Combined therapy of ruthenium dendrimers and anti-cancer drugs against human leukemic cells

被引:13
|
作者
Michlewska, Sylwia [1 ,2 ]
Maroto, Marta [3 ,4 ]
Holota, Marcin [2 ]
Kubczak, Malgorzata [2 ]
Sanz del Olmo, Natalia [3 ,4 ]
Ortega, Paula [3 ,4 ,5 ]
Shcharbin, Dzmitry [6 ]
de la Mata, Francisco Javier [3 ,4 ,5 ]
Bryszewska, Maria [2 ]
Ionov, Maksim [2 ]
机构
[1] Univ Lodz, Fac Biol & Environm Protect, Lab Microscop Imaging & Specialized Biol Tech, Banacha 12-16, PL-90237 Lodz, Poland
[2] Univ Lodz, Fac Biol & Environm Protect, Dept Gen Biophysics, Pomorska 141-143, PL-90236 Lodz, Poland
[3] Univ Alcala, Dept Organ & Inorgan Chem, Madrid, Spain
[4] Res Inst Chem Andres M del Rio IQAR, Madrid, Spain
[5] Networking Res Ctr Bioengn Biomat & Nanomed CIBER, Madrid, Spain
[6] NASB, Inst Biophys & Cell Engn, Minsk 220072, BELARUS
基金
欧盟地平线“2020”;
关键词
MYELOID-LEUKEMIA; CANCER; METHOTREXATE; COMPLEXES; CHILDREN;
D O I
10.1039/d1dt01388b
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Carbosilane ruthenium(ii) dendrimers have been complexed with conventional anti-cancer drugs. Due to its features, the presence of ruthenium within a dendrimer structure improves the anti-cancer properties of nanocomplexes containing 5-flurouracyl, methotrexate and doxorubicin. These dendrimers could be promising carriers of anti-cancer medicines. Ruthenium dendrimers that are positively charged can also enhance the cytotoxicity to cancer cells; moreover, they can form stable complexes with drugs. Results indicate that ruthenium dendrimers combined with doxorubicin and methotrexate significantly reduced the viability of leukaemia 1301 and HL-60 cancer cells.
引用
收藏
页码:9500 / 9511
页数:12
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