色谱
色譜
색보
CHINESE JOURNAL OF CHROMATOGRAPHY
2010年
3期
247-252
,共6页
吴翊民%吴庆政%王晓春%谢增鸿%吴晓苹
吳翊民%吳慶政%王曉春%謝增鴻%吳曉蘋
오익민%오경정%왕효춘%사증홍%오효평
加压毛细管电色谱%亲水作用%整体柱%激光诱导荧光检测%核黄素类物质%血清
加壓毛細管電色譜%親水作用%整體柱%激光誘導熒光檢測%覈黃素類物質%血清
가압모세관전색보%친수작용%정체주%격광유도형광검측%핵황소류물질%혈청
pressurized capillary electrochromatography (pCEC)%hydrophilic interaction (HI)%monolith%laser induced fluorescence detection (LIF)%riboflavin and its derivatives%serum
一种新型的亲水作用毛细管电色谱(HI-CEC)整体柱被应用于加压毛细管电色谱-激光诱导荧光检测(pCEC-LIF)联用法对核黄素类物质的分离分析.采用自组装的pCEC-LIF系统,实现了对痕量核黄素(RF)、黄素单核苷酸(FMN)和黄素腺嘌呤二核苷酸(FAD)的快速分析.在最优的分离检测条件下,3种化合物在8.0 min内完全分离,RF、FMN和FAD的检出限(LOD,S/N=3)分别为5.0×10~(-11) mol/L、8.0×10~(-10) mol/L 和2.5×10~(-9) mol/L,测定线性范围可达3个数量级,精密度良好.方法简便、全分析时间短、灵敏度和选择性高,血清样品分析实验结果良好,可望进一步应用于体液及细胞中核黄素类物质的痕量检测.
一種新型的親水作用毛細管電色譜(HI-CEC)整體柱被應用于加壓毛細管電色譜-激光誘導熒光檢測(pCEC-LIF)聯用法對覈黃素類物質的分離分析.採用自組裝的pCEC-LIF繫統,實現瞭對痕量覈黃素(RF)、黃素單覈苷痠(FMN)和黃素腺嘌呤二覈苷痠(FAD)的快速分析.在最優的分離檢測條件下,3種化閤物在8.0 min內完全分離,RF、FMN和FAD的檢齣限(LOD,S/N=3)分彆為5.0×10~(-11) mol/L、8.0×10~(-10) mol/L 和2.5×10~(-9) mol/L,測定線性範圍可達3箇數量級,精密度良好.方法簡便、全分析時間短、靈敏度和選擇性高,血清樣品分析實驗結果良好,可望進一步應用于體液及細胞中覈黃素類物質的痕量檢測.
일충신형적친수작용모세관전색보(HI-CEC)정체주피응용우가압모세관전색보-격광유도형광검측(pCEC-LIF)련용법대핵황소류물질적분리분석.채용자조장적pCEC-LIF계통,실현료대흔량핵황소(RF)、황소단핵감산(FMN)화황소선표령이핵감산(FAD)적쾌속분석.재최우적분리검측조건하,3충화합물재8.0 min내완전분리,RF、FMN화FAD적검출한(LOD,S/N=3)분별위5.0×10~(-11) mol/L、8.0×10~(-10) mol/L 화2.5×10~(-9) mol/L,측정선성범위가체3개수량급,정밀도량호.방법간편、전분석시간단、령민도화선택성고,혈청양품분석실험결과량호,가망진일보응용우체액급세포중핵황소류물질적흔량검측.
A novel hydrophilic interaction capillary electrochromatographic (HI-CEC) monolith with covalently bonded zwitterionic functional groups was applied for the separation of riboflavins (RF) and its derivatives.With a homemade pressurized capillary electrochromatography-laser induced fluorescence detection (pCEC-LIF) system,trace levels of RF and its derivatives,flavin mononucleotide (FMN) and flavin adenine dinucleotide (FAD),can be baseline separated within 8.0 min in isocratic elution mode.The effect of experimental parameters on separation was investigated.Under the optimum conditions,analytes could be determined over nearly three orders of magnitudes with the detection limits (LODs) as low as 5.0×10~(-11) mol/L (RF),8.0×10~(-10) mol/L (FMN),2.5×10~(-9) mol/L (FAD),and the relative standard deviations (RSDs) were less than 8.2% .This method is rapid,simple,repeatable and more sensitive than the most of reported methods,and satisfied results has been achieved in serum sample.Furthermore,it can be further applied for trace analysis of RF and its derivatives in biological fluid and cells.