中国临床药理学杂志
中國臨床藥理學雜誌
중국림상약이학잡지
The Chinese Journal of Clinical Pharmacology
2015年
21期
2134-2136
,共3页
安静%刘洪涛%董占军%张笑丹
安靜%劉洪濤%董佔軍%張笑丹
안정%류홍도%동점군%장소단
利福平%利福喷丁%利福布汀%超高效液相色谱串联质谱%血药浓度
利福平%利福噴丁%利福佈汀%超高效液相色譜串聯質譜%血藥濃度
리복평%리복분정%리복포정%초고효액상색보천련질보%혈약농도
rifampicin%rifapentine%rifabutine%UPLC-MS/MS%blood concentration
目的:建立超高效液相色谱质谱联用法( UPLC-MS/MS)同时测定儿童血浆中利福平、利福喷丁和利福布汀的浓度方法。方法以扎来普隆为内标,血浆样品经乙腈沉淀蛋白处理后检测。 ACQUITY UPLC HSS T3色谱柱(2.1 mm ×100 mm,1.8μm)为分析柱,以乙腈-水(15 mmol? L-1甲酸铵-0.05%甲酸)为流动相,梯度洗脱,用电喷雾离子化源(ESI),以正离子多反应监测(MRM),检测专属性、标准曲线与定量下限、精密度与回收率、基质效应和稳定性。结果利福平、利福喷丁和利福布汀的线性范围分别为100~5000,20~2000,20~2000 ng? mL -1。日内、日间精密度相对标准偏差( RSD )均小于15%。结论本法灵敏、简便、准确,可同时对利福平、利福喷丁及利福布汀进行治疗药物监测。
目的:建立超高效液相色譜質譜聯用法( UPLC-MS/MS)同時測定兒童血漿中利福平、利福噴丁和利福佈汀的濃度方法。方法以扎來普隆為內標,血漿樣品經乙腈沉澱蛋白處理後檢測。 ACQUITY UPLC HSS T3色譜柱(2.1 mm ×100 mm,1.8μm)為分析柱,以乙腈-水(15 mmol? L-1甲痠銨-0.05%甲痠)為流動相,梯度洗脫,用電噴霧離子化源(ESI),以正離子多反應鑑測(MRM),檢測專屬性、標準麯線與定量下限、精密度與迴收率、基質效應和穩定性。結果利福平、利福噴丁和利福佈汀的線性範圍分彆為100~5000,20~2000,20~2000 ng? mL -1。日內、日間精密度相對標準偏差( RSD )均小于15%。結論本法靈敏、簡便、準確,可同時對利福平、利福噴丁及利福佈汀進行治療藥物鑑測。
목적:건립초고효액상색보질보련용법( UPLC-MS/MS)동시측정인동혈장중리복평、리복분정화리복포정적농도방법。방법이찰래보륭위내표,혈장양품경을정침정단백처리후검측。 ACQUITY UPLC HSS T3색보주(2.1 mm ×100 mm,1.8μm)위분석주,이을정-수(15 mmol? L-1갑산안-0.05%갑산)위류동상,제도세탈,용전분무리자화원(ESI),이정리자다반응감측(MRM),검측전속성、표준곡선여정량하한、정밀도여회수솔、기질효응화은정성。결과리복평、리복분정화리복포정적선성범위분별위100~5000,20~2000,20~2000 ng? mL -1。일내、일간정밀도상대표준편차( RSD )균소우15%。결론본법령민、간편、준학,가동시대리복평、리복분정급리복포정진행치료약물감측。
Objective To establish a method for the simultaneous deter-mination of rifampicin, rifapentine and rifabutine in child plasma by UPLC-MS/MS.Methods Zaleplon was used as internal standard. The proteins of plasma samples were precipitated with acetonitrile.The fluid was separated on the ACQUITY UPLC HSS T3 column ( 2.1 mm × 100 mm,1.8 μm) .The mobile phase consisted of acetonitrile and 15 mol? L-1 ammonium formate -0.05% formic acid solution in gradient elution.Electrospray ionization ( ESI) source was applied and operated in the positive multiple reaction monitoring ( MRM) mode.The specificity, standard curve and lower limit of quantitation, precision and recovery rate and stability as well as the matrix effect were investigated.Results The linear ranges of rifampicin, rifapentine, rifabutine were 100-5000, 20-2000, 20-2000 ng? mL-1 , respectively.The intra-day and inter-day precision ( RSDs) were less than 15%.Conclusion The method is sensi-tive, simple and accurate.The therapeutic drug monitoring of three antitu-berculosis drugs could be performed at the same time.