现代医药卫生
現代醫藥衛生
현대의약위생
MODERN MEDICINE HEALTH
2014年
15期
2252-2253
,共2页
何银舟%葛婷婷%柴尧%程建明
何銀舟%葛婷婷%柴堯%程建明
하은주%갈정정%시요%정건명
色谱法,高压液相%车前%复方%皂苷类/分析
色譜法,高壓液相%車前%複方%皂苷類/分析
색보법,고압액상%차전%복방%조감류/분석
Chromatography,high pressure liquid%Plantago asiatica%Compounds(TCD)%Saponins/analysis
目的:建立荔之咽滴丸中高车前苷含量的高效液相色谱(HPLC)测定方法,为荔之咽滴丸的质量控制提供依据。方法色谱柱:Hedera ODS-2(250.0 mm×4.6 mm,5μm);流动相:甲醇∶0.5%冰醋酸水溶液(50∶50);柱温:30℃;流速:1.0 mL/min;检测波长:335 nm;进样量:10μL。结果高车前苷在0.20~2.52μg时呈良好的线性关系,相关系数(r)=0.9998;平均回收率为99.80%,其相对标准偏差(RSD)为2.35%。结论 HPLC用于测定荔之咽滴丸中高车前苷含量,方法简便、准确、专属性强、重复性好,能起到控制荔之咽滴丸中高车前苷含量的作用。
目的:建立荔之嚥滴汍中高車前苷含量的高效液相色譜(HPLC)測定方法,為荔之嚥滴汍的質量控製提供依據。方法色譜柱:Hedera ODS-2(250.0 mm×4.6 mm,5μm);流動相:甲醇∶0.5%冰醋痠水溶液(50∶50);柱溫:30℃;流速:1.0 mL/min;檢測波長:335 nm;進樣量:10μL。結果高車前苷在0.20~2.52μg時呈良好的線性關繫,相關繫數(r)=0.9998;平均迴收率為99.80%,其相對標準偏差(RSD)為2.35%。結論 HPLC用于測定荔之嚥滴汍中高車前苷含量,方法簡便、準確、專屬性彊、重複性好,能起到控製荔之嚥滴汍中高車前苷含量的作用。
목적:건립려지인적환중고차전감함량적고효액상색보(HPLC)측정방법,위려지인적환적질량공제제공의거。방법색보주:Hedera ODS-2(250.0 mm×4.6 mm,5μm);류동상:갑순∶0.5%빙작산수용액(50∶50);주온:30℃;류속:1.0 mL/min;검측파장:335 nm;진양량:10μL。결과고차전감재0.20~2.52μg시정량호적선성관계,상관계수(r)=0.9998;평균회수솔위99.80%,기상대표준편차(RSD)위2.35%。결론 HPLC용우측정려지인적환중고차전감함량,방법간편、준학、전속성강、중복성호,능기도공제려지인적환중고차전감함량적작용。
Objective To establish determination method of homoplantaginin content in the Lizhiyan dropping pills by high performance liquid chromatography(HPLC),in ordetr to provide a basis for the quality control of Lizhiyan dropping pills. Methods The chromatographic column:Hedera ODS-2(250.0 mm × 4.6 mm,5μm);mobile phase:methanol∶0.5%glacial acetic acid(50∶50);column temperature:30℃;flow rate:1.0 mL/min;detection wavelength:335 nm;injection volume:10μL. Results Homoplantaginin showed a good linear relationship when the injection volume was within 0.20-2.52 μg with the correlation coeffi-cient of 0.999 8;the average recovery rate was 99.8%,and the relative standard deviation (RSD) was 2.35%. Conclusion This method is simple,accurate,specific and repeatable,and it has contribution to control the content of homoplantaginin in the Lizhiyan dropping pills.