33 results match your criteria: "Sweden and Lund Institute of Advanced Neutron and X-ray Science LINXS[Affiliation]"

Apolipoprotein A-I primes beta cells to increase glucose stimulated insulin secretion.

Biochim Biophys Acta Mol Basis Dis

March 2020

Lund Institute of Advanced Neutron and X-ray Science (LINXS), Lund, Sweden; Lund Institute of Advanced X-ray and Neutron Science (LINXS), Lund, Sweden. Electronic address:

The increase of plasma levels of high-density lipoproteins and Apolipoprotein A-I (ApoA-I), its main protein component, has been shown to have a positive action on glucose disposal in type 2 diabetic patients. The current study investigates the unexplored function of ApoA-I to prime beta cells for improved insulin secretion. INS-1E rat clonal beta cells as well as isolated murine islets were used to study the effect of ApoA-I on responsiveness of the beta cells to high glucose challenge.

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Simple models based on isotropic interparticle attractions often fail to capture experimentally observed structures of colloidal gels formed through spinodal decomposition and subsequent arrest: the resulting gels are typically denser and less branched than their experimental counterparts. Here, we simulate gels formed from soft particles with directional attractions ("patchy particles"), designed to inhibit lateral particle rearrangement after aggregation. We directly compare simulated structures with experimental colloidal gels made using soft attractive microgel particles, by employing a "skeletonization" method that reconstructs the three-dimensional backbone from experiment or simulation.

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Preparation of colloidal molecules with temperature-tunable interactions from oppositely charged microgel spheres.

Soft Matter

October 2019

Division of Physical Chemistry, Lund University, POB 124, SE-22100 Lund, Sweden. and NanoLund, POB 118, SE-22100 Lund, Sweden and Lund Institute of Advanced Neutron and X-ray Science (LINXS), Scheelevägen 19, SE-22370 Lund, Sweden.

The self-assembly of small colloidal clusters, so-called colloidal molecules, into crystalline materials has proven extremely challenging, the outcome often being glassy, amorphous states where positions and orientations are locked. In this paper, a new type of colloidal molecule is therefore prepared, assembled from poly(N-isopropylacrylamide) (PNIPAM)-based microgels that due to their well documented softness and temperature-response allow for greater defect tolerance compared to hard spheres and for convenient in situ tuning of size, volume fraction and inter-particle interactions with temperature. The microgels (B) are assembled by electrostatic adsorption onto oppositely charged, smaller-sized microgels (A), where the relative size of the two determines the valency (n) of the resulting core-satellite ABn-type colloidal molecules.

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Article Synopsis
  • Small clusters of spherical colloids called colloidal molecules show potential as building blocks for new materials but struggle with ordered assembly due to limited control over particle interactions.
  • The study introduces temperature-responsive microgel particles that change from a repulsive to an attractive state at a specific temperature, enabling better control over interactions.
  • A microfluidics device is used to create uniform emulsion droplets with microgels, which, after undergoing evaporation and cross-linking, form clusters that exhibit attractive interactions similar to those found in biological molecules like proteins.
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The peculiar linear temperature-dependent swelling of core-shell microgels has been conjectured to be linked to the core-shell architecture combining materials of different transition temperatures. Here the structure of pNIPMAM-core and pNNPAM-shell microgels in water is studied as a function of temperature using small-angle neutron scattering with selective deuteration. Photon correlation spectroscopy is used to scrutinize the swelling behaviour of the colloidal particles and reveals linear swelling.

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The present study focuses on the development of multiresponsive core-shell microgels and the manipulation of their swelling properties by copolymerization of different acrylamides-especially -isopropylacrylamide (NIPAM), -isopropylmethacrylamide (NIPMAM), and NNPAM-and acrylic acid. We use atomic force microscopy for the dry-state characterization of the microgel particles and photon correlation spectroscopy to investigate the swelling behavior at neutral (pH 7) and acidic (pH 4) conditions. A transition between an interpenetrating network structure for microgels with a pure poly--propylacrylamide (PNNPAM) shell and a distinct core-shell morphology for microgels with a pure poly--isopropylmethacrylamide (PNIPMAM) shell is observable.

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Soft particles in an electric field - a zero average contrast study.

Soft Matter

August 2019

Division of Physical Chemistry, Department of Chemistry, Lund University, SE-22100 Lund, Sweden and Lund Institute of advanced Neutron and X-ray Science (LINXS), Lund University, Lund, Sweden.

We report on the structural properties of ionic microgel particles subjected to alternating electric fields, using small-angle neutron scattering. The experiments were performed under so-called zero average contrast conditions, which cancel the structure factor contribution to the scattered intensity, allowing us to obtain direct information on the single particle size and structure as particles align in field-induced strings. Our results reveal only a marginal compression of the particles as they align in strings, and indicate considerable particle overlap at higher field strengths.

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We investigate the collective behavior of suspended thermoresponsive microgels that expel solvent and subsequently decrease in size upon heating. Using a binary mixture of differently thermoresponsive microgels, we demonstrate how distinctly different gel structures form, depending on the heating profile used. Confocal laser scanning microscopy (CLSM) imaging shows that slow heating ramps yield a core-shell network through sequential gelation, while fast heating ramps yield a random binary network through homogelation.

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