Nano-based apigenin delivery systems for cancer applications

被引:1
|
作者
Cunha, Izi Vieira Nunes [1 ]
Campos, Angela Machado [1 ]
Caon, Thiago [1 ]
机构
[1] Univ Fed Santa Catarina, Postgrad Program Pharm, Campus Reitor Joao David Ferreira Lima S-N, BR-88040900 Florianopolis, SC, Brazil
关键词
Apigenin; Cancer; Drug delivery; Nanoparticles; IN-VITRO EVALUATION; GOLD NANOPARTICLES; CELL-DEATH; HEPATOCELLULAR-CARCINOMA; PHOSPHOLIPID COMPLEX; SOLID DISPERSIONS; INDUCED APOPTOSIS; DNA-DAMAGE; PATHWAY; LIPOSOMES;
D O I
10.1016/j.jddst.2024.105334
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Apigenin (APG) has been considered in the treatment of various types of cancer due to its capacity to modulate cell proliferation, apoptosis, cell cycle arrest, invasion, metastasis and autophagy by regulating different cell signaling pathways. Moreover, this molecule exhibits high selectivity to cancer cells compared to healthy cells, a key aspect in relation to other anticancer therapies. On the other hand, APG is characterized by low aqueous solubility, slow oral absorption, high metabolization and association rate with plasma proteins. As a consequence, low plasma concentrations are often found after oral administration. Nanotechnology emerges as an alternative to overcome pharmacokinetic or physicochemical limitations, providing a targeted and controlled drug delivery, increased oral bioavailability and aqueous solubility as well as improved side effect profile. In this review, studies addressing the anticancer properties of APG nanoparticles were analyzed in detail. The synergism of action between drugs already used clinically and APG nanoparticles allow to reduce the dose of the drug administrated, which would minimize adverse effects. In vivo studies, in turn, showed its potential in reducing tumor volume, encouraging trials with humans.
引用
收藏
页数:15
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