Preparation and characterization of biodegradable magnetic carriers by single emulsion-solvent evaporation

This paper describes a single emulsion-solvent evaporation protocol to prepare PEGylated biodegradable/biocompatible magnetic carriers by utilizing hydrophobic magnetite and a mixture of poly(D,L lactide-co-glycolide) (PLGA) and poly(lactic acid-block-polyethylene glycol) (PLA-PEG) (26:1 by mass) polymers. We characterized the magnetic microspheres in terms of morphology, composite microstructure, size and size distribution, and magnetic properties. Results show that the preparation produces magnetic microspheres with a good spherical morphology, small size (mean diameter of 1.2–1.5 μm) by means of large size distributions, and magnetizations up to 20–30 emu/g of microspheres.     

Theoretical analysis of a simple yet efficient portable magnetic separator design for separation of magnetic nano/micro-carriers from human blood flow

A technology that could physically remove substances from the blood such as biological, chemical, or radiological toxins could dramatically improve treatment of disease. One method in development proposes to use magnetic-polymer spheres to selectively bind toxins and remove them by magnetic filtration. Although magnetic filtration is a developed technology, the clinical boundary conditions described here require a new filter design. We investigated the removal of toxin-bound magnetic carriers from the blood stream using 2-D FEMLAB simulations. The magnetic separator consisted of a permanent magnet with parallel ferromagnetic prisms on the faces and in contact with a straight tube carrying the magnetic-polymer spheres in suspension. We varied the following parameters: blood flow velocity, the size, and number of ferromagnetic prisms, and the ferromagnetic material in both prisms and magnets. The capture efficiency reached maximum values when the depth of the prisms equaled the diameter of the tubing and the saturation magnetization of the prism material equaled twice that of the magnet. With this design a piece of 2 mm (diameter) tube carrying the fluid resulted in 95% capture of 2.0 μm magnetic-polymer spheres at 10 cm/s flow velocity.     

Synthesis of Cyclic Peptides by Photochemical Decarboxylation of N‐Phthaloyl Peptides in Aqueous Solution

The synthesis of a variety of cyclic peptides from N‐phthaloyl‐protected di‐, tri‐, tetra‐, and pentapeptides with different aminocarboxylic acid tethers by photodecarboxylation – initiated by intramolecular electron transfer – has been explored in aqueous media. The progress and the chemoselectivity of the follow‐up processes after CO₂ extrusion were traced by the respective pH/time‐profiles, as well as by the overall change in pH after completion of the reaction. The competition between cyclization and simple oxidative decarboxylation depends on spacer length and geometry, H‐bonding interaction between the electron accepting phthalimide C?O groups and amide H‐atoms, as well as the geometric reorganization coupled with the radical combination step and the formation of the lactam rings. With progressing reaction, hydrolysis of the phthalimide chromophore becomes an increasingly important side reaction due to the constant increase in pH. The use of phosphate‐buffered aqueous media consequently improved the cyclization yields. The ground‐state interactions between amide groups and the terminal COO^? group with the imide C?O groups were studied for the model system [N‐(phthaloyl)glycyl]sarcosine ( 1 ) by NMR spectroscopy where the amide (E/Z)‐equilibrium depends on the presence of carboxylate vs. free carboxylic acid, demonstrating the role of H‐bonding and metal coordination.     

Ueber die Vieltheiligkeit der ebenen algebraischen Curven

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