PEGylated bottom-up synthesized graphene nanoribbons loaded with camptothecin as potential drug carriers

被引:1
|
作者
Hou, H. [1 ]
Cardo, L. [1 ]
Merino, J. P. [1 ,2 ]
Xu, F. [3 ]
Wetzl, C. [1 ,2 ]
Arnaiz, B. [1 ]
Luan, X. [3 ]
Mai, Y. [3 ]
Criado, A. [1 ,4 ]
Prato, M. [1 ,5 ,6 ]
机构
[1] Basque Res & Technol Alliance BRTA, Ctr Cooperat Res Biomat CIC BiomaGUNE, Paseo Miramon 182, Donostia San Sebastia 20014, Spain
[2] Univ Basque Country UPV EHU, Donostia San Sebastian 20018, Spain
[3] Shanghai Jiao Tong Univ, Frontiers Sci Ctr Transformat Mol, Sch Chem & Chem Engn, Shanghai Key Lab Elect Insulat & Thermal Ageing, 800 Dongchuan Rd, Shanghai 200240, Peoples R China
[4] Univ A Coruna, CICA Ctr Interdisciplinar Quim & Biol, Rua Carballeiras, La Coruna 15071, Spain
[5] Univ Trieste, Dept Chem & Pharmaceut Sci, Via L Giorgieri 1, I-34127 Trieste, Italy
[6] Basque Fdn Sci, Ikerbasque, Bilbao 48013, Spain
基金
中国国家自然科学基金;
关键词
Bottom -up synthesis; Chemical modification; Drug carrier; Folic acid; Graphene nanoribbon; SOLID LIPID NANOPARTICLES; FOLIC-ACID; DELIVERY; NANOCARRIER; TOXICITY; THERAPY;
D O I
10.1016/j.mtchem.2023.101668
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
This work discusses the potential use of bottom-up synthesized graphene nanoribbons (GNRs) as nano-carriers for drug delivery systems (DDSs). GNRs have a high loading capacity for anticancer drugs due to their high specific surface area and non-covalent adsorption with hydrophobic anticancer drug molecules. Herein, we synthesized GNRs using a bottom-up approach, modified with PEG2000 (GNR-PEG) and PEG2000 carrying folic acid chains (GNR-PEG-FA), and then loaded with camptothecin (CPT). The targeting ability mediated by folic acid of the GNR derivative was evaluated using cellular assays, and the cytotoxicity of GNR systems loaded with CPT was assessed by in vitro studies. They suggest that the functionalization of GNR derivatives with folic acid significantly affects their interaction with cells expressing different levels of folic acid receptors. The authors also explore the possibility to employ GNRs in photothermal therapy (PTT). GNR-PEG and GNR-PEG-FA display minor or no toxicity in standard cell cultures, but they show remarkable thermal response upon NIR irradiation, causing complete loss of cell viability within a few hours of treatment. This work highlights the potential of GNRs as DDSs and emphasizes the importance of further research on their biocompatibility and as a platform for PTT.
引用
收藏
页数:7
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