中国药师
中國藥師
중국약사
CHINA PHARMACIST
2014年
11期
1833-1834,1835
,共3页
刘艳红%程帆%刘地发%杨小玲
劉豔紅%程帆%劉地髮%楊小玲
류염홍%정범%류지발%양소령
超高效液相色谱法%穿心莲内酯磺化物%穿心莲内酯磺化物E%穿心莲内酯磺化物F%含量测定
超高效液相色譜法%穿心蓮內酯磺化物%穿心蓮內酯磺化物E%穿心蓮內酯磺化物F%含量測定
초고효액상색보법%천심련내지광화물%천심련내지광화물E%천심련내지광화물F%함량측정
UPLC%Andrographolide sulfonates%Andrographolide sulfonate E%Andrographolide sulfonate F%Determination
目的:建立超高效液相色谱法( UPLC)同时测定穿心莲内酯磺化物中穿心莲内酯磺化物E、穿心莲内酯磺化物F含量。方法:色谱柱:Shimadzu Shim-pack XR-ODSⅢ(2.0 m ×75 mm,1.6μm);流动相:乙睛(A),磷酸二氢钾缓冲液(B:每1000 ml水中加入磷酸二氢钾1.361 g与庚烷-1-磺酸钠1.0 g)梯度洗脱;流速:0.4 ml·min-1;检测波长:225 nm;柱温:30℃。结果:穿心莲内酯磺化物E在4.39~43.88 g·ml-1(r=1.0000)、穿心莲内酯磺化物F在4.43~44.32μg·ml-1(r=1.0000)范围内,呈良好的线性关系。穿心莲内酯磺化物E平均回收率为98.71%, RSD=1.41%(n=6);穿心莲内酯磺化物F平均回收率为99.29%,RSD=0.76%(n=6)。结论:本法重复性好、灵敏度高、定量准确,可用于穿心莲内酯磺化物的质量控制。
目的:建立超高效液相色譜法( UPLC)同時測定穿心蓮內酯磺化物中穿心蓮內酯磺化物E、穿心蓮內酯磺化物F含量。方法:色譜柱:Shimadzu Shim-pack XR-ODSⅢ(2.0 m ×75 mm,1.6μm);流動相:乙睛(A),燐痠二氫鉀緩遲液(B:每1000 ml水中加入燐痠二氫鉀1.361 g與庚烷-1-磺痠鈉1.0 g)梯度洗脫;流速:0.4 ml·min-1;檢測波長:225 nm;柱溫:30℃。結果:穿心蓮內酯磺化物E在4.39~43.88 g·ml-1(r=1.0000)、穿心蓮內酯磺化物F在4.43~44.32μg·ml-1(r=1.0000)範圍內,呈良好的線性關繫。穿心蓮內酯磺化物E平均迴收率為98.71%, RSD=1.41%(n=6);穿心蓮內酯磺化物F平均迴收率為99.29%,RSD=0.76%(n=6)。結論:本法重複性好、靈敏度高、定量準確,可用于穿心蓮內酯磺化物的質量控製。
목적:건립초고효액상색보법( UPLC)동시측정천심련내지광화물중천심련내지광화물E、천심련내지광화물F함량。방법:색보주:Shimadzu Shim-pack XR-ODSⅢ(2.0 m ×75 mm,1.6μm);류동상:을정(A),린산이경갑완충액(B:매1000 ml수중가입린산이경갑1.361 g여경완-1-광산납1.0 g)제도세탈;류속:0.4 ml·min-1;검측파장:225 nm;주온:30℃。결과:천심련내지광화물E재4.39~43.88 g·ml-1(r=1.0000)、천심련내지광화물F재4.43~44.32μg·ml-1(r=1.0000)범위내,정량호적선성관계。천심련내지광화물E평균회수솔위98.71%, RSD=1.41%(n=6);천심련내지광화물F평균회수솔위99.29%,RSD=0.76%(n=6)。결론:본법중복성호、령민도고、정량준학,가용우천심련내지광화물적질량공제。
Objective:To establish an UPLC method for the simultaneous determination of andrographolide sulfonate E and an-drographolide sulfonate F in andrographolide sulfonates. Methods: The sample was separated on a Shimadzu Shim-pack XR-ODSⅢcolumn (2. 0 m × 75 mm, 1. 6 μm) with acetonitrile( A) and potassium dihydrogen phosphate buffer solution( B:1. 361 g potassium dihydrogen phosphate and 1. 0g heptane-1-sodium sulfonate were dissolved in 1 000 ml water) as the mobile phase with gradient elu-tion, and the flow rate was 0. 4 ml·min-1 ,the column temperature was 30℃, and the detection wavelength was set at 225nm. Re-sults:The linear range of andrographolide sulfonate E was 4. 39-43. 88μg·ml-1(r=1. 000 0) and the average recovery was 98. 71%(RSD=1. 41%, n=6). The linear range of andrographolide sulfonate F was 4. 43-44. 32 g·ml-1(r=1. 000 0) and the average re-covery was 99. 29%(RSD=0. 76%, n=6). Conclusion:The method is reproducible, sensitive and accurate, which can be used in the quality control of andrographolide sulfonates.