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
2014年
6期
556-558
,共3页
贾萌萌%何晓梦%周莹%吴义来%李虎群%黎维勇
賈萌萌%何曉夢%週瑩%吳義來%李虎群%黎維勇
가맹맹%하효몽%주형%오의래%리호군%려유용
硝苯地平%高效液相色谱-质谱联用%血药浓度%药代动力学
硝苯地平%高效液相色譜-質譜聯用%血藥濃度%藥代動力學
초분지평%고효액상색보-질보련용%혈약농도%약대동역학
nifedipine%HPLC-MS/MS%plasma concentration%phar-macokinetic
目的:建立测定人血浆中硝苯地平的高效液相色谱-质谱联用( HPLC-MS/MS)方法。方法血浆样品经乙腈沉淀蛋白提取分离,色谱柱为Utimat AQ-C18,流动相为乙腈-20 mmol · L-1醋酸铵(58∶42),流速为0.30 mL· min-1,柱温:40℃,电喷雾负离子源( ESI -),用多反应离子检测( MRM)。结果硝苯地平线性范围为0.03~80.00 ng · mL-1,定量下限为0.03 ng · mL-1,提取回收率在94.7%~102.3%,日内、日间RSD均小于9.8%。结论本方法专属性强,灵敏度高,操作简便、快速、准确,适用于硝苯地平缓释片药代动力学研究。
目的:建立測定人血漿中硝苯地平的高效液相色譜-質譜聯用( HPLC-MS/MS)方法。方法血漿樣品經乙腈沉澱蛋白提取分離,色譜柱為Utimat AQ-C18,流動相為乙腈-20 mmol · L-1醋痠銨(58∶42),流速為0.30 mL· min-1,柱溫:40℃,電噴霧負離子源( ESI -),用多反應離子檢測( MRM)。結果硝苯地平線性範圍為0.03~80.00 ng · mL-1,定量下限為0.03 ng · mL-1,提取迴收率在94.7%~102.3%,日內、日間RSD均小于9.8%。結論本方法專屬性彊,靈敏度高,操作簡便、快速、準確,適用于硝苯地平緩釋片藥代動力學研究。
목적:건립측정인혈장중초분지평적고효액상색보-질보련용( HPLC-MS/MS)방법。방법혈장양품경을정침정단백제취분리,색보주위Utimat AQ-C18,류동상위을정-20 mmol · L-1작산안(58∶42),류속위0.30 mL· min-1,주온:40℃,전분무부리자원( ESI -),용다반응리자검측( MRM)。결과초분지평선성범위위0.03~80.00 ng · mL-1,정량하한위0.03 ng · mL-1,제취회수솔재94.7%~102.3%,일내、일간RSD균소우9.8%。결론본방법전속성강,령민도고,조작간편、쾌속、준학,괄용우초분지평완석편약대동역학연구。
Objective To establish a HPLC-MS/MS method for deter-mination of nifedipine in human plasma.Methods After protein precip-itation, the plasma was separated on an Utimat AQ -C18 column, with a mobile phase of acetonitrile -20 mmol · L-1 ammonium acetate ( 58∶42 ) .The flow rate was 0.30 mL · min-1 and the column temperature 40 ℃.Quantification was performed in the negative ion multiple -reac-tion-monitoring ( MRM ) mode.Results Determination of nifedipine had good linearity in the concentration range of 0.03 -80 ng · mL-1.The lower limit of quantization was 0.03 ng · mL-1 , extraction recovery rate was from 94.71% to 102.3%, and the intra -day and inter -day RSD were both less than 9.8%.Conclusion This method is specific , simple, sensitive, rapid, accurate and suitable for determination of nife-dipine in human plasma.