Liposomal Formulations for Nose-to-Brain Delivery: Recent Advances and Future Perspectives

被引:116
作者
Hong, Soon-Seok [1 ]
Oh, Kyung Taek [2 ]
Choi, Han-Gon [3 ]
Lim, Soo-Jeong [1 ]
机构
[1] Sejong Univ, Dept Integrated Biosci & Biotechnol, 209 Neungdong Ro, Seoul 05006, South Korea
[2] Chung Ang Univ, Coll Pharm, 84 Heukseok Ro, Seoul 06974, South Korea
[3] Hangang Univ, Coll Pharm, 55 Hanyangdaehak Ro, Ansan 15588, South Korea
基金
新加坡国家研究基金会;
关键词
liposomes; intranasal; formulation; brain delivery; nanoparticle; INTRANASAL DELIVERY; DRUG-DELIVERY; CATIONIC LIPOSOMES; ALZHEIMERS-DISEASE; NASAL CAVITY; RAT-BRAIN; BARRIER; THERAPEUTICS; PROTEINS; PATHWAYS;
D O I
10.3390/pharmaceutics11100540
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Restricted drug entry to the brain that is closely associated with the existence of the blood brain barrier (BBB) has limited the accessibility of most potential active therapeutic compounds to the brain from the systemic circulation. Recently, evidences for the presence of direct nose-to-brain drug transport pathways have been accumulated by several studies and an intranasal drug administration route has gained attention as a promising way for providing direct access to the brain without the needs to cross to the BBB. Studies aiming for developing nanoparticles as an intranasal drug carrier have shown considerable promise in overcoming the challenges of intranasal drug delivery route. This review gives a comprehensive overview of works having investigated liposomes as a potential vehicle to deliver drugs to the brain through nose-to-brain route while considering the excellent biocompatibility and high potential of liposomes for clinical development. Herein, studies are reviewed with special emphasis on the impact of formulation factors, such as liposome composition and surface modification of liposomes with targeting moieties, in addition to intranasal environmental factors that may affect the extent/site of absorption of intranasally administered, liposome-encapsulated drugs.
引用
收藏
页数:18
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