Nestmann Earle R, Alluri Venkata Krishnaraju, Dodda Sundararaju, Davis Barbara A
Health Science Consultants Mississauga Ontario Canada.
Laila Nutraceuticals R&D Center Vijayawada India.
Food Sci Nutr. 2019 Jan 29;7(2):817-833. doi: 10.1002/fsn3.931. eCollection 2019 Feb.
LI12542F6, a botanical extract composed of and , was evaluated for mutagenicity in bacteria clastogenicity in mouse bone marrow, acute oral and dermal toxicity in the rat, irritation (dermal, eye) in rabbit, and subacute and subchronic toxicity (28 and 90 days) in the rat. All studies followed standard OECD test protocols, in accordance with the principles of Good Laboratory Practice (GLP). LI12542F6 did not induce mutations in the bacterial assay using and strains, nor did it induce genotoxic effects in erythrocytes from mouse bone marrow. LI12542F6 was found to have oral and dermal LD values greater than the limit dose of 2,000 mg/kg body weight in the rat. In an eye irritation/corrosion test, LI12542F6 caused conjunctival redness, corneal opacity, and chemosis and is classified as Category 2A ("irritating to eyes - reversible eye effect"). Doses in the 28-day and 90-day rat oral toxicity studies were 0, 500, 1,000, and 1,500 and 0, 1,000, 1,500, and 2,000 mg/kg body weight/day, respectively, administered by gavage. Both studies featured a recovery period. Minor effects were random and not treatment related except for local irritation of the forestomach in the 28-day study, evidenced by histopathologic examination, in mid- and high-dose animals. The frequency and severity of these effects were reduced in the recovery group; irritation was not found in the forestomach of rats in the 90-day study. The no observed adverse effect level (NOAEL) was greater than the highest dose tested, that is, >2,000 mg/kg in the 90-day study. This botanical composition will be marketed commercially for muscle health as Myotor™.
LI12542F6是一种由[具体成分1]和[具体成分2]组成的植物提取物,对其进行了细菌致突变性、小鼠骨髓染色体断裂性、大鼠急性经口和经皮毒性、家兔刺激性(皮肤、眼睛)以及大鼠亚急性和亚慢性毒性(28天和90天)的评估。所有研究均遵循经合组织(OECD)标准测试方案,符合良好实验室规范(GLP)原则。LI12542F6在使用[具体菌株1]和[具体菌株2]的细菌试验中未诱导突变,在小鼠骨髓红细胞中也未诱导遗传毒性效应。发现LI12542F6的经口和经皮半数致死剂量(LD)值高于大鼠2000mg/kg体重的极限剂量。在眼刺激/腐蚀试验中,LI12542F6导致结膜发红、角膜混浊和球结膜水肿,被归类为2A类(“眼睛刺激性 - 可逆性眼效应”)。大鼠28天和90天经口毒性研究的剂量分别为0、500、1000和1500mg/kg体重/天以及0、1000、1500和2000mg/kg体重/天,通过灌胃给药。两项研究均设有恢复期。除28天研究中高剂量和中剂量动物的前胃局部刺激外,轻微影响是随机的且与治疗无关,组织病理学检查证实了这一点。恢复期组这些影响的频率和严重程度有所降低;90天研究中大鼠的前胃未发现刺激。未观察到有害作用水平(NOAEL)高于测试的最高剂量,即在90天研究中>2000mg/kg。这种植物成分将作为Myotor™进行商业销售,用于肌肉健康。