Evidence map›Paper›PMID 38202484›Full record

ArticleNanomaterials (Basel, Switzerland)2023

Tissue Distribution, Pharmacokinetics, and Effect of Hematological and Biochemical Parameters of Acute Intravenous Administration of Silver Nanoparticles in Rats.

Elsayed I Salim, Khaled Y Abdel-Halim, Mostafa E El-Mahalawy, Haitham A Badr, Hafiz Ahmed

Abstract read
In one paragraph

Article in Nanomaterials (Basel, Switzerland), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Article
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  4. Review
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  8. Review
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

5 authors.

Elsayed I SalimResearch Laboratory of Molecular Carcinogenesis, Department of Zoology, Faculty of Science, Tanta University, Tanta 31527, Egypt.
Khaled Y Abdel-HalimMammalian & Aquatic Toxicology Department, Central Agricultural Pesticides Laboratory (CAPL), Agricultural Research Center (ARC), Dokki, Giza 12618, Egypt.
Mostafa E El-MahalawyResearch Laboratory of Molecular Carcinogenesis, Department of Zoology, Faculty of Science, Tanta University, Tanta 31527, Egypt.
Haitham A BadrBiochemistry Department, Faculty of Agriculture, Zagazig University, Zagazig 44519, Egypt.ORCID 0000-0002-2403-3785
Hafiz AhmedGlycoMantra Inc., 1450 South Rolling Road, Baltimore, MD 21227, USA.

Funding

Targeting galectin-3 to overcome insulin resistance in type 2 diabetesR44DK125126 · NIDDK · GLYCOMANTRA, INC. · PI AHMED, HAFIZ · 2023 to 2024
$3.7M
Targeting galectin-3 to intervene COVID-19R43AI162182 · NIAID · GLYCOMANTRA, INC. · PI AHMED, HAFIZ · 2022 to 2023
$597k
Targeting galectin-3 to overcome insulin resistance in type 2 diabetesR43DK125126 · NIDDK · GLYCOMANTRA, INC. · PI AHMED, HAFIZ · 2020 to 2020
$300k
NIAID NIH HHS R43 AI162182NIDDK NIH HHS R43 DK125126NIDDK NIH HHS R44 DK125126NIH HHS AI162182
6 · The paper itself

Abstract

The widespread biomedical and commercial applications of silver nanoparticles (AgNPs) have increased their potential for human and environmental exposure and toxicity to human health. The bio-distribution and toxicity of AgNPs in rodents following inhalation, intratracheal instillation, and oral ingestion are well documented; however, little is known about the bio-distribution of intravenously (IV)-administered AgNPs and their organ-specific pathophysiological effects. Here, we investigate the pharmacokinetic pattern and tissue distribution of AgNPs in male rats following IV administration. The animals were humanely sacrificed after 10 min, 1 h, 6 h, 12 h, 24 h, and 168 h of AgNP administration, and the silver (Ag) content was measured from blood samples and various tissues following acid digestion. The AgNPs were readily absorbed and subsequently distributed into most organs predominantly in the colon, small intestine, kidney, and heart after 6 h; however, they were the highest in the spinal cord after 168 h. White blood cells (WBCs) were significantly increased (42-60%) in AgNP-administered animals at all time points except 10 min. Regarding platelets, all AgNP-administered animals showed counts 7.8-39.2% lower, with the lowest count at 168 h post-administration. In the case of lymphocytes (LYMs), the AgNP-treated animals exhibited a count 19.5-41% lower at 10 min and 1 h post-administration; however, the animals at 168 h post-administration showed a count 30.5% more. The mean corpuscular hemoglobin (MCH) counts from the AgNP-treated animals were decreased by 50-62%. The concentrations of aspartate transaminase (AST), urea, and creatinine were increased in the AgNP-treated animals. Taken together, the results suggest that the acute IV administration of AgNPs alters metabolic and hematological parameters in animals and may pose a health risk to humans.

Indexed as

hematological and biochemical alterationspharmacokineticsratssilver nanoparticlestissue distribution

Identifiers

PMID38202484
PMCPMC10780562

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.