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采用液相色谱-串联质谱法测定人母乳样本中丁丙诺啡和去甲丁丙诺啡的浓度。

Buprenorphine and norbuprenorphine concentrations in human breast milk samples determined by liquid chromatography-tandem mass spectrometry.

作者信息

Grimm Dominik, Pauly Eva, Pöschl Johannes, Linderkamp Otwin, Skopp Gisela

机构信息

Department of Pediatrics, Division of Neonatology, Ruprecht-Karls University, Heidelberg, 69120 Heidelberg, Germany.

出版信息

Ther Drug Monit. 2005 Aug;27(4):526-30. doi: 10.1097/01.ftd.0000164612.83932.be.

Abstract

Buprenorphine (BUP) is considered to be safe during pregnancy. However, the extent of BUP transfer into breast milk has not been investigated thoroughly. Because the drug concentration in the milk is 1 of the determinants in the assessment of the exposure risk, a rapid and sensitive LC-MS/MS method has been developed and evaluated to measure BUP and norbuprenorphine (norBUP) concentrations in milk. A solid-phase and 2 liquid-liquid extraction procedures have been compared. The lower limits of detection and quantification were 0.05 ng/mL and 0.18 ng/mL for BUP and 0.05 ng/mL and 0.20 ng/mL for norBUP, respectively, using a sample volume of 0.5 mL milk. BUP and norBUP concentrations determined from 10 random breast milk samples collected over 4 successive days from a lactating woman during buprenorphine maintenance therapy ranged from 1.0 to 14.7 and 0.6 to 6.3 ng/mL, respectively. Drug exposure of the infant may be considered to be low. Further investigations may seek to extend these preliminary findings to evaluate an infant's level of BUP exposure through breast milk.

摘要

丁丙诺啡(BUP)被认为在孕期是安全的。然而,丁丙诺啡向母乳中的转移程度尚未得到充分研究。由于乳汁中的药物浓度是评估暴露风险的决定因素之一,因此已开发并评估了一种快速灵敏的液相色谱-串联质谱(LC-MS/MS)方法来测定乳汁中丁丙诺啡和去甲丁丙诺啡(norBUP)的浓度。比较了一种固相萃取和两种液液萃取方法。使用0.5 mL乳汁样本时,丁丙诺啡的检测下限和定量下限分别为0.05 ng/mL和0.18 ng/mL,去甲丁丙诺啡的检测下限和定量下限分别为0.05 ng/mL和0.20 ng/mL。在丁丙诺啡维持治疗期间,从一名哺乳期妇女连续4天收集的10份随机母乳样本中测定的丁丙诺啡和去甲丁丙诺啡浓度分别为1.0至14.7 ng/mL和0.6至6.3 ng/mL。婴儿的药物暴露可能被认为较低。进一步的研究可能会寻求扩展这些初步发现,以评估婴儿通过母乳接触丁丙诺啡的水平。

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