2011
DOI: 10.3358/shokueishi.52.183
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Single and 13-Week Oral Toxicity Study of Fucoxanthin Oil from Microalgae in Rats

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Cited by 47 publications
(30 citation statements)
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“…Furthermore, histological study suggested no abnormality was found in different tissues including liver, kidney, spleen, and gonadal, after repeating dose of 500 and 1000 mg/kg for 30 day in mice [10]. In addition, the genotoxic/mutagenic effects were also not found in mouse bone marrow cells [24,25]. Thus, compared to existing cancer cytotoxic chemotherapy, fucoxanthin can generate growth inhibition effects to multiple types of cancer cell with low toxicity.…”
Section: Resultsmentioning
confidence: 99%
“…Furthermore, histological study suggested no abnormality was found in different tissues including liver, kidney, spleen, and gonadal, after repeating dose of 500 and 1000 mg/kg for 30 day in mice [10]. In addition, the genotoxic/mutagenic effects were also not found in mouse bone marrow cells [24,25]. Thus, compared to existing cancer cytotoxic chemotherapy, fucoxanthin can generate growth inhibition effects to multiple types of cancer cell with low toxicity.…”
Section: Resultsmentioning
confidence: 99%
“…showed no signs of genotoxicity in the bacterial reverse mutation test and micronucleus test in mice [26]. In addition, in a rat study, the 50% lethal single dose of FX was more than 2 g/kg of body weight and no elevated mortality or abnormalities were observed in a 13-week oral administration of FX in a dose of 200 mg/kg [27].…”
Section: Fx Sources and Toxicitymentioning
confidence: 92%
“…This result suggested that the no observed adverse effect level of FX-containing oil extracted from microalga Chaetoseros sp. was 200 mg/kg body weight under the tested subchronic dose condition [24]. …”
Section: Toxicitymentioning
confidence: 99%