18色譜柱(250 mm×4.6 mm,5 μm),流動相甲醇-0.1%磷酸(38:62),檢測波長276 nm,體積流量1.0 mL/min,柱溫30℃,進(jìn)樣量5 μL。結(jié)果 木蝴蝶苷B在0.064 6~1.292 0 μg與峰面積線性關(guān)系良好。木蝴蝶苷B平均回收率為100.67%,RSD值為1.12%。結(jié)論 本法測定快速、結(jié)果準(zhǔn)確、重復(fù)性好、專屬性強(qiáng),可用于測定芪貞慢咽寧顆粒中木蝴蝶苷B。;Objective To establish an HPLC method to determine oroxin B in Qizhen Manyanning Granules. Methods The determination was carried out on Kromasil 100-5 C18 column (250 mm×4.6 mm, 5 μm). The mobile phase consisted of methanol-0.1% phosphoric acid (38:62), and UV detection wavelength was set at 276 nm. The flow rate was 1.0 mL/min and the column temperature was 30℃ with the injection volume of 5 μL. Results There was a good linear relationship between peak area and the content of oroxin B in the rang of 0.064 6-1.292 0 μg. The average recovery of oroxin B was 100.67% with RSD 1.12%. Conclusion The method is rapid, accurate and reproducible for the quantification of oroxin B in Qizhen Manyanning Granules."/>

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首頁 > 過刊瀏覽>2016年第31卷第9期 >2016,31(9):1335-1337. DOI:10.7501/j.issn.1674-5515.2016.09.005
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HPLC法測定芪貞慢咽寧顆粒中木蝴蝶苷B

Determination of oroxin B in Qizhen Manyanning Granules by HPLC

發(fā)布日期:2016-09-23