Advances in Intrathecal Nanoparticle Delivery: Targeting the Blood-Cerebrospinal Fluid Barrier for Enhanced CNS Drug Delivery

被引:0
|
作者
Madadi, Ahmad Khalid [1 ]
Sohn, Moon-Jun [1 ,2 ]
机构
[1] Inje Univ, Grad Sch Med, Dept Biomed Sci, 75 Bokji Ro, Busan 47392, South Korea
[2] Inje Univ, Coll Med, Hybrid Res Ctr, Dept Neurosurg Neurosci & Radiosurg,Ilsan Paik Hos, Juhwa Ro 170, Goyang 10380, South Korea
基金
新加坡国家研究基金会;
关键词
blood-cerebrospinal fluid barrier; nanoparticles; targeted drug strategies; CNS penetration; pharmacokinetics; CENTRAL-NERVOUS-SYSTEM; DENSITY-LIPOPROTEIN RECEPTOR; NEWTON NIMODIPINE MICROPARTICLES; HYDROXYPROPYL-BETA-CYCLODEXTRIN; MAMMALIAN CEREBRAL EPITHELIUM; CHOROID-PLEXUS; BRAIN-BARRIER; IN-VIVO; LIPOSOMAL CYTARABINE; MEDIATED DELIVERY;
D O I
10.3390/ph17081070
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The blood-cerebrospinal fluid barrier (BCSFB) tightly regulates molecular exchanges between the bloodstream and cerebrospinal fluid (CSF), creating challenges for effective central nervous system (CNS) drug delivery. This review assesses intrathecal (IT) nanoparticle (NP) delivery systems that aim to enhance drug delivery by circumventing the BCSFB, complementing approaches that target the blood-brain barrier (BBB). Active pharmaceutical ingredients (APIs) face hurdles like restricted CNS distribution and rapid clearance, which diminish the efficacy of IT therapies. NPs can be engineered to extend drug circulation times, improve CNS penetration, and facilitate sustained release. This review discusses key pharmacokinetic (PK) parameters essential for the effectiveness of these systems. NPs can quickly traverse the subarachnoid space and remain within the leptomeninges for extended periods, often exceeding three weeks. Some designs enable deeper brain parenchyma penetration. Approximately 80% of NPs in the CSF are cleared through the perivascular glymphatic pathway, with microglia-mediated transport significantly contributing to their paravascular clearance. This review synthesizes recent progress in IT-NP delivery across the BCSFB, highlighting critical findings, ongoing challenges, and the therapeutic potential of surface modifications and targeted delivery strategies.
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页数:33
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