国际医药卫生导报
國際醫藥衛生導報
국제의약위생도보
INTERNATIONAL MEDICINE & HEALTH GUIDANCE NEWS
2012年
13期
1947-1948
,共2页
根痛平滴丸%芍药苷%葛根素%高效液相色谱法%含量
根痛平滴汍%芍藥苷%葛根素%高效液相色譜法%含量
근통평적환%작약감%갈근소%고효액상색보법%함량
Root pain ping pills%Paeoniflorin%Puerarin%High performance liquid chromatography%Content
目的 通过采用高效液相色谱法来测定根痛平滴丸中芍药苷和葛根素的含量.方法 应用AgelaTMC18色谱柱,水-甲醇-乙腈为流动相,流速为0.96 ml/min,柱温为30℃,250 nm的检测波长,测定根痛平滴丸中芍药苷和葛根素的含量并作相关分析.结果 本品中每丸含芍药苷不小于0.80 mg,葛根素不小于0.28 mg,芍药苷于59~1150 mg/L,葛根素于9.0~180 mg/L的范围内线性关系好.结论 采用高效液相色谱法测定药物成分含量,操作简单、结果精确,回收率良好和重现性满意,用于根痛平滴丸质量控制可获得良好效果.
目的 通過採用高效液相色譜法來測定根痛平滴汍中芍藥苷和葛根素的含量.方法 應用AgelaTMC18色譜柱,水-甲醇-乙腈為流動相,流速為0.96 ml/min,柱溫為30℃,250 nm的檢測波長,測定根痛平滴汍中芍藥苷和葛根素的含量併作相關分析.結果 本品中每汍含芍藥苷不小于0.80 mg,葛根素不小于0.28 mg,芍藥苷于59~1150 mg/L,葛根素于9.0~180 mg/L的範圍內線性關繫好.結論 採用高效液相色譜法測定藥物成分含量,操作簡單、結果精確,迴收率良好和重現性滿意,用于根痛平滴汍質量控製可穫得良好效果.
목적 통과채용고효액상색보법래측정근통평적환중작약감화갈근소적함량.방법 응용AgelaTMC18색보주,수-갑순-을정위류동상,류속위0.96 ml/min,주온위30℃,250 nm적검측파장,측정근통평적환중작약감화갈근소적함량병작상관분석.결과 본품중매환함작약감불소우0.80 mg,갈근소불소우0.28 mg,작약감우59~1150 mg/L,갈근소우9.0~180 mg/L적범위내선성관계호.결론 채용고효액상색보법측정약물성분함량,조작간단、결과정학,회수솔량호화중현성만의,용우근통평적환질량공제가획득량호효과.
Objective To detect the contents of paeoniflorin and pueratin in root pain ping pills by using high performance liquid chromatography.Methods Agela TMC 18 column was used and water methanol acetonitrile was used as mobile phase,with a flow rate of 0.96 ml / min,column temperature of 30°C,and detection wavelength of 250 nm,to determine the contents of paeoniflorin and puerarin in root pain ping pills; and the related analysis was conducted.Results Paeoniflorin was not less than 0.80 mg and puerarin was not less than 0.28 mg in each pill.Paeoniflorin in 59~ 1150 mg / L and puerarin in 9~180 mg/ L had a good linear relation.Conclusions High performance liquid chromatography for detecting drug content is simple to operate and accurate and has good reproducibility and a satisfied recovery rate.It has a good effect for quality control of root pain ping pillat.