中国药品标准
中國藥品標準
중국약품표준
DRUG STANDARDS OF CHINA
2014年
4期
262-265
,共4页
肖浩%严小红%江英桥%侯惠婵
肖浩%嚴小紅%江英橋%侯惠嬋
초호%엄소홍%강영교%후혜선
广升麻%高效液相色谱法%指纹图谱
廣升痳%高效液相色譜法%指紋圖譜
엄승마%고효액상색보법%지문도보
Radix Serratulae Chinensis%HPLC%fingerprint
目的:建立广升麻的HPLC指纹图谱,为广升麻的质量控制提供依据。方法:采用高效液相色谱法,以β-蜕皮甾酮为内参照物,采用色谱柱Agilent C18(3.0 mm ×100 mm,1.8μm),乙腈-0.1%甲酸溶液梯度洗脱,流量为0.4 mL· min-1,检测波长为310 nm,柱温30℃。结果:获得了较为理想的广升麻药材HPLC指纹图谱,确定了13个共有峰。结论:该方法简便、准确、可靠,为评价广升麻药材的质量提供依据。
目的:建立廣升痳的HPLC指紋圖譜,為廣升痳的質量控製提供依據。方法:採用高效液相色譜法,以β-蛻皮甾酮為內參照物,採用色譜柱Agilent C18(3.0 mm ×100 mm,1.8μm),乙腈-0.1%甲痠溶液梯度洗脫,流量為0.4 mL· min-1,檢測波長為310 nm,柱溫30℃。結果:穫得瞭較為理想的廣升痳藥材HPLC指紋圖譜,確定瞭13箇共有峰。結論:該方法簡便、準確、可靠,為評價廣升痳藥材的質量提供依據。
목적:건립엄승마적HPLC지문도보,위엄승마적질량공제제공의거。방법:채용고효액상색보법,이β-세피치동위내삼조물,채용색보주Agilent C18(3.0 mm ×100 mm,1.8μm),을정-0.1%갑산용액제도세탈,류량위0.4 mL· min-1,검측파장위310 nm,주온30℃。결과:획득료교위이상적엄승마약재HPLC지문도보,학정료13개공유봉。결론:해방법간편、준학、가고,위평개엄승마약재적질량제공의거。
Objective:To establish HPLC fingerprint of Radix Serratulae Chinensis.Methods: β-ecdysone was used as the internal standard substance.The reversed phase HPLC system was consisted of a C18 column (3.0 mm ×100 mm,1.8 μm) and a mixture of acetonitrile-0.1%formic acid solution as the mobile phase with gradient elution mode at the flow rate of 0.4 mL· min-1.The absor-bance was monitored at 310 nm and the column temperature was 30℃.Results:A satisfactory method for HPLC fingerprint determina-tion of Radix Serratulae Chinensis was established , 13 characteristic peaks in the HPLC fingerprint were indicated.Conclusion:The method is simple , accurate with good repeatability and can be used as a quality control method for Radix Serratulae Chinensis .