0
Article ? AI-assigned paper type based on the abstract. Classification may not be perfect — flag errors using the feedback button. Tier 2 ? Original research — experimental, observational, or case-control study. Direct primary evidence. Human Health Effects Nanoplastics Sign in to save

Histological, Haematological, and thyroid hormones toxicity of oral exposure to CuO/ZnO core/shell nanoparticles in female rats

Research Square (Research Square) 2022 Score: 35 ? 0–100 AI score estimating relevance to the microplastics field. Papers below 30 are filtered from public browse.
Raghad S. Mohammed, Kadhim A. Aadim, Khalid A. Ahmed

Summary

Researchers assessed the in vivo toxicity of CuO/ZnO core/shell nanoparticles (30 nm) in female albino rats via 30-day oral administration at doses from 5 to 40 mg/L, finding significant alterations in white blood cells, red blood cells, hemoglobin, hematocrit, and thyroid hormone levels, indicating systemic toxicity at low doses.

Models
Study Type In vivo

Abstract Advancements in nanomedicine helped scientists design a new class of nanoparticles known as hybrid nanoparticles (core/shell) for diagnostic and therapeutic purposes. An essential requirement for the successful use of nanoparticles in biomedical applications is their low toxicity. Therefore, toxicological profiling is necessary to understand the mechanism of nanoparticles. The current study aimed to assess the toxicological potential of CuO/ZnO core/shell nanoparticles with a size of 30 nm in Albino female rats. In vivo toxicity was evaluated by oral administration of 0, 5, 10, 20, and 40 (mg/L) of CuO/ZnO core/shell nanoparticles to a female rate for 30 consecutive days. The toxicological evaluation revealed significant (p < 0.01) alteration in white blood cells (WBC) at a 5 (mg/L) dose. Also, increase in red blood cells (RBC) at 5, 10 (mg/L) doses, while hemoglobin (Hb) levels and hematocrit (HCT) increased at all doses. This maybe indicates that the CuO/ZnO core/shell nanoparticles stimulated the rate of blood corpuscle generation. The anaemia diagnostic indices (mean corpuscular volume MCV and mean corpuscular haemoglobin MCH) remained unchanged throughout the experiment for all the doses tested 5, 10, 20, and 40 (mg/L). Significant (p < 0.01) growth retardation in all groups treated due to rats' infection by Hyperthyroidism induced by thyroxine (T4) level increase. The histological examination indicates that the low concentrations of CuO/ZnO core/shell nanoparticles are safe for desired biomedical applications.

Sign in to start a discussion.

More Papers Like This

Article Tier 2

Subchronic intraperitoneal toxicity of Sio2NPs on body weight andthyroid gland hormones in female Rats

Researchers investigated the subchronic intraperitoneal toxicity of silica nanoparticles (SiO2NPs) on body weight and thyroid hormone levels in female rats, finding significant decreases in body weight and alterations in thyroid function hormones (T3, T4, TSH) at both low and high doses after 10, 20, and 30 days of exposure. The results indicate that SiO2NPs can disrupt thyroid hormone regulation in a dose- and time-dependent manner.

Article Tier 2

Silica Nanoparticle Acute Toxicity on Male Rattus norvegicus Domestica: Ethological Behavior, Hematological Disorders, Biochemical Analyses, Hepato-Renal Function, and Antioxidant-Immune Response

Researchers assessed the acute toxicity of silica nanoparticles in male rats, finding significant hematological disorders, liver and kidney damage, oxidative stress, and immune system disruption at higher doses after 24 and 96 hours of exposure.

Article Tier 2

Synthesis and Characterization of Silica, Silver-Silica, and Zinc Oxide-Silica Nanoparticles for Evaluation of Blood Biochemistry, Oxidative Stress, and Hepatotoxicity in Albino Rats

Researchers synthesized silica nanoparticles combined with silver and zinc oxide and tested their effects on rat blood chemistry and liver health. The nanoparticles caused dose-dependent changes in liver enzymes and oxidative stress markers, with the silver-silica composite showing the strongest effects. This study contributes to understanding how engineered nanoparticles interact with biological systems, relevant to the broader field of particle toxicology.

Article Tier 2

Tissue distribution, placental transfer and excretion of silver nanoparticles in pregnant rats after a single oral dose

Researchers quantitatively tracked silver nanoparticles in organs, fluids, and fetal blood of pregnant rats following a single oral dose, finding placental transfer and time-dependent tissue distribution over 24 hours.

Article Tier 2

Evaluation of distribution, chemical speciation, and toxic effects of CuO and ZnO nanoparticles in Daphnia magna and Danio rerio

Copper oxide and zinc oxide nanoparticles were toxic to both water fleas (Daphnia magna) and zebrafish at low concentrations, accumulating in tissues and causing oxidative damage. These nanoparticles are used in plastics as stabilizers and antimicrobials, making their aquatic toxicity relevant to assessing risks from plastic-derived nanoparticle release.

Share this paper