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用 β-环糊精衍生物调节非离子型蠕虫状胶束的黏弹性:一个高度有区别的过程。

Tuning the viscoelasticity of nonionic wormlike micelles with β-cyclodextrin derivatives: a highly discriminative process.

机构信息

Institute of Pharmaceutical Science, King's College London, Franklin-Wilkins Building, 150 Stamford Street, London SE1 9NH, United Kingdom.

出版信息

Langmuir. 2013 Jun 25;29(25):7697-708. doi: 10.1021/la4015338. Epub 2013 Jun 4.

Abstract

We report the influence of five β-cyclodextrin (β-CD) derivatives, namely: randomly methylated β-cyclodextrin (MBCD), heptakis (2,6-di-O-methyl)-β-cyclodextrin (DIMEB), heptakis (2,3,6-tri-O-methyl)-β-cyclodextrin (TRIMEB), 2-hydroxyethyl-β-cyclodextrin (HEBCD) and 2-hydroxypropyl-β-cyclodextrin (HPBCD), on the self-assembly of mixtures of nonionic surfactants: polyoxyethylene cholesteryl ether (ChEO10) and monocaprylin (MCL). Mixtures of ChEO10/MCL in water form highly viscoelastic wormlike micelle solutions (WLM) over a range of concentrations; herein, the composition was fixed at 10 wt % ChEO10/3 wt % MCL. The addition of methylated β-CDs (MBCD, DIMEB, TRIMEB) induced a substantial disruption of the solid-like viscoelastic behavior, as shown from a loss of the Maxwell behavior, a large reduction in G' and G″ in oscillatory frequency-sweep measurements, and a drop of the viscosity. The disruption increased with the degree of substitution, following: MBCD < DIMEB < TRIMEB. Cryo-TEM images confirmed a loss of the WLM networks, revealing short rods and disc-like aggregates, which were corroborated by small-angle neutron scattering (SANS) measurements. Critical aggregation concentrations (CAC), measured by fluorescence spectroscopy, increased in the presence of DIMEB for both ChEO10 and MCL, suggesting the existence of interactions between methylated β-CDs and both surfactants involved in WLM formation. Instead, hydroxyl-β-CDs had a very different effect on the WLM. HPBCD only slightly reduced the solid-like behavior, without suppressing it. Quite remarkably, the addition of HEBCD reinforced the solid-like characteristics and increased the viscosity 10-fold. Cryo-TEM images confirmed the subsistence of WLM in ChEO10/MCL/HEBCD solutions, while SANS data revealed a slight elongation and thickening of the worms, and an increase of associated water molecules. CAC data showed that HPBCD had little effect on either surfactant, while HEBCD strongly affected the CAC of MCL and only slightly affected the ChEO10. For both DIMEB and HEBCD, time-resolved SANS measurements showed that morphology changes underlying these macroscopic changes occur in less than 100 ms.

摘要

我们报告了 5 种β-环糊精(β-CD)衍生物的影响,即:随机甲基化β-环糊精(MBCD)、七(2,6-二-O-甲基)-β-环糊精(DIMEB)、七(2,3,6-三-O-甲基)-β-环糊精(TRIMEB)、2-羟乙基-β-环糊精(HEBCD)和 2-羟丙基-β-环糊精(HPBCD),对非离子表面活性剂混合物:聚氧乙烯胆甾醇醚(ChEO10)和单辛酸甘油酯(MCL)自组装的影响。ChEO10/MCL 在水中形成高度粘弹性蠕虫状胶束溶液(WLM),浓度范围很广;在此,固定组成 10wt%ChEO10/3wt%MCL。甲基化β-CDs(MBCD、DIMEB、TRIMEB)的加入导致固态粘弹性行为的实质性破坏,这表现为失去麦克斯韦行为、在振荡频率扫描测量中 G'和 G″的大幅度降低以及粘度下降。破坏作用随取代度的增加而增加,遵循:MBCD<DIMEB<TRIMEB。低温透射电镜(Cryo-TEM)图像证实了 WLM 网络的丢失,显示出短棒和盘状聚集体,这与小角中子散射(SANS)测量结果相符。通过荧光光谱法测量的临界聚集浓度(CAC)在 DIMEB 存在下均增加了对于 ChEO10 和 MCL,这表明甲基化β-CDs 与参与 WLM 形成的两种表面活性剂之间存在相互作用。相反,羟基-β-CDs 对 WLM 有非常不同的影响。HPBCD 仅略微降低固态行为,而不会抑制它。值得注意的是,添加 HEBCD 增强了固态特性并使粘度增加了 10 倍。低温透射电镜(Cryo-TEM)图像证实了 ChEO10/MCL/HEBCD 溶液中 WLM 的存在,而小角中子散射(SANS)数据显示蠕虫略微伸长和变粗,以及相关水分子的增加。CAC 数据表明 HPBCD 对两种表面活性剂几乎没有影响,而 HEBCD 强烈影响 MCL 的 CAC,对 ChEO10 的影响很小。对于 DIMEB 和 HEBCD,时间分辨 SANS 测量表明,这些宏观变化背后的形态变化在不到 100ms 内发生。

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