analysis of the amount of proteins recovered from each nanoparticle revealed similarities in the protein adsorption profile as a function of size and porosity. The mechanism of uptake was highly dependent on size rather than porosity or the adsorbed proteins.

Indexed as

cellular uptakecytotoxicityprotein adsorptionprotein coronasilica nanoparticles

Identifiers

PMID27998138
PMCPMC5538804

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.