中国药业
中國藥業
중국약업
China Pharmaceuticals
2015年
17期
55-56
,共2页
肖琦%阳文武%李柏群%张钦%田毅%陈爽
肖琦%暘文武%李柏群%張欽%田毅%陳爽
초기%양문무%리백군%장흠%전의%진상
足光散%苦参碱%高效液相色谱法
足光散%苦參堿%高效液相色譜法
족광산%고삼감%고효액상색보법
Zuguang Powder%martine%HPLC
目的:建立测定足光散中苦参碱含量的高效液相色谱法。方法采用迪马 Diamonsil C18柱(250 mm ×4.6 mm,5μm),以甲醇-0.025 mol/L磷酸二氢钾(7:93)为流动相,流速为0.8 mL/min,测定波长为220 nm。结果供试品溶液主峰的保留时间与对照品溶液主峰的保留时间一致,阴性对照无相应的色谱峰出现。苦参碱质量浓度在21.60~216.00μg/mL( r=0.9999,n=3)范围内与峰面积线性关系良好;平均回收率为98.00%( RSD=1.29%,n=6)。结论该法准确、重复性好,可用于足光散中苦参碱含量的测定。
目的:建立測定足光散中苦參堿含量的高效液相色譜法。方法採用迪馬 Diamonsil C18柱(250 mm ×4.6 mm,5μm),以甲醇-0.025 mol/L燐痠二氫鉀(7:93)為流動相,流速為0.8 mL/min,測定波長為220 nm。結果供試品溶液主峰的保留時間與對照品溶液主峰的保留時間一緻,陰性對照無相應的色譜峰齣現。苦參堿質量濃度在21.60~216.00μg/mL( r=0.9999,n=3)範圍內與峰麵積線性關繫良好;平均迴收率為98.00%( RSD=1.29%,n=6)。結論該法準確、重複性好,可用于足光散中苦參堿含量的測定。
목적:건립측정족광산중고삼감함량적고효액상색보법。방법채용적마 Diamonsil C18주(250 mm ×4.6 mm,5μm),이갑순-0.025 mol/L린산이경갑(7:93)위류동상,류속위0.8 mL/min,측정파장위220 nm。결과공시품용액주봉적보류시간여대조품용액주봉적보류시간일치,음성대조무상응적색보봉출현。고삼감질량농도재21.60~216.00μg/mL( r=0.9999,n=3)범위내여봉면적선성관계량호;평균회수솔위98.00%( RSD=1.29%,n=6)。결론해법준학、중복성호,가용우족광산중고삼감함량적측정。
Objective To establish a method for content determination of martine in Zuguang Powder by HPLC. Methods The Diamonsil C18 column(250 mm ×4. 6 mm,5 μm) was used with the mobile Phase of methanol-0. 025 mol/L Potassium dihydrogen PhosPhate(7:93) at a flow rate of 0. 8 mL/min,the detection wavelength was set at 220 nm. Results The test solution Peak retention time and Peak retention time of the reference solution was consistent with the negative control without the corresPonding Peaks. Martine was linear within 21. 60-216. 00 μg/mL( r=0. 999 9,n=3),and the average recovery rate of martine was 98. 00%( RSD=1. 29%,n=6). Conclusion The method is accurate and better rePeatable,and can be used for the content determination of martine in Zuguang Powder.