Liposome-Assisted Drug Delivery in the Treatment of Multiple Sclerosis

被引:1
|
作者
Greco, Giuliana [1 ,2 ]
Sarpietro, Maria Grazia [2 ,3 ]
机构
[1] Univ Catania, Dept Biomed & Biotechnol Sci, I-95123 Catania, Italy
[2] Univ Catania, NANOMED Res Ctr Nanomed & Pharmaceut Nanotechnol, I-95125 Catania, Italy
[3] Univ Catania, Dept Drug & Hlth Sci, I-95125 Catania, Italy
来源
MOLECULES | 2024年 / 29卷 / 19期
关键词
multiple sclerosis; BBB; EAE models; nanocarriers; liposomes; drug delivery; EXPERIMENTAL ALLERGIC ENCEPHALOMYELITIS; GUINEA-PIGS; FATTY-ACID; T-CELLS; MYELIN; SUPPRESSION; PATHOGENESIS; INFLAMMATION; ANTIBODIES; PEPTIDE;
D O I
10.3390/molecules29194689
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
Multiple sclerosis (MS) is an immune-mediated demyelinating disease of the nervous system that leads to neurological dysfunctions and severe disabilities. It is worth noting that conventional pharmacotherapy is poorly selective and causes toxicity problems and several systemic side effects. Thus, there is a need to develop new approaches to this medical challenge. The use of nanocarriers for drug delivery represents a good strategy to overcome several issues such as high therapeutic drug doses with side effects, such as diarrhea, nausea, and abdominal pain, and drug degradation processes; in addition, nanocarriers can provide controlled and targeted drug release. This review describes the application of liposomes for the delivery of pharmaceutical actives to target MS. Firstly, MS is explained. Then, liposomes are described along with their preparation, characterization, and stability. The literature about the use of liposomes for the treatment of MS is then analyzed.
引用
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页数:22
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