Laboratoire CRRET/CNRS UMR 7149, Université Paris 12 val de Marne, PRES Paris Est, 61, Avenue du Général de Gaulle 94010, Créteil Cedex, France.
Food Chem Toxicol. 2010 Jul;48(7):1965-8. doi: 10.1016/j.fct.2010.04.045. Epub 2010 May 7.
Heparan sulfate mimetic polymers promotes tissue repair when injected locally in doses of 1-2mg/kg by various routes. These biopolymers, have been extensively studied for their diverse biological activities. However, there is no detailed report investigating the toxicity of OTR4120. In this study, the acute and subchronic (30 days) toxicity of varying levels of OTR4120 was investigated in mice after intraperitoneal administration. The results showed that no significant toxicological changes were observed when 50mg/kg body weight per day OTR4120 was administered to mice. But when the dose was increased to 60 and 70 mg/kg body weight per day, the clotting time was significantly prolonged. Alanine aminotransferase (ALT), aspartate aminotransferase (AST) and alkaline phosphatase (ALP) activities were reduced female and male at dose 70 mg/kg body weight per day. These blood biochemistry data suggest that OTR4120 have a hepatoprotective effect. Based on these results, it can be concluded that the no adverse effect level of OTR4120 is 50 mg/kg body weight per day.
硫酸乙酰肝素模拟聚合物通过各种途径以 1-2mg/kg 的剂量局部注射时可促进组织修复。这些生物聚合物因其多种生物学活性而被广泛研究。然而,目前尚无详细报告研究 OTR4120 的毒性。在这项研究中,通过腹腔内给药研究了不同水平的 OTR4120 的急性和亚慢性(30 天)毒性。结果表明,当每天给小鼠 50mg/kg 体重的 OTR4120 时,未观察到明显的毒理学变化。但是,当剂量增加到每天 60 和 70mg/kg 体重时,凝血时间明显延长。丙氨酸氨基转移酶(ALT)、天冬氨酸氨基转移酶(AST)和碱性磷酸酶(ALP)的活性在每天 70mg/kg 体重的雌性和雄性中降低。这些血液生化学数据表明 OTR4120 具有肝保护作用。基于这些结果,可以得出结论,OTR4120 的无不良影响水平为每天 50mg/kg 体重。