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Inclusion complex of GA-13315 with cyclodextrins: Preparation, characterization, inclusion mode and properties

机译:GA-13315与环糊精的包合物:制备,表征,包合方式和性质

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摘要

GA-13315 (13-chlorine-3,15-dioxy-gibberIlic acid methyl ester) was semi-synthesized by GA3 (gib-berellic acid) as a potential anticancer drug. To pursue its promising application, cyclodextrin was used for forming complexes to overcome its drawbacks such as poor water solubility and stability. So, GA-13315/CD complexes were prepared with native β-cyclodextrin and its derivatives (hydroxypropyl-β-cyclodextrin (HPβCD)) and their inclusion complexation behavior, characterization and binding ability in both solution and the solid state was studied by means of UV, XRD, DSC, SEM,~1H and 2D NMR spectroscopy. Furthermore, preliminary in vitro cytotoxicity assay showed that the complexes still maintain antitumor activities, compared with GA-13315 or adriamycin (ADM, positive control) as the positive control. The results showed that the water solubility and stability of GA-13315 were obviously improved in the inclusion complex with cyclodextrins, suggesting the inclusion complexes as promising future therapeutic agents.
机译:GA-13315(13-氯-3,15-二氧-赤霉烯酸甲酯)是由GA3(赤霉素-硬脂酸)半合成的潜在抗癌药物。为了追求其有希望的应用,环糊精被用于形成复合物以克服其缺点,例如差的水溶性和稳定性。因此,用天然的β-环糊精及其衍生物(羟丙基-β-环糊精(HPβCD))制备了GA-13315 / CD复合物,并通过液相色谱法研究了它们在溶液和固体中的包合络合行为,表征和结合能力。 UV,XRD,DSC,SEM,〜1H和2D NMR光谱此外,初步的体外细胞毒性试验表明,与GA-13315或阿霉素(ADM,阳性对照)作为阳性对照相比,该复合物仍保持抗肿瘤活性。结果表明,GA-13315在环糊精包合物中的水溶性和稳定性均得到明显改善,表明该包合物作为有前途的治疗剂。

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