Department of Pharmaceutics, Delhi Institute of Pharmaceutical Sciences and Research, Sector-3, MB Road, PushpVihar, Delhi-110017, India.
Department of Pharmaceutical Chemistry, Delhi Institute of Pharmaceutical Sciences and Research, Sector-3, MB Road, PushpVihar, Delhi, India.
Curr Top Med Chem. 2020;20(30):2777-2788. doi: 10.2174/1568026620666201019112557.
Parkinson's disease (PD) is one of the most prevalent and severe neurodegenerative disease affecting more than 6.1 million people globally. It is characterized by age-related progressive deterioration of neurological functions caused by neuronal damage or neuronal death. During PD, the dopamineproducing cells in the substantia nigra region of the brain degenerate, which leads to symptoms like resting tremors and rigidity. Treatment of PD is very challenging due to the blood-brain barrier, which restricts the drug from reaching the brain. Conventional drug delivery systems possess a limited capacity to cross the blood barrier, leading to low bioavailability and high toxicity (due to off-site drug release). Therefore, it becomes necessary to accelerate the development of novel drug delivery systems, including nanoparticles, microemulsions, matrix systems, solid dispersions, liposomes, and solid lipid nanoparticles for the treatment of PD. Exosomes are biological lipid bilayer membrane vesicles produced by nearly all mammalian cells. The characteristics of vesicles are unique to their cell of origin and are primarily involved in intracellular communication. Exosomes, due to their nanoscale size, could easily permeate across the central nervous system, which makes them ideal for targeting the neurons in the substantia nigra. Exosomes could be efficient drug carrier systems for brain targeting, which can increase the efficacy of the drug and minimize the side effects. The review aims at providing a broad updated view of exosomes and their application in the treatment of PD.
帕金森病(PD)是一种最常见和最严重的神经退行性疾病,影响着全球超过 610 万人。它的特征是与年龄相关的神经功能进行性恶化,由神经元损伤或死亡引起。在 PD 中,大脑黑质区域产生多巴胺的细胞退化,导致静止性震颤和僵硬等症状。由于血脑屏障的存在,药物无法到达大脑,因此 PD 的治疗极具挑战性。传统的药物输送系统穿越血脑屏障的能力有限,导致生物利用度低和毒性高(由于药物在非靶部位释放)。因此,有必要加速新型药物输送系统的开发,包括纳米颗粒、微乳液、基质系统、固体分散体、脂质体和固体脂质纳米颗粒,以治疗 PD。外泌体是几乎所有哺乳动物细胞产生的生物脂质双层膜囊泡。囊泡的特征与其起源细胞独特相关,主要参与细胞内通讯。由于其纳米级尺寸,外泌体可以很容易地穿透中枢神经系统,这使得它们成为靶向黑质神经元的理想选择。外泌体可以作为脑靶向的有效药物载体系统,提高药物的疗效,最小化副作用。本综述旨在提供对外泌体及其在 PD 治疗中的应用的广泛更新观点。