期刊论文详细信息
Molecules
Progress in Drug Delivery to the Central Nervous System by the Prodrug Approach
Barbara Pavan2  Alessandro Dalpiaz1  Nunzia Ciliberti1  Carla Biondi2  Stefano Manfredini1 
[1] University of Ferrara, Department of Pharmaceutical Sciences, via Fossato di Mortara 19, 44100, Ferrara, Italy;University of Ferrara, Department of Biology, General Physiology Section, via L. Borsari 46, 44100, Ferrara, Italy
关键词: Brain delivery;    nasal administration;    prodrugs;    SVCT2;    carrier-mediated transport;   
DOI  :  10.3390/molecules13051035
来源: mdpi
PDF
【 摘 要 】

This review describes specific strategies for targeting to the central nervous system (CNS). Systemically administered drugs can reach the brain by crossing one of two physiological barriers resistant to free diffusion of most molecules from blood to CNS: the endothelial blood-brain barrier or the epithelial blood-cerebrospinal fluid barrier. These tissues constitute both transport and enzymatic barriers. The most common strategy for designing effective prodrugs relies on the increase of parent drug lipophilicity. However, increasing lipophilicity without a concomitant increase in rate and selectivity of prodrug bioconversion in the brain will result in failure. In these regards, consideration of the enzymes present in brain tissue and in the barriers is essential for a successful approach. Nasal administration of lipophilic prodrugs can be a promising alternative non-invasive route to improve brain targeting of the parent drugs due to fast absorption and rapid onset of drug action. The carrier-mediated absorption of drugs and prodrugs across epithelial and endothelial barriers is emerging as another novel trend in biotherapeutics. Several specific transporters have been identified in boundary tissues between blood and CNS compartments. Some of them are involved in the active supply of nutrients and have been used to explore prodrug approaches with improved brain delivery. The feasibility of CNS uptake of appropriately designed prodrugs via these transporters is described in detail.

【 授权许可】

CC BY   
© 2008 by the authors; licensee Molecular Diversity Preservation International, Basel, Switzerland.

【 预 览 】
附件列表
Files Size Format View
RO202003190058988ZK.pdf 224KB PDF download
  文献评价指标  
  下载次数:2次 浏览次数:16次