A comprehensive toxicological safety assessment of an aqueous extract of Polypodium leucotomos (Fernblock®)

被引:21
|
作者
Murbach, Timothy S. [1 ]
Beres, Erzsebet [2 ]
Vertesi, Adel [2 ]
Glavits, Robert [2 ]
Hirka, Gabor [2 ]
Endres, John R. [1 ]
Clewell, Amy E. [1 ]
Szakonyine, Ilona Pasics [2 ]
机构
[1] AIBMR Life Sci Inc, Puyallup, WA 98373 USA
[2] Taxi Coop Zrt, H-1124 Budapest, Hungary
关键词
Polypodium leucotomos; Safety assessment; Toxicity; Fernblock; NOAEL; Photoprotection; GENE-TOX PROGRAM; HUMAN SKIN; IN-VITRO; PHOTOPROTECTIVE PROPERTIES; IDIOPATHIC PHOTODERMATOSES; ANTIOXIDANT ACTIVITY; HYDROPHILIC EXTRACT; LIPID-PEROXIDATION; MUTAGENICITY TEST; P53; EXPRESSION;
D O I
10.1016/j.fct.2015.11.008
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
A battery of toxicological studies was conducted in accordance with internationally accepted standards to investigate the genotoxicity and repeated-dose oral toxicity of Fernblock (R), a commercial aqueous extraction of the leaves of the tropical fern Polypodium leucotomos used for its oral and topical photoprotective properties. No evidence of mutagenicity was observed in a bacterial reverse mutation test or in vitro mammalian chromosomal aberration test nor was any genotoxic activity observed in an in vivo mouse micronucleus test. Two repeated-dose oral toxicity studies were conducted in male and female Wistar rats. In the first study, no mortality or toxic effects were observed and no target organs were identified at doses administered for 14 days by gavage up to the maximum dose of 5000 mg/kg bw/day. Based on these results, a 90-day study was conducted at 0, 300, 600, and 1200 mg/kg bw/day. No mortality or treatment-related adverse effects were observed and no target organs were identified. The NOAEL from the 90-day study was determined to be 1200 mg/kg bw/day, the highest dose tested. (C) 2015 The Authors. Published by Elsevier Ltd.
引用
收藏
页码:328 / 341
页数:14
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