海峡药学
海峽藥學
해협약학
STRAIT PHARMACEUTICAL JOURNAL
2015年
7期
30-32
,共3页
紫草素%正交设计%提取工艺%HPLC
紫草素%正交設計%提取工藝%HPLC
자초소%정교설계%제취공예%HPLC
Alkannin%Orthogonal Design%Extraction process%HPLC
目的:正交法优选新疆紫草中紫草素的提取方法。方法以紫草素的含量为指标,用HPLC法测定紫草素的含量,色谱柱:Hedera ODS-2色谱柱(4.6mm ×250mm,5μm);流动相:甲醇:0.05%甲酸-水(80:20);流速:1mL? min -1;检测波长:516nm;进样量:20μL;柱温:30℃。考察提取时间、加醇倍量、温度对紫草素的提取的影响。结果紫草素线性范围是2.5~40.0μg? mL -1, r=0.9999;平均加样回收率为99.96%。紫草中紫草素的最佳提取工艺为:提取4h,10倍量95%乙醇,温度50℃。结论该工艺合理,稳定可行,可为紫草素的提取工艺提供依据。
目的:正交法優選新疆紫草中紫草素的提取方法。方法以紫草素的含量為指標,用HPLC法測定紫草素的含量,色譜柱:Hedera ODS-2色譜柱(4.6mm ×250mm,5μm);流動相:甲醇:0.05%甲痠-水(80:20);流速:1mL? min -1;檢測波長:516nm;進樣量:20μL;柱溫:30℃。攷察提取時間、加醇倍量、溫度對紫草素的提取的影響。結果紫草素線性範圍是2.5~40.0μg? mL -1, r=0.9999;平均加樣迴收率為99.96%。紫草中紫草素的最佳提取工藝為:提取4h,10倍量95%乙醇,溫度50℃。結論該工藝閤理,穩定可行,可為紫草素的提取工藝提供依據。
목적:정교법우선신강자초중자초소적제취방법。방법이자초소적함량위지표,용HPLC법측정자초소적함량,색보주:Hedera ODS-2색보주(4.6mm ×250mm,5μm);류동상:갑순:0.05%갑산-수(80:20);류속:1mL? min -1;검측파장:516nm;진양량:20μL;주온:30℃。고찰제취시간、가순배량、온도대자초소적제취적영향。결과자초소선성범위시2.5~40.0μg? mL -1, r=0.9999;평균가양회수솔위99.96%。자초중자초소적최가제취공예위:제취4h,10배량95%을순,온도50℃。결론해공예합리,은정가행,가위자초소적제취공예제공의거。
OBJECTIVE To optimize the extraction of alkannin from Arnebia euchroma ( Royel) Johnst by or-thogonal design.METHODS Referring to the content of alkannin ,HPLC was employed for the content determina-tion with Hedera ODS-2(4.6mm ×250mm,5μm)and the mobile phase of methanol-0.05%formic acid solution (80∶20 ) at detection wavelength of 516 nm.The column temperature was 30℃and flow rate was 1.0 mL? min -1 .Factors of temperature、times amount of 95%ethanol and extraction time were studied .RESULTS Alkannin had linear in the range between 2.5~40.0μg? mL-1 , r=0.9999;The recovery was 99.96%.The optimal process of extraction was as follows:the extraction time was 4h,adding 10 times 95% ethanol,at 50℃.CONCLUSION The extract process is reasonable and practicable ,which can be used as basis for the extraction process of alkannin .