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Cytotoxicity evaluation of symmetrically branched glycerol trimer in human hepatocellular carcinoma HepG2 cells

机译:对称分支甘油三聚体对人肝细胞癌HepG2细胞的细胞毒性评价

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An appropriate balance between lipophilicity and hydrophilicity is necessary for pharmaceuticals to achieve fine Absorption, Distribution, Metabolism and Excretion (ADME) properties including absorption and distribution, in particular. We have designed and proposed symmetrically branched oligoglycerols (BGL) as an alternative approach to improve the lipophilic-hydrophilic balance. We have previously shown that stability in circulation and water-solubility of such molecules as proteins, liposomes and hydrophobic compounds are much improved by conjugation to BGL. Albeit these successful applications of BGL, little was known whether BGL could be used in safety. Thus we conducted evaluation of the cytotoxicity of a representative BGL, symmetrically branched glycerol trimer (BGL003) in the cultured cells to clarify its biological safeness. Here we demonstrate that water-solubility of an extremely hydrophobic agent, fenofibrate was more than 2,000-fold improved just by conjugated with BGL003. BGL003 did not exhibit any significant cytotoxicity in human hepatocarcinoma HepG2 cells. Thus BGL003 should be safe and suitable strategy to endow hydrophobic molecules with much hydrophilicity.
机译:亲脂性和亲水性之间的适当平衡对于药物实现特别是吸收和分布(包括吸收和分布)的良好吸收,分布,代谢和排泄(ADME)特性是必需的。我们已经设计并提出了对称支化低聚甘油(BGL)作为改善脂溶性-亲水性平衡的替代方法。先前我们已经表明,通过与BGL结合,可以大大改善诸如蛋白质,脂质体和疏水性化合物之类的分子在循环中的稳定性和水溶性。尽管BGL取得了这些成功的应用,但对于BGL是否可用于安全性却鲜为人知。因此,我们在培养的细胞中评估了代表性BGL,对称分支甘油三聚体(BGL003)的细胞毒性,以阐明其生物学安全性。在这里,我们证明,仅通过与BGL003偶联,一种极其疏水的药剂非诺贝特的水溶性就提高了2,000倍以上。 BGL003在人肝癌HepG2细胞中未显示任何明显的细胞毒性。因此,BGL003应该是赋予疏水性分子高度亲水性的安全且合适的策略。

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