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Analytical characterization of a ferulic acid/gamma-cyclodextrin inclusion complex.

机译:阿魏酸/γ-环糊精包合物的分析表征。

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Ferulic acid (FA) is a well-known antioxidant of natural source with promising properties as photoprotective agent (approved in Japan as sunscreen) and its derivatives (alkyl ferulates) are under screening for the prevention of photoinduced skin tumours. In the present work we describe the preparation of a solid inclusion complex between ferulic acid and gamma-cyclodextrin (gamma-CD) and its characterization by different analytical techniques: differential scanning calorimetry (DSC), X-ray diffractometry (XRD), nuclear magnetic resonance spectroscopy (1H NMR) and by supporting information of molecular modelling. All these approaches indicate that ferulic acid is able to form an association complex with gamma-CD but only 1H NMR and molecular modelling studies give an unequivocal evidence that the antioxidant molecule is embedded into the gamma-CD cavity to form an inclusion complex. In detail it is entrapped inside the hydrophobic core of gamma-CD with the lipophilic aromatic ring and the ethylenic moieties, leaving the more polar functional groups close to wider rim or outside the cavity.
机译:阿魏酸(FA)是一种广为人知的天然抗氧化剂,具有光化学防护剂(在日本获得防晒霜认可)及其衍生物(烷基阿魏酸酯)的良好前景,可预防光致皮肤肿瘤。在当前的工作中,我们描述了阿魏酸和γ-环糊精(γ-CD)之间的固体包合物的制备及其通过不同分析技术的表征:差示扫描量热法(DSC),X射线衍射法(XRD),核磁共振光谱法(1H NMR)并通过分子建模支持信息。所有这些方法表明,阿魏酸能够与γ-CD形成缔合复合物,但只有1H NMR和分子模型研究明确表明抗氧化剂分子嵌入γ-CD腔中形成包合物。详细地,它被亲脂性芳族环和烯键部分包裹在γ-CD的疏水核内部,使极性更强的官能团靠近较宽的边缘或在空腔外部。

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