Computational, In Vitro, and In Vivo Models for Nose-to-Brain Drug Delivery Studies

被引:3
|
作者
Boyuklieva, Radka [1 ,2 ]
Zagorchev, Plamen [2 ,3 ]
Pilicheva, Bissera [1 ,2 ]
机构
[1] Med Univ Plovdiv, Fac Pharm, Dept Pharmaceut Sci, Plovdiv 4002, Bulgaria
[2] Med Univ Plovdiv, Res Inst, Plovdiv 4002, Bulgaria
[3] Med Univ Plovdiv, Fac Pharm, Dept Med Phys & Biophys, Plovdiv 4002, Bulgaria
关键词
nose-to-brain delivery; computational models; in vitro models; ex vivo models; in vivo models; NONHUMAN PRIMATE MODELS; AIR-LIQUID-INTERFACE; INTRANASAL DELIVERY; OLFACTORY DEPOSITION; CELL MONOLAYER; NASAL; PERMEABILITY; NANOPARTICLES; DIFFUSION; SYSTEM;
D O I
10.3390/biomedicines11082198
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Direct nose-to-brain drug delivery offers the opportunity to treat central nervous system disorders more effectively due to the possibility of drug molecules reaching the brain without passing through the blood-brain barrier. Such a delivery route allows the desired anatomic site to be reached while ensuring drug effectiveness, minimizing side effects, and limiting drug losses and degradation. However, the absorption of intranasally administered entities is a complex process that considerably depends on the interplay between the characteristics of the drug delivery systems and the nasal mucosa. Various preclinical models (in silico, in vitro, ex vivo, and in vivo) are used to study the transport of drugs after intranasal administration. The present review article attempts to summarize the different computational and experimental models used so far to investigate the direct delivery of therapeutic agents or colloidal carriers from the nasal cavity to the brain tissue. Moreover, it provides a critical evaluation of the data available from different studies and identifies the advantages and disadvantages of each model.
引用
收藏
页数:19
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