广州化工
廣州化工
엄주화공
GUANGZHOU CHEMICAL INDUSTRY AND TECHNOLOGY
2015年
16期
140-142
,共3页
高效液相色谱法%骨刺片%柚皮苷%芍药苷%含量测定
高效液相色譜法%骨刺片%柚皮苷%芍藥苷%含量測定
고효액상색보법%골자편%유피감%작약감%함량측정
HPLC%Gu CI Tablet%Naringin%Paeoniflorin%contentdetermination
测定骨刺片中柚皮苷、芍药苷的含量。采用HPLC法测定柚皮苷、芍药苷的含量。色谱柱: Inertsil ODS-SP C18(250 mm×4.60 mm,5μm);检测波长:283 nm;流动相:乙腈-0.1%醋酸溶液梯度洗脱;柱温30℃,流速0.8 mL/min;进样量:10μL· mL-1。柚皮苷:线性范围为35.19μg· mL-1~1.7595 mg· mL-1, r=0.99990,平均回收率为102.50%, RSD为0.5%(n=6)。芍药苷:线性范围为35.74μg· mL-1~1.7870 mg· mL-1, r=0.99990,平均回收率为99.79%, RSD为0.9%(n=6)。该方法简便、快速、准确,为提高和完善该制剂的质量标准提供了依据。
測定骨刺片中柚皮苷、芍藥苷的含量。採用HPLC法測定柚皮苷、芍藥苷的含量。色譜柱: Inertsil ODS-SP C18(250 mm×4.60 mm,5μm);檢測波長:283 nm;流動相:乙腈-0.1%醋痠溶液梯度洗脫;柱溫30℃,流速0.8 mL/min;進樣量:10μL· mL-1。柚皮苷:線性範圍為35.19μg· mL-1~1.7595 mg· mL-1, r=0.99990,平均迴收率為102.50%, RSD為0.5%(n=6)。芍藥苷:線性範圍為35.74μg· mL-1~1.7870 mg· mL-1, r=0.99990,平均迴收率為99.79%, RSD為0.9%(n=6)。該方法簡便、快速、準確,為提高和完善該製劑的質量標準提供瞭依據。
측정골자편중유피감、작약감적함량。채용HPLC법측정유피감、작약감적함량。색보주: Inertsil ODS-SP C18(250 mm×4.60 mm,5μm);검측파장:283 nm;류동상:을정-0.1%작산용액제도세탈;주온30℃,류속0.8 mL/min;진양량:10μL· mL-1。유피감:선성범위위35.19μg· mL-1~1.7595 mg· mL-1, r=0.99990,평균회수솔위102.50%, RSD위0.5%(n=6)。작약감:선성범위위35.74μg· mL-1~1.7870 mg· mL-1, r=0.99990,평균회수솔위99.79%, RSD위0.9%(n=6)。해방법간편、쾌속、준학,위제고화완선해제제적질량표준제공료의거。
To determine the content of Naringin and Paeoniflorin in Gu CI Tablet , Naringin and Paeoniflorin were determined on a Inertsil ODS-SP C18 (250 mm ×4.60 mm, 5 μm) column used with the mobile phase of acetonitrile-0.1%acetic acid solution with gradient elution , 283 nm as the detection wavelength , 30 ℃ as the column temperature and 0.8 mL· min-1 as the flow rate.Result showed that the linear range of Naringin was 35.35 μg· mL-1 ~1.7675 mg· mL-1 ( r=0.99990 ).The average recovery was 102.50%( RSD=0.5%, n=6 ).The linear range of Paeoniflorin was 36.19 μg· mL-1 ~1.8095 mg· mL-1 ( r=0.99990 ).The average recovery was 99.79%( RSD=0.9%, n=6 ).The method is simple , accurate and repeatable , and can provide the basis for the improvement and optimization of the quality standard of Gu CI Tablet.