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作 者:曹宏娟 吴江颖[1] 李国飞[2] CAO Hong-juan;WU Jiang-ying;LI Guo-fei(Department of Intervention,The Fourth Affiliated Hospital of China Medical University,Shenyang 110032,China;Department of Pharmacy,Shengjing Hospital of China Medical University,Shenyang 110004,China)
机构地区:[1]中国医科大学附属第四医院介入科,沈阳110032 [2]中国医科大学附属盛京医院药学部,沈阳110004
出 处:《中国药学杂志》2022年第15期1278-1282,共5页Chinese Pharmaceutical Journal
摘 要:目的 建立同时测定人血浆中吗啡、羟考酮、哌替啶及芬太尼4种治疗药物浓度的方法,并用于治疗药物的监测。方法 血浆样本经乙腈沉淀蛋白后,以氘代吗啡作为内标,应用超高效液相色谱-串联质谱法(UPLC-MS/MS)测定药物浓度。以Agilent Eclipse XDB-C18柱(2.1 mm×50.0 mm, 1.7μm)为色谱柱,甲醇-水(2.0 mmol·L醋酸铵)为流动相等度洗脱,流速为0.3 mL·min^(-1),电喷雾离子源,应用多重反应监测模式进行正离子扫描分析。结果 吗啡、羟考酮、哌替啶及芬太尼的血药浓度在50.0~10 000.0 ng·mL^(-1)内线性关系良好,日内及日间精密度均小于15.0%,提取回收率及基质效应均在85.0%~115.0%内,稳定性等符合要求。结论 该方法灵敏、快速、专属性强,可以用于吗啡、羟考酮、哌替啶及芬太尼治疗药物浓度监测及药动学等方面的研究。OBJECTIVE To establish a UPLC-MS/MS method to simultaneously determine the concentrations of morphine, oxycodone, pethidine and fentanyl in human plasma for therapeutic drug monitoring(TDM). METHODS Morphine-D3 was used as the isotope internal standard. The analytes were extracted from plasma by using acetonitrile and separated using an Agilent Eclipse XDB-C18 column(2.1×50 mm, 1.7 μm) with water containing 2 mmol·Lammonium acetate and methanol as the mobile phase. The flow rate was 0.3 mL·min^(-1). With positive ion electrospray ionization, the analytes were monitored on a triple quadrupole mass spectrometer in MRM mode. RESULTS Calibration curves were obtained over the concentration ranges of 50.0-10 000.0 ng·mL^(-1)for all the analytes, and the intra-and inter-day precision RSDs were <15.0%. The recovery and matrix effect were within the range of 85.0% to 115.0%. Stability was in line with relevant requirements.CONCLUSION The method is proved to be sensitive, rapid, and can be used for TDM and pharmacokinetic studies of morphine, oxycodone, pethidine, and fentanyl.
关 键 词:超高效液相色谱串联质谱 方法学验证 镇痛药物 血浆药物浓度 治疗药物监测
分 类 号:R917[医药卫生—药物分析学]
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