Pharmacokinetics of Therapeutic Nanoparticles in the CNS

描述（由申请人提供）：中枢神经系统（CNS）内神经元的进行性变性对这些细胞控制的正常功能具有深远的负面影响，特别是对个体的整体功能。有许多影响大脑的神经退行性疾病，包括阿尔茨海默病、帕金森病、亨廷顿病等。作为中枢神经系统的另一部分，视网膜的神经元变性也发生在许多疾病中，包括老年性黄斑变性、色素性视网膜炎、糖尿病视网膜病变等。这些神经退行性疾病似乎都是由独特的原发性缺陷引起的，这些缺陷导致神经元慢性或急性暴露于活性氧中间体（ROI）。这些氧化代谢的有毒产物激活了细胞自杀途径-细胞凋亡。这一研究领域的一个普遍目标是找到破坏或清除ROI的分子，以期减缓或停止这些疾病的进展。我们假设特定的无机纳米颗粒，由于它们的活性、尺寸（~5nm）、纳米粒子状态、不溶解性和无机性质，将能够进入细胞并清除ROI，从而防止细胞凋亡的激活和死亡。我们的初步数据表明，这些特定的纳米颗粒可以在试管中破坏ROI，在培养的视网膜神经元中破坏ROI，并可以防止体内ROI介导的视网膜变性。该项目的总体目标是确定这些纳米颗粒的药代动力学（分布和周转），以验证我们的假设，即只要它们存在，它们就会通过进入细胞并防止ROI增加而起作用。第一个问题是：注射后纳米粒在眼睛细胞内停留多久？一个推论是纳米颗粒在任何浓度和长时间内是否有毒。纳米颗粒的改性制剂也将进行测试。透射电子显微镜将用于直接检测纳米颗粒，而白化大鼠光损伤模型将用于检测其保护视网膜功能的能力的保留。特异性目的二将测试纳米粒的功能机制是通过阻止凋亡途径的激活而不是诱导其他拯救途径的假设。我们的数据表明，纳米颗粒也将有效抑制在各种神经退行性疾病中发生的roi诱导的细胞死亡的进展。它们在视网膜中的药代动力学特征对于验证它们在人类中的潜在治疗应用非常重要。使用这些无机纳米颗粒作为多种疾病的直接治疗代表了一种新的策略，并表明它们可能代表了一种独特的技术。在美国，有数百万人患有某种形式的神经退行性疾病，如阿尔茨海默病、帕金森病、痴呆症、年龄相关性黄斑变性、糖尿病视网膜病变等。我们的初步数据表明，我们的稀土元素无机纳米颗粒可以预防活性氧诱导的大鼠视网膜变性。为了实现我们的具体目标，表征这些纳米颗粒的药代动力学（摄取、分布和消除）对于最终抑制神经元变性和保存依赖于中枢神经系统的人类的智力、视力和整体身体活动是必要的。

DESCRIPTION (provided by applicant): Progressive degeneration of neurons within the central nervous system (CNS) has a profound negative effect on the normal functions controlled by those cells and especially on the overall functioning of the individual. There are numerous neurodegenerative diseases which affect the brain including Alzheimer's disease, Parkinson's disease, Huntington's disease, etc. Degeneration of neurons in the retina, another part of the CNS, also occurs in many diseases including Age Related Macular Degeneration, Retinitis Pigmentosa, Diabetic Retinopathy, etc. Each of these neurodegenerative diseases appears to arise from unique primary defects which result in a chronic or an acute exposure of the neurons to Reactive Oxygen Intermediates (ROI). These toxic products of oxidative metabolism activate a cell suicide pathway - apoptosis. A universal goal in this area of research has been to find molecules which destroy or scavenge ROI in anticipation that the progression of these diseases can be slowed or halted. We hypothesized that specific inorganic nanoparticles, because of their activity, size (~5nm), nanoparticle status, insolubility and inorganic nature, would be able to enter cells and scavenge ROI and thereby prevent the activation of apoptosis and the death of the cells. Our preliminary data demonstrate that these specific nanoparticles can destroy ROI in test tubes, in retinal neurons in culture and can prevent ROI-mediated retinal degeneration in vivo. The overall objective of this project is to determine the pharmacokinetics (distribution and turnover) of these nanoparticles in order to test our hypothesis that they are acting by entering cells and preventing increases in ROI for as long as they are present. Specific Aim One will ask the question: How long after injection do the nanoceria particles remain within the cells of the eye? A corollary is whether the nanoparticles are toxic at any concentration and over prolonged periods of time. Modified preparations of the nanoparticles will also be tested. Transmission electron microscopy will be used to directly detect the nanoparticles whereas the albino rat light-damage model will be used to detect the retention of their ability to protect retinal function. Specific Aim Two will test the hypothesis that the mechanism by which the nanoceria particles function is by preventing the activation of apoptotic pathways rather than inducing other rescue pathways. Our data suggest that the nanoparticles will also be effective in inhibiting the progression of ROI-induced cell death that occurs in a variety of neurodegenerative diseases. The characterization of their pharmacokinetics in the retina is very important for validating their potential therapeutic applications in humans. The use of these inorganic nanoparticles as direct therapy for multiple diseases represents a novel strategy and suggests they may represent a unique technology. There are millions of people in the USA who have some form of neurodegenerative disease such as, Alzheimer's disease, Parkinson's disease, Dementia, Age Related Macular Degeneration, Diabetic Retinopathy, etc. Our preliminary data demonstrate that our rare earth element inorganic nanoparticles prevent Reactive Oxygen Species induced retinal degeneration in rats. Achievement of our specific aims, the characterization of the pharmacokinetics (uptake, distribution, and elimination) of these nanoparticles, is necessary for the eventual inhibition of neuronal degeneration and the preservation of mental abilities, vision, and overall physical activities in humans which are dependent on the central nervous system.