首页> 美国卫生研究院文献>Antibiotics >Development of a Novel Pharmaceutical Formula of Nanoparticle Lipid Carriers of Gentamicin/α-Tocopherol and In Vivo Assessment of the Antioxidant Protective Effect of α-Tocopherol in Gentamicin-Induced Nephrotoxicity
【2h】

Development of a Novel Pharmaceutical Formula of Nanoparticle Lipid Carriers of Gentamicin/α-Tocopherol and In Vivo Assessment of the Antioxidant Protective Effect of α-Tocopherol in Gentamicin-Induced Nephrotoxicity

机译:庆大霉素/α-生育酚的纳米脂质载体的新型药物配方的开发和庆大霉素诱导的肾毒性的体内评估α-生育酚的抗氧化保护作用。

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Gentamicin is a potent antibiotic with a nephrotoxicity drawback which limits its use. D-α-tocopherol polyethylene glycol succinate (α-tocopherol) is widely used as a surfactant and have potent antioxidant properties. This study aimed to assess the protective effect of α-tocopherol on gentamicin-induced nephrotoxicity by loading gentamicin on nanostructured lipid carriers (NLC). In vivo, the product was administered intravenously to three groups of rabbits (control, gentamicin and gentamicin/α-tocopherol NLC) for 10 consecutive days. Blood was collected on days 1, 5 and 10 to assess renal function. A significant difference in all plasma parameters related to kidney function were observed in the gentamicin group compared to the control by day 5 and 10, confirming the nephrotoxicity effect. On the other hand, the same parameter levels of the NLC group were significantly different compared to the gentamicin group, confirming the protective effect on kidney function. Gentamicin also caused significant decreases in plasma levels of glutathione sulfhydryl (GSH) and superoxide dismutase (SOD) activity. However, gentamicin-α-tocopherol NLC significantly elevates both plasma levels of GSH as well as SOD activity. The present work indicates that, loading of gentamicin on NLC by using α-tocopherol, is an innovative strategy to protect against aminoglycoside-induced nephrotoxicity due to its antioxidant activity.
机译:庆大霉素是一种强效抗生素,具有肾毒性缺点,限制了其用途。 D-α-生育酚聚乙二醇琥珀酸酯(α-生育酚)被广泛用作表面活性剂并具有有效的抗氧化性能。这项研究旨在通过将庆大霉素加载到纳米结构脂质载体(NLC)上来评估α-生育酚对庆大霉素诱导的肾毒性的保护作用。在体内,将产品静脉内连续三天给三组兔子(对照组,庆大霉素和庆大霉素/α-生育酚NLC)给药。在第1、5和10天收集血液以评估肾功能。在第5天和第10天,与对照组相比,庆大霉素组与肾脏功能有关的所有血浆参数均存在显着差异,证实了其肾毒性作用。另一方面,与庆大霉素相比,NLC组的相同参数水平存在显着差异,从而证实了对肾脏功能的保护作用。庆大霉素还引起血浆谷胱甘肽巯基(GSH)和超氧化物歧化酶(SOD)活性的显着降低。然而,庆大霉素-α-生育酚NLC显着提高了血浆GSH水平和SOD活性。目前的工作表明,通过使用α-生育酚将庆大霉素负载在NLC上,是一种创新的策略,可防止氨基糖苷由于其抗氧化活性而引起的肾毒性。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号