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HPLC-MS法分析甲苯磺酸拉帕替尼中痕量基因毒性杂质 被引量:12
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作者 张莉 黄丽娜 +1 位作者 黎其荣 杨伟涵 《药物分析杂志》 CAS CSCD 北大核心 2015年第2期317-319,共3页
目的:建立液相色谱-质谱联用方法测定甲苯磺酸拉帕替尼中基因毒性杂质的含量。方法:采用色谱柱C18(4.6 mm×250 mm,5μm),以0.1%甲酸溶液-乙腈(20∶80)为流动相,流速1.0 mL·min^-1,电喷雾离子化(ESI)正离子模式下选择m... 目的:建立液相色谱-质谱联用方法测定甲苯磺酸拉帕替尼中基因毒性杂质的含量。方法:采用色谱柱C18(4.6 mm×250 mm,5μm),以0.1%甲酸溶液-乙腈(20∶80)为流动相,流速1.0 mL·min^-1,电喷雾离子化(ESI)正离子模式下选择m/z252离子进行检测。结果:基因毒性杂质4-(3-氟苯甲氧基)-3-氯苯胺质量浓度在0.08~8 ng·mL^-1范围内,与峰面积线性关系良好(r=1.000);检测限为0.003 6 ng,定量限为0.010 7 ng;样品中基因毒性杂质测定结果的重复性良好,RSD(n=6)为7.5%;基因毒性杂质平均回收率(n=9)为96.6%。结论:本方法操作简便,结果可靠,可以用于甲苯磺酸拉帕替尼中基因毒性杂质4-(3-氟苯甲氧基)-3-氯苯胺含量的检测。 展开更多
关键词 酪氨酸激酶抑制剂 甲苯磺酸拉帕替尼 基因毒性杂质 氟苯甲氧基氯苯胺 液相色谱-质谱联用 痕量杂质检测 杂质控制
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LC-MS法分析多立培南的酸降解产物 被引量:3
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作者 程玉宝 杨伟涵 +1 位作者 张莉 黎其荣 《今日药学》 CAS 2015年第6期401-403,共3页
目的建立液相色谱-质谱法快速分析多立培南在酸性条件下的降解产物。方法借助高效液相色谱-单四级杆质谱仪测定多立培南的酸降解产物,并根据质谱所获得降解产物相对分子质量信息,结合反应机制及相关文献推测降解产物结构。结果多立培南... 目的建立液相色谱-质谱法快速分析多立培南在酸性条件下的降解产物。方法借助高效液相色谱-单四级杆质谱仪测定多立培南的酸降解产物,并根据质谱所获得降解产物相对分子质量信息,结合反应机制及相关文献推测降解产物结构。结果多立培南与酸降解产物能有效分离,3个主要降解产物分别为多立培南开环物、开环二聚物、闭环二聚物。结论该方法快速、灵敏、专属性强,能够有效控制多立培南的质量,并且对多立培南聚合物可以进行准确监控。 展开更多
关键词 多立培南 液相色谱-质谱法 降解产物
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HPLC-MS/MS法分析氟胞嘧啶中痕量基因毒性杂质N,N-二甲基苯胺 被引量:11
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作者 张云峰 钱建钦 王建 《药物分析杂志》 CAS CSCD 北大核心 2017年第2期265-271,共7页
目的:建立液相色谱-质谱联用方法测定氟胞嘧啶中痕量基因毒性杂质N,N-二甲基苯胺的含量。方法:采用C_(18)(2.1 mm×100 mm,1.8μm)色谱柱,以水(含0.1%甲酸)-甲醇(含0.1%甲酸)(95∶5)为流动相,流速0.2 m L·min^(-1),电喷雾离子... 目的:建立液相色谱-质谱联用方法测定氟胞嘧啶中痕量基因毒性杂质N,N-二甲基苯胺的含量。方法:采用C_(18)(2.1 mm×100 mm,1.8μm)色谱柱,以水(含0.1%甲酸)-甲醇(含0.1%甲酸)(95∶5)为流动相,流速0.2 m L·min^(-1),电喷雾离子化(ESI),正离子模式下MRM采集。结果:N,N-二甲基苯胺质量浓度在0.4~10 ng·m L^(-1)范围内,与峰面积线性关系良好(r=0.999 5);检测限为0.1 ng·m L^(-1),定量限为0.4 ng·m L^(-1);平均回收率(n=9)为101.3%。3批样品中N,N-二甲基苯胺的含量均小于0.02μg·g^(-1)。结论:本方法可用于氟胞嘧啶中痕量基因毒性杂质N,N-二甲基苯胺含量的检测。 展开更多
关键词 氟胞嘧啶 基因毒性杂质 N N-二甲基苯胺 液相色谱-质谱联用 杂质控制
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Rapid and sensitive liquid chromatography–tandem mass spectrometric method for the quantitative determination of potentially harmful substance 5,5′-oxydimethylenebis (2-furfural) in traditional Chinese medicine injections 被引量:4
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作者 Qingce Zang Yang Gao +5 位作者 Luojiao Huang Jiuming He Sheng Lin Hongtao Jin Ruiping Zhang Zeper Abliz 《Acta Pharmaceutica Sinica B》 SCIE CAS CSCD 2018年第2期235-241,共7页
With the rapid development and wide application of traditional Chinese medicine injection(TCMI), a number of adverse events of some TCMIs have incessantly been reported and have drawn broad attention in recent years. ... With the rapid development and wide application of traditional Chinese medicine injection(TCMI), a number of adverse events of some TCMIs have incessantly been reported and have drawn broad attention in recent years. Establishing effective and practical analytical methods for safety evaluation and quality control of TCMI can help to improve the safety of TCMIs in clinical applications. In this study, a sensitive and rapid high-performance liquid chromatography–tandem mass spectrometry(HPLC–MS/MS)method has been developed and validated for the quantitative determination of potentially harmful substance5,5′-oxydimethylenebis(2-furfural, OMBF) in TCMI samples. Chromatographic separation was performed on a C18 reversed-phase column(150 mm × 2.1 mm, 5 μm) by gradient elution, using methanol–water containing 0.1% formic acid as mobile phase at the flow rate of 0.3 m L/min. MS/MS detection was performed on a triple quadrupole mass spectrometer with positive electrospray ionization in the multiple reaction-monitoring mode. The method was sensitive with a limit of quantification of 0.3 ng/m L and linear over the range of 0.3–30 ng/m L(r = 0.9998). Intra-and inter-day precision for analyte was o9.52% RSD withrecoveries in the range 88.0–109.67% at three concentration levels. The validated method was successfully applied to quantitatively determine the compound OMBF in TCMIs and glucose injections. Our study indicates that this method is simple, sensitive, practicable and reliable, and could be applied for safety evaluation and quality control of TCMIs and glucose injections. 展开更多
关键词 5 5′-Oxydimethylenebis (2-furfural) lcms/ms Quantitative analytical method Traditional Chinese medicine injection Quality control
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