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首页> 外文期刊>Journal of Pharmaceutical and Biomedical Analysis: An International Journal on All Drug-Related Topics in Pharmaceutical, Biomedical and Clinical Analysis >Co-existing colloidal phases of human duodenal aspirates: Intraindividual fluctuations and interindividual variability in relation to molecular composition
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Co-existing colloidal phases of human duodenal aspirates: Intraindividual fluctuations and interindividual variability in relation to molecular composition

机译:人类十二指肠患者的共同存在胶体阶段:与分子组成有关的Intrining Indivitual波动和与间接变异

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We investigated the ultrastructural pattern of colloidal phases in human duodenal fluids. Aspirates were collected from three volunteers in both fasted and fed nutritional states. Analysis methods comprised the combination of asymmetric flow field-flow fractionation (AF4) and multi-angle laser light scattering (MALLS). Furthermore, dynamic light scattering (DLS) and diffusion-ordered NMR spectroscopy (DOSY-NMR) were employed as alternative analytical approaches for comparison. By AF4/MALLS, up to four, and in some cases up to five distinct co-existing fractions could be differentiated in the sub-micron size-range, which, in accordance with a previous study (Elvang et al., 2018), may be assigned to three main types, namely small bile salt micelles, intermediate size mixed bile salt/phospholipid micelles and large phospholipid aggregates / vesicles. Although more or less the same colloidal phases were found to co-exist in all aspirates, their prevalence was found to vary, both over time and between the three individual human volunteers. Any uniform changes of patterns of colloidal phases over time, however, could not be identified. On the other hand, prevalence of specific colloidal phases was identified for aspirates of individual volunteers, which correlated reasonably well with the prevalence of certain lipid species in their molecular composition. It remains to be investigated whether such prevalence of specific colloidal phases influences drug solubilizing capacity as well as drug absorption. If so, this may help to better understand the substantial inter-individual variability seen in many drug absorption profiles.
机译:我们调查了人十二指肠液中胶体阶段的超微结构模式。从禁食和美联储营养状态的三个志愿者收集吸气。分析方法包括非对称流场 - 流分馏(AF4)和多角激光散射(商场)的组合。此外,使用动态光散射(DLS)和扩散有序的NMR光谱(DOSY-NMR)作为替代分析方法进行比较。通过AF4 / MALLS,最多四种,在某些情况下,在亚微米尺寸范围内,在某些情况下可能会差异化五个不同的共存分数,这是根据先前的研究(Elvang等,2018),可以分配给三种主要类型,即小胆汁盐胶束,中间尺寸混合胆汁盐/磷脂胶束和大磷脂聚集体/囊泡。尽管在所有吸气中发现了或多或少地发现相同的胶体相,但发现它们的患病率随着时间的推移和三个个体人类志愿者而异。然而,不能识别随时间随时间的任何均匀变化。另一方面,针对单独志愿者的吸气鉴定了特异性胶体相的患病率,其在其分子组合物中具有一定脂质物种的患病率相关。仍有待研究特定胶体阶段的这种患病率是否影响药物溶解的能力以及吸毒。如果是,这可能有助于更好地理解在许多吸毒谱中看到的大量间间可变性。

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