A Novel Nanoconjugate of Landomycin A with C60 Fullerene for Cancer Targeted Therapy: In Vitro Studies

被引:21
|
作者
Bilobrov, V. [1 ]
Sokolova, V. [2 ,3 ]
Prylutska, S. [1 ]
Panchuk, R. [4 ]
Litsis, O. [1 ]
Osetskyi, V. [1 ]
Evstigneev, M. [5 ]
Prylutskyy, Yu. [1 ]
Epple, M. [2 ,3 ]
Ritter, U. [6 ]
Rohr, J. [7 ]
机构
[1] Taras Shevchenko Natl Univ Kyiv, Volodymyrska Str 64, UA-01601 Kiev, Ukraine
[2] Univ Duisburg Essen, Inorgan Chem, Univ Str 5-7, D-45117 Essen, Germany
[3] Univ Duisburg Essen, Ctr Nanointegrat Duisburg Essen CeNIDE, Univ Str 5-7, D-45117 Essen, Germany
[4] Natl Acad Sci Ukraine, Inst Cell Biol, Drahomanov Str 14-16, UA-79005 Lvov, Ukraine
[5] Sevastopol State Univ, Dept Phys, Univ Skaya Str 33, UA-299053 Sevastopol, Crimea, Ukraine
[6] Tech Univ Ilmenau, Inst Chem & Biotechnol, Weimarer Str 25, D-98693 Ilmenau, Germany
[7] Univ Kentucky, Coll Pharm, South Limestone Str 789, Lexington, KY 40536 USA
关键词
C-60; fullerene; Landomycin A; Complexation; Cytotoxicity; Membranotropic effect; Molecular modelling; Dynamic light scattering; Fourier transform infrared spectroscopy; Scanning electron microscopy; Fluorescence microscopy; AQUEOUS-SOLUTION; DRUG; GENERATION; CISPLATIN; MODEL; BIODISTRIBUTION; COMPLEXATION; NANOPARTICLE; ASSOCIATION; DOXORUBICIN;
D O I
10.1007/s12195-018-0548-5
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Introduction Landomycins are a subgroup of angucycline antibiotics that are produced by Streptomyces bacteria and possess strong antineoplastic potential. Literature data suggest that enhancement of the therapeutic activity of this drug may be achieved by means of creating specific drug delivery systems. Here we propose to adopt C-60 fullerene as flexible and stable nanocarrier for landomycin delivery into tumor cells.MethodsThe methods of molecular modelling, dynamic light scattering and Fourier transform infrared spectroscopy were used to study the assembly of C-60 fullerene and the anticancer drug Landomycin A (LA) in aqueous solution. Cytotoxic activity of this nanocomplex was studied in vitro towards two cancer cell lines in comparison to human mesenchymal stem cells (hMSCs) using 3-(4,5-dimethyl-2-thiazolyl)-2,5-diphenyl-2-H-tetrazolium bromide (MTT) test and a live/dead assay. The morphology of the cells incubated with fullerene-drug nanoparticles and their uptake into target cells were studied by scanning electron microscopy and fluorescence light microscopy.ResultsThe viability of primary cells (hMSCs, as a model for healthy cells) and cancer cell lines (human osteosarcoma cells, MG-63, and mouse mammary cells, 4T1, as models for cancer cells) was studied after incubation with water-soluble C-60 fullerenes, LA and the mixture C-60+LA. The C-60+LA nanocomplex in contrast to LA alone showed higher toxicity towards cancer cells and lower toxicity towards normal cells, whereas the water-soluble C-60 fullerenes at the same concentration were not toxic for the cells.ConclusionsThe obtained physico-chemical data indicate a complexation between the two compounds, leading to the formation of a C-60+LA nanocomposite. It was concluded that immobilization of LA on C-60 fullerene enhances selectivity of action of this anticancer drug in vitro, indicating on possibility of further preclinical studies of novel C-60+LA nanocomposites on animal tumor models.
引用
收藏
页码:41 / 51
页数:11
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