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Drug-protein binding and blood-brain barrier permeability.

机译:药物-蛋白质结合和血脑屏障通透性。

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The permeability surface area (PS) product, an index of permeability of the blood-brain barrier (BBB), was measured by using the in situ perfusion method. In the cerebral circulation, the fraction of drug that permeates into the brain through the BBB is not only the unbound fraction but also the fraction dissociated from the protein in the perfusate. The sum of these two fractions, the apparent exchangeable fraction, was estimated by fitting the parameters of the BBB permeability under the condition of varying BSA concentrations in the perfusate. The unbound fraction of drugs in a buffer containing 0.5 mM BSA was measured by using the ultrafiltration method in vitro, and the apparent exchangeable fraction was measured in vivo by using the intracarotid artery injection method. The apparent exchange fraction was 100% for S-8510, 96.5% for diazepam, 90.9% for caffeine, 38.3% for S-312-d, 33.1% for propranolol, and 6.68% for (+)-S-145 Na, and each of these was higher than the corresponding unbound fraction in vitro in all drugs. The apparent exchangeable fractions, for example, were 8 times higher for diazepam and 38 times for S-312-d than the unbound fractions in vitro. The apparent exchangeable fraction of drugs was also estimated from the parameters obtained with the perfusion method. Because drugs can be infused for an arbitrary length of time in the perfusion method, substances with low permeability can be measured. The apparent exchangeable fractions obtained with this method were almost the same as those obtained with the intracarotid artery injection method.
机译:通透性表面积(PS)乘积是血脑屏障(BBB)的通透性指标,是通过使用原位灌注方法测量的。在脑循环中,通过BBB渗透到大脑中的药物部分不仅是未结合的部分,而且是与灌注液中的蛋白质解离的部分。通过在灌注液中BSA浓度变化的条件下拟合BBB渗透率的参数,可以估算出这两个馏分的总和,即表观可交换馏分。通过体外使用超滤方法测量含有0.5 mM BSA的缓冲液中药物的未结合部分,并通过颈内动脉注射方法在体内测量表观可交换部分。 S-8510的表观交换分数为100%,地西epa为96.5%,咖啡因为90.9%,S-312-d为38.3%,普萘洛尔为33.1%,(+)-S-145 Na为6.68%。在所有药物中,每一种均高于体外相应的未结合部分。例如,在体外,地西epa的表观可交换级分是非结合级分的8倍,S-312-d是38倍。药物的表观可交换分数也由灌注方法获得的参数估算。由于可以通过灌注方法在任意时间长度内注入药物,因此可以测量渗透性低的物质。用这种方法获得的表观可交换级分与用颈动脉内注射方法获得的表观可交换级分几乎相同。

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