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蛋白质结合、脂相分配和不对称转运对药物向人和鼠乳汁中转移的贡献。

Contribution of protein binding, lipid partitioning, and asymmetrical transport to drug transfer into milk in mouse versus human.

机构信息

Department of Pediatrics, The University of Tokyo Hospital Faculty of Medicine, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-8655, Japan.

出版信息

Pharm Res. 2013 Sep;30(9):2410-22. doi: 10.1007/s11095-013-1085-5. Epub 2013 May 31.

Abstract

PURPOSE

Drug transfer into milk is a general concern during lactation. Because data are limited in human subjects, particularly for new drugs, experimental animal models of lactational drug transfer are critical. This study analyzed drug transfer into milk in a mouse model, as well as the contribution of similar and dissimilar host factors.

METHODS

Milk/plasma drug concentration ratios (M/P) in humans were obtained from the literature, while those in mice were determined experimentally after intraperitoneal implantation of osmotic pumps containing drugs of interest. Unbound drug fractions in plasma and milk were determined in vitro for both species.

RESULTS

M/P values were determined for 27 drugs in mice and compared with those in human. These values were increased in mice for 21 drugs; the geometric mean ratio of M/P between mice and humans was 2.03 (95% CI, 1.42-2.89) for all 27 drugs. These results were reasonably explained by the relatively high protein and lipid content in mouse milk. Moreover, species-specific asymmetrical transport systems were suggested for 9 drugs.

CONCLUSIONS

In addition to species-specific differences in milk protein and lipid content, variances in asymmetrical drug transport across the mammary epithelium may yield discordant M/P values in humans and mice.

摘要

目的

哺乳期药物向乳汁中的转移是一个普遍关注的问题。由于人类研究数据有限,特别是对于新药,实验性的哺乳期药物转移动物模型非常重要。本研究分析了一种小鼠模型中的药物向乳汁中的转移情况,以及相似和不同宿主因素的贡献。

方法

从文献中获得了人类乳汁/血浆药物浓度比(M/P),并在小鼠体内通过植入含有研究药物的渗透泵后实验性地确定了 M/P。对于这两种物种,均在体外测定了血浆和乳汁中游离药物部分。

结果

在小鼠中确定了 27 种药物的 M/P 值,并与人类进行了比较。对于 21 种药物,小鼠中的 M/P 值增加;所有 27 种药物的 M/P 值的几何平均值比(小鼠与人类的比值)为 2.03(95%置信区间,1.42-2.89)。这些结果可以通过小鼠乳汁中相对较高的蛋白质和脂质含量得到合理的解释。此外,还提示了 9 种药物存在种属特异性的不对称转运系统。

结论

除了乳汁中蛋白质和脂质含量的种属特异性差异外,跨乳腺上皮的不对称药物转运的差异也可能导致人类和小鼠之间的 M/P 值不一致。

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