Research and Development Centre, Ambe Phytoextracts Private Limited, Pauri Garhwal, Uttarakhand, India.
Department of Pharmaceutics, National Institute of Pharmaceutical Education and Research, Hyderabad, Telangana, India.
ScientificWorldJournal. 2022 Mar 28;2022:6224107. doi: 10.1155/2022/6224107. eCollection 2022.
Acute and subacute toxicity analysis of AND-2-HyP--CYD complex was conducted in Sprague-Dawley (SD) rats following oral and inhalation routes of administration.
Single dose acute toxicity was carried out at 2000 mg/kg of AND-2-HyP--CYD complex, while the doses of 200, 400, and 666 mg/kg were administered, over a period of 28 days under repeated dose oral toxicity study. Hence, LD50 (lethal dose) was found to be >2000 mg/kg in addition to NOAEL (no observed adverse effect level) of 666 mg/kg. Correspondingly, single dose acute inhalation toxicity of AND-2-HyP--CYD complex was carried out at 5 mg/L/4 h/day and subacute inhalation toxicity at 0.5, 1, and 1.66 mg/L/4 h/day over a period of 28 days. The NOAEL and LOAEL (lowest observed adverse effect level) were estimated to be 0.5 mg/L/4 h/day and 1 mg/L/4 h/day, respectively.
The findings of the present study would further be useful in assessing and utilizing the medicinal and therapeutic benefits of AND-2-HyP--CYD complex.
通过经口和吸入途径给予 Sprague-Dawley(SD)大鼠,对 AND-2-HyP--CYD 复合物进行急性和亚急性毒性分析。
在单次剂量急性毒性试验中,给予 2000mg/kg 的 AND-2-HyP--CYD 复合物;在重复经口毒性研究中,给予 200、400 和 666mg/kg 的剂量,持续 28 天。因此,发现 LD50(致死剂量)>2000mg/kg,此外,NOAEL(无观察到不良效应水平)为 666mg/kg。相应地,AND-2-HyP--CYD 复合物的单次急性吸入毒性试验在 5mg/L/4h/day 下进行,亚急性吸入毒性试验在 0.5、1 和 1.66mg/L/4h/day 下进行,持续 28 天。NOAEL 和 LOAEL(最低观察到不良效应水平)分别估计为 0.5mg/L/4h/day 和 1mg/L/4h/day。
本研究的结果将有助于评估和利用 AND-2-HyP--CYD 复合物的药用和治疗益处。