Fujii Hajime, Nishioka Hiroshi, Wakame Koji, Magnuson Bernadene A, Roberts Ashley
Amino Up Chemical Co., Ltd., Kiyota-ku, Sapporo 004-0839, Japan.
Food Chem Toxicol. 2008 Dec;46(12):3553-62. doi: 10.1016/j.fct.2008.06.005. Epub 2008 Jun 18.
Oligonol is a phenolic product derived from lychee fruit extract and green tea extract, containing catechin-type monomers and oligomers of proanthocyanidins, produced by a manufacturing process which converts polyphenol polymers into oligomers. The safety of Oligonol was assessed in acute and subchronic studies and genotoxicity assays. In a single dose acute study of Oligonol, male and female rats were administered 2000mg/kg body weight (bw) Oligonol in water by gavage. Oligonol caused no adverse effects and body weight gain and food consumption were within normal range, thus the LD(50) of Oligonol was determined to be greater than 2000mg/kg. A 90 day subchronic study (100, 300 and 1000mg/kgbw/day, oral gavage) in male and female rats reported no significant adverse effects in food consumption, body weight, mortality, clinical chemistry, haematology, gross pathology and histopathology. Similarly, no adverse effects were observed in mice fed diets providing 2, 20 or 200mg/kgbw Oligonol or 200mg/kgbw lychee polyphenol for 90 days. Oligonol did not show any potential to induce gene mutations in reverse mutation tests using Salmonella typhimurium TA98, TA100, TA1535, TA1537 and Escherichia coli WP2uvrA strains. Oligonol did not induce chromosomal aberrations in cultured Chinese hamster lung cells, but it showed increased polyploidy. In a micronucleus assay in mice, Oligonol did not induce any micronuclei or suppress bone marrow, indicating it does not cause chromosome aberrations. The results from these safety studies and previous reports support the safety of Oligonol for human consumption.
低聚原花青素是一种从荔枝果提取物和绿茶提取物中获得的酚类产品,含有儿茶素型原花青素单体和低聚物,其生产工艺是将多酚聚合物转化为低聚物。通过急性和亚慢性研究以及遗传毒性试验对低聚原花青素的安全性进行了评估。在低聚原花青素的单次剂量急性研究中,雄性和雌性大鼠经口灌胃给予水中2000mg/kg体重的低聚原花青素。低聚原花青素未引起不良反应,体重增加和食物消耗在正常范围内,因此低聚原花青素的半数致死量(LD50)被确定大于2000mg/kg。在雄性和雌性大鼠中进行的为期90天的亚慢性研究(100、300和1000mg/kg体重/天,经口灌胃)报告称,在食物消耗、体重、死亡率、临床化学、血液学、大体病理学和组织病理学方面均未观察到显著不良反应。同样,在给予含2、20或200mg/kg体重低聚原花青素或200mg/kg体重荔枝多酚的饲料90天的小鼠中,也未观察到不良反应。在使用鼠伤寒沙门氏菌TA98、TA100、TA1535、TA1537和大肠杆菌WP2uvrA菌株的回复突变试验中,低聚原花青素没有显示出任何诱导基因突变的潜力。低聚原花青素在培养的中国仓鼠肺细胞中未诱导染色体畸变,但显示多倍体增加。在小鼠微核试验中,低聚原花青素未诱导任何微核或抑制骨髓,表明它不会引起染色体畸变。这些安全性研究和先前报告的结果支持低聚原花青素供人类食用的安全性。