Improving the Therapeutic Performance of Glycyrrhiza Glabra Hydroalcoholic Extract Using Liposomal Nano-carriers and Their Characterization

M. Akhlaghi, Lida Eftekharivash, Mohammad Taebpour, Saeid Afereydoon, Marziyeh Ebrahimpour, Maryam Zarezadeh Mehrizi, Mahboobeh Zarezadeh Mehrizi, Bibi fatemeh Haghirosadat
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Abstract

Background: The use of plants as therapeutic drugs has long been common among human beings. The Glycyrrhiza glabra is one of the medicinal plants with many therapeutic properties. However, using this herb in traditional methods faces some challenges. The use of pharmaceutical nano-carriers such as liposomes is one of the new strategies to overcome these challenges. In this regard, the current study aimed to synthesize and characterize liposomal nano-carriers containing the G. glabra hydroalcoholic extract to improve its therapeutic effects. Materials and Methods: After the extraction of the G. glabra root by the Soxhlet method, nano-liposomes containing G. glabra extracts were synthesized by the thin-film preparation method. Then, the encapsulation efficiency (EE) rate and drug release pattern of nanoliposome were examined using the spectrophotometry method. Next, physicochemical properties such as size, zeta potential, morphology, and non-interaction of the nano-system with the extract were investigated by dynamic-light-scattering (DLS), atomic force microscope (AFM), and Fourier transform infrared spectroscopy (FTIR) methods, and finally, the toxicity of the nano-system on human foreskin fibroblast cells was assessed using the MTT method. Results: Nano-liposomes containing licorice extracts with the EE of 2.3±75.32% were from the type of slow release and controlled release, having a size of 111.4±1.2 nm, a surface charge of -53.6±6.3, and a dispersion index of 0.210±0.13, and they had no interaction with the loaded extract. The results of the MTT test also demonstrated that the synthesized nano-liposomes were non-toxic on normal cells. Conclusion: Overall, the findings proved that synthesized nano-liposomes with proper physicochemical properties can be a suitable carrier for the G. glabra extract and thus cause stability and improve the therapeutic effects of this herbal extract as a medicinal plant.
利用纳米脂质体载体提高甘草水醇提取物的治疗效果及其表征
背景:利用植物作为治疗药物在人类中早已司空见惯。甘草是一种具有多种治疗作用的药用植物。然而,在传统方法中使用这种草药面临着一些挑战。使用药物纳米载体如脂质体是克服这些挑战的新策略之一。因此,本研究旨在合成并表征含有光天牛水醇提取物的纳米脂质体载体,以提高其治疗效果。材料与方法:采用索氏法提取光天草根后,采用薄膜制备法合成含光天草提取物的纳米脂质体。采用分光光度法测定纳米脂质体的包封率和药物释放规律。其次,通过动态光散射(DLS)、原子力显微镜(AFM)和傅里叶变换红外光谱(FTIR)等方法研究纳米体系的大小、zeta电位、形态和与提取物的非相互作用等理化性质,最后采用MTT方法评估纳米体系对人包皮成纤维细胞的毒性。结果:含甘草提取物的纳米脂质体为缓释型和控释型,EE为2.3±75.32%,粒径为111.4±1.2 nm,表面电荷为-53.6±6.3,分散指数为0.210±0.13,与载药提取物无相互作用。MTT试验结果还表明,合成的纳米脂质体对正常细胞无毒。结论:综上所述,合成的纳米脂质体具有适当的理化性质,可作为光草提取物的合适载体,从而提高光草提取物作为药用植物的稳定性和疗效。
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