广州化工
廣州化工
엄주화공
GUANGZHOU CHEMICAL INDUSTRY AND TECHNOLOGY
2012年
13期
124-126
,共3页
蒙汉富%陈晓军%梁山丹%黄园%廖九明%庞继梅%梁霞
矇漢富%陳曉軍%樑山丹%黃園%廖九明%龐繼梅%樑霞
몽한부%진효군%량산단%황완%료구명%방계매%량하
复方板蓝根口服液%高效液相色谱法%表告依春%含量测定
複方闆藍根口服液%高效液相色譜法%錶告依春%含量測定
복방판람근구복액%고효액상색보법%표고의춘%함량측정
compound banlangen oral solution%HPLC%epigoitrin%content determination
建立了高效液相色谱法测定复方板蓝根口服液中表告依春的含量。采用高效液相色谱法。色谱柱为Aigleng C18柱(250 mm×4.6 mm,5μm);流动相:甲醇-0.01 mol/L磷酸二氢钠缓冲液(氢氧化钠试液调节pH 7.2)(7∶93)流速:1.0 mL/min,检测波长240 nm;柱温:30℃。结果显示:表告依春色谱峰分离良好,表告依春进样量在0.01938~0.3876μg范围内线性关系良好,回归方程:A=7154.3C-22.73,r=0.9999;平均回收率为99.7%,RSD为0.77%(n=6)。该测定方法简便,准确,重现性好,精度高,可用于该制剂的质量控制。
建立瞭高效液相色譜法測定複方闆藍根口服液中錶告依春的含量。採用高效液相色譜法。色譜柱為Aigleng C18柱(250 mm×4.6 mm,5μm);流動相:甲醇-0.01 mol/L燐痠二氫鈉緩遲液(氫氧化鈉試液調節pH 7.2)(7∶93)流速:1.0 mL/min,檢測波長240 nm;柱溫:30℃。結果顯示:錶告依春色譜峰分離良好,錶告依春進樣量在0.01938~0.3876μg範圍內線性關繫良好,迴歸方程:A=7154.3C-22.73,r=0.9999;平均迴收率為99.7%,RSD為0.77%(n=6)。該測定方法簡便,準確,重現性好,精度高,可用于該製劑的質量控製。
건립료고효액상색보법측정복방판람근구복액중표고의춘적함량。채용고효액상색보법。색보주위Aigleng C18주(250 mm×4.6 mm,5μm);류동상:갑순-0.01 mol/L린산이경납완충액(경양화납시액조절pH 7.2)(7∶93)류속:1.0 mL/min,검측파장240 nm;주온:30℃。결과현시:표고의춘색보봉분리량호,표고의춘진양량재0.01938~0.3876μg범위내선성관계량호,회귀방정:A=7154.3C-22.73,r=0.9999;평균회수솔위99.7%,RSD위0.77%(n=6)。해측정방법간편,준학,중현성호,정도고,가용우해제제적질량공제。
HPLC for determining the content of Epigoitrin in Compound Banlangen Oral Solution was established. Stationary phase was Aigleng C18 chromatographic column (4.6 ×250mm, 5μm), mobile phase was methanol -0.01 mol/L sodium dihydrogen phosphate buffer solution ( Adijusted to pH 7.2 with sodium hydroxide solution) ( 7 : 93 ), de- tection wavelength was 240 nm, flow rate was 1.0 mL/min and column temperature was 30℃. Epigoitrin had a good separation of peaks, the calibration curve were linear over the range of 0.01938 -0.3876 μg, and the regression equation was A = 7154.3C - 22.73, r = 0.9999. The average recovery was 99.7% with RSD = 0.77% (n = 6). This method was simple, accurate, with good reproducibility and high precision, and can be used to control the quality of Compound Ban- langen Oral Solution.