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Nanodelivery of drugs for therapeutic strategies in CNS disorders. Current and Future perspectives

机译:CNS疾病治疗策略的药物纳米次数。 当前和未来的观点

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In this innovation, we examined sleep deprivation (SD) induced brain pathology and therapeutic strategies to induce neuroprotction using nanodelivery of cerebrolysin. SD is a serious problem in military and we have previously shown that SD of 12 to 48 h causes blood-brain barrier (BBB) disruption, brain edema formation and neuronal damages after 48 h SD. Measurement of BDNF showed 50 to 60 % decline in different brain areas in SD. Nanowired delivery of cerebrolysin 4 to 6 h after the onset of SD significantly reduced brain pathology and enhanced regional BDNF levels after 48 h SD. However, normal cerebrolysin given after the onset of SD has only minimal effects on regional BDNF level and brain pathology seen at 48 h SD. This indicates that nanodelivery of drugs have superior effects in achieving neuroprotection. Thus, we feel that our policy makers, researchers, clinicians and nanotechnologists should consider exploring the dose response relationship of nanoparticles from wide variety of nanocarriers on cellular toxicity both in vivo and in vitro situations urgently. These studies will help create a database for suitable nanocarriers to use for drug delivery to the CNS as effective therapeutic tools for clinical practice. Only after these data, nanoneuropharmacology could be developed as a distinct discipline in the near future
机译:在这项创新中,我们检查了睡眠剥夺(SD)诱导的大脑病理和治疗策略,以使用大脑蛋白的纳米次数诱导神经间隙。 SD是军事中的一个严重问题,我们之前已经表明,12至48小时的SD会导致血脑屏障(BBB)中断,脑水肿形成和48小时后的神经元损伤。 BDNF的测量显示SD中不同脑区的下降50%至60%。在48小时后,纳米乳蛋白酶4至6小时明显减少脑病理和增强的区域BDNF水平。然而,SD发作后给出的正常脑蛋白对48小时SD的区域BDNF水平和脑病学具有最小的影响。这表明药物的纳米次数在实现神经保护作用方面具有优异的效果。因此,我们觉得我们的政策制定者,研究人员,临床医生和纳米技术学家应考虑迫切地和体外情况探讨纳米颗粒在各种纳米载体中的纳米粒子的剂量反应关系。这些研究将有助于为合适的纳米载体创建一个数据库,以用于药物递送给CNS作为临床实践的有效治疗工具。只有在这些数据之后,纳尼科医生才能在不久的将来发展成为一种独特的纪律

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