Nano graphene oxide: A novel carrier for oral delivery of flavonoids

被引:89
作者
Rahmanian, Nazanin [1 ,2 ]
Hamishehkar, Hamed [3 ]
Dolatabadi, Jafar Ezzati Nazhad [4 ]
Arsalani, Nasser [2 ]
机构
[1] Tabriz Univ Med Sci, Biotechnol Res Ctr, Tabriz, Iran
[2] Univ Tabriz, Dept Organ & Biochem, Res Lab Polymer, Fac Chem, Tabriz, Iran
[3] Tabriz Univ Med Sci, Drug Appl Res Ctr, Tabriz, Iran
[4] Tabriz Univ Med Sci, Res Ctr Pharmaceut Nanotechnol, Tabriz, Iran
关键词
Graphene oxide; Nanoparticle; Drug delivery; Quercetin; Cytotoxicity; SOLID LIPID NANOPARTICLES; TARGETED DELIVERY; IN-VITRO; DRUG; QUERCETIN; CYTOTOXICITY; DISSOLUTION; FORMULATION; NANOSHEETS; REDUCTION;
D O I
10.1016/j.colsurfb.2014.09.036
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
The interesting physical and chemical properties of graphene oxide (GO) have led to much excitement among biomedical scientists in recent years. It is known that many potent, often aromatic medicines are water insoluble, and this has hindered their administration to treat diseases. Nano GO was synthesized and investigated for its biological application as a carrier for quercetin, a focused bioactive flavonoid widely used as a health supplement and a drug candidate. Different techniques were used to fully evaluate the synthesis, cytotoxicity, and quercetin loading capacity of nano GO. AFM and TEM results confirmed the preparation of planar nanoparticles without aggregation which was verified by reported size results (30 nm) obtained with a particle size analyzer. FTIR and DSC results proved the drug-carrier interaction. In vitro cytotoxicity assays showed that nano GO had no cytotoxicity on A549 cells in different amounts after incubation for 72 h, confirming its suitability as a drug carrier. Our results showed that nano GO can be proposed as a new carrier due to its small size, large specific surface area, low cost, and useful non-covalent interactions with aromatic low-soluble flavonoids such as quercetin. Moreover, it may find widespread applications in biomedicine. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:331 / 338
页数:8
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