毛细管电泳法测定产程和分娩过程中青霉素G含量

Andrea Thomas , Omon K. Ukpoma , Jennifer A. Inman , Anil K. Kaul , James H. Beeson , Kenneth P. Roberts
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引用次数: 12

摘要

在本研究中,毛细管电泳(CE)方法作为一种手段,以测量青霉素G (PCN G)在分娩和分娩的B群链球菌(GBS)阳性孕妇。这项发展研究的志愿者在分娩开始时被给予500万单位的PCN G。在分娩期间和分娩后收集尿液、血液和羊水样本。样品采用Waters tC18 SepPak 3cc固相萃取(SPE)半纯化,采用磷酸钠/甲醇阶梯梯度洗脱。采用毛细管电泳或反相高效液相色谱(RP-HPLC)结合二极管阵列吸光度检测,在30 min内分离样品。建立线性动态范围的校准曲线,定量。tC18固相萃取方法提供了大量的样品清理和高回收率的PCN G(~ 90%)。结果发现,在使用反相高效液相色谱时,SPE对于保持分离柱的完整性至关重要,但对于没有固定相存在的CE样品分析则不是必需的。定量结果从母体尿液中PCN - G的毫摩尔浓度到羊水中的微摩尔浓度不等。血清和脐带血PCN G水平低于定量限制,这可能是由于抗生素给药后样本收集的时间延长。这些结果表明CE可以作为一种简单有效的表征分娩过程中PCN G在母体到胎儿体内药代动力学分布的方法。预计类似的方法有可能提供一种快速、简单和具有成本效益的方法来监测妊娠期间PCN G和其他药物的临床疗效。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Quantification of penicillin G during labor and delivery by capillary electrophoresis

In this study, a capillary electrophoresis (CE) method was developed as a means to measure levels of penicillin G (PCN G) in Group B Streptococcus (GBS) positive pregnant women during labor and delivery. Volunteers for this developmental study were administered five million units of PCN G at the onset of labor. Urine, blood, and amniotic fluid samples were collected during labor and post delivery. Samples were semi-purified by solid-phase extraction (SPE) using Waters tC18 SepPak 3 cc cartridges with a sodium phosphate/methanol step gradient for elution. Capillary electrophoresis or reversed-phase high-performance liquid chromatography (RP-HPLC) with diode-array absorbance detection were used to separate the samples in less than 30 min. Quantification was accomplished by establishing a calibration curve with a linear dynamic range. The tC18 SPE methodology provided substantial sample clean-up with high recovery yields of PCN G (∼ 90%). It was found that SPE was critical for maintaining the integrity of the separation column when using RP-HPLC, but was not necessary for sample analysis by CE where no stationary phase is present. Quantification results ranged from millimolar concentrations of PCN G in maternal urine to micromolar concentrations in amniotic fluid. Serum and cord blood levels of PCN G were below quantification limits, which is likely due to the prolonged delay in sample collection after antibiotic administration. These results show that CE can serve as a simple and effective means to characterize the pharmacokinetic distribution of PCN G from mother to unborn fetus during labor and delivery. It is anticipated that similar methodologies have the potential to provide a quick, simple, and cost-effective means of monitoring the clinical efficacy of PCN G and other drugs during pregnancy.

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