Dual drug-loaded paclitaxel-thymoquinone nanoparticles for effective breast cancer therapy

被引:64
作者
Soni, Parth [1 ]
Kaur, Jasmine [1 ]
Tikoo, Kulbhushan [1 ]
机构
[1] NIPER, Dept Pharmacol & Toxicol, Lab Epigenet & Dis, Sect 67, Sas Nagar 160062, Punjab, India
关键词
Paclitaxel; Thymoquinone; Breast cancer; PLGA; Nanomedicine; IN-VITRO; PLGA NANOPARTICLES; MULTIDRUG-RESISTANCE; ANTICANCER ACTIVITY; CONTROLLED-RELEASE; ANTITUMOR-ACTIVITY; DELIVERY; APOPTOSIS; CELLS; BIOAVAILABILITY;
D O I
10.1007/s11051-014-2821-4
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The present study highlights the beneficial synergistic blend of anticancer drug paclitaxel (PTX) and thymoquinone (TQ) in MCF-7 breast cancer cells. We aimed to augment the therapeutic index of PTX using a polymeric nanoparticle system loaded with PTX and TQ. PLGA nanoparticles encapsulating the two drugs, individually or in combination, were prepared by single emulsion solvent evaporation method. The formulated nanoparticles were homogenous with an overall negative charge and their size ranging between 200 and 300 nm. Entrapment efficiency of PTX and TQ in the dual drug-loaded nanoparticles was found to be 82.4 +/- 2.18 and 65.8 +/- 0.45 %, respectively. The release kinetics of PTX and TQ from the nanoparticles exhibited a biphasic pattern characterised by an initial burst, followed by a gradual and continuous release. The anticancer activity of nanoparticles encapsulating both the drugs was higher as compared to the free drugs in MCF-7 breast cancer cells. The combination index for the dual drug-loaded NPs was found to be 0.688 which is indicative of synergistic interaction. Thus, here, we propose the synthesis and use of dual drug-loaded TQ and PTX NPs which exhibits enhanced anticancer activity and can additionally help to alleviate the toxic effects of PTX by lowering its effective dose.
引用
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页数:12
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