广州化工
廣州化工
엄주화공
GUANGZHOU CHEMICAL INDUSTRY AND TECHNOLOGY
2012年
15期
161-163
,共3页
郑永刚%郁长治%王欢%唐辉
鄭永剛%鬱長治%王歡%唐輝
정영강%욱장치%왕환%당휘
天山花楸%黄酮苷%槲皮素%山柰素%HPLC
天山花楸%黃酮苷%槲皮素%山柰素%HPLC
천산화추%황동감%곡피소%산내소%HPLC
Sorbus tianschanica%flavonoids%quercetin%kaempferol%HPLC
为了建立天山花楸叶中总黄酮苷含量的测定方法,对样品酸水解处理再进行HPLC分析,色谱柱为Waters-C18(150 mm×4.6 mm,5μm),柱温25℃,使用可变波长检测器;流动相为甲醇-乙腈-0.4%磷酸水溶液,梯度洗脱程序为0 min(12∶20∶68)-10 min(52∶0∶48)-18 min(72∶0∶28);流速1.0 mL/min,检测波长为360 nm。结果表明:槲皮素浓度在5.98~47.84μg/mL之间与色谱峰面积呈良好的线性关系,回归方程A=66.96C-5.9964,r=0.9995。平均回收率94.86%,RSD=1.9%;山柰素浓度在4.04~28.28μg/mL之间与色谱峰面积呈良好的线性关系,回归方程A=50.114C-19.529,r=0.9999,平均回收率93.89%,RSD=2.7%;其黄酮苷百分含量为(12.62±0.40)%。该方法干扰少,灵敏,简便,重现性好,可为天山花楸叶的药用开发利用提供质量控制方法。
為瞭建立天山花楸葉中總黃酮苷含量的測定方法,對樣品痠水解處理再進行HPLC分析,色譜柱為Waters-C18(150 mm×4.6 mm,5μm),柱溫25℃,使用可變波長檢測器;流動相為甲醇-乙腈-0.4%燐痠水溶液,梯度洗脫程序為0 min(12∶20∶68)-10 min(52∶0∶48)-18 min(72∶0∶28);流速1.0 mL/min,檢測波長為360 nm。結果錶明:槲皮素濃度在5.98~47.84μg/mL之間與色譜峰麵積呈良好的線性關繫,迴歸方程A=66.96C-5.9964,r=0.9995。平均迴收率94.86%,RSD=1.9%;山柰素濃度在4.04~28.28μg/mL之間與色譜峰麵積呈良好的線性關繫,迴歸方程A=50.114C-19.529,r=0.9999,平均迴收率93.89%,RSD=2.7%;其黃酮苷百分含量為(12.62±0.40)%。該方法榦擾少,靈敏,簡便,重現性好,可為天山花楸葉的藥用開髮利用提供質量控製方法。
위료건립천산화추협중총황동감함량적측정방법,대양품산수해처리재진행HPLC분석,색보주위Waters-C18(150 mm×4.6 mm,5μm),주온25℃,사용가변파장검측기;류동상위갑순-을정-0.4%린산수용액,제도세탈정서위0 min(12∶20∶68)-10 min(52∶0∶48)-18 min(72∶0∶28);류속1.0 mL/min,검측파장위360 nm。결과표명:곡피소농도재5.98~47.84μg/mL지간여색보봉면적정량호적선성관계,회귀방정A=66.96C-5.9964,r=0.9995。평균회수솔94.86%,RSD=1.9%;산내소농도재4.04~28.28μg/mL지간여색보봉면적정량호적선성관계,회귀방정A=50.114C-19.529,r=0.9999,평균회수솔93.89%,RSD=2.7%;기황동감백분함량위(12.62±0.40)%。해방법간우소,령민,간편,중현성호,가위천산화추협적약용개발이용제공질량공제방법。
An method for determination of the content of flavonoid glycosides extracted from Sorbus tianschnica was established.The samples,which were hydrolyzed with acid,were analyzed by RP-HPLC.The analysis was carried out on a waters-C18(4.6 mm×150 mm,5 μm) column,The mobile phase was composed of A(methanol)-phase B(acetonitrile)-phase C(0.4% phosphoric acid water solution) in gradient elution 0 min(12:20:68)-10 min(52:0:48)-18 min(72:0:28) by flow rate of 1.0 mL/min in this method,the detection wave length was set at 360 nm,the VWD was used and the column temperature was 25 ℃.The linear relationship of quercetin was good 5.98~47.84 μg/mL,A=66.96C-5.9964,and r=0.9995.The average recovery was 94.86%,(RSD=1.9%),the linear relationship of kaempferol was good 4.04~28.28 μg/mL,A=50.114C-19.529,and r=0.9999.The average recovery was 93.89%,(RSD=2.7%).The content of flavonoid glycosides was(12.62±0.40)%.This method was simple,sensitive and less interference,reproducible,the utilization of quality control method with the leaf of Sorbus tianschanica.