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

IF 2.5 4区 医学 Q3 PHARMACOLOGY & PHARMACY DARU Journal of Pharmaceutical Sciences Pub Date : 2024-06-01 Epub Date: 2024-01-03 DOI:10.1007/s40199-023-00495-7
Salah Jaafar Abdulkareem, Davoud Jafari-Gharabaghlou, Mahdi Farhoudi-Sefidan-Jadid, Elnaz Salmani-Javan, Fatemeh Toroghi, Nosratollah Zarghami
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Abstract

Purpose: Despite 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.

Methods: Niosomal 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.

Results: Both 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 μM and 14.6 mM, respectively while in nano formulated form their IC50 values decreased to 56.7 μM and 78.3 μM, 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.

Conclusion: The 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.

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青蒿素和二甲双胍通过聚乙二醇化niosomal纳米颗粒联合给药:治疗肺癌细胞的潜在抗癌效果。
目的:尽管治疗手段不断进步,但肺癌仍是全球关注的问题,因此有必要开发新的治疗方法。最近发现二甲双胍(MET)和青蒿素(ART)等双胍类药物具有抗癌特性。因此,在当前的研究中,我们研究了将二甲双胍(MET)和青蒿素(ART)共同封装在纳米颗粒中对肺癌细胞的抗癌作用,以建立一种创新的治疗技术:方法:采用薄膜水合法合成了Niosomal纳米颗粒(Nio-NPs),并通过傅立叶变换红外光谱分析了其理化性质。用 FE-SEM 和 AFM 评估了 Nio-NPs 的形态。MTT 试验用于评估游离 MET、游离 ART、它们与 Nio-NPs 的封装形式以及它们的组合对 A549 细胞的细胞毒性作用。细胞凋亡试验用于检测细胞程序性死亡所涉及的生物过程。使用细胞周期测定法评估了细胞周期对药物反应的停滞。药物治疗 48 小时后,采用 qRT-PCR 方法评估了 hTERT、Cyclin D1、BAX、BCL-2、Caspase 3 和 7 基因的表达水平:结果:MET和ART都能以剂量依赖的方式降低肺癌细胞的存活率。纯 ART 和 MET 的 IC50 值分别为 195.2 μM 和 14.6 mM,而纳米制剂的 IC50 值分别降至 56.7 μM 和 78.3 μM。与单一疗法相比,MET 和 ART 的组合能协同减少肺癌细胞的增殖。重要的是,MET和ART联用对A549肺癌细胞的抗增殖作用更强,IC50值更低。实时荧光定量PCR检测结果显示,与单一疗法相比,纳米制剂MET和ART联合疗法可显著改变hTERT、Cyclin D1、BAX、BCL-2、Caspase 3和Caspase 7基因的表达:本研究结果表明,Nio-NPs 封装的 MET 和 ART 组合疗法可用于治疗肺癌,并能提高肺癌治疗的效率。
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DARU Journal of Pharmaceutical Sciences
DARU Journal of Pharmaceutical Sciences PHARMACOLOGY & PHARMACY-
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期刊介绍: DARU Journal of Pharmaceutical Sciences is a peer-reviewed journal published on behalf of Tehran University of Medical Sciences. The journal encompasses all fields of the pharmaceutical sciences and presents timely research on all areas of drug conception, design, manufacture, classification and assessment. The term DARU is derived from the Persian name meaning drug or medicine. This journal is a unique platform to improve the knowledge of researchers and scientists by publishing novel articles including basic and clinical investigations from members of the global scientific community in the forms of original articles, systematic or narrative reviews, meta-analyses, letters, and short communications.
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