Flavonoids nanostructures promising therapeutic efficiencies in colorectal cancer

被引:22
|
作者
Hassani, Sepideh [1 ,2 ]
Maghsoudi, Hossein [1 ,2 ]
Fattahi, Fahimeh [3 ,4 ]
Malekinejad, Faezeh [1 ,2 ]
Hajmalek, Nooshin [5 ]
Sheikhnia, Farhad [1 ,2 ]
Kheradmand, Fatemeh [2 ]
Fahimirad, Shohreh [4 ]
Ghorbanpour, Mansour [6 ]
机构
[1] Urmia Univ Med Sci, Student Res Comm, Orumiyeh, Iran
[2] Urmia Univ Med Sci, Sch Med, Dept Clin Biochem, Orumiyeh, Iran
[3] Iran Univ Med Sci, Oncopathol Res Ctr, Tehran, Iran
[4] Arak Univ Med Sci, Mol & Med Res Ctr, Arak, Iran
[5] Babol Univ Med Sci, Sch Med, Dept Clin Biochem, Babol, Iran
[6] Arak Univ, Fac Agr & Nat Resources, Dept Med Plants, Arak 3815688349, Iran
关键词
Colorectal cancer; Flavonoid; Polyphenol; Nano-formulation; VITRO ANTIOXIDANT ACTIVITY; COLON-CANCER; IN-VITRO; DELIVERY-SYSTEM; DRUG-DELIVERY; EPIGALLOCATECHIN-3-GALLATE EGCG; INHIBITS PROLIFERATION; CELL-PROLIFERATION; INDUCED APOPTOSIS; GALLATE EGCG;
D O I
10.1016/j.ijbiomac.2023.124508
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
Colorectal cancer is among the frequently diagnosed cancers with high mortality rates around the world. Polyphenolic compounds such as flavonoids are secondary plant metabolites which exhibit anti-cancer activities along with anti-inflammatory effects. However, due to their hydrophobicity, sensitivity to degradation and low bioavailability, therapeutic effects have shown poor therapeutic effect. Nano delivery systems such as nanoliposomes, nanomicelles, silica nanoparticles have been investigated to overcome these difficulties. This review provides a summary of the efficiency of certain flavonoids and polyphenols (apigenin, genistein, resveratrol, quercetin, silymarin, catechins, luteolin, fisetin, gallic acid, rutin, and curcumin) on colorectal cancer models. It comprehensively discusses the influence of nano-formulation of flavonoids on their biological functions, including cellular uptake rate, bioavailability, solubility, and cytotoxicity, as well as their potential for reducing colorectal cancer tumor size under in vivo situations.
引用
收藏
页数:22
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