240 research outputs found
Softening of the stiffness of bottlebrush polymers by mutual interaction
We study bottlebrush macromolecules in a good solvent by small-angle neutron
scattering (SANS), static light scattering (SLS), and dynamic light scattering
(DLS). These polymers consist of a linear backbone to which long side chains
are chemically grafted. The backbone contains about 1600 monomer units (weight
average) and every second monomer unit carries side-chains with ca. 60 monomer
units. The SLS- and SANS data extrapolated to infinite dilution lead to the
form factor of the polymer that can be described in terms of a worm-like chain
with a contour length of 380 nm and a persistence length of 17.5 nm. An
analysis of the DLS data confirm these model parameters. The scattering
intensities taken at finite concentration can be modeled using the polymer
reference interaction site model. It reveals a softening of the bottlebrush
polymers caused by their mutual interaction. We demonstrate that the
persistence decreases from 17.5 nm down to 5 nm upon increasing the
concentration from dilute solution to the highest concentration 40.59 g/l under
consideration. The observed softening of the chains is comparable to the
theoretically predicted decrease of the electrostatic persistence length of
linear polyelectrolyte chains at finite concentrations.Comment: 4 pages, 4 figure
Case of chest-wall rigidity in a preterm infant caused by prenatal fentanyl administration
The inability to appropriately ventilate neonates shortly after their birth could be related in rare cases to chest-wall rigidity caused by the placental transfer of fentanyl. Although this adverse effect is recognized when fentanyl is administered to neonates after their birth, the prenatal phenomenon is less known. Treatment with either naloxone or muscle relaxants reverses the fentanyl effect and may prevent unnecessary excessive ventilatory settings
An antiviral trap made of protein nanofibrils and iron oxyhydroxide nanoparticles
Minimizing the spread of viruses in the environment is the first defence line when fighting outbreaks and pandemics, but the current COVID-19 pandemic demonstrates how difficult this is on a global scale, particularly in a sustainable and environmentally friendly way. Here we introduce and develop a sustainable and biodegradable antiviral filtration membrane composed of amyloid nanofibrils made from food-grade milk proteins and iron oxyhydroxide nanoparticles synthesized in situ from iron salts by simple pH tuning. Thus, all the membrane components are made of environmentally friendly, non-toxic and widely available materials. The membrane has outstanding efficacy against a broad range of viruses, which include enveloped, non-enveloped, airborne and waterborne viruses, such as SARS-CoV-2, H1N1 (the influenza A virus strain responsible for the swine flu pandemic in 2009) and enterovirus 71 (a non-enveloped virus resistant to harsh conditions, such as highly acidic pH), which highlights a possible role in fighting the current and future viral outbreaks and pandemics
Interaction of cylindrical polymer brushes in dilute and semi-dilute solution
We present a systematic study of flexible cylindrical brush-shaped macromolecules in a good solvent by small-angle neutron scattering (SANS), static light scattering (SLS), and by dynamic light scattering (DLS) in dilute and semi-dilute solution. The SLS and SANS data extrapolated to infinite dilution lead to the shape of the polymer that can be modeled in terms of a worm-like chain with a contour length of 380 nm and a persistence length of 17.5 nm. SANS data taken at higher polymer concentration were evaluated by using the polymer reference interaction site model (PRISM). We find that the persistence length reduce from 17.5 nm at infinite dilution to 5.3 nm at the highest concentration (volume fraction 0.038). This is comparable with the decrease of the persistence length in semi-dilute concentration predicted theoretically for polyelectrolytes. This finding reveals a softening of stiffness of the polymer brushes caused by their mutual interaction
The N3RO trial: a randomised controlled trial of docosahexaenoic acid to reduce bronchopulmonary dysplasia in preterm infants <â29 weeksâ gestation
Background: Bronchopulmonary dysplasia (BPD) is a major cause of mortality and long-term respiratory and neurological morbidity in very preterm infants. While survival rates of very preterm infants have increased over the past two decades there has been no decrease in the rate of BPD in surviving infants. Evidence from animal and human studies has suggested potential benefits of docosahexaenoic acid (DHA), an n-3 long chain polyunsaturated fatty acid, in the prevention of chronic lung disease. This randomised controlled trial aims to determine the effectiveness of supplementary DHA in reducing the rate of BPD in infants less than 29 weeksâ gestation.
Methods/design: This is a multicentre, parallel group, randomised, blinded and controlled trial. Infants born less than 29 weeksâ gestation, within 3 days of first enteral feed and with parent informed consent are eligible to participate. Infants will be randomised to receive an enteral emulsion containing DHA or a control emulsion without DHA. The DHA emulsion will provide 60 mg/kg/day of DHA. The study emulsions will continue to 36 weeksâ postmenstrual age (PMA). The primary outcome is BPD as assessed by the requirement for supplemental oxygen and/or assisted ventilation at 36 weeksâ PMA. Secondary outcomes include the composite of death or BPD; duration of respiratory support and hospitalisation, major neonatal morbidities. The target sample size is 1244 infants (622 per group), which will provide 90 % power to detect a clinically meaningful absolute reduction of 10 % in the incidence of BPD between the DHA and control emulsion (two tailed α =0.05).
Discussion: DHA supplementation has the potential to reduce respiratory morbidity in very preterm infants. This multicentre trial will provide evidence on whether an enteral DHA supplement reduces BPD in very preterm infants
Coupling of Rotational Motion with Shape Fluctuations of Core-shell Microgels Having Tunable Softness
The influence of shape fluctuations on deformable thermosensitive microgels
in aqueous solution is investigated by dynamic light scattering (DLS) and
depolarized dynamic light scattering (DDLS). The systems under study consist of
a solid core of polystyrene and a thermosensitive shell of cross-linked
poly(N-isopropylacrylamide) (PNIPA) without and with embedded palladium
nanoparticles. PNIPA is soluble in water, but has a lower critical solution
temperature at 32 C (LCST). Below the LCST the PNIPA shell is swollen. Here we
find that besides translational and rotational diffusion, the particles exhibit
additional dynamics resulting from shape fluctuations. This leads to a
pronounced apparent increase of the rotational diffusion coefficient. Above the
transition temperature the shell collapses and provides a rather tight envelope
of the core. In this state the dynamics of the shell is frozen and the
core-shell particles behave like hard spheres. A simple physical model is
presented to capture and explain the essentials of the coupling of rotational
motion and shape fluctuations.Comment: 9 pages, 7 figure
3D Brownian Diffusion of Submicron-Sized Particle Clusters
We report on the translation and rotation of particle clusters made through
the combination of spherical building blocks. These clusters present ideal
model systems to study the motion of objects with complex shape. Because they
could be separated into fractions of well-defined configurations on a
sufficient scale and their overall dimensions were below 300 nm, the
translational and rotational diffusion coefficients of particle duplets,
triplets and tetrahedrons could be determined by a combination of polarized
dynamic light scattering (DLS) and depolarized dynamic light scattering (DDLS).
The use of colloidal clusters for DDLS experiments overcomes the limitation of
earlier experiments on the diffusion of complex objects near surfaces because
the true 3D diffusion can be studied. When the exact geometry of the complex
assemblies is known, different hydrodynamic models for calculating the
diffusion coefficient for objects with complex shapes could be applied. Because
hydrodynamic friction must be restricted to the cluster surface the so-called
shell model, in which the surface is represented as a shell of small friction
elements, was most suitable to describe the dynamics. A quantitative comparison
of the predictions from theoretical modeling with the results obtained by DDLS
showed an excellent agreement between experiment and theory
A Common Type 2 Diabetes Risk Variant Potentiates Activity of an Evolutionarily Conserved Islet Stretch Enhancer and Increases C2CD4A and C2CD4B Expression
Genome-wide association studies (GWASs) and functional genomics approaches implicate enhancer disruption in islet dysfunction and type 2 diabetes (T2D) risk. We applied genetic fine-mapping and functional (epi)genomic approaches to a T2D- and proinsulin-associated 15q22.2 locus to identify a most likely causal variant, determine its direction of effect, and elucidate plausible target genes. Fine-mapping and conditional analyses of proinsulin levels of 8,635 non-diabetic individuals from the METSIM study support a single association signal represented by a cluster of 16 strongly associated (p < 10â17) variants in high linkage disequilibrium (r2 > 0.8) with the GWAS index SNP rs7172432. These variants reside in an evolutionarily and functionally conserved islet and ÎČ cell stretch or super enhancer; the most strongly associated variant (rs7163757, p = 3 Ă 10â19) overlaps a conserved islet open chromatin site. DNA sequence containing the rs7163757 risk allele displayed 2-fold higher enhancer activity than the non-risk allele in reporter assays (p < 0.01) and was differentially bound by ÎČ cell nuclear extract proteins. Transcription factor NFAT specifically potentiated risk-allele enhancer activity and altered patterns of nuclear protein binding to the risk allele in vitro, suggesting that it could be a factor mediating risk-allele effects. Finally, the rs7163757 proinsulin-raising and T2D risk allele (C) was associated with increased expression of C2CD4B, and possibly C2CD4A, both of which were induced by inflammatory cytokines, in human islets. Together, these data suggest that rs7163757 contributes to genetic risk of islet dysfunction and T2D by increasing NFAT-mediated islet enhancer activity and modulating C2CD4B, and possibly C2CD4A, expression in (patho)physiologic states
Self-assembled amyloid fibrils with controllable conformational heterogeneity
Amyloid fibrils are a hallmark of neurodegenerative diseases and exhibit a conformational diversity that governs their pathological functions. Despite recent findings concerning the pathological role of their conformational diversity, the way in which the heterogeneous conformations of amyloid fibrils can be formed has remained elusive. Here, we show that microwave-assisted chemistry affects the self-assembly process of amyloid fibril formation, which results in their conformational heterogeneity. In particular, microwave-assisted chemistry allows for delicate control of the thermodynamics of the self-assembly process, which enabled us to tune the molecular structure of ??-lactoglobulin amyloid fibrils. The heterogeneous conformations of amyloid fibrils, which can be tuned with microwave-assisted chemistry, are attributed to the microwave-driven thermal energy affecting the electrostatic interaction during the self-assembly process. Our study demonstrates how microwave-assisted chemistry can be used to gain insight into the origin of conformational heterogeneity of amyloid fibrils as well as the design principles showing how the molecular structures of amyloid fibrils can be controlledopen0
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