scholarly journals Acute and subacute repeated oral toxicity study of fragmented microplastics in Sprague-Dawley rats

2021 ◽  
Vol 228 ◽  
pp. 112964
Author(s):  
Jinsik Kim ◽  
Muthuchamy Maruthupandy ◽  
Kyu Sup An ◽  
Kwang Hun Lee ◽  
Soyeon Jeon ◽  
...  
2013 ◽  
Vol 32 (5) ◽  
pp. 385-394 ◽  
Author(s):  
Antoinette Y. Odendaal ◽  
Narendra S. Deshmukh ◽  
Tennille K. Marx ◽  
Alexander G. Schauss ◽  
John R. Endres ◽  
...  

This toxicological assessment evaluated the safety of a hydroethanolic extract prepared from Caralluma fimbriata (CFE), a dietary supplement marketed worldwide as an appetite suppressant. Studies included 2 in vitro genotoxicity assays, a repeated dose oral toxicity study, and a developmental study in rats. No evidence of in vitro mutagenicity or clastogenicity surfaced in the in vitro studies at concentrations up to 5000 μg of extract/plate (Ames test) or 5000 μg of extract/mL (chromosomal aberration test). No deaths or treatment-related toxicity were seen in the 6-month chronic oral toxicity study in Sprague-Dawley rats conducted at 3 doses (100, 300, and 1000 mg/kg body weight (bw)/d). The no observed effect level for CFE in this study was considered to be 1000 mg/kg bw/d. A prenatal developmental toxicity study conducted at 3 doses (250, 500, and 1000 mg/kg bw/d) in female Sprague-Dawley rats resulted in no treatment-related external, visceral, or skeletal fetal abnormalities, and no treatment-related maternal or pregnancy alterations were seen at and up to the maximum dose tested. CFE was not associated with any toxicity or adverse events.


2016 ◽  
Vol 81 ◽  
pp. 275-283 ◽  
Author(s):  
A.M. Saillenfait ◽  
F. Marquet ◽  
J.P. Sabaté ◽  
D. Ndiaye ◽  
A.M. Lambert-Xolin

2014 ◽  
Vol 9 (5) ◽  
pp. 603-612 ◽  
Author(s):  
Jae Hyuck Sung ◽  
Soo Jin Park ◽  
Min Sook Jeong ◽  
Kyung Seuk Song ◽  
Kyu Sup Ahn ◽  
...  

2013 ◽  
Vol 2013 ◽  
pp. 1-14 ◽  
Author(s):  
Kwan Yuet Ping ◽  
Ibrahim Darah ◽  
Yeng Chen ◽  
Subramaniam Sreeramanan ◽  
Sreenivasan Sasidharan

DespiteEuphorbia hirtaL. ethnomedicinal benefits, very few studies have described the potential toxicity. The aim of the present study was to evaluate thein vivotoxicity of methanolic extracts ofE. hirta. The acute and subchronic oral toxicity ofE. hirtawas evaluated in Sprague Dawley rats. The extract at a single dose of 5000 mg/kg did not produce treatment related signs of toxicity or mortality in any of the animals tested during the 14-day observation period. Therefore, the LD 50 of this plant was estimated to be more than 5000 mg/kg. In the repeated dose 90-day oral toxicity study, the administration of 50 mg/kg, 250 mg/kg, and 1000 mg/kg/day ofE. hirtaextract per body weight revealed no significant difference (P>0.05) in food and water consumptions, body weight change, haematological and biochemical parameters, relative organ weights, and gross findings compared to the control group. Macropathology and histopathology examinations of all organs including the liver did not reveal morphological alteration. Analyses of these results with the information of signs, behaviour, and health monitoring could lead to the conclusion that the long-term oral administration ofE. hirtaextract for 90 days does not cause sub-chronic toxicity.


Food Research ◽  
2021 ◽  
Vol 5 (1) ◽  
pp. 390-393
Author(s):  
Rohini J. ◽  
Rabeta M.S. ◽  
Wan Ezumi M.F.

In this study, the extract of Ocimum tenuiflorum was formulated to promote wound healing and no acute toxicity study has been reported on this type of formulation. Acute oral toxicity results of the rats after administration of 5000 mg/kg body weight (BW) formulation showed no toxic effects and behavioural changes of the rats after 14 days of observation. On day 14, the rats were anaesthetized to collect the vital organs for histopathological examination. The microscopy study of the visceral organs of wound healing powder group shows no sign of toxicity in comparison to untreated rats organs. In conclusion, the result of the acute oral toxicity test of wound healing drink showed no sign of toxicity, as corroborated by a histopathological study.


Author(s):  
Hansol Won ◽  
Jin Hee Lee ◽  
Ji-Hyun Seok ◽  
Kikyung Jung ◽  
Jun-Young Yang ◽  
...  

2017 ◽  
Vol 2017 ◽  
pp. 1-8 ◽  
Author(s):  
Sae-Rom Yoo ◽  
Hyekyung Ha ◽  
Mee-Young Lee ◽  
Hyeun-Kyoo Shin ◽  
Su-Cheol Han ◽  
...  

Traditional herbal medicines have been used for centuries in Asian countries. However, recent studies have led to increasing concerns about the safety and toxicity of herbal prescriptions. Bojungikgi-tang (BJIGT), a herbal decoction, has been used in Korea to improve physical strength. To establish the safety information, BJIGT water extract was evaluated in a 4-week repeated-dose oral toxicity test in Crl:CD Sprague Dawley rats. BJIGT was orally administered in daily doses of 0, 500, 1000, and 2000 mg/kg/day for 4 weeks via oral gavage in male and female rats. We examined the mortality, clinical signs, body weight change, food intake, organ weights, hematology, serum biochemistry, and urinalysis parameters. No significant changes were observed in mortality, clinical sings, body weight, food intake, organ weights, hematology, serum biochemistry, and urinalysis parameters between the control group and the BJIGT-treated groups in the rats of both sexes. The results indicate that BJIGT did not induce toxic effects at a dose level up to 2000 mg/kg in rats. Thus, this concentration is considered the nonobservable effect dose in rats and is appropriate for a 13-week subchronic toxicity study.


Molecules ◽  
2012 ◽  
Vol 17 (4) ◽  
pp. 4326-4342 ◽  
Author(s):  
Adlin Afzan ◽  
Noor Rain Abdullah ◽  
Siti Zaleha Halim ◽  
Badrul Amini Rashid ◽  
Raja Hazlini Raja Semail ◽  
...  

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