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Influence of Chronobiology on the Nanoparticle-Mediated Drug Uptake into the Brain

机译:时序生物学对纳米颗粒介导的脑部药物吸收的影响

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摘要

Little attention so-far has been paid to the influence of chronobiology on the processes of nanoparticle uptake and transport into the brain, even though this transport appears to be chronobiologically controlled to a significant degree. Nanoparticles with specific surface properties enable the transport across the blood–brain barrier of many drugs that normally cannot cross this barrier. A clear dependence of the central antinociceptive (analgesic) effects of a nanoparticle-bound model drug, i.e., the hexapeptide dalargin, on the time of day was observable after intravenous injection in mice. In addition to the strongly enhanced antinociceptive effect due to the binding to the nanoparticles, the minima and maxima of the pain reaction with the nanoparticle-bound drug were shifted by almost half a day compared to the normal circadian nociception: The maximum in the pain reaction after i.v. injection of the nanoparticle-bound dalargin occurred during the later rest phase of the animals whereas the normal pain reaction and that of a dalargin solution was highest during the active phase of the mice in the night. This important shift could be caused by an enhanced endo- and exocytotic particulates transport activity of the brain capillary endothelial cells or within the brain during the rest phase.
机译:迄今为止,尽管时间生物学对纳米生物学的摄取和向大脑的传输过程的影响很少受到关注,尽管这种传输似乎在很大程度上是按时间生物学控制的。具有特定表面特性的纳米颗粒可以使许多通常无法通过该屏障的药物跨血脑屏障转运。在小鼠中静脉内注射后,可以观察到纳米颗粒结合的模型药物,即六肽达拉根的中枢抗伤害感受(镇痛)作用在一天中的明显依赖性。除了由于与纳米颗粒的结合而大大增强了止痛作用外,与正常的昼夜节律感受相比,与纳米颗粒结合的药物引起的疼痛反应的最小值和最大值也偏移了将近半天: iv后纳米颗粒结合的达拉金注射液在动物的其余休息阶段发生,而正常的疼痛反应和达拉金溶液的疼痛反应在小鼠的活跃期最高。这种重要的变化可能是由于在休息阶段大脑毛细血管内皮细胞或大脑内部的胞内和胞外颗粒运输活动增强所致。

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