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安非他酮的胎盘转运与代谢

Transplacental transfer and metabolism of bupropion.

作者信息

Earhart Angela D, Patrikeeva Svetlana, Wang Xiaoming, Abdelrahman Doaa Reda, Hankins Gary D V, Ahmed Mahmoud S, Nanovskaya Tatiana

机构信息

Department of Obstetrics & Gynecology, University of Texas Medical Branch, Galveston, Texas 77555-0587, USA.

出版信息

J Matern Fetal Neonatal Med. 2010 May;23(5):409-16. doi: 10.1080/14767050903168424.

Abstract

OBJECTIVE

In order to evaluate the potential use of bupropion as smoking cessation therapy during pregnancy, the aim of this investigation was to determine transplacental transfer and metabolism of bupropion and its distribution among placental tissue and maternal and fetal circuits of the dually perfused placental lobule.

METHODS

Placentas obtained from healthy term pregnancies were perfused with bupropion at two concentrations 150 ng/ml and 450 ng/ml, along with the marker compound antipyrine 20 microg/ml. Radioactive isotopes of the two drugs were co-transfused to enhance their detection limits. Concentrations of bupropion and its metabolite were determined by liquid chromatography and liquid scintillation spectrometry.

RESULTS

The fetal/maternal concentration ratio of bupropion was 1.07 +/- 0.22. Following 4 h of its perfusion, 48 +/- 6% of bupropion was retained by placental tissue, 32 +/- 5% remained in the maternal circuit, and 20 +/- 6% was transferred to the fetal circuit. A metabolite of bupropion, threohydrobupropion, was identified.

CONCLUSIONS

Bupropion was transferred from the maternal to fetal circuit and was biotransformed by placental tissue enzymes to its metabolite threohydrobupropion. Bupropion and its metabolite did not affect placental tissue viability or functional parameters. These data suggest that bupropion has the potential of being used for smoking cessation during pregnancy and should be further investigated for its safety and efficacy.

摘要

目的

为了评估安非他酮在孕期作为戒烟疗法的潜在用途,本研究旨在确定安非他酮的胎盘转运及代谢情况,以及其在双灌注胎盘小叶的胎盘组织、母体和胎儿循环中的分布。

方法

从健康足月妊娠中获取胎盘,用两种浓度(150纳克/毫升和450纳克/毫升)的安非他酮以及标记化合物安替比林(20微克/毫升)进行灌注。两种药物的放射性同位素共同输注以提高其检测限。通过液相色谱法和液体闪烁光谱法测定安非他酮及其代谢物的浓度。

结果

安非他酮的胎儿/母体浓度比为1.07±0.22。灌注4小时后,48±6%的安非他酮被胎盘组织保留,32±5%留在母体循环中,20±6%转移至胎儿循环。鉴定出安非他酮的一种代谢物——苏-安非他酮。

结论

安非他酮从母体循环转移至胎儿循环,并被胎盘组织酶生物转化为其代谢物苏-安非他酮。安非他酮及其代谢物不影响胎盘组织活力或功能参数。这些数据表明安非他酮有在孕期用于戒烟的潜力,应进一步研究其安全性和有效性。

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