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首页> 外文期刊>Journal of chromatography, B. Analytical technologies in the biomedical and life sciences >Sensitive liquid chromatography/tandem mass spectrometry method for the determination of the lipophilic antipsychotic drug chlorpromazine in rat plasma and brain tissue
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Sensitive liquid chromatography/tandem mass spectrometry method for the determination of the lipophilic antipsychotic drug chlorpromazine in rat plasma and brain tissue

机译:灵敏液相色谱/串联质谱法测定大鼠血浆和脑组织中的亲脂性抗精神病药物氯丙嗪

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摘要

A simple, sensitive and robust liquid chromatography/electrospray ionization tandem mass spectrometry (LC-ESI-MS/MS) method was developed and validated for quantification of chlorpromazine in rat plasma and brain tissue. Chlorpromazine was extracted from rat plasma and brain homogenate using liquid-liquid extraction. The compounds were separated on a Waters AtlantiS((TM)) dC-18 (30 turn x 2.1 nun i.d., 3 mu m) column using a mobile phase of acetonitrile/20 mM ammonium formate (pH 4.25 adjusted with formic acid) with gradient elution. Chlorpromazine was detected in positive ion mode using multiple reaction monitoring (MRM). The method was validated and the specificity, linearity, lower limit of quantitation (LLOQ), precision, accuracy, recoveries and stability were determined. The LLOQ was 0.2 ng/ml for plasma and 0.833 ng/g for brain tissue. The method was linear over the concentration range from 0.2 to 200.0 ng/ml for plasma and from 0.833 to 833.3 ng/g for brain tissue. The correlation coefficient (R-2) values were more than 0.998 for both plasma and brain homogenate. The precision and accuracy for intra-day and inter-day were better than 7.54%. The relative and absolute recovery was above 84.9% and matrix effects were lower than 5.6%. This validated method has been successfully used to quantify the rat plasma and brain tissue concentration of chlorpromazine after chronic treatment. (C) 2007 Elsevier B.V. All rights reserved.
机译:开发了一种简单,灵敏且稳定的液相色谱/电喷雾串联质谱(LC-ESI-MS / MS)方法,并验证了该方法可用于定量大鼠血浆和脑组织中的氯丙嗪。从大鼠血浆中提取氯丙嗪,并使用液液提取法从脑匀浆中提取氯丙嗪。使用乙腈/ 20 mM甲酸铵(pH 4.25,用甲酸调节)的流动相,在Waters AtlantiS(TM)dC-18(30 turn x 2.1 nun id,3μm)色谱柱上分离化合物洗脱。使用多反应监测(MRM)以阳离子模式检测氯丙嗪。验证了该方法的有效性,并确定了特异性,线性,定量下限(LLOQ),精密度,准确性,回收率和稳定性。血浆的LLOQ为0.2 ng / ml,脑组织的LLOQ为0.833 ng / g。该方法在血浆浓度范围为0.2至200.0 ng / ml和脑组织浓度范围为0.833至833.3 ng / g范围内是线性的。血浆和脑匀浆的相关系数(R-2)值均大于0.998。日内和日间的准确性和准确性均优于7.54%。相对和绝对回收率高于84.9%,基质效应低于5.6%。这种经过验证的方法已成功用于量化慢性治疗后大鼠血浆和脑组织中氯丙嗪的浓度。 (C)2007 Elsevier B.V.保留所有权利。

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