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Intracellular ROS protection efficiency and free radical-scavenging activity of quercetin and quercetin-encapsulated liposomes

机译:槲皮素和槲皮素包裹的脂质体的细胞内ROS保护效率和清除自由基的活性

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Abstract Quercetin (3,5,7,3’,4’-pentahydroxyflavone) is a natural bio-flavonoid originating from fruits, vegetables, seeds, berries, and tea. The antioxidant activity of quercetin and its protective effects against cardiovascular disorders, anti-cancer, anti-inflammatory, and anti-viral activities have been extensively documented; however, the clinical request of quercetin in cancer treatment is significantly limited due to its very poor delivery features. In order to increase the hydrophilicity and drug delivery capability, we encapsulated quercetin into liposomes. Our data indicated that liposomal quercetin can significantly improve the solubility and bioavailability of quercetin and can be used as an effective antioxidant for ROS protection within the polar cytoplasm, and the nano-sized quercetin encapsulated by liposomes enhanced the cellular uptake (cancer cell human MCF_7). Quercetin has many pharmaceutical applications, many of which arise from its potent antioxidant properties. The present research examined the antioxidant activities of quercetin in polar solvents by a comparative study using reduction of ferric iron in aqueous medium, intracellular ROS/toxicity assays, and reducing DPPH assays. Cell viability and ROS assays demonstrated that quercetin was able to penetrate into the polar medium inside the cells and to protect them against the highly toxic and deadly belongings of cumene hydroperoxide. The purpose of this study was to determine whether a liposomal formulation of quercetin can suggestively improve its solubility and bioavailability and can be a possible request in the treatment of tumor. The authors encapsulated quercetin in a liposomal delivery system. They studied the in vitro effects of this compound on proliferation using human MCF-7 carcinoma cells. The activity of liposomal quercetin was equal to or better than that of free quercetin at equimolar concentrations. Our data indicated that liposomal quercetin can significantly improve the solubility and bioavailability of quercetin and can be a potential application in the treatment of tumor.
机译:摘要槲皮素(3,5,7,3’,4’-五羟基黄酮)是一种天然的生物类黄酮,起源于水果,蔬菜,种子,浆果和茶。槲皮素的抗氧化活性及其对心血管疾病,抗癌,抗炎和抗病毒活性的保护作用已得到广泛的文献证明;然而,槲皮素由于其非常差的递送功能而在癌症治疗中的临床需求受到极大限制。为了增加亲水性和药物递送能力,我们将槲皮素封装到脂质体中。我们的数据表明脂质体槲皮素可以显着提高槲皮素的溶解度和生物利用度,并且可以用作极性细胞质内ROS保护的有效抗氧化剂,脂质体包裹的纳米级槲皮素可以增强细胞摄取(癌细胞人MCF_7) 。槲皮素具有许多药物应用,其中许多来自其强大的抗氧化特性。本研究通过使用水性介质中三价铁的还原,细胞内ROS /毒性测定和DPPH还原测定的对比研究,研究了槲皮素在极性溶剂中的抗氧化活性。细胞活力和ROS分析表明槲皮素能够渗透到细胞内部的极性介质中,并保护它们免受氢过氧化枯烯的高毒性和致命性伤害。这项研究的目的是确定槲皮素的脂质体制剂是否可以暗示地改善其溶解度和生物利用度,并且可能是治疗肿瘤的可能要求。作者将槲皮素封装在脂质体递送系统中。他们使用人MCF-7癌细胞研究了该化合物对体外增殖的影响。在等摩尔浓度下脂质体槲皮素的活性等于或优于游离槲皮素的活性。我们的数据表明脂质体槲皮素可以显着提高槲皮素的溶解度和生物利用度,并且可能在肿瘤治疗中具有潜在的应用价值。

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