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首页> 外文期刊>International Journal of Nanomedicine >Free radical scavenging in vitro and biological activity of diphenyl diselenide-loaded nanocapsules: DPDS-NCS antioxidant and toxicological effects
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Free radical scavenging in vitro and biological activity of diphenyl diselenide-loaded nanocapsules: DPDS-NCS antioxidant and toxicological effects

机译:载有二苯二硒化物的纳米胶囊的体外自由基清除和生物活性:DPDS-NCS抗氧化剂和毒理作用

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Abstract: Selenium compounds, such as diphenyl diselenide (DPDS), have been shown to exhibit biological activity, including antioxidant effects. However, the use of DPDS in pharmacology is limited due to in vivo pro-oxidative effects. In addition, studies have shown that DPDS-loaded nanocapsules (DPDS-NCS) have greater bioavailability than free DPDS in mice. Accordingly, the aim of this study was to investigate the antioxidant properties of DPDS-NCS in vitro and biological activity in mice. Our in vitro results suggested that DPDS-NCS significantly reduced the production of reactive oxygen species and Fe(II)-induced lipid peroxidation (LPO) in brain. The administration of DPDS-NCS did not result in death or change the levels of endogenous reduced or oxidized glutathione after 72?hours of exposure. Moreover, ex vivo assays demonstrated that DPDS-NCS significantly decreased the LPO and reactive oxygen species levels in the brain. In addition, the highest dose of DPDS-NCS significantly reduced Fe(II)- and sodium nitroprusside-induced LPO in the brain and Fe(II)-induced LPO in the liver. Also, δ-aminolevulinate acid dehydratase within the brain was inhibited only in the highest dose of DPDS-NCS. In conclusion, our data demonstrated that DPDS-NCS exhibited low toxicity in mice and have significant antioxidant characteristics, indicating that nanoencapsulation is a safer method of DPDS administration.
机译:摘要:硒化合物,例如二苯基二硒化物(DPDS),已显示出生物活性,包括抗氧化作用。然而,由于体内促氧化作用,DPDS在药理学中的使用受到限制。此外,研究表明,在小鼠体内,装载有DPDS的纳米胶囊(DPDS-NCS)的生物利用度高于游离DPDS。因此,本研究的目的是研究DPDS-NCS的体外抗氧化特性和小鼠的生物学活性。我们的体外研究结果表明,DPDS-NCS显着降低了活性氧的生成和Fe(II)诱导的脑脂质过氧化(LPO)。暴露72小时后,DPDS-NCS的给药不会导致死亡或改变内源性还原型或氧化型谷胱甘肽的水平。此外,离体测定表明DPDS-NCS显着降低了大脑中LPO和活性氧的含量。此外,DPDS-NCS的最高剂量显着降低了脑中Fe(II)和硝普钠诱导的LPO和肝脏中Fe(II)诱导的LPO。而且,仅在最高剂量的DPDS-NCS中,大脑中的δ-氨基乙酰丙酸酯酸脱水酶才被抑制。总之,我们的数据表明DPDS-NCS在小鼠中表现出低毒性并且具有显着的抗氧化特性,表明纳米囊封法是DPDS管理的一种更安全的方法。

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