Shah Mansi, Bourner Luke, Ali Shariq, Al-Enazy Sanaalarab, Youssef Menatallah M, Fisler Morgan, Rytting Erik
Department of Obstetrics & Gynecology, University of Texas Medical Branch, 301 University Boulevard, Galveston, TX 77555-1062, USA.
Department of Pharmacology and Toxicology, University of Texas Medical Branch, Galveston, TX 77555-1062, USA.
Separations. 2018 Mar;5(1). doi: 10.3390/separations5010009. Epub 2018 Jan 24.
Assessment of drug transport across the placenta is important in understanding the effect of drugs on placental and fetal health. These phenomena can be studied in both in vitro cell lines and ex vivo placental perfusions. We have successfully developed a sensitive yet simple high performance liquid chromatography (HPLC) method coupled with fluorescence detection to determine the concentration of doxorubicin (DXR) in cell culture media for transport studies in human trophoblast cells (BeWo, b30 clone) and in fetal media for placental perfusion experiments. The method was developed based on a protein precipitation technique and was validated in both media types for linearity, intra-day, and inter-day precision and accuracy. The relationship of peak area to concentration was linear with values of 0.99 or greater obtained over the concentration range of 1.5 to 15,000 ng/mL. Despite the high concentrations of albumin in fetal perfusion media (30 mg/mL), the lower limits of detection and quantification for DXR were found to be 1.5 and 5 ng/mL, respectively. This analytical method may be used to study the transport of DXR across BeWo cells and human placenta during placental perfusion studies.
评估药物通过胎盘的转运对于理解药物对胎盘和胎儿健康的影响至关重要。这些现象可以在体外细胞系和离体胎盘灌注实验中进行研究。我们成功开发了一种灵敏且简单的高效液相色谱(HPLC)方法,该方法结合荧光检测,用于测定人滋养层细胞(BeWo,b30克隆)细胞培养基中阿霉素(DXR)的浓度,以进行转运研究,同时也用于胎盘灌注实验中胎儿培养基中DXR浓度的测定。该方法基于蛋白质沉淀技术开发,并在两种培养基类型中针对线性、日内和日间精密度及准确度进行了验证。在1.5至15,000 ng/mL的浓度范围内,峰面积与浓度的关系呈线性,相关系数值为0.99或更高。尽管胎儿灌注培养基中白蛋白浓度很高(30 mg/mL),但DXR的检测限和定量下限分别为1.5和5 ng/mL。这种分析方法可用于在胎盘灌注研究中研究DXR通过BeWo细胞和人胎盘的转运情况。