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Validated HPLC method for the determination of tinidazole in human serum and its application in a clinical pharmacokinetic study.

机译:经验证的HPLC方法测定人血清中的替硝唑及其在临床药代动力学研究中的应用。

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摘要

A high performance liquid chromatographic (HPLC) method for the determination of tinidazole in human serum using metronidazole as internal standard (IS) is described. Protein precipitation is used for the preparation of sample. Mobile phase consisting of 0.002 M phosphate buffer, methanol and acetonitrile mixture (85:7.5:7.5/v/v/v) was used at a flow rate of 1 ml/min on a C18 column. The eluate was monitored using an UV/Vis detector set at 320 nm. Ratio of peak area of analyte to IS was used for quantification of serum samples. The absolute recovery was greater than 95% over a concentration range of 0.5 to 30 micrograms/ml and the limit of quantitation was 0.05 microgram/ml. The intra-day relative standard deviation (RSD) measured at 0.5, 5, 15 and 30 micrograms/ml ranged from 0.36 to 6.14%. The inter-day RSD ranged from 1.14 to 4.21%. The method is simple, sensitive and has been successfully used in a pharmacokinetic study conducted in healthy human volunteers.
机译:描述了一种高效液相色谱(HPLC)方法,以甲硝唑为内标(IS)测定人血清中的替硝唑。蛋白质沉淀用于制备样品。在C18色谱柱上以1 ml / min的流速使用由0.002 M磷酸盐缓冲液,甲醇和乙腈混合物(85:7.5:7.5 / v / v / v)组成的流动相。使用设置为320 nm的UV / Vis检测器监控洗脱液。分析物的峰面积与IS的比值用于定量血清样品。在0.5至30微克/毫升的浓度范围内,绝对回收率大于95%,定量限为0.05微克/毫升。以0.5、5、15和30微克/毫升测量的日内相对标准偏差(RSD)为0.36%至6.14%。日间相对标准偏差为1.14%至4.21%。该方法简单,灵敏,已成功用于健康人类志愿者的药代动力学研究中。

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