Department of Pharmacology & Toxicology, National Institute of Pharmaceutical Education and Research, Hyderabad, Telangana State, India.
Department of Pharmaceutics, National Institute of Pharmaceutical Education and Research, Hyderabad, Telangana State, India.
Curr Neuropharmacol. 2023;21(3):493-516. doi: 10.2174/1570159X20666220507022701.
Blood-Brain Barrier (BBB) acts as a highly impermeable barrier, presenting an impediment to the crossing of most classical drugs targeted for neurodegenerative diseases including Parkinson's disease (PD). About the nature of drugs and other potential molecules, they impose unavoidable doserestricted limitations eventually leading to the failure of therapy. However, many advancements in formulation technology and modification of delivery approaches have been successful in delivering the drug to the brain in the therapeutic window. The nose to the brain (N2B) drug delivery employing the nanoformulation, is one such emerging delivery approach, overcoming both classical drug formulation and delivery-associated limitations. This latter approach offers increased bioavailability, greater patient acceptance, lesser metabolic degradation of drugs, circumvention of BBB, ample drug loading along with the controlled release of the drugs. In N2B delivery, the intranasal (IN) route carries therapeutics firstly into the nasal cavity followed by the brain through olfactory and trigeminal nerve connections linked with nasal mucosa. The N2B delivery approach is being explored for delivering other biologicals like neuropeptides and mitochondria. Meanwhile, this N2B delivery system is associated with critical challenges consisting of mucociliary clearance, degradation by enzymes, and drug translocations by efflux mechanisms. These challenges finally culminated in the development of suitable surfacemodified nano-carriers and Focused- Ultrasound-Assisted IN as FUS-IN technique which has expanded the horizons of N2B drug delivery. Hence, nanotechnology, in collaboration with advances in the IN route of drug administration, has a diversified approach for treating PD. The present review discusses the physiology and limitation of IN delivery along with current advances in nanocarrier and technical development assisting N2B drug delivery.
血脑屏障(BBB)作为一种高度不可渗透的屏障,对大多数针对神经退行性疾病(包括帕金森病(PD))的经典药物的穿越构成了障碍。关于药物和其他潜在分子的性质,它们施加了不可避免的剂量限制限制,最终导致治疗失败。然而,许多制剂技术的进步和传递方法的修改已经成功地将药物递送到治疗窗口中的大脑。采用纳米制剂的从鼻到脑(N2B)药物传递是一种新兴的传递方法,克服了经典药物制剂和传递相关的限制。这种方法提供了更高的生物利用度、更高的患者接受度、更少的药物代谢降解、绕过 BBB、药物加载量大以及药物的控释。在 N2B 传递中,鼻内(IN)途径首先将治疗剂携带到鼻腔中,然后通过与鼻黏膜相连的嗅觉和三叉神经连接传递到大脑。N2B 传递方法正在被探索用于传递其他生物制剂,如神经肽和线粒体。同时,这种 N2B 传递系统与关键挑战有关,包括粘液纤毛清除、酶降解和外排机制的药物转运。这些挑战最终导致了合适的表面改性纳米载体的开发和聚焦超声辅助 IN 作为 FUS-IN 技术,这扩展了 N2B 药物传递的视野。因此,纳米技术与药物管理 IN 途径的进步相结合,为治疗 PD 提供了多样化的方法。本综述讨论了 IN 传递的生理学和局限性以及纳米载体和技术发展的最新进展,这些进展有助于 N2B 药物传递。