首页|HPLC法测定瘀血痹颗粒中丹酚酸B、羟基红花黄色素A、姜黄素和齐墩果酸含量

HPLC法测定瘀血痹颗粒中丹酚酸B、羟基红花黄色素A、姜黄素和齐墩果酸含量

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目的 建立一种可用于瘀血痹颗粒中丹酚酸B、羟基红花黄色素A、姜黄素和齐墩果酸含量测定的HPLC法.方法 采用Shimadzu CLC-ODS C18色谱柱;以乙腈(流动相A)-0.3%磷酸溶液(流动相B)为流动相,程序洗脱;测定波长:丹酚酸B为286 nm,羟基红花黄色素A为403 nm,姜黄素为430 nm,齐墩果酸为205 nm;体积流量1.0 mL·min-1;柱温30℃;进样体积:10μL.结果 丹酚酸B、羟基红花黄色素A、姜黄素和齐墩果酸分别在质量浓度0.096 6~9.660 0、0.125 8~12.580 0、0.098 1~9.810 0、0.958 0~95.800 0 μg·mL-1 内具有良好的线性,平均回收率分别为 99.89%、100.39%、99.94%和 100.01%,RSD 值分别为 0.60%、0.99%、1.01%和0.71%.结论 该方法适用于瘀血痹颗粒制剂的质量控制.
Establishment of HPLC method for determination of salvianolic acid B,hydroxyl safflower yellow A,curcumin and oleanolic acid in Yuxuebi granules
AIM To establish an HPLC method for determining salvianolic acid B,hydroxyl safflower yellow A,curcumin,and oleanolic acid in Yuxuebi granules.METHODS Shimadzu CLC-ODS C18 chromatographic column separation was used.Acetonitrile(mobile phase A)-0.3%phosphoric acid solution(mobile phase B)was used as the mobile phase.Detection wavelengths were set at 286 nm for salvianolic acid B,403 nm for hydroxyl safflower yellow A,430 nm for curcumin,and 205 nm for oleanolic acid.The volume flow rate was set at 1.0 mL·min-1.The column temperature was set at 30℃,and the injection volume was 10 μL.RESULTS The mass concentration showed good linear relationships with the chromatographic peak area in the range of 0.096 6-9.660 0 μg·mL-1(salvianolic acid B),0.125 8-12.580 0μg·mL-1(hydroxyl safflower yellow A),0.098 1-9.810 0 μg·mL-1(curcumin)and 0.958 0-95.800 0 μg·mL-1(oleanolic acid).The average recoveries were 99.89%,100.39%,99.94%,100.01%,with RSD values of 0.60%,0.99%,1.01%,and 0.71%,respectively.CONCLUSION This method could apply to the quality control of Yuxuebi granule preparation.

HPLCYuxuebi granulesalvianolic acid Bhydroxyl safflower yellow Acurcuminoleanolic acid

崔健、李海萍、殷佳蕊

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北京市大兴区人民医院药剂科,北京 102600

HPLC 瘀血痹颗粒 丹酚酸B 羟基红花黄色素A 姜黄素 齐墩果酸

2024

中国临床药学杂志
中国药学会

中国临床药学杂志

CSTPCD
影响因子:0.502
ISSN:1007-4406
年,卷(期):2024.33(2)
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