18色譜柱(250 mm×4.6 mm, 5 μm);流動相:乙腈-水(70:30);檢測波長:276 nm;柱溫:50 ℃;體積流量:0.8 mL/min;進樣量:10 μL。結(jié)果 依維莫司在63~1 008 μg/mL線性關(guān)系良好(r=0.999 7), 平均回收率為100.45%, RSD值為0.64%(n=9)。結(jié)論 所建立的操作簡便, 專屬性強, 可用于依維莫司原料藥的質(zhì)量控制。;Objective To establish an HPLC method for determination of everolimus in everolimus active pharmaceutical ingredient. Methods The separation was performed on a Hypersil-ODS C18 column with acetonitrile -water (70:30) as mobile phases. The detection wavelength was set at 276 nm. The column temperature was 50 ℃. The flow rate was 0.8 mL/min with injection volume of 10 μL. Results Everolimus had good linearity in the ranges of 63 — 1 008 μg/mL (r= 0.999 7). The average recovery was 100.45% with RSD 0.64% (n=9). Conclusion The method is simple and specific, and can be used effectively for quality control of everolimus active pharmaceutical ingredient."/>

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首頁 > 過刊瀏覽>2015年第30卷第6期 >2015,30(6):663-665. DOI:10.7501/j.issn.1674-5515.2015.06.012
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HPLC法測定依維莫司原料藥中依維莫司

Determination of everolimus in everolimus active pharmaceutical ingredient by HPLC

發(fā)布日期:2015-06-19