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
  • 在线访问环境研究 (OARE)
  • 打开 J 门
  • 学术钥匙
  • 期刊目录
  • 访问全球在线农业研究 (AGORA)
  • 参考搜索
  • 哈姆达大学
  • 亚利桑那州EBSCO
  • OCLC-世界猫
  • 学者指导
  • SWB 在线目录
  • 普布隆斯
  • 欧洲酒吧
分享此页面

抽象的

Screening the extraction performance of aprotic polar and non-polar solvents on the proportional variances of saturated fatty acids in cassava cell cultures and their cytotoxicity assessment

Nermeen M. Arafa

Cassava plant is one of the major economical crops, involved in lots of industrial applications and therapeutic purposes as suppression of cancer cells activity. Present work targeted to assess saturated fatty acids and their derivatives in cassava cell cultures. The extraction adequacy of aprotic polar (ethylacetate) and non-polar (chloroform, n-hexane) solvents was evaluated. Stem explants of in vitro growing plantlets were induced calli on MS-medium+1mg/l NAA+0.5mg/l BA. Medium containing 5 mg/l 2.4-D and 0.2 mg/l BA was selected for callus productivity.Chloroform callus extract contained mostly fatty acid methyl esters (FAMEs) and fatty acid propyl esters (FAPEs). In contrast n-hexane extract contained higher amounts of fatty acid constituents in free form such as palmitic acid (23.55%). However ethylacetate extract included the highest value of lauric acid (28.34%) in free form as well other fatty acids such as caprylic acid (14.525%), capric acid (2.53%) and enanthic acid (6.41%). Ethylacetate extract conferred the optimal efficiency to suppress the breast cancer cells prevalence (2.63 ug IC50), followed by hexanoic extract (3.44 ug IC50) then chloroformic extract (6 ug IC50) recording the least value for cancer cells propagation. In conclusion, stem calli of cassava plantlets possess essential saturated fatty acids for considerable effectiveness against breast cancer prevalence. For callus induction, stem explants of in vitro growing plantlets were cultured on MS-medium supplemented with 1mg/l NAA+0.5mg/l BA. Stem derived calli were sub-cultured on MS-medium contained 8 mg/l 2,4-D for callus production. Using 5 mg/l 2.4-D + 0.2 mg/l BA visually observed to be the best treatment in callus proliferation after 30 days of cultivation.