Co-delivery of artemisinin and metformin via PEGylated niosomal nanoparticles: potential anti-cancer effect in treatment of lung cancer cells

被引:3
|
作者
Abdulkareem, Salah Jaafar [1 ,2 ]
Jafari-Gharabaghlou, Davoud [1 ,2 ]
Farhoudi-Sefidan-Jadid, Mahdi [1 ,2 ]
Salmani-Javan, Elnaz [1 ,2 ]
Toroghi, Fatemeh [3 ]
Zarghami, Nosratollah [1 ,2 ,4 ]
机构
[1] Tabriz Univ Med Sci, Dept Clin Biochem, Tabriz, Iran
[2] Tabriz Univ Med Sci, Fac Med, Lab Med, Tabriz, Iran
[3] Hamedan Univ Med Sci, Res Ctr Mol Med, Hamadan, Iran
[4] Istanbul Aydin Univ, Fac Med, Dept Med Biochem, Istanbul, Turkiye
关键词
Metformin; Artemisinin; Lung cancer; Niosome; Combination therapy; MOLECULAR TARGET THERAPY; IN-VITRO; LOADED PLGA; CYCLIN-D; DRUG; CYTOTOXICITY; HTERT; DERIVATIVES; EXPRESSION; PREVENTION;
D O I
10.1007/s40199-023-00495-7
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
PurposeDespite the advances in treatment, lung cancer is a global concern and necessitates the development of new treatments. Biguanides like metformin (MET) and artemisinin (ART) have recently been discovered to have anti-cancer properties. As a consequence, in the current study, the anti-cancer effect of MET and ART co-encapsulated in niosomal nanoparticles on lung cancer cells was examined to establish an innovative therapy technique.MethodsNiosomal nanoparticles (Nio-NPs) were synthesized by thin-film hydration method, and their physicochemical properties were assessed by FTIR. The morphology of Nio-NPs was evaluated with FE-SEM and AFM. The MTT assay was applied to evaluate the cytotoxic effects of free MET, free ART, their encapsulated form with Nio-NPs, as well as their combination, on A549 cells. Apoptosis assay was utilized to detect the biological processes involved with programmed cell death. The arrest of cell cycle in response to drugs was assessed using a cell cycle assay. Following a 48-h drug treatment, the expression level of hTERT, Cyclin D1, BAX, BCL-2, Caspase 3, and 7 genes were assessed using the qRT-PCR method.ResultsBoth MET and ART reduced the survival rate of lung cancer cells in the dose-dependent manner. The IC50 values of pure ART and MET were 195.2 mu M and 14.6 mM, respectively while in nano formulated form their IC50 values decreased to 56.7 mu M and 78.3 mu M, respectively. The combination of MET and ART synergistically decreased the proliferation of lung cancer cells, compared to the single treatments. Importantly, the combination of MET and ART had a higher anti-proliferative impact against A549 lung cancer cells, with lower IC50 values. According to the result of Real-time PCR, hTERT, Cyclin D1, BAX, BCL-2, Caspase 3, and Caspase 7 genes expression were considerably altered in treated with combination of nano formulated MET and ART compared to single therapies.ConclusionThe results of this study showed that the combination of MET and ART encapsulated in Nio-NPs could be useful for the treatment of lung cancer and can increase the efficiency of lung cancer treatment.
引用
收藏
页码:133 / 144
页数:12
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