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Development of solid lipid nanoparticles containing total flavonoid extract from Dracocephalum moldavica L. and their therapeutic effect against myocardial ischemia–reperfusion injury in rats

机译:毛白杨总黄酮提取物固体脂质纳米粒的制备及其对大鼠心肌缺血再灌注损伤的治疗作用

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Total flavonoid extract from Dracocephalum moldavica L. (TFDM) contains effective components of D. moldavica L. that have myocardial protective function. However, the cardioprotection function of TFDM is undesirable due to its poor solubility. In order to improve the solubility and efficacy of TFDM, we developed TFDM-loaded solid lipid nanoparticles (TFDM-SLNs) and optimized the formulation of TFDM-SLNs using central composite design and response surface methodology. The physicochemical properties of TFDM-SLNs were characterized, and the pharmacodynamics was investigated using the myocardial ischemia–reperfusion injury model in rats. The nanoparticles of optimal formulation for TFDM-SLNs were spherical in shape with the average particle size of 104.83?nm and had a uniform size distribution with the polydispersity index value of 0.201. TFDM-SLNs also had a negative zeta potential of -28.7 mV to ensure the stability of the TFDM-SLNs emulsion system. The results of pharmacodynamics demonstrated that both TFDM and TFDM-SLN groups afforded myocardial protection, and the protective effect of TFDM-SLNs was significantly superior to that of TFDM alone, based on the infarct area, histopathological examination, cardiac enzyme levels and inflammatory factors in serum. Due to the optimal quality and the better myocardial protective effect, TFDM-SLNs are expected to become a safe and effective nanocarrier for the oral delivery of TFDM.
机译:霉菌Dracocephalum Moldavica L.(TFDM)的总黄酮提取物含有霉菌D. Moldavica L.的有效成分,具有心肌保护功能。但是,TFDM的心脏保护功能由于其不良的溶解性而不理想。为了提高TFDM的溶解度和功效,我们开发了装载TFDM的固体脂质纳米颗粒(TFDM-SLNs),并使用中心复合设计和响应面方法优化了TFDM-SLN的配方。对TFDM-SLNs的理化性质进行了表征,并使用大鼠心肌缺血-再灌注损伤模型研究了其药效学。 TFDM-SLNs最佳配方的纳米颗粒为球形,平均粒径为104.83?nm,粒径分布均匀,多分散指数值为0.201。 TFDM-SLNs还具有负的zeta电位-28.7 mV,以确保TFDM-SLNs乳液体系的稳定性。药效学结果表明,TFDM和TFDM-SLN组均可提供心肌保护,并且从梗死面积,组织病理学检查,心脏酶水平和炎症因子方面来看,TFDM-SLNs的保护作用明显优于单独的TFDM。血清。由于其最佳的质量和更好的心肌保护作用,TFDM-SLNs有望成为口服TFDM的安全有效的纳米载体。

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