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新型硅制剂——以阿拉伯胶稳定的单甲基硅三醇(MMST)的毒理学评价

A toxicological evaluation of monomethylsilanetriol (MMST) stabilized in acacia gum, a novel silicon preparation.

机构信息

AIBMR Life Sciences, Inc, 1425 Broadway, Suite 458, Seattle, WA, 98122, USA.

Toxi-Coop Zrt, Magyar Jakobinusok tere 4/B, H-1122, Budapest, Hungary.

出版信息

Regul Toxicol Pharmacol. 2020 Nov;117:104782. doi: 10.1016/j.yrtph.2020.104782. Epub 2020 Sep 6.

DOI:10.1016/j.yrtph.2020.104782
PMID:32905813
Abstract

Monomethylsilanetriol (MMST), a silicon-containing compound, has been sold in dietary supplements. However, toxicological studies on its safety profile are not readily available. To assess the safety of MMST stabilized in acacia gum, a novel delivery form of MMST, in accordance with internationally accepted standards, the genotoxic potential and repeated-dose oral toxicity of Living Silica® Acacia Gum Stabilized Monomethylsilanetriol (formerly known as Orgono Acacia Gum Powder®), a food grade product consisting of 80 ± 10% acacia gum and 2.8% (SD ± 10%) elemental silicon from MMST, was investigated. A bacterial reverse mutation test, an in vitro mammalian chromosomal aberration test, an in vivo mammalian micronucleus test, and a 90-day repeated-dose oral toxicity study in rats were performed. No evidence of mutagenicity or genotoxic activity was observed under the applied test systems. In the 90-day study, male and female Hsd.Han Wistar rats were administered daily doses of 0, 500, 1000, and 2000 mg/kg bw/day by gavage. No mortality or treatment-related adverse effects were observed, and no target organs were identified. Therefore, the no observed adverse effects level (NOAEL) was determined as 2000 mg/kg bw/day (201 mg MMST/kg bw/day), the highest dose tested.

摘要

单甲基硅三醇(MMST)是一种含硅化合物,已作为膳食补充剂销售。然而,其安全性的毒理学研究并不容易获得。为了根据国际公认的标准评估 MMST 在阿拉伯胶中稳定的安全性,即 MMST 的新型传递形式,对一种食品级产品进行了遗传毒性潜力和重复剂量口服毒性研究,该产品由 80±10%阿拉伯胶和 2.8%(SD±10%)来自 MMST 的元素硅组成,名为 Living Silica® Acacia Gum Stabilized Monomethylsilanetriol(以前称为 Orgono Acacia Gum Powder®)。进行了细菌回复突变试验、体外哺乳动物染色体畸变试验、体内哺乳动物微核试验和大鼠 90 天重复剂量口服毒性试验。在应用的测试系统下,没有观察到致突变性或遗传毒性活性的证据。在 90 天的研究中,雄性和雌性 Hsd.Han Wistar 大鼠通过灌胃每天给予 0、500、1000 和 2000mg/kg bw/day 的剂量。未观察到死亡率或与治疗相关的不良影响,也未确定靶器官。因此,未观察到不良影响水平(NOAEL)确定为 2000mg/kg bw/day(201mg MMST/kg bw/day),即测试的最高剂量。

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