河南大学学报(医学版)
河南大學學報(醫學版)
하남대학학보(의학판)
JOURNAL OF HENAN UNIVERSITY (MEDICAL SCIENCE)
2013年
4期
254-257
,共4页
宋卫中%周伟%丁平%刘蔚
宋衛中%週偉%丁平%劉蔚
송위중%주위%정평%류위
高效液相色谱法%保济丸%厚朴酚%和厚朴酚
高效液相色譜法%保濟汍%厚樸酚%和厚樸酚
고효액상색보법%보제환%후박분%화후박분
HPLC%baoji pills%Magnolol%Honokiol
目的:保济丸中厚朴酚、和厚朴酚的含量测定。方法采用 Hypersil ODS 色谱柱(4.6 mm ×250 mm ,25 um),以甲醇-水(78∶22)为流动相,检测波长为294 nm ,测定厚朴酚及和厚朴酚含量。结果厚朴酚在0.226 mg ~0.133 mg 线性关系良好( r =0.9999),平均回收率为97.96%,RSD 为1.80%。和厚朴酚在0.32 mg ~1.60 mg 线性关系良好( r =0.9999),平均回收率为95.88%,RSD 为1.56%。结论该方法稳定,结果可靠,重复性好,可作为保济丸质量控制标准之一。
目的:保濟汍中厚樸酚、和厚樸酚的含量測定。方法採用 Hypersil ODS 色譜柱(4.6 mm ×250 mm ,25 um),以甲醇-水(78∶22)為流動相,檢測波長為294 nm ,測定厚樸酚及和厚樸酚含量。結果厚樸酚在0.226 mg ~0.133 mg 線性關繫良好( r =0.9999),平均迴收率為97.96%,RSD 為1.80%。和厚樸酚在0.32 mg ~1.60 mg 線性關繫良好( r =0.9999),平均迴收率為95.88%,RSD 為1.56%。結論該方法穩定,結果可靠,重複性好,可作為保濟汍質量控製標準之一。
목적:보제환중후박분、화후박분적함량측정。방법채용 Hypersil ODS 색보주(4.6 mm ×250 mm ,25 um),이갑순-수(78∶22)위류동상,검측파장위294 nm ,측정후박분급화후박분함량。결과후박분재0.226 mg ~0.133 mg 선성관계량호( r =0.9999),평균회수솔위97.96%,RSD 위1.80%。화후박분재0.32 mg ~1.60 mg 선성관계량호( r =0.9999),평균회수솔위95.88%,RSD 위1.56%。결론해방법은정,결과가고,중복성호,가작위보제환질량공제표준지일。
Objective Magnolol and Honokiol were identified in baojiwan pills .Methods To detemine the contents of Magnolol in baoji pills by HPLC ,Hypersil ODS column was used ,and methanol water( 78 ∶ 22) as a mobilephase , the detection wave length was at 294 nm . To detemine the contents of Honokiol in baoji pills by HPLC ,Hypersil ODS column was used ,and methanol water( 78 ∶ 22) as a mobilephase ,the detection wave length was at 294 nm . Results Magnolol showed a good linear relationship at a range of 0 .266 mg - 1 .33mg ( r = 0 .9999) , The average recovery was 97 .96% and RSD was1 .80% .Honokiol showed a good linear relationship at a range of 0 .32 mg -1 .6 mg( r = 0 .9999 ) ,The average recovery was 95 .88% and RSD was 1 .56 % .Conclusion The method is accurate and reliable ,and can be used to conrrol the quality of baoji pills .