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肼屈嗪的经胎盘转运及母乳中的浓度。

Transplacental passage and breast milk concentrations of hydralazine.

作者信息

Liedholm H, Wåhlin-Boll E, Hanson A, Ingemarsson I, Melander A

出版信息

Eur J Clin Pharmacol. 1982;21(5):417-9. doi: 10.1007/BF00542329.

Abstract

The concentration of "real" and "apparent" (= "real" hydralazine + acid-labile hydrazones) hydralazine in maternal and umbilical plasma obtained at delivery of 6 women treated with hydralazine and atenolol for pregnancy hypertension were measured by gas chromatography. In one of the patients, the concentrations of the same substances were subsequently measured in breast milk. "Apparent" hydralazine reached higher levels in umbilical than in maternal blood. The concentration of "real" hydralazine seemed to be at least as high in the fetus as in the mother. On the other hand, even though the fraction of "real" (i.e. presumably active) hydralazine was greater in milk than in plasma, the total concentration was smaller, and the estimated dose per milk feed of 75 ml would not exceed 0.013 mg. Thus, hydralazine treatment of the pregnant woman would expose her fetus to effective concentrations of the drug, but breast feeding would not result in a clinically relevant concentration in the infant.

摘要

采用气相色谱法测定了6例因妊娠高血压接受肼屈嗪和阿替洛尔治疗的孕妇分娩时母体和脐血中“真实”和“表观”(=“真实”肼屈嗪+酸不稳定腙)肼屈嗪的浓度。其中1例患者随后还测定了母乳中相同物质的浓度。“表观”肼屈嗪在脐血中的水平高于母体血液。“真实”肼屈嗪在胎儿体内的浓度似乎至少与母亲体内一样高。另一方面,尽管母乳中“真实”(即可能具有活性)肼屈嗪的比例高于血浆,但总浓度较低,估计每75毫升母乳的给药剂量不会超过0.013毫克。因此,孕妇接受肼屈嗪治疗会使胎儿暴露于有效浓度的药物中,但母乳喂养不会导致婴儿体内出现具有临床意义的浓度。

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