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Meratrim®的安全性和毒理学评价:一种用于体重管理的草药配方

Safety and toxicological evaluation of Meratrim®: an herbal formulation for weight management.

作者信息

Saiyed Zainulabedin M, Sengupta Krishanu, Krishnaraju Alluri V, Trimurtulu Golakoti, Lau Francis C, Lugo James P

机构信息

InterHealth Nutraceuticals Research Center, Benicia, CA, United States.

Laila Nutraceuticals, Vijayawada, India.

出版信息

Food Chem Toxicol. 2015 Apr;78:122-9. doi: 10.1016/j.fct.2015.02.010. Epub 2015 Feb 11.

DOI:10.1016/j.fct.2015.02.010
PMID:25680508
Abstract

Meratrim is a unique dietary ingredient consisting of extracts from Sphaeranthus indicus flower heads and Garcinia mangostana fruit rind. Clinical studies have demonstrated that Meratrim is effective and well-tolerated in weight management. Herein we assessed the broad spectrum safety of Meratrim in a battery of in vitro and animal toxicological studies including a sub-chronic repeated-dose 13-week oral toxicity study to determine the no-observable-adverse-effect-level (NOAEL). The LD50 levels of Meratrim in Sprague-Dawley (SD) rats, as determined by the acute oral and dermal toxicity studies, were >5000 and >2000 mg/kg body weight, respectively. The primary skin and eye irritation tests classified Meratrim as non-irritating to the skin and mildly irritating to the eye. Genotoxicity studies showed that Meratrim is non-mutagenic. In the repeated-dose 13-week oral toxicity study, SD rats were orally gavaged with Meratrim at 0, 250, 500 or 1000 mg/kg/day. No morbidity, mortality, or significant adverse events were observed either during the course of the study or on the 13th week. The NOAEL of Meratrim was concluded to be 1000 mg/kg of body weight/day in male and female SD rats. These results, combined with the tolerability of Meratrim in the human clinical trials, demonstrate the broad spectrum safety of Meratrim.

摘要

Meratrim是一种独特的膳食成分,由印度圆叶薄荷的头状花序提取物和山竹果皮提取物组成。临床研究表明,Meratrim在体重管理方面有效且耐受性良好。在此,我们通过一系列体外和动物毒理学研究评估了Meratrim的广谱安全性,其中包括一项为期13周的亚慢性重复剂量口服毒性研究,以确定无可见不良反应水平(NOAEL)。急性口服和皮肤毒性研究确定,Meratrim在Sprague-Dawley(SD)大鼠中的半数致死量(LD50)水平分别>5000和>2000mg/kg体重。原发性皮肤和眼睛刺激性试验将Meratrim分类为对皮肤无刺激性,对眼睛有轻度刺激性。遗传毒性研究表明,Meratrim无致突变性。在为期13周的重复剂量口服毒性研究中,给SD大鼠口服灌胃0、250、500或1000mg/kg/天的Meratrim。在研究过程中或第13周时,均未观察到发病、死亡或重大不良事件。Meratrim在雄性和雌性SD大鼠中的NOAEL被确定为1000mg/kg体重/天。这些结果,结合Meratrim在人体临床试验中的耐受性,证明了Meratrim的广谱安全性。

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