Yang Han-Mo
Division of Cardiology, Department of Internal Medicine, Seoul National University Hospital, 101 Daehak-ro, Chongno-gu, Seoul 03080, Republic of Korea.
Pharmaceutics. 2025 Aug 11;17(8):1041. doi: 10.3390/pharmaceutics17081041.
The increasing global health crisis of neurodegenerative diseases such as Alzheimer's, Parkinson's, amyotrophic lateral sclerosis, and Huntington's disease is worsening because of a rapidly increasing aging population. Disease-modifying therapies continue to face development challenges due to the blood-brain barrier (BBB), which prevents more than 98% of small molecules and all biologics from entering the central nervous system. The therapeutic landscape for neurodegenerative diseases has recently undergone transformation through advances in targeted drug delivery that include ligand-decorated nanoparticles, bispecific antibody shuttles, focused ultrasound-mediated BBB modulation, intranasal exosomes, and mRNA lipid nanoparticles. This review provides an analysis of the molecular pathways that cause major neurodegenerative diseases, discusses the physiological and physicochemical barriers to drug delivery to the brain, and reviews the most recent drug targeting strategies including receptor-mediated transcytosis, cell-based "Trojan horse" approaches, gene-editing vectors, and spatiotemporally controlled physical methods. The review also critically evaluates the limitations such as immunogenicity, scalability, and clinical translation challenges, proposing potential solutions to enhance therapeutic efficacy. The recent clinical trials are assessed in detail, and current and future trends are discussed, including artificial intelligence (AI)-based carrier engineering, combination therapy, and precision neuro-nanomedicine. The successful translation of these innovations into effective treatments for patients with neurodegenerative diseases will require essential interdisciplinary collaboration between neuroscientists, pharmaceutics experts, clinicians, and regulators.
由于全球老龄化人口迅速增加,阿尔茨海默病、帕金森病、肌萎缩侧索硬化症和亨廷顿舞蹈症等神经退行性疾病引发的全球健康危机日益严重。由于血脑屏障(BBB)的存在,疾病修饰疗法继续面临开发挑战,血脑屏障会阻止超过98%的小分子和所有生物制剂进入中枢神经系统。最近,通过靶向药物递送技术的进步,神经退行性疾病的治疗格局发生了转变,这些技术包括配体修饰的纳米颗粒、双特异性抗体转运体、聚焦超声介导的血脑屏障调节、鼻内递送外泌体和mRNA脂质纳米颗粒。本综述分析了导致主要神经退行性疾病的分子途径,讨论了药物递送至大脑的生理和物理化学障碍,并综述了最新的药物靶向策略,包括受体介导的转胞吞作用、基于细胞的“特洛伊木马”方法、基因编辑载体和时空控制物理方法。本综述还批判性地评估了免疫原性、可扩展性和临床转化挑战等局限性,提出了提高治疗效果的潜在解决方案。详细评估了最近的临床试验,并讨论了当前和未来的趋势,包括基于人工智能(AI)的载体工程、联合治疗和精准神经纳米医学。要将这些创新成功转化为神经退行性疾病患者的有效治疗方法,神经科学家、药剂学专家、临床医生和监管机构之间需要进行必要的跨学科合作。