18</sub> C 250mm×4.6mm , 5μm )色譜柱分離,以甲醇-乙腈 -0.7% 磷酸(30:2:68)作為流動相進行等度洗脫,柱溫 30<sup>q</sup>C ,進樣體積 10μL ,流速 1.0mL/min ,以 403nm 為檢測波長進行檢測。結(jié)果:羥基紅花黃色素A在 32.55~651ng 范圍內(nèi)線性關(guān)系良好( R<sup>2</sup>=1 ),加樣回收率為 100.17%~102.64% ,相對標準偏差(RSD)值為 0.87% 。結(jié)論:該方法操作簡便、準確、重復性好,測定結(jié)果穩(wěn)定,可以作為參芪通絡顆粒中羥基紅花黃色素A的含量測定方法。-龍源期刊網(wǎng)" />

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HPLC法測定參芪通絡顆粒中羥基紅花黃色素A的含量

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【中圖分類號】R284.1 【文獻標志碼】A 【文章編號】1007-8517(2025)11-0052-03

DOI: 10.3969/j . issn.1007-8517.2025.11. zgmzmjyyzz202511011

Determination of Hydroxysafflower Yellow A in Shenqi Tongluo Granules by HPLC

LIN Qunfeng'XU Jie2*ZHANG Huijing2 LI Ning2LI Qiang2 1. , , ,; 2. , ,

Abstract:ObjectiveToestablishahighpeformance liquidchromatographymethodforthequantificationof hydroxysafflower Yellow A in Shenqi Tongluo granules. Methods After dissolved with 50% methanol,ultrasonic, filtered,the test sample was loaded onto a YMC - Triart C18 ( 250mm×4.6mm , 5μm )column to separate with a mobile phase of methanol -acetonitrile -0.7% (2 phosphoric acid(30:2:68),the detection wavelength was 403nm ,the column temperature was 30 C ,the injection volume was 10 (20 μL , the flow rate was 1.0mL/min . Results The calibration curve of hydroxysafflower yellow A showed a good linearity( R2=1 ) in the range of32.55-651 ng.The recoverieswere in the range of100.17%-102.64 % , the relative stard deviations(RSD) was 0.87% .Conclusion The method issimple,accurate,reproduciblestable,can beused forthedeterminationof hydroxysafflower yellow A in Shenqi Tongluo granules.

KeyWords:Shenqi Tongluo Granules;Hydroxysafflower Yellow A;Content Determination;HPLC

參芪通絡顆粒處方來源于壽光市中醫(yī)醫(yī)院臨床經(jīng)驗方。(剩余4235字)

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