Jeffrey P, Summerfield S G
Neurology & GI Centre of Excellence for Drug Discovery, GlaxoSmithKline, Harlow, UK.
Xenobiotica. 2007 Oct-Nov;37(10-11):1135-51. doi: 10.1080/00498250701570285.
Whilst blood-brain barrier permeability is an important determinant in achieving efficacious central nervous system drug concentrations, it should not be viewed or measured in isolation. Recent studies have highlighted the need for an integrated approach where optimal central nervous system penetration is achieved through the correct balance of permeability, a low potential for active efflux, and the appropriate physicochemical properties that allow for drug partitioning and distribution into brain tissue. Integrating data from permeability studies performed incorporating an assessment of active efflux by P-glycoprotein in combination with drug-free fraction measurements in blood and brain has furthered the understanding of the impact of the blood-brain barrier on central nervous system uptake and the underlying physicochemical properties that contribute to central nervous system drug disposition. This approach moves away from screening and ranking compounds in assays designed to measure or predict central nervous system penetration in the somewhat arbitrary units of brain-blood (or plasma) ratios.
虽然血脑屏障通透性是实现有效中枢神经系统药物浓度的重要决定因素,但不应孤立地看待或衡量它。最近的研究强调了采用综合方法的必要性,即通过通透性的正确平衡、低主动外排潜力以及允许药物在脑组织中分配和分布的适当物理化学性质来实现最佳的中枢神经系统渗透。将通透性研究的数据与通过P-糖蛋白评估主动外排以及血液和脑组织中游离药物分数测量相结合,进一步加深了对血脑屏障对中枢神经系统摄取的影响以及有助于中枢神经系统药物处置的潜在物理化学性质的理解。这种方法摒弃了在旨在以脑血(或血浆)比率的任意单位测量或预测中枢神经系统渗透的试验中对化合物进行筛选和排名的做法。