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ID:9253261
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页数:29页
时间:2018-04-25
《川芎嗪衍生物tbn的hplc含量测定方法》由会员上传分享,免费在线阅读,更多相关内容在学术论文-天天文库。
1、QuantitativeHPLCAnalyticalMethodforTetramethylpyrazineDerivativeTBNStudentNameMAKSAUHANGStudentNo.MajorSupervisorProfessorWang,YuqiangDate(dd/mm/yyyy)暨南大学本科生毕业论文论文题目川芎嗪衍生物TBN的HPLC含量测定方法学院国际学院学系药学系专业药学姓名学号指导教师StatementofOriginalityIherebydeclarethatthethesispresentedist
2、heresultofresearchperformedbymepersonally,underguidancefrommysupervisor.Thisthesisdoesnotcontainanycontent(otherthanthosecitedwithreferences)thathasbeenpreviouslypublishedorwrittenbyothers,nordoesitcontainanymaterialpreviouslypresentedtoothereducationalinstitutionsford
3、egreeorcertificatepurposetothebestofmyknowledge.Ipromisethatallfactspresentedinthisthesisaretrueandcreditable.Signed:_________________Date:QuantitativeHPLCanalyticalmethodfortetramethylpyrazinederivativeTBNAbstract:Ahigh-performanceliquidchromatography(HPLC)methodforan
4、ewtetramethylpyrazinederivative,TBN,wasdeveloped.Analyticalperformanceparameterssuchaslinearity,precision,accuracy,specificity,limitofdetection(LOD)andlimitofquantification(LOQ)weredeterminedundertheguidelineofInternationalConferenceonHarmonizationQ2B[1].TBNwasanalyzed
5、byRP-HPLCwithC18columnusingmethanol-water(35:65)asmobilephase.Theflowrateis0.8ml/minandthedetectorwassetto295nm.Thelinearityofcalibrationcurveisgood(r2>0.999)andtheLODandLOQwere12.096ng/mland40.32ng/mlrespectively.Therelativestandarddeviation(RSD)ofprecisionandaccuracy
6、were0.1245%and0.6895%,respectively,andthesamplerecoverywas99.08%(RSD:0.40%).ThismethodisreliableandeasyforTBNanalysis.KeyWords:tetramethylpyrazinederivative,TBN,HPLC川芎嗪衍生物TBN的HPLC含量测定方法摘要:目的:建立川芎嗪衍生物(TBN)高效液相含量测定方法。方法:选用C-18色谱柱;甲醇-水(35:65);流速:0.8ml/min;检测波长为295nm。结果:TB
7、N在12.42-310.5mg/ml范围内线性关系良好(r2>0.999);定量限和检测限分别为12.096ng/ml及40.32ng/ml;精密度及准确度RSD分别为0.1245%及0.6895%;加样回收率结果为99.08%(RSD:0.40%)。结论:本方法简便可靠,可作为TBN之定量分析方法。关键词:川芎嗪衍生物,TBN,高效液相Contents1.Introduction32.Materials32.1.Chemicals32.2.Apparatus33.ExperimentalMethod33.1.TBNstandard
8、preparation33.1.1.ColumnchromatographyforTBNpurification33.1.2.Semi-preparativecolumnchromatography33.2.Developmentof
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