GET THE APP

Comparative study on acute toxicity of aluminium oxide nanopartic | 57526
Journal of Clinical Toxicology

Journal of Clinical Toxicology
Open Access

ISSN: 2161-0495

+44 1478 350008

Comparative study on acute toxicity of aluminium oxide nanoparticle and aluminium chloride anhydrous in rat


15th Euro Global Summit on Toxicology and Applied Pharmacology

July 02-04, 2018 | Berlin, Germany

Je Hein Kim

Korea Institute of Toxicology, Republic of South Korea

Posters & Accepted Abstracts: J Clinic Toxicol

Abstract :

In order to compare the toxicity between aluminium oxide nanoparticle and aluminium chloride anhydrous, test articles were administered by oral gavage to 6-week-old Crl:CD (SD) rats of both sexes. Those were separated into 7 groups (n=10 for each group) and each test article was given three dose of 800, 2000, 5000 mg/kg body weight or vehicle solution. Aluminium oxide nanoparticle were dispersed into the 1% hydroxylpropyl methylcellulose (HPMC) solution. During the study, clinical signs, mortality, body weight, hematology, serum biochemistry, gross findings, and organ weights were measured. In aluminium chloride anhydrous group, six and four animals were dead at day 1 and day 2 in high-dose group (5000 mg/kg). In the middledose group (2000 mg/kg), five, three and two dead animals were found at day 2, day 3 and day 3, respectively. In contrast, no treatment-related clinical signs observed in aluminium oxide nanoparticle group and no significant changes of body weight, organ weight were noted in all treated animals. In hematology and serum biochemistry, PLT, CREA were increased in male 800 mg/kg and higher GLU was seen at female 800 mg/kg dose group of aluminium chloride anhydrous group. In the aluminium oxide nanoparticle, increased ALB was noted at female 800 mg/kg and Glu was increased at 5000 mg/kg. In conclusion, aluminium chloride anhydrous has higher toxicity than aluminium oxide nanoparticle in rat.
Recent Publications:
1. H K Lee et al. (2018) Nemopilema nomurai jellyfish venom exerts an anti-metastatic effect by inhibiting Smad- and NF-�?ºB-mediated epithelialâ�?�?mesenchymal transition in HepG2 cells. Scientific Reports 8:2808.
2. I C Lee et al. (2016) Comparative toxicity and biodistribution assessments in rats following subchronic oral exposure to copper nanoparticles and microparticles. Particle and Fibre Toxicology. 13(1):56.
3. Y Heo et al. (2015) Evaluation of phototoxic and skin sensitization potentials of PLA2-free bee venom. Evidencebased Complementary and Alternative Medicine. 2015:157367.

Biography :

Je Hein Kim has completed his Master´s Degree from Gyeongsang National University, Republic of South Korea. He is a Researcher at the Korea Institute of Toxicology, a world-class prestigious contract research organization and has experience in toxicology. His research interest include: Food Toxicology and Genetic Toxicology.

E-mail: jehein@kitox.re.kr

Top