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Acute and subchronic (28-day) oral toxicity study in rats fed with novel surfactants

机译:用新型表面活性剂喂养的大鼠的急性和亚慢性(28天)口服毒性研究

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摘要

The toxicity of 2 new synthetic lipids, 1,2-dioleoyl-rac-glycerol-3-dodecaethylene glycol, GDO-12 (lipid >1) and 1,2-distearoyl-rac-glycerol-3-dodecaethylene glycol, GDS-12 (lipid >2) has been evaluated in acute and subchronic toxicity studies. Acute oral toxicity studies in male and female rats documented no deaths or treatment-related signs at high doses. The lipids were individually administered (by gavage) to male and female Sprague-Dawley rats at concentrations of 250, 500, and 1000 mg/Kg bodyweight for 28 days. All animals survived the duration of the study, with no significant changes in clinical signs, hematological parameters, organ weights, ophthalmology evaluations, or histopathological findings. These studies establish that both GDO-12 (lipid >1) and GDS-12 (lipid >2) are nontoxic in rats following oral administration. The no-observed-adverse-effect level ranged between 250 mg/Kg and 1000 mg/Kg following oral administration.
机译:两种新的合成脂质的毒性:1,2-二油酰基-rac-甘油-3-十二烷基乙二醇,GDO-12(脂质> 1 )和1,2-二硬脂基-rac-甘油-3-已经在急性和亚慢性毒性研究中评估了十二碳二烯二醇GDS-12(脂质> 2 )。在雄性和雌性大鼠中的急性口服毒性研究表明,高剂量时无死亡或与治疗相关的症状。分别以250、500和1000 mg / Kg体重的浓度分别对雄性和雌性Sprague-Dawley大鼠施用脂质(通过管饲法),持续28天。所有动物在研究期间均存活,临床体征,血液学参数,器官重量,眼科评估或组织病理学发现无明显变化。这些研究证实,口服给药后,GDO-12(脂质> 1 )和GDS-12(脂质> 2 )均对大鼠无毒。口服后未观察到的不良反应水平在250 mg / Kg和1000 mg / Kg之间。

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