Fabrication and characterization of liposomal nanoparticles containing hydroalcoholic extract of Artemisia absintium and its toxicity on MCF-7 breast cancer cell line

Mohammad Taebpour, M. Majdizadeh, B. Haghiralsadat, Medical Nanotechnology
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引用次数: 1

Abstract

Introduction: The use of chemotherapy drugs has side effects, and the use of herbal compounds in the treatment of cancer faces challenges. Nanoparticles, especially liposomes, with appropriate properties in drug delivery, such as slow drug release and low toxicity at the target cell site, can solve some of these problems. Therefore, the aim of the present study was to develop a liposomal system containing Artemisia absinthium extract and to investigate its toxicity against the MCF-7 cell line. Methods: Three liposomal systems containing extracts with different molar percentages of soybean phosphatidylcholine (80% and 60%) along with cholesterol were prepared using the thin-film hydration method. The most suitable formulation was selected according to the loading percentage and release rate. Extract release from the selected formulation, particle size, and zeta potential were investigated. Finally, the toxicity of the extractloaded system, the free extract, and the unloaded system against the MCF-7 cell line was measured. Results: Extract loading, particle size, dispersion index, and zeta potential for the selected formulation are 49.2% ± 0.4%, 121.9 nm, 0.129, and −10.6 mV. The system showed a slow release at temperatures similar to healthy and cancer cells. Also, the liposome-encapsulated extract was more toxic against MCF-7 cells compared with the free extract, and extract-free liposomes had little toxicity against MCF-7 cells. Conclusion: The liposomal system containing Artemisia absinthium extract has a higher toxicity than the free extract against breast cancer cells, which can be due to the physicochemical properties of the system, including targeted release.
艾草水醇提取物纳米脂质体的制备、表征及其对MCF-7乳腺癌细胞系的毒性
导论:化疗药物的使用存在副作用,使用草药化合物治疗癌症面临挑战。纳米颗粒,尤其是脂质体,在药物传递方面具有适当的特性,如药物在靶细胞部位释放缓慢和毒性低,可以解决这些问题。因此,本研究的目的是建立含苦艾提取物的脂质体体系,并研究其对MCF-7细胞系的毒性。方法:采用薄膜水合法制备大豆磷脂酰胆碱(80%和60%)和胆固醇的不同摩尔百分比提取物脂质体体系。根据载药率和释药率选择最合适的配方。考察了所选制剂的释放度、粒径和zeta电位。最后,测定了载提取物体系、游离提取物体系和未载提取物体系对MCF-7细胞系的毒性。结果:所选制剂的萃取量、粒径、分散指数和zeta电位分别为49.2%±0.4%、121.9 nm、0.129和−10.6 mV。在与健康细胞和癌细胞相似的温度下,该系统显示出缓慢的释放。同时,脂质体包封提取物对MCF-7细胞的毒性较游离提取物大,而无提取物脂质体对MCF-7细胞的毒性较小。结论:含艾草提取物脂质体体系对乳腺癌细胞的毒性高于不含艾草提取物的脂质体体系,这可能与该体系的理化性质有关,包括靶向释放。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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