首页> 外文期刊>Analytical Biochemistry: An International Journal of Analytical and Preparative Methods >Quantification of cholesterol solubilized in bile salt micellar aqueous solutions using ~(13)C nuclear magnetic resonance
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Quantification of cholesterol solubilized in bile salt micellar aqueous solutions using ~(13)C nuclear magnetic resonance

机译:使用〜(13)C核磁共振定量分析胆汁盐胶束水溶液中溶解的胆固醇

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摘要

In this work, we develop a methodology to quantitatively follow the solubilization of cholesterol on glycodeoxycholic acid (GDCA) micelles using ~(13)C nuclear magnetic resonance (NMR). The amount of solubilized cholesterol enriched in ~(13)C at position 4, [4- ~(13)C] cholesterol, was quantified from the area of its resonance, at 44.5 ppm, using the CH _2 groups from GDCA as an internal reference. The loading of the micelles with cholesterol leads to a quantitative upper field shift of most carbons in the nonpolar surface of GDCA, and this was used to follow the solubilization of unlabeled cholesterol. The solubilization followed a pseudo first-order kinetics with a characteristic time constant of 3.6 h, and the maximum solubility of cholesterol in 50 mM total lipid (GDCA + cholesterol) is 3.0 ± 0.1 mM, corresponding to a mean occupation number per micelle ≥1. The solubilization profile indicates that the affinity of cholesterol for the GDCA micelles is unaffected by the presence of the solute, leading essentially to full solubilization up to the saturation limit. The relaxation times of GDCA carbons at 50 mM give information regarding its aggregation and indicate that GDCA is associated in small micelles (hydrodynamic [Rh] = 1.1 nm) without any evidence for formation of larger secondary micelles. This was confirmed by dynamic light scattering results.
机译:在这项工作中,我们开发了一种方法,可以使用〜(13)C核磁共振(NMR)定量地跟踪胆固醇在糖脱氧胆酸(GDCA)胶束上的溶解。使用来自GDCA的CH _2基作为内部变量,从其共振区域44.5 ppm处定量测定4位〜(13)C中富含的可溶胆固醇的量[4-〜(13)C]胆固醇参考。胆固醇负载在胶束中会导致GDCA非极性表面中大多数碳的定量上场偏移,这被用来追踪未标记胆固醇的溶解。增溶遵循伪一级动力学,特征时间常数为3.6 h,胆固醇在50 mM总脂质(GDCA +胆固醇)中的最大溶解度为3.0±0.1 mM,相当于每个胶束的平均占领数≥1 。增溶曲线表明胆固醇对GDCA胶束的亲和力不受溶质的影响,从根本上导致完全增溶直至饱和极限。 GDCA碳在50 mM处的弛豫时间提供了有关其聚集的信息,并表明GDCA在小胶束中缔合(流体动力学[Rh] = 1.1 nm),而没有证据表明会形成较大的次级胶束。动态光散射结果证实了这一点。

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