278 research outputs found
Restricting detergent protease action to surface of protein fibres by chemical modification
Due to their excellent properties, such as
thermostability, activity over a broad range of pH and
efficient stain removal, proteases from Bacillus sp. are
commonly used in the textile industry including industrial
processes and laundry and represent one of the most
important groups of enzymes. However, due to the action
of proteases, severe damage on natural protein fibres such
as silk and wool result after washing with detergents
containing proteases. To include the benefits of proteases in
a wool fibre friendly detergent formulation, the soluble
polymer polyethylene glycol (PEG) was covalently
attached to a protease from Bacillus licheniformis. In
contrast to activation of PEG with cyanuric chloride (50%)
activation with 1,1âČ-carbonyldiimidazole (CDI) lead to
activity recovery above 90%. With these modified
enzymes, hydrolytic attack on wool fibres could be
successfully prevented up to 95% compared to the native
enzymes. Colour difference (ÎE) measured in the three dimensional colour space showed good stain removal
properties for the modified enzymes. Furthermore, half-life
of the modified enzymes in buffers and commercial
detergents solutions was nearly twice as high as those of
the non-modified enzymes with values of up to 63 min. Out
of the different modified proteases especially the B.
licheniformis protease with the 2.0-kDa polymer attached
both retained stain removal properties and did not
hydrolyse/damage wool fibres
PEG-Albumin Plasma Expansion Increases Expression of MCP-1 Evidencing Increased Circulatory Wall Shear Stress: An Experimental Study
Treatment of blood loss with plasma expanders lowers blood viscosity, increasing cardiac output. However, increased flow velocity by conventional plasma expanders does not compensate for decreased viscosity in maintaining vessel wall shear stress (WSS), decreasing endothelial nitric oxide (NO) production. A new type of plasma expander using polyethylene glycol conjugate albumin (PEG-Alb) causes supra-perfusion when used in extreme hemodilution and is effective in treating hemorrhagic shock, although it is minimally viscogenic. An acute 40% hemodilution/exchange-transfusion protocol was used to compare 4% PEG-Alb to Ringerâs lactate, Dextran 70 kDa and 6% Hetastarch (670 kDa) in unanesthetized CD-1 mice. Serum cytokine analysis showed that PEG-Alb elevates monocyte chemotactic protein-1 (MCP-1), a member of a small inducible gene family, as well as expression of MIP-1α, and MIP-2. MCP-1 is specific to increased WSS. Given the direct link between increased WSS and production of NO, the beneficial resuscitation effects due to PEG-Alb plasma expansion appear to be due to increased WSS through increased perfusion and blood flow rather than blood viscosity
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PEGâpeptide conjugates
The remarkable diversity of the self-assembly behavior
of PEGâpeptides is reviewed, including self-assemblies formed by PEGâpeptides with ÎČ-sheet and α-helical (coiled-coil) peptide sequences. The modes of self-assembly in solution and in the solid state are discussed. Additionally, applications in bionanotechnology and synthetic materials science are summarized
Controlling and characterising the deposits from polymer droplets containing microparticles and salt
It is very well known that as suspension droplets evaporate, a pinned contact line leads to strong outwards capillary flow resulting in a robust coffee ring-stain at the periphery of the droplet. Conversely tall pillars are deposited in the centre of the droplet when aqueous droplets of poly(ethylene oxide) evaporate following a boot-strapping process in which the contact line undergoes fast receding, driven by polymer precipitation. Here we map out the phase behaviour of a combined particle-polymer system, illustrating a range of final deposit shapes, from ring-stain to flat deposit to pillar. Deposit topologies are measured using profile images and stylus profilometery, and characterised using the skewness of the profile as a simple analytic method for quantifying the shapes: pillars produce positive skew, flat deposits have zero skew and ring-stains have a negative value. We also demonstrate that pillar formation can be disrupted using potassium sulphate salt solutions, which change the water from a good solvent to a thetapoint solvent, consequently reducing the size of the polymer coils. This inhibits polymer crystallisation, interfering with the bootstrap process and ultimately preventing pillars from forming. Again, the deposit shapes are quantified using the skew parameter
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PEGylated systems in pharmaceutics
This review addresses the use of poly(ethylene glycol) (PEG) and PEG conjugation for the design of novel dosage forms and the modification of biomolecules. The peculiarities of PEGylated nanoparticles, liposomes, proteins, enzymes, and small drug and polyelectrolyte molecules and their influence on systemic drug delivery, including overcoming of various biological barriers and adhesion to mucosal tissues (mucoadhesion), are considered
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