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http://dx.doi.org/10.5487/TR.2007.23.4.373

Mouse Single Oral Dose Toxicity Studies of PGB-1, a Novel Polyglucosamine Polymer Produce from Enterobacter sp. BL-2  

Lee, Yong-Hyun (Department of Genetic Engineering, College of Natural Sciences, Kyungpook National University)
Son, Mi-Kyung (Department of Genetic Engineering, College of Natural Sciences, Kyungpook National University)
Jung, Young-Mi (ENZ Bio Co., Ltd.)
Kim, Tae-Kwon (ENZ Bio Co., Ltd.)
Park, Dong-Chan (ENZ Bio Co., Ltd.)
Lee, Hyeung-Sik (Department of Herbal Biotechnology, Daegu Haany University)
Kim, Pan-Soo (Department of Technical Support, Gyeonggi Bio-center)
Ku, Sae-Kwang (Department of Anatomy and Histology, College of Oriental Medicine, Daegu Haany University)
Publication Information
Toxicological Research / v.23, no.4, 2007 , pp. 373-382 More about this Journal
Abstract
This study was conducted to obtain acute information of the oral dose toxicity of PGB-1, a novel polyglucosamine polymer produced from a new strain Enterobacter sp. BL-2 in male and female mice. In order to calculated 50% lethal dose ($LD_{50}$) and approximate lethal dose (LD), test material was once orally administered to male and female ICR mice at dose levels of 2000, 1000, 500, 250, 125 and 0 (vehicle control) ml/kg (body wt.). The mortality and changes on body weight, clinical signs, gross observation and organ weight and histopathology of principle organs were monitored 14 days after dosing with PGB-1. We could not find any mortalities, clinical signs, body weight changes and gross findings. In addition, significant changes in the organ weight and histopathology of principal organs were not observed except for some sporadic findings. The results obtained in this study suggest that PGB-1 may not be toxic in mice and may be therefore safe for clinical use. The $LD_{50}$ and approximate LD in mice after single oral dose of PGB-1 were considered over 2000 mg/kg in both female and male mice.
Keywords
Polyglucosamine; PGB-1; Polymer; Enterobacter; Single oral dose toxicity; Mice; Histopathology;
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