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Cubic liquid crystalline nanoparticles containing a polysaccharide from Ulva fasciata with potent antihyperlipidaemic activity

机译:含有来自Ulva fasciata的多糖的立方液晶纳米颗粒具有有效的抗高血脂活性

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摘要

The present study involves the preparation of cubic liquid crystalline nanoparticles (cubsomes) for liver targeting to assess the potential of a formulated bioactive polysaccharide isolated from the hot aqueous extract of Ulva fasciata as an alternative natural agent with anti-hyperlipidaemic activity. Cubosomal nanoparticles were prepared by disrupting the cubic gel phase of the polysaccharide and water in the presence of a surfactant. Different lipid matrices and stabilizers were tested. All the formulations were in the nanosize range and showed sufficient negative charge to inhibit the aggregation of the cubosomes. Drug entrapment efficiencies (EEs%) were determined and in vitro release studies were performed. Transmission electron microscopy (TEM) and differential scanning calorimetry were used to analyze the loaded cubosomal nanoparticles containing glyceryl monostearate (GMO 2.25 g), poloxamer 407 (0.25 g) and 50 mg of the polysaccharide. A preclinical study comparing the cubic liquid crystalline nanoparticles containing polysaccharide to fluvastatin as a reference drug in hyperlipidaemic rats was conducted. The rats treated with the polysaccharide- loaded cubosomes showed significant decreases in total cholesterol (TC), triglycerides (TG) and total lipid (TL) compared to the untreated HL rats. In addition, oxidative stress and antioxidant biomarkers were measured in the HL rats. Compared to the untreated HL rats, the cubosome treated rats showed a significant reduction in malondialdehyde (MDA), whereas insignificant changes were detected in nitric oxide (NO), glutathione (GSH) levels and total antioxidant capacity (TAC). Further, vascular and intercellular adhesion molecules (VCAM, ICAM), and myeloperoxidase were demonstrated. A histopathological examination was conducted to study the alterations in histopathological lesions and to document the biochemical results. In conclusion, this study demonstrates the superiority of using a natural lipid regulator such as polysaccharide loaded cubosomes instead of fluvastatin.
机译:本研究涉及制备用于肝脏靶向的立方液晶纳米颗粒(立方脂质体),以评估从Ulva fasciata热水提取物中分离出的具有生物活性的多糖作为具有抗高血脂活性的替代天然药物的潜力。通过在表面活性剂的存在下破坏多糖和水的立方凝胶相来制备立方纳米颗粒。测试了不同的脂质基质和稳定剂。所有制剂均在纳米尺寸范围内,并显示出足够的负电荷以抑制立方体的聚集。确定了药物包封效率(EEs%),并进行了体外释放研究。使用透射电子显微镜(TEM)和差示扫描量热法分析了负载的立方微粒,其中包含单硬脂酸甘油酯(GMO 2.25微克),泊洛沙姆407(0.25微克)和50微克的多糖。进行了临床前研究,比较了高脂血症大鼠中含有多糖和氟伐他汀作为参考药物的立方液晶纳米颗粒。与未治疗的HL大鼠相比,用多糖负载的立方体处理的大鼠的总胆固醇(TC),甘油三酸酯(TG)和总脂质(TL)明显降低。另外,在HL大鼠中测量了氧化应激和抗氧化剂生物标志物。与未处理的HL大鼠相比,用立方体处理的大鼠的丙二醛(MDA)明显降低,而一氧化氮(NO),谷胱甘肽(GSH)和总抗氧化能力(TAC)的变化却很小。此外,还证实了血管和细胞间粘附分子(VCAM,ICAM)和髓过氧化物酶。进行了组织病理学检查以研究组织病理学病变的改变并记录生化结果。总而言之,这项研究证明了使用天然脂质调节剂(例如多糖负载的cubosomes)代替氟伐他汀的优越性。

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