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首页> 外文期刊>Clinical and experimental pharmacology & physiology >Enhanced antitumour activity of doxorubicin and simvastatin combination loaded nanoemulsion treatment against a Swiss albino mouse model of Ehrlich ascites carcinoma
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Enhanced antitumour activity of doxorubicin and simvastatin combination loaded nanoemulsion treatment against a Swiss albino mouse model of Ehrlich ascites carcinoma

机译:增强多柔比星和辛伐他汀组合的抗肿瘤活性加载纳米乳液治疗ehrlich腹水癌的瑞士白化动物癌

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Summary Doxorubicin ( DOX ) is the most commonly used anticancer drug; however, it has limited use because prolonged administration may result in severe cardiotoxicity. Simvastatin ( SIM ), generally prescribed for hypercholesterolaemia, has also shown salubrious results in the monotherapy or combinational drug therapy of different cancers in various models. Nanoparticle drug delivery systems are a novel way of improving therapeutics and also improving the absorption and specificity of drugs towards tumour cells. In this study, we exploited this technology to increase drug specificity and minimize imminent adverse effects. In this study, the antitumour activity of the combination formulas of DOX and SIM , either loaded in water ( DOX ‐ SIM ‐Solution) or nanoemulsions ( NE s) ( DOX ‐ SIM ‐ NE ), was evaluated in a Swiss albino mouse model of Ehrlich ascites carcinoma. The anticancer effect was assessed by quantifying the change in body weight, mean survival time, and percent increase in lifespan (% ILS ), determining haematological and serum biochemical parameters (liver function test, kidney function test and lipid profile parameters) as well as studying the histopathological alterations in liver tissues. We observed a clear increase in % ILS of the DOX ‐ SIM ‐Solution group (265.30) that was double the % ILS of the DOX ‐ SIM ‐ NE group (134.70). However, DOX ‐ SIM ‐ NE had a non‐toxic effect on the haematological parameters, whereas DOX ‐ SIM ‐Solution increased the levels of haemoglobin and lymphocytes. Furthermore, the encapsulation of SIM and DOX into NE s improved the levels of all serum biochemical parameters compared to the DOX ‐ SIM ‐Solution. A reduction in the side effects of DOX ‐ SIM ‐ NE on the liver was also established using light microscopy, which revealed that the morphologies of the hepatocytes of the mice were less affected by administration of the DOX ‐ SIM ‐ NE treatment than with the DOX ‐ SIM ‐Solution treatment. The study showed that incorporating SIM into the DOX ‐loaded‐ NE formulation remarkably improved its efficiency and simultaneously reduced its adverse effects.
机译:发明内容Doxorubicin(Dox)是最常用的抗癌药物;然而,它使用有限,因为长时间给药可能导致严重的心脏毒性。一般为高胆固醇血症规定的辛伐他汀(SIM)也表现出各种模型中不同癌症的单一疗法或组合药物治疗的挠性症。纳米粒子药物递送系统是一种改善治疗方法的新方法,并还提高了对肿瘤细胞的药物的吸收和特异性。在这项研究中,我们利用这种技术来增加药物特异性并最大限度地减少迫在眉睫的不良反应。在该研究中,在瑞士白化小鼠模型中评估了DOX和SIM的组合公式的抗肿瘤活性,无论是在水(DOX - SIM-SOME)或纳米乳液(NEX - SIM - NE)中的Ehrlich腹水癌。通过量化体重,平均存活时间和寿命增加(%ILS)增加的变化来评估抗癌效果,确定血液神经和血清生物化学参数(肝功能试验,肾功能试验和脂质分布参数)以及研究肝组织中的组织病理学改变。我们观察到Dox - Sim-Solulation组%ILS的显然增加(265.30),这是DOX - SIM - NE组的%ILS(134.70)。然而,DOX - SIM - NE对血液学参数具有无毒的影响,而DOX - SIM-Solution升高了血红蛋白和淋巴细胞的水平。此外,与DOX-SIM-SOLUTS相比,将SIM和DOX的封装改善了所有血清生物化学参数的水平。使用光学显微镜也建立了DOX - SIM - NE对肝脏副作用的降低,表明小鼠的肝细胞的形态受到DOX - SIM - NE治疗的影响小于DOX - Sim-凝固处理。该研究表明,将SIM掺入DOX -LOWARED-NE的制剂显着提高了其效率,同时降低了其不利影响。

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