Multi-functionalization of reduced graphene oxide nanosheets for tumor theragnosis: Synthesis, characterization, enzyme assay, in-silico study, radiolabeling and in vivo targeting evaluation

被引:0
|
作者
Sakr, Tamer M. [1 ,2 ]
Elsabagh, Mohammed F. [1 ,3 ]
Fayez, Hend [3 ]
Sarhan, Mona O. [3 ]
Syam, Yasmin M. [4 ]
Anwar, Manal M. [4 ]
Motaleb, Mohammed A. [3 ]
Zaghary, Wafaa A. [5 ]
机构
[1] Egyptian Atom Energy Author, Radioisotopes Prod Facil, Egyptian Res Reactor Complex 2, Cairo 13759, Egypt
[2] Egyptian Atom Energy Author, Hot Labs Ctr, Radioact Isotopes & Generator Dept, Cairo 13759, Egypt
[3] Egyptian Atom Energy Author, Hot Labs Ctr, Labeled Cpds Dept, Cairo 13759, Egypt
[4] Natl Res Ctr, Dept Therapeut Chem, Cairo, Egypt
[5] Helwan Univ, Fac Pharm, Dept Pharmaceut Chem, Cairo, Egypt
关键词
Nanographene sheets; Technetium-99m; Nano synthesis; Tumor imaging; Radiolabeling; Active targeting; In-silico study; PRAP-1; inhibitor; Tumor theragnosis; BIOLOGICAL EVALUATION; MOLECULAR DOCKING; IMAGING AGENT; NANOPARTICLES; CANCER; INHIBITOR; DELIVERY; PARP-1; VASCULATURE; CHITOSAN;
D O I
10.1007/s40199-023-00487-7
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
BackgroundIn this study, a combination of nanotechnology, organic synthesis and radiochemistry were utilized in order to design an efficient nano-system conjugated with a suitable radionuclide and an antitumor agent for possible application as tumor theragnostic agent.MethodFour novel compounds (3 and 4a-c) bearing tetrahydroquinazoline-7-sulfonohydrazide or 1,2,3,4-tetrahydroquinazoline-7-sulfonamide scaffold were designed. Then, docking study predicted that the compounds can be considered as potential inhibitors for PARP-1. Following that; the four compounds were synthesized and properly characterized using 1HNMR, 13CNMR, IR and Mass spectroscopy. The cytotoxic effect of the four compounds was evaluated against breast cancer cell line (MDA-MB-436), where compound 3 showed the most promising cytotoxic effect. The inhibitory effect of the four compounds was evaluated in vitro against PARP-1.ResultCarboxylated graphene oxide nanosheets (NGO-COOH) were synthesized by a modified Hummer's method and has size of range 40 nm. The NGO-COOH nanosheets were proven to be safe and biocompatible when tested in vitro against normal human lung fibroblast cells (MRC-5). The prepared NGO-COOH nanosheets were conjugated with compound 3 then radiolabeled with 99mTc to yield 99mTc-NGO-COOH-3 with a radiochemical yield of 98.5.0 +/- 0.5%. 99mTc-NGO-COOH-3 was injected intravenously in solid tumor bearing mice to study the degree of localization of the nano-system at tumor tissue. The results of the study revealed, excellent localization and retention of the designed nano-system at tumor tissues with targeting ratio of 9.0.ConclusionStirred a new candidate tumor theragnostic agent that is safe, selective and stable.
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页码:77 / 95
页数:19
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  • [1] Multi-functionalization of reduced graphene oxide nanosheets for tumor theragnosis: Synthesis, characterization, enzyme assay, in-silico study, radiolabeling and in vivo targeting evaluation
    Tamer M. Sakr
    Mohammed F. Elsabagh
    Hend Fayez
    Mona O. Sarhan
    Yasmin M. Syam
    Manal M. Anwar
    Mohammed A. Motaleb
    Wafaa A. Zaghary
    DARU Journal of Pharmaceutical Sciences, 2024, 32 : 77 - 95