Evaluation of Recent Intranasal Drug Delivery Systems to the Central Nervous System

被引:63
|
作者
Crowe, Tyler P. [1 ]
Hsu, Walter H. [2 ]
机构
[1] Univ Iowa, Carver Coll Med, Iowa City, IA 52242 USA
[2] Iowa State Univ, Dept Biomed Sci, Ames, IA 50011 USA
关键词
intranasal; nose-to-brain; CNS; drug delivery; nanocarriers; TO-BRAIN TRANSPORT; SOLID LIPID NANOPARTICLES; NASAL MUCOCILIARY CLEARANCE; IN-SITU GELS; SURFACE-CHARGE; CHITOSAN NANOPARTICLES; CEREBROSPINAL-FLUID; PLGA NANOPARTICLES; STEM-CELLS; PARACELLULAR PERMEABILITY;
D O I
10.3390/pharmaceutics14030629
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Neurological diseases continue to increase in prevalence worldwide. Combined with the lack of modifiable risk factors or strongly efficacious therapies, these disorders pose a significant and growing burden on healthcare systems and societies. The development of neuroprotective or curative therapies is limited by a variety of factors, but none more than the highly selective blood-brain barrier. Intranasal administration can bypass this barrier completely and allow direct access to brain tissues, enabling a large number of potential new therapies ranging from bioactive peptides to stem cells. Current research indicates that merely administering simple solutions is inefficient and may limit therapeutic success. While many therapies can be delivered to some degree without carrier molecules or significant modification, a growing body of research has indicated several methods of improving the safety and efficacy of this administration route, such as nasal permeability enhancers, gelling agents, or nanocarrier formulations. This review shall discuss promising delivery systems and their role in expanding the clinical efficacy of this novel administration route. Optimization of intranasal administration will be crucial as novel therapies continue to be studied in clinical trials and approved to meet the growing demand for the treatment of patients with neurological diseases.
引用
收藏
页数:26
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