Effect of supromolecular interactions with cationic surfactant decamethoxine on adsorption of curcumine on highly dispersed silica

N. Lipkovska, V. Barvinchenko
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Abstract

Curcumin, a sparingly soluble polyphenol of plant origin, has antitumor, anti-inflammatory, antithrombotic, antidiabetic and antimicrobial properties. Currently, an important task is the development of medicinal composites based on curcumin, which provide an increase in its solubility and, accordingly, bioavailability. The aim of the work is to determine the optimal conditions for the adsorption of curcumin on the surface of a silica enterosorbent as soluble supramolecular complexes with a cationic dimeric surfactant decamethoxine. The UV/Vis spectroscopy data indicate that supramolecular interactions with decamethoxine lead to changes in the spectral characteristics of curcumin in solutions and on silica surface. The bathochromic shift of the absorption spectrum of curcumin in decamethoxine solutions characterizes the polarization of its carbonyl group in supramolecular complexes. The hypsochromic shift in the absorption spectra of curcumin adsorbed from decamethoxine solutions on silica is explained by the violation of its conjugated π-bond system, resulted probably from the change in the spatial orientation of the curcumin molecule at the adsorption of its complexes on the sorbent surface. Curcumin is adsorbed on highly dispersed silica much more effectively from decamethoxine solutions than from aqueous solutions. The adsorption of curcumin is maximal (92 %) at a concentration of decamethoxine 0.002 M, and decreases sharply to 9 % in the micellar region of concentrations (≥ 0.008 M). The dependence of curcumin adsorption on decamethoxine concentration is described by a domed curve, which indicates a significant contribution of hydrophobic interactions to the formation of supramolecular complexes of curcumin with cationic surfactant and their adsorption on silica surface. The results obtained are of practical importance and can be used in the development of new, more effective medicines containing bioactive curcumin, antiseptic decamethoxine and silica enterosorbent.
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阳离子表面活性剂十甲氧胺的超分子相互作用对姜黄素在高分散二氧化硅上吸附的影响
姜黄素是一种植物源性难溶多酚,具有抗肿瘤、抗炎、抗血栓、抗糖尿病和抗菌等特性。目前,一个重要的任务是开发基于姜黄素的药用复合材料,从而提高其溶解度和生物利用度。本研究的目的是确定姜黄素在二氧化硅肠道吸附剂表面作为可溶性超分子配合物与阳离子二聚体表面活性剂十甲氧胺的最佳吸附条件。紫外/可见光谱数据表明,姜黄素与十胺甲素的超分子相互作用导致其在溶液和二氧化硅表面的光谱特性发生变化。姜黄素在十甲氧胺溶液中吸收光谱的色移表征了其在超分子配合物中羰基的极化。十甲氧辛溶液在二氧化硅上吸附姜黄素时,其吸收光谱的次色移可以解释为其共轭π键系统的破坏,这可能是由于姜黄素配合物在吸附剂表面吸附时分子的空间取向发生了变化。姜黄素在高度分散的二氧化硅上的吸附,在十甲氧胺溶液中比在水溶液中更有效。在十甲氧辛浓度为0.002 M时,姜黄素的吸附量最大(92%),在浓度≥0.008 M胶束区,姜黄素的吸附量急剧下降至9%。在十甲氧辛浓度下,姜黄素的吸附量随浓度的变化呈圆形曲线,表明疏水相互作用对姜黄素与阳离子表面活性剂的超分子配合物的形成及其在二氧化硅表面的吸附有重要的贡献。所得结果具有实际意义,可用于开发新的、更有效的含有生物活性姜黄素、防腐十甲氧胺和二氧化硅肠吸收剂的药物。
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