重庆医学
重慶醫學
중경의학
CHONGQING MEDICAL JOURNAL
2014年
3期
311-313,316
,共4页
王洪波%张梦亮%张芸辉%杨艳%张宝昌
王洪波%張夢亮%張蕓輝%楊豔%張寶昌
왕홍파%장몽량%장예휘%양염%장보창
肌苷%肌酐普拉诺贝%液相色谱-质谱联用法%血浆%药代动力学
肌苷%肌酐普拉諾貝%液相色譜-質譜聯用法%血漿%藥代動力學
기감%기항보랍낙패%액상색보-질보련용법%혈장%약대동역학
inosine%inosine pranobex%liquid chromatography-tandem mass spectrometry%plasma%pharmacokinetics
目的:建立LC-M S/M S测定人血浆中肌苷浓度的方法并应用于异丙肌苷药代动力学研究。方法以阿德福韦为内标,采用甲醇∶10 mmol/L 乙酸铵(15∶85,v/v )为流动相,以Agilent SB-C18柱(5μm粒径,150.0 mm ×4.6 mm I .D .)为分析柱,通过电喷雾电离源(ESI),M RM扫描方式进行检测。用于定量分析的离子反应分别为m/z母离子为267.3,子离子为135.0(肌苷)和m/z母离子为272.0,子离子为134.1(阿德福韦)。结果血浆中肌苷定量的线性范围10~3000 ng/m L ,定量下限为10 ng/mL。日内、日间精密度(RSD)小于5%,平均回收率大于90%,无基质效应。结论本法专属性强,样品处理方便,灵敏度高,适用于肌苷临床药动学研究。
目的:建立LC-M S/M S測定人血漿中肌苷濃度的方法併應用于異丙肌苷藥代動力學研究。方法以阿德福韋為內標,採用甲醇∶10 mmol/L 乙痠銨(15∶85,v/v )為流動相,以Agilent SB-C18柱(5μm粒徑,150.0 mm ×4.6 mm I .D .)為分析柱,通過電噴霧電離源(ESI),M RM掃描方式進行檢測。用于定量分析的離子反應分彆為m/z母離子為267.3,子離子為135.0(肌苷)和m/z母離子為272.0,子離子為134.1(阿德福韋)。結果血漿中肌苷定量的線性範圍10~3000 ng/m L ,定量下限為10 ng/mL。日內、日間精密度(RSD)小于5%,平均迴收率大于90%,無基質效應。結論本法專屬性彊,樣品處理方便,靈敏度高,適用于肌苷臨床藥動學研究。
목적:건립LC-M S/M S측정인혈장중기감농도적방법병응용우이병기감약대동역학연구。방법이아덕복위위내표,채용갑순∶10 mmol/L 을산안(15∶85,v/v )위류동상,이Agilent SB-C18주(5μm립경,150.0 mm ×4.6 mm I .D .)위분석주,통과전분무전리원(ESI),M RM소묘방식진행검측。용우정량분석적리자반응분별위m/z모리자위267.3,자리자위135.0(기감)화m/z모리자위272.0,자리자위134.1(아덕복위)。결과혈장중기감정량적선성범위10~3000 ng/m L ,정량하한위10 ng/mL。일내、일간정밀도(RSD)소우5%,평균회수솔대우90%,무기질효응。결론본법전속성강,양품처리방편,령민도고,괄용우기감림상약동학연구。
Objective To develop a LC-MS/MS method for the determination of inosine in human plasma and to apply it in the isoprinosine pharmacokinetic researches .Methods With adefovir as the internal standard ,methanol -10 mmol/L ammonium ace-tate(15 :85 ,v/v) was adopted as the mobile phase .The chromatographic column was the Agilent SB-C18 column(5 μm ,150 mm × 4 .6 mm I .D .) .Electrospray ionization(ESI) source was applied and the detection was conducted by the multiple-reaction monito-ring(MRM) mode .The ion reactions for the quantitative analysis were m/z 135 .0-267 .3(inosine) and m/z 134 .1-272 .0(adefo-vir) .Results The linear range of plasma inosine was 10-3 000 ng/mL .The lower detection limit was 10 ng/mL .The inter-and in-tra-day precisions(RSD) were less than 5% .The average recovery rate was above 90% without the matrix effect .Conclusion This method has the strong specificity ,convenience in treating the sample and high sensitivity ,and is suitable for the inosine pharmacokinetic re-searches .