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Bio-Analytical Liquid Chromatographic Method for the Determination of Linezolid in Plasma

机译:生物分析液相色谱法测定血浆中利奈唑胺

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摘要

An isocratic selective and sensitive high performance liquid chromatographic method for the estimation of linezolid in human plasma by precipitation of plasma proteins with 5 % perchloric acid, after precipitation the supernatant was separated and injecting 10 uL of sample volume. The chromatography separation was achieved on a Hypersil BDS C_(18) (4.6 ID x 250 mm, 5 μ particle size) column using a mixture of 20 Mm potassium dihydrogen phosphate buffer (pH 3.5 ± 0.1) and acetonitrile in a ratio of 85:15 (v/v) as the mobile phase. The column elutes were monitored at 252 nm. The total chromatographic run time was 12.5 min and the elution of linezolid and zidovudine (IS) retention times 10.5 and 5.2 respectively. The method was found to be linear in the concentration range of 50.0 to 20059.9 ng/mL. The method was successfully applied to in vitro pharmacokinetic-bioequivalence studies.
机译:等度选择性和灵敏的高效液相色谱法,通过用5%高氯酸沉淀血浆蛋白来估算人血浆中的利奈唑胺,沉淀后分离上清液并注入10 uL样品量。色谱分离是在Hypersil BDS C_(18)(4.6 ID x 250 mm,5μm粒径)色谱柱上使用比例为85:20的20 Mm磷酸二氢钾缓冲液(pH 3.5±0.1)和乙腈的混合物完成的15(v / v)作为流动相。在252 nm处监测柱洗脱液。总色谱运行时间为12.5分钟,洗脱的利奈唑胺和齐多夫定(IS)保留时间分别为10.5和5.2。发现该方法在50.0至20059.9 ng / mL的浓度范围内是线性的。该方法已成功应用于体外药代动力学-生物等效性研究。

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