To save content items to your account,
please confirm that you agree to abide by our usage policies.
If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account.
Find out more about saving content to .
To save content items to your Kindle, first ensure email@example.com
is added to your Approved Personal Document E-mail List under your Personal Document Settings
on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part
of your Kindle email address below.
Find out more about saving to your Kindle.
Note you can select to save to either the @free.kindle.com or @kindle.com variations.
‘@free.kindle.com’ emails are free but can only be saved to your device when it is connected to wi-fi.
‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.
The dissolution of a single droplet, containing a mixture of oils, in water is experimentally studied. The oils in the droplet varied in terms of their solubility in water and their hydrophobicity. We demonstrate that the polarity of the droplet constituents strongly influences the dissolution dynamics. A binary-component droplet, containing two polar components (one soluble the other insoluble) exhibits a retarded dissolution as compared to a droplet containing only the soluble component. We argue that in this case the mixture in the droplet can be assumed homogeneous, leading to a smaller effective contact area of the soluble liquid in the droplet with the bulk water, and thus delayed dissolution. On the other hand, it is shown that this is not the case when a polar, soluble component is mixed with an insoluble non-polar component, in which case segregation between the different liquids inside the droplet occurs, leading to Marangoni flows and superspreading of the droplet. The segregation is confirmed by volumetric measurements and by the use of a solvatochromic dye in combination with confocal microscopy, which clearly showed that during dissolution local concentration differences inside the droplet developed.
Arachidonic acid (AA) is considered essential in fetal development and some of its metabolites are thought to be important mediators of the immune responses. Therefore, we studied whether prenatal exposure to AA is associated with some immune-related clinical conditions and plasma markers in childhood. In 280 children aged 7 years, atopy, lung function and plasma inflammation markers were measured and their relationships with early AA exposure were studied by linear and logistic regression analyses. AA exposure was deduced from AA concentrations in plasma phospholipids of the mothers collected at several time points during pregnancy and at delivery, and in umbilical cord plasma and arterial and venous wall phospholipids. In unadjusted regression analyses, significant positive associations were observed between maternal AA concentrations at 16 and 32 weeks of pregnancy (proxies for fetal AA exposure) and peak expiratory flow decline after maximal physical exercise and plasma fibrinogen concentrations of their children, respectively. However, after correction for relevant covariables, only trends remained. A significant negative relationship was observed between AA concentrations in cord plasma (reflecting prenatal AA exposure) and the average daily amplitude of peak expiratory flow at rest, which lost significance after appropriate adjustment. Because of these few, weak and inconsistent relationships, a major impact of early-life exposure to AA on atopy, lung function and selected plasma inflammation markers of children at 7 years of age seems unlikely.
Email your librarian or administrator to recommend adding this to your organisation's collection.