国际标准期刊号: 2155-9872

分析与生物分析技术杂志

开放获取

我们集团组织了 3000 多个全球系列会议 每年在美国、欧洲和美国举办的活动亚洲得到 1000 多个科学协会的支持 并出版了 700+ 开放获取期刊包含超过50000名知名人士、知名科学家担任编委会成员。

开放获取期刊获得更多读者和引用
700 种期刊 15,000,000 名读者 每份期刊 获得 25,000 多名读者

索引于
  • CAS 来源索引 (CASSI)
  • 哥白尼索引
  • 谷歌学术
  • 夏尔巴·罗密欧
  • 学术期刊数据库
  • 打开 J 门
  • Genamics 期刊搜索
  • 期刊目录
  • 研究圣经
  • 中国知网(CNKI)
  • 乌尔里希的期刊目录
  • 电子期刊图书馆
  • 参考搜索
  • 研究期刊索引目录 (DRJI)
  • 哈姆达大学
  • 亚利桑那州EBSCO
  • OCLC-世界猫
  • 学者指导
  • SWB 在线目录
  • 虚拟生物学图书馆 (vifabio)
  • 普布隆斯
  • 欧洲酒吧
  • ICMJE
分享此页面

抽象的

Acute Toxicity of Aqueous Leaf extract of Newbouldia laevis in Swiss Albino Mice

Ene AC, Aniche CB, Ajuzieogu GI, Elezua VC, Ezeifeka FC

The acute toxicity of aqueous leaf extract of Newbouldia laevis was evaluated in Swiss albino mice. For the first phase, the mice were divided into four groups of three animals each at random. The aqueous leaf extract of Newbouldia laevis was administered both orally and intraperitoneally to the groups in doses of 0, 10, 100, and 1000 mg/kg body weight, respectively. The animals were separated into four groups of three animals each for the second phase of administration, and single doses of the extract at 0, 1600, 2900, and 5000 mg/kg body weight were administered. Animals in both phases were closely monitored for 24 hours and 14 days, respectively. For the animals that got the extract through the oral route, no death was recorded in any of the groups in both phase. The LD50 of the aqueous leaf extract of Newbouldia laevis when administered orally was calculated to be up to 5000 mg/kg. The results indicate that the extract may be safe to be used at high doses through the oral route. For the intraperitoneal administration, no death was recorded in any of the groups in phase I, however, all the animals that got the extract in phase II died within 24 hours after intraperitoneal administration. The LD50 of the aqueous leaf extract of Newbouldia laevis when administered intraperitoneally was calculated to be 1264.9 mg/kg. The results indicate that the extract may be toxic at a high dose in short-term exposure and non-toxic when taken at low doses through the intraperitoneal route.

免责声明: 此摘要通过人工智能工具翻译,尚未经过审核或验证。