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Solid inclusion inclusion complexes of oleanolic acid with amino -appended beta-cyclodextrins (ACDs).: Preparation, characterization, water solubility. and anticancer activity

机译:齐墩果酸与氨基附加的β-环糊精(ACD)的固体包合物包合物:制备,表征,水溶性。和抗癌活性

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摘要

Oleanolic acid (OA) is a pentacydic triterpenoid acid of natural abundance in plants which possesses important biological activities. However, its medicinal applications were severely impeded by the poor water solubility and resultan low bioavailability and potency. In this work, studies on solid inclusion complexes of OA with a series of amino-appended beta-cyclodextrins (ACDs) were conducted in order to address this issue. These complexes were prepared by suspension method and were well characterized by NMR, SEM, XRD, TG, DSC and Zeta potential measurement. The 2:1 inclusion mode of ACDs/OA complexes was elucidated by elaborate 2D NMR (ROESY). Besides, water solubility of OA was dramatically promoted by inclusion complexation with ACDs. Moreover, in vitro anticancer activities of OA against human cancer cell lines HepG2, HT29 and HCT116 were significantly enhanced after formation of inclusion complexes, while the apoptotic response results indicated their induction of apoptosis of cancer cells. This could provide a novel approach to development of novel pharmaceutical formulations of OA. (C) 2016 Elsevier B.V. All rights reserved.
机译:齐墩果酸(OA)是植物中自然丰富的五酰基三萜酸,具有重要的生物活性。然而,其不良的水溶性严重阻碍了其在医学上的应用,并导致了较低的生物利用度和效力。在这项工作中,对OA与一系列氨基附加的β-环糊精(ACD)的固体包合配合物进行了研究,以解决这个问题。这些配合物是通过悬浮法制备的,并通过NMR,SEM,XRD,TG,DSC和Zeta电势进行了很好的表征。详细的2D NMR(ROESY)阐明了ACD / OA复合物的2:1包容模式。此外,与ACD的包合络合极大地促进了OA的水溶性。此外,包涵体复合物形成后,OA对人癌细胞HepG2,HT29和HCT116的体外抗癌活性显着增强,而凋亡反应结果表明它们诱导了癌细胞的凋亡。这可以提供开发OA的新药物制剂的新颖方法。 (C)2016 Elsevier B.V.保留所有权利。

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