Surveying the content of evodiamine,rutaecarpine and obaculactone in super instant drinking tablet of evodia rutaecarpine with HPLC
Xiao Hu
Abstract
Xiao Hu
Abstract
Objective To determine the content of evodiamine,rutaecarpine and Obaculactone with HPLC.Methods Hypersil ODS2 C 18 column(4.6 mm×250 mm,5μm);Shimadzu LC-20AD HPLC;mobile phase:acetonitrileWater-tetrahydrofuran-glacial acetic acid(34:64.7:1.1:0.2);flow rate:1.0 mL/min;detection wave-length:225 nm;column temperature:30℃.Results The amount of evodiamine,rutaecarpineand obaculactone was respectively at the ranges of 0.101 6~2.032μg(r 2 =0.999 9,n=6),0.097 4 ~ 1.948μg(r 2 =0.999 9,n=6),0.701 0~14.02μg(r 2 =0.999 9,n=6),which showed a good linear correlation between the ranges and the peak areas.The average recovery rate of evodiamine,rutaecarpine and obaculactone was 100.37%(RSD=1.29%,n=6),99.11%(RSD=0.83%,n=6) and 99.30%(RSD=0.52%,n=6).Conclusion The method is easy,fast,accurate and repeatable and should be used in the quality control of super instant drinking tablet of evodia rutaecarpine.
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Objective To determine the content of evodiamine,rutaecarpine and Obaculactone with HPLC.Methods Hypersil ODS2 C 18 column(4.6 mm×250 mm,5μm);Shimadzu LC-20AD HPLC;mobile phase:acetonitrileWater-tetrahydrofuran-glacial acetic acid(34:64.7:1.1:0.2);flow rate:1.0 mL/min;detection wave-length:225 nm;column temperature:30℃.Results The amount of evodiamine,rutaecarpineand obaculactone was respectively at the ranges of 0.101 6~2.032μg(r 2 =0.999 9,n=6),0.097 4 ~ 1.948μg(r 2 =0.999 9,n=6),0.701 0~14.02μg(r 2 =0.999 9,n=6),which showed a good linear correlation between the ranges and the peak areas.The average recovery rate of evodiamine,rutaecarpine and obaculactone was 100.37%(RSD=1.29%,n=6),99.11%(RSD=0.83%,n=6) and 99.30%(RSD=0.52%,n=6).Conclusion The method is easy,fast,accurate and repeatable and should be used in the quality control of super instant drinking tablet of evodia rutaecarpine.
Key concepts: Rutaecarpine, Evodiamine, Chromatography, Medicine, High-performance liquid chromatography, Content determination, Tincture (heraldry), Traditional medicine