Acetylcholinesterase inhibitors and nanoparticles on Alzheimer's disease: a review

被引:4
|
作者
Silva, Sara [1 ,2 ,3 ]
Almeida, Antonio J. [3 ]
Vale, Nuno [1 ,4 ]
机构
[1] Ctr Hlth Technol & Serv Res CINTESIS, OncoPharma Res Grp, Rua Dr Placido Costa, P-4200450 Porto, Portugal
[2] Univ Porto, Fac Pharm, Rua Jorge Viterbo Ferreira 228, P-4050313 Porto, Portugal
[3] Univ Lisbon, Res Inst Med iMed ULisboa, Fac Pharm, P-1649003 Lisbon, Portugal
[4] Univ Porto, Fac Med, P-4200319 Porto, Portugal
关键词
Alzheimer's disease; Acetylcholinesterase inhibitors; Memantine; Nanoparticles; Delivery system; SOLID-LIPID NANOPARTICLES; RIVASTIGMINE HYDROGEN TARTRATE; DRUG-DELIVERY-SYSTEM; CHITOSAN NANOPARTICLES; INTRANASAL DELIVERY; TARGETED DELIVERY; NASAL DELIVERY; CHOLINESTERASE-INHIBITORS; APOLIPOPROTEIN-E; RAT MODEL;
D O I
10.1007/s11051-020-05118-9
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Alzheimer's disease (AD) is a multifactorial neurodegenerative disease clinically characterized by progressive loss of memory, impairment cognitive function, and neuropsychiatric and behavior dysfunction. The molecular pathology of the disease is characterized with extracellular accumulation of amyloid beta plaques and neurofibrillary tangles composed of hyperphosphorylated Tau. Even with crescent number of AD patients worldwide, the current treatment approved does not alter the course of the disease but rather controls the symptoms. In addition to this, also present poor solubility and low bioavailability. Therefore, several studies have been exploring new delivery systems to efficiently deliver those drugs and enhance biological activity. Among them, nanoparticulated systems have demonstrated great potential as a drug delivery system in neurodegenerative disease. In this review, we will reflect on the current progress of nanoparticulated systems with an overall particle size ranging from 2 up to 200 nm and potential to deliver AD drugs for AD treatment.
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页数:19
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