化学与生物工程
化學與生物工程
화학여생물공정
CHEMISTRY & BIOENGINEERING
2015年
4期
21-25
,共5页
胡淑曼%付志飞%张培育%李玥嬴%管华诗%刘红兵
鬍淑曼%付誌飛%張培育%李玥嬴%管華詩%劉紅兵
호숙만%부지비%장배육%리모영%관화시%류홍병
龙葵%澳洲茄边碱%响应面法%提取工艺%抗肿瘤活性
龍葵%澳洲茄邊堿%響應麵法%提取工藝%抗腫瘤活性
룡규%오주가변감%향응면법%제취공예%항종류활성
Solanum nigrum L.%solamargine%response surface methodology%extraction process%antitumor activit y
利用响应面法优化龙葵中澳洲茄边碱的提取工艺。采用单因素实验结合 Box-Behnken 中心组合设计,以澳洲茄边碱提取率为指标,考察乙醇体积分数、提取时间、料液比等因素对提取效果的影响。确定龙葵中澳洲茄边碱的最优提取工艺为:乙醇体积分数80%、提取时间2.1 h、料液比1∶12(g∶mL)、提取2次,在此条件下,澳洲茄边碱提取率为0.721 mg·g-1,与理论值(0.712 mg·g-1)相符,表明工艺可行,预测性较好。从龙葵中提取的澳洲茄边碱能明显抑制 K562、HL-60、BGC-823、MCF-7、Hela 等肿瘤细胞的增殖,具有较强的体外抗肿瘤活性。
利用響應麵法優化龍葵中澳洲茄邊堿的提取工藝。採用單因素實驗結閤 Box-Behnken 中心組閤設計,以澳洲茄邊堿提取率為指標,攷察乙醇體積分數、提取時間、料液比等因素對提取效果的影響。確定龍葵中澳洲茄邊堿的最優提取工藝為:乙醇體積分數80%、提取時間2.1 h、料液比1∶12(g∶mL)、提取2次,在此條件下,澳洲茄邊堿提取率為0.721 mg·g-1,與理論值(0.712 mg·g-1)相符,錶明工藝可行,預測性較好。從龍葵中提取的澳洲茄邊堿能明顯抑製 K562、HL-60、BGC-823、MCF-7、Hela 等腫瘤細胞的增殖,具有較彊的體外抗腫瘤活性。
이용향응면법우화룡규중오주가변감적제취공예。채용단인소실험결합 Box-Behnken 중심조합설계,이오주가변감제취솔위지표,고찰을순체적분수、제취시간、료액비등인소대제취효과적영향。학정룡규중오주가변감적최우제취공예위:을순체적분수80%、제취시간2.1 h、료액비1∶12(g∶mL)、제취2차,재차조건하,오주가변감제취솔위0.721 mg·g-1,여이론치(0.712 mg·g-1)상부,표명공예가행,예측성교호。종룡규중제취적오주가변감능명현억제 K562、HL-60、BGC-823、MCF-7、Hela 등종류세포적증식,구유교강적체외항종류활성。
Response surface methodology(RSM)was employed to optimize the extraction process of solama-rgine from Solanum nigrum L..Using extraction rate of solamargine as index,the effects of ethanol volume fraction,extraction time and solid-liquid ratio on extraction efficiency were investigated by single factor experi-ment and Box-Behnken central composite design.The optimum extraction conditions were obtained as follows:ethanol volume fraction 80%,extraction time 2.1 h,solid-liquid ratio 1 ∶ 12(g∶mL),extracting for 2 times. Under above conditions,the extraction rate was 0.721 mg· g-1 ,which was well met with the predictive of 0.712 mg·g-1 .Results showed that the process was feasible and had good predictability.Solamargine extracted from Solanum nigrum L.had obvious inhibitory effects on K562,HL-60,BGC-823,MCF-7 and Hela cell lines, and exhibited significant antitumor activities in vitro .