福建分析测试
福建分析測試
복건분석측시
FUJIAN ANALYSIS & TESTING
2015年
1期
46-49
,共4页
姚志敏%陈秀红%林童%魏玉海
姚誌敏%陳秀紅%林童%魏玉海
요지민%진수홍%림동%위옥해
沙棘粉%儿茶素%均匀设计法%HPLC
沙棘粉%兒茶素%均勻設計法%HPLC
사극분%인다소%균균설계법%HPLC
sea buckthorn powder%catechin%uniform design%HPLC
目的:筛选优化沙棘粉中儿茶素的提取方法,并用HPLC测定其含量。方法:以均匀设计法优化提取条件,采用Agilent ZORBAX SB-C18柱,以甲醇—乙酸溶液(用乙酸调pH值至3.2)(25:75)为流动相,流速1 mL/min;柱温25℃,检测波长280nm。结果:优选出的最佳提取条件:甲醇浓度为74.0%,水浴温度为70℃,超声时间为30min。儿茶素在0.50~10.0μg/mL 浓度范围内线性良好,相关系数(r)为0.9999,平均回收率为97.25%(RSD=1.77%)。结论:本试验建立的含量测定方法操作简便、重现性好且具有较强的专属性。
目的:篩選優化沙棘粉中兒茶素的提取方法,併用HPLC測定其含量。方法:以均勻設計法優化提取條件,採用Agilent ZORBAX SB-C18柱,以甲醇—乙痠溶液(用乙痠調pH值至3.2)(25:75)為流動相,流速1 mL/min;柱溫25℃,檢測波長280nm。結果:優選齣的最佳提取條件:甲醇濃度為74.0%,水浴溫度為70℃,超聲時間為30min。兒茶素在0.50~10.0μg/mL 濃度範圍內線性良好,相關繫數(r)為0.9999,平均迴收率為97.25%(RSD=1.77%)。結論:本試驗建立的含量測定方法操作簡便、重現性好且具有較彊的專屬性。
목적:사선우화사극분중인다소적제취방법,병용HPLC측정기함량。방법:이균균설계법우화제취조건,채용Agilent ZORBAX SB-C18주,이갑순—을산용액(용을산조pH치지3.2)(25:75)위류동상,류속1 mL/min;주온25℃,검측파장280nm。결과:우선출적최가제취조건:갑순농도위74.0%,수욕온도위70℃,초성시간위30min。인다소재0.50~10.0μg/mL 농도범위내선성량호,상관계수(r)위0.9999,평균회수솔위97.25%(RSD=1.77%)。결론:본시험건립적함량측정방법조작간편、중현성호차구유교강적전속성。
Objective:Screening methods to optimize the extraction of catechins sea buckthorn powder,and determine its content by HPLC. Methods:With uniform design to optimize ultrasonic extraction conditions,using Agilent ZORBAX SB-C18 column with methanol - acetic acid solution(pH value adjusted to 3.2 with acetic acid)(25:75)as the mobile phase, flow rate 1 mL / min;column temperature was 25 ℃ The detection wavelength 280nm. Results:The optimum extraction con?ditions optimized concentration of 74.0% for methanol,water bath temperature of 70 ℃,ultrasonic time of 30min. Catechin at 0.50 ~ 10.0μg / mL concentration range good linearity,the correlation coefficient(r)was 0.9999,the average recovery was 97.25%(RSD=1.77%). Conclusion:Method for the determination of the trial established simple,reproducible and has a strong specificity.