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渗透率文献数据的Meta分析显示了常用方法的可能性和局限性。

Meta-Analysis of Permeability Literature Data Shows Possibilities and Limitations of Popular Methods.

作者信息

Storchmannová Kateřina, Balouch Martin, Juračka Jakub, Štěpánek František, Berka Karel

机构信息

Department of Physical Chemistry, Faculty of Science, Palacký University Olomouc, 17. listopadu 12, 771 46 Olomouc, Czech Republic.

Department of Chemical Engineering, University of Chemistry and Technology, Technická 3, Prague 6, 166 28 Prague, Czech Republic.

出版信息

Mol Pharm. 2025 Mar 3;22(3):1293-1304. doi: 10.1021/acs.molpharmaceut.4c00975. Epub 2025 Feb 20.

Abstract

Permeability is an important molecular property in drug discovery, as it co-determines pharmacokinetics whenever a drug crosses the phospholipid bilayer, e.g., into the cell, in the gastrointestinal tract, or across the blood-brain barrier. Many methods for the determination of permeability have been developed, including cell line assays (CACO-2 and MDCK), cell-free model systems like parallel artificial membrane permeability assay (PAMPA) mimicking, e.g., gastrointestinal epithelia or the skin, as well as the black lipid membrane (BLM) and submicrometer liposomes. Furthermore, many in silico approaches have been developed for permeability prediction: meta-analysis of publicly available databases for permeability data (MolMeDB and ChEMBL) was performed to establish their usability. Four experimental and two computational methods were evaluated. It was shown that repeatability of the reported permeability measurement is not great even for the same method. For the PAMPA method, two different permeabilities are reported: intrinsic and apparent. They can vary in degrees of magnitude; thus, we suggest being extra cautious using literature data on permeability. When we compared data for the same molecules using different methods, the best agreement was between cell-based methods and between BLM and computational methods. Existence of unstirred water layer (UWL) permeability limits the data agreement between cell-based methods (and apparent PAMPA) with data that are not limited by UWL permeability (computational methods, BLM, intrinsic PAMPA). Therefore, different methods have different limitations. Cell-based methods provide results only in a small range of permeabilities (-8 to -4 in cm/s), and computational methods can predict a wider range of permeabilities beyond physical limitations, but their precision is therefore limited. BLM with liposomes can be used for both fast and slow permeating molecules, but its usage is more complicated than standard transwell techniques. To sum up, when working with in-house measured or published permeability data, we recommend caution in interpreting and combining them.

摘要

通透性是药物研发中一项重要的分子特性,因为每当药物穿过磷脂双分子层时,例如进入细胞、在胃肠道中或穿过血脑屏障时,它都会共同决定药物的药代动力学。已经开发出许多测定通透性的方法,包括细胞系测定法(Caco-2和MDCK)、无细胞模型系统,如模拟胃肠道上皮或皮肤的平行人工膜通透性测定法(PAMPA),以及黑色脂质膜(BLM)和亚微米脂质体。此外,还开发了许多用于通透性预测的计算机模拟方法:对公开可用的通透性数据库(MolMeDB和ChEMBL)进行荟萃分析以确定其可用性。评估了四种实验方法和两种计算方法。结果表明,即使对于相同的方法,所报道的通透性测量的重复性也不太好。对于PAMPA方法,报道了两种不同的通透性:固有通透性和表观通透性。它们在数量级上可能有所不同;因此,我们建议在使用通透性的文献数据时格外谨慎。当我们使用不同方法比较相同分子的数据时,基于细胞的方法之间以及BLM和计算方法之间的一致性最好。未搅动水层(UWL)通透性的存在限制了基于细胞的方法(和表观PAMPA)与不受UWL通透性限制的数据(计算方法、BLM、固有PAMPA)之间的数据一致性。因此,不同的方法有不同的局限性。基于细胞的方法仅在较小的通透性范围内(厘米/秒为-8至-4)提供结果,而计算方法可以预测超出物理限制的更宽的通透性范围,但其精度因此受到限制。带有脂质体的BLM可用于快速和慢速渗透分子,但它的使用比标准的Transwell技术更复杂。总之,在处理内部测量或已发表的通透性数据时,我们建议在解释和组合这些数据时要谨慎。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d09/11881145/087724fe7fd6/mp4c00975_0001.jpg

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