Fabrication and evaluation of mannose decorated curcumin loaded nanostructured lipid carriers for hepatocyte targeting: In vivo hepatoprotective activity in Wistar rats

Q2 Agricultural and Biological Sciences Current Research in Pharmacology and Drug Discovery Pub Date : 2022-01-01 DOI:10.1016/j.crphar.2022.100083
Manish Kumar Gupta , Vipul Sansare , Birendra Shrivastava , Santosh Jadhav , Prashant Gurav
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引用次数: 3

Abstract

Curcumin is a well-recognized antioxidant phytoactive isolated from the rhizomes of Curcuma longa. Numerous landmark investigations have proved the antioxidant and hepatoprotective potential of curcumin. The aim of present study was to target curcumin loaded nanocarriers to hepatocytes using asialoglycoprotein receptors targeting strategy. Mannose, a water-soluble carbohydrate, was hydrophobized by anchoring stearylamine with an objective to conjugate mannose on the surface of curcumin loaded nanostructured lipid carriers for targeting asialoglycoprotein receptors on hepatocytes. Mannose conjugated stearylamine was synthesized and characterized using various analytical techniques. The synthesized targeting ligand was incorporated curcumin loaded nanostructured lipid carriers and characterized by photon correlation spectroscopy. Zeta potential measurement was used to confirm the conjugation of the synthesized ligand to the surface of drug-loaded nanostructured lipid carriers. CCl4 induced hepatotoxicity in male Wistar rats was used as an experimental animal model to evaluate the hepatoprotective potential of formulated drug encapsulated nanostructured lipid carriers. The hepatoprotective potential was assessed by measuring serum liver injury markers and oxidative stress parameters in the liver post–mitochondrial supernatant. Mannose conjugated nanostructured lipid carriers showed acceptable particle size which revealed its suitability for hepatocyte targeting. In addition to this, mannose conjugated nanocarriers revealed significantly better (p ​< ​0.05) reduction of serum liver injury markers and proinflammatory cytokines compared to the unconjugated one which confirmed hepatocytes targeting potential of the synthesized ligand. Asialoglycoprotein receptors targeting could be a landmark strategy for hepatocyte targeting. Thus, the synthesized mannose anchored stearylamine could be a promising novel targeting ligand having hepatocyte targeting potential.

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甘露糖修饰姜黄素负载纳米脂质载体的制备和评价:Wistar大鼠体内肝保护活性
姜黄素是从姜黄根茎中分离出来的一种公认的抗氧化植物活性物质。许多具有里程碑意义的研究已经证明了姜黄素的抗氧化和保护肝脏的潜力。本研究的目的是利用asialal糖蛋白受体靶向策略将姜黄素纳米载体靶向到肝细胞。甘露糖是一种水溶性碳水化合物,通过锚定硬脂胺疏水,目的是将甘露糖偶联在姜黄素负载的纳米结构脂质载体表面,以靶向肝细胞上的asialal糖蛋白受体。合成了甘露糖共轭硬脂胺,并用各种分析技术对其进行了表征。合成的靶配体是姜黄素负载的纳米结构脂质载体,并通过光子相关光谱对其进行了表征。Zeta电位测定证实了合成的配体与载药的纳米结构脂质载体表面的结合。以CCl4诱导的雄性Wistar大鼠肝毒性为实验动物模型,评价药物包封纳米结构脂质载体对肝脏的保护作用。通过测定血清肝损伤标志物和肝脏线粒体后上清中的氧化应激参数来评估肝保护潜力。甘露糖缀合的纳米结构脂质载体显示出可接受的粒径,表明其适合肝细胞靶向。除此之外,甘露糖缀合纳米载体显示出明显更好的(p <0.05)血清肝损伤标志物和促炎细胞因子与未结合的相比降低,证实了合成配体的肝细胞靶向潜力。亚洲糖蛋白受体靶向可能是肝细胞靶向的一个里程碑式的策略。因此,合成的甘露糖锚定的硬脂胺可能是一种有前景的新型靶向配体,具有靶向肝细胞的潜力。
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来源期刊
Current Research in Pharmacology and Drug Discovery
Current Research in Pharmacology and Drug Discovery Agricultural and Biological Sciences-Animal Science and Zoology
CiteScore
6.40
自引率
0.00%
发文量
65
审稿时长
40 days
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